Director, GCP Audits
Uxbridge, London
Gilead Sciences, Inc.
Posted 13 days ago
Job Viewed
Job Description
At Gilead, we're creating a healthier world for all people. For more than 35 years, we've tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer - working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world's biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact.
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.
**Job Description**
Job Description
At Gilead we believe every employee deserves a great leader. As a people leader now or in the future, we expect that you will model and create an environment of inclusion, be intentionally focused on the hiring, development, growth, and retention of talent, and empower teams to align and achieve goals.
**Director, GCP Audits**
Location: Cambridge or Stockley Park, UK
The Director, Good Clinical Practice (GCP) Audits serves a pivotal role within Gilead's R&D Quality Organization, serving as the primary point of contact for assigned R&D groups across designated geographic regions and therapeutic areas. This position is responsible for executing internal and investigator site GCP audits, in support of the R&D Quality Annual Audit plan.
This position requires close collaboration with cross-functional stakeholders, including R&D Clinical Quality Business Partners (CQBPs), the Quality Governance, Risk, Audit & Analytics (GRA&A) team, and other relevant departments. The Director is instrumental in proactively identifying, evaluating, and mitigating clinical compliance risks while supporting the overall compliance of clinical processes and portfolio. In partnership with GVP and E-System/Digital Audit groups, this role helps shape, communicate, and implement the R&D Quality Annual Audit Program.
Reporting to the Head of GCP/GLP Audits, the Director contributes to the strategic development and operational execution of the GCP audit function. Responsibilities include developing audit tools and procedures, resource planning, ensuring the effectiveness of corrective and preventive actions (CAPAs), and providing updates through quality forums and internal communications regarding audit outcomes and CAPA status.
Beyond auditing, the Director supports regulatory inspections, readiness, and partners with the R&D Quality Extended Leadership team with responsibilities for helping build and shape quality capabilities, enhance process improvements and transparency. This role is vital to maintaining global compliance, reinforcing audit excellence, and ensuring the consistent delivery of high-quality audits, supporting Gilead's mission to advance transformative therapies.
**PRIMARY RESPONSIBILITIES**
_GCP Audit Program Leadership_
+ Accountable for the successful oversight and completion of a broad spectrum of GCP audit activities and deliverables across large sites, countries, or multiple regions.
+ Lead internal and external R&D quality audits for assigned R&D groups or locations.
+ Provide matrix management and leadership to project teams.
+ Develop and drive continuous improvements in R&D quality processes, systems, and standards to meet regulatory requirements and organizational goals and contribute to the overall quality mindset and culture.
_GCP Audit Operations_
+ Act as a primary point-of-contact to assigned R&D groups and advise on: GCP regulatory requirements; relevant Gilead policies and procedures supporting audits and clinical activities.
+ Evaluate SOPs, other procedures, data and reporting of assigned R&D groups / locations to ensure ongoing regulatory compliance, R&D quality and fit-for-purpose to both Gilead business needs and regulatory requirements.
+ Execute the strategic audit plan. Plan, schedule, and conduct GCP audits in accordance with the audit plan.
+ Prepare and deliver high quality audit reports and follow up on CAPAs to ensure timely resolution and CAPA effectiveness.
+ Lead/Support risk assessment activities, in partnership with risk program and SMEs.
+ Support the overall inspection readiness of the GCP Audit program, including preparation and participation for inspections.
+ Oversee and manage the work of contractor auditors, ensuring effective oversight and completion of assigned tasks.
+ Track resources and ensure compliance with regulatory timelines and quality standards for audit deliverables.
+ Provide accurate and thorough input and recommendations into resource allocation and budgets.
_Quality Management_
+ Evaluate, and advise on systems, processes, documentation, and CAPAs for assigned R&D groups to ensure ongoing compliance and alignment with regulatory requirements.
+ Play a key role in preparing the assigned R&D groups for inspections or external reviews including ensuring alignment with Gilead business needs and regulatory requirements.
+ Support Head of GCP/GLP Audits to implement an Effectiveness Check strategy, in partnership with GVP and E-system/Digital Audit Heads for Audit related CAPAs.
+ Stay current with evolving global clinical regulations and guidance.
+ Support the development of GCP Audit material/insights for quality forums and management reviews.
_Training & Development_
+ Develop and deliver on GCP training for assigned R&D groups ensuring teams are equipped with the knowledge and skills to maintain compliance and audit excellence.
+ Establish relationships with key stakeholders, including contract auditors, cross-functional leaders, and regulatory teams to facilitate training, knowledge sharing and continuous improvement initiatives.
**BASIC QUALIFICATION:**
**Education & Experience**
+ PharmD/PhD w relevant experience
+ MA/MS/MBA with relevant experience
+ BA/BS with relevant experience or advanced degree in life sciences/related fields with significant experience in quality compliance or related fields.
+ Proficiency in clinical regulatory requirements (Global) is a must.
+ Expert-level experience working with GCP processes and systems is required.
+ Proficient in GxP Auditing with a successful track record of leading clinical/investigator site audits.
+ Broad experience participating in cross-functional projects and teams with responsibilities related to pharmacovigilance and quality system activities.
+ Significant experience leading quality, compliance or related projects in the biopharma or related industry, including leading continuous improvements such as new or updated business processes, systems and/or SOPs.
+ Significant experience advising business functions in the biopharma industry on quality and compliance requirements, evolving regulations, risk minimization and mitigation.
+ Experience working with total quality management methodologies, such as Lean Six Sigma, is preferred.
+ Certification as a Quality Auditor is preferred.
**Rest of World Education & Experience**
BA/BS or advanced degree in life sciences or related field with significant relevant experience in the biopharma industry, including significant relevant experience working in quality, compliance, pharmacovigilance, or a related field.Extensive experience leading GCP audits, in the biopharma or related industry.
**Knowledge & Other Requirements**
+ Expert knowledge of the drug development process and GCP, including global regulations (FDA, EMA, ICH) and their application to cross-functional clinical development.
+ Proficient in GxP Auditing with a successful track record of leading clinical/investigator site audits.
+ Thorough knowledge of standards, systems, policies, and procedures that enable QMS operations and compliance within the biopharma industry, specifically those related to GCP.
+ Proven effectiveness in making appropriate decisions independently for relatively complex projects or related issues, as evidenced by past decision-making track record.
+ Proven abilities to assume increasing scope and complexity, as evidenced by past successes with team and project leadership, strategic cross-functional partnering, and key contributions to strategy, operational and infrastructure development.
+ Advanced business knowledge and analytical skills, as evidenced by strengths in assessing complex information and understanding the quality and compliance implications on the portfolio.
+ Track record of successful interaction and collaboration with other functions and with senior leadership, on key projects and deliveries supporting quality and compliance.
