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QA Auditor - GLP

HAR Labcorp Early Development Laboratories Limited

Eye

On-site

GBP 35,000 - 55,000

Full time

Yesterday
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Job summary

A leading global life sciences company is seeking a Quality Assurance Auditor in Eye, Suffolk. The role involves conducting audits, ensuring regulatory compliance, and improving processes within a supportive team environment. Candidates should have a strong background in GLP or GCP and excellent communication and organisational skills.

Benefits

Comprehensive benefits package
Career development opportunities
Flexible working options after training
Access to wellbeing programs

Qualifications

  • Proven work history in a regulatory environment (GLP or GCP).
  • Strong verbal and written communication skills with the ability to provide clear feedback.
  • Experience using Microsoft Office packages.

Responsibilities

  • Conduct protocol review, data and report audits, process inspections.
  • Ensure regulatory compliance and follow SOPs.
  • Support quality topics and process improvement initiatives.

Skills

Attention to detail
Organisational skills
Process improvement
Communication

Job description

Social network you want to login/join with:

HAR Labcorp Early Development Laboratories Limited

Location:

Eye, United Kingdom

Job Category:

Other

-

EU work permit required:

Yes

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Job Reference:

19b4d1e864e6

Job Views:

4

Posted:

04.07.2025

Expiry Date:

18.08.2025

col-wide

Job Description:

Are you proactive, enjoy working with people and have a keen interest in Auditing?

Are you committed to supporting process improvement and change?

Do you want a role with training and a structured career progression path?

If so, read on!

Labcorp is a leading global life sciences company. With a missionto improve health and improve lives, Labcorp delivers world-class diagnostic solutions, brings innovative medicines to patients faster and uses technology to improve the delivery of care.

We are seeking an experienced Quality Assurance Auditor based at our site in Eye, Suffolk.

Your main responsibilities will be to:

Follow applicable policies and Standard Operating Procedures (SOPs)

Navigate to the regulations and able to read/understand specific regulations

Conduct Protocol review, data and report audits, process inspections

Explain the role of QA (sufficient for client audits)

Establish relationships with local QA colleagues

Retrieve data for client visits/regulatory inspections

Ensure Regulatory Compliance and Quality Assurance (RC&QA) responsibilities, as indicated in applicable controlled documents, are followed

Work with operational management to support Quality topics and/or working on projects with QA team on other sites

Contribute to local Quality initiatives and process improvement initiatives aimed at improving compliance and/or efficiency of the local QA organization

Create and/or re-write QA SOPs based on findings from local quality initiatives.

What we can offer you:

A competitive salary together with a comprehensive benefits package including health cover and pension

Unsurpassed career development opportunities in a supportive and experienced team

A culture of CARE with access to various employee resource groups and wellbeing programs

Flexible working on completion of training

What you need to apply:

A proven work history in a regulatory environment working to GLP or GCP

Excellent attention to detail paired with organisational and process improvement skills

Ability to work independently and with others

Strong verbal and written communication skills with the ability to provide clear feedback

Experience using Microsoft Office packages to include Outlook, Word, SharePoint, PowerPoint and Excel

Ability to remain flexible

If you are looking to work within a stable team, where there are real opportunities to learn, develop and progress then we would like to hear from you!

At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions —because we know that knowledge has the potential to make life better for all. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. Here, you can join our more than 70,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives. Join us and see how you can embrace possibilities and change lives!

Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.

We encourage all to apply

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