887 Healthcare Regulatory Bodies jobs in the United Kingdom

Food Microbiologist/ Quality Assurance

Join our expert team at Campden BRI, delivering high-impact consultancy services to clients across the food industry. This role blends technical excellence with client-facing delivery, offering a dynamic mix of research, training, and strategic support.

We're looking for a Food Microbiologist with hands-on experience in food manufacturing, ideally within a Quality Assurance or Hygiene function. This is a dynamic opportunity for someone passionate about food safety and eager to expand their expertise across multiple disciplines.

In this role, you'll embark on a structured learning and development pathway designed to evolve your capabilities into a Safety, Quality, and Hygiene Specialist. You'll play a vital role in supporting our team to deliver and enhance factory hygiene services through both consultancy, technical support and the delivery of training and workshops.

Position

• Conducting assessments and providing guidance on Cleaning Systems
• Evaluating and improving personnel hygiene practices
• Advising on hygienic design of equipment and facilities
• Reviewing and optimizing building and air handling systems for contamination control
• Designing environmental sampling programs
• Validating cleaning and disinfection protocols to ensure regulatory compliance and conformity to commercial standards
• Delivering training sessions to upskill factory teams on hygiene best practices
• Troubleshooting hygiene-related issues and offering actionable solutions

Requirements

• A collaborative environment where your scientific insight drives real-world impact
• Access to cutting-edge knowledge across a number of disciplines
• Opportunities to work across diverse product categories and manufacturing setups
• Mentorship from industry-leading experts in food safety and hygiene
• Career progression into consultancy, auditing, or technical leadership roles

Benefits

• Hybrid working
• Reward platform with employee discounts and rewards
• 25 days holiday + 8 bank holidays
• Buy and sell holiday scheme
• A generous work save pension scheme, with employee contributions matched by the company up to 10%
• Culture focus around work/life balance (early finish Fridays)
• Subsidised onsite restaurant
• £30,000-£45,000 pa dependent on experience

Click 'apply now' or send your CV to

Cure Talent are delighted to be partnered with an innovative medical device company developing novel technology ahead of a planned US launch in 2028. As they prepare for significant regulatory milestones, we have an exciting opportunity for a Regulatory Affairs & Quality Assurance Manager to join their growing team.

As the new RAQA Manager, you will lead global regulatory strategy and compliance activities, focusing on FDA De Novo submissions, Q-Sub interactions, and wider international registrations. Alongside this, you will oversee the Quality Management System in line with ISO 13485, managing the transition from a paper-based system to an eQMS (Greenlight Guru), while acting as the Management Representative to senior leadership.

Key Responsibilities

• Lead and execute regulatory strategy to support market entry, including De Novo and 510(k) submissions and FDA Q-Sub meetings.
• Prepare, review, and manage regulatory submissions and technical documentation in line with FDA, UK, and international requirements.
• Liaise directly with regulatory authorities, notified bodies, and external partners to support submissions, audits, and inspections.
• Maintain and improve the Quality Management System in compliance with ISO 13485 and 21 CFR Part 820.
• Lead the transition from a paper-based QMS to an eQMS (Greenlight Guru).
• Oversee supplier management, CAPA, nonconformance, change control, document management, and audit processes.
• Promote regulatory and quality awareness across the business and provide training to R&D and manufacturing teams.
• Act as Management Representative, reporting on QMS performance, risk areas, and quality objectives to senior leadership.
• Line manage and support QA staff responsible for day-to-day QMS maintenance and documentation.
• Review and approve documentation related to product development, validation, risk management, and sterilisation.

Experience and Skills Required

• Proven experience in Regulatory Affairs and Quality Assurance within the medical device sector.
• Strong understanding of international frameworks and FDA pathways, including De Novo and 510(k).
• In-depth knowledge of ISO 13485, 21 CFR Part 820, QMSR, ISO 14971, and ISO 9001.
• Experience leading or supporting QMS implementation projects, ideally eQMS (Greenlight Guru).
• Skilled in CAPA, audit management, risk management, validation, and change control.
• Excellent communication, organisation, and stakeholder management skills.
• Life sciences or engineering degree; relevant professional certifications advantageous.

If you’re an experienced RAQA professional seeking an opportunity to lead both regulatory strategy and QMS improvement for cutting-edge medical technologies, we’d love to hear from you.

Cure Talent are delighted to be partnered with an innovative medical technology company developing advanced wearable and AI-driven healthcare solutions. As they continue to expand their global regulatory footprint, we have an exciting opportunity for an RAQA Manager to join their growing team.