+ Demonstrates ability to execute against the strategic and tactical objectives provided by senior leaders both within Quality and outside of the function.
+ Demonstrates ability to integrate varied concepts and data to develop relevant solutions.
+ Proven abilities to anticipate problems of varying complexity and lead the resolution of these in a collaborative manner, across functions.
+ Strong leadership presence with demonstrated ability to lead without authority and influence programs, projects and/or initiatives.
+ Strong critical and strategic thinking skill and risk-based mindset.
+ Proven track record of successful change management implementation across highly matrixed organizations.
+ Ability to travel (up to 20%)
When you join Gilead, you join our mission to change the world by enabling people to live healthier and more fulfilling lives. Come join a mission-driven bio-pharmaceutical organization that values inclusion and diversity, has a strong portfolio of products, and is constantly #CreatingPossible
**ABOUT R&D QUALITY**
Gilead R&D Quality is a phenomenal place to develop your skills and expertise. Our strong pipeline of therapies will provide you opportunities to be challenged and stretched while supported and developed by our diverse and expert team. We are a committed team of highly skilled Quality professionals dedicated to helping deliver life-saving therapies for unmet needs. We bring our passion for science, discovery, and creative thinking into everything we do.
We are an inclusive and diverse community, who are supported by strong leaders that are committed to giving each of us a voice while achieving our mission. Our collaborative and supportive structure will help you develop your skills, experience, and your career. Are you ready to explore how you can play a vital role on the team and help deliver life-saving therapies to patients around the world?
**ABOUT GILEAD**
Gilead Sciences, Inc. is a research-based biopharmaceutical company that discovers, develops and commercializes innovative medicines in areas of unmet medical need. With each new discovery and investigational drug candidate, we seek to improve the care of patients living with life-threatening diseases around the world. Gilead's therapeutic areas of focus include HIV/AIDS, liver diseases, cancer and inflammation, and serious respiratory and cardiovascular conditions.
**Equal Employment Opportunity (EEO)**
It is the policy of Gilead Sciences, Inc. and its subsidiaries and affiliates (collectively "Gilead" or the "Company") to recruit select and employ the most qualified persons available for positions throughout the Company. Except if otherwise provided by applicable law, all employment actions relating to issues such as compensation, benefits, transfers, layoffs, returns from layoffs, company-sponsored training, education assistance, social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds, which may include an individual's gender, race, color, national origin, ancestry, religion, creed, physical or mental disability, marital status, sexual orientation, medical condition, veteran status, and age, unless such protection is prohibited by federal, state, municipal, provincial, local or other applicable laws). Gilead also prohibits discrimination based on any other characteristics protected by applicable laws.
**For Current Gilead Employees and Contractors:**
Please apply via the Internal Career Opportunities portal in Workday.
Gilead Sciences, Inc. is a biopharmaceutical company that has pursued and achieved breakthroughs in medicine for more than three decades, with the goal of creating a healthier world for all people. The company is committed to advancing innovative medicines to prevent and treat life-threatening diseases, including HIV, viral hepatitis and cancer. Gilead operates in more than 35 countries worldwide, with headquarters in Foster City, California.
Every member of Gilead's team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we're looking for the next wave of passionate and ambitious people ready to make a direct impact.
We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.
**Job Description**
Job Description
At Gilead we believe every employee deserves a great leader. As a people leader now or in the future, we expect that you will model and create an environment of inclusion, be intentionally focused on the hiring, development, growth, and retention of talent, and empower teams to align and achieve goals.
**Director, GCP Audits**
Location: Cambridge or Stockley Park, UK
The Director, Good Clinical Practice (GCP) Audits serves a pivotal role within Gilead's R&D Quality Organization, serving as the primary point of contact for assigned R&D groups across designated geographic regions and therapeutic areas. This position is responsible for executing internal and investigator site GCP audits, in support of the R&D Quality Annual Audit plan.
This position requires close collaboration with cross-functional stakeholders, including R&D Clinical Quality Business Partners (CQBPs), the Quality Governance, Risk, Audit & Analytics (GRA&A) team, and other relevant departments. The Director is instrumental in proactively identifying, evaluating, and mitigating clinical compliance risks while supporting the overall compliance of clinical processes and portfolio. In partnership with GVP and E-System/Digital Audit groups, this role helps shape, communicate, and implement the R&D Quality Annual Audit Program.
Reporting to the Head of GCP/GLP Audits, the Director contributes to the strategic development and operational execution of the GCP audit function. Responsibilities include developing audit tools and procedures, resource planning, ensuring the effectiveness of corrective and preventive actions (CAPAs), and providing updates through quality forums and internal communications regarding audit outcomes and CAPA status.
Beyond auditing, the Director supports regulatory inspections, readiness, and partners with the R&D Quality Extended Leadership team with responsibilities for helping build and shape quality capabilities, enhance process improvements and transparency. This role is vital to maintaining global compliance, reinforcing audit excellence, and ensuring the consistent delivery of high-quality audits, supporting Gilead's mission to advance transformative therapies.
**PRIMARY RESPONSIBILITIES**
_GCP Audit Program Leadership_
+ Accountable for the successful oversight and completion of a broad spectrum of GCP audit activities and deliverables across large sites, countries, or multiple regions.
+ Lead internal and external R&D quality audits for assigned R&D groups or locations.
+ Provide matrix management and leadership to project teams.
+ Develop and drive continuous improvements in R&D quality processes, systems, and standards to meet regulatory requirements and organizational goals and contribute to the overall quality mindset and culture.
_GCP Audit Operations_
+ Act as a primary point-of-contact to assigned R&D groups and advise on: GCP regulatory requirements; relevant Gilead policies and procedures supporting audits and clinical activities.
+ Evaluate SOPs, other procedures, data and reporting of assigned R&D groups / locations to ensure ongoing regulatory compliance, R&D quality and fit-for-purpose to both Gilead business needs and regulatory requirements.
+ Execute the strategic audit plan. Plan, schedule, and conduct GCP audits in accordance with the audit plan.
+ Prepare and deliver high quality audit reports and follow up on CAPAs to ensure timely resolution and CAPA effectiveness.
+ Lead/Support risk assessment activities, in partnership with risk program and SMEs.
+ Support the overall inspection readiness of the GCP Audit program, including preparation and participation for inspections.
+ Oversee and manage the work of contractor auditors, ensuring effective oversight and completion of assigned tasks.
+ Track resources and ensure compliance with regulatory timelines and quality standards for audit deliverables.
+ Provide accurate and thorough input and recommendations into resource allocation and budgets.
_Quality Management_
+ Evaluate, and advise on systems, processes, documentation, and CAPAs for assigned R&D groups to ensure ongoing compliance and alignment with regulatory requirements.
