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QA Officer

Quantum Pharmaceutical Ltd

Bilton

On-site

GBP 30,000 - 40,000

Full time

Yesterday
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Job summary

A leading pharmaceutical company in Bilton is seeking a meticulous Quality Assurance Officer to ensure compliance with Good Manufacturing Practices. Key responsibilities include managing quality assurance activities, documentation oversight, and leading audits. The ideal candidate holds a Bachelor’s degree and has 2+ years of relevant experience. The position offers competitive rewards, professional growth opportunities, and a dynamic work environment within a supportive team focused on innovation and quality.

Benefits

Active Social and Charity Committee
Cycle to Work Scheme
Electric Vehicle Scheme
Eye Care Vouchers

Qualifications

  • 2+ years' experience in Quality, Manufacturing, or related fields.
  • Experience in the pharmaceutical, healthcare, or life sciences industry.
  • English and Mathematics GCSE grades A-C (or equivalent).

Responsibilities

  • Managing quality assurance activities and compliance with standards.
  • Ensuring documentation meets Good Manufacturing Practices.
  • Leading internal and external audits and evaluations.

Skills

Analytical problem solving
Communication
Self-direction
Knowledge of regulations

Education

Bachelor’s degree

Tools

Electronic Quality Management Systems (eQMS)
Microsoft Office
Job description
  • Job Ref: JM1489824QuaQO
  • Location: 30 Bilton Way, Luton
  • Postcode: LU1 1UU
  • Type of contract: Permanent
  • Posted Date: Monday, February 2, 2026
  • Closing Date: Friday, February 27, 2026

Are you passionate about innovation and quality in the pharmaceutical industry? Do you thrive in a dynamic and supportive work environment? Quantum Pharmaceutical, part of the Target Healthcare Group, is looking for talented individuals to join our team and help us achieve our mission.

"To become the UK’s leading provider of aseptic products by driving innovation, delivering unmatched quality and service, and building strong partnerships, setting new industry standards."

Transform Healthcare with Us!

  • Impact - Ensure the safety and efficacy of life‑saving medicines.
  • Innovation - Work with cutting‑edge technology and groundbreaking processes in a rapidly growing environment.
  • Career Growth - Enjoy unparalleled opportunities for continuous learning and professional advancement.
  • Collaborative Excellence - Be part of a passionate, international team dedicated to making a real difference in healthcare.
  • Competitive Rewards - Receive a top‑tier salary, comprehensive benefits, and enjoy a balanced work‑life environment.
The Role

Our Quality Assurance department is the heart of our operation, ensuring every product meets the highest standards of Good Manufacturing Practices. As we expand, we are seeking a meticulous and dedicated Quality Assurance Officer to join our elite team.

Key Responsibilities
  • Managing quality assurance activities such as Deviations and CAPA management, Change Management while assuring compliance with established standards, regulations, specifications, and SOPs.
  • Ensuring that documentation follows current Good Manufacturing Practices, current Good Documentation Practices, and external regulations. Assure the safety and quality of the products, processes, and systems.
  • Developing and maintaining procedures, and policies to assure compliance with cGMP’s. Ensuring all documents are created, distributed, stored, and archived in line with regulatory requirements.
  • Ensuring all systems, operations, products, processes, procedures, and documentation for adequacy and effectiveness to ensure Quality and Regulatory Compliance to related CAPA.
  • Leading, participating in, and reviewing all types of investigations, Root Cause Analysis and Quality Risk Management.
  • Applying problem solving logically and in an organised manner. Must have experience with Root Cause Analysis tools and the ability to apply tools.
  • Leading and assisting with both internal and external audits and audit reports.
  • Assessing and implementing regulatory changes.
  • Identifying any relevant quality‑related training needs, provide training tools and deliver training.
What We Are Looking For
  • Experience of operating in a similar role is desirable.
  • Bachelor’s degree with 2 or more years’ experience in Quality, Manufacturing, or related field.
  • Experience working in pharmaceutical / healthcare / life sciences industry advantageous.
  • Ability to communicate efficiently verbally and in writing with all levels of the organisation and with external clients.
  • Detailed knowledge of applicable regulations and standards. Strong analytical/problem solving skills.
  • Knowledge of electronic Quality Management systems (eQMS) will be advantageous.
  • Demonstrable experience of working autonomously and making decisions with minimal direction.
  • Ability to travel to other sites and for vendor audits.
  • English and Mathematics GCSE grades A-C (or equivalent).
  • High computer literacy; experience operating with all Microsoft Office software.
Benefits Of Working With Us

Joining the Target Healthcare Group means being part of an inspired, enthusiastic team committed to our vision and values. We believe in cultivating a nurturing, dynamic workplace culture.

  • Other benefits include:
  • Active Social and charity committee
  • Cycle to Work Scheme
  • Electric Vehicle Scheme
  • Eye Care Vouchers

If you are passionate about quality and aspire to make a significant impact in healthcare, we want you on our team. Join Target Healthcare Group and become a key player in our mission to transform healthcare.

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