QA Auditor - GLP

Labcorp; Huntingdon; On-site; GBP 44,000 - 56,000; Full time

Job summary

An established industry player is seeking a dedicated QA Auditor to enhance quality assurance processes. This role offers the opportunity to work in a dynamic environment, conducting audits and inspections while ensuring compliance with GLP standards. You'll play a crucial part in supporting process improvements and providing training to operational teams. With a commitment to career development and a supportive culture, this position promises a rewarding journey in the life sciences sector. Join a team that values innovation and excellence in healthcare delivery.

Benefits

Competitive salaries

Comprehensive benefits package

Flexible and hybrid work options

Career development opportunities

Access to well-being programs

Subsidised on-site canteen

Gym facilities

Free parking

Qualifications

• Proven work history in a regulatory environment working to GLP or GCP.
• Ability to influence process improvement initiatives.

Responsibilities

• Conducting regulated study protocol reviews and data audits.
• Reviewing Standard Operating Procedures and conducting internal inspections.

Skills

GLP or GCP experience

Data collection systems (Pristima, Veeva)

Knowledge of UK and OECD GLP standards

Process improvement

Clear communication skills

Critical thinking skills

Job description

Labcorp Huntingdon, England, United Kingdom

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Labcorp Huntingdon, England, United Kingdom

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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
• Co-hosting 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
• Cross-site 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 well-being programs and various employee resource groups
• Subsidised on-site canteen/ restaurant, Gym facilities (small monthly cost) and free parking
  
  

Skills / Experience

• A proven work history in a regulatory environment working to GLP or GCP
• Experience using data collection systems such as Pristima and Veeva is advantageous
• Knowledge of the UK and OECD GLP quality systems/standards and able to apply regulations in order to monitor compliance
• Experience 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 paired with critical thinking skills
  
  

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.

We encourage all to apply

If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.

2514029

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance

• Industries

  Hospitals and Health Care

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