+ Play a key role in preparing the assigned R&D groups for inspections or external reviews including ensuring alignment with Gilead business needs and regulatory requirements.
+ Support Head of GCP/GLP Audits to implement an Effectiveness Check strategy, in partnership with GVP and E-system/Digital Audit Heads for Audit related CAPAs.
+ Stay current with evolving global clinical regulations and guidance.
+ Support the development of GCP Audit material/insights for quality forums and management reviews.
_Training & Development_
+ Develop and deliver on GCP training for assigned R&D groups ensuring teams are equipped with the knowledge and skills to maintain compliance and audit excellence.
+ Establish relationships with key stakeholders, including contract auditors, cross-functional leaders, and regulatory teams to facilitate training, knowledge sharing and continuous improvement initiatives.
**BASIC QUALIFICATION:**
**Education & Experience**
+ PharmD/PhD w relevant experience
+ MA/MS/MBA with relevant experience
+ BA/BS with relevant experience or advanced degree in life sciences/related fields with significant experience in quality compliance or related fields.
+ Proficiency in clinical regulatory requirements (Global) is a must.
+ Expert-level experience working with GCP processes and systems is required.
+ Proficient in GxP Auditing with a successful track record of leading clinical/investigator site audits.
+ Broad experience participating in cross-functional projects and teams with responsibilities related to pharmacovigilance and quality system activities.
+ Significant experience leading quality, compliance or related projects in the biopharma or related industry, including leading continuous improvements such as new or updated business processes, systems and/or SOPs.
+ Significant experience advising business functions in the biopharma industry on quality and compliance requirements, evolving regulations, risk minimization and mitigation.
+ Experience working with total quality management methodologies, such as Lean Six Sigma, is preferred.
+ Certification as a Quality Auditor is preferred.
**Rest of World Education & Experience**
BA/BS or advanced degree in life sciences or related field with significant relevant experience in the biopharma industry, including significant relevant experience working in quality, compliance, pharmacovigilance, or a related field.Extensive experience leading GCP audits, in the biopharma or related industry.
**Knowledge & Other Requirements**
+ Expert knowledge of the drug development process and GCP, including global regulations (FDA, EMA, ICH) and their application to cross-functional clinical development.
+ Proficient in GxP Auditing with a successful track record of leading clinical/investigator site audits.
+ Thorough knowledge of standards, systems, policies, and procedures that enable QMS operations and compliance within the biopharma industry, specifically those related to GCP.
+ Proven effectiveness in making appropriate decisions independently for relatively complex projects or related issues, as evidenced by past decision-making track record.
+ Proven abilities to assume increasing scope and complexity, as evidenced by past successes with team and project leadership, strategic cross-functional partnering, and key contributions to strategy, operational and infrastructure development.
+ Advanced business knowledge and analytical skills, as evidenced by strengths in assessing complex information and understanding the quality and compliance implications on the portfolio.
+ Track record of successful interaction and collaboration with other functions and with senior leadership, on key projects and deliveries supporting quality and compliance.
+ Demonstrates ability to execute against the strategic and tactical objectives provided by senior leaders both within Quality and outside of the function.
+ Demonstrates ability to integrate varied concepts and data to develop relevant solutions.
+ Proven abilities to anticipate problems of varying complexity and lead the resolution of these in a collaborative manner, across functions.
+ Strong leadership presence with demonstrated ability to lead without authority and influence programs, projects and/or initiatives.
+ Strong critical and strategic thinking skill and risk-based mindset.
+ Proven track record of successful change management implementation across highly matrixed organizations.
+ Ability to travel (up to 20%)
When you join Gilead, you join our mission to change the world by enabling people to live healthier and more fulfilling lives. Come join a mission-driven bio-pharmaceutical organization that values inclusion and diversity, has a strong portfolio of products, and is constantly #CreatingPossible
**ABOUT R&D QUALITY**
Gilead R&D Quality is a phenomenal place to develop your skills and expertise. Our strong pipeline of therapies will provide you opportunities to be challenged and stretched while supported and developed by our diverse and expert team. We are a committed team of highly skilled Quality professionals dedicated to helping deliver life-saving therapies for unmet needs. We bring our passion for science, discovery, and creative thinking into everything we do.
We are an inclusive and diverse community, who are supported by strong leaders that are committed to giving each of us a voice while achieving our mission. Our collaborative and supportive structure will help you develop your skills, experience, and your career. Are you ready to explore how you can play a vital role on the team and help deliver life-saving therapies to patients around the world?
**ABOUT GILEAD**
Gilead Sciences, Inc. is a research-based biopharmaceutical company that discovers, develops and commercializes innovative medicines in areas of unmet medical need. With each new discovery and investigational drug candidate, we seek to improve the care of patients living with life-threatening diseases around the world. Gilead's therapeutic areas of focus include HIV/AIDS, liver diseases, cancer and inflammation, and serious respiratory and cardiovascular conditions.
**Equal Employment Opportunity (EEO)**
It is the policy of Gilead Sciences, Inc. and its subsidiaries and affiliates (collectively "Gilead" or the "Company") to recruit select and employ the most qualified persons available for positions throughout the Company. Except if otherwise provided by applicable law, all employment actions relating to issues such as compensation, benefits, transfers, layoffs, returns from layoffs, company-sponsored training, education assistance, social and recreational programs are administered on a non-discriminatory basis (i.e. without regard to protected characteristics or prohibited grounds, which may include an individual's gender, race, color, national origin, ancestry, religion, creed, physical or mental disability, marital status, sexual orientation, medical condition, veteran status, and age, unless such protection is prohibited by federal, state, municipal, provincial, local or other applicable laws). Gilead also prohibits discrimination based on any other characteristics protected by applicable laws.
**For Current Gilead Employees and Contractors:**
Please apply via the Internal Career Opportunities portal in Workday.
Gilead Sciences, Inc. is a biopharmaceutical company that has pursued and achieved breakthroughs in medicine for more than three decades, with the goal of creating a healthier world for all people. The company is committed to advancing innovative medicines to prevent and treat life-threatening diseases, including HIV, viral hepatitis and cancer. Gilead operates in more than 35 countries worldwide, with headquarters in Foster City, California.
This advertiser has chosen not to accept applicants from your region.
0
GCP Data Architect
London, London
HCLTech
Posted today
Job Viewed
Job Description
Get AI-powered advice on this job and more exclusive features.nDirect message the job poster from HCLTech
Responsibilities
Maintain architecture principles, guidelines and standards
Project & Program Management
Data Warehousing
Data Analytics & Data Science for solutioning
Relevant technology domainsnRelevant technology domains:
Experience in designing & implementing solutions in mentioned areas
Strong Google Cloud Platform Data Components
– BigQuery, BigTable, CloudSQL, Dataproc, Data Flow, Data Fusion, etc.
