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ID: POS08426

Quality Control Analyst (m/f/d)

Pharma & Biotech
Asap
4 months
Neuchatel, Switzerland
Temporary Employment
K-Recruiting Schweiz AG
Contact:

Cristina Croppi

+49 89 1890998-625

cristina.croppi@k-recruiting.com

Quality Control Analyst (M/F/D)

 

Tasks:

  • Perform QC analyses and sample collections in compliance with SOPs, cGMPs, and pharmacopoeial standards

  • Complete documentation (forms, logbooks, results systems) per Good Manufacturing and Documentation Practices

  • Notify supervisors of non-conforming/invalid results and initiate quality events within deadlines

  • Proactively report planning deviations and escalate procedural deviations as required

  • Comply with and promote EHS rules; address unsafe behaviors and open EHS events promptly

  • Participate in maintaining a safe, compliant lab environment during all activities

  • Execute validation and qualification protocols for methods, systems, equipment, and consumables

  • Perform recalculations, supervise external results, and reconcile controlled documents

  • Ensure equipment calibration/maintenance is current and report any issues.

  • Conduct GEMBAs, review alarms, and uphold 5S lab organization standards.

  • Train analysts and apprentices on equipment and GMP; act as a backup trainer

  • Maintain up-to-date training status (e.g., SABA) and complete modules on time.

  • Act as SME for methods/equipment, resolving complex issues and supporting CAPAs

  • Back up supervisor or QC lifecycle roles and contribute to risk analyses and regulatory submissions

  • Manage logbooks, trend reports, and data systems (RAM, Bolton) with strong data integrity focus

  • Assess result validity/conformity and escalate priority conflicts as needed.

  • Support and initiate corrective and preventive actions in collaboration with lab leadership

 

Qualification:

  • Minimum CFC (Swiss Federal Certificate) in microbiology or equivalent experience in the pharmaceutical or biotech industry.

  • 2–5 years of experience in a cGMP lab or minimum 2 years as Analyst I.

  • At least 5 years of experience in a cGMP lab or minimum 5 years as Analyst II

  • Good to excellent knowledge of lab methods.

  • Good understanding of cGMP requirements.

  • Knowledge of Data Integrity and its application in a regulated environment.

  • Comfortable with standard office and IT tools (MS Office suite).

  • French and technical English required.

  • English level: minimum B2

 

Requirements: 

Start: 21.07.2025

Duration: 4 months

Capacity: 5 days per week

Location: Neuchatel, Switzerland 

Have we peaked your interest? Let's go
Contact
Cristina Croppi
+49 89 1890998-625
cristina.croppi@k-recruiting.com