At a Glance
- Tasks: Write clear GMP documentation and coordinate with teams to meet project timelines.
- Company: Join OXB, a mission-driven company focused on life-changing therapies.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on core values: Responsible, Responsive, Resilient, Respectful.
- Why this job: Make a real difference in advancing therapies that change lives.
- Qualifications: Experience in technical writing and understanding of GMP standards.
The predicted salary is between 40000 - 50000 £ per year.
Join Us in Changing Lives 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.
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. Your responsibilities in this role would be:
- 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
GMP Technical Writer employer: Oxford BioMedica Limited
At OXB, we pride ourselves on fostering a collaborative and innovative work environment where our employees are empowered to make a meaningful impact in the field of life sciences. As a GMP Technical Writer, you will benefit from a culture that values responsibility, responsiveness, resilience, and respect, alongside opportunities for professional growth and development. Located in a vibrant area, our company offers competitive benefits and a supportive atmosphere that encourages creativity and teamwork, making it an excellent place for passionate individuals to thrive.
StudySmarter Expert Advice🤫
We think this is how you could land GMP Technical Writer
✨Tip Number 1
Network like a pro! Reach out to folks in the industry, attend relevant events, and connect with people 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 practising common questions and showcasing your knowledge about GMP documentation. We recommend using the STAR method (Situation, Task, Action, Result) to structure your answers and highlight your experience effectively.
✨Tip Number 3
Follow up after interviews! A quick thank-you email can go a long way in leaving a positive impression. It shows you're genuinely interested in the role and appreciate the opportunity to chat.
✨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 keen on joining our mission at OXB.
We think you need these skills to ace GMP Technical Writer
Some tips for your application 🫡
Show Your Passion:When writing your application, let your enthusiasm for the role shine through. We want to see how your values align with ours—Responsible, Responsive, Resilient, and Respectful. Share why you’re excited about contributing to life-changing therapies!
Be Clear and Concise:Just like the GMP documentation you'll be creating, your application should be straightforward and to the point. Avoid jargon and keep your sentences clear. We appreciate a well-structured application that’s easy to read!
Tailor Your Experience:Make sure to highlight your relevant experience in technical writing and GMP documentation. We want to know how your background prepares you for this role, so don’t hesitate to draw connections between your past work and the responsibilities listed in the job description.
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 shows you’re serious about joining our team!
How to prepare for a job interview at Oxford BioMedica Limited
✨Know Your GMP Basics
Before the interview, brush up on Good Manufacturing Practices (GMP) and understand how they apply to documentation like Batch Manufacturing Records (BMRs) and Standard Operating Procedures (SOPs). Being able to discuss these concepts confidently will show that you’re serious about the role.
✨Showcase Your Writing Skills
Prepare samples of your previous technical writing work, especially any GMP-related documents. If you can, bring along examples that highlight your ability to write clearly and concisely. This will give the interviewers a tangible sense of your skills and style.
✨Demonstrate Team Collaboration
Since the role involves coordinating with manufacturing teams and subject matter experts, be ready to share examples of how you've successfully collaborated in the past. Highlight your communication skills and how you manage document updates while keeping everyone in the loop.
✨Be Ready for Scenario Questions
Expect questions that assess how you would handle specific situations, such as managing document changes or dealing with tight deadlines. Think of scenarios from your past experience where you demonstrated resilience and responsiveness, and be prepared to discuss them in detail.
