Records Management Jobs in Visp
1 - 12 von 12
Suchergebnisse - Records Management Jobs in Visp
Lonza Group Ltd.-Visp
documentation package
• Involvement in MES Syncade Recipe change management
• Collaborate with Operations team to clarify ambiguities in the executed batch records
• Support in the management of Quality Records (Change Request, CAPAs, Deviations/Investigations...
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Swisslinx-Visp
Requirements:
Project Strategy & Lifecycle Management:
• Define technical project scope, success criteria, and strategic roadmap in alignment with GMP and operational goals.
• Drive project lifecycle from conceptual design through to performance qualification...
Lonza Group Ltd.-Visp
elektronische Master Batch Records (EMBR); Überprüfung auf Widerspruchsfreiheit mit Zulassungsdokumenten, Prozessbeschreibungen, Transferdokumenten, Prüfplänen, Parameterlisten etc.
3. Kontrolle der ausgefüllten Reinigungsprotokolle auf Vollständigkeit...
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Lonza-Visp
and maintain Quality Systems and related processes at the Visp site including deviation, CAPA and complaint management, change control, document management, training, inspection management, risk management, Quality councils and management review.
You...
Careforce24-Visp
operational teams, quality assurance, and the Engineering team responsible for overseeing the Engineering, Procurement, and Construction Management (EPCM) contractor.
Project Duration: Approx. 6 Months
Starting Date: ASAP
Key Responsibilities
Project Scope...
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TN Switzerland-Visp
managing the preparation and ensuring the submission of CMC documentation supporting clinical trial applications and marketing submissions.
3. Review and evaluate the regulatory impact of the change requests for the Small Molecule Drug Substances and Drug...
Records Management Stellenangebote – Weitere Orte:
Swisslinx-Visp
Ensure cGMP compliance through the investigation process, and to drive their quality records to completion......
efinancialcareers.nl -
EPM Scientific - Phaidon International-Visp
documentation and equipment complies with client standards
• Authoring DR, CAPA, and Investigation in Trackwise to participate in Deviation Record Board
• Managing the resolution of test deviations, CAPA, and TCR
• Ensuring that test results and deviations are...
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Lonza-Visp
Drug Master Files (DMFs), Site Master Files (SMF) or other records on behalf of customers.
• Utilize prior analytical (Quality Control, Analytical Development) and/or manufacturing process (Operation) or Quality Assurance or Program Management...
Lonza-Visp
and maintain Quality Systems and related processes at the Visp site including deviation, CAPA and complaint management, change control, document management, training, inspection management, risk management, Quality councils and management review.
You...
ten23 health-Visp
and evaluation of cleaning agents.
8. Oversee change and deviation management for cleanrooms and hygiene-related procedures.
9. Coordinate with external cleaning staff to ensure efficient and effective cleaning services.
10. Analyze environmental monitoring data...
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Lonza Biologics Porriño SLU-Visp
DMFs), Site Master Files (SMF) or other records on behalf of customers.
• Utilize prior analytical (Quality Control, Analytical Development) and/or manufacturing process (Operation) or Quality Assurance or Program Management experience to question...
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