GMP Quality Manager: Facilities & Equipment Validation in Weybridge
GMP Quality Manager: Facilities & Equipment Validation

GMP Quality Manager: Facilities & Equipment Validation in Weybridge

Weybridge Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead qualification and validation activities in a GMP environment.
  • Company: Global healthcare company with a focus on innovation.
  • Benefits: Full-time role with a fixed-term contract until 2026.
  • Why this job: Join a dynamic team and ensure compliance in cutting-edge R&D.
  • Qualifications: Bachelor's degree in a scientific discipline and GMP experience.
  • Other info: Collaborate with cross-functional teams in a supportive environment.

The predicted salary is between 36000 - 60000 £ per year.

A global healthcare company is seeking a Quality Manager for their new R&D facility in Weybridge, UK. This role involves leading qualification and validation activities in a GMP environment, ensuring compliance with regulatory standards, and collaborating with cross-functional teams.

The ideal candidate has a strong technical background and a Bachelor's degree in a scientific discipline, alongside significant experience in a GMP-regulated setting. This is a full-time position with a fixed-term contract until 2026.

GMP Quality Manager: Facilities & Equipment Validation in Weybridge employer: Gsk

Join a leading global healthcare company in Weybridge, where innovation meets compliance. As a GMP Quality Manager, you will thrive in a collaborative work culture that prioritises employee growth and development, offering unique opportunities to lead critical validation activities in a state-of-the-art R&D facility. With a commitment to excellence and a supportive environment, this role promises meaningful contributions to healthcare advancements while enjoying the benefits of a dynamic team.
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Contact Detail:

Gsk Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land GMP Quality Manager: Facilities & Equipment Validation in Weybridge

✨Tip Number 1

Network like a pro! Reach out to professionals in the GMP field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that Quality Manager role.

✨Tip Number 2

Prepare for interviews by brushing up on your technical knowledge and regulatory standards. We recommend practising common interview questions related to facilities and equipment validation to show you’re the right fit for the team.

✨Tip Number 3

Showcase your experience! When discussing your background, highlight specific projects where you led qualification and validation activities. We want to see how you’ve made an impact in previous roles.

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. We’re excited to see your skills in action and how you can contribute to our new R&D facility.

We think you need these skills to ace GMP Quality Manager: Facilities & Equipment Validation in Weybridge

GMP Compliance
Qualification and Validation
Regulatory Standards Knowledge
Cross-Functional Collaboration
Technical Background in Scientific Discipline
Experience in GMP-Regulated Setting
Project Management
Attention to Detail

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in GMP environments and any relevant qualifications. We want to see how your background aligns with the role of Quality Manager, so don’t hold back on showcasing your technical skills!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for our R&D facility in Weybridge. Share specific examples of your past experiences that demonstrate your ability to lead qualification and validation activities.

Showcase Your Teamwork Skills: Collaboration is key in this role, so be sure to mention any cross-functional projects you've worked on. We love to see how you’ve successfully partnered with others to achieve common goals in a GMP setting.

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 this exciting opportunity. Plus, it’s super easy!

How to prepare for a job interview at Gsk

✨Know Your GMP Inside Out

Make sure you brush up on your Good Manufacturing Practice (GMP) knowledge. Understand the key regulations and standards that govern the industry, as well as any recent changes. This will show your potential employer that you're not just familiar with the basics but are also committed to staying updated.

✨Showcase Your Technical Expertise

Prepare to discuss your technical background in detail. Be ready to share specific examples of your experience with facilities and equipment validation. Highlight any projects where you led qualification activities, and be prepared to explain the challenges you faced and how you overcame them.

✨Collaboration is Key

Since this role involves working with cross-functional teams, think of examples where you've successfully collaborated with others. Be ready to discuss how you communicate effectively with different departments and how you handle conflicts or differing opinions to achieve a common goal.

✨Ask Insightful Questions

Prepare some thoughtful questions about the company's R&D facility and their approach to quality management. This not only shows your interest in the role but also gives you a chance to assess if the company culture aligns with your values and work style.

GMP Quality Manager: Facilities & Equipment Validation in Weybridge
Gsk
Location: Weybridge
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  • GMP Quality Manager: Facilities & Equipment Validation in Weybridge

    Weybridge
    Full-Time
    36000 - 60000 £ / year (est.)
  • G

    Gsk

    10000+
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