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Quality Assurance/Quality Control Consultant - Oferta z Jobs.pl

Produkcja, Przemysł » Produkcja, Przemysł - inne

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Quality Assurance/Quality Control Consultant

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  • Quality Assurance/Quality Control Consultant 6 Month-Immediate Start- Switzerland Level: Quality Assurance(QA)/ Quality Control (QC) Consultant Contract: 6-12 Month Contract Salary: Negotiable Location: Switzerland Language: English & German Summary QA consultant is required to complete an urgent contract for 6-12 months based in Switzerland. The successful candidate should have experience with cGMP to support product development. This is an immediate start role and the details are as follows: Responsibilities * Responsible for review and update of Quality control process documentation, SOP's, WOI's, TEI's, FOB's, RARs and other quality related documentation * Review and assess local and global change controls * Review and asses deviation reports escalating as needed * Support in completions of PQRs * Ensure the definition of appropriate CAPA's as required * Manage and develop quality systems * Review of MBRs, batch production records and supporting documents * Set batch status in LIM's and SAP including QP release * Perform QA release of batches and intermediates * Set batch status in LIMS and SAP excluding QP release * Take over equivalent competencies for other products if delegations approved by the qualified person * Requesting blocking of equipment, processes and products * Definition of quality related corrective and preventive actions * Performance measurement fulfilment of duties and tasks as described before and as to be defined in the yearly performance talks * Responsible for quality matters related to activities performed in the production and during process development * Assure efficient and effective quality assurance activities at required cGMP levelQualifications * Minimum 3 years industry experience in testing * Degree in applicable field (biological or pharmaceutical field) * Strong knowledge of Quality assurance * Inspection experience * Know how of biological manufacturing process * Knowledge of cGMP * Knowledge of risk management activities * Collecting and implementing stakeholder feedback for test methods instruction from scientific experts, EHS, QA and Quality Systems * Revision of existing and writing of new SOPs for QC processes * Fluent in spoken and written English and German d To make an application or to find out more please contact: Amie Touray (0)#LI-AT1


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