Skip to main content

MSAT Engineer

  1. West Coast
  1. Contract
Competitive
  1. Drug Safety / Pharmacovigilance
03-05-2023
31271

This vacancy has now expired

MSAT Process Engineer – Cell & Gene Therapy – 6 Month Contract – Philadelphia

Are you looking for your next Process Engineer opportunity? Quanta have the new position for you.

Working alongside our client, a global innovator in Cell & Gene Therapy, as their newest MSAT Process Engineer you will be responsible for providing support to CDMOs, particularly related to development and GMP manufacturing of gene-edited cell therapy drug products.

Led by mission-driven and visionary scientists, our client is truly passionate about their impact on the discoveries of cell gene and therapy. Your role here will make a difference to the world and is a contract you can be proud of.

MSAT Process Engineer Responsibilities:
  • Will interface with Contract Development and Manufacturing Organizations (CDMOs) that are part of our supply chain and primarily oversee activities related to GMP manufacture of our gene edited autologous drug products.
  • The ideal candidate has deep early and late-stage process development experience, experience with transferring processes to Manufacturing and interfacing with in-house and/or external Manufacturing organizations.
  • Experience with cell therapy manufacturing and process development, risk analysis, investigation methodologies, change control systems and related QA documentation is a plus.
About you:
  • BSc/MSc in Chemical/Biochemical Engineering or related discipline
  • Cell Therapy experience – HSC/CAR-T/IPSC’s and CRISPR/Cas9
  • Experience interfacing directly with CDMOs
  • Comprehensive knowledge of GMP, aseptic processing, ATMP requirements
  • Experience developing and scaling up multiple products across different product lines.
  • Experience in working with CDMOs and third parties for process development and cGMP manufacturing.
Are you a good fit for this MSAT Process Engineer position? We want to hear from you. Apply now!

The candidate must have the rights to work in the location stated in the job advert.

Please note, Quanta part of QCS Staffing does not sponsor Visa applications.

To view Quanta's privacy policy, please visit our website
Save as a job alert
List #1

Similar Jobs

Documentation Specialist

Salary

Competitive

Location

Paris

Salary

Competitive

Sector

Drug Safety / Pharmacovigilance

Job type

Permanent

Location

France

Description

Documentation Specialist – Life Sciences – Paris – Permanent This is a unique opportunity for a Documentation Specialist to join our client – an esteemed partner for regulatory and

Reference

31189

Expiry Date

06/30/2023

Kathryn Taylor Read more
Clinical Studies Project Manager

Salary

Competitive

Location

Paris

Salary

Competitive

Sector

Drug Safety / Pharmacovigilance

Job type

Contract

Location

France

Description

Clinical Studies Project Manager – Pharmacovigilance – 6 Month Contract – Paris This is a unique opportunity for a Clinical Studies Project Manager to join our client – an esteemed partner

Reference

30603

Expiry Date

06/30/2023

Kathryn Taylor Read more
QPPV

Salary

Competitive

Location

Belgium

Salary

Competitive

Sector

Drug Safety / Pharmacovigilance

Job type

Permanent

Location

Antwerp

Description

QPPV – Life Sciences – Permanent – Belgium  Our client, a prominent consulting and solutions firm specialising in risk management and compliance services for the pharmaceutical industry, has

Reference

31472

Expiry Date

06/29/2023

Kathryn Taylor Read more

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.