Skip to main content

This job has expired

Experienced QC Scientist

Employer
Labcorp
Location
York, United Kingdom
Salary
Competitive
Start date
27 Oct 2021
Closing date
29 Oct 2021

View more

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

Job Details


Do you have solid experience of Client Study Management and looking for your next opportunity within this exciting, growing team?

Are you interested in expanding your career development opportunities and management responsibility?

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

Our UK site in York is currently recruiting for an Experienced QC Scientist/Study Manager/Director to join the CMC (Chemistry, Manufacturing Controls) division and will be responsible for the managing of batch testing, release testing, sample analysis, stability, assay development, assay establishment or validation/transfers with monoclonal antibodies.

Labcorp Drug Development 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 Labcorp Drug Development helped develop.

Labcorp Drug Development can offer you:
  • Competitive salaries and a comprehensive benefits package including health cover and contributory pension
  • Unrivalled opportunities to develop a successful career in the scientific industry, utilizing multiple analytical techniques
  • Unsurpassed career development opportunities, with the ability to develop your management skills
  • 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:

  • Act as a Subject Matter Expert (SME) within BioCMC with knowledge of standard and non-standard study designs and the ability to draw scientific conclusions
  • Working method knowledge e.g. instruments used within the laboratories and ability to make decisions on assay results, suggest assay/technique advancements/improvements to the client, and follow through with the client as necessary
  • Assist in the preparation/review of training modules in areas of expertise and mentors and develops others in the group
  • In-depth knowledge of study process from award to finalisation archiving and amendments to final reports and to write and review Analytical Procedures, Policies, SOPs and Guides where appropriate.
  • Employ effective general management, communication and interpersonal skills to work within the project teams, with the Client and other project stake-holders e.g. supporting functions at Labcorp Drug Development
  • Participate in client regulatory audits and perform revenue recognition where required
  • Responsible for on-time delivery of data, project documents, and quality documents

Relocation assistance may be available for this role
Education/Qualifications:
  • The post holder should ideally have a relevant degree and extensive industry experience/PhD and industry experience in CMC Drug Development
Experience:
  • Technical expertise in at least one of the following scientific disciplines - HPLC, ELISA, Cell Based Assays, Capillary Electrophoresis and compendial techniques
  • Experience in similar types of study management and client management
  • An in-depth understanding of health and safety policies and a good understanding on GMP/GLP/GCP and an up to date knowledge of regulatory guidelines
  • Able to communicate effectively at all levels with internal employees and external clients, with the ability to get things done by influencing others.
  • Commercial awareness, interpersonal and negotiating skills and able to learn and maintain knowledge of process excellence processes

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
Send job

Get job alerts

Create a job alert and receive personalised job recommendations straight to your inbox.

Create alert