Professional Summary
Strong experience in Big Data
Good Python skills, experience with data visualization tools such as Google Data Studio or Power BI
Strong migration experience of production Hadoop clusters to Google Cloud
Certifications
Google Professional Cloud Architect
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Information Technology and Customer Service
Industries
IT Services and IT Consulting and Banking
#J-18808-Ljbffrn
Responsibilities
Maintain architecture principles, guidelines and standards
Project & Program Management
Data Warehousing
Data Analytics & Data Science for solutioning
Relevant technology domainsnRelevant technology domains:
Experience in designing & implementing solutions in mentioned areas
Strong Google Cloud Platform Data Components
– BigQuery, BigTable, CloudSQL, Dataproc, Data Flow, Data Fusion, etc.
Professional Summary
Strong experience in Big Data
Good Python skills, experience with data visualization tools such as Google Data Studio or Power BI
Strong migration experience of production Hadoop clusters to Google Cloud
Certifications
Google Professional Cloud Architect
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Information Technology and Customer Service
Industries
IT Services and IT Consulting and Banking
#J-18808-Ljbffrn
This advertiser has chosen not to accept applicants from your region.
1
Data Architect - GCP
London, London
ZipRecruiter
Posted 2 days ago
Job Viewed
Job Description
Overview
A GCP Data Architect is required to join a Google partner who are helping various private sector clients migrate from an on-prem data warehouse to GCP. The GCP Data Architect is required to design data architecture patterns, evaluate different approaches and technologies, and communicate with various design working groups and architecture forums.nResponsibilities
Design data architecture patterns, evaluate different approaches and technologies, and communicate with design working groups and architecture forums.nQualifications
Extensive experience with GCP and BigQuery essential (at least 2 years experience - relevant certifications a bonus)nGood communication, stakeholder management and negotiation skills (consultative approach)nExperience with other technologies such as Hadoop, Hbase, Hive, DataProc, DataFlow and/or GKE would be usefulnAdditional Information
If interested in discussing further, please apply immediately and we'll endeavour to get in touch with successful applicants ASAP.nPlease note this role is entirely remote. The client would ideally like someone to visit their London office every few weeks but this is negotiable.nEames Consulting is acting as an Employment Business in relation to this vacancy.
#J-18808-Ljbffrn
A GCP Data Architect is required to join a Google partner who are helping various private sector clients migrate from an on-prem data warehouse to GCP. The GCP Data Architect is required to design data architecture patterns, evaluate different approaches and technologies, and communicate with various design working groups and architecture forums.nResponsibilities
Design data architecture patterns, evaluate different approaches and technologies, and communicate with design working groups and architecture forums.nQualifications
Extensive experience with GCP and BigQuery essential (at least 2 years experience - relevant certifications a bonus)nGood communication, stakeholder management and negotiation skills (consultative approach)nExperience with other technologies such as Hadoop, Hbase, Hive, DataProc, DataFlow and/or GKE would be usefulnAdditional Information
If interested in discussing further, please apply immediately and we'll endeavour to get in touch with successful applicants ASAP.nPlease note this role is entirely remote. The client would ideally like someone to visit their London office every few weeks but this is negotiable.nEames Consulting is acting as an Employment Business in relation to this vacancy.
#J-18808-Ljbffrn
This advertiser has chosen not to accept applicants from your region.
2
Senior Software Engineer – GCP Focus
London, London
N Consulting Limited
Posted 1 day ago
Job Viewed
Job Description
LocationSheffield (priority), Birmingham, Edinburgh., United Kingdom# Senior Software Engineer – GCP Focus at N Consulting LtdLocationSheffield (priority), Birmingham, Edinburgh., United KingdomSalary£300 - £400 /dayJob TypeContractDate PostedSeptember 7th, 2025Apply Now# **Job Opportunity: Senior Software Engineer – GCP Focus*** Locations (priority order):** Sheffield > Birmingham > Edinburgh
** Contract Duration:** 6+ months (extensions possible based on performance)
** Work Model:** Hybrid (2–3 days/week onsite from one of the offices)
** Important:** Candidates must be **open and comfortable with FTE conversion**.# **Role Overview**We are looking for a **highly motivated Senior Software Engineer** with strong expertise in **Google Cloud Platform (GCP)** and modern software engineering practices. This role involves designing, developing, and maintaining resilient backend services, frontend clients, and infrastructure automation in a secure and highly regulated financial services environment.# **Key Responsibilities**Design, build, and maintain **secure, scalable, and performant backend REST API services** and frontend clients using **Python, Golang, Docker, and cloud-native services**.Manage **database schema changes** with Liquibase, ensuring compliance and audit alignment.Build and maintain **CI/CD pipelines**, embedding security and regulatory controls.Oversee **GCP cloud infrastructure** (compute, storage, networking, IAM), optimizing for resilience, performance, and cost.Collaborate with **architecture, infrastructure, and cybersecurity teams** to meet governance and risk standards.Support live systems, conduct root-cause analysis, and resolve performance issues.# **Qualifications & Experience**Bachelor’s/Master’s in Computer Science or equivalent professional experience.**5+ years’ software engineering experience** with distributed systems.Proficiency in **Golang and Python**.Strong hands-on experience with **GCP cloud-native services** (AWS exposure desirable).Infrastructure as Code (Terraform/Ansible) and **DevOps CI/CD pipelines** (Jenkins, GitLab CI, etc.).Database expertise (Relational & NoSQL), plus Liquibase or equivalent.Knowledge of **Linux, Kubernetes, containers, serverless functions, microservices, and distributed tracing**.Strong background in **security, compliance, and audit controls** in regulated environments.Excellent communication skills for both technical and business stakeholders.# **Essential Skills**Public cloud architecture (GCP strongly preferred).Infrastructure build/configuration (compute, storage, networking).RESTful API services, enterprise logging/monitoring (Splunk, ELK, Prometheus, Grafana).Messaging and streaming integration services.Non-functional testing and troubleshooting.Cryptography knowledge (authentication, encryption).Agile development experience.# **Desirable Skills**Experience in **financial services** or other highly regulated industries.**GCP certifications** (e.g., Google Cloud Engineer, GCP Cloud DevOps Engineer). **Hybrid role (2–3 days onsite per week).**
**Contract: 6+ months (with extension potential).**
**Locations: Sheffield (priority), Birmingham, Edinburgh.**
**Candidates must be open to FTE conversion.**n#J-18808-Ljbffrn
** Contract Duration:** 6+ months (extensions possible based on performance)
** Work Model:** Hybrid (2–3 days/week onsite from one of the offices)
** Important:** Candidates must be **open and comfortable with FTE conversion**.# **Role Overview**We are looking for a **highly motivated Senior Software Engineer** with strong expertise in **Google Cloud Platform (GCP)** and modern software engineering practices. This role involves designing, developing, and maintaining resilient backend services, frontend clients, and infrastructure automation in a secure and highly regulated financial services environment.