Senior QA Logistics Lead - Cold Chain & GMP Compliance

Lonza

Oberwallis

On-site

Vertraulich

Full time

7 days ago
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Benefits offered by this job

Competitive salary
Lifestyle benefits
Inclusive workplace

Job summary

Lonza Visp site is seeking a QA Logistics professional to provide quality oversight of supply chain activities, warehousing, cold chain, and material flow, ensuring GMP and regulatory compliance. You will manage deviations, change controls, and CAPAs in TrackWise, while partnering with Logistics, Warehousing, Manufacturing, and Quality Control to support compliant site operations.

The role emphasizes maintenance and improvement of quality procedures, audits, and continuous improvement

Qualifications

  • Academic degree in Pharmaceutical Sciences/Biochemistry or Supply Chain/Logistics or related field.
  • Experience in Quality Assurance within pharmaceutical environments and cGMP.
  • Knowledge of GMP/GDP regulatory requirements.

Responsibilities

  • Provide QA oversight for logistics, warehousing, cold chain, and material flow activities.
  • Oversee deviations, change controls, and CAPAs within TrackWise.
  • Maintain quality systems for logistics processes to stay GMP/GDP compliant.
  • Assess GMP impact of cold-chain alarms, temperature excursions, and incidents.
  • Collaborate with cross‑functional stakeholders to support compliant site activities.
  • Improve quality procedures and support audits/regulatory interactions.

Skills

Communication skills
Collaborative mindset
Organizational skills
Problem solving
Stakeholder communication

Education

Degree in Pharmaceutical Sciences or Biochemistry or Supply Chain/Logistics

Tools

TrackWise

Job description

Lonza Visp site is seeking a QA Logistics professional to provide quality oversight of supply chain activities, warehousing, cold chain, and material flow, ensuring GMP and regulatory compliance. You will manage deviations, change controls, and CAPAs in TrackWise, while partnering with Logistics, Warehousing, Manufacturing, and Quality Control to support compliant site operations.

The role emphasizes maintenance and improvement of quality procedures, audits, and continuous improvement

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