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- Tasks: Oversee batch release processes and promote a quality culture in the organisation.
- Company: Leading European specialty pharmaceutical company in the UK.
- Benefits: Competitive salary up to £90,000 plus bonuses and career growth opportunities.
- Why this job: Join a dynamic team and make a real impact in the pharmaceutical industry.
- Qualifications: Minimum 2 years of QP experience and strong GMP knowledge.
- Other info: Work on-site in Essex, 4 days a week.
The predicted salary is between 54000 - 72000 £ per year.
A leading European specialty pharmaceutical company in the UK is seeking an experienced Qualified Person (QP) for a full-time permanent position. This role involves overseeing batch release processes and driving a quality culture across the organization.
The ideal candidate will have:
- A minimum of 2 years of experience as a QP in the pharmaceutical industry
- A strong background in GMP
The position requires working 4 times a week on-site in Essex, offering a remuneration package of up to £90,000 plus bonuses.
On-Site Qualified Person (QP) – East London/Essex employer: Cpl Life Sciences
Contact Detail:
Cpl Life Sciences Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land On-Site Qualified Person (QP) – East London/Essex
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those who know about QP roles. A friendly chat can lead to insider info on job openings that aren't even advertised yet.
✨Tip Number 2
Prepare for interviews by brushing up on your GMP knowledge and batch release processes. We recommend practising common interview questions with a friend or in front of the mirror to boost your confidence.
✨Tip Number 3
Showcase your passion for quality culture during interviews. Share examples of how you've driven quality initiatives in past roles. This will help you stand out as a candidate who truly cares about the industry.
✨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 the initiative to connect directly with us.
We think you need these skills to ace On-Site Qualified Person (QP) – East London/Essex
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience as a Qualified Person (QP) and your background in GMP. We want to see how your skills match the job description, so don’t be shy about showcasing your relevant achievements!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for this role. Share your passion for quality in the pharmaceutical industry and how you can contribute to our quality culture.
Be Clear and Concise: When filling out your application, keep it straightforward. We appreciate clarity, so avoid jargon and get straight to the point about your qualifications and experiences that relate to the QP role.
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 position. Plus, it’s super easy!
How to prepare for a job interview at Cpl Life Sciences
✨Know Your GMP Inside Out
Make sure you brush up on Good Manufacturing Practice (GMP) regulations before the interview. Be ready to discuss how you've applied these principles in your previous roles, especially in batch release processes.
✨Showcase Your Quality Culture Experience
Prepare examples of how you've driven a quality culture in your past positions. Think about specific initiatives or changes you implemented that improved quality standards and how they benefited the organisation.
✨Be Ready for Technical Questions
Expect technical questions related to your experience as a Qualified Person. Review common scenarios you might face in the role and be prepared to explain your decision-making process and outcomes.
✨Ask Insightful Questions
At the end of the interview, have a few thoughtful questions ready about the company's approach to quality assurance and their future goals. This shows your genuine interest in the role and helps you assess if it's the right fit for you.
