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 have an exciting opportunity for a Head of Quality Assurance. This is a newly created role as part of our newly created Senior Quality Leadership Team. You will own and drive the site quality improvement agenda. You will be the decision maker for the function with autonomy to make operational decisions.

You will manage the Batch Release, Quality Systems and GMP training teams.

You will be an experienced QA professional with substantial experience leading teams in an operational quality environment (of which a significant amount should include managing QA teams) and you will be able to demonstrate strong leadership, coaching and influencing skills.

We are looking for someone with in depth experience across multiple quality systems who is able to lead multiple quality improvement activities within cross functional teams, as well as the ability to advise and act on complex quality issues – e.g. business processes, root cause analysis, document control and traceability.

You will be able to demonstrate good foundational knowledge and understanding of current UK and EU GMP standards and regulations as well as experience of fronting multiple Health Authority inspections and internal audits.

Practical experience (ideally from aseptic manufacturing) as well as the ability to influence decision making and working collaboratively with peers and other key stakeholders is also key.

Experience with electronic QMS systems would also be really beneficial.

You will be involved in the following:

• Defining and driving the vision and strategy for the site QA function
• Being accountable for the performance of the Quality Assurance function; responsible for setting the quality standards, targets, measures, and has oversight for the provision of the metrics
• Ensuring all products, processes and operations within the Worthing site are fit for purpose, adhere to relevant regulatory requirements and match the Company’s marketing commitments
• Being accountable for ensuring that the function signs off accurate and fit for purpose Deviation/Complaint investigations to identify root cause and establish appropriate actions
• Ensuring the PQS meets the requirements of the licences, and current standards, legislation and guidance and directs the site in the use of the PQS and where required supports the development and implementation of the electronic QMS
• Leading Quality Council and Change Management forums, and (where required) escalation of adverse trends/metrics/performance to the Executive
• Driving ownership for delivered quality and compliance and ensures all QA processes are lean and efficient through use of performance management tools
• Playing a lead role in support of audits/inspections by customers, internal auditors and external regulatory bodies. Ensure the QA function and site is continually inspection ready and supports development of site CAPA and responses
• Developing and improving the site processes for Document Control and Training
• Reviewing and approval of reports, procedures, policies, critical and major non-conformances, complaints (etc) as required and determines the acceptability of data
• Supporting reviews / compilation of reports in support of PQR’s, MAA or BLA
• Leading the Quality Assurance teams, ensuring high levels of team and personal engagement and leading the teams through change
• Owning budget adherence and cost control measures as appropriate
• Leading complex initiatives outside the Quality Unit duties and at a site level to meet business strategy
• Developing talent through coaching and mentoring
• Ensuring that an effective system for continuous improvement is maintained across the company and its operation meets with regulatory and customer expectations

We are looking for a Senior QA Release Officer to provide quality guidance and support for manufacturing, production and packaging operations.  As part of the role you will release products manufactured under our Specials License.  The role also acts as the point of contact cross functionally with regard to quality release questions, providing support for external GMP requirements and providing data integrity support.

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 (in line with regulations). This experience will ideally have been gained in a steriles manufacturing environment.

You will be a confident communicator who is calm under pressure and comfortable working with a number of stakeholders.

We are looking for someone who can provide guidance for the team and also work closely with the QA Manager to support GMP compliance.

You will be involved in the following:

• Reviewing and releasing of products manufactured under our Specials License
• Ensuring timely review of all bulk, finished product and specifics batch documentation for QP release
• Preparation of Certificate of Analysis
• Acting as the QA point of contact for cross functional queries with regards to batch release and review.
• Managing day to day workload within the team
• Acting as champion for investigations and assisting QA Manager in improving and ensuring root causes assessed adequately
• Ensuring the continued support and compliance to QA systems in terms of change control, non-conformances, customer complaints and annual product review
• Providing Quality guidance in support of site operations
• Supporting compliance with all GMP regulations as instructed by QA Manager
• Maintaining up to date knowledge of current industry practices for quality systems

This is a site based role.

We are looking for a Senior Vendor Quality Compliance Officer to lead our site Vendor Qualification process and conduct all Vendor Qualification activities.

You will already be experienced and proficient in a Vendor Qualification role and be ready to progress to the next level, bringing your experience with you to coach and develop others.

