Job Description

• 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; fiona.koh@gmprecruit.com

We regret that only shortlisted candidates will be notified.

GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | EA Personnel: Fiona Koh | Registration No: R1109239