Senior QA Specialist – Logistics 80-100% (f/m/d)

Lonza Group; Oberwallis; Teletrabalho; CHF 120 000 - 180 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Relocation assistance

Competitive salary

Comprehensive benefits package

Resumo da oferta

Lonza Group in Visp, Switzerland, seeks a Senior QA Specialist – Logistics to lead quality oversight of logistics, warehousing, cold chain, and material flow activities. The role ensures compliance with GMP, GDP, and Lonza standards across the site, addressing deviations, change controls, and CAPAs within TrackWise.

The successful candidate will collaborate with cross-functional teams, review cold-chain events, and support audits and regulatory interactions.

Qualificações

• Academic degree or equivalent in pharma/science or supply chain.
• Experience in Quality Assurance within pharmaceutical industries or GMP environments.
• Knowledge of Swiss/EU/US GMP regulations for audits and compliance.
• Strong communication and collaboration skills across functions.
• Fluent in English; German is an advantage.

Responsabilidades

• Provide QA oversight for logistics, warehousing, cold chain, and material flow activities to ensure GMP/compliance.
• Provide QA oversight for supply chain and logistics operations, managing deviations, change controls, and CAPAs in TrackWise.
• Own and maintain quality-relevant logistics processes ensuring GMP, GDP, and Lonza standards compliance.
• Review GMP impact of cold-chain alarms, temperature excursions, storage and transport incidents.
• Collaborate with Logistics, Warehousing, Supply Chain, Manufacturing, QC and other stakeholders for compliant site activities.
• Maintain and improve quality procedures related to logistics and warehousing activities.
• Support audits, inspections, and regulatory interactions with documentation and SME input.
• Contribute to inspection readiness and continuous improvement through risk-based quality oversight.

Conhecimentos

Quality Assurance

Logistics

Cross-functional collaboration

GMP compliance

Audit readiness

Problem solving

English proficiency

Formação académica

Academic degree in Pharmaceutical Sciences/Biochemistry or Supply Chain/Logistics or related field

Ferramentas

TrackWise

Descrição da oferta de emprego

Senior QA Specialist – Logistics 80-100% (f/m/d)

Location: the actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.

The QA Logistics group sits within QA Supply Chain and provides key quality oversight and support for the Switzerland Visp site. This group supports warehousing operations, cold-chain management, and the movement and storage of raw materials and products.

This position will focus on implementing and managing robust cross-functional support for supply chain and logistics operations across the site. You will be responsible for ensuring Quality Assurance oversight of supply chain processes, warehousing activities, cold-chain management, and associated quality systems, while maintaining compliance with Lonza standards, industry best practices, and national and international regulatory requirements.

What you will get:

• An agile career and a dynamic work culture.
• An inclusive and ethical workplace.
• Compensation programs that recognize high performance.

In addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits. Our full list of tailored local benefits can be found below.

• Provide QA oversight for logistics, warehousing, cold chain, and material flow activities to ensure compliance with GMP and regulatory requirements.
• Provide Quality Assurance oversight for supply chain and logistics operations across the site, ensuring appropriate management and quality assessment of deviations, change controls, and CAPAs within TrackWise.
• Own and maintain quality-relevant logistics processes, ensuring procedures, controls, and quality system requirements remain compliant with applicable GMP, GDP, and Lonza standards.
• Review and assess the GMP impact of cold-chain alarms, temperature excursions, storage and transportation incidents, and other logistics-related quality events.
• Partner with Logistics, Warehousing, Supply Chain, Manufacturing, Quality Control, and other stakeholders to support compliant site activities and effective issue resolution.
• Maintain and improve quality procedures, standards, and processes related to logistics and warehousing activities.
• Support audits, inspections, and regulatory interactions by providing documentation, subject matter expertise, and follow-up actions.
• Contribute to inspection readiness and continuous improvement initiatives through risk-based quality oversight and process improvements.

What we are looking for:

• Academic degree in Pharmaceutical Sciences/ Biochemistry or Supply Chain/Logistics or related field or Relevant work experience in Quality Assurance and/or Production/Supply Chain/Logistics and/or Quality Control in pharmaceutical industries and cGMP-controlled environments.
• Knowledge of Swiss, EU, and US GMP regulations relevant to audit/inspections and compliance systems.
• Strong verbal and written communication skills (English required, German is an advantage).
• Ability to communicate quality and compliance requirements to varying levels and functions of the organization.
• Strong collaborative mindset and the ability to build relationships quickly.
• Strong organizational skills, and ability to balance multiple priorities simultaneously.
• Ability to solve problems, understand details and strategic picture, providing practical solutions.
• Experience partnering with cross-functional stakeholders in a manufacturing, supply chain, or operational environment.

About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Why Lonza:

We are a place of unique opportunity, where your ideas, expertise and ambition can make a real difference. Here, will have the freedom to grow, the support to succeed and the chance to contribute to work that matters.

We are the makers of the medicines of tomorrow.