About Us
Allergy Therapeutics are a market leading, pioneering immunology business with specialist experience in the research and development of allergy treatments.
We believe that transformational outcomes for patients are achieved by directly treating the cause, rather than just managing symptoms. Our vaccines are aluminium free. Driving convenience; our ultra-short course treatments make life easier and increase adherence.
Our adjuvant technologies not only advance the results of allergy immunotherapy but also drive beneficial immune responses in cancer and infectious disease.
We are a proud and passionate team with a vision that delivers growth and transforms the way we think about immunology.
We are continuing to grow and it's an exciting time to be joining us. You will contribute to our ongoing success and be part of our future which is looking very bright
You'll join a team of like-minded people who are passionate about what they do and providing positive outcomes for our patients.
We are looking for a Production Document Coordinator who will be responsible for managing and controlling the flow of the department's batch records and controlled documents.
The Production Document Coordinator will act as the Data Integrity Subject Matter Expert (SME) for Production, ensuring compliance of documentation associated with Production.
About you
We are looking for someone who has experience of document management as well as report writing.
You will have excellent attention to detail and be confident working alongside stakeholders at all levels.
Experience in data integrity and non-conformance investigations would be beneficial although not essential.
The role
You will be involved in the following:
* Ensuring timely, accurate, and complete review of Production batch records for delivery to QA Release
* Managing the control of documents in and out of Production, including SOPs, Work Instructions, Batch Records, and Controlled Forms including introduction of new documents, management of changes and periodic reviews.
* Maintaining up to date knowledge of current data integrity (DI) practices
* Completing DI assessments for Production
* Conducting periodic reviews of Production documentation to maintain compliance
* Completing GMP and GDocP training, and maintain trained status
* Supporting the Production Team Leaders in the completion of non-conformances and CAPAs
This is a site-based role.
Job Types: Full-time, Permanent
Pay: £25,570.00 per year
Benefits:
* Company pension
* Cycle to work scheme
* Free parking
* Health & wellbeing programme
* Life insurance
* On-site parking
* Private medical insurance
* Referral programme
Application question(s):
* Do you have experience in a similar role?
Work authorisation:
* United Kingdom (required)
Work Location: In person