Document Controller
Oxford Biomedica
Date: 5 days ago
City: Oxford
Contract type: Full time
We want you to feel inspired every day. We’re future-focused and our business is growing. We succeed together through passion, commitment and teamwork, and so can you.
We are currently recruiting for a Document Controller to join the Quality Assurance team. The purpose of this role is to provide GxP documentation to support manufacturing, research and validation activities whilst ensuring maintenance of Document Control systems across the business.
Oxford Biomedica’s Quality Assurance (QA) team is responsible for the company’s quality processes and systems, in compliance with GMP guidelines. The team are accountable for internal and external audits, quality compliance and control.
Your responsibilities in this role would be:
Oxford Biomedica is a quality and innovation-led viral vector CDMO (Contract Development and Manufacturing Organization) with a mission to enable its clients to deliver life changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, we have more than 25 years of experience in viral vectors; the driving force behind the majority of gene therapies.
Oxford Biomedica collaborates with some of the world’s most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno-associated virus, and adenoviral vectors. Oxford Biomedica’s world-class capabilities span from early-stage development to commercialisation. These capabilities are supported by robust quality-assurance systems, analytical methods, and depth of regulatory expertise.
What’s in it for you:
Collaborate. Contribute. Change lives
We are currently recruiting for a Document Controller to join the Quality Assurance team. The purpose of this role is to provide GxP documentation to support manufacturing, research and validation activities whilst ensuring maintenance of Document Control systems across the business.
Oxford Biomedica’s Quality Assurance (QA) team is responsible for the company’s quality processes and systems, in compliance with GMP guidelines. The team are accountable for internal and external audits, quality compliance and control.
Your responsibilities in this role would be:
- Provide working copies and controlled copies of paper documents such as batch records, logbooks and labels for numerous company functions such as the Manufacturing department.
- Maintenance of current documentation in the electronic document management system and paper based filing system.
- Provide administration support for the electronic document management system and troubleshooting for document writing.
- Preparation of documentation for the offsite archive and recall documents upon request.
- Maintenance of stationery stock.
- Participate in continuous improvement initiatives to enhance working practices.
- QA Administrative departmental support.
- A level of English and Mathematics and ideally Science preferably to A Level.
- Proficient in Microsoft Office Word, Excel, Outlook and Powerpoint
- An understanding and GMP or GXP and pharmaceutical industry QA / Documentation is preferred.
- The ability to prioritise daily workload in order to meet deadlines.
- Able to work on own initiative.
- Demonstrate a good attention to detail.
Oxford Biomedica is a quality and innovation-led viral vector CDMO (Contract Development and Manufacturing Organization) with a mission to enable its clients to deliver life changing therapies to patients around the world. One of the original pioneers in cell and gene therapy, we have more than 25 years of experience in viral vectors; the driving force behind the majority of gene therapies.
Oxford Biomedica collaborates with some of the world’s most innovative pharmaceutical and biotechnology companies, providing viral vector development and manufacturing expertise in lentivirus, adeno-associated virus, and adenoviral vectors. Oxford Biomedica’s world-class capabilities span from early-stage development to commercialisation. These capabilities are supported by robust quality-assurance systems, analytical methods, and depth of regulatory expertise.
What’s in it for you:
- Highly total reward packages
- Wellbeing programmes
- Development opportunities
- Welcoming, friendly, supportive colleagues
- A diverse and inclusive working environment
- Our values are: Deliver Innovation, Be Inspiring and Have Integrity
- State of the art laboratory and manufacturing facilities
Collaborate. Contribute. Change lives
How to apply
To apply for this job you need to authorize on our website. If you don't have an account yet, please register.
Post a resumeSimilar jobs
Scientist III, Product Feasibility Group - 12 Months Maternity Cover
Oxford Biomedica,
Oxford
4 days ago
We are at the centre of the rapidly growing cell and gene therapy sector. We deliver life-changing therapies to patients, and so can you. We are currently recruiting for a Scientist III to join the Product Feasibility Team within Process Development. The purpose of this role is to execute and report laboratory-based experiments and analytical investigations to support early client...
Flight Dynamics Engineer
Holt Executive Ltd,
Oxford
5 days ago
Holt Executive are currently partnered with a global leader in Space Sustainability, a dynamic and rapidly growing technology innovator who are making hugely positive contributions to tackle the growing problem of orbital space debris.They require a Flight Dynamics Engineer to bring robust, innovative concepts into the trajectory planning and optimization processes, whilst developing relative orbit determination mechanisms, streamlining the operational...
Data and Information Resources Acquisition Specialist - 29740
Environment Agency,
Oxford
1 week ago
Job DescriptionAt the Environment Agency we aspire for inclusivity to thrive in our workforce. We embrace equal opportunities and flexible work arrangements, ensuring everyone can contribute and succeed.We are looking for a motivated, self-starter to help us: Manage the renewal, contracts and supplier management for some of the Information Resources we subscribe to, e.g. Science Direct. Ensure information library subject...