Technician – Quality Control Microbiology Laboratory

Gi Life SciencesNeuchâtelEURESippubblikat 23/09/2026
Meħtieġ:LeadJunior

Ref 2580076 \| Date: 21 Sept 2026

![Gi Life Sciences]( )

Technician – Quality Control Microbiology Laboratory

Technician – Quality Control Microbiology Laboratory

Temporary mission – 6 months (start ASAP)

Location: Neuchâtel area

Your role

As a Technician in the QC Microbiology Laboratory, you support day\-to\-day lab operations and ensure compliant sample handling and microbiology activities in a GMP\-regulated environment. You may also perform selected non\-product testing, support investigations, review data, and mentor junior colleagues to ensure efficient and high\-quality laboratory execution.

Your responsibilities

  • Support lab operations (housekeeping, alarm acknowledgement, reagent preparation, inventory management, ordering materials/reagents, execution of work orders).
  • Ensure accurate sample/material labelling and maintain sample tracking, labelling, and chain\-of\-custody records according to procedures.
  • Maintain a safe, compliant, and well\-organized laboratory in line with GMP requirements.
  • Perform non\-product testing as required ( , raw material visual inspection, environmental monitoring sampling, utility monitoring).
  • Perform data review for assigned laboratory activities and ensure right\-first\-time documentation.
  • Communicate sample management activities and priorities with lab and manufacturing teams.
  • Support deviation and laboratory investigations through data gathering and participation in interviews as needed.
  • Support and/or draft updates to laboratory documents (SOPs, work instructions) for managerial review and approval.
  • Record and monitor performance metrics; contribute to lab planning and scheduling inputs.
  • Train and mentor colleagues on task execution and general job duties.
  • Contribute to and lead simple projects; support complex projects within the team.
  • Actively participate in Operational Excellence (OpEx) and Continuous Improvement (CI) initiatives.
  • Support audit/inspection readiness and, if needed, represent the department during internal/external audits and regulatory inspections.
  • Model company values and complete all tasks safely and compliantly.

Your profile

  • Strong experience with Environmental Monitoring (EM) sampling is required.
  • Experience in a GMP\-regulated laboratory environment; ability to interpret and apply cGMP, USP, regulatory requirements and industry best practices.
  • Comfortable working in a fast\-paced environment, managing multiple priorities and meeting deadlines.
  • Strong attention to detail, organization skills, and critical thinking.
  • Good working knowledge of electronic systems (MS Office/email) and lab data systems ( , LIMS).
  • Education/experience (one of the following or equivalent):
  • High school diploma/GED with ≥3 years relevant experience, or
  • Associate degree in a technical/scientific discipline with ≥2 years experience, or
  • Bachelor’s degree (non\-technical) with ≥1 year experience.
  • Languages: English and/or French.

jpid1ce4dbejm jpit0939jm jpiy26jm

Persuna ta' kuntatt

Imsemmija minn min iħaddem fl-avviż — għal mistoqsijiet u l-applikazzjoni tiegħek.

  • Gi Life Sciences