Career vacancies

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

We are looking for someone with strong expertise in method development and validation of biochemistry and chemistry analytical techniques including spectroscopy, ELISA, SDS-PAGE, chromatography, GC as examples.

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

This is a site-based role

We are looking for a Sterility Assurance Officer to provide expert sterility assurance guidance and support across manufacturing, production and engineering operations at our Worthing sites.

We are looking for someone with experience in a manufacturing, testing or QA environment and you must have experience within steriles manufacturing.

You will be a confident communicator, able to provide training and guidance and raise any issues where applicable.

We are looking for someone with experience of leading quality improvement projects who is able to apply their knowledge of GxP regulations and guidance to the role.

You will be involved in the following:

• Providing support for IMP manufacture as required
• Training, supporting and advancing standards and understanding of aseptic behaviours
• Providing support and guidance for Compliance improvement projects / continuous improvement
• Promoting, encouraging and championing the good aseptic behaviours essential for the manufacture of sterile pharmaceuticals
• Leading and supporting Non-Conformance / Complaint / OOX investigations (including GEMBA and write ups)
• Providing support for CAPA actions and Change Control actions
• Providing support for Risk Assessments and Quality Risk Management projects
• Supporting and driving improvements for the Sterility Assurance program
• Compiling environmental monitoring trend reports for presentation in various reports and forums.
• Supporting the self-inspection / internal audit schedule in the area(s)
• Providing quality metrics relevant to the area(s)
• Providing support for shutdowns and new equipment, e.g. validation review, snagging, and GxP advice and guidance with a focus on Sterility Assurance
  
  

We have a vacancy for a Procurement Manager who will play a key role in managing our Purchasing Function and work with the Procurement Lead to drive the department forward for the future.

We are looking for someone who has gained some experience in a purchasing role, who has had some experience in managing or coaching others and perhaps is looking for the first step into a Procurement Manager role.

This is a key role which will help shape the future of the department and also involves some of the transactional activities so you will see the process end to end.

Experience with inventory management and contract negotiation are key as well as materials and capacity requirements.

You will be working cross functionally but also with wider external stakeholders so you must be able to demonstrate that you can build good working relationships.

You will be involved in the following:

• Working with Procurement Lead to develop the function and implement proposals
• Working with Procurement Lead to build strategic inventories to protect supply
• Working with the legal team to draft supply contracts with key suppliers
• Leading the Purchasing team to manage the vendor lifecycle and performance
• Monitoring supplier delivery and quality performance
• Monitoring and challenging new supplier introduction
• Managing change control process for the department
• Supporting the procurement strategy for new product introduction
• Leading and participating in projects related to the purchasing function as required
• Responding to supplier quality non-conformances and CAPA’s within the defined timeframe
• Working with Procurement Lead and wider stakeholders to create purchasing KPI’s and report on these as required
• Responsible for ensuring that supply is not adversely affected due to late delivery of material requirements
• Working with Procurement Lead to simplify purchasing and business systems
• Responsible for ensuring team maintains compliance with purchasing policies
• Contributing to annual budgets for cost centre and inventory
• Analysing and reporting on variances to budget

This is a hybrid role with some UK/EU travel

We are looking for a QA Release Officer to provide quality guidance and support for manufacturing, production and packaging operations.

You will be experienced within a similar role having gained this experience within a pharmaceutical manufacturing environment, with a minimum of 2 years’ experience in a GMP environment.

You will be able to manage a number of batch releases and be flexible to changing priorities.

We are looking for someone with good report writing skills who has a knowledge of basic statistical tools and methods.

You will be involved in the following:

• Ensuring timely review of all bulk, finished product and specifics batch documentation for release
• Provide Quality guidance in support of site operations
• Review of non-conformances
• Effectively manage the batch release process to ensure product is released in a timely manner
• Review production records before QP release to ensure issues are highlighted/resolved promptly
• Release of named patient products
• Perform sample receipt and review
• Generate certificates
• Complete documentation and filing activities
• Provide QA input at meetings and for projects or as and when required
• Escalate issues to the QP’s as and when required
• Provide training on QA related topics across the business as and when required
• Provide QA metrics and/or data as required
• Perform, or assist with audits as required
• Liaise with other departments to risk assess and monitor the effect of changes in processes and/or working practices
• QA preparation, review and/or issue of documents as required
• Support QA systems in terms of change control and customer complaints when required.

This is a site-based role.