We are looking for someone who has a background in Quality Assurance who can demonstrate excellent communication skills, working with both external and internal stakeholders.

You will be responsible for the following:

• Leading the qualification of vendors in accordance with GxP requirements and corporate procedures
• Performing QA reviews for all Non GXP vendors
• Maintenance of Approved Vendor list
• Leading the full life cycle of vendor approval process, keep the VAF tracker and support the maintenance of the audit schedules
• Performing ongoing vendor qualification process
• Performing self-inspection of the team
• Providing vendor qualification data for annual product review
• Performing risk assessments for high, medium, and low risk vendors
• Reviewing and creating SOPs as appropriate
• Management of CAPAs and NCs raised from audits and internal processes
• Acting as the first point of contact for external vendors, and internal departments for vendor management enquiries
• Conducting license checks (GMP, WDA, MIA, GDP) of vendors
• Preparing/assessing TSE compliance and prepare the TSE report

Please note that this is a hybrid/homeworking role with the requirement to be on-site at least once a month. You may also be required to travel as part of this role.

We are looking for a Corporate Governance Coordinator to provide key support across a full range of governance activities and work closely with the Company Secretary, CFO (and on occasion the CEO) and Board to ensure that ATL manages its obligations in line with governance frameworks and in line with statutory and regulatory requirements.

We are looking for someone with strong administration experience, gained within a corporate environment.

We are keen to speak to people who can work autonomously and are able to demonstrate tenacity and resilience, and who can work comfortably with key stakeholders (internally and externally).

You may have experience within a different role and sector, if you are able to take information, assimilate this effectively and can show real attention to detail then we would love to hear from you

You will be involved in the following:

Company Secretarial Support

• Responsible for / provide support with collating and delivering agendas, meeting papers, board packs and minutes for all Board meetings
• Track actions arising from all Board and Committee Meetings
• Maintain Board and Committee records
• Support in the planning and coordination of key meetings
• Deal with queries from stakeholders and escalating where appropriate
• Support drafting high quality governance documents, including annual reports, policies etc
• Provide key support to the Company Secretary to deliver activities on time and to a high standard
• Provide full administration support across the governance function (e.g. updating and maintaining insider lists)
• Undertake project work as required
• Maintain annual corporate meetings calendar with key dates and topics to be presented
• Assist with the maintenance of all group companies registers (Directors, Share Registers; registered addresses and signatories)
• Support corporate transactions (as required) which includes drafting of board resolutions and circulating any supporting materials for Board members

Legal Support

• Assist in the update of Governance policies such as Our Code, Conflict of Interest, Speak up etc.
• Support as required in the following areas:
  • Corporate Governance
  • GDPR
  • Fundraising or other corporate activities
  • Litigation/claims/disputes
  • Contracts management processes

Please note that this is a hybrid role with a requirement to be on-site on an ad hoc basis

We are looking for a Laboratory Technician to work within our QC Chemistry Lab. You will provide support for a team of QC Scientists. Your main duties will include the daily setup and preparation of the laboratory for routine tasks and analytical tests, and the regular maintenance of the laboratory to ensure it is kept to the required standards and state of readiness.

You will have a relevant qualification in Chemistry and you will have some practical experience within a laboratory and, ideally, GMP environment. This could be through previous work experience or a placement opportunity gained as part of a degree course.

We are looking for a real team player who is flexible and will work closely with the QC Chemistry teams to ensure that there are zero delays in testing activity by providing excellent support to the team to deliver their activities.

This is a great opportunity for someone who is looking for a laboratory support-based role.

You will be involved in the following:

• Daily Calibration/Verification of laboratory equipment (e.g. balances, pH meters, pipettes)
• Preparation of laboratory reagents in accordance with SOP’s and SAM’s
• Management of QC Chemistry inventory (including ordering)
• Sampling of chemical and allergen raw materials, in accordance with approved procedures
• Coordination of routine external maintenance activities for QC equipment
• Receipt, booking in and management of laboratory testing samples via the LIMS system
• Organisation and disposal of laboratory waste
• Maintaining laboratory housekeeping tasks
• Maintenance of the cleanliness of laboratories (including coordination of glassware washing)
• Preparation and coordination of despatch of samples for external analysis
• Supporting the QC Admin with administrator tasks, as required

Please note that this role is based on-site. You should be able to work 7am – 3pm (with a requirement to be flexible based on business need)