Job Scope:

• Participate in the preparation, operation and completion of assigned process stages to ensure the production of bulk drug substances is within establish timing and quality standards.
• Ensure good housekeeping of the facilities to keep them in good operational order in line with cGMP, safety and environmental requirements.
• Participate in commissioning and qualification activities as required

·         Assist Lead Biotechnologist or Shift Supervisor or Operations Superintendent in detailed team operations planning

• Conduct classroom and on-the-job (OJT) training as assigned

·         Perform timely review of documentation and make necessary corrections.

• Have good quality mindset and integrity to ensure products are manufactured with the highest quality
• Participate in deviation investigation process
• Reporting and documentation - Ensure that batch record, checklist and logbooks are correctly recorded, cGMP complied and maintained. Perform VS review of completed documentation to ensure adherence to GDP

Requirements:

• Nitec/Higher Nitec/Diploma in the fields of Biotechnology/Chemical Engineering/Life Science
• Minimum 0 - 2 years of relevant experience in Biologics/Chemical/Pharmaceutical/ Food or other regulated industry
• Basic knowledge of cGMP
• Familiar with purification/fermentation/conjugation/isolator operations/material and buffer operations is an advantage
• 12 hours permanent day shift (8am-8pm) and in clean room environment
• Location: Tuas

To apply, please visit to www.gmprecruit.com and search for Job Code: 22757
To find out more about this opportunity, please contact Constance at constance.lim@gmprecruit.com
We regret that only shortlisted candidates will be notified.
GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | EA Personnel: Constance Lim Wen Shi | Registration No: R1551808