QA manager sterile production environment

☞ Randstad

View: 160

Update day: 21-03-2024

Location: Plan-les-Ouates Genève GE

Category: Pharmaceutical / Chemical / Biotech

Industry:

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Job content

Jobdescription

To complete the Quality Assurance & Quality Control department of an international company leader in the pharma sector, we are looking for a
Quality Manager

You will be in charge of the Quality Assurance in the sterile productionSite.

Activities
You will be in charge of releasing the incoming raw materials and consumable;
You will be responsible for the batch records (production and packaging) reviewing;
You will assure the Technical Release of the semi-finished and finished product in compliance to applicable regulations, regulatory dossiers and product specifications;
You will manage all deviations (production, packaging and QC) and complaints investigation;
You will Review/approve for issuance of GMP documents related to production area, preventive maintenance plan, SOPs and validation/qualification documentation related to production area;
You will ensure that activities related to the product quality and sterile operation quality are conform with the company policies and Corporate Quality directives;
You establish compilations and trending of GMP data;
You evaluate any signal detection which could have a potential product quality impact;
You will manage directly the operation and packaging QA team. Your profile
You have a University degree in Pharmacy, Chemistry or Biochemistry with 5 to 10 years experience in GMP environment inspected by FDA, Swiss and other Health Authorities.
Experience in sterile production environment MANDATORY
You are fluent in English (both oral and written).
You have an experience of 5 years as manager.
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Deadline: 05-05-2024

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