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Quality Assurance Auditor - GLP

Labcorp Drug Development
Derby, United Kingdom
Start date
6 May 2022
Closing date
4 Jun 2022

View more

Full Time
Contract Type
Experience Level
Experienced (non-manager)
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Job Details

Are you already working in a GLP / GCP environment and want to consider Quality Assurance as your next career move?

Do you want to be part of a company that helps build a healthier and safer world?

Are you looking for industry recognised training and development opportunities?

Labcorp is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries.

As a Good Laboratory Practice (GLP)Quality Assurance Auditor at Labcorp Drug Development, based at Shardlow, Derbyshire you will play an essential part in making this happen.

The Shardlow site is the epicenter of aquatic ecotoxicology and biodegradation. They focus on crop protection and chemical testing.

Responsibilities will include:

- Performing protocol, data, report, and in-lab phase inspections for a specific study type to verify conformance to applicable Standard Operating Procedures (SOP's) and Good Laboratory Practice (GLP) regulatory requirements.

- Evaluating responses to Good Laboratory Practice (GLP) inspection reports and performing follow-up with respondents, management, or others, if needed, to ensure resolution.

- Ensuring that systems used in Good Laboratory Practice (GLP) quality assurance are properly maintained.

- Notifying management of service failures. - Performing study sign-off including but not limited to quality assurance statement preparation (internal/external) and report finalisation.

- Performing Standard Operating Procedures (SOP's) reviews.

- Participating in internal facility and supplemental inspections, under supervision.

- Deliver basic quality/regulatory training, under supervision. Identifying opportunities for process improvement and harmonisation efforts that promote best practices.

What Labcorp can offer you:

- Competitive salaries and a comprehensive benefits package including health cover and contributorypension.

- Unrivalled opportunities to develop a successful career in the scientific industry.

- Unsurpassed career development opportunities.


- A minimum of a Bachelor's Degree in Life Sciences preferred (or equivalent Life Science experience).

- Experience may be substituted for education.


- Proven work history in a regulatory environment.

- Ability to apply basic relevant regulatory knowledge

- GLP/GCP. - Ability to follow instruction e.g. QA documents (SOPs).

- Ability to assimilate/interpret operational documents such that audit can be performed to required level.

- Ability to critically assess data and apply procedures and regulations. - Adaptability to an ever changing work environment.

- Ability to recognise gaps in procedures and regulations and consult with more senior QA individuals.

Labcorp is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.

For more information about how we collect and store your personal data, please see our Privacy Statement .


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 in our pursuit of answers.


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Find Us
Maidenhead Office Park
Westacott Way
Littlewick Green
United Kingdom
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