Senior QA Specialist, Project Management 80-100% (f/m/d)

Lonza; Oberwallis; Vor Ort; Vertraulich; Vollzeit

Benefits dieser Stelle

Agile culture

Inclusive workplace

Competitive compensation

Role-based benefits

Zusammenfassung

Lonza in Visp, Switzerland is seeking a Senior QA Specialist to manage GMP-focused projects within BioConjugates. You will ensure API production complies with GMP, support contract manufacturing, and advise development, production, and analytical teams on quality systems.

You will review manufacturing documentation, drive change control, investigate deviations and OOS results, and contribute to continuous improvement of Quality Management Systems while acting as the quality contact during client

Qualifikationen

• Academic degree in Life Sciences or related field.
• Experience in GMP environments within biopharma.
• Experience with project management and stakeholder management.
• Strong communication and teamwork abilities.

Aufgaben

• Ensure API production complies with GMP.
• Support contract manufacturing and advise on GMP across departments.
• Check manufacturing documentation for conformity and change control.
• Investigate deviations and OOS results.
• Contribute to continuous improvement of Quality Management Systems.
• Serve as quality contact for client GMP audits.

Kenntnisse

Project management

Stakeholder management

Communication

Teamwork

Customer focus

Ausbildung

Life Sciences degree

Jobbeschreibung

Senior QA Specialist, Project Management 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.

This role has been created to support the growing business in BioConjugates.

We are looking for a Senior QA Specialist (f/m/d) who wants to manage projects and will support our growing business in BioConjugates. Join us and apply for this exciting opportunity in Visp, Switzerland.

What you will get:

• An agile career and dynamic working culture
• An inclusive and ethical workplace
• Compensation programs that recognize high performance
• A variety of benefits dependant on role and location

As a member of the quality assurance team (PCP Conjugates), you will be responsible to ensure production of APIs is in accordance with Good Manufacturing Practice (GMP).

You will support the contract manufacturing and advise members of development, production, and analytical departments on all aspects of GMP.

You will be responsible for checking manufacturing documentation for conformity, change control, and investigation of deviations and OOS-results.

You will combine regulatory awareness with an entrepreneurial mindset to achieve effective quality solutions.

You will support continuous improvement programs to establish effective Quality Management Systems.

In addition, you will be the quality contact for our clients and will be present during their GMP audits.

What we are looking for:

• Academic degree in Life Sciences (e.g. Microbiology/ Biotechnology/ Chemistry or a related field).
• Significant experience in the biopharmaceutical industry in a GMP environment.
• Relevant experience is preferred, with a focus on independence, sociability, and customer focus.
• Experience in a customer-focused environment, managing stakeholders and their needs independently.
• First experience in project management is preferred.
• Strong communication skills and the ability to combine regulatory awareness with a proactive and team-oriented mindset.
• Excellent English (written and verbal) for customer interaction and a good command of German (B2 level) to communicate with colleagues on a daily basis.

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.