Browse by job sector

Senior Scientist

  1. London
Remote work
  1. Contract
Competitive
  1. CAPEX Projects
33875
Apply to this job Save job
Senior Scientist, Drug Product Development - Remote, UK - 2.5-Year Contract 

We are looking for an experienced Senior Scientist for a fantastic 2.5 year contract remote based.

You will be working with our client, a global biopharmaceutical organisation committed to improving the lives of people afflicted with neurological and immunological disease.

This is a superb opportunity if you are looking to advance your career in the field with a supportive and innovative company that will put you first.



Primary Purpose / Regulatory Responsibilities:
  • Establishment of robust, fit for purpose biologicals drug product manufacturing processes for the different development phases (FIM, Ph2, Ph3).
  • Defining and selecting drug product manufacturing processes and parameters for clinical manufacture.
  • Build close collaboration with the External DP Clinical Manufacturing Team for the establishment of drug product processes and manufacturing of stability and clinical DP batches.
  • Support the development and implementation of the DP CMC development strategy within BCPDS.
  • Represent the DP development project team on the TST.
  • Support the definition of DP processes for different types of formulation (liquid in vials,
  • PFS or other container, solid (either lyophilized or spray dried), and any other more innovating formulation addressing parenteral route of administration or other requirements for clinical development and future commercial manufacture.
  • Provide all appropriate support to drug product process development activities (eg filter selection and sizing, target fill volume assessment, compatibility assessments, clinical blinding, etc) as required for clinical development.

Experience:
  • Minimum 3 years experience in sterlie drug product development and/or manufacturing within the pharmaceutical industry is required. Experience within the biopharmaceutical
  • industry is an advantage
  • Good knowledge and technical experience in parenteral liquid drug product development and cGMP manufacturing under aseptic conditions (such as vial, cartridge and pre-filled syringe filling) would be required.
  • Good technical knowledge of sterile DP development covering DP components, process transfer, scale and optimisation. Good knowledge of cGMP.
  • An understanding of the issues and challenges of product development at phase 1 is an advantage

If this role is of interest to you, please apply now! 

 #LI-KT1
Apply to this job Save job
Save as a job alert
List #1

Similar Jobs

Maintenance / Project engineer

Salary

Competitive

Location

Bedford

Salary

Competitive

Sector

CAPEX Projects

Job type

Contract

Location

East Anglia

Description

Maintenance / Project Engineer -  Life Sciences - Bedford - 6-Months  How would you like the opportunity to work with in one of the largest biopharmaceutical projects in the country? If yes,

Reference

35167

Expiry Date

01/01/0001

Bobby Andrews

Author

Bobby Andrews
Bobby Andrews

Author

Bobby Andrews
Read more
Read more
Procurement

Salary

Competitive

Location

San Juan

Salary

Competitive

Sector

CAPEX Projects

Job type

Contract

Location

Argentina

Description

Procurement - Pharmaceuticals - San Juan - 12-Month Contract  This is a fantastic opportunity for a Procurement to join our major, global pharmaceutical client on their latest new-build project

Reference

35286

Expiry Date

01/01/0001

Kristen Scott

Author

Kristen Scott
Kristen Scott

Author

Kristen Scott
Read more
Read more
Quality Engineer

Salary

Competitive

Location

County Mayo

Salary

Competitive

Sector

CAPEX Projects

Job type

Contract

Location

Midlands (Ireland)

Description

Quality Engineer - Westport, County Mayo Located on the picturesque west coast of Ireland, our Global pharmaceutical client is looking for Quality Engineerto join their state of the art

Reference

34865

Expiry Date

01/01/0001

James Smithson

Author

James Smithson
James Smithson

Author

James Smithson
Read more
Read more

Insights

life sciences testing laboratory

Why you should work in Commissioning, Qualification and Validation
Read more

02/07/2023

Your next step as a Validation Engineer
Read more

07/20/2021

pharmaceutical factory construction

Working in an organisation from Start Up Phase

Read more

06/28/2021

VIEW ALL

Send us your CV

Our candidates are the cornerstone of our organisation and we are always looking to connect with new professionals who are seeking their next contract assignment or career opportunity.

Send your CV
Upload your CV