Job Description

Responsibilities

: " Our client is a global Pharmaceutical company headquartered in the UK. It currently has 1 opening for Senior QA Validation Specialist. This role requires candidates to: Provide validation strategy and QA oversight on computer system validation (lab equipment, process equipment, IT, automation system - DeltaV, PEMS, AMS) and equipment/system validation (vessels, fermenter, washing machine, washing cabinet, chambers, Isolator) and SIP Review and approve validation protocols and reports including validation lifecycle documents, but not limited to the following: URS, FS, SLIA, RA, IQ, OQ, PQ, RTM Review and approve change control and provide validation impact assessment for changes Review and approve deviation and CAPA. Be part of the core member for the deviation investigation and RCA Review and approve SOPs, if required Requirements: Bachelor's Degree in Chemical Engineering or equivalent At least 5 years of experience in Computer System Validation (CSV) and Equipment Validation Relevant QA oversight experience in CSV and Equipment Validation Be familiar with validation life-cycle documents such as IQ, OQ, PQ etc To have sound knowledge and experience in Data Integrity principle and practice To have sound knowledge and be familiar with regulatory requirements and industry practices on validation Must be comfortable with contract basis role ", "identifier":{ "@type": "PropertyValue", "name":"Psc Biotech Pte. Ltd.", "value": "*******" }, "datePosted": "2022-08-02", "validThrough": "2022-09-01", "url": "********************", "employmentType" : "FULL_TIME",
Benefits