As the new RAQA Manager, you will take ownership of regulatory compliance and market access activities across UKCA, FDA, and upcoming CE marking, while overseeing the Quality Management System in line with ISO 13485 and FDA 21 CFR Part 820. The role also includes line management of one team member, offering an excellent opportunity to shape both regulatory and quality strategy across the business.

Key Responsibilities

• Maintain existing UKCA and FDA submissions and lead CE marking activities.
• Prepare, update, and manage regulatory documentation and technical files.
• Liaise with regulatory authorities, notified bodies, and external stakeholders.
• Oversee the Quality Management System in compliance with ISO 13485, MDR, and FDA 21 CFR Part 820.
• Manage internal and supplier audits, CAPA, NCR, change control, and risk management activities.
• Maintain document control and training records in line with regulatory requirements.
• Line manage and mentor one direct report.

Experience and Skills Required

• Proven Regulatory Affairs and Quality experience within the medical device industry.
• Strong knowledge of UKCA marking, CE marking, and FDA 510(k) submissions.
• In-depth understanding of ISO 13485, MDR, and FDA 21 CFR Part 820.
• Experience leading or supporting audits and inspections.
• Knowledge of risk management, change control, and product lifecycle processes.
• Experience with MDSAP, UDI, or PMS activities is advantageous.
• Familiarity with connected medical devices or digital health technologies is desirable.
• Previous line management or mentoring experience preferred.

If you’re an experienced RAQA professional seeking a dynamic role where you can lead both regulatory and quality activities in an innovative medical technology environment, we’d love to hear from you.

Contract type: Permanent

Start date: Immediate start - pending successful CTC clearance

Salary: £23.38 plus £ph Supervisory uplift plus .50 site bonus (this will go up to .37 during outages)

We are the leading provider of infrastructure services.

At Altrad, we transform our nation’s critical infrastructure to operate safely and sustainably.

With over 11,000 talented people, we provide the full spectrum of critical engineering and construction services for industries both onshore and offshore.

Join a Leading Organisation in the Nuclear Industry.

Role details:

We currently have an opportunity for multiple QA Engineers to join our team at Sizewell B Nuclear Power station. Successful candidates will be required to undergo CTC clearance.

Key Responsibilites:

• Ensure that all activities are controlled in a responsible, safety conscious climate, meeting Altrad’s requirements and current legislation. Application of all relevant Engineering Standards & Specifications to achieve a world class HSEQ performance, meeting all technical and environmental legislative requirements.
• Ensure safety of people and the environment.
• Have knowledge and familiarisation of associated mechanical, civils and quality procedures.
• Scope, Time and Cost to be fully understood, communicated, monitored and controlled & when required proactive mitigation is evident.
• Ensure high standards of workmanship within the facilities.
• Always use best practices & continually look for innovations that support continuous quality improvement.
• Continuous Improvement tools and techniques are deployed to improve efficiency and effectiveness for both Altrad and the Client.
• Suitable and sufficient risk assessments are followed and signed onto.
• Record and report delays to Project Team.
• Accurate recording of all required HSEQ documentation.
• Undertake responsibility for the development and implementation of the Altrad Integrated Management System (AIMS) within the working location.
• Ensure project work is carried out in accordance with the relevant Client Specifications & British standards.
• Development, approval, and monitoring of project quality Inspection Test Plans (ITPS) and Subcontractor Quality Plans (QPs).
• Support Project Managers/Engineers with project setup documentation i.e. Quality Plans/ITPs and ensuring QP/ITP sign offs are completed concurrent to the works completed.
• Managing the LTR strategy requirements, inclusive co-ordination, compiling, checking, approval and storage of • Projects/Delivery Partners/Sub-Contractor LTRs for submission on time.
• Ensure inspection certificates are completed in line with the QP/ITP schedule and are issued for inclusion in the LTR concurrent to the works completed.
• Undertake periodic Quality Management System audits both internal and external to ensure that the system and procedures are adhered to.
• Monitor Vendor Performance and carry out Supplier/Subcontractor assessments and audits as appropriate.
• Support and lead continuous improvement activities.
• Undertake special projects as assigned

Key Requirements:

• May possess several types of qualifications ranging from the Diploma, Associate and Degree level that may include:
• CQI Certificate or Bachelor’s Degree in Quality/HNC Engineering desirable.
• NVQ Qualification in Nuclear/Engineering related area.
• Demonstrable experience in a Quality Engineering (QA/QC) related position.
• Ideally a CSWIP 3.1 qualification, ISO:9001 internal auditor preferred.
• Valid Site Safety Passport

Why Join Us?

• Work on high-impact projects within a leading organisation
• Competitive salary and benefits package.
• Opportunities for career growth and professional development.
• Collaborative and dynamic work environment with a focus on innovation and excellence.