# **Key Responsibilities**Design, build, and maintain **secure, scalable, and performant backend REST API services** and frontend clients using **Python, Golang, Docker, and cloud-native services**.Manage **database schema changes** with Liquibase, ensuring compliance and audit alignment.Build and maintain **CI/CD pipelines**, embedding security and regulatory controls.Oversee **GCP cloud infrastructure** (compute, storage, networking, IAM), optimizing for resilience, performance, and cost.Collaborate with **architecture, infrastructure, and cybersecurity teams** to meet governance and risk standards.Support live systems, conduct root-cause analysis, and resolve performance issues.# **Qualifications & Experience**Bachelor’s/Master’s in Computer Science or equivalent professional experience.**5+ years’ software engineering experience** with distributed systems.Proficiency in **Golang and Python**.Strong hands-on experience with **GCP cloud-native services** (AWS exposure desirable).Infrastructure as Code (Terraform/Ansible) and **DevOps CI/CD pipelines** (Jenkins, GitLab CI, etc.).Database expertise (Relational & NoSQL), plus Liquibase or equivalent.Knowledge of **Linux, Kubernetes, containers, serverless functions, microservices, and distributed tracing**.Strong background in **security, compliance, and audit controls** in regulated environments.Excellent communication skills for both technical and business stakeholders.# **Essential Skills**Public cloud architecture (GCP strongly preferred).Infrastructure build/configuration (compute, storage, networking).RESTful API services, enterprise logging/monitoring (Splunk, ELK, Prometheus, Grafana).Messaging and streaming integration services.Non-functional testing and troubleshooting.Cryptography knowledge (authentication, encryption).Agile development experience.# **Desirable Skills**Experience in **financial services** or other highly regulated industries.**GCP certifications** (e.g., Google Cloud Engineer, GCP Cloud DevOps Engineer). **Hybrid role (2–3 days onsite per week).**
**Contract: 6+ months (with extension potential).**
**Locations: Sheffield (priority), Birmingham, Edinburgh.**
**Candidates must be open to FTE conversion.**n#J-18808-Ljbffrn
This advertiser has chosen not to accept applicants from your region.
3
Principal Platform Engineer GCP - Start-up
W1T London, London
client server
Posted today
Job Viewed
Job Description
Principal Platform Engineer London / WFH to £100k
Are you a technologist with start-up experience and a first class education looking for a new opportunity?
You could be joining a small Fintech start-up run by small, successful and proven team of finance technology entrepreneurs, backed by Silicon Valley investors, as they build out the product, currently in stealth mode.
As a Principal Platform Engineer you'll have an impactful role with lots of influence. Initially you'll assess the current tech set up based on GCP, Python, TypeScript, PostgreSQL and Terraform; establish the production environment and extend the platform to enable scalability.
You'll collaborate closely with the CTO and Lead Software Engineer to establish and build systems from scratch and will build a team of high performing engineers, progressing quickly to Head of Technology.
Location / WFH:
You'll be based in Central London, with flexibility to work from home twice a week.
About you:
You have experience in a similar Principal Platform Engineer role within start-up / scale-up environments with strong commercial acumennYou have achieved a 2.1 or above BSc from a well renowned top world university, e.g. Russel Group, Ivy League in a relevant technical disciplinenYou have a software engineering background with a strong knowledge of modern best practices, architecture and design experiencenYou have strong, current technical skills including: GCP, Python, TypeScript, PostgreSQL and TerraformnYou're collaborative and pragmatic with strong leadership and stakeholder management skillsnYou have experience of building teams and developing people
What's in it for you:
Strating salary £100knEquity
Apply now to find out more about this Principal Platform Engineer opportunity.
At Client Server we believe in a diverse workplace that allows people to play to their strengths and continually learn. We're an equal opportunities employer whose people come from all walks of life and will never discriminate based on race, colour, religion, sex, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. The clients we work with share our values.n
Are you a technologist with start-up experience and a first class education looking for a new opportunity?
You could be joining a small Fintech start-up run by small, successful and proven team of finance technology entrepreneurs, backed by Silicon Valley investors, as they build out the product, currently in stealth mode.
As a Principal Platform Engineer you'll have an impactful role with lots of influence. Initially you'll assess the current tech set up based on GCP, Python, TypeScript, PostgreSQL and Terraform; establish the production environment and extend the platform to enable scalability.
You'll collaborate closely with the CTO and Lead Software Engineer to establish and build systems from scratch and will build a team of high performing engineers, progressing quickly to Head of Technology.
Location / WFH:
You'll be based in Central London, with flexibility to work from home twice a week.
About you:
You have experience in a similar Principal Platform Engineer role within start-up / scale-up environments with strong commercial acumennYou have achieved a 2.1 or above BSc from a well renowned top world university, e.g. Russel Group, Ivy League in a relevant technical disciplinenYou have a software engineering background with a strong knowledge of modern best practices, architecture and design experiencenYou have strong, current technical skills including: GCP, Python, TypeScript, PostgreSQL and TerraformnYou're collaborative and pragmatic with strong leadership and stakeholder management skillsnYou have experience of building teams and developing people
What's in it for you:
Strating salary £100knEquity
Apply now to find out more about this Principal Platform Engineer opportunity.
At Client Server we believe in a diverse workplace that allows people to play to their strengths and continually learn. We're an equal opportunities employer whose people come from all walks of life and will never discriminate based on race, colour, religion, sex, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. The clients we work with share our values.n
This advertiser has chosen not to accept applicants from your region.
4
Associate Director Inspection Management (GCP)
Uxbridge, London
Regeneron Pharmaceuticals
Posted 10 days ago
Job Viewed
Job Description
The Associate Director, Global Development Quality Inspection Management (GDQIM) acting as an Inspection Management Lead (IML) is a key position that is responsible for the effective management of GCP, GVP and GLP inspections. The GDQIM IML will engage with key stakeholders, build strategic partnerships working and liaising with Clinical Study teams, relevant functions and other GDQ functions to support teams with inspection preparation activities on all Regeneron-sponsored clinical trials.
**In this role, a typical day might include the following:**
Ensuring and managing the notification of all relevant internal and external stakeholders of upcoming and/or anticipated regulatory inspections.
- Ensuring the preparation, management and integration of inspection management processes and training activities into the clinical development programs and all relevant stakeholders.
