Analyst Jobs in Visp
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Suchergebnisse - Analyst Jobs in Visp
Panda International-Visp
QC Analyst
We are looking for a dedicated QC Analyst to join our state-of-the-art facility in Visp, Switzerland. In this role, you will be responsible for ensuring compliance with GMP and safety standards, while executing and managing daily...
appcast.io -
Lonza-Visp
and implementing reliability strategies, conducting failure analysis and improving maintenance processes to enhance overall plant reliability, efficiency and reduce downtime. Key responsibilities: Design and implement reliability improvement plans Develop, monitor...
Lonza Group Ltd.-Visp
Laboratory Analyst / Laborant, Quality Control 4-Schichtbetrieb (m/w/d)
Lonza ist heute ein weltweit führendes Unternehmen im Bereich Life Sciences, welches auf drei Kontinenten tätig ist. Wir sind in der Wissenschaft tätig, jedoch gibt es keine...
appcast.io -
Lonza-Visp
and implementing reliability strategies, conducting failure analysis and improving maintenance processes to enhance overall plant reliability, efficiency and reduce downtime. Key responsibilities: Design and implement reliability improvement plans Develop, monitor...
Lonza-Visp
and collaborate with a vibrant and international team. Your primary responsibilities will revolve around conducting routine analysis of biopharmaceuticals using HPLC. This role offers a lot of variety with many different projects and a wide variety of HPLC...
Lonza Group Ltd.-Visp
meetings and workshops as required.
8. Respond to ad hoc requests for data, data analysis, and presentation materials.
9. Provide support to the project controls functional group as and when required.
Key Requirements:
1. Bachelor’s Degree in the field...
appcast.io -
Lonza-Visp
technology and instruments, and collaborate with a vibrant and international team. Your primary responsibilities will revolve around conducting routine analysis of biopharmaceuticals using HPLC. This role offers a lot of variety with many different projects...
Lonza-Visp
want to be part of.
Equipment used for the analysis of chemical and biological products has to be properly tested and is released/approved by authorized people for its intended use. The increasing computerization of laboratory equipment adds complexity...
Arxada-Visp
in laboratory scale and actively support their implementation in commercial scale. This includes the experimental planning and execution as well as data analysis, writing of research reports, preparation of customer presentations and documentation...
CTC Resourcing Solutions-Visp
Technical Documentation, Process, GAP Analysis, Risk Assessment, among others.
• The validation documentation deliverables include URS, DQ, FMEA, Risk Assessments, FAT, SAT, Protocols (IQ, IOQ, OQ, PQ).
• Prepare validation documents.
• Execution of IQ/OQ...
appcast.io -
Coopers Group GmbH-Visp
Your responsibilities:
Validation activities: Facilities, Utilities, Validation Life Cycle.
Execution, Technical Documentation, Process, GAP Analysis, Risk Assessment, among others.
The validation documentation deliverables include URS, DQ, FMEA...
Vaxcyte-Visp
and documentation are in place. Ensure that all testing activities are well-documented and comply with Good Documentation Practices (GDP).
• Review and approval of analytical data, test reports, and certificates of analysis (CoAs) generated by contract laboratories...
appcast.io -
Lonza-Visp
with the project cross-functional team (PD, Ops, QA, QC, etc.)
• Change control management
• Support production campaigns and leading process troubleshooting on the manufacturing floor as needed
• Process optimization by regular data analysis and compilation...
surfingwave.app -
Visp
developments
• Support nimble project management and clear decisions through excellent cost documentation and timely communication
• Actively participate in the tender/bid process--from initial tender/bid documentation through analysis and reporting
• Oversee...
icims.com -
Lonza AG-Visp
in cooperation with the Bioprocess engineer, Plant Lead, QA, and MSAT.
• Monitor and change processes under change control during the start-up, qualification and production phase. Participate in risk and process deviation analyses.
• Provide support outside...
xing.com -
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