Quite simply, a journey with Altrad begins with a desire to create a better tomorrow…

Opus People Solutions on behalf of our client in the East Midlands have an exciting opportunity for an Auditor to join their team.

Rate of Pay: £40-45 per hour

Working Arrangements: Hybrid, 2 days a week in the office

Length of Assignment: Minimum 6 months.

Provide a range of services for children. These include early help, safeguarding and support for children in need and children looked after. We need a consistent, rigorous understanding of the quality and effectiveness of the help we provide these vulnerable children.

Auditors will play a key role in evaluating practice, analysing audit findings, identifying areas for improvement, recommending improvement options and reporting to senior leaders. They will also undertake coaching, make presentations and contribute to training events.

Responsibilities:

• Undertake in-depth case audits, working alongside social workers and team managers to evaluate the quality and impact of practice in improving children’s lives.
• Obtain and evaluate the views of children, families and professional partners about the quality and impact of practice.
• Undertake extensive thematic case sampling to understand and report on the quality specified elements of practice.
• Go beyond auditing by using the audit process to coach social workers and managers in good practice, helping them build on existing strengths and eliminate weaknesses.
• Train and coach managers in effective auditing.
• Undertake audits of supervision at child level and practitioner level.
• Moderate case audit and case sampling completed by others so we can be confident that evaluations and judgements are are evidence-based with a consistent understanding of what good looks like.
• Analyse and collate audit findings across CFN so they can be reported routinely to senior leaders to inform the full range of practice improvement and workforce development activities.
• Present audit findings and lessons from audit to groups of practitioners, managers and senior leaders as required.

Experience:

• Qualified Social Worker
• Social Work England Registered
• Team Manager Experience
• 3 Years post qualifying experience

If you thrive to make a difference and have 3 years experience and this is the role for you, then we would love to hear from you.

Job Overview

We're seeking a detail-oriented QA Engineer to ensure the quality, reliability, and performance of our fintech and financial education platforms. You will design and execute tests, identify issues, and collaborate with development teams to deliver a seamless user experience.

Key Responsibilities:

• Develop and execute manual and automated test plans for web and mobile applications.
• Identify, document, and track software defects and issues.
• Collaborate with developers and product teams to resolve bugs and improve system performance.
• Conduct regression, integration, and performance testing.
• Maintain testing documentation and provide clear reporting on quality metrics.
• Recommend process improvements to enhance software quality and efficiency.
• Stay updated on QA tools, methodologies, and industry best practices.

Requirements:

• Proven experience as a QA Engineer, Software Tester, or similar role.
• Experience with automated testing tools (Selenium, Cypress, JUnit, etc.) is preferred.
• Strong knowledge of QA methodologies, processes, and best practices.
• Excellent analytical, problem-solving, and attention-to-detail skills.
• Understanding of software development life cycle (SDLC) and Agile methodologies.
• Experience in fintech, SaaS, or educational platforms is advantageous.

Benefits:

• Work on innovative fintech and financial education platforms.
• Collaborative and innovation-focused team environment.
• Professional development and career growth opportunities.

Job Types: Full-time, Permanent

Pay: £40,000.00-£55,000.00 per year

Benefits:

• Company pension
• Work from home

Work Location: Hybrid remote in London E14

QA Pack Development & Review

o Prepare, assemble, and maintain QA documentation for all electrical works, including as installed packs (AIPs), inspection and test plans (ITPs), and compliance records.

o Review and validate NIC submissions from ensuring compliance with BS EN standards.

o Ensure all QA documentation aligns with client requirements, internal procedures, TfL standards, and regulatory standards.

Site QA Management

o Manage a team of site QA engineers, allocating tasks and responsibilities.

o Coordinate inspections, audits, and commissioning tests, resolution of non-conformances, and hit deadlines.

Compliance & Standards

o Ensure all electrical installations comply with TfL standards, BS/EN standards, and project specifications.

Candidate Requirements

• Experience as a Quality Assurance Manager or Senior QA Engineer within electrical contracting on large-scale infrastructure or rail projects.

• Familiarity with TfL (LU) standards and procedures.

• Experience managing site QA teams and coordinating multiple site locations.

• Knowledge of BS EN standards, and electrical installation practices.

• Organisational, communication, and leadership skills.

• Ability to produce high-quality "redlined" drawings such as schematics, schedules, elevation drawings, etc. with PDF editors or CAD from the information received from the site survey

• Lead testing efforts for international e-commerce projects, ensuring high product quality across web and mobile platforms.
• Analyze product requirements to define test scope, design test cases, and create comprehensive test plans.
• Execute manual and automated tests, identifying issues and driving them to resolution.
• Apply diverse testing methods (functional, regression, white-box, automation, performance) to improve test coverage and efficiency.
• Design, develop, and maintain automated test frameworks to reduce manual testing effort.
• Collaborate with product managers, developers, and business teams to ensure requirements are met with high reliability.
• Continuously improve testing processes, tools, and methodologies through knowledge sharing and innovation.

