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For Companies At a Glance
- Tasks: Lead quality actions and ensure regulatory compliance for batch releases.
- Company: Join a global biopharmaceutical leader with a respected product portfolio and growth potential.
- Benefits: Enjoy a competitive salary, annual bonus, generous pension, and wellness allowance.
- Why this job: Be part of a diverse culture recognized as one of the 'Best Workplaces' while making a real impact.
- Qualifications: Must be eligible to act as a QP with experience in sterile manufacturing environments.
- Other info: This is a hybrid role requiring at least 3 days on-site each week.
The predicted salary is between 48000 - 72000 £ per year.
Job Description
Walker James Group are currently representing a global biopharmaceutical company as they seek to add an experienced Qualified Person to their team.
Our client is a leader in their field, with an incredibly well established and respected product portfolio that has provided a platform for continued and sustained growth. With further treatments in development, they have an impressive outlook for 2025 and beyond which is also the driver behind significant investment at this particular site, as they seek to expand their capability and production output, which in-turn will be hugely impactful for their patients.
As a Qualified Person (QP) you will take a leading role across quality actions for the site, supporting in the regulatory compliance and QP certification of batch releases in accordance with UK and EU requirements. Furthermore you will:
- Be well versed in Quality Assurance, working closely alongside product development teams to stringently manage the introduction and disposition of clinical materials.
- Offer leadership and mentoring throughout, your actions will foster a culture of 'Commitment to Quality' which will be underpinned by the necessary framework instilled across the Quality function.
- Assist throughout regular audits for varying governance.
- Be eligible to act as a QP within the pharmaceutical industry as well as having proven experience operating at a technically high level within a sterile manufacturing environment.
On offer is a competitive salary which is complemented by an extensive benefits package, incl. annual bonus, generous pension and wellness allowance amongst others.
You will be joining this business at a really exciting time in their journey. This site alone has seen repeated recognition in the 'Best Workplaces' awards, attributed to a diverse and inclusive culture whilst creating an environment where employees feel valued and empowered to be impactful in their work.
Please note this is a hybrid role where the expectation will be for a minimum of 3 days per week on site.
Qualified Person employer: Walker James Group
Contact Detail:
Walker James Group Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Qualified Person
✨Tip Number 1
Make sure to familiarize yourself with the latest UK and EU regulatory requirements for Qualified Persons. Understanding these regulations will not only help you in interviews but also demonstrate your commitment to compliance and quality assurance.
✨Tip Number 2
Network with professionals in the biopharmaceutical industry, especially those who are already working as Qualified Persons. Engaging with them can provide valuable insights into the role and may even lead to referrals or recommendations.
✨Tip Number 3
Highlight any experience you have in sterile manufacturing environments during your conversations. This is a key aspect of the role, and showcasing your relevant background will set you apart from other candidates.
✨Tip Number 4
Prepare to discuss how you foster a culture of 'Commitment to Quality' in your previous roles. Be ready to share specific examples of how you've led teams or initiatives that emphasize quality assurance and compliance.
We think you need these skills to ace Qualified Person
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Qualified Person position. Understand the key responsibilities and required qualifications, as this will help you tailor your application effectively.
Highlight Relevant Experience: In your CV and cover letter, emphasize your experience in Quality Assurance and any previous roles where you acted as a Qualified Person. Use specific examples that demonstrate your ability to manage quality actions and regulatory compliance.
Showcase Leadership Skills: Since the role involves mentoring and fostering a culture of 'Commitment to Quality', be sure to include examples of your leadership experience. Highlight how you've successfully led teams or initiatives in past positions.
Tailor Your Cover Letter: Craft a personalized cover letter that addresses the specific needs of the company. Mention why you are excited about the opportunity to join their team and how your skills align with their goals for growth and quality assurance.
How to prepare for a job interview at Walker James Group
✨Understand Regulatory Compliance
Make sure you are well-versed in UK and EU regulatory requirements. Be prepared to discuss how your experience aligns with these standards and how you can ensure compliance in batch releases.
✨Showcase Quality Assurance Experience
Highlight your background in Quality Assurance, especially in sterile manufacturing environments. Provide specific examples of how you've managed clinical materials and contributed to a culture of 'Commitment to Quality'.
✨Demonstrate Leadership Skills
As a Qualified Person, you'll need to lead and mentor teams. Prepare to share instances where you've successfully led quality initiatives or mentored colleagues, emphasizing the positive outcomes of your leadership.
✨Prepare for Audit Scenarios
Since regular audits are part of the role, be ready to discuss your experience with audits. Think of examples where you've contributed to successful audit outcomes and how you handle governance challenges.
