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Full-time, Part-time
bachelor degree
Flexible work options, Learning and development opportunities, Relocation support, Compensation programs
Posted 6d ago
~40 hrs/week
Responsibilities
The operator will execute biopharmaceutical production operations while ensuring strict adherence to cGMP, safety, and quality standards. They will also identify and resolve process deviations while maintaining accurate documentation and supporting team training.
Requirements
Candidates must have an educational background in biotechnology, chemistry, or a related life sciences discipline. Previous experience in a regulated manufacturing environment and a strong understanding of cGMP principles are required.
Full job description
Operator / Biotechnologist (m/f/d) 50%-100%
Location: Visp, Switzerland
The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.
Join our growing manufacturing teams in Visp and contribute to the production of life-changing medicines. This is an exciting opportunity for biotechnologists at various career stages to work in a highly innovative life sciences environment while developing technical expertise and supporting global healthcare advancements.
This is a fully site-based role. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.
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 dependent on role and location.
Flexible work options, including part-time opportunities where applicable.
Ongoing learning and development opportunities to support career growth.
Contribute to the manufacture of biopharmaceutical products while ensuring compliance with safety, quality, and cGMP requirements.
Execute production operations across different manufacturing processes, including documentation and process-related calculations.
Identify, investigate, and help resolve process deviations to support continuous manufacturing excellence.
Collaborate closely with cross-functional teams, including production, quality, and engineering stakeholders.
Maintain accurate production records and support regulatory and quality standards.
Assist in onboarding and training new team members, sharing technical knowledge and best practices.
Support continuous improvement activities that enhance operational performance, safety, and product quality.
What we are looking for
Education in biotechnology, biopharmaceutical sciences, chemistry, or a related life sciences discipline.
Experience working in a pharmaceutical, biotechnology, or regulated manufacturing environment.
Understanding of cGMP principles and quality-focused manufacturing practices.
Ability to identify and solve process-related issues in a structured and compliant manner.
Strong attention to detail and commitment to safety and quality standards.
Effective communication skills in English; German language skills are advantageous.
Flexibility to work in shift patterns, including 4-shift operations where required.
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.
Lonza is a pioneer and world leader in the CDMO industry, setting the pace with cutting-edge science, smart technology, and lean manufacturing. United by a common purpose, we turn our customers’ breakthrough innovations into viable therapies and manufacture the medicines of tomorrow.
Founded in Switzerland in 1897, our company is the first and original CDMO, and today we are more dynamic, agile and forward-focused than ever before. As one of the largest Western CDMOs, we bring together a global team of around 18,500 colleagues across five continents to deliver comprehensive, integrated solutions for our customers' complex needs.
For our customers and their patients, we bring quality, safety and reliability to bring life-enhancing and life-saving treatments to market at speed and at scale. For our colleagues, we strive to create a sense of belonging and inclusion where every person can thrive and bring their best.
How many Manufacturing jobs are open in Visp, Switzerland right now?
There are currently 120 open manufacturing positions in Visp, Switzerland listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Manufacturing roles in Visp, Switzerland?
Companies currently hiring include Lonza, Arxada - NA Wood Protection Business Unit, Vaxcyte, ten23 health, Fusion Consulting, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Manufacturing jobs in Visp, Switzerland?
Yes — 11 of the 120 open manufacturing positions offer remote or hybrid work (0 remote, 11 hybrid).
How do I apply for Manufacturing jobs in Visp, Switzerland?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.