Responsible for checking manufacturing documentation for conformity, processing change controls, and reviewing and approving deviations and OOS results.
plans (timing, phasing of approach, perform possible extra preliminary investigations, deliverables, organization of documentation and quality assurance) Coordination
Senior Engineering Project Manager
Proclinical Staffing
Visp
Vollzeit
Maintain comprehensive projectdocumentation, including risk assessments, design reviews, and performance qualification (PQ) records.
Zu den Ersten gehören
Operator / Senior Operator
Lonza AG
Visp
Vollzeit
What you’ll do: during the project phase: Support the project team in defining and setting up innovative vaccine production processes.
Zu den Ersten gehören
Senior Scientist Quality Control Biochemistry 80-100%
Lonza AG
Visp
Vollzeit84.000 CHF – 105.500 CHF
Quality Control, Quality Assurance, Project Leaders) Key requirements : PhD in Biochemistry or similar field, or MSc with several years of work experience in Quality
Zu den Ersten gehören
Data Center Manager (f/m/d)
Lonza AG
Visp
Vollzeit89.500 CHF – 122.000 CHF
Documentation of physical installation including rack layout.
Zu den Ersten gehören
Manufacturing Specialist
Lonza AG
Visp
Vollzeit
implementation and control of defined measures Assist document preparation (e.g. electronic batch records, SOPs) specific to the assigned production area Review production documentation
Zu den Ersten gehören
Manufacturing Specialist Mammalian (m/f/d)
Lonza AG
Visp
Vollzeit98.000 CHF – 112.000 CHF
implementation and control of defined measures Assist document preparation (e.g. electronic batch records, SOPs) specific to the assigned production area Review production documentation
(including QA for QC and QA On The Floor), other QA teams and will interact with the the other Operational teams at BioAtrium like Production, Engineering and Project
Senior Principal Scientist in Advanced Synthesis R&D 80-100% (m/f/d)
Lonza AG
Visp
Vollzeit
Contribute to the planning, execution, and documentation of academic research projects in collaboration with internal teams and external institutions.
Biotechnologist (f/m/d) (80-100%)
Lonza AG
Visp
Vollzeit86.500 CHF – 102.500 CHF
Review production documentation and work on deviations, change requests and implementation of CAPAs to ensure high-quality GMP standards.
Manufacturing Specialist Mammalian 100% (m/f/d)
Lonza AG
Visp
Vollzeit98.000 CHF – 112.000 CHF
implementation and control of defined measures Assist document preparation (e.g. electronic batch records, SOPs) specific to the assigned production area Review production documentation
PMO Manager MCRB
Lonza AG
Visp
Vollzeit89.500 CHF – 112.000 CHF
Support the development and rollout of documentation, templates, reporting standards, and local training.
Reviews production documentation and works on deviations, change requests and implementation of CAPAs to ensure high-quality GMP standards.
MSAT Bioconjugates Process Expert (f/m/d) 80-100%
Lonza AG
Visp
Vollzeit86.000 CHF – 106.500 CHF
team (tech transfer, scale up, GMP documentation, equipment) What we're looking for: Master or PhD or equivalent experience in Bioconjugation, Biotechnology, chemical
Technical Document Manager
Proclinical
Visp
Vollzeit72.500 CHF – 98.500 CHF
the coordination and management of technical projectdocumentation within a regulated GMP framework.
Technical Support Associate
Proclinical
Visp
Vollzeit67.000 CHF – 92.000 CHF
Provide raw data documentation, evaluate results, and propose input for designing subsequent experiments.
Manufacturing Specialist Vibe-X (m/f/d)
Lonza AG
Visp
Vollzeit97.500 CHF – 118.000 CHF
What you’ll do: during the project phase Support the project team in defining and setting up innovative vaccine production processes.