Allergy Therapeutics offers a wide range of career opportunities.

If you’d like to join our team of fanastic people who are passionate in our ambition to transform lives through the extraordinary ideas we develop and bring to market, please get in touch.

All queries and applications should be sent by email to;

Please send us an email with your CV attached and details of the role you are looking to apply for.

If you would like to learn more about us, head over to our careers areas to find out more about each area of our business area.

As an equal opportunities employer we welcome applications from anyone with the skills, experience and commitment to succeed.

Recruitment Agencies 

We do work with a number of key agency partners but we are not looking to extend our Preferred Supplier List at this time. If you would like to be considered in the future, please use the email address above to send your details through to us.

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.