Projektleiter/in Analytik

Lonza Group Ltd.; Oberwallis; Vor Ort; Vertraulich; Vollzeit

Benefits dieser Stelle

Agile career

Inclusive workplace

Performance-based compensation

Ownership of projects

Cross-functional collaboration

Continuous improvement

Local benefits in Visp

Zusammenfassung

Lonza Group Ltd. in Visp, Switzerland, is seeking a QC Project Lead to ensure QC activities align with project goals, manufacturing schedules, and customer expectations.

You will act as the primary interface between customers and internal stakeholders, coordinating analytical activities and driving execution in a GMP-regulated environment. You'll lead cross‑functional collaboration across laboratories, QA, Production, and project teams, managing QC risks, deviations, investigations, CAPAs, and

Qualifikationen

• Degree (MSc, with experience or a PhD) in Biochemistry, Biology, Chemistry or life sciences.
• Experience in Quality Control, Analytics, Manufacturing Support, or GMP-regulated environments.
• Strong project coordination and stakeholder management in cross-functional environments.
• Fluency in English; German is an advantage.

Aufgaben

• Serve as QC single point of contact for assigned customer projects.
• Coordinate and drive QC deliverables to support milestones and timelines.
• Bridge laboratories, QA, Production, MSAT and project teams for decisions and execution.
• Manage QC risks, deviations, investigations, CAPAs and change controls per GMP.
• Represent QC during customer interactions, audits, inspections and meetings.
• Provide visibility on priorities, analytical scope, timelines, and costs.
• Ensure customer requirements meet compliance, quality, and business objectives.
• Drive proactive communication and issue resolution to sustain momentum and satisfaction.
• Support continuous improvement of QC processes and operations.

Kenntnisse

Quality Control

Project coordination

GMP compliance

Analytical testing

Cross-functional collaboration

Communication

Ausbildung

MSc or PhD in Life Sciences

Jobbeschreibung

The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. In this role, you will act as the Quality Control (QC) Project Lead for customer programs, ensuring that QC activities are aligned with project objectives, manufacturing schedules, and customer expectations. You will serve as the key interface between customers and internal stakeholders, coordinating analytical activities, managing risks, and driving execution in a fast-paced GMP-regulated environment.

What you will get:

• An agile scientific career in a dynamic, GMP-regulated environment.
• An inclusive and ethical workplace that values collaboration and accountability.
• Compensation programs that recognize performance and technical expertise.
• Opportunities to deepen your expertise and take ownership of impactful projects.
• Exposure to cross‑functional collaboration and regulatory interactions.
• A supportive culture that encourages continuous improvement and learning.
• Competitive local benefits.
• Benefits in Visp

What you will do:

• Serve as the Quality Control (QC) single point of contact for assigned customer projects.
• Coordinate and drive QC deliverables to support project milestones, manufacturing schedules, and customer timelines.
• Act as the bridge between laboratories, QA, Production, MSAT, and project teams to enable effective decision-making and execution.
• Manage QC-related risks, deviations, investigations, CAPAs, and change controls in accordance with GMP requirements.
• Represent QC during customer interactions, audits, inspections, and cross-functional project meetings.
• Provide clear visibility on project priorities, analytical scope, timelines, and associated costs.
• Ensure customer requirements are met while balancing compliance, quality standards, and business objectives.
• Drive proactive communication and issue resolution to maintain project momentum and customer satisfaction.
• Support continuous improvement initiatives to enhance QC processes, efficiency, and operational excellence.

What we are looking for:

• Degree (MSc,with experience or a PhD) in Biochemistry, Biology, Chemistry, or another life sciences discipline.
• Experience in Quality Control, Analytics, Manufacturing Support, or a related GMP-regulated environment, ideally within biologics.
• Strong project coordination and stakeholder management skills with the ability to navigate complex cross-functional environments.
• Customer-focused mindset with excellent communication, influencing, and relationship-building capabilities.
• Ability to understand analytical testing requirements and translate them into project deliverables and priorities.
• Independent, organized, and solution-oriented working style with a strong sense of ownership and accountability.
• Proven ability to prioritize effectively and drive execution in a dynamic, fast-paced environment.
• Fluency in English is required; German is considered an advantage.

About Lonza

At Lonza, our people are our greatest strength. With more than 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.