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Senior Analyst - PCR Analyst - 9 month FTC

Employer
Labcorp
Location
Huntingdon, United Kingdom
Salary
Competitive
Start date
11 May 2021
Closing date
9 Jun 2021

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Discipline
Medical Affairs, Scientific Advisor
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)
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Job Details


Do you have solid Analytical experience and looking for your next opportunity?

Are you interested in expanding your career development opportunities?

Do you want to be a part of the world's leading drug development company?

Our UK site in Alconbury, Cambridgeshire is currently recruiting for an Experienced QC Analyst to join the CMC (Chemistry, Manufacturing Controls) d ivision and will be responsible for performing analytical work on studies using qPCR and/or RTqPCR, DNA/RNA extraction via manual and/or automated methods and provide specialist technical advice and training to department staff and study sponsors.

Covance by Labcorp has helped pharmaceutical and biotech companies develop one-third of all prescription medicines in the market today. Chances are, you or someone you know has benefitted from a medicine or medical device that Covance by Labcorp helped develop.

What Covance by Labcorp can offer you:
  • Ability to work with a variety of different clients on wide ranging projects
  • Opportunity to work in a rapidly expanding and leading edge field

Job responsibilities include:

  • Performing allocated analytical work on projects and studies, ensuring that work is performed to satisfactory scientific standards, in accordance with the project plan or protocol, GMP, GLP and the relevant SOPs
  • Developing, improving and validating analytical procedures, ensuring that these meet the objectives of the study and the scientific standards
  • Interpreting and analysing the results obtained from relevant studies and provide advice to department staff in data interpretation
  • Producing accurate scientific reports of the work undertaken by self or under one's supervision, ensuring that these reflect the requirements of the project plan or protocol, GMP/GLP and the relevant SOPs and to report on work performed to Team Leader
  • Developing, improving and validating analytical procedures, ensuring that these meet the objectives of the study and the scientific standards required
  • Liaising, on a limited basis, with the client, Company, Sponsors
  • To provide specialist technical advice and training to department staff and study sponsors

Please note, this is a Fixed Term Contract until February 2022

Education/Qualifications:
  • Degree (B.Sc.) or above, or equivalent industry experience
Experience:
  • Experience of working in a regulatory environment, ideally GLP or GMP ideally in a CRO or Pharmaceutical/research company
  • Exprience in performing qPCR and/or RTqPCR, DNA/RNA extraction via manual and/or autiomated methods
  • Experienced scientist in field of expertise, ideally with method development / trouble shooting and validation experience
  • Able to prioritise and excellet 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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