Summary
UP$5000
Monday to Friday
9am to 6pm
Central (Company will relocate to TaiSeng after Jun 2023)
Biotechnological Manufacturing industry
Responsibilities
Compile quality metric data required for reporting
Write and issue SOP for site qualification and validation project
Identify deviations and potential risks in manufacturing systems, processes and methods, and their possible causes.
Assess impact to validation for changes that occur during the project and define appropriate validation requirements and approach to meet these requirements.
Review and approve the validation deliverables related to Facility/Utilities/equipment, computerized system (automation) as well as laboratory equipment/system, further to ensure compliance with company procedures, regulatory requirements and cGMP expectations and meeting project schedule.
Requirements
Candidate with working understanding of Lab/GMP Operations, QC, QA, Process Development, Supply Chain and related functions.will have an advantage.
Possess foundational understanding of ICH Q7,Q8, Q9, FDA 21 CFR, Eudralex, PIC/S cGMP guideline.
To Apply, kindly click on the "APPLY NOW" button.
We regret to inform that only shortlisted candidates will be contacted.
Staffking Pte Ltd (20C0358) | Quek Weixiang Gary (R1981768)
Not Specified
