About LabCorp Drug Development:

As a leading contract research organization, LabCorp provides comprehensive drug development solutions for a range of industries. We are a global leader in nonclinical safety assessment, clinical trial testing and clinical trial management services. Together with our clients, we support the development of innovative, life-changing treatments.

The Role:

Our largest UK site in Harrogate, North Yorkshire is currently recruiting for a Quality Control Data Auditor to join the Molecular Biology CMC team.   

Within the CMC (Chemistry Manufacturing Controls) business unit; the Molecular Biology department is dedicated to the development, validation and execution of molecular techniques, such as QPCR, RTqPCR and Digital PCR to support Cell Therapies, Gene Therapies and Vaccines. We structure ourselves to deliver scientific expertise to our clients; collaborating closely with them to support the development of medicinal products through the drug development process and onto market.

The Quality Control Data Auditor position is an office based role with responsibility for checking data and reports in order to highlight any errors that need to be resolved prior to approval.

Job Responsibilities include:

• Checking data and reports, in terms of accuracy of transcription, detail, manual calculations, procedural and regulatory compliance

• Conducting all work in compliance with applicable GLP/GCP regulatory requirements specified in the study plans, protocols, or work agreements

• Liaising with the Supervisors or QC Scientists to understand the requirements of the job in terms of priorities and deadlines

• Follows the relevant training, methods and SOPs as closely as possible. Highlights any deviations, problems or errors to the Supervisor ASAP

• Supervising and training junior staff in data checking and additional responsibilities as necessary

• Archiving study data

• Highlighting errors found in data or reports so they can be addressed promptly by the analyst concerned; ensuring the integrity of the data

• Inputting data on to Laboratory Management Information Systems

• Reviewing or writing SOPs as required

 What Labcorp Drug Development can offer you:

• A comprehensive onboarding training plan covering technical and regulatory training packages

• Unsurpassed career development opportunities

• Ability to work with a variety of different clients on wide ranging projects

• Competitive salaries and a comprehensive benefits package including a contributory pension

Key Information:

• Position includes a 6-month onboarding & probationary period during which working hours are 8:45am – 5pm, based at our site in Harrogate.

• Following the initial onboarding period; you will move to one of the following shift patterns 6:00am – 2:15pm or 8:45am – 5:00pm.

Education/Experience:

• Excellent communication skills

• Experience of working in a scientific environment

• Ideally a scientific degree or equivalent but not essential

• Ability to multitask and prioritise workload, with excellent attention to detail

• An understanding of health and safety policies and a good understanding of GLP/GCP regulatory guidelines

• Writing reports or administrative experience would be beneficial

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.