Supply Chain Quality Specialist

Lonza; Oberwallis; Hybrid; Vertraulich; Vollzeit

Benefits dieser Stelle

Agile career development

Inclusive workplace

Competitive hourly rate

Zusammenfassung

Lonza in Visp, Switzerland, seeks a GMP-focused QA/Supply Chain professional for a hybrid, fixed-term role. You will manage TrackWise change requests and concept changes, coordinate with QA, manufacturing, IT and engineering, and drive compliant, efficient drug manufacturing operations.

You will develop SOPs and work instructions, monitor change activities, and support audit readiness while enabling continuous improvement in a regulated environment. Fluency in English; German is a plus.

Qualifikationen

• GMP-regulated QA or supply chain background.
• Experience managing Change Requests, Concept Changes, Change Controls, Deviations, or CAPAs.
• Hands-on TrackWise experience highly valued.
• Ability to write and maintain clear procedures, operating standards, and work instructions.
• Strong cross-functional stakeholder management and communication skills.

Aufgaben

• Support end-to-end management of GMP-related Change Requests and Concept Changes in TrackWise to drive compliant supply chain execution.
• Partner with cross-functional stakeholders across Supply Chain, QA, Manufacturing, Engineering, and IT to perform risk assessments.
• Standardize recurring ways of working by developing, documenting, and maintaining clear SOPs, operating standards, and work instructions.
• Proactively monitor open change activities, follow up on action items, and ensure timely closure of records in line with QMS standards.
• Translate lessons learned and best practices into sustainable procedures, fostering continuous improvement and process simplification.
• Support audit and inspection readiness initiatives, ensuring documentation and quality systems meet strict regulatory expectations.
• Serve as a key subject matter expert, guiding cross-functional teams on TrackWise workflows and compliance standards.

Kenntnisse

TrackWise

Change Requests

Quality Assurance

Cross-functional collaboration

SOP writing

Documentation

English fluency

German knowledge

Jobbeschreibung

Are you passionate about bridging the gap between Supply Chain operations and Quality Assurance in a world-leading life sciences environment? In this dynamic hybrid position based in Visp, Switzerland, you will coordinate GMP-related Change Requests and Concept Changes in TrackWise, standardizing operating procedures to ensure compliant, seamless, and efficient drug manufacturing operations.

This is a hybrid role. Working together in person supports close, real‑time collaboration and team alignment, enabling us to deliver our best work. You will spend 1–2 days per week on‑site in Visp, with the flexibility to work remotely for the remainder of your time.

This is a fixed term contract position until the end of 2026 with a possibility for extension.

What you will get:

• An agile career and dynamic working culture.
• An inclusive and ethical workplace.
• Competitive hourly rate / compensation package.

Compensation for this role will be determined by the candidate’s qualifications, skills, experience, and relevant knowledge.

What you will do:

• Support the end‑to‑end management of GMP‑related Change Requests and Concept Changes in TrackWise to drive compliant supply chain execution.
• Partner with cross‑functional stakeholders across Supply Chain, QA, Manufacturing, Engineering, and IT to perform thorough impact and risk assessments.
• Standardize recurring ways of working by developing, documenting, and maintaining clear SOPs, operating standards, and work instructions.
• Proactively monitor open change activities, follow up on action items, and ensure timely closure of records in line with QMS standards.
• Translate lessons learned and best practices into sustainable procedures, fostering continuous improvement and process simplification.
• Support audit and inspection readiness initiatives, ensuring documentation and quality systems meet strict regulatory expectations.
• Serve as a key subject matter expert, guiding cross‑functional teams on TrackWise workflows and compliance standards.

What we are looking for:

• Background in Quality Assurance, Quality Systems, Supply Chain, or Procurement within a regulated GMP environment.
• Solid experience managing Change Requests, Concept Changes, Change Controls, Deviations, or CAPAs.
• Hands‑on experience with quality management software, with TrackWise experience being highly valued.
• Proven ability to write and maintain clear procedures, operating standards, and technical work instructions.
• Strong cross‑functional stakeholder management, facilitation, and communication skills to drive actions forward.
• Ability to work independently in a hybrid setup (working remotely with 1–2 days per week on‑site in Visp), combining structured analytical thinking with proactive follow‑up.
• Professional fluency in English; local language capabilities (German) are a plus.

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.

As Lonza’s talent acquisition partner, please note, Randstad is responsible for the engagement and contracting of this contingent role.