Labcorp Drug Development Job - 39840727 | CareerArc
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Company: Labcorp Drug Development
Location: England, United Kingdom
Career Level: Associate
Industries: Healthcare, Pharmaceutical, Biotech

Description

Job Overview:

Are you interested in starting a career as a trainee Quality Assurance professional? 

 

Do you have experience working in a regulated laboratory?

 

Do you want to work for a company that helps build a healthier and safer world?

 

As one of the world's premier Contract Research Organisations, we provide research services for a multitude of organisations.

 

We strive to make a difference to people's everyday lives by bringing essential products to the market and as a Good Manufacturing Practice (GMP) Quality Associate at Labcorp Drug Development, based at Harrogate, North Yorkshire, you will play an essential part in making this happen.

 

The Quality Associate is responsible for supporting the local implementation and operation of the GMP Quality Management System. The role aims to ensure the site remains in a state of GMP compliance by participation in investigations, audits, data reviews, validation projects and the delivery of GMP related training, etc. This role is a trainee position; therefore, the following duties will require training/supervision:                                                             

 

Responsibilities will include:

 

  • Performs a preliminary regulatory review to provide recommendations regarding the compliance status of study related documentation (i.e. protocols, reports, certificates of analysis, etc) prior to QA approval
  • Reviews and approves site quality documents (Standard Operating Procedures (SOP's), Policies, etc.) to ensure compliance with GMP, Covance document management procedures and other applicable quality standards
  • Supports the GMP QA internal audit programme by participating as trainee in audits of GMP-related systems, processes and facilities
  • Participates in projects as trainee to ensures facilities, utilities, equipment and computer systems are appropriately validated/qualified
  • Review of metrology methods and specifications for accuracy/relevance and compliance with appropriate standards
  • Participates as a trainee in investigations (deviations, OOS, customer complaints, etc.) assisting senior GMP QA personnel to assign cause and resolution of quality defects
  • Participates as a trainee to continual improvement initiatives aimed at improving the efficiency/ effectiveness of GMP operations
  • Delivery of basic GMP training in due course

 

 

What Labcorp Drug Development can offer you:

 

  • Competitive salary and benefits package
  • Unparalleled opportunities for career development and progression within a global organisation with global clients
  • Excellent relocation package (subject to criteria)
  • Flexible working arrangements
Education/Qualifications:
  • Bachelor's Degree, in a Biology or Chemistry discipline. A secondary/High School education with at least 2 years' relevant work experience in a regulated industry may be accepted in lieu of Bachelor's Degree.
  • Relevant GMP regulated analytical laboratory experience may be substituted for education.
Experience:
  • Experience of auditing in a GMP regulated drug development/pharmaceutical setting or experience of working in a GMP analytical laboratory environment
  • Basic Awareness of Good Manufacturing Practice Regulations, quality management systems / principles, tools
    and standards.
  • General awareness of industry quality systems/standards, e.g. ICHQ10
  • Detail orientated with knowledge of quality metrics and previous auditing experience
    preferred.
  • Good communication, decision making, negotiating, and problem solving skills
  • Experience in process improvement preferable
  • Customer service orientated, i.e. ability to interact effectively with clients
  • Ability to work under minimal supervision
  • Computer literate
  • Good verbal and written communication in English


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