Our Swindon facility houses our Zydis® fast dissolving tablet development and manufacturing operation as well as a CMC pharmaceutical analytical lab services unit that offers ASAP stability.

Position Summary

We have an opportunity for a QC Scientist 1 to join our team. In this role, you will perform finished product quality control release testing under supervision using a range of analytical techniques. You will support stability and process validation testing, ensuring compliance with GMP standards and accurate documentation. This position offers the chance to work in a dynamic laboratory environment, contributing to the delivery of high-quality pharmaceutical products.

Shift: Monday - Friday 37.5 hours per week.
Location: Swindon, UK
100% Onsite

The Role

• Perform finished product QC release testing under supervision using techniques such as balances, pH meter, UV, Karl Fischer, FT-IR, TLC, and dissolution.
• Conduct analytical testing for stability and process validation following test plans, with guidance as needed.
• Use LIMS for data entry and Qumas for document access.
• Follow written instructions accurately, maintaining minimal method deviations.
• Deliver consistent analytical output with acceptable Right First Time (RFT) performance in notebooks and testing.
• Manage daily tasks with supervision, including interpreting product tracking sheets, identifying correct specifications, and completing work within set timeframes.
• Recognize out-of-specification results and understand out-of-trend procedures.
• Participate in lab rotas and support ordering via VMI and Kanban systems.
• Maintain lab cleanliness and organization in line with 5S principles.
• Comply with GMP standards, including documentation and Compliancewire tasks.
• Adhere to EH&S protocols, raise SOSs, and follow Risk & COSHH assessments.

The Candidate

Minimum Requirements

• Knowledge of High-Performance Liquid Chromatography (HPLC).
• Degree in a scientific subject or equivalent technical knowledge.

Preferred Skills & Background

• Ability to work independently and collaboratively in a team environment.
• Strong attention to detail and commitment to data integrity.
• Knowledge of Good Manufacturing Practice (GMP).

Why You Should Join Catalent

• Our Swindon facility houses our Zydis® fast dissolving tablet development and manufacturing operation as well as a CMC pharmaceutical analytical lab services unit that offers ASAP stability.
• Competitive Salary – Reflecting your experience and skills.
• Bonus & Benefits – Includes a site performance bonus, a pension scheme matching up to 8% and life assurance. Enjoy a generous holiday entitlement that increases with tenure, with the option to purchase additional leave. Plus, gain access to Reward Gateway, offering discounts at many national retailers.
• Career Development – Access high-quality training, mentoring, and cross-functional opportunities within Catalent’s global network. Benefit from a subscription to LinkedIn Learning, providing access to 10,000+ online courses.
• Health & Wellbeing – Includes an employee assistance programme, on-site canteen facilities, and an active safety and “Patient First” culture. Take advantage of a Cycle to Work Scheme and an Electric Vehicle car scheme.
• Excellent Location – Just a two-minute drive from J16 of the M4, with free on-site parking.

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. 

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

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 [email protected]. 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.