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Senior Quality Associate x2

Job in 3000, Bern, Canton de Berne, Switzerland
Listing for: CSL
Full Time position
Listed on 2026-08-04
Job specializations:
  • Quality Assurance - QA/QC
  • Healthcare
    Data Scientist, Medical Science
Salary/Wage Range or Industry Benchmark: 120000 - 180000 CHF Yearly CHF 120000.00 180000.00 YEAR
Job Description & How to Apply Below

The Opportunity

The Senior Quality Associate ensures that internal operations across Global Pathogen Safety (GPS) laboratories in Bern are conducted in compliance with the OECD Principles of Good Laboratory Practice (GLP), GCLP (ISO/IEC 17025), and Good Research Laboratory Practice. The role may be required to support biosecurity and biosafety to CSL operations in Bern in alignment with relevant global, regional, and country-specific regulations, as well as CSL internal policies and procedures.

It supports the implementation and improvement of GLP/GCLP/GRLP-aligned quality systems and processes across laboratory networks, advancing global quality strategies for GPS activities. Additionally, this position may be required to provide quality oversight for nonclinical development activities in Research EU and collaborate globally to ensure consistent CSL quality standards. This position supports inspection readiness, audits, and regulatory interactions, helping ensure timely and compliant completion of quality actions, such as corrective and preventive actions (CAPAs).

In addition, the Senior Quality Associate models the CSL Way and fosters a strong, proactive quality culture, driving sustainable improvements in quality systems, processes, and cross-site collaboration.

Your Tasks & Responsibilities
  • Establish procedures, standards, and systems to meet local and regulatory requirements with stakeholders.
  • Liaise with stakeholder departments regarding quality assurance and compliance related issues
  • Maintain documentation in line with OECD principles of GLP, ISO 17025 standards and internal CSL standard – Good Research Laboratory Practice (GRLP)
  • Review and approve study plans, protocols, and reports for GLP compliance; prepare QA statements for final reports.
  • Plan and conduct inspections (GLP/GRLP process, facility, study, document) to ensure compliance and report findings and recommendations.
  • Report inspection results to Facility Management, Study Director, and Principal Investigator as needed.
  • Advise CSL facility owners and project managers on biosecurity and biosafety compliance (as required)
  • Ensure inspection readiness; host/participate in regulatory agency inspections and provide support, direction and guidance relating to responses
  • Support internal audit program and perform internal inspections per guidelines.
  • Ensure CSL facilities comply with all biosafety, biosecurity, and regional regulatory requirements.
Your Skills And Experience Education
  • BS degree in relevant biological science, science, or related discipline
Experience
  • Minimum 3 years’ experience working in at least one of the following: OGTR, Department of Agriculture, applicable EU Directives, and/or similarly governed laboratories
  • R&D Quality Assurance or relevant process development facilities
  • Understanding and application of standards for microbiology and pathogen safety and containment
  • Knowledge of OECD Principles of GLP
  • Experience and knowledge in the application of Quality Systems
Competencies
  • Commitment to improvement
  • Strong planning and organizational skills
  • Good presentation, negotiation, and decision-making skills
  • Strong customer focus
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Position Requirements
10+ Years work experience
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