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Manufacturing Technician; Support Operations

Job in 3930, Visp, Canton du Valais, Switzerland
Listing for: Proclinical Staffing
Full Time position
Listed on 2026-02-05
Job specializations:
  • Manufacturing / Production
    Quality Engineering, Operations Engineer, Pharmaceutical Manufacturing, Validation Engineer
Salary/Wage Range or Industry Benchmark: 30000 - 80000 CHF Yearly CHF 30000.00 80000.00 YEAR
Job Description & How to Apply Below
Position: Manufacturing Technician (Support Operations)
Location: Visp

Join a high‑performing CMO where your manufacturing expertise keeps support operations running with precision, efficiency, and flawless coordination.

Proclinical is seeking a Manufacturing Technician to provide technical and logistical support for manufacturing operations. This role focuses on ensuring smooth, GMP-compliant processes across upstream (USP), downstream (DSP), and in-process control (IPC) areas. You will play a key role in calibration, material readiness, equipment handling, sample management, and maintaining safe and efficient operations.

Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.

Responsibilities:

  • Perform daily calibration of equipment used in IPC and DSP, including preparation and use of WFI.
  • Conduct checks on single-use assemblies and execute column buffer exchange activities.
  • Operate autoclaves, including loading, cycle execution, and unloading sterilized materials.
  • Manage materials and chemicals, including completing checklists, notifying engineers of discrepancies, and ethanol aliquotation following GMP and safety standards.
  • Maintain clean and GMP-compliant production spaces through room cleaning and inoculation area tasks.
  • Deliver samples to designated areas such as QC and IPC.
  • Support 6S principles to ensure organized and audit-ready work spaces.
  • Complete accurate GMP documentation for all tasks and adhere to safety, quality, and environmental procedures.
  • Collaborate with QA, QC, and Bioprocess Engineers to ensure seamless operations.

Key Skills and Requirements:

  • Training or qualifications in Chemical Engineering, Biotechnology, Laboratory Technology, or Pharmaceutical Production Technology.
  • Strong understanding of GMP principles and cleanroom operations.
  • Ability to read and follow SOPs, batch records, and technical instructions in English.
  • Hands-on experience with bioreactors, media-buffer preparation, chromatography systems, ultrafiltration-diafiltration (UF-DF), and autoclave operations is advantageous.
  • Familiarity with GMP documentation, batch execution, and deviation reporting is a plus.
  • Experience working in clean rooms of Grade C-D or higher is preferred.
  • Fluency in English is required;
    German proficiency is an advantage.

If you are having difficulty in applying or if you have any questions, please contact Emile De Beer at

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data -

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