23 Quality Assurance Manager jobs in Winnersh

Our client, a leading pharmaceutical company with a commitment to innovation and quality, is seeking a highly experienced Senior Quality Assurance Manager for their facility in Reading, Berkshire, UK . This pivotal role is responsible for ensuring that all pharmaceutical products meet the highest standards of quality, safety, and efficacy, in full compliance with regulatory requirements. The ideal candidate will possess extensive experience in pharmaceutical quality systems, GMP (Good Manufacturing Practice), and regulatory affairs. You will lead and manage the QA department, overseeing all aspects of quality control, batch release, validation, and auditing. Key responsibilities include developing, implementing, and maintaining robust quality management systems, conducting internal and external audits, managing deviations and CAPAs (Corrective and Preventive Actions), and ensuring regulatory compliance across all manufacturing and R&D operations. You will play a crucial role in preparing for regulatory inspections from agencies such as the MHRA, FDA, and EMA. Strong leadership, analytical skills, and the ability to make critical quality decisions are essential. This role requires a thorough understanding of pharmaceutical manufacturing processes, quality control methodologies, and the regulatory landscape. You will be expected to drive a culture of quality excellence throughout the organization and mentor a team of QA professionals. This is an on-site position requiring active participation in day-to-day operations at our Reading facility.
Key Responsibilities:

• Oversee and manage all pharmaceutical Quality Assurance activities.
• Develop, implement, and maintain the Quality Management System (QMS).
• Ensure compliance with GMP, GCP, GLP, and other relevant regulatory standards.
• Conduct internal audits and manage external audits from regulatory agencies and partners.
• Review and approve batch records, specifications, and validation protocols.
• Manage deviations, investigations, CAPAs, and change control processes.
• Provide QA support for manufacturing, R&D, and other functional areas.
• Train personnel on quality policies, procedures, and regulatory requirements.
• Lead and mentor the QA team, fostering professional development.
• Contribute to regulatory submissions and ensure ongoing compliance.

Qualifications:

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field.
• Minimum of 8 years of experience in Quality Assurance within the pharmaceutical industry.
• Demonstrated experience with GMP, regulatory affairs, and quality systems.
• Proven track record in managing QA operations and leading audit activities.
• Strong knowledge of pharmaceutical manufacturing processes and quality control.
• Excellent understanding of regulatory guidelines (MHRA, FDA, EMA).
• Exceptional leadership, analytical, problem-solving, and decision-making skills.
• Strong written and verbal communication abilities.

This is a high-level opportunity to contribute significantly to the quality and integrity of life-saving medications.

Our client is seeking a highly qualified and experienced Pharmaceutical Quality Assurance Manager to lead their QA functions from a remote capacity. This pivotal role will ensure that all pharmaceutical products and processes comply with regulatory standards, Good Manufacturing Practices (GMP), and internal quality policies. You will be responsible for developing, implementing, and maintaining the company’s Quality Management System (QMS), overseeing batch record review, deviation management, change control, and CAPA (Corrective and Preventive Actions) processes. Your expertise will be crucial in conducting internal audits, supporting external inspections, and ensuring continuous improvement of quality processes.

Key responsibilities include managing a remote QA team, fostering a strong quality culture, and providing guidance on all quality-related matters. You will work closely with manufacturing, R&D, and regulatory affairs departments to ensure product quality and compliance throughout the product lifecycle. Experience in risk management and performing quality risk assessments is essential. You will also be involved in supplier qualification and audits. The ideal candidate will possess a degree in Pharmacy, Chemistry, Life Sciences, or a related field, with significant experience in pharmaceutical Quality Assurance, preferably in a managerial role. A strong understanding of global pharmaceutical regulations (FDA, EMA, MHRA) is mandatory. Excellent leadership, analytical, problem-solving, and communication skills are required to effectively manage a remote team and complex quality systems. If you are a dedicated and meticulous QA professional ready to lead quality assurance remotely in the pharmaceutical industry, this is an exceptional opportunity.

Our client, a prestigious automotive manufacturer renowned for its commitment to quality and innovation, is seeking a highly experienced Senior Quality Assurance Manager for their facility in **Reading, Berkshire, UK**. This is a critical, hands-on role overseeing all aspects of quality control and assurance within the manufacturing process, ensuring the production of flawless vehicles.

