Career vacancies

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 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 looking for a qualified electrical engineer (NVQ in electrical installation, 18th edition wiring regulations and their test and inspect 2391,2392 or 2394/5 (or equivalent) qualification) who ideally has experience of working within a cleanroom/pharma environment (we would be happy to receive applications from candidates from other regulated backgrounds).

You will have demonstrable commercial electrical experience in a range of work, including installations, remedial work and test and inspections of electrical installations.

The role

You will be involved in the following:

• Completing all planned and unplanned maintenance activities, adhering to HSE rules (permits to work, pre‑work risk assessments, method statements, and PPE as required)
• Taking responsibility for all site Portable Appliance Testing
• Taking responsibility for electrical installation and condition reporting
• Supporting all departments in delivering a professional and safe maintenance and repair service, keeping them updated on progress and plans
• Ensuring all electrical emergencies are responded to quickly and efficiently
• Completing daily plant checks for all facilities, including the Energy Centre
• Participating in both major and minor projects through to successful completion, ensuring all relevant documentation is completed, and validation meets the correct standards before handing over to trades and production
• Working collaboratively with other Engineers and Validation/Production Team Leaders/Managers to ensure operational demands are met and a consistent approach is taken across all areas
• Ensuring appropriate SOPs are in place for electrical engineering activities, kept up to date with statutory and regulatory guidance, and written to provide clear work instructions
• Undertaking on‑call duties to cover breakdowns outside normal working hours

We are increasing capacity at our Worthing site which is our primary site for the manufacture and testing of our products, and we are hiring for  additional team members in our Packaging department.

The salary on this role is £26,230 per annum.

We would be keen to hear from candidate who have experience in a Packaging environment. An eye for detail is really important as you will be inspecting products before they are packaged for our patients.

You will be comfortable working in a team and have a proactive approach to your work, with a real customer focus.

The working hours are 37.5 per week with paid overtime available during busy periods.

You will be involved in:

• Working to daily inspection, labelling and packaging schedules
• Performing line clearances at the beginning and end of a task
• Confirming all products and packaging delivered to the line are checked for correct batch number and product
• Reconciling stock received, stock output and any rejects
• Performing manual and semi-automated inspection of vials and syringes
• Performing manual and semi-automated labelling of vials and syringes
• Performing manual packaging
• Ensuring all inspection, labelling and packaging activities are carried out in a GMP compliant manner
• Completing all necessary documentation to GMP standards
• Assisting with stock checks and stock control
• Ensuring all ILP materials are scrapped in line with procedures
• Preparing and collecting work for the ILP team to pack