QA Officer

ROLE OVERVIEW

We are currently looking for a Quality Assurance Officer to join a leading pharmaceutical manufacturer based in our client’s site. This is an excellent opportunity for an experienced QA professional to become an integral part of a dedicated team, supporting essential quality systems and ensuring compliance with industry standards. The successful candidate will report to the Quality Assurance Manager and contribute to maintaining the company's high-quality standards in a dynamic environment.

This full-time, permanent role offers a chance to develop your expertise within a supportive organisation committed to excellence in pharmaceutical quality practices, working closely with cross-functional teams to uphold regulatory compliance and continuous improvement.

KEY DUTIES AND RESPONSIBILITIES

Your duties as the Quality Assurance Officer will be varied however the key duties and responsibilities are as follows:

• To provide support to the Quality Assurance Manager / Responsible Person as directed, ensuring effective QA processes are upheld.
• To assist in the implementation and maintenance of GxP cross-company QA procedures, including training and documentation updates.
• To support internal audits, external supplier audits, and contribute to the management of deviations, CAPAs, and supplier quality incidents.
• To assist in creating, reviewing, and updating quality-related documentation, including GDP and WDA(H) documentation.
• As the Quality Assurance Officer, you will help prepare reports for operational and management review meetings and maintain supplier documentation accurately.

ROLE REQUIREMENTS

To be successful in your application to this exciting role as the Quality Assurance Officer we are looking to identify the following on your profile and past history:

• A Degree or higher level in a relevant scientific discipline (e.g., Pharmaceutical Chemistry / Quality Assurance / Quality Management).
• Proven experience in a pharmaceutical quality environment with knowledge of GDP/GMP, GxP, regulatory, and accreditation systems.
• Strong analytical skills to evaluate complex data and investigative reports.
• Excellent interpersonal skills to communicate effectively across all levels of the organisation.
• Ability to plan, organise, and manage multiple projects efficiently while working under pressure with a proactive, can-do attitude.

WHAT’S IN IT FOR YOU?

Joining our client offers you the opportunity to work within a reputable company that values professional growth and development. You will be part of a collaborative team that recognises dedication and expertise, with learning and progression supported at all levels.

Key Words: Quality Assurance / Pharmaceutical / GxP / GMP / GCP / QA / Compliance / Documentation / Audits / CAPA / Supplier Quality / Training / Regulatory Standards / Continuous Improvement / Quality Systems / Cross-functional Teams

"Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career".

Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.