As the Senior QA Manager, you will be responsible for establishing, implementing, and maintaining the company's Quality Management System (QMS), ensuring it aligns with international standards such as IATF 16949. You will lead a team of QA professionals, driving continuous improvement initiatives, and ensuring that all products meet stringent quality specifications and customer expectations. Your role will involve working closely with production, engineering, and supply chain departments to identify and resolve quality issues proactively.

Key responsibilities include:

• Developing, implementing, and managing the Quality Management System (QMS) for automotive manufacturing.
• Leading and mentoring the quality assurance team, including inspectors and technicians.
• Establishing quality control procedures for raw materials, in-process production, and finished goods.
• Conducting internal audits and supporting external quality audits from customers and certification bodies.
• Analyzing quality data, identifying root causes of defects, and implementing corrective and preventive actions (CAPA).
• Collaborating with engineering and production teams to resolve quality issues and improve manufacturing processes.
• Managing supplier quality and ensuring that supplied components meet required specifications.
• Developing and delivering quality training programs for employees across all departments.
• Driving a culture of quality excellence throughout the organization.
  
  The ideal candidate will possess a Bachelor's degree in Engineering, Manufacturing Technology, or a related technical field, with a minimum of 10 years of progressive experience in quality assurance, specifically within the automotive manufacturing industry. A strong understanding of IATF 16949 and other relevant automotive quality standards (e.g., APQP, PPAP, FMEA) is mandatory. Proven experience in leading QA teams and implementing robust QMS is essential. Excellent analytical, problem-solving, and decision-making skills are required, along with strong leadership and communication abilities. Experience with statistical process control (SPC) and quality tools is highly beneficial. This is an outstanding opportunity for a seasoned quality professional to make a significant impact on product quality and operational excellence within a leading automotive company.

Join us as we shape the future of healthcare through innovation, integrity, and excellence. We are seeking an experienced leader to take on the role of Senior Director, Global Development Quality Management (GVP). This pivotal position offers the opportunity to drive strategy, lead quality initiatives, and collaborate globally to ensure compliance and excellence in drug development and pharmacovigilance practices.
As a member of the GDQGO Leadership Team, you will play an integral role in advancing our mission while fostering innovation, quality, and collaboration across global functions.
**A Typical Day:**
In this role, you will:
+ Lead the GDQM (GVP) sub-function, providing strategic direction and operational oversight.
+ Ensure proactive, risk-based approaches to quality and compliance within Regeneron's Quality Management System (QMS).
+ Collaborate with cross-functional teams to support Good Pharmacovigilance Practice (GVP), Good Clinical Practice (GCP), and Medical and Regulatory Affairs.
+ Oversee timely issue escalation, risk management activities, and inspection readiness.
+ Manage team resources, including hiring strategies, onboarding, and performance reviews.
+ Represent the GDQGO sub-function during regulatory inspections and cross-functional forums.
+ Drive process improvement initiatives and champion innovation to enhance quality objectives.
**This Role May Be For You If you:**
+ Are a strategic thinker with expert knowledge in GVP Quality and local affiliate QMS oversight.
+ Have a proven ability to lead cross-functional teams and build strong stakeholder relationships.
+ Thrive in a collaborative environment and are skilled at balancing strategic vision with operational execution.
+ Are adept at identifying risks and embedding proactive quality management approaches.
+ Possess exceptional communication skills and can effectively deliver key messages to executive leadership and cross-functional teams.
+ Excel at managing resources, fostering team growth, and driving large-scale quality initiatives.
**To Be Considered:**
We are looking for candidates with:
+ Extensive experience in quality management, particularly in GVP, GCP, and regulatory affairs.
+ A strong track record of leadership in global functions and cross-functional collaboration.
+ Expertise in risk-based quality management and inspection readiness strategies.
+ A passion for driving innovation and process improvement in quality systems.
+ Preferred qualifications include familiarity with Regeneron's global PV system and experience representing quality functions during regulatory inspections.
**Why Join Us?**
At Regeneron, we believe in the power of collaboration, innovation, and a commitment to excellence. As the Head of Global Development Quality Management (GVP), you will have the opportunity to make a meaningful impact on our mission to bring life-changing medicines to patients worldwide.
Join us and be part of a team that exemplifies quality, integrity, and leadership in every interaction.
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.

Join a leading pharmaceutical company as a Remote Pharmaceutical Quality Control Analyst. This critical role is pivotal in ensuring the quality, safety, and efficacy of our pharmaceutical products. As a fully remote position, you will leverage your analytical skills and scientific knowledge to conduct essential quality checks and contribute to our stringent quality assurance processes. You will work with a talented team of scientists and quality professionals, all collaborating virtually to uphold the highest industry standards.

