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 are looking for a Services Technician to provide a key role in preparing components and equipment and ensuring all orders are sterilised and ready for production manufacturing processes.

There will also be requirements for technician to be involved with critical cleaning and disinfecting activities as well as movement of goods between buildings in a company van.

Candidate must be happy working in a small team within production areas, this will include working within a clean room environment and there will also be an element of heavy lifting so you must be comfortable with this.

A clean driver’s licence must be held to drive the company van.

You will be involved in the following:

• Completion of work requests to meet production demand.
• Operate machinery to sterilise/sanitise equipment.
• Cleaning and disinfecting our grade A/B and C areas.
• Managing consumable stock levels around production areas.
• Ensuring all activities are carried out in a GMP compliant manner

There is a requirement to be fully gowned for part of the shift so you must be comfortable working in these conditions.

This role is offered on a rotating shift basis (1 week will be 6.00am – 2.00pm with the following week 1.00pm – 9.00pm) and the salary is £24,570 per annum + 15% shift premium.

We are looking for a Production Compliance Lead to be the key point of contact for the Production teams with regards compliance activities. Responsible for developing, implementing, and maintaining compliance standards to meet expectations within the relevant Production department.

This is a site based role.

You will have experience in a GMP Production role as well as experience of root cause analysis.

We are looking for a real team player who is happy working with stakeholders from different areas with excellent communication skills.

You will be able to demonstrate strong analytical and problem-solving skills.

You will be involved in the following:

Quality Management System

• Participating in the development and maintenance of departmental SOPs to support the operations
• Acting as Lead Investigator for departmental non-conformances and complaint investigations, working across the teams to ensure effective root cause analysis identified in timely manner
• Delivering Corrective and Preventive Actions (CAPA) and Effectiveness Checks to agreed deadlines
• Take ownership of change control for department
• Author, implement and manage lifecycle of Protocols and Method Statements

Audits and Inspections

• Act as key contributor to departmental Inspection Readiness program
• Ensure team compliance to Plan Do Check Act (PDCA) cycle

Risk Management

• Identify and assess potential compliance risks within the teams
• Support local risk management process

Regulatory Compliance

• Collaborate with cross-functional teams to interpret and implement regulatory requirements effectively
• Work with Operational Quality, Sterility Assurance and Production Teams to ensure best practice embedded within team both procedurally and culturally.

Training

• Work with Production SMEs to ensure departmental SOPs are maintained in line with current and best practice.

Continuous Improvement

• Contribute to departmental program of Continuous Improvement including 5S and other Lean initiatives as appropriate.

We’re looking for a proactive and detail-oriented Analytical Method Development Scientist to join our dynamic team for a 12-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 an Intellectual Property & Patent Clerk to take responsibility for administration and oversight of key documentation underpinning the R&D product lifecycle across all functions. This includes but is not limited to Patent protection, Data integrity for external use including scientific, regulatory and commercial.

You will have previous experience of Intellectual Property systems and processes as well as experience of pharmaceutical product development and route to CTA, MAA or BLA.

You will have a degree in life sciences, engineering or business administration and any further qualification in Project Management would be beneficial, although not essential.

You will be a confident communicator, able to work with stakeholders at all levels both internally and externally and ideally with experience working in a matrix organisation.

You will be involved in the following:

• Supporting the development and management of the Company’s intellectual property strategy in R&D
• Managing communications with outside counsel for IP matters.
• Reviewing papers, posters and other communications in conjunction with R&D to remove confidential data
• Collating and presenting knowledge of competitor IP, due diligence and freedom to operate opinions with outside counsel
• Enabling efficient collaboration with others cross-functionally to collectively advance product development plans toward securing future IP
• Work with project sponsors and the R&D Project managers with the initiation, updating and management of all Project plans to ensure IP considerations are captured
• Coordinating and presenting project progress by supporting agreed timelines for core teams in liaison with other departments and clients, ensuring that milestones are achieved and budgets are upheld
• Supporting with the Identification and tracking of project risks, issues, assumptions, and decisions so the project sponsor can escalate
• Assisting in the leading of internal and client communications/meetings, ensuring meetings are organized, recording of meeting minutes, tracking action items, preparing meeting agendas, project team activities/actions and disseminating project information
• Actively participating in the development and the consistent application of R&D Project management systems and tools (SharePoint, Roadmap, TPP, PDP)
• Working as an active member of the R&D Project Management team, participate in regular Project Management functional meetings
• Assisting R&D Project Managers in execution of project management training initiative across R&D

This is a remote role.

We are looking for a Junior Infrastructure Engineer who will provide 3^rd line Technical Support to the business and manage project deliverables in line with project plans.  The role is responsible for supporting both the functional and operational efficiency of the IT department and business.

This is a 12-month fixed term hybrid role so you must be able to commute to Worthing.

We are looking for someone who has experience performing some system administration functions within a corporate environment.

You will have a good understanding of Active Directory administration and an excellent working knowledge of ServiceNow.

You must have excellent troubleshooting skills with ability to troubleshoot Windows 10 enterprise workstation and Windows Server platform 2012/2016/2019/2022.

You will be involved in:

Infrastructure Projects

• Completing individual project deliverables within time scales set in the project plan
• Providing expertise while working with users to establish and meet business needs. Ensuring the correct application of operational procedures
• Providing technical solutions to Business requirements
• Contributing to the development of appropriate system architectures in specific business, infrastructure or functional areas, selecting appropriately from predictive (plan-driven) approaches or adaptive (iterative/agile) approaches
• Implementing agreed infrastructure changes and maintenance routines
• Providing advice and guidance on the application and operation of physical, procedural and technical security controls

Infrastructure Maintenance

• Identifying operational problems and contributes to their resolution and managed in accordance with agreed standards and procedures
• Ensuring daily/weekly/monthly infrastructure maintenance checks are completed
• Ensuring system security is always maintained

We are looking for an Inspection, Labelling & Packaging (ILP) Team Leader who will managing and leading a team.

We are looking for someone who has experience of managing a team, who is able to lead and motivate. You will have experience of GMP and have worked in a packaging/inspection role previously.

The role involves:

• Leading, motivating, and managing a team; demonstrating leadership and maintaining high morale
• Fostering a positive “can do” attitude within the team and driving forward initiatives as requested by management
• Developing formal training and education plans for all individuals within the team
• Ensuring team members are trained and work compliantly to all relevant SOPs
• Ensuring appropriate SOPs are in place, up to date, and accurately map the processes they detail
• Monitoring and managing Change Requests, Non-Conformances, and Protocol Deviations, ensuring timely resolution
• Maintaining data integrity assessments and oversee the completion of Non Conformance reports, CAPAs, and effectiveness checks
• Prioritising tasks and managing working schedules to ensure customer delivery dates are met while maintaining GMP requirements
• Continuously striving for time/cost/labour reductions and process improvements, including safety and quality enhancements
• Developing, implementing, and continuously improving ILP processes according to lean principles such as Visual Management, 5S, and Standard Work

This is a site based role.