QA Auditor Ii

3 weeks ago


Huntingdon, Cambridgeshire, United Kingdom Labcorp Full time

Do you have GLP or GCP experience in industry?

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 mission
to 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 looking for a
Good Laboratory (GLP) Quality Assurance Auditor based at our site in
Huntingdon, Cambridgeshire.

Duties Include:

  • Conducting regulated study protocol reviews, data and report audits for Toxicology, Safety Assessment and Pharmacology studies.
  • Conducting internal (study, process, facility) inspections.
  • Reviewing Standard Operating Procedures.
  • Performing Supplier and Test Site qualifications.
  • Cohosting client visits and regulatory inspections.
  • Development and delivery of training to operational groups and QA.
  • Providing advice and guidance on aspects of quality and compliance.
  • Crosssite QA and operational relationship, providing recommendations for improving compliance and/or efficiency
  • Working with operational management to support Quality topics and/or working on projects with QA team on other sites
  • Managing local Quality initiatives aimed at improving compliance and/or efficiency of the local QA organization
  • Ensuring Regulatory Compliance and Quality Assurance (RC&QA) responsibilities, as indicated in applicable controlled documents, are followed

What Labcorp can offer you:

  • Competitive salaries and a comprehensive benefits package including health cover and contributory pension.
  • Flexible and hybrid work once the training has been completed.
  • Unrivalled opportunities to develop a successful career in the scientific industry, QA specialist roles, management training and senior apprenticeships.
  • Unsurpassed career development opportunities and the chance to progress quickly up the career development framework.
  • A culture of CARE with access to wellbeing programs and various employee resource groups.
  • Subsidised onsite canteen/ restaurant, Gym facilities (small monthly cost) and free parking.

Experience:

  • A proven work history in a regulatory environment working to GLP or GCP.
  • Experienced using data collection systems such as Pristima and Veeva is advantageous.
  • Experienced in process improvement.
  • Clear communication skills, including ability to provide clear feedback.
  • Ability to clearly articulate processes in order to provide training.
  • Ability to influence process improvement initiatives / offer solutions.

Labcorp is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, Labcorp strives for diversity and inclusion 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 of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), 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.

We encourage all to apply.

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