At a Glance
- Tasks: Write GMP documentation like Batch Manufacturing Records and Standard Operating Procedures.
- Company: Join OXB, a leader in life-changing therapies and innovative viral vector solutions.
- Benefits: Enjoy competitive rewards, wellbeing programmes, and career development opportunities.
- Other info: Be part of a supportive and collaborative culture in state-of-the-art facilities.
- Why this job: Make a real impact in the biotech field while working with cutting-edge technology.
- Qualifications: Experience in GMP documentation and strong attention to detail required.
The predicted salary is between 35000 - 45000 £ per year.
At OXB, our people are at the heart of everything we do. We’re on a mission to enable life-changing therapies to reach patients around the world and we’re looking for passionate individuals who embody our core values every day: Responsible, Responsive, Resilient, and Respectful.
Your responsibilities in this role would be:
- Writing clear and concise GMP documentation such as Batch Manufacturing Records (BMRs) and Standard Operating Procedures (SOPs) to support lentiviral vector manufacturing for clinical and commercial use
- Coordinating and prioritising document creation, updates and reviews with manufacturing teams and subject matter experts to meet project timelines
- Initiating and managing document updates based on change controls and manufacturing schedules across all suites
- Ensuring consistency across GMP documents, assessing the impact of changes and escalating issues to relevant experts
- Participating in project meetings and communicating document update progress to stakeholders across departments
- Acting as subject matter expert for GMP documentation in support of manufacturing activities and regulatory audits
- Identifying and driving improvements in GMP documentation in collaboration with manufacturing teams and experts
- Maintaining high ethical standards and delivering high quality work consistently
We are looking for:
- Experience of authoring clear and concise GMP documentation such as SOPs or BMRs.
- Strong knowledge of GMP and regulatory documentation requirements.
- Competent user of MS Office applications especially MS Word.
- Attention to detail to ensure documentation is free of errors and a keen interest in scientific writing in a highly regulated field.
- Experience working with electronic document management systems and an understanding of document workflows.
About Us: OXB is a quality and innovation-led viral vector CDMO 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 30 years of experience in viral vectors; the driving force behind the majority of gene therapies. OXB 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 (AAV) and adenoviral vectors. OXB’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.
Why Join Us?
- Competitive total reward packages
- Wellbeing programmes that support your mental and physical health
- Career development opportunities to help you grow and thrive
- Supportive, inclusive, and collaborative culture
- State-of-the-art labs and manufacturing facilities
- A company that lives its values: Responsible, Responsive, Resilient, Respect
We want you to feel inspired every day. At OXB, we’re future-focused and growing fast. We succeed together through passion, commitment, and teamwork.
Ready to Make a Difference? Collaborate. Contribute. Change lives.
GMP Technical Writer in Banbury employer: Oxford BioMedica (UK) Limited
At OXB, we pride ourselves on being a leading employer in the biopharmaceutical sector, where our commitment to innovation and quality is matched by our dedication to employee wellbeing and growth. Our supportive and inclusive culture fosters collaboration and creativity, while our state-of-the-art facilities provide an inspiring environment for you to thrive. With competitive rewards, comprehensive wellbeing programmes, and ample career development opportunities, joining OXB as a GMP Technical Writer means becoming part of a mission-driven team that is making a real difference in the lives of patients worldwide.
Contact Details:
Oxford BioMedica (UK) Limited Recruitment Team
StudySmarter Expert Advice🤫
We think this is how you could land GMP Technical Writer in Banbury
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and its values. At OXB, they value being Responsible, Responsive, Resilient, and Respectful, so think about how you can demonstrate these traits during your chat.
✨Tip Number 3
Practice your answers to common interview questions, especially those related to GMP documentation. Be ready to showcase your experience with SOPs and BMRs, as well as your attention to detail.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in joining the OXB team.
We think you need these skills to ace GMP Technical Writer in Banbury
Some tips for your application 🫡
Tailor Your Application:Make sure to customise your CV and cover letter to highlight your experience with GMP documentation. Use keywords from the job description to show that you understand what we're looking for.
Showcase Your Writing Skills:Since this role is all about clear and concise writing, consider including samples of your previous work or a brief writing exercise. This will help us see your style and attention to detail.
Highlight Relevant Experience:Don’t forget to mention any specific experience you have with SOPs, BMRs, or electronic document management systems. We want to know how your background aligns with our needs!
Apply Through Our Website:For the best chance of success, make sure to apply directly through our website. It’s the easiest way for us to keep track of your application and get back to you quickly!
How to prepare for a job interview at Oxford BioMedica (UK) Limited
✨Know Your GMP Inside Out
Make sure you brush up on your knowledge of Good Manufacturing Practices (GMP) and regulatory documentation requirements. Be ready to discuss specific examples of how you've authored SOPs or BMRs in the past, as this will show your expertise and passion for the role.
✨Showcase Your Attention to Detail
During the interview, highlight your attention to detail by discussing how you ensure documentation is free of errors. You might want to share a story about a time when your meticulousness made a significant impact on a project or helped avoid potential issues.
✨Familiarise Yourself with Document Management Systems
Since experience with electronic document management systems is crucial, be prepared to talk about any systems you've used before. If you can, mention how you’ve navigated document workflows and how that experience can benefit the team at OXB.
✨Emphasise Collaboration Skills
As a GMP Technical Writer, you'll need to coordinate with various teams. Share examples of how you've successfully collaborated with subject matter experts or manufacturing teams in the past. This will demonstrate your ability to work well in a team-oriented environment, which aligns with OXB's values.
