Process Validation Specialist
vor 6 Stunden
Today, Lonza is a global leader in life sciences operating across three 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. The Process Validation Specialist is responsible for defining the validation strategy and executing process validation activities to support the implementation of commercial manufacturing processes at Lonza Visp. The Process Validation Specialist also reviews the validation status as part of continued process performance verification. Additionally, the role includes assessing the validation impact of deviations and change request in commercial projects. Key responsibilities: Process Validation: Develops, executes, and documents validation protocols; ensures ongoing CPV/PQR. Deviation & Change Control: Manages deviations and change controls per compliance standards. Customer Collaboration: Represents validation in projects; liaises with customer technical/quality teams. Audit Support: Serves as validation representative in audits and inspections. Training & Compliance: Follows training, policies, and cGMP; applies ICH, FDA, EMA, PIC guidance. Mentoring: Supports colleagues through knowledge sharing and technical advice. Key requirements: PhD or Master`s Degree in Chemistry or an related field Experience in process manufacturing, in GMP environment is preferred Ability working within a virtual team and managing the collaboration of different departments Fluent language skills in English are required 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. #J-18808-Ljbffr
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MSAT Process Validation Specialist
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Zermatt, Schweiz Lonza VollzeitA global biopharmaceutical company is seeking an MSAT Process Validation Specialist for their Visp site in Switzerland. This role involves defining validation strategies, preparing documentation for a vaccine manufacturing process, and ensuring compliance with industry standards. The ideal candidate will hold a master's degree and have strong skills in...
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Senior QA Specialist – Process Validation
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Zermatt, Schweiz Lonza VollzeitA leading life sciences company in Visp is seeking a Senior QA Specialist for process validation in biopharmaceutical manufacturing. The ideal candidate will have advanced degrees in Chemistry or Biotechnology and extensive experience in validation functions. Responsibilities include ensuring compliance with manufacturing processes and leading validation...
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MSAT Process Validation Specialist
Vor 4 Tagen
Zermatt, Schweiz Lonza VollzeitProcess Validation Expert MSAT (m/f/d) Today, Lonza is a global leader in life sciences operating across three c ontinents. 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...
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Process Validation Lead
vor 6 Stunden
Zermatt, Schweiz Lonza VollzeitA global leader in life sciences is seeking a Process Validation Specialist in Zermatt, Switzerland. In this role, you will define validation strategies and manage process validations for commercial manufacturing. Candidates should have a PhD or Master's in Chemistry, experience in process manufacturing in a GMP environment, and fluency in English. You will...
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Senior QA Specialist, Process Validation 80-100%
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MSAT Process Validation Lead – Team Leadership
vor 1 Woche
Zermatt, Schweiz Lonza VollzeitA global leader in life sciences seeks a Process Validation Team Lead in Zermatt, Switzerland. The role involves leading a team responsible for process validation of mammalian manufacturing processes, ensuring compliance with regulatory standards. Candidates should possess a relevant degree, minimum 5 years of process validation experience in a cGMP...
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Zermatt, Schweiz Lonza VollzeitA leading life sciences company in Zermatt, Switzerland, is seeking a Process Validation Expert to manage validation activities for biopharmaceutical manufacturing processes. The ideal candidate will have a degree in biotechnology or related fields and at least one year of experience in process validation within a cGMP environment. Responsibilities include...
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Mammalian Process Validation Expert – MSAT
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Zermatt, Schweiz Lonza VollzeitA global life sciences leader is seeking a skilled professional in Zermatt for a process validation role within the biopharmaceutical sector. The successful candidate will be responsible for ensuring compliance with regulatory standards and managing complex validation projects. Required qualifications include a relevant degree and at least one year of...
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Process Validation Expert MSAT
vor 3 Wochen
Zermatt, Schweiz Lonza VollzeitToday, Lonza is a global leader in life sciences operating across three 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,...
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Senior QA Specialist
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Zermatt, Schweiz Lonza VollzeitA leading life sciences company in Switzerland is seeking an experienced professional to support validation specialists and review documentation for cleaning validation. The ideal candidate will hold a Master degree or PhD in Chemistry or Biotechnology, have significant experience in biopharmaceutical manufacturing, and fluency in English is required. This...