Biotech Jobs in Sitten
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Suchergebnisse - Biotech Jobs in Sitten
Swisslinx AG-Sitten
Swisslinx AG in Visp, Switzerland, is seeking a biotechnology expert to support upstream manufacturing in a GMP environment. You will combine strong technical expertise in biotechnology and mammalian cell culture with leadership and operational...
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appcast.io -
KPC International-Sitten
KPC International in Visp, Switzerland, is seeking a Deviation Specialist to own and investigate deviations at a large-scale mammalian cell culture facility. You will define root causes, assess impact on product and systems, and draft CAPAs to...
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CTC Resourcing Solutions-Sitten
CTC Resourcing Solutions is seeking a USP Biotechnologist Manager for a contract role in Valais, Switzerland, to lead production support and people development for active pharmaceutical ingredient operations. You will partner with Production Leaders,...
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appcast.io -
Panda International-Sitten
and drive CAPAs through to completion.
You will collaborate with SMEs and cross-functional stakeholders to ensure investigations meet cGMP requirements while contributing to continuous improvement initiatives in a regulated biotech environment.
#J-18808...
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Rebrid-Zürich, 156 km von Sitten
liegt auf agilen, inspirierenden und fordernden Unternehmen aus verschiedenen Branchen (Fintech, Biotech, IT, Industrie, E-Commerce).
Trust Work wächst und bietet Chancen, wenn du engagiert, selbstbestimmt und unternehmerisch arbeiten willst...
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BioTalent-Sitten
Experience
• 3–5 years in project engineering or project management
• Experience in pharmaceutical, biotech, or chemical industries
• Hands‑on experience with process equipment in GMP environments
• Proven ability to deliver engineering projects
Technical...
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Vispact-Sitten
und COMOS für Bestellung, technische Bewertung und Kapazitätsplanung
• Technische Ausbildung (FH/HF/Uni) in Verfahrenstechnik, Maschinenbau, Chemietechnik oder verwandtem Fachbereich
• Idealerweise Berufserfahrung im regulierten Umfeld (Pharma / Biotech...
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BioTalent-Sitten
compliant and validated.
• Participate in audits and regulatory inspections.
• Support quality systems including deviations, CAPAs, and change management.
Requirements
• 2–6 years of Validation/Qualification experience.
• GMP pharmaceutical, biotech...
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Proclinical Staffing-Sitten
validation, temperature mapping, and controlled storage rooms.
• Support continuous improvement initiatives and other assigned duties.
Key Skills and Requirements:
• Experience in GMP-regulated pharmaceutical, biotech, or cell and gene therapy environments...
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KPC International-Sitten
related field.
• Previous experience in Deviations and cGMP in a regulated pharmaceutical/API industry is a strong advantage.
• Knowledge of biotech. manufacturing processes and analytical methods is an advantage.
• Experience with Human and Organizational...
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Lonza Group AG-Sitten
University Degree or equivalent experience, or vocational education (EFZ, FH, HF, BSc.)
• Proven experience in the operation and maintenance of pharmaceutical plants or the biotech industry
• Proficiency in SAP, COMOS (Plant Engineering Software), DeltaV...
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Lonza-Sitten
Engineer managing large-scale (>250M CHF) pharmaceutical or biotech capital projects in EPCm environments.
• Direct experience representing the Client owner side within the pharmaceutical or life sciences industry.
• Strong proficiency in capital project...
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Lonza-Sitten
organizations for new biotech manufacturing processes.
• Responsible for review and final release of records like Standard Operating Procedures (SOPs), Master Manufacturing Batch Records, Material Specifications, Deviations, Change Requests, Effectiveness...
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Lonza-Sitten
therapies, we look forward to welcoming you on board.
Lonza is a leading global partner in the healthcare industry, empowering innovative medicines and solutions through scientific expertise and advanced manufacturing across pharma, biotech, and nutrition...
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