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- Tasks: Ensure compliance with UK/EU GMP and oversee batch disposition decisions.
- Company: Upperton Pharma Solutions, a growing CDMO in Nottingham.
- Benefits: 30 days holiday, birthday off, private medical insurance, and pension package.
- Why this job: Join a dynamic team making a real impact in pharmaceutical manufacturing.
- Qualifications: Eligibility as a UK Qualified Person and experience in GMP-licensed environments.
- Other info: Modern offices, employee events, and excellent career growth opportunities.
The predicted salary is between 36000 - 60000 £ per year.
Upperton Pharma Solutions is a Nottingham-based CDMO that specialises in the development and manufacture of pharmaceutical products, providing a complete service from early-stage feasibility to GMP clinical manufacture. Formulations cover a range of delivery routes, typically including oral (tablets & capsules), nasal and inhaled. Continued growth and investment into the business has led to the creation of exciting new job opportunities in our new GMP Manufacturing headquarters in Beeston, Nottingham. Upperton Pharma Solutions is undergoing a period of significant expansion to meet international customer demand and offer a comprehensive drug development portfolio.
The Qualified Person (QP) has legal responsibility under UK and EU law, including EU Directives 2001/83, 2001/20 and 2003/94, ensuring that each batch of medicinal product has been manufactured and checked in compliance with UK/EU GMP in accordance with CTA, PSF and IMPD.
Main duties and responsibilities:
- Complete batch dispositions decisions as required and ensure that the appropriate systems are in place to support batch disposition.
- Support the site in developing policies and procedures to comply with GMP.
- Ensure the site team have an up to date and appropriate level of GMP knowledge.
- Bring to the attention of senior management any GMP non-compliance or concerns about future non-compliances.
- Ensuring that the appropriate systems are in place for final batch disposition.
- Supporting the company in client interactions as required.
- Providing GMP expertise in problem solving and change management.
- Supporting regulatory inspections and customer audits.
- Provide technical support to the site team in matters of regulatory compliance and product safety.
- Complete site training as required to ensure appropriate GMP system maintenance and site regulatory knowledge.
- Assess site compliance through customer audit and appropriate management review.
- Support the site in obtaining competent authority registrations.
- Monitor product quality as needed through tracking and trending of site quality indicators.
- Conduct investigations and reports as required.
Essential Skills and experience:
- Eligibility to act as a UK Qualified Person, recognised by the Joint professional bodies: Eligible to be named on a UK Manufacturing and Importation Authorisation (MA).
- Full understanding of the legal responsibilities of UK QP and commitment to compliance with the QP Code of Practice.
- Significant experience working within UK GMP-licensed pharmaceutical manufacturing.
- Strong practical experience with:
- Batch certificates and release decision making.
- Deviation and OOS management.
- Root cause analysis and CAPA.
- Change control and quality risk management.
What you will get in return:
- 30 days holiday and your birthday off!
- Company contributory pension package.
- Life insurance.
- Private Medical Insurance through Vitality.
- Free onsite car parking.
- Modern offices located just 2 minutes from Beeston train station.
We also organise employee events throughout the year, like our annual Christmas party, summer party and charity fundraising events.
Qualified Person (QP) in Nottingham employer: UPPERTON LIMITED
Contact Detail:
UPPERTON LIMITED Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Qualified Person (QP) in Nottingham
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharmaceutical industry, especially those who work at Upperton Pharma Solutions. A friendly chat can sometimes lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on your GMP knowledge and understanding the specific responsibilities of a Qualified Person. We recommend practising common interview questions and scenarios related to batch disposition and compliance.
✨Tip Number 3
Showcase your problem-solving skills! During interviews, be ready to discuss how you've tackled challenges in previous roles, especially around deviation management and quality risk. Real-life examples will make you stand out.
✨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 joining our team at Upperton Pharma Solutions.
We think you need these skills to ace Qualified Person (QP) in Nottingham
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Qualified Person role. Highlight your experience with UK GMP regulations and any relevant qualifications. We want to see how your background aligns with what we do at Upperton Pharma Solutions!
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 your skills can contribute to our team. Remember, we love seeing genuine enthusiasm for what we do!
Showcase Your Compliance Knowledge: Since compliance is key in this role, make sure to mention your understanding of UK and EU laws related to GMP. We’re looking for someone who can confidently navigate these regulations, so don’t hold back on your expertise!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, it shows us that you’re serious about joining our team at Upperton Pharma Solutions!
How to prepare for a job interview at UPPERTON LIMITED
✨Know Your GMP Inside Out
Make sure you brush up on your knowledge of Good Manufacturing Practice (GMP) regulations. Familiarise yourself with the specific UK and EU laws that apply to the role of a Qualified Person, as well as the relevant directives. This will not only show your expertise but also demonstrate your commitment to compliance.
✨Prepare for Scenario Questions
Expect to be asked about real-life scenarios related to batch disposition decisions, deviation management, and CAPA processes. Think of examples from your past experience where you successfully navigated these situations. Being able to articulate your thought process will impress the interviewers.
✨Showcase Your Communication Skills
As a QP, you'll need to communicate effectively across all levels of the organisation. Prepare to discuss how you've handled challenging conversations or provided feedback in previous roles. Highlighting your ability to challenge constructively will set you apart.
✨Ask Insightful Questions
At the end of the interview, don’t shy away from asking questions. Inquire about the company’s approach to regulatory inspections or how they support their team in maintaining GMP compliance. This shows your genuine interest in the role and helps you gauge if the company is the right fit for you.