Proven expertise in document management or technical documentation for CapEx or OpEx projects.
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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
Creation, revision and review of cGMP documentation (SOP’s, Quality Instructions, protocols, reports…) based on a standard format related to quality control activities
Responsible for checking manufacturing documentation for conformity, processing change controls, and reviewing and approving deviations and OOS results.
We are looking for a Senior QA Specialist (f/m/d) who wants to manage projects and will support our growing business in BioConjugates.
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
expertise Ability to interface and communicate directly with customers and regulatory bodies Excellent written and oral communication to include accurate and legible documentation
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
Manufacturing Specialist Vibe-X (m/f/d)
Lonza AG
Visp
Vollzeit97.500 CHF – 118.000 CHF
Manufacturing Specialist Vibe-X (m/f/d) Switzerland, Visp Today, Lonza is a global leader in life sciences operating across three continents.
Manufacturing Specialist (m/f/d)
Lonza AG
Visp
Vollzeit93.500 CHF – 117.000 CHF
Manufacturing Specialist (m/f/d) Switzerland, Visp The actual location of this job is in Visp, Switzerland.
Lab Technician
Proclinical Staffing
Visp
Vollzeit66.500 CHF – 89.000 CHF
Strong organizational skills for documentation and administrative tasks. Ability to maintain laboratory equipment and ensure operational efficiency.
Biotechnologist
Proclinical
Visp
Vollzeit69.000 CHF – 98.500 CHF
Prepare and maintain production documentation, including MBR forms and GMP logbooks.
Biotechnologist (3-Month Contract)
Proclinical Staffing
Visp
Vollzeit71.500 CHF – 103.500 CHF
Compile GMP documentation related to cleaning activities. Collaborate with the manufacturing team to ensure timely and compliant batch production.
Senior Engineering Project Manager
Proclinical Staffing
Visp
Vollzeit
Maintain comprehensive project documentation, including risk assessments, design reviews, and performance qualification (PQ) records.
QC operator
Proclinical Staffing
Visp
Vollzeit
play a key role in performing environmental monitoring in classified areas, including air, surfaces, and utility systems, while maintaining accurate and timely documentation
Automation Expert
Proclinical Staffing
Visp
Vollzeit72.500 CHF – 99.500 CHF
Skilled in managing change records and commissioning documentation. Proficient in troubleshooting and resolving equipment/system issues.
Technical Support Associate
Proclinical Staffing
Visp
Vollzeit66.500 CHF – 90.500 CHF
Provide raw data documentation, evaluate results, and propose input for designing subsequent experiments.