Salary: up to $4500 + shift allowance
Duration: 1 year contract
Working Days & Hours: 12 hrs rotating shift 3223
Location: Tuas (islandwide pickup)
Job Description:
Pursue ongoing training to increase knowledge & understanding
- Attain good understanding of cGMP requirements & compliance within a GMP manufacturing setting
- Perform assigned tasks (by Section Lead/ Manager) both with and without supervision
- Perform equipment monitoring & basic 6S housekeeping
- Perform basic laboratory tasks (e.g. sampling, pH/ conductivity/ osmolality measurements etc.)
- Perform routine sanitization tasks to maintain facility standards
- Achieve & consistently maintain a training status of ≥ 95%
- 100% trained & signed off on all Performance Measures (PMs)
- Demonstrate aseptic technique in the handling of product/ materials
- Perform all assigned tasks independently
- Able to multi-task on equipment preparations & operations to ensure adherence to schedule
- Display basic process & equipment troubleshooting ability under routine scenarios (Biotech I/ II)
- Display superior process & equipment troubleshooting ability under both routine & non-routine scenarios (Biotech III)
- Provide guidance to juniors where applicable (Biotech II/ III)
- Provide coaching and mentoring to juniors where applicable (Biotech III)
- · Attain trainer qualifications for > 50% of PMs in area of manufacturing operations (Biotech II)
- Attain trainer qualifications for 100% of PMs in area of manufacturing operations (Biotech III)
- Attain full competency in the performance of all operations relevant to manufacturing areas assigned (Biotech III)
- Able to make decisions based on significant knowledge & experience (Biotech III) Technical Process Expertise (All areas)
- Exhibit full understanding of critical process/ operational parameters and target/ acceptable ranges
- Understand process flow from scheduling & resource loading perspective
- Exhibit basic understanding of the entire process e.g. interactions between different process parameters (Biotech I/ II)
- Exhibit detailed understanding of the entire process e.g. interactions between different process parameters (Biotech III)
- Display basic awareness of operational factors which influence the process (Biotech I)
- Display in-depth awareness of operational factors which influence the process (Biotech II/ III)
- Work effectively interdepartmentally, providing manufacturing insights & support to MSAT, Lot Review and Deviation Investigation groups Systems & cGMP Expertise (All areas)
- Use Standard Operating Procedures (SOPs), logbooks & Batch Records (BRs) or other GMP documents effectively & competently
- Understand in general the BR and logbook review process/ workflow
- Perform logbook & 1st level BR review effectively & competently
- Trained & competent in the submission of samples via LIMS
- Attain operating knowledge of DeltaV Control System
- Operate DeltaV Control System independently for daily routines, historian data retrieval/ trending/ printing
- Understand the deviation system/ workflow overview
- Initiate clear & concise Deviations with or without guidance
- Understand the material movement system & competent in ordering of consumables, BRs traceable and emergency materials requisition
- Execute validation and adhoc activities as per instructed
- Raise & follow through to completion Work Notifications
- Initiate Quality Tag-outs
- Understand the document change workflow overview & able to initiate document revisions
- Complete document revisions independently (Biotech II/ III)
Job Requirements: Min Diploma/Degree in Biotechnology/Pharmaceutical Engineering/Life Sciences or similar
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