- Providing effective guidance, consultancy, and support to the Clinical Study Teams (and any other key stakeholders) in advance of an impending inspection.
- Assisting with the identification of opportunities to conduct mock inspections and/or Investigator Site Preparation Visits, in collaboration with the GD Quality Assurance (GDQA) team and other relevant functional groups.
- Identifying and discussing with the Clinical Study Teams potential issues and/or gaps, in advance of an impending inspection, that may require strategies to mitigate risk and/or provide additional clarification to an inspector.
- Ensuring the preparation, management and conduct of inspection preparation sessions which include mock inspections, trainings, and clinical site preparation visits working with GDQA team to identify and mitigate risks to clinical programs.
- Serving as the back room lead/co-lead or front room co-lead, responsible for explaining, managing,and ensuring the execution of all activities, including managing the tracking of requests and inquiries, and coordinating requests for responses from relevant personnel during any regulatory inspection conducted worldwide.
- Responsible for managing the preparation and provision of timely inspection updates and daily/end of inspection summaries to GD Executive and Senior Management, in addition to any other key relevant internal and external stakeholders.
- Responsible for managing inspection response development, and Corrective Actions/Preventive Actions (CAPA) follow-up activities alongside other GDQIM colleagues, cross-functional stakeholders, and process owners.
- Ensuring and managing the development, collection, reporting and analysis of inspection-related quality data, trends, and metrics.
**This role may be for you if have:**
- Advanced knowledge, understanding and application of GCP, and/or GVP
guidelines including the management of significant/complex quality issues
and compliance activities.
- Extensive experience with participating in, and supporting, Regulatory
Agency Inspections of Investigator Sites, Sponsors and Clinical Research
Organizations (CROs) in a GxP environment, including inspection
preparation, facilitation, and follow-up.
- Effective management of interpersonal relationships, stakeholder
engagement, and collaborations.
- Demonstrated ability to interface and collaborate effectively with other
Managers and Directors within, and external to, the organization.
- Extensive experience in providing training and presenting information on
key quality and regulatory compliance information.
**To be considered for this opportunity we are looking for:**
Bachelor's degree with a minimum of 10 years of relevant
healthcare/pharmaceutical industry experience.
- Experience working in either a quality/compliance role (e.g., Quality
Management, Quality Assurance etc.), or in a Clinical Development role
with expertise and/or transferable skills related to Good Clinical Practice
(GCP), and/or Good Pharmacovigilance Practice (GVP).
- Experience in training, supervising, line management, mentoring and
development of staff, and leading a small team
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.
For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.
Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.
**In this role, a typical day might include the following:**
Ensuring and managing the notification of all relevant internal and external stakeholders of upcoming and/or anticipated regulatory inspections.
- Ensuring the preparation, management and integration of inspection management processes and training activities into the clinical development programs and all relevant stakeholders.
- Providing effective guidance, consultancy, and support to the Clinical Study Teams (and any other key stakeholders) in advance of an impending inspection.
- Assisting with the identification of opportunities to conduct mock inspections and/or Investigator Site Preparation Visits, in collaboration with the GD Quality Assurance (GDQA) team and other relevant functional groups.
- Identifying and discussing with the Clinical Study Teams potential issues and/or gaps, in advance of an impending inspection, that may require strategies to mitigate risk and/or provide additional clarification to an inspector.
- Ensuring the preparation, management and conduct of inspection preparation sessions which include mock inspections, trainings, and clinical site preparation visits working with GDQA team to identify and mitigate risks to clinical programs.
- Serving as the back room lead/co-lead or front room co-lead, responsible for explaining, managing,and ensuring the execution of all activities, including managing the tracking of requests and inquiries, and coordinating requests for responses from relevant personnel during any regulatory inspection conducted worldwide.
- Responsible for managing the preparation and provision of timely inspection updates and daily/end of inspection summaries to GD Executive and Senior Management, in addition to any other key relevant internal and external stakeholders.
- Responsible for managing inspection response development, and Corrective Actions/Preventive Actions (CAPA) follow-up activities alongside other GDQIM colleagues, cross-functional stakeholders, and process owners.
- Ensuring and managing the development, collection, reporting and analysis of inspection-related quality data, trends, and metrics.
**This role may be for you if have:**
- Advanced knowledge, understanding and application of GCP, and/or GVP
guidelines including the management of significant/complex quality issues
and compliance activities.
- Extensive experience with participating in, and supporting, Regulatory
Agency Inspections of Investigator Sites, Sponsors and Clinical Research
Organizations (CROs) in a GxP environment, including inspection
preparation, facilitation, and follow-up.
- Effective management of interpersonal relationships, stakeholder
engagement, and collaborations.
- Demonstrated ability to interface and collaborate effectively with other
Managers and Directors within, and external to, the organization.
- Extensive experience in providing training and presenting information on
key quality and regulatory compliance information.
**To be considered for this opportunity we are looking for:**
Bachelor's degree with a minimum of 10 years of relevant
healthcare/pharmaceutical industry experience.
- Experience working in either a quality/compliance role (e.g., Quality
Management, Quality Assurance etc.), or in a Clinical Development role
with expertise and/or transferable skills related to Good Clinical Practice
(GCP), and/or Good Pharmacovigilance Practice (GVP).
- Experience in training, supervising, line management, mentoring and
development of staff, and leading a small team
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.
For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.
Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.
This advertiser has chosen not to accept applicants from your region.
5
Senior Cloud Engineer AWS GCP - Fintech
EC2A London, London
client server
Posted today
Job Viewed
Job Description
Senior Cloud Engineer (AWS GCP IaaS PaaS) London / WFH to £110k
Are you a cloud technologist? You could be progressing your career in an impactful Senior Cloud Engineer role at a global FinTech / CFD trading company that has been consistently voted as one of the UKs top employers.
As a Senior Cloud Engineer you will join a small team and be instrumental in designing, implementing and maintaining cloud infrastructure in AWS and GCP, creating environments and tools that empower software engineering teams with key technical enablers, building automation and self service capabilities that streamline operations across the globe.
You'll architect and design IaaS and PaaS on a multi-cloud (AWS / GCP) platform, deploy scalable, resilient cloud solutions, create developer friendly tools and platforms, implement IaC practices and connect with on-prem infrastructure. You'll collaborate with the team to seek continual improvement and to optimise cloud resources to balance performance and cost efficiency.
Location / WFH:
There's a hybrid model with two days a week work from home, when you are in the office you'll be based in the City with an upbeat team environment, casual dress code and a range of facilities including roof terrace, restaurant and break out areas.
