Job Description Summary

We are seeking a dedicated QC Finished Product Analyst to join our team on a 12‑month fixed‑term contract, working on a 4‑cycle shift pattern. In this role, you will play a key part in ensuring that all finished product testing is carried out to the highest cGMP and cGLP standards, supporting product release, compliance, and continuous improvement across the QC function. This position offers the opportunity to work with a wide range of analytical techniques while collaborating closely with cross‑functional teams in a fast‑paced, highly regulated environment.

Job Description

Responsibilities

• Carry out routine analysis on Finished Product samples ensuring compliance with cGLP/cGMP and that turnaround times are met. The testing carried out includes but is not limited to:   HPLC, Osmolality, Organic Iodine, Inorganic Iodine, Thin Layer Chromatography, Free aromatic amines, pH, RI, Trom’s, EDTA, Technical tests, Extractable volume., complaints etc..

• Assisting in the maintenance of the stability program

• Actively involved in Investigations e.g. LIR’s. etc..

• Logging of samples in LIMS

• Entering results on LIMS, checking results are within specification and also task approval.

• Ensure compliance with EHS at all times, actively participate in EHS activities.

• Perform routine instrument calibration checks at appropriate times.

• Preparation and control of Standard Operating Procedures and ensuring compliance with cGMP guidelines at all times.

• Completion of Documentation for Batch Release process.

• Assisting in the provision of trends, CPV etc..

• Assist in audits.

• Generation/ reporting of Key performance indicators for the group.

• Be proactive in approach planning for future and implement improvements in an effective manner.

• Develop areas of expertise in analytical testing in order to solve technical issues.

• Ensure compliance with current pharmacopoeias and all regulatory/company guidelines.

• Interaction with other departments e.g. QA, BU, Sterility assurance etc.

• Keep colleagues informed of current issues and developments as appropriate.

• Assist in the training and up skilling of colleagues.

• Reasonable level of overtime will be required to facilitate the business needs.

• Liaising with internal and external customers e.g., planning/ QA/ BU etc.

• Carry out additional duties as deemed necessary by your Group Leader/ Supervisor.

Qualifications and Requirements

• A third level Science Qualification

• Basic pharmaceutical experience in a GMP regulated laboratory environment.

Desired Characteristics

• Strong oral and written communication skills. Ability to document, plan, market, and execute programs.

Inclusion and Diversity

GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

Behaviors

We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership – always with unyielding integrity.

Total Rewards

Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration and support.

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Additional Information