Senior QA Specialist - Product Quality Review 80-100% (f/m/d)

Lonza; Zermatt; Hybrid; CHF 80’000 - 100’000; Vollzeit

Zusammenfassung

A leading life sciences company is seeking a Process Validation Specialist in Zermatt, Switzerland. This role involves ensuring compliance with internal SOPs and requires an academic degree in Chemistry/Biotechnology, with proficiency in both English and German. Ideal candidates will have experience in GMP manufacturing and excellent communication skills. This position offers the opportunity to contribute to impactful work in the life sciences sector.

Leistungen

Agile career opportunities

Inclusive and ethical workplace

High performance compensation programs

Qualifikationen

• Experience in GMP manufacturing is required.
• Proficiency in writing scientific reports in English.

Aufgaben

• Ensure the trainings required for the Process Validation Specialist are completed.
• Support project teams to ensure compliance with Lonza SOPs.
• Maintenance of the PQR status overview list.
• Contact person for PQR/CPV during customer audits.

Kenntnisse

Fluent English

Fluent German

Excellent communication skills

Critical thinking

Ausbildung

Academic degree in Chemistry/Biotechnology or related field

Jobbeschreibung

Location: Visp, HybridWork Model. Relocation assistance is available for eligible candidates and their families, if needed.

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

What you’ll 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

The full list of our global benefits can be also found on https://www.lonza.com/careers/benefits.

What you’ll do:

• Ensure the trainings required to the Process Validation Specialist with focus on Product Quality Review are completed
• Active participation and contribution to the validation team to ensure the experience is shared and the practices are further developed
• Support the project teams to ensure compliance with Lonza SOP CHVI-348, CHVI-301000 and related documents
• Preparation and approval of the monthly PQR Newsletter
• Maintenance of the PQR status overview list CHVI-204288
• Participation in the preparation of process specific PQRs review and approval of PQRs
• Evaluation and approval of change requests, deviation and SOPs concerning PQRs
• Contact person for PQR/CPV during customer audits

What we’re looking for:

• Academic degree in Chemistry/ Biotechnology or any related field
• Fluent English AND German are required
• Proficiency in writing scientific reports in English
• Experience in GMP manufacturing is required
• Excellent communication skills
• Someone who challenges the status quo and looks for opportunities to make improvements in his/her area of the business and beyond

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.