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

This is a site-based role, working on a rotating shift basis of week 1: 6am - 2pm, week 2: 10am - 6pm and week 3: 2pm - 10pm. 

We are looking for an experienced QC Microbiology Scientist to work as part of the team delivering QC testing activities with a particular focus on Environmental Monitoring (~70% of the role).

You will have a relevant Microbiology related qualification and have gained practical microbiology experience within a lab.

The role has a GMP focus and you must be comfortable with changing priorities whilst maintaining lab compliance at all times.

You will be involved in the following:

• Performing environmental monitoring of the Classified Areas to support manufacturing
• Performing routine analytical testing on raw and source materials following Pharmacopeia
• Preparing and testing samples in support of in process monitoring for production
• Preparing reagents and solutions for use in analysis
• Performing routine analytical testing of finished products for the purposes of release in accordance with the standard analytical methods and the weekly test schedule
• Performing any additional analysis in support of development projects or as part of investigations for out of specifications/out of expectations
• Entering data onto the LIMS system
• Acting as checker for analyst methods and test results and validate in LIMS

Laboratory support

• Supporting and training colleagues in analytical methods as required
• Assisting with laboratory equipment validation
• Assisting with investigation of OOS and deviations after undertaking the appropriate training
• Appropriately raising and reporting any potential or confirmed OOS and deviations and notify the relevant departments
• Undertaking and completing tasks such as Root Cause Analysis, NC report writing or laboratory Hypothesis investigation in order to determine a suitable root cause for a deviation or OOS (if applicable)
• Performing bench freeze on all carried out analysis/testing
• Performing and reporting assay and product trending
• Undertaking the drafting, completion and checking of SAMs, risk assessments or SOPs as and when required, which aid in the training of personnel in the laboratory
• Liaising with various departments within the company, such as Production and Planning to deliver updates on testing and raise any concerns or issues that arise that may affect scheduling and product release

This is a site based role, working on a shift basis. The shift options are fixed lates (2pm - 10pm Monday to Friday) or a rotating shift of week 1: 6am - 2pm and week 2: 2pm - 10pm. Please indicate when applying which shift is your preference. 

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

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

We are looking for people with experience within a technical/production environment 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 can improve your skills and grow a career with us.

The working hours are 37.5 per week on a shift base system, with paid overtime available during busy periods.

We have 2 shifts that we are currently recruiting for:

Late shift of 14:00 to 22:00 (Monday to Friday) and

Rotating shift (06:00 – 14:00 week 1, 14:00 – 22:00 Week 2)

Our minimum starting salary is £26,230 - £27,230 with the potential to earn £29,230 to £30,230 within 3-6 months subject to successful sterile training. We also have a shift premium of 15% for working the above shifts.

We are currently recruiting a Packaging (Inspection, Labelling and Packaging) Manager to lead the function. You will be responsible for ensuring compliant, safe and efficient processing of our products to our patients.

This is a 37.5 hour per week role, working Monday to Friday 7am – 3pm, based onsite in Worthing.

We are looking for someone who has a strong background in a similar Inspection/Packaging leadership role in the pharmaceutical industry.

We would really like to hear from candidates who also have experience in Sterile Manufacturing processes.

You will have a GMP background and be a strong leader, able to drive change and efficiencies by using lean principles such as Visual Management, 5S and Standard Work.

You will be involved in the following:

Sterile Product Inspection & Operational Oversight

• Oversee the inspection, labelling and packaging of all products, with particular responsibility for compliant inspection of sterile products
• Ensure sterile inspection activities are performed by trained personnel using controlled environments and appropriate visual standards
• Monitor operational performance, addressing risks to product quality and patient safety

Leadership & People Management

• Lead, motivate and manage the ILP team
• Develop training and education plans and support multi‑skilling across the team

Production Planning & Delivery

• Plan, organise and publish working schedules to meet customer delivery dates while maintaining GMP standards
• Coordinate packaging schedules and resources using S&OP data

Continuous Improvement & Lean Leadership

• Identify and implement new and efficient ways of working to improve time, cost, labour, safety and quality
• Embed Lean principles such as Visual Management, 5S and Standard Work

We are currently recruiting for a Team Leader for our Aqueous Production area, covering our late shift of 14:00 to 22:00 (Monday to Friday).

The salary for this role is £37,000 per annum with a 15 % shift premium – totalling £42,550 per annum.

We are looking for a proactive leader who has worked within a Production team or in either a scientific role or within another technical discipline. Any experience of working within a GMP environment would be beneficial but not essential.

You will work well with colleagues and stakeholders and maintain a consistent and high performing operation.

We are looking for strong people skills and someone who can work in a fast-paced environment with changing priorities.

You will be part of a fantastic team and part of a company who aim to transform patients’ lives and the lives of those around them. Working as part of an innovative team, we can offer opportunities to develop your skills and grow your future career with us.

The role will involve:

• Ensuring adherence to company policies, procedures and system in accordance with the MHRA and HS&E standards and guidelines.
• Leading, motivating, and managing a teamwhile demonstrating leadership and maintaining high morale
• Fostering a positive “can do” attitude within the team and drive forward initiatives as requested by management
• Delivering Dispensary, Stock Solutions and MATA schedules, as required by demand, whilst maintaining GMP requirements.
• Prioritising tasks effectively, organise and manage working schedules to ensure customer delivery dates are met whilst maintaining GMP requirements
• Developing formal training and education plans for all individuals within the team
• Ensuring multi skilling of team members through cross team working
• Monitoring and managing Change Requests, Non-Conformances, and Protocol Deviations, ensuring timely resolution.
• Working collaboratively with other Team Leaders/Supervisors/Managers within ATL to ensure consistency across all areas and meet business needs
• Delivering production area and manufacturing projects under the management of Primary Production Manager
• Continuously striving for time/cost/labour reductions, and process improvements, including safety and quality enhancements