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Senior QA Specialist, QA Operations; f​/m​/d

Job in Stalden, Valais, Switzerland
Listing for: Lonza
Full Time position
Listed on 2026-06-19
Job specializations:
  • Quality Assurance - QA/QC
    QA Specialist / Manager, Quality Control / Manager, Quality Engineering, Quality Technician/ Inspector
Salary/Wage Range or Industry Benchmark: 80000 - 100000 CHF Yearly CHF 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Position: Senior QA Specialist, QA Operations 80-100% (f/m/d)
Location: Stalden

Senior QA Specialist, QA Operations 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.

We are looking for a Senior QA Specialist (m/f/d) to join multifunctional QA Operations team in the Bioconjugates Business unit, who will support to establish and maintain quality management & compliance processes. You will work closely with various quality, engineering and operational functions to ensure cGMP compliant manufacturing and documentation

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.

Responsible for project specific QA Operation tasks during Commissioning / Qualification.

Responsible for review and final release of records such as Standard Operating Procedures (SOPs), Master Manufacturing.

Batch Records, Material Specifications, Quality Risk Assessments, Deviations, CAPAs, Change Requests, Effectiveness Checks, Testing Protocols & Reports…etc.

Managing independently stakeholders and their needs in a customer focused environment.

Participate and support regulatory inspections and customer audits.

What we are looking for:

Academic degree in Biotechnology/ Biochemistry or a related field.

Significant experience in biopharmaceutical manufacturing, preferably in a QA function.

Strong background in cGMP and broad knowledge in biotechnological manufacturing processes, validation approaches and risk management.

Sound experience in representing Quality and Compliance in projects.

Good communication skills and experience in interaction with all kinds of interfaces within the organization.

Experience in the use of the following systems would be preferred:
Track Wise, LIMS, DMS and SAP.

Excellent written and spoken English - knowledge of written and spoken German would be 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.

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Position Requirements
10+ Years work experience
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