QC Microbiology Scientist

vor 13 Stunden


Visp Valais, Schweiz Panda International Vollzeit

Scientist QC Microbiology

Visp, Switzerland – 9-Month Contract (Extension Possible)

Job Description

As a Scientist QC Microbiology, you will join the Quality Control Microbiology department at a leading global biotechnology and pharmaceutical manufacturing site in Visp, Switzerland.

In this role, you will act as a technical representative of the QC Microbiology department both internally and externally, supporting customer meetings, audits, inspections, and project-related activities. You will serve as the scientific SME for project-specific and routine microbial analyses, ensuring high-quality execution, timely delivery, and cross-functional alignment across business units.

Key Responsibilities

Technical & Scientific Expertise (QC Microbiology)

  • Represent the QC Microbiology department during internal discussions, customer meetings, audits, site visits, and inspections for assigned projects.
  • Act as the scientific SME for microbial and project-specific analyses, including monitoring, evaluating, and coordinating the implementation of improvements.
  • Provide expert input into method-related topics, study designs, validation/verification activities, deviations, CAPAs, and analytical transfers.

Project & Work Package Coordination

  • Coordinate and ensure timely completion of assigned work packages for different business units (BUs).
  • Facilitate effective communication and alignment across interdisciplinary teams (e.g., QC, QA, Validation, MSAT, Operations).
  • Support documentation, data review, and reporting activities related to microbial testing and project workstreams.

Essential Skills

  • Minimum 2 years of experience in QC Microbiology, Microbial Analytics, or related laboratory roles within pharma/biotech or regulated GMP environments.
  • Strong understanding of microbial methods, aseptic techniques, and GMP requirements.
  • Ability to communicate effectively across teams and represent QC in cross-functional and customer-facing settings.
  • Strong organizational skills and ability to manage multiple project tasks with tight timelines.
  • Analytical, detail-oriented, and proactive in identifying improvements and risks.
  • German language skills preferred; strong English required.
  • Availability for on-site work (100% on-site preferred; maximum 2 days remote per week).

Preferred Experience

  • Prior experience in large-scale biologics manufacturing or exposure to global CDMO environments.
  • Knowledge of method validations, method transfers, and microbial trending.
  • Familiarity with deviations, CAPAs, and audit/inspection preparation.
  • Strong technical writing skills and proficiency with QC/QA documentation systems.

Additional Insights

  • Start Date:
    ASAP
  • Contract Duration:
    9 months (extension possible)
  • Location:
    Visp, Switzerland (100% preferred; max 2 days remote)

Interested?

Send your CV to
Khanyi Mabena
at
k.-
, or contact directly at

to learn more.



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