Job Description

Do you enjoy being in an environment that is focused around delivering meaningful work at a dynamic pace? Our number one value is Patient First. Everything we do surrounds this philosophy and we see our employees as our primary asset when it comes to achieving this essential business value.

We have an exciting opportunity for a QC Team manager to join The Quality Control department in Swindon. Our Swindon facility houses our Zydis\xc2\xae fast dissolving tablet development and manufacturing operation as well as a CMC pharmaceutical analytical lab services unit that offers ASAP stability.

The team manager will coordinate the activities which comprise of the Finished Product Testing non-test items and packaging components and QC Inspection activities within the Quality Control group, to ensure that the company\xe2\x80\x99s final products are tested, and stage approved in accordance with the relevant specifications and with cGMP, and to a standard acceptable to any auditing bodies.

Shift role; 4 on 4 off.

07.00 \xe2\x80\x93 19.00

The Job:

• To ensure that products (including stability studies) are tested in accordance with defined procedures and methods, and the requirements of cGMP (GLP), and that any deviations are documented, and appropriate action is taken.
• Daily Supervision of the QC Chemistry team, comprising of around 10 - staff, including performance management and supporting staff in attaining their personal development plans.
• To ensure that all QC analysts are trained appropriately for their duties, and that the training is documented.
• To ensure that all specifications and methods of test are kept current, by reference to customers licensing activities and to changes in compendial requirements.
• To participate in internal and external audits related to the laboratory activities whilst taking a leading approach to audit preparations.
• To arrange for investigation, documentation, and follow-up of any anomalous events within the Final Product / Stability testing areas within the laboratory which may have a bearing on cGMP or product quality.
• To be responsible for resource planning for QC analysts using the information supplied from the monthly commitments and Finite meetings.
• To maintain close dialogue with Supply Chain, ensuring that any issues of quality are resolved in timely fashion.
• To work in a manner compliant with EH&S demonstrating a leading performance with respect to SOS\xe2\x80\x99s and Positive Safety behaviors, including actions to resolve.
• To perform any other duties required by line management.

The Candidate:

• Must have experience in a quality environment, for pharmaceutical or medical devices.
• Appropriate Science based Degree or relevant industrial experience.
• HPLC Experience
• People management/supervisory experience

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve. As a result of the global pandemic, we have modified many of our recruitment and on-boarding processes to maintain everyone\xe2\x80\x99s safety. The Human Resources teams will communicate all necessary safety processes and procedures throughout each stage.

personal initiative. dynamic pace. meaningful work.

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Catalent is an Equal Opportunity Employer and does not discriminate based on any characteristic protected by local law.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Catalent