• Bachelor's degree or higher in Computer Science, Software Engineering, or a related field.
• 2+ years of experience in software testing, with strong understanding of testing theory, strategy, and design methods.
• Proficiency in at least one programming language (e.g., Java, Python) with experience in automation test development.
• Hands-on experience with SQL databases (e.g., MySQL), including ability to write and optimize complex queries.
• Strong analytical thinking, problem-solving, and communication skills, with the ability to understand business requirements and translate them into test strategies.
• Ability to thrive in a fast-paced, international team environment.
• Effective communication skills in Chinese and English.

• Experience with test automation frameworks (e.g., Selenium, Appium, JUnit, PyTest).
• Familiarity with Agile development and CI/CD pipelines.
• Prior experience in e-commerce platforms or large-scale consumer applications.
• Knowledge of performance testing or security testing.

• A dynamic and challenging work environment in a leading global e-commerce company.
• The opportunity to collaborate with an international, cross-functional team and directly influence product quality.
• Competitive salary and benefits package, including health insurance, retirement plans, and performance bonuses.

(NASDAQ: JD and HKEX: 9618), also known as JINGDONG, has evolved from a pioneering e-commerce platform into a leading technology and service provider with supply chain at its core. Renowned for its supply chain innovation and excellence, has expanded into sectors including retail, technology, logistics, healthcare, and more, aiming to transform traditional business models with cutting-edge digital solutions. Ranked 47th on the Fortune Global 500, is China's largest retailer by revenue. In 2023, reported revenues of US$152.8 billion and served approximately 600 million active customers.

We are dedicated to building a digitally intelligent, cross-border supply chain and global retail infrastructure. Leveraging our global supply chain capabilities, continues to expand in markets where our competitive strengths shine. Currently, operates globally, with business activities in countries such as China, the U.S., U.K., Netherlands, France, Germany, Spain, Brazil, Hungary, Japan, South Korea, Australia, Thailand, Vietnam, Malaysia, Indonesia, Saudi Arabia, the UAE, and many others, reaching customers in every corner of the world.

QA Associate

Location
: Slough (Fully Onsite)

Contract Length
: 9 months (with potential to extend)

Pay Rate
: £21.92 per hour

Role Purpose & Scope

As a member of the QA Operations Documentation Control Team, your primary responsibility will be to perform Batch Consolidation (auditing) for QC Biochemistry and Microbiology testing activities related to Drug Product (DP) and Drug Substance (DS). You will ensure all QC testing activities are complete and meet release specifications. You will also proactively issue GMP documents and labels to Manufacturing in line with schedules and timelines.

Key Responsibilities

• Coordinate and perform batch consolidation for QC Biochemistry and Microbiology testing.
• Ensure all testing activities are complete and meet release specifications.
• Issue GMP documents and labels to Manufacturing, ensuring accuracy and timeliness.
• Liaise with internal departments to gather required information and maintain effective communication.
• Support QA Operations in continuous improvement of quality systems and processes.
• Assist in audit preparation and provide documentation during audits.
• Lead and manage quality records (Deviations, CAPAs, Change Controls, Investigations).
• Author, review, and approve GMP documentation.
• Maintain the archiving system and coordinate document retrieval.
• Ensure training compliance and maintain an up-to-date training profile.
• Prioritise workload to meet strict deadlines and support Manufacturing needs.
• Perform other duties as assigned.

Technical & Interpersonal Skills

• Strong attention to detail and accurate data entry
• Proficiency in MS Office (Word, Excel, Outlook, Access)
• Familiarity with database systems
• Effective verbal and written communication
• Risk-based decision-making
• Ability to prioritise workload and meet deadlines
• Strong organisational and planning skills
• Experience with PQS (Pharmaceutical Quality Systems) is desirable

Core Competencies

Agility

• Learns from experience, adapts to change, and embraces new challenges

Business Acumen

• Understands how their role contributes to business success

Collaboration

• Shares knowledge, listens actively, and respects others

Customer Focus

• Understands and responds to internal/external customer needs

Driving Results

• Delivers high-quality work on time, monitors KPIs, and overcomes challenges

Leadership

• Takes responsibility, seeks feedback, and contributes to a positive work environment

Qualifications

Education: BSc in Biology or a related field (or equivalent experience)

Experience: Entry-level (0–4 years); prior QA/GMP experience is beneficial but not essential