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Visp, Valais/Wallis, Schweiz/Suisse/Svizzera/Svizra
Onsite
Location: the actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.
You will represent Quality Assurance in cross-functional teams, establish and maintain interfaces with the Manufacturing teams, QC, Support Functions, Project- and Site Engineering project / technology transfer to effectively execute tasks related to Drug Product processes.
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
The full list of our global benefits can be also found on https://www.lonza.com/careers/benefits.
What you will do:
Represent Quality Assurance in cross-functional teams, establish and maintain interfaces with the Manufacturing teams, QC, Support Functions, Project- and Site Engineering project / technology transfer to effectively execute tasks related to Drug Product processes
Act as point of contact for Drug Product QA related questions and issues related to the manufacturing operations
Ensure manufacturing shop floor QA oversight
Assess, review and approve quality records e.g. deviations, change control, CAPAs, investigations, effectiveness checks, extensions, complaints, APR/PQRs in line with current local SOPs
Review and approve GMP-relevant documents (SOPs, protocols, risk assessments, manufacturing process descriptions, equipment recipes)
Review and approve executed manufacturing batch records or other executed GMP documents (logbooks, forms, protocols)
Responsible to present Drug Product QA topics during the conduction of internal audits as well as customer audits and regulatory inspections within DPS Visp / Biologics / Visp site
Provide GXP-related trainings to Module D Operations personnel (eg. GMP, Good Documentation Practice, Good Aseptic Behavior)
Support continuous improvement programs to establish an effective Quality Management System for DPS Visp
What we are looking for:
University degree or equivalent in Chemistry / Biology / Biotechnology or a related field
Long-term experience working in the GMP environment of the pharmaceutical industry, preferably in Drug Product
Experience working in a QA department is strongly required
Fluent English language skills are required, German language is an advantage
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.
Ready to shape the future of life sciences? Apply now.