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View: 112

Update day: 03-04-2024

Location: Visp Valais VS

Category: Executive management Production / Operation

Industry: Staffing Recruiting

Position: Associate

Job type: Full-time

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Job content

We are looking for a Production Quality Specialist for our client Lonza AG in Visp.Responsibilities

Review of the executed Batch Records (e.g. cleaning logs, production documentation review, temperature reports, test procedures (HEPT, FIT), Autoclave and Washing machine protocols, used material, calibration records, sample results recorded in LIMS, logbooks, etc.)
Support preparation of documentation package to enable fast release by QA
Review comments added to the executed Batch Records, clarify with the operations team and evaluate with the responsible QA Manager
Initiate and support accomplishment of Deviations and investigations for Batch Record review related observations
Collect and evaluate KPI data on a regular basis
Support the initiation of CRs and TCRs
Previous experience in GDP and GMP regulated pharmaceutical / API industry is an advantage
English fluent
Experiences with MES System is necessary
Ability to identify non-compliance and gaps from quality standards
Very good communication skills and interaction with all kinds of interfaces within the organization; strong team orientation
Open-minded for new ideas and suggestions; solution-oriented
Agile, highly motivated and dynamic drive
Ability to produce reliable results under stress

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