About you:
You have strong cloud platform engineering experience including design and administration of complex AWS cloud infrastructure platforms at scalenYou have experience of building the VPC, creating control towers and managing AWS foundational infrastructurenYou have some GCP knowledge (you'll be working with both going forward)nYou have a good knowledge of IaC tools such as Terraform, Ansible, CDK, Pulumi, DevOps principles and CI/CDnYou're collaborative and pragmatic with great communication and stakeholder management skills
What's in it for you:
As a Senior Cloud Engineer you will earn a competitive package:
Salary to £110k + BonusnPension, Private Medical Care, Life AssurancenOption to buy or sell holiday daysnWellness benefits and gym subsidynChildcare vouchersnEnhanced paternity leave including shared parental pay and leavenEmployee led LGBTQ+, Women's, Black and Parents & Carers networks with an annual budget for organising events and projects that foster an open, diverse and inclusive culturenPlus a range of other perks
Apply now to find out more about this Senior Cloud Engineer (AWS GCP IaaS PaaS) opportunity.
At Client Server we believe in a diverse workplace that allows people to play to their strengths and continually learn. We're an equal opportunities employer whose people come from all walks of life and will never discriminate based on race, colour, religion, sex, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. The clients we work with share our values.n
Are you a cloud technologist? You could be progressing your career in an impactful Senior Cloud Engineer role at a global FinTech / CFD trading company that has been consistently voted as one of the UKs top employers.
As a Senior Cloud Engineer you will join a small team and be instrumental in designing, implementing and maintaining cloud infrastructure in AWS and GCP, creating environments and tools that empower software engineering teams with key technical enablers, building automation and self service capabilities that streamline operations across the globe.
You'll architect and design IaaS and PaaS on a multi-cloud (AWS / GCP) platform, deploy scalable, resilient cloud solutions, create developer friendly tools and platforms, implement IaC practices and connect with on-prem infrastructure. You'll collaborate with the team to seek continual improvement and to optimise cloud resources to balance performance and cost efficiency.
Location / WFH:
There's a hybrid model with two days a week work from home, when you are in the office you'll be based in the City with an upbeat team environment, casual dress code and a range of facilities including roof terrace, restaurant and break out areas.
About you:
You have strong cloud platform engineering experience including design and administration of complex AWS cloud infrastructure platforms at scalenYou have experience of building the VPC, creating control towers and managing AWS foundational infrastructurenYou have some GCP knowledge (you'll be working with both going forward)nYou have a good knowledge of IaC tools such as Terraform, Ansible, CDK, Pulumi, DevOps principles and CI/CDnYou're collaborative and pragmatic with great communication and stakeholder management skills
What's in it for you:
As a Senior Cloud Engineer you will earn a competitive package:
Salary to £110k + BonusnPension, Private Medical Care, Life AssurancenOption to buy or sell holiday daysnWellness benefits and gym subsidynChildcare vouchersnEnhanced paternity leave including shared parental pay and leavenEmployee led LGBTQ+, Women's, Black and Parents & Carers networks with an annual budget for organising events and projects that foster an open, diverse and inclusive culturenPlus a range of other perks
Apply now to find out more about this Senior Cloud Engineer (AWS GCP IaaS PaaS) opportunity.
At Client Server we believe in a diverse workplace that allows people to play to their strengths and continually learn. We're an equal opportunities employer whose people come from all walks of life and will never discriminate based on race, colour, religion, sex, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status. The clients we work with share our values.n
This advertiser has chosen not to accept applicants from your region.
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6
Manager GCP Quality, Technology and Compliance
Uxbridge, London
Regeneron Pharmaceuticals
Posted 1 day ago
Job Viewed
Job Description
We're looking for a quality-minded systems expert to help shape how regulated processes are managed across Global Development.
As Manager, GDQTC, you'll support our Veeva Quality Suite-based eQMS _which manages the quality events, actions and audits of our Global Development organization_ . Working across Clinical, Regulatory, and IT teams, you'll ensure the eQMS continues to meet the needs of a complex, fast-evolving environment. This role offers the opportunity to blend quality process ownership with system-level thinking-driving meaningful improvements in how we maintain GCP and GVP compliance across Regeneron's global development operations.
**A Typical Day:**
+ Managing and triaging user requests via the Quality Support Mailbox
+ Coordinating eQMS system upgrades and configuration changes with Global Development IT
+ Supporting issue management workflows including deviations, CAPAs, investigations, and change controls
+ Gathering and refining business requirements to guide system enhancements
+ Creating dashboards, storyboards, and reports for audit readiness and quality oversight
+ Liaising with stakeholders across Clinical, Regulatory, Medical, and Quality functions
+ Ensuring adherence to SDLC principles and validation expectations for all system changes
+ Identifying and driving process improvements tied to system use, support, and compliance
**This Role May Be For You:**
+ You've managed or owned quality workflows-like deviations and CAPAs-within an electronic QMS
+ You're adept at managing the full system lifecycle, from implementing new features to overseeing data standards and vendor performance
+ You're familiar with the Veeva Quality Suite, especially QualityDocs and QMS modules
+ You bring hands-on experience with GCP and/or GVP-regulated processes
+ You're a strong communicator who enjoys cross-functional collaboration and stakeholder engagement
+ You thrive in structured environments and bring rigor to how systems and data are handled
+ You've supported system changes under regulated SDLC practices (validation, change control, etc.)
+ You enjoy working at the intersection of quality, technology, and operations
+ You're analytical and enjoy using data to inform decisions and improvements
**To Be Considered:**
You'll need a bachelor's degree and at least 6 years of experience in the pharmaceutical or healthcare industry. The ideal candidate has supported quality issue management processes-such as deviations, CAPAs, and investigations-within a GCP or GVP setting. Experience with the Veeva Quality Suite (especially QualityDocs and QMS modules) is strongly preferred, and formal Veeva Vault Platform certifications (e.g., White/Gray Belt) are highly desirable. Familiarity with related clinical systems is a bonus.
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.
For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.
Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.
As Manager, GDQTC, you'll support our Veeva Quality Suite-based eQMS _which manages the quality events, actions and audits of our Global Development organization_ . Working across Clinical, Regulatory, and IT teams, you'll ensure the eQMS continues to meet the needs of a complex, fast-evolving environment. This role offers the opportunity to blend quality process ownership with system-level thinking-driving meaningful improvements in how we maintain GCP and GVP compliance across Regeneron's global development operations.
