QA Specialist: GMP/PQS in CGT Biopharma in Hounslow
QA Specialist: GMP/PQS in CGT Biopharma

QA Specialist: GMP/PQS in CGT Biopharma in Hounslow

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

  • Tasks: Ensure compliance in Pharmaceutical Quality Systems and manage critical documentation.
  • Company: Leading biopharmaceutical services company in the South West of the UK.
  • Benefits: Competitive salary, career development, and a chance to influence quality culture.
  • Why this job: Join a respected organisation and make a real impact on quality assurance.
  • Qualifications: Relevant scientific degree and experience in GMP environments.
  • Other info: Collaborative environment with opportunities for professional growth.

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

A leading biopharmaceutical services company in the South West of the UK is seeking a Quality Assurance Specialist. This role involves ensuring compliance within the Pharmaceutical Quality System, working closely with Quality, Production, and QC teams, and managing critical documentation and deviation processes.

Candidates should have a relevant scientific degree and experience in GMP environments, and will have the chance to influence quality culture in a respected organization.

QA Specialist: GMP/PQS in CGT Biopharma in Hounslow employer: Hyper Recruitment Solutions LTD

Join a leading biopharmaceutical services company in the South West of the UK, where you will be part of a dynamic team dedicated to ensuring the highest standards of quality in the industry. With a strong emphasis on employee development and a collaborative work culture, this role offers you the opportunity to make a meaningful impact on quality assurance practices while enjoying a supportive environment that values innovation and professional growth.
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Contact Detail:

Hyper Recruitment Solutions LTD Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land QA Specialist: GMP/PQS in CGT Biopharma in Hounslow

✨Tip Number 1

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

✨Tip Number 2

Prepare for interviews by brushing up on GMP regulations and quality assurance processes. We recommend practising common interview questions related to compliance and documentation management to show you’re ready to hit the ground running.

✨Tip Number 3

Showcase your experience! Bring examples of how you've influenced quality culture in previous roles. We want to see how you can make an impact in our organisation, so don’t hold back!

✨Tip Number 4

Apply through our website! It’s the best way to ensure your application gets noticed. We’re always on the lookout for passionate candidates who are eager to contribute to our team.

We think you need these skills to ace QA Specialist: GMP/PQS in CGT Biopharma in Hounslow

Quality Assurance
GMP Compliance
Pharmaceutical Quality System
Documentation Management
Deviation Management
Collaboration with Quality Teams
Collaboration with Production Teams
Collaboration with QC Teams
Scientific Degree
Influencing Quality Culture

Some tips for your application 🫡

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

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about quality assurance in biopharma and how you can contribute to our team. We love seeing candidates who are genuinely excited about the role.

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.

Apply Through Our Website: We encourage you to apply directly through our website for a smoother process. It helps us keep track of applications and ensures you’re considered for the role. Plus, it’s super easy to do!

How to prepare for a job interview at Hyper Recruitment Solutions LTD

✨Know Your GMP Inside Out

Make sure you brush up on Good Manufacturing Practice (GMP) regulations and guidelines. Familiarise yourself with the specific requirements of the Pharmaceutical Quality System, as this will show your potential employer that you’re serious about compliance and quality.

✨Showcase Your Teamwork Skills

Since this role involves working closely with Quality, Production, and QC teams, be prepared to discuss examples of how you've successfully collaborated in the past. Highlight any experiences where you’ve influenced quality culture or resolved conflicts within a team.

✨Prepare for Documentation Questions

Expect questions about managing critical documentation and deviation processes. Think of specific instances where you’ve handled documentation effectively or dealt with deviations, and be ready to explain your thought process and the outcomes.

✨Ask Insightful Questions

At the end of the interview, don’t forget to ask questions that demonstrate your interest in the company and the role. Inquire about their approach to quality assurance and how they foster a positive quality culture. This shows you’re not just looking for any job, but are genuinely interested in contributing to their success.

QA Specialist: GMP/PQS in CGT Biopharma in Hounslow
Hyper Recruitment Solutions LTD
Location: Hounslow
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