Biotech Jobs in Sitten
1 - 13 von 13
Suchergebnisse - Biotech Jobs in Sitten
Swisslinx AGSittenappcast.io
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...
BioTalentSitten
BioTalent, a global biotechnology organisation, is seeking a QA Validation Specialist to support a major facility expansion. The role focuses on QA oversight of qualification and validation activities within a GMP-regulated environment.
You will...
CTC Resourcing SolutionsSittenappcast.io
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,...
KPC InternationalSitten
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...
RebridZürich, 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...
Panda InternationalSitten
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...
VispactSitten
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...
Proclinical StaffingSitten
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...
BioTalentSitten
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...
BioTalentSitten
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...
KPC InternationalSitten
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...
LonzaSitten
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...
LonzaSitten
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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