Key Responsibilities:

• Performing analytical testing of raw materials, in-process samples, and finished pharmaceutical products
• Documenting test results accurately and meticulously according to Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP)
• Interpreting analytical data and identifying any deviations from specifications
• Investigating out-of-specification (OOS) results and deviations
• Preparing and maintaining calibration logs for laboratory equipment
• Assisting in the validation of analytical methods and equipment
• Ensuring compliance with all relevant regulatory requirements (e.g., FDA, EMA)
• Contributing to the continuous improvement of quality control processes
• Collaborating with other departments, including R&D and Manufacturing, to resolve quality issues
• Maintaining a safe and organized work environment in your home laboratory setup

The ideal candidate will hold a degree in Chemistry, Pharmacy, Biology, or a related life science field, coupled with demonstrable experience in a quality control laboratory setting. Proficiency with analytical instrumentation such as HPLC, GC, UV-Vis, and dissolution testers is highly desirable. You must possess excellent analytical and problem-solving skills, a strong understanding of GMP/GLP guidelines, and meticulous attention to detail. Effective communication and collaboration skills are essential for working within a remote team environment. Experience with data analysis software and electronic lab notebooks is also beneficial. This is an exceptional opportunity to advance your career in pharmaceutical quality assurance while enjoying the flexibility of a remote work arrangement.

The Quality Engineer role is focused on Accreditation Management of Credentials (3rd Party authorisation) associated to sites within the EMEA region. Accreditation Management acts as a leader to gatekeep accreditation(s) and have oversight of company operated activities or service fulfilment and in a support role for Conformity Assessment Body activity.
Day to Day activities (examples):
+ Organise, plan and facilitate assessments
+ Act as the host for an (onsite) assessment; organise rooms, refreshments, personnel to be involved
+ Act as the main contact for Accreditors, Regulators and External Scheme Owners so all activities are channelled through and are known to Accreditation Management & Strategy (AMS)
+ Work with the Customer Operating Unit (COU) to collect information regarding accreditor/regulator applications and act as signatory on the application (unless another function is designated to do this)
+ Support the CAB with internal and external assessments
+ Support/guide a process owner in document compilation
+ Own only controlled documents which are directly related to accreditation e.g. use of an accreditor symbol, the application process, accreditor schedule management
+ Management of Credentials (accreditation/certification).
+ Facilitate Internal and External Accreditors, Regulators, and Scheme Audits. Act as primary contact responsible for engaging with Accreditors, Regulators and External Scheme Owners. Establish and maintain accreditation (inc. scope extensions and reductions.
+ When required, facilitate resolution of customer complaints.
+ Facilitate understanding of the Corrective Action Request (CAR) process and possibly serve as CAR Champion.
+ Participate and provide inputs for Regulatory Services owned processes (CAR, Internal Compliance Assessments and External Assessments), when requested for Management Review, per applicable standard requirements.
+ Assess Management System compliance, including control of documentation and records, via the Internal Compliance Assessments Process.
+ When necessary, review and approve Management System documentation, to facilitate compliance. Maintain oversight of the management system.
+ Oversee the development of new Management Systems.
+ Merger & Acquisitions - Management System Integration per the approved playbook or specific Master Plan.
+ Support capacity for improvements, management review, risks etc
+ Preferred - University degree (or equivalent) in Engineering, or related field plus generally five years of directly related experience.
+ Fluent in English and local language place of residence (verbal and written) skills.
+ Detailed knowledge of quality management systems and process improvement principles, tools and techniques including quality and business excellence models (e.g., ISO 9001, 17025, 17065, Lean Sigma, Baldrige / Shingo).
+ Demonstrated knowledge of auditing and CAPA Principles.
+ Demonstrated ability to conduct internal quality audits, root cause analysis and plan/implement corrective action.
+ Demonstrated ability to analyze data, to interact with all levels of the organization, and to present and facilitate discussions of the findings.
+ Ability to lead improvement teams to develop mid-level to complex processes and process maps.
#LI-HH1
UL LLC has been and will continue to be an equal opportunity employer. To assure full implementation of this equal employment policy, we will take steps to assure that:
Persons are recruited, hired, assigned and promoted without regard to race, color, age, sex or gender, sexual orientation, gender identity, gender expression, transgender status, religion, creed, national origin, ethnicity, citizenship, ancestry, disability, genetic information, military or veteran status, pregnancy, marital or familial status, or any other protected category under applicable law.

