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AD QA Compliance/External Quality

JR United Kingdom

Slough

On-site

GBP 35,000 - 55,000

Full time

8 days ago

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Job summary

A leading life sciences recruiter seeks a skilled professional for the AD QA Compliance role in Slough. The position focuses on overseeing quality standards in biotech manufacturing, engaging in team management, validation, and compliance with industry requirements. Candidates must possess a robust understanding of quality assurance and GMP, ensuring processes align with current regulations.

Qualifications

  • Strong understanding of quality assurance in manufacturing.
  • Familiarity with GMP regulations.
  • Ability to apply sterile manufacturing principles.

Responsibilities

  • Manage teams for validation and supplier quality.
  • Ensure quality systems meet current regulations.
  • Continuously improve quality processes.

Skills

Quality Assurance
Good Manufacturing Practices (GMP)
Sterile Manufacturing

Job description

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AD QA Compliance/External Quality, slough

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Client:

Hobson Prior

Location:

slough, United Kingdom

Job Category:

Other

-

EU work permit required:

Yes

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Job Views:

4

Posted:

31.05.2025

Expiry Date:

15.07.2025

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Job Description:

Are you ready to make a groundbreaking impact in the world of biotechnology? Join a growing company that's shaping the future of healthcare and science.

Hobson Prior is seeking an experienced professional for a role focused on ensuring quality standards in biotech manufacturing. You will lead teams responsible for validation and supplier quality, ensuring compliance with industry regulations. This position requires a proactive approach to maintaining and improving quality systems.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

  • Manage teams responsible for validation and supplier quality.
  • Ensure quality systems are up-to-date and meet current regulations.
  • Continuously improve processes to maintain high standards.

Key Skills and Requirements:

  • Strong understanding of quality assurance in manufacturing.
  • Familiarity with guidelines and regulations for good manufacturing practices (GMP).
  • Ability to apply principles of sterile manufacturing effectively.

For more information, please contact Raif Valery.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.hobsonprior.com/privacy-policy

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