Salary: up to $5.5k
Job Duration: 6 months
Working Days & Hours: 5 Days (8am – 4.30pm)
Location: 5 Days (8am – 4.30pm)
Job Description:
- Able to lead project for Method validation/verification/transfer to introduce new/remediated QC methods for testing existing and new products independently
- Subject matter expert in method validation, verification and transfer; covering wide arrays of methods and complex techniques
- Author of Method validation/verification/transfer Protocols, Reports, Reports, ensuring GMP compliance in ICH Q2(R1), USP <1225>, USP <1226>, EU GMP Chapter 6, and WHO Annex
- Ensure timely release of methods to support commercial production, manufacturing investigations and product investigations
- Ensure RFT in the method introduction process
- Maintain validated status of assays by establishing a control and monitoring strategy to ensure that the method is in the state of control, and the data generated from the method is reliable. Project Management: Analytical Equipment Qualification
- Able to lea project for Analytical Equipment Qualification to qualify/ re-qualify QC equipment for testing existing and new products independently
- Subject matter expert to provide technical advice to Local QC in laboratory related troubleshooting, e.g. lab equipment failure
- Author of equipment qualification documents as indicated in global procedures
Job Requirements: Min Degree in Pharmaceutical Science/Chemistry w 3 years of relevant experience
Interested candidates, please submit your resume to: [email protected]
Ally Audrey Lok Xin Woon
Recruit Express Pte Ltd (Healthcare & Lifescience)
Company EA Licence number : 99C4599
Personnel EA License: R21102307
