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 Sterile Services Cleaner to join our team, providing key cleaning services to our sites in Worthing.

You will have previous experience in a similar role and whilst experience in a clean room environment would be beneficial this is not essential as long as you are willing to be trained in these areas.

You will take pride in what you do and work methodically, paying attention to the detail.

We are looking for team players who are comfortable working in a sterile gowning environment.

You will be involved in the following:

• Ensuring that all classified areas in both buildings are cleaned and disinfected each day
• Completing any special daily cleaning requirements and record in logbook
• Assisting in ensuring equipment, laundry and consumables are available to all Production areas
• Carrying out the transfer process in Noon Grade C and B areas.
• Operating or emptying Autoclaves, VHPs and Oven chambers.
• Carrying out cleaning activities in a compliant manner
• Completing all necessary documentation to appropriate standards
• Ensuring end of day checks are carried out

This role is part time, working 20 hours per week (Monday – Friday 5pm – 9pm), the annual salary is £12,480 + 15% shift premium

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 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
• Ensure the continued support of QA systems in terms of change control, non-conformances, customer complaints, and specifics batch release
• 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, non-conformances, customer complaints, and specifics batch release when required.

This is a full-time role, based onsite in Worthing

We are looking for a QC Chemistry Scientist Level II to work as part of the team delivering QC testing activities.

This is a weekend role working 30 hours Friday – Monday (inclusive). The salary will be equivalent to a full-time salary made up with the gross salary plus shift premium.

You will ideally have a Chemistry degree, although we would accept applications from someone with an alternative science related subject (or equivalent experience). You will have experience of working within a Chemistry lab and you will also have previous experience of working within a GMP environment.

You will be involved in the following:

• Performing QC sampling and inspection of raw and source materials
• Preparing reagents and solutions for use in analysis
• Performing routine analytical testing on raw and source materials following European Pharmacopoeia
• Preparing and testing samples in support of In-Process monitoring for production processes
• Performing routine analytical testing of finished products for the purposes of release in accordance with a wide variety of Standard Analytical Methods, for example UV-vis, Karl Fischer, Kjeldahl, HPLC and GC techniques
• Performing analytical testing of stability trials
• Performing any additional analysis in support of development projects or as part of investigations for Out of Specification results
• 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 approval in LIMS system

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 notifying 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

Please note that this is a site-based role.