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Analytical Development & Quality Control Manager

Switzerland   •  CHF60 - CHF73 per hour  •  Contract/Temporary, Full time

Job Responsibilities:
Design, plan, organise, interpret and report results of scientific experiments for the preparation and timely delivery of drug substance (DS) or drug products (DP), processes and procedures. Lead and manage all project and local network activities as well as support/coach/mentor team members, participate in subteams and contribute to overall GPDQA strategies and goals. AD/QC Manager must ensure that products are delivered according to quality standards defined during development and in compliance with GMP and regulatory guidelines.
The Manager working in AD/QC will have the following responsibilities and tasks:

  • Responsible for a project portfolio of up to 4 small projects (typically up to phase 2) or 1-2 highly complex or late-stage projects (typically phase 3 and commercial).
  • Proactively communicate key issues and other critical topics in a timely manner to the appropriate management level and/or to any other relevant project team member(s) Manages a team of direct reports or for matrix organization lead with indirect leadership
  • Leads cross-functional teams related to analytical topics
  • Acts as a Subject-Matter expert (SME) on different analytical areas
  • Organization of laboratory activities. Follow the processes defined in the Guidelines and SOP?s.
  • Development, optimization and implementation of analytical methods, e.g., for purity-, stability-, cleaning verification/validation-, excipients-, content-, and potentially genotoxic impurity determinations as well as write-up of these documents for implementation.
  • Representation of AD/QC in technical project team and CMC team meetings

Candidate's requirements:

  • College-, or university-degree or equivalent education in the field of chemistry, biochemistry, pharmacy, biology or chemical engineering with 12+ years BS, 9+ years MS or 2+ years of PhD experience in the pharmaceutical industry with demonstrated previous success in a managerial function.
  • In addition to knowledge of the GMP/regulatory requirements, a strong background in analytical chemistry is required.
  • Personality and disposition to manage professionals effectively in a matrix system. High flexibility, superior communication, time-management and team working skills.
  • Diligent attention to details.
  • Willingness to limited travel.
  • Ability to work independently and to take initiative.
  • Proficient in English.
  • Strong skills in timeline development and management.
  • Excellent problem-solving skills, excellent team-player, including an ability to work with diverse teams

For more information, please contact Fandi Hatib on +441727 817600 or email fhatib@achieva.co.uk

  • Agency: Achieva Group Limited
  • Reference: FH-38
  • Posted: 15th June 2022
  • Expires: 13th July 2022

Achieva Group Limited

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