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 Data Intelligence and 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 Mechanical Engineer on a 6-month fixed term basis. This is a key role, working with the wider team to complete engineering tasks and projects across all Worthing facilities.

You will have previous experience in an Engineering role within a GMP environment. Experience within Steriles Manufacturing would also be beneficial but not essential.

You will be able to work to targets and deadlines and be able to work with stakeholders at all levels.

We are looking for someone who can demonstrate broad skills and knowledge across engineering function processes.

You will be involved in the following:

• Working collaboratively with other Engineers, Team Leaders / Supervisors / Managers within the business to ensure operational demands are met and a consistent approach is taken across all areas
• Ensuring all Maximo Work Orders are raised, actioned, and completed / closed in a timely manner
• Ensuring all related actions for Change requests, Deviations, NC’s, CAPA’s and Protocols are raised and closed out in a timely manner
• Raising and managing purchase requisitions and invoices for Engineering works and Engineering Stock control
• Managing Engineering Stock with the Engineering Team Leaders to ensure no out of stocks whilst maintaining good budget compliance
• Assisting in the delivery of Engineering projects as required
• Supporting the delivery of new product launches and clinical trial material for the business
• Providing back up to all trade groups and be able to undertake electrical / instrument / mechanical repairs as required
• Participating in both major and minor projects to their successful completion, to complete relevant documentation and ensure validation to the correct standards before ensuring a smooth handover to trades and production

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 QC Chemistry Scientist Level III to work as part of the team delivering QC testing activities.

You will have a relevant degree in a Science related subject and have gained significant pharma lab experience. Experience in leading non-conformances and/or out of specification investigations is also essential.

We would welcome applications from candidates with experience in HPLC and/or Raw Material (Pharmacopoeia) testing and those who have experience of training other team members. Experience performing department self-inspections would also be beneficial.

You will be involved in the following:

• Performing routine analytical testing on raw and source materials following Pharmacopoeia
• 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
• Ensuring analysis is performed in according with SOPs, Good Quality Control Lab Practice (GQCLP) and Good Manufacturing Practice (GMP)
• Acting as a 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 and reporting assay and product trending
• To undertake 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
• Supporting projects run by Stability, Science or Process Improvement as requested

Please note that this role is based on-site in Worthing.

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 9-month fixed term contract role, based onsite in Worthing.

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 have an exciting opportunity for a QA Operations Officer to provide operational quality guidance and support for warehousing, manufacturing, production, inspection, labelling, packaging and despatch operations across our Worthing sites.

You will be an experienced Quality professional with at least 2 years’ experience in a Pharmaceutical Manufacturing, Testing or QA environment.

You will have experience in the application of GxP regulations and guidance and be comfortable working with a number of stakeholders. You will have a strong working knowledge of Annex 1 and it’s application to aseptic manufacture.

You will be an experienced auditor and have the ability to write technical reports.

You will be involved in the following:

• Promoting compliance with GMP/GDP as instructed by management, the Quality department, or as per the current Regulations and Guidance applicable
• Supporting compliance with GCP regulations as required
• Undertaking compliance spot checks in the area(s), including review of CCTV (where applicable)
• Providing support and guidance for compliance improvement projects / continuous improvement
• Undertaking early review of documentation and records in order to ensure ‘right first time’ (RFT) batch reviews
• Providing support for Non-Conformance / Complaint / OOx investigations (including GEMBA)
• Providing support for CAPA actions and Change Control actions
• Providing support for Risk Assessments
• Supporting the self-inspection / Internal Audit schedule in the area(s)
• Providing support for shutdowns and new equipment, e.g. validation review, snagging, and GxP advice and guidance
• Being the link between the Operations team and the Batch Release team

We are looking for a Health, Safety & Environmental Advisor to be responsible for ensuring compliance with health, safety, and environmental regulations, promoting a culture of safety, and minimizing risks associated with our operations. This role involves conducting regular safety audits, providing training, and collaborating with various departments to enhance safety performance.

You will have experience in a similar role. Experience within pharmaceuticals would be beneficial but other technical backgrounds would also be relevant.

We are looking for someone with strong knowledge of HSE regulations and best practice as well as proficiency in using HSE management software.

You will be a confident communicator with the ability to conduct thorough investigations and risk assessments. The role will also involve training so you must be experienced in delivering key HSE training to groups of people.

You will be involved in the following:

• Delivering induction training for all new staff and contractors
• Developing, implementing, and maintaining HSE policies and procedures
• Conducting regular inspections and audits to ensure compliance with safety regulations and industry standards
• Providing training and support to employees on HSE best practices and safety protocols
• Investigating incidents and accidents to identify root causes and recommend corrective actions
• Collaborating with management to promote a culture of safety within the organisation
• Conducting risk assessments and develop strategies to mitigate identified risks
• Ensuring compliance with all relevant health, safety, and environmental legislation
• Preparing and presenting reports on HSE activities and performance to senior management
• Staying up to date with new legislation and industry developments affecting the pharmaceutical sector