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Scientific Quality Control - Assurance - FTC until Feb 2022

Employer
Labcorp
Location
Huntingdon, United Kingdom
Salary
Competitive
Start date
14 Jul 2021
Closing date
3 Aug 2021

View more

Discipline
Finance / Administration, Administration
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details


Do you want to be in a role that co-ordinates accurate work from within a laboratory?

Are you someone who takes pride in their work, has great attention to detail and also used to working to tight deadlines?

Do you want to the opportunity work for a global organisation who strive to make a difference to people's everyday lives by bringing essential products to the market?

As a Quality Control team member within the CMC (Chemistry, Manufacturing & Controls) team based in Alconbury, Cambridgeshire you will have responsibility to undertake routine checking of analytical qPCR data and reports generated in the department

The job responsibilies will include:

  • Prepare accurate data tables and graphs, and maintain associated records and help maintain laboratory records
  • Respond to Quality Assurance audit comments as appropriate
  • Understand UK and international GLP, GMP and GCP regulations and their application to the work area
  • Interpreting and analysing the results obtained from relevant studies and provide advice to department staff in data interpretation
  • Developing, improving and validating qPCR analytical procedures, ensuring that these meet the objectives of the study and the scientific standards required by clients and regulatory authorities
  • Liaising, on a limited basis, with the client, Company, Sponsors, preparing faxes and other communications as necessary
  • Liaising with the Project Manager / Study Director / responsible Scientist on the performance of technical work involving projects, Studies performed within area of responsibility

What Labcorp Drug Development can offer you:
  • Competitive salaries and a comprehensive benefits package including health cover and contributory pension
  • Unsurpassed career development opportunities. With the support of exceptional people from across the globe and an energized purpose, you will be empowered to own your career journey with mentoring, training and personalized development planning
  • Ability to work with a variety of different people and clients on wide ranging projects

Please note this is a fixed term contract until February 2022
Education/Qualifications:
  • Degree (B.Sc.) or above, or equivalent industry experience.
Experience:
  • Experience in drug development process within either a CRO or Pharmaceutical company
  • Experience of working in a regulatory environment, ideally GLP or GMP
  • Experienced scientist in PCR and good trouble shooting skills
  • Excellent eye for detail- experience of performing quality control checking / review of raw data, reports etc.
  • Able to prioritise, with time management skills

Company

At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions —because we know that knowledge has the potential to make life better for all. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. Here, you can join our more than 70,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives. Join us in our pursuit of answers.

 

 

 

 

Company info
Website
Location
Maidenhead Office Park
Westacott Way
Littlewick Green
Maidenhead
SL6 3QH
United Kingdom

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