Quality Engineer (Contract)

Quality Engineer (Contract)

Temporary 30 - 40 £ / hour (est.) Home office (partial)
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At a Glance

  • Tasks: Support quality and regulatory compliance in a leading life sciences organisation.
  • Company: Join a global leader committed to quality and innovation in health.
  • Benefits: Competitive hourly rate, flexible remote work, and potential contract extension.
  • Other info: Collaborative culture with opportunities for professional growth.
  • Why this job: Make a real impact in a fast-paced, quality-driven environment.
  • Qualifications: Degree in Life Sciences or Engineering; experience in regulated industries.

The predicted salary is between 30 - 40 £ per hour.

Your new company

You will be joining a leading global organisation within the life sciences sector, recognised for its commitment to quality, innovation, and improving global health outcomes. The company operates within a highly regulated environment and fosters a collaborative, high-performing culture focused on continuous improvement and operational excellence.

Your new role

As a Q&RA Engineer, you will play a key role in supporting quality and regulatory compliance across operations. You will work closely with cross-functional teams to maintain and improve quality systems, ensuring products and processes meet stringent regulatory standards. Key responsibilities include:

  • Supporting compliance with GMP/GxP and ISO standards
  • Leading and contributing to deviation investigations and root cause analysis
  • Managing change control and CAPA processes
  • Authoring and reviewing quality documentation (SOPs, reports, etc.)
  • Supporting internal and external audits and regulatory inspections
  • Analysing quality data and reporting on trends and metrics
  • Collaborating with manufacturing, QA, and engineering teams to drive improvements

This is a primarily remote role with occasional on-site presence required.

What you'll need to succeed

To be successful in this position, you will have:

  • A degree in Life Sciences, Engineering, or a related discipline
  • Experience within a regulated industry (pharmaceutical, biotech, or medical devices)
  • Strong knowledge of GMP/GxP and ISO standards
  • Experience with quality systems, including deviations, CAPA, and change control
  • Familiarity with QMS platforms (e.g. MasterControl or similar)
  • Strong investigation and root cause analysis skills
  • Excellent technical writing and documentation skills
  • Strong communication skills and ability to work cross-functionally
  • The ability to work both independently and collaboratively

Must have Full Right to Work in the UK for duration of contract. No Sponsorship Provided.

What you'll get in return

In return, you will receive:

  • Competitive hourly rate
  • Flexible, primarily remote working arrangement
  • Opportunity to work within a well-established and reputable organisation
  • Exposure to a fast-paced, quality-driven environment
  • Potential for contract extension

What you need to do now

If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.

Quality Engineer (Contract) employer: Hays Life Sciences

Join a leading global organisation in the life sciences sector, where your contributions as a Quality Engineer will directly impact quality and regulatory compliance. Enjoy a flexible, primarily remote working arrangement within a collaborative culture that prioritises continuous improvement and operational excellence, while benefiting from competitive pay and opportunities for contract extension.

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Contact Details:

Hays Life Sciences Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Quality Engineer (Contract)

Tip Number 1

Network like a pro! Reach out to your connections in the life sciences sector and let them know you're on the hunt for a Quality Engineer role. You never know who might have the inside scoop on job openings or can put in a good word for you.

Tip Number 2

Prepare for those interviews by brushing up on your GMP/GxP and ISO standards knowledge. Be ready to discuss how you've applied these in past roles, as well as your experience with quality systems. We want you to shine!

Tip Number 3

Don’t forget to showcase your technical writing skills! Bring along examples of SOPs or reports you've authored to demonstrate your expertise. This will help you stand out as a candidate who knows their stuff.

Tip Number 4

Apply through our website for the best chance at landing that Quality Engineer gig! We’re all about making the process smooth and easy for you, so don’t miss out on the opportunity to join a fantastic team.

We think you need these skills to ace Quality Engineer (Contract)

GMP/GxP Compliance
ISO Standards Knowledge
Deviation Investigations
Root Cause Analysis
Change Control Management
CAPA Processes
Quality Documentation Authoring

Some tips for your application 🫡

Tailor Your CV:Make sure your CV highlights your experience in regulated industries and your knowledge of GMP/GxP and ISO standards. We want to see how your background aligns with the role, so don’t be shy about showcasing relevant projects or achievements!

Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re passionate about quality engineering and how you can contribute to our mission of improving global health outcomes. Keep it concise but impactful!

Showcase Your Technical Writing Skills:Since excellent technical writing is key for this role, include examples of your documentation work in your application. Whether it’s SOPs or reports, we want to see your ability to communicate complex information clearly.

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 the role. Plus, it’s super easy – just click ‘apply now’!

How to prepare for a job interview at Hays Life Sciences

Know Your Standards

Make sure you brush up on GMP/GxP and ISO standards before the interview. Being able to discuss these in detail will show that you understand the regulatory environment and can contribute to maintaining compliance.

Showcase Your Experience

Prepare specific examples from your past roles where you've successfully managed deviations, CAPA processes, or change control. This will help demonstrate your hands-on experience and problem-solving skills in a regulated industry.

Communicate Clearly

Since this role involves cross-functional collaboration, practice articulating your thoughts clearly. Be ready to explain complex concepts in simple terms, as effective communication is key in a team-oriented environment.

Ask Insightful Questions

Prepare thoughtful questions about the company's quality systems and how they approach continuous improvement. This shows your genuine interest in the role and helps you assess if the company culture aligns with your values.