Biotechnologist (1 year contract) | MNC | Tuas

Roles & Responsibilities

Jobscope :

• 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.
• Identify areas for improvement and participate in continuous improvement projects to enhance operational effectiveness and efficiencies
• Participate in commissioning and qualification activities as required
• 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 :

To apply, please visit www.gmprecruit.com and search for Job Reference : 24837

To learn more about this opportunity, please contact Fiona Koh

We regret that only shortlisted candidates will be notified.

GMP Technologies (S) Pte Ltd | EA Licence : 11C3793 | EA Personnel : Fiona Koh| Registration No : R11092398

Tell employers what skills you have

Pharmaceutical Manufacturing

Housekeeping

Documentation

Investigation

Environmental Health

Biotechnology

Pharmaceutical industry experience

Communication Skills

Plant Operations

Team Player

biopharmaceutical

Manufacturing

Chemical Engineering

Commissioning

cleanroom envirnoment