Biotech jobs in United Kingdom

Catalent are currently recruiting for a Quality Specialist to join the Bathgate site. The Quality Specialist will carry out functions relevant to the Quality (GMP) objectives and policies of Catalent.

This role will see you join the dedicated Quality function that is an integral part of our success here at Catalent. In this role, you will be responsible for the movement, control, and tracking of documentation to adhere to the production schedule.

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply.

Working hours: shift 7am – 3pm & 10am - 6pm – alternating

The Role:

• To be responsible for the movement, control, and tracking of documentation, ensuring a timely flow to adhere to the production schedule.

• Review and approve Material Specifications to ensure compliance with pharmacopoeia and client requirements.

• To review and approve Incoming Bulk, Intermediate and Finished Materials to ensure compliance with pharmacopoeia and client requirements.

• Review and approve Randomisations to ensure compliance with GMP and client requirements.

• Review and approve GMP information to ensure accuracy and compliance with company procedures.

• Review and approve production (Pre and Post Packaging Batch) Records to ensure compliance with GMP and company procedures.

• Liaise with relevant department staff and management on quality issues and timelines.

• Review and approve observation and deviation reports to ensure compliance with GMP.

• Perform internal audits as scheduled and monitor/trend findings. Walkthroughs.

The Candidate:

• Educated to HNC level in relevant scientific topic or equivalent in a pharmaceutical environment.

• Experience of Pharmaceutical/Clinical Trials Packaging and GMP Processes.

• Excellent verbal/written communication skills.

• A high level of concentration and a good eye for detail is essential.

• The ability to be decisive when required on material/product quality issues to ensure compliance.

Benefits:

• Annual Salary

• Pension

• Life Assurance

• Bupa Healthcare

• Opportunities to join Employee Resource groups and be involved in charity events.

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 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 DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability.