QA Analytical Specialist

Our client is active in the biopharmaceutical markets and they are looking to strengthen their Quality team in Switzerland.

Responsibilities

  • You will be responsible for review and QA disposition of data for in process and finished bulk drug substance intended for cGMP use
  • You will provide QA oversight of analytical and microbial laboratory activities
  • You will collaborate with laboratories, manufacturing, QA batch disposition and other internal stakeholders to achieve site, operational and department specific goals
  • You will perform timely review and QA disposition of test data for in process and finished bulk drug substance samples
  • You will provide QA support for Investigations, Deviations, CAPAs, Change Controls and Projects related to laboratory processes, instruments, specifications, methods and SOPs associated with testing of in process samples and finished bulk drug substance intended for cGMP use
  • You will attend relevant operational meetings, support client audits and regulatory inspections

Requirements

  • You will hold a Bachelor’s degree as a minimum and have relevant experience in a QA, QC or cGMP environment in Biopharmaceuticals
  • You must have a strong understanding of cGMP regulations
  • Having experience in Quality Systems, Quality Control and release of biopharmaceuticals for cGMP use is advantageous
  • Fluent in English, spoken & written and a good level of French is required

Interested? Please do not hesitate in sending your CV and/or the best contact details for yourself to info@thetechrg.com and our team of skilled consultants would be very happy to contact you with more details.

Proud to be working in partnership with Talentory AG.

To apply for this job email your details to info@thetechrg.com.