Senior Pharma Validation Engineer

The Senior Validation Engineer is responsible for the qualification or requalification of laboratory equipment within the targeted schedule. **Responsibilities**: - Responsible for managing and writing of qualification related documentation but not limited to Qualification Plan and IQ, OQ, PQ and ERES Test Scripts for QC laboratory equipment (lab bench and...

**Responsibilities**: - Monitor day-to-day Validation activities in accordance with approved SOPs / Plan / Policies for a large scale, multi-product, GMP biotech contract manufacturing facility - Participate in review and approval of Validation Protocols / Reports including site discrepancies and deviations investigation / closure - Support / participate in...

A leading company in temperature mapping solutions in Singapore is seeking a qualified professional to plan and execute temperature mapping studies and ensure validation compliance within GMP environments. Key responsibilities include performing CQV and supporting documentation for regulatory compliance. The ideal candidate holds a degree in Engineering or...

Join to apply for the Senior Process Engineer (Pharma) role at Wood 2 days ago Be among the first 25 applicants Join to apply for the Senior Process Engineer (Pharma) role at Wood Get AI-powered advice on this job and more exclusive features. Job DescriptionWood is currently recruiting for a Process Engineer with extensive experience in pharmaceutical and...

**Responsibilities**: - Support general validation activities (equipment qualification, system qualification, and cleaning validation). - Develop, review and/or approve validation lifecycle document and protocols/reports in accordance with relevant policies, standards, procedures and guidelines, and completed in a timely fashion - Manage qualification...

About Us Headquartered in Denmark, NNIT Singapore Pte Ltd is a rapidly expanding leader in life science consulting, delivering innovative solutions across Singapore and the broader Asian region since 2011. We provide comprehensive, end-to-end services tailored to life science clients, covering every aspect of the value chain-from laboratory environments and...

**Responsibilities**: - Support equipment qualification, system qualification, and cleaning validation. - Develop, review and/or approve validation lifecycle document and protocols/reports in accordance with relevant policies, standards, procedures and guidelines, and completed in a timely fashion. - Review Turnover / Vendor Packages as part of the project...

**Responsibilities**: - Support equipment/system qualification and cleaning validation - Develop validation lifecycle document and protocols/reports in accordance with relevant policies, standards, procedures and guidelines, and completed in a timely fashion - Manage qualification/validation execution and lead the validation deviation investigations...

**Responsibilities**: - Support equipment/system qualification and cleaning validation - Develop validation lifecycle document and protocols/reports in accordance with relevant policies, standards, procedures and guidelines, and completed in a timely fashion - Manage qualification/validation execution and lead the validation deviation investigations...

Job Scope - Performing technical assessment and sizing for safety relief valves, rupture discs, vent devices and others. - Originating and checking PRD sizing calculations for Pressure Relief Valves, Bursting/Rupture Discs and Conservation & Breather Vents as per International Standards in API. - Specification for purchasing PRDs - Drafting Pressure Relief...