Job Description

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. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.


We are seeking a proactive and detail-oriented

Technical Change Expert

to join our Team. This pivotal role supports the development and execution of change controls and the updating of GMP documentation--including Batch Manufacturing Records (BMR) and Artwork changes--within a defined scope. You will play a key role in driving process capability improvements and ensuring business continuity across the Supply Chain function.

The Role:

Change Management & Documentation

Develop and execute change controls, technical documentation, and artwork updates. Manage implementation of approved technical product and process changes to agreed timelines. Collaborate with cross-functional teams including R&D, Engineering, Quality, and Supply Chain.

Compliance & Safety

Ensure all technical changes comply with current GMP standards. Conduct risk assessments to ensure safety of people, processes, and equipment. Report and investigate any EH&S incidents in line with company policy.

Operational Excellence

Maintain visual systems to track project status, priorities, and timelines. Ensure timely completion of training and adherence to change control due dates. Support effective transfer of process changes into production operations.

The Candidate:

Strong numeracy, verbal, and written communication skills. Excellent problem-solving skills and attention to detail. Ability to work under pressure and meet tight deadlines. Confident communicator with the ability to engage effectively with internal and external stakeholders. Experience in a supply chain environment, preferably within pharmaceutical Background in production/operations is a plus. A technical supply chain or commercial qualification (e.g. CIPS, APICS, IOM) is advantageous. Experience in a supply chain environment, preferably within pharmaceutical or food industries. Self-starter with a passion for continuous improvement and change management.

Why You Should Join Catalent:

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 DisabilityAccommodations@catalent.com. 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.