QC Instrument Expert Global Pharma Manufacturing Site Pest County
6 days ago
For investment projects, you play a determinative role in the procurement process of the new machine park and the support during the installation period. Day-to-day work requires close cooperation with internal and external departments such as supplier companies or QC Managers.
Your key responsibilities:
Create and continuously update documentation related to the inspection of devices and processes within your area of controlDesign validation plans for computer systems used in product quality control testsPrepare calibration and qualification plans and reports for analytical instrumentsEnsure quality assurance perspectives are considered when ordering new equipment and defining user requirements (URS)Collaborate in the development of procedures and the commissioning of instrumentsFollow, implement, and continually improve data integrity guidelines within quality controlParticipate in the development of economic and efficiency indicators characteristic of the area (data provision and analysis)Continuously monitor the GMP requirements, ensure compliance, and provide necessary training and updatesProactively identify and assess risks, and manage existing risks in line with corporate and cGMP guidelines We appreciate your application if you have:
University degree as chemist, chemical engineer, bioengineer, pharmacist, or specialized teaching diploma3+ years of professional experience in pharma/chemical industry - primarily analytical experience, especially experience gained in quality control Maintenance/qualification knowledge and practice related to analytical equipmentKnowledge of validation / qualification documentationGMP knowledgeUser-level computer skillsIntermediate professional English language skill Should you be interested in this position please let us know by submitting your CV via the advertisement - our colleagues will soon contact you with the details.
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