Lead QC & Site Development - New GMP Lab Build

Bachem Holding AG; Stein; On-site; CHF 180,000 - 240,000; Full time

Benefits offered by this job

Dynamic and growing work environment

Internal development opportunities

Pension fund contributions support

Staff restaurant and on-campus leisure

Job summary

Bachem Holding AG is building a new Sisslerfeld manufacturing site in Northwestern Switzerland. We are seeking a Lead QC Sisslerfeld Site Development (a) 100% to establish and lead the ramp-up of the Quality Control organization, setting up laboratories, systems and processes while ensuring regulatory compliance.

You will build and lead the QC team, drive qualification and validation, support QMS implementation, and oversee GMP-compliant operations with audits and inspections during the project

Qualifications

• PhD or MSc in a scientific discipline with chemistry/pharma focus.
• 7+ years in QC/QA with leadership experience in GMP environments.
• Experience with Swissmedic and international regulatory audits.

Responsibilities

• Build, lead, and develop the QC organization for the Sisslerfeld site.
• Drive qualification, validation, and implementation of analytical methods and lab systems.
• Ensure regulatory compliance and inspection readiness across QA functions.
• Coordinate with stakeholders to ensure operational readiness from project to operations.
• Oversee QC lab operations, CAPAs, deviations, and change controls during ramp-up.

Skills

Leadership

Regulatory compliance

Quality systems

GMP knowledge

Cross-functional collaboration

German and English proficiency

Education

PhD or MSc in Chemistry, Pharmacy, or related field

Job description

Bachem Holding AG is building a new Sisslerfeld manufacturing site in Northwestern Switzerland. We are seeking a Lead QC Sisslerfeld Site Development (a) 100% to establish and lead the ramp-up of the Quality Control organization, setting up laboratories, systems and processes while ensuring regulatory compliance.

You will build and lead the QC team, drive qualification and validation, support QMS implementation, and oversee GMP-compliant operations with audits and inspections during the project