- In charge of sample specimen for raw material, intermediate and final product.
- Follow related procedure for GMP sampling.
- Timely report the various issue associated with sampling process. Ensure GMP compliance.
- Involved in the procedure update and ensure execution.
- Communicate with QC project team, processing team and warehouse. Ensure the smoothness of analytical activities.
- Assist necessary Lab investigation, keep good Lab environment, meet 5S and EHS requirements, ensure Lab safety and the safety of Lab staff.
- Follow the requirements of Lab events, OOX, Deviation and involve the investigation if necessary.
- Participate in customer audits and government inspections, promptly address identified issues, and ensure GMP compliance
- Timely track work progress, strengthen communication with internal and external clients, and establish stable and good relationships
- Perform any other ad hoc duties as required by the Department
Requirements:
- ITE or Diploma in Pharmacy or Chemistry related major
- Understand pharmaceutical production, testing, and quality management familiar with GMP regulations.
- Proficient in English or Mandarin, proficient in both Mandarin and English are preferred.
- Good computer skills.
- At least one-year experience of Lab related work
- Strong ability to handle on-site issues, with good coordination, communication, and execution skills
- Detail-oriented, proactive, and able to work under pressure
- Ability to determine problems, gather information, understand facts, and draw correct and effective conclusions through scientific reasoning.
- Be able to work shift hours
To find out more about this opportunity, please contact Fiona Koh [Confidential Information]
We regret that only shortlisted candidates will be notified.
GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | EA Personnel: Fiona Koh | Registration No: R1109239
