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 GLP/GCP Quality Assurance Auditor at Labcorp based in Harrogate, North Yorkshire, you will play an essential part in making this happen.
We are looking for someone who is able to apply basic regulatory knowledge and critically assess data, whilst working in an ever-changing environment.
Responsibilities will include:
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Navigating, reading and understanding specific regulations
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Conducting work as identified on the audit activity table
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Timely notification to management regarding identification of critical issues
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Building successful relationships on a one-to-one basis
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Being able to answer questions relating to audit findings (successful interaction/relationships on small scale outside QA function)
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Making suggestions for improving compliance and/or efficiency of the local QA organization and business units supported
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Ensuring Regulatory Compliance and Quality Assurance (RC&QA) responsibilities, as indicated in applicable controlled documents, are followed
What Labcorp can offer you:
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Competitive salary and a comprehensive benefits package including health cover and contributory pension
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Unrivalled opportunities to develop a successful career in the scientific industry
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Unsurpassed, structured career development opportunities
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Flexible working
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A culture of CARE with access to well-being programs and various employee resource groups
Education:
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A minimum of a Bachelor’s Degree in Life Sciences preferred (or equivalent Life Science experience)
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Experience may be substituted for education
Skills / Experience:
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Proven work history in a regulatory environment working to GLP / GCP preferred
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Ability to apply basic relevant regulatory knowledge
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Ability to follow instruction e.g. QA documents (SOPs)
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Ability to assimilate/interpret operational documents such that audit can be performed to required level
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Ability to critically assess data and apply procedures and regulations
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Adaptability to an ever-changing work environment
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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, 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. 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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What We Do
We believe in harnessing science for human good. And so we work day and night, around the world, to deliver answers for all your health questions—whether you’re a provider, drug developer, hospital, medical researcher or patient. That means everything from advancing diagnostic testing to helping launch new drugs, to offering new perspectives through data - all drawing from a deep well of scientific expertise. So when you need trusted information to make clear, confident health decisions, consider us your source.