Perform analytical testing accurately and efficiently and in accordance to Standard Operating Procedures (SOPs).
Perform equipment verification and calibration in accordance to procedures.
Document all results in accordance to Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) requirements.
Conduct OJT training for new hires.
Troubleshoot all operating deviations and issues and coordinate with other function when required.
Perform chemical analysis using wet chemistry methods and analytical instrumentation, including HPLC, GC, particle size analyzer etc.
Ensure that tests assigned are performed in a timely manner in accordance with validated test protocols and procedures.
Perform instrument calibration, maintenance and troubleshooting. Able to prioritize based on operation needs.
Support laboratory operations, including sample receipt, sample subdivision and labeling, waste disposal, stability sample packing.
Advise on the significance of test results and follow up with appropriate course of actions.
Actively participate in Safety initiatives, typically a role model for other analyst. Ability to perform investigation related to EHS.
Participate in 5S team initiatives and practice good housekeeping.
Coordinate work flow and laboratory activities according to QC sample and testing plans.
Lead and conduct laboratory investigations/incidents such as out of specification investigation and equipment troubleshooting investigations, identify root causes and implement appropriate corrective action and preventive measures.
Participate in Analytical Method Transfer Exercise and independently resolve issues associated with test methods.
Review test reports and ensure that all laboratory documents are in a constant state of regulatory compliance and inspection readiness.
Develop test methods or instrument Standard Operating Procedures (SOPs), write and update Quality Procedures.
Plan and deliver technical training to colleagues. Developed and review training materials as required e.g. Basic lab techniques.
Close coordination with cross function colleagues / Vendors to achieve desire outcome ( e.g. Lab equipment installation/ Validation/ Service contract / External contract lab testing fulfillment).
Commitment to work and positive influencer/role model/motivate others for overall operational excellence.
Participate actively and contribute to site project teams.
Contribute to the continuous improvements in laboratory activities.
Requirements
Diploma in Science (preferably Chemical Process Technology) or equivalent.
A minimum of 3 years QC experience in pharmaceutical industry
Interested candidates please send a copy of your resume to
*All information will be treated with strictest confidence. We regret that only short-listed applicants will be notified.
Industry
Education & Training Healthcare / Pharmaceutical / Life Science / Medical Device Public Sector / Government & Statutory Boards Semiconductor / Electronics / Engineering
Specialization
Engineering Healthcare - Pharmaceutical / Life Science / Medical Device / Clinical Research / Regulatory Affairs Professional Services
Location
Central, North, East, West
Employment Type
Contract / Temp Permanent
Salary
S$4,001 - S$6,000 / mth
If you meet the requirements of this role, please email a detailed resume in Word document to Lynn Ho Lin Ying (Outsourcing Team).
Interested candidates please send a copy of your resume to