At a Glance
- Tasks: Write clear GMP documentation to support life-changing therapies.
- Company: Join OXB, a pioneer in viral vector development and manufacturing.
- Benefits: Enjoy competitive rewards, wellbeing programmes, and career growth opportunities.
- Other info: Be part of a supportive and inclusive culture in state-of-the-art facilities.
- Why this job: Make a real impact in healthcare while working with innovative teams.
- Qualifications: Experience in GMP documentation and strong attention to detail required.
The predicted salary is between 35000 - 45000 £ per year.
Join Us in Changing Lives
Location: Oxford, GB
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.
We’re currently recruiting for a GMP Technical Writer to join our Manufacturing team. In this role, you will author GMP related documentation including Batch Manufacturing Records (BMRs) and Standard Operating Procedures (SOPs), playing a key part in advancing our mission and making a real difference.
Responsibilities
- Writing clear and concise GMP documentation such as BMRs and 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.
Qualifications
- 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.
Benefits
- 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 Oxford employer: OXB
At OXB, we pride ourselves on being an exceptional employer, offering a supportive and inclusive culture that fosters collaboration and innovation. Our commitment to employee wellbeing is reflected in our comprehensive benefits package and career development opportunities, ensuring that every team member can thrive while contributing to life-changing therapies. Located in Oxford, our state-of-the-art facilities provide an inspiring environment where passionate individuals can make a real difference in the world of gene therapy.
StudySmarter Expert Advice🤫
We think this is how you could land GMP Technical Writer in Oxford
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect with current employees at OXB. A friendly chat can sometimes lead to opportunities that aren’t even advertised.
✨Tip Number 2
Prepare for interviews by practising common questions related to GMP documentation. We recommend using the STAR method (Situation, Task, Action, Result) to structure your answers and showcase your experience effectively.
✨Tip Number 3
Showcase your passion for scientific writing and attention to detail during interviews. Bring examples of your previous work, like SOPs or BMRs, to demonstrate your skills and how you can contribute to OXB’s mission.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, it shows you’re genuinely interested in being part of our team at OXB.
We think you need these skills to ace GMP Technical Writer in Oxford
Some tips for your application 🫡
Tailor Your Application:Make sure to customise your CV and cover letter for the GMP Technical Writer role. Highlight your experience with GMP documentation like SOPs and BMRs, and show us how your skills align with our mission at OXB.
Showcase Your Attention to Detail:Since this role requires a keen eye for detail, include examples in your application that demonstrate your ability to produce error-free documentation. We want to see how you ensure clarity and precision in your writing!
Familiarise Yourself with Our Values:Before applying, take a moment to understand our core values: Responsible, Responsive, Resilient, and Respectful. Reflect these values in your application to show us you’re a great fit for our team culture.
Apply Through Our Website:We encourage you to submit your application through our website. It’s the best way for us to receive your details and ensures you’re considered for the role. Plus, it’s super easy!
How to prepare for a job interview at OXB
✨Know Your GMP Inside Out
Make sure you brush up on your knowledge of Good Manufacturing Practices (GMP) and regulatory documentation requirements. Be prepared to discuss specific examples of how you've authored clear and concise GMP documents like Batch Manufacturing Records (BMRs) or Standard Operating Procedures (SOPs). This will show that you understand the importance of quality and compliance in 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 difference in a project. This aligns perfectly with OXB's commitment to high-quality work.
✨Familiarise Yourself with Document Workflows
Since you'll be working with electronic document management systems, it’s crucial to demonstrate your understanding of document workflows. Be ready to explain how you've managed document updates and coordinated with teams in the past. This will show that you can handle the responsibilities of the role effectively.
✨Embrace Collaboration
OXB values teamwork, so be prepared to discuss how you've collaborated with others in previous roles. Share examples of how you’ve worked with manufacturing teams and subject matter experts to meet project timelines. This will illustrate that you embody their core values of being Responsible, Responsive, Resilient, and Respectful.
