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 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.

We are looking for a Team Leader in our Sterile services team to supervise a team of Services technicians on shift as well as an evening cleaning team. This includes the direct recruitment, resourcing, development and performance of all team members to ensure that standards are always achieved.

The Services team is split into 5 sections: Component Preparation, Van Duties, Clean Suite Servicing, Equipment Preparation & Cleaning.

Please note that this role is offered on a rotating shift basis (week 1: 6.00am – 2.00pm/week 2: 1.00pm – 9.00pm) with a 15% shift premium included.

You will have experience managing a team of people ideally in a similar role although we would consider applications from those who have management experience in a transferable sector.

You will have experience of working in a GMP environment and be able to apply these to what you do consistently and ensure that your team do the same.

You will be involved in the following:

• Ensuring the completion of all Sterile Services duties are carried out effectively
• Co –managing recruitment requirements and headcount for the team
• Managing team absence in accordance with the Company Absence Procedure
• Deputising for Sterile Services Manager as and when required
• Working collaboratively with other Team Leaders/Supervisors/Managers within ATL to ensure business needs are met and a consistent approach is taken across all areas
• Ensuring management of all waste streams are upheld
• Developing formal training and development plans for all individuals within the team
• Ensuring any Change Requests/Non-Conformances/CAPAs and Protocol Deviations are raised and closed out in a timely manner