Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Support quality department with release activities and major QA projects.
- Company: Growing pharmaceutical manufacturer in North West England.
- Benefits: Competitive package and dynamic work environment.
- Other info: Collaborative role with regular interaction across various departments.
- Why this job: Join a fast-paced team and make a real impact in the pharmaceutical industry.
- Qualifications: Degree in a relevant scientific discipline and 5 years' GMP QA experience.
The predicted salary is between 50000 - 65000 £ per year.
BioTalent are currently representing a growing pharmaceutical manufacturer based in the North West in their search for an experienced Qualified Person. You will be integral to the Quality department supporting on the week to week release activities alongside other major QA projects for the site. This position requires individuals to have prior experience working on a license and preferably with terminally sterilised products.
Key requirements:
- Review and evaluate batch records and authorise batch disposition.
- Manage the site QMS, monitor compliance with GMP and drive quality improvements.
- Review and approve deviations and laboratory investigations in compliance with GMP.
- Investigate and respond to complaints.
- Highly collaborative, regular interaction with senior management, Regulatory groups, QPPV, Supply chain, site-based QA, distributors, testing labs, warehouses, sales departments, customers and regulators.
- Ability to work independently with limited supervision, self-driven, responsive and results orientated.
Duties:
- The successful candidate will be qualified to degree level (as a minimum) in a relevant scientific discipline.
- The candidate must be eligible to act as a Qualified Person for medicinal products (as defined in EU Directive 2001/83/EC) and have been named on a UK MIA.
- Robust technical knowledge of EU GMP, regulations and guidelines.
- Experienced in the operation of an EU regulatory approved QMS.
- At least 5 years’ experience in a GMP QA role within the pharmaceutical industry and experience of managing quality systems.
- Ability to work independently with limited supervision, self-driven, responsive and results orientated.
This is an excellent opportunity for an individual who is looking to work in a fast paced, dynamic environment supported by a wider QA team.
Shortlisting for this role has begun with a view to holding first stage interviews over the next couple of weeks.
Qualified Person in Liverpool employer: BioTalent
Contact Detail:
BioTalent Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Qualified Person in Liverpool
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those who work in QA roles. A friendly chat can lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of EU GMP regulations and quality systems. We recommend doing mock interviews with friends or using online platforms to get comfortable with common questions.
✨Tip Number 3
Showcase your experience! When you get the chance to speak with potential employers, highlight your past achievements in managing quality systems and driving improvements. We want to see how you can add value to their team.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take that extra step to connect with us directly.
We think you need these skills to ace Qualified Person in Liverpool
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Qualified Person role. Highlight your experience with batch records, QMS management, and any relevant GMP knowledge. We want to see how your background fits perfectly with what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about the pharmaceutical industry and how your skills align with our needs. We love seeing genuine enthusiasm and a clear understanding of the role.
Showcase Your Experience: When detailing your experience, focus on specific achievements in your previous roles. Mention any quality improvements you've driven or compliance challenges you've overcome. We appreciate candidates who can demonstrate their impact!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re proactive and keen to join our team!
How to prepare for a job interview at BioTalent
✨Know Your GMP Inside Out
Make sure you brush up on your knowledge of EU GMP regulations and guidelines. Be prepared to discuss how you've applied these in your previous roles, especially in relation to batch records and quality systems.
✨Showcase Your Experience
Highlight your experience as a Qualified Person and any specific projects you've worked on. Be ready to share examples of how you've managed quality improvements or handled deviations and complaints.
✨Demonstrate Collaboration Skills
Since this role involves regular interaction with various departments, think of examples that showcase your ability to work collaboratively. Discuss how you've effectively communicated with senior management, regulatory groups, and other stakeholders.
✨Prepare Questions
Have a few thoughtful questions ready to ask at the end of the interview. This shows your interest in the role and the company. You might want to ask about their current QA projects or how they measure success within the team.