Career vacancies

We are looking for Production Technicians to work across a number of our Production Teams.

These are key roles, where you will positively affect the lives of our patients.

You will assist with the manufacture of our patient products. This includes vial collation, set up, updating our systems, completing batch documentation and manufacturing across our Grade A, B and C sterile areas.

You will work in a clean room environment so you must be comfortable in this environment, all Personal Protective Equipment (PPE) will be supplied.

You will be involved with the following:

• Manufacturing batches to time and GMP standards
• Transferring batches out of the clean suites
• Undertaking weekly stock checks for filling consumables
• Completing batch records
• Carry out clean down procedures prior and post manufacturing
• Removing expired stock from clean suite in line with procedures

For all roles you must be able to work between 7am – 3pm Monday to Friday at our site in Dominion Way, Worthing and also be able to demonstrate flexibility to adjust hours during our busy periods (overtime payments would apply for any additional hours worked)

We are looking for people with experience in a Production role and any experience gained in a GMP environment would also be a real bonus!

You will be dexterous and have a good eye for detail.  Full training will be provided.

We are looking for real team players who can demonstrate the skills and qualities for this role.

You will be part of a fantastic team and part of a company who aim to improve the lives of our patients!  You will also have the opportunity to improve your skills and grow your career.

We’re looking for a proactive and detail-oriented Analytical Method Development Scientist to join our dynamic team for a 10-month fixed term contract.

We are looking for someone with strong expertise in method development and validation (HPLC, GC, wet chemistry and general biochemical knowledge).

You will have experience of the application of ICH Q2 guidelines and regulatory requirements in method development and validation within the pharmaceutical industry.

You will have strong analytical and problem-solving skills with a hands-on approach, bringing a professional, adaptable, and team-oriented mindset.

You will be involved in the following:

• Developing and validating analytical methods in line with ICH Q2 guidelines and familiarised with other guidelines
• Utilizing advanced analytical instrumentation for method development and troubleshooting
• Solving complex analytical problems with a proactive and solution-driven approach
• Ensuring high-quality data generation and regulatory compliance
• Collaborating across teams to drive innovation and continuous improvement

We are looking for a Sterile Services Cleaner to join our team, providing key cleaning services to our sites in Worthing.

You will have previous experience in a similar role and whilst experience in a clean room environment would be beneficial this is not essential as long as you are willing to be trained in these areas.

You will take pride in what you do and work methodically, paying attention to the detail.

We are looking for a team player who is comfortable working in a sterile gowning environment.

You will be involved in the following:

• Ensuring that all classified areas in both buildings are cleaned and disinfected each day
• Completing any special daily cleaning requirements and record in logbook
• Assisting in ensuring equipment, laundry and consumables are available to all Production areas
• Carrying out the transfer process in Noon Grade C and B areas.
• Operating or emptying Autoclaves, VHPs and Oven chambers.
• Carrying out cleaning activities in a compliant manner
• Completing all necessary documentation to appropriate standards
• Ensuring end of day checks are carried out

This role is part time, working 20 hours per week (Monday – Friday 5pm – 9pm), the annual salary is £13,104 (£24,570 Full Time Equivalent) + 15% shift premium

We are looking for a Production Document Coordinator who will be responsible for managing and controlling the flow of the department’s batch records and controlled documents.

The Production Document Coordinator will act as the Data Integrity Subject Matter Expert (SME) for Production, ensuring compliance of documentation associated with Production.

We are looking for someone who has experience of document management as well as report writing.

You will have excellent attention to detail and be confident working alongside stakeholders at all levels.

Experience in data integrity and non-conformance investigations would be beneficial although not essential.

You will be involved in the following:

• Ensuring timely, accurate, and complete review of Production batch records for delivery to QA Release
• Managing the control of documents in and out of Production, including SOPs, Work Instructions, Batch Records, and Controlled Forms including introduction of new documents, management of changes and periodic reviews.
• Maintaining up to date knowledge of current data integrity (DI) practices
• Completing DI assessments for Production
• Conducting periodic reviews of Production documentation to maintain compliance
• Completing GMP and GDocP training, and maintain trained status
• Supporting the Production Team Leaders in the completion of non-conformances and CAPAs

This is a site-based role.