Quality Assurance Administrator

Are you a detail-oriented professional with a passion for ensuring quality? Do you thrive in a dynamic environment where your contributions make a real difference? If so, we have an exciting opportunity for you!

Position : Quality Assurance Administrator
Contract Type : Temporary
Location : Merstham
Hours : 8 AM - 4 PM

Booking Duration - 3 months, could be extended

Start Date : As soon as next week!

Our client is seeking a Quality Assurance Administrator to join their Imaging Department, where you will play a pivotal role in maintaining the highest standards for client work. This position is perfect for someone who enjoys a challenging yet rewarding role and is looking to grow their skills in a supportive environment.

Key Responsibilities :

• Conduct thorough quality checks on client projects to ensure accuracy and compliance with standards.
• Communicate effectively with team members and clients to address any quality concerns.
• Self-manage your workload and prioritise tasks to meet deadlines.
• utilise Microsoft Excel and other platforms for data management and reporting.

What We're Looking For :

• A keen eye for detail and a commitment to quality.
• Strong communication skills to liaise with various stakeholders.
• Proficiency in Microsoft platforms, especially Excel.
• The ability to work independently while being a collaborative team player.

Why Join Us?

• Supportive Team Environment : Work alongside a friendly team who values your input and expertise.
• Exciting Project : Be a part of a project launching on September 8th! Your work will have an immediate impact.

If you're ready to take on this exciting challenge, we want to hear from you! Please send your CV to us today, and let's arrange an interview to discuss how you can contribute to our client's success.

Apply Now!

Adecco is a disability-confident employer. It is important to us that we run an inclusive and accessible recruitment process to support candidates of all backgrounds and all abilities to apply. Adecco is committed to building a supportive environment for you to explore the next steps in your career. If you require reasonable adjustments at any stage, please let us know and we will be happy to support you.

Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer.

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Position: Director of Quality Assurance & Regulatory Affairs

Location: Middlesex

Salary: 85K + benefits

Purpose of the Role

To lead global quality and regulatory strategy, ensuring compliance across the company's product portfolio. This role is pivotal in enabling market access, maintaining high standards, and embedding quality throughout the product lifecycle.

Strategic Leadership

• Represent role model or servant leader model leadership as a member of senior site management team.
• Develop and implement the QARA strategy aligned with business goals and regulatory compliance requirements.
• Collaborate with Engineering, Operations, and Commercial teams to integrate quality and compliance from concept to delivery.
• Represent the company in regulatory compliance audits and external engagements.

Regulatory Affairs

• Oversee global product registrations and submissions, including CE marking and international approvals for company products
• Support in defining regulatory pathways early in product development, including Intended Use and Risk Classification.
• Ensure compliance with ISO 13485, MDR, FDA 21 CFR Part 820, and other relevant standards.

Quality Assurance

• Maintain and enhance the Quality Management System (QMS).
• Lead internal and supplier audits, investigations, and corrective actions.
• Analyse QA data to drive continuous improvement and risk mitigation.

Project Oversight

• Lead QARA team in managing regulatory documentation and audit readiness.
• Support change control and post-market surveillance activities.

Team Development

• Mentor and develop QARA team members.
• Ensure training programmes reflect current regulatory and quality practices.

Skills & Experience

• Proven leadership in QARA within medical devices or regulated industries.
• Strong engineering background
• Experience with CE marking, Medical Device Requirements, both EU and UK, regulatory submissions, electrical safety requirements, software validation, and international compliance.
• Excellent communication and stakeholder engagement skills.
• Familiarity with electronic QMS and project management tools.

Desirable Qualifications

• Degree in Engineering, Life Sciences, or related field (Master's preferred).
• Experience working directly with regulatory bodies.
• Lead Auditor Certification

About Us

We are dedicated to fostering a diverse and inclusive community. In line with our Diversity and Inclusion policy, we welcome applications from all qualified individuals, regardless of age, gender, ethnicity, sexual orientation, or disability. As a Disability Confident Employer, and part of the Nicholas Associates Group, we are committed to supporting candidates with disabilities, and we're happy to discuss flexible working options.

We are committed to protecting the privacy of all our candidates and clients. If you choose to apply, your information will be processed in accordance with the Nicholas Associates Group of companies Privacy Notice.