**A Typical Day:**
+ Managing and triaging user requests via the Quality Support Mailbox
+ Coordinating eQMS system upgrades and configuration changes with Global Development IT
+ Supporting issue management workflows including deviations, CAPAs, investigations, and change controls
+ Gathering and refining business requirements to guide system enhancements
+ Creating dashboards, storyboards, and reports for audit readiness and quality oversight
+ Liaising with stakeholders across Clinical, Regulatory, Medical, and Quality functions
+ Ensuring adherence to SDLC principles and validation expectations for all system changes
+ Identifying and driving process improvements tied to system use, support, and compliance
**This Role May Be For You:**
+ You've managed or owned quality workflows-like deviations and CAPAs-within an electronic QMS
+ You're adept at managing the full system lifecycle, from implementing new features to overseeing data standards and vendor performance
+ You're familiar with the Veeva Quality Suite, especially QualityDocs and QMS modules
+ You bring hands-on experience with GCP and/or GVP-regulated processes
+ You're a strong communicator who enjoys cross-functional collaboration and stakeholder engagement
+ You thrive in structured environments and bring rigor to how systems and data are handled
+ You've supported system changes under regulated SDLC practices (validation, change control, etc.)
+ You enjoy working at the intersection of quality, technology, and operations
+ You're analytical and enjoy using data to inform decisions and improvements
**To Be Considered:**
You'll need a bachelor's degree and at least 6 years of experience in the pharmaceutical or healthcare industry. The ideal candidate has supported quality issue management processes-such as deviations, CAPAs, and investigations-within a GCP or GVP setting. Experience with the Veeva Quality Suite (especially QualityDocs and QMS modules) is strongly preferred, and formal Veeva Vault Platform certifications (e.g., White/Gray Belt) are highly desirable. Familiarity with related clinical systems is a bonus.
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.
For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.
Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.
This advertiser has chosen not to accept applicants from your region.
7
Cloud Infrastructure Engineer
London, London
Prism Digital
Posted 1 day ago
Job Viewed
Job Description
Overview
This range is provided by Prism Digital. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.nBase pay range
Direct message the job poster from Prism DigitalnSalary - £60,000nHolborn / TCR office 3 days a weeknMy client is a world-leading independent production and distribution group that produces some of the most popular TV programmes in the world.nThey are looking for a Cloud Infrastructure Engineer who will support circa 30 internal companies with approximately 1,500 users and hundreds of freelancers. You will operate in a fast-paced and dynamic work environment. You will be working for a fun organisation, diversity-focused and dress-down culture based in the Holborn / Tottenham Court Road location. The role is on a hybrid model with non-negotiable in-office requirements, currently every Tuesday.nYou will work alongside 3 other senior engineers, and 2 project-based engineers reporting to the IT Manager.nA bit of a unique opportunity here as you will be a “modern Windows engineer” as our client is hosting 95% of their infrastructure in AWS. You will be involved in project work as well as dealing with 3rd line support tickets. There’s a separate 1st / 2nd line support team so you won’t have to tackle any of these tickets.nYou will be working with the infrastructure team that’s predominantly cloud-based. It’s a unique setup being a Windows/Microsoft environment inside the AWS ecosystem. Everything is glued together using Terraform so there’s great tooling at work here.nResponsibilities
Support circa 30 internal companies with approximately 1,500 users and hundreds of freelancers.nWork in a fast-paced, dynamic environment as part of a small team of engineers reporting to the IT Manager.nOperate as a modern Windows engineer with 95% of infrastructure hosted in AWS.nEngage in project work and 3rd line support (note: 1st/2nd line support is handled by a separate team).nContribute to a predominantly cloud-based infrastructure setup in a Windows/Microsoft environment within AWS, using Terraform.nWork on migration projects and automation initiatives involving AWS, Okta, Terraform, and Office 365/SharePoint.nParticipate in Windows VM provisioning and AWS EC2-related tasks; manage 100+ Windows VMs across multiple accounts.nHandle S3 backups and storage; utilize Okta and Okta Workflows for automation.nAssist with onboarding for newly acquired businesses and security access processes.nRequired / Qualifications
AWS – solid experience is an absolute mustnWindows Server administration ) in an IaaS setup within AWSnOkta & Okta WorkflowsnTerraformnOffice 365 / SharePointnBenefits
Hybrid working – in-office on Tuesdays is essentialn25 days of holidaynPension contributionnFree fresh fruit and office snacksnTraining opportunities with open access to UdemynApply ASAP if you would relish the opportunity to work in an exciting production environment alongside creative experts in the field.
#J-18808-Ljbffrn
This range is provided by Prism Digital. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.nBase pay range
Direct message the job poster from Prism DigitalnSalary - £60,000nHolborn / TCR office 3 days a weeknMy client is a world-leading independent production and distribution group that produces some of the most popular TV programmes in the world.nThey are looking for a Cloud Infrastructure Engineer who will support circa 30 internal companies with approximately 1,500 users and hundreds of freelancers. You will operate in a fast-paced and dynamic work environment. You will be working for a fun organisation, diversity-focused and dress-down culture based in the Holborn / Tottenham Court Road location. The role is on a hybrid model with non-negotiable in-office requirements, currently every Tuesday.nYou will work alongside 3 other senior engineers, and 2 project-based engineers reporting to the IT Manager.nA bit of a unique opportunity here as you will be a “modern Windows engineer” as our client is hosting 95% of their infrastructure in AWS. You will be involved in project work as well as dealing with 3rd line support tickets. There’s a separate 1st / 2nd line support team so you won’t have to tackle any of these tickets.nYou will be working with the infrastructure team that’s predominantly cloud-based. It’s a unique setup being a Windows/Microsoft environment inside the AWS ecosystem. Everything is glued together using Terraform so there’s great tooling at work here.nResponsibilities
Support circa 30 internal companies with approximately 1,500 users and hundreds of freelancers.nWork in a fast-paced, dynamic environment as part of a small team of engineers reporting to the IT Manager.nOperate as a modern Windows engineer with 95% of infrastructure hosted in AWS.nEngage in project work and 3rd line support (note: 1st/2nd line support is handled by a separate team).nContribute to a predominantly cloud-based infrastructure setup in a Windows/Microsoft environment within AWS, using Terraform.nWork on migration projects and automation initiatives involving AWS, Okta, Terraform, and Office 365/SharePoint.nParticipate in Windows VM provisioning and AWS EC2-related tasks; manage 100+ Windows VMs across multiple accounts.nHandle S3 backups and storage; utilize Okta and Okta Workflows for automation.nAssist with onboarding for newly acquired businesses and security access processes.nRequired / Qualifications
AWS – solid experience is an absolute mustnWindows Server administration ) in an IaaS setup within AWSnOkta & Okta WorkflowsnTerraformnOffice 365 / SharePointnBenefits
Hybrid working – in-office on Tuesdays is essentialn25 days of holidaynPension contributionnFree fresh fruit and office snacksnTraining opportunities with open access to UdemynApply ASAP if you would relish the opportunity to work in an exciting production environment alongside creative experts in the field.
#J-18808-Ljbffrn
This advertiser has chosen not to accept applicants from your region.
8