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- Tasks: Provide QP certification and support audit activities in a life sciences environment.
- Company: Global life sciences organisation improving lives through quality and compliance.
- Benefits: Part-time hybrid role with flexible hours and a collaborative culture.
- Other info: Opportunity for growth in a purpose-driven team focused on patient impact.
- Why this job: Make a real impact in healthcare while enjoying a structured work-life balance.
- Qualifications: Must be a qualified QP with experience in GMP and regulatory compliance.
The predicted salary is between 50000 - 60000 £ per year.
BioTalent have partnered with a global life sciences and healthcare organisation that plays a critical role in supporting the development, storage, and distribution of products that help improve lives around the world. This business operates at the intersection of science, quality, and patient impact, providing specialist services that support pharmaceutical, biotech, and clinical supply operations. Their work contributes to important areas such as clinical development, product integrity, regulatory compliance, and supply chain excellence.
They are now looking to appoint an experienced Qualified Person (QP) to join the UK team on a 2-year fixed-term contract, working part-time (22.5 hours per week) in a hybrid arrangement across Monday to Wednesday.
The Opportunity
This is a key quality leadership role, supporting regulated operations within a specialist life sciences environment. The successful candidate will provide QP certification and declarations, contribute technical expertise across operations, and support audit and compliance activities. This is an excellent opportunity for a QP who enjoys working in a high-quality, collaborative, and purpose-driven environment, with the flexibility of a structured Mon–Wed hybrid setup.
Key Responsibilities
- Provide QP certification in line with regulatory requirements and client technical agreements
- Perform QP GMP declarations, including on-site audits where required to support importation activities
- Deliver UK QP oversight activities
- Conduct internal and external audits as needed
- Provide and support GMP training across the business
- Offer guidance to internal teams on QP roles and responsibilities
- Support Business Development, Sales, and Project Management during pre-contract assessments for new opportunities
- Maintain awareness of relevant regulatory developments and advise colleagues where appropriate
- Support the preparation and review of Technical Agreements
- Contribute QP expertise during client and regulatory inspections/audits
- Undertake travel and off-site work where required
Ideal Background
- Eligible and operating as a Qualified Person (QP) in the UK
- Proven experience acting as a QP for IMPs
- Experience with biological products would be highly advantageous
- Strong understanding of GMP, regulatory expectations, and quality oversight
- Comfortable working cross-functionally with operational, commercial, and quality teams
- Prior exposure to pharmaceutical development processes would be beneficial
Qualified person in Colchester employer: BioTalent
Contact Detail:
BioTalent Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Qualified person in Colchester
✨Tip Number 1
Network like a pro! Reach out to your connections in the life sciences and healthcare sectors. Attend industry events or webinars, and don’t be shy about introducing yourself. You never know who might have the inside scoop on job openings!
✨Tip Number 2
Prepare for interviews by brushing up on your QP knowledge and regulatory requirements. Think about real-life examples from your experience that showcase your skills. Practice common interview questions with a friend to boost your confidence!
✨Tip Number 3
Showcase your passion for quality and patient impact during interviews. Employers love candidates who are genuinely interested in their mission. Share why you want to work in a high-quality, collaborative environment and how you can contribute to their goals.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we’re always looking for talented individuals like you to join our team and make a difference in the life sciences field.
We think you need these skills to ace Qualified person in Colchester
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience as a Qualified Person and any relevant skills that match the job description. We want to see how your background aligns with our needs, so don’t be shy about showcasing your expertise in GMP and regulatory compliance!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about the role and how you can contribute to our mission of improving lives. Keep it concise but impactful – we love a good story that connects your experience to our values.
Showcase Your Collaborative Spirit: Since this role involves working cross-functionally, make sure to highlight any teamwork experiences in your application. We value collaboration, so share examples of how you've successfully worked with different teams in the past!
Apply Through Our Website: We encourage you to apply directly through our website for a smoother process. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team!
How to prepare for a job interview at BioTalent
✨Know Your Regulatory Stuff
Make sure you brush up on the latest GMP regulations and quality oversight practices. Being able to discuss how you’ve applied these in your previous roles will show that you’re not just familiar with the rules, but that you can also implement them effectively.
✨Showcase Your QP Experience
Prepare specific examples of your experience as a Qualified Person, especially related to IMPs and biological products. Highlight any audits you've conducted or training you've provided, as this will demonstrate your hands-on expertise and leadership in quality assurance.
✨Understand the Company’s Mission
Familiarise yourself with the organisation's role in the life sciences and healthcare sector. Be ready to discuss how your values align with their mission of improving lives through quality and compliance, which will show your genuine interest in the position.
✨Ask Insightful Questions
Prepare thoughtful questions about the company’s operations, particularly around their audit processes and regulatory challenges. This not only shows your enthusiasm for the role but also your proactive approach to understanding how you can contribute to their success.