QA Specialist: Launching a New GMP Drug Facility in Wrexham
QA Specialist: Launching a New GMP Drug Facility

QA Specialist: Launching a New GMP Drug Facility in Wrexham

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

  • Tasks: Ensure documentation and processes meet GMP standards for a new drug facility.
  • Company: Leading biopharmaceutical company focused on innovation.
  • Benefits: Competitive salary, health benefits, and opportunities for professional growth.
  • Why this job: Join a team dedicated to operational excellence and continuous improvement.
  • Qualifications: Experience in pharma or biopharma with strong GMP knowledge.
  • Other info: Exciting opportunity in a dynamic environment with career advancement potential.

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

A leading biopharmaceutical company is seeking a QA Specialist to support the launch of a new drug product facility at their Wrexham site. You will be responsible for ensuring all documentation, processes, and systems meet GMP standards and are ready for operational excellence.

Ideal candidates will have:

  • Experience in pharma or biopharma
  • Strong knowledge of GMP and validation
  • Experience in sterile manufacturing

This is an exciting opportunity to join a team committed to innovation and continuous improvement.

QA Specialist: Launching a New GMP Drug Facility in Wrexham employer: Ipsen

Join a leading biopharmaceutical company in Wrexham, where innovation meets operational excellence. As a QA Specialist, you will thrive in a collaborative work culture that prioritises employee growth and development, offering comprehensive training and career advancement opportunities. Enjoy the unique advantage of working in a state-of-the-art facility dedicated to launching groundbreaking drug products, all while contributing to meaningful healthcare solutions.
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Contact Detail:

Ipsen Recruiting Team

StudySmarter Expert Advice 🀫

We think this is how you could land QA Specialist: Launching a New GMP Drug Facility in Wrexham

✨Tip Number 1

Network like a pro! Reach out to folks in the biopharma industry, especially those who work in QA or GMP. A friendly chat can lead to insider info about job openings and even referrals.

✨Tip Number 2

Prepare for interviews by brushing up on your GMP knowledge and validation processes. We recommend practising common interview questions related to sterile manufacturing to show you're ready for the role.

✨Tip Number 3

Don’t just apply anywhere; focus on companies that align with your values and career goals. Check out our website for tailored job listings that match your skills in QA and biopharma.

✨Tip Number 4

Follow up after interviews! A quick thank-you email can keep you top of mind and show your enthusiasm for the position. It’s a small gesture that can make a big difference.

We think you need these skills to ace QA Specialist: Launching a New GMP Drug Facility in Wrexham

GMP Knowledge
Validation Experience
Sterile Manufacturing Experience
Documentation Management
Process Improvement
Operational Excellence
Biopharmaceutical Industry Experience
Attention to Detail
Team Collaboration
Quality Assurance
Regulatory Compliance
Problem-Solving Skills
Adaptability
Communication Skills

Some tips for your application 🫑

Tailor Your CV: Make sure your CV highlights your experience in pharma or biopharma, especially any roles related to GMP and validation. We want to see how your background aligns with the QA Specialist position, so don’t hold back on showcasing relevant skills!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re excited about this opportunity and how your experience in sterile manufacturing makes you a perfect fit for our new GMP drug facility. Let us feel your passion!

Showcase Your Attention to Detail: As a QA Specialist, attention to detail is key. Make sure your application is free from typos and errors. We appreciate candidates who take the time to ensure their documents are polished and professional, reflecting the high standards we uphold.

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 role. Plus, it shows us you’re keen to join our innovative team!

How to prepare for a job interview at Ipsen

✨Know Your GMP Inside Out

Make sure you brush up on your Good Manufacturing Practice (GMP) knowledge. Be ready to discuss specific examples of how you've applied GMP standards in your previous roles, especially in sterile manufacturing. This will show that you’re not just familiar with the concepts but can also implement them effectively.

✨Showcase Your Validation Experience

Prepare to talk about your experience with validation processes. Think of concrete examples where you ensured compliance and operational excellence. Highlight any challenges you faced and how you overcame them, as this demonstrates your problem-solving skills and adaptability.

✨Research the Company and Its Products

Take some time to learn about the biopharmaceutical company and their new drug product facility. Understanding their mission, values, and recent innovations will help you tailor your answers and show genuine interest in the role. It’s a great way to connect your experience with their goals.

✨Prepare Questions That Matter

Have a list of thoughtful questions ready to ask at the end of the interview. Inquire about the team dynamics, the specific challenges they face in launching the new facility, or how they measure success in the QA department. This shows that you’re engaged and serious about contributing to their success.

QA Specialist: Launching a New GMP Drug Facility in Wrexham
Ipsen
Location: Wrexham
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  • QA Specialist: Launching a New GMP Drug Facility in Wrexham

    Wrexham
    Full-Time
    36000 - 60000 Β£ / year (est.)
  • I

    Ipsen

    1000-5000
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