Duration: 12 months (Renewable)
Work location: Tuas South Ave 6 (Nearest MRT Tuas Crescent)
Working hours: Monday – Friday, 8:30am – 6:00pm
Responsibilities
- Indexing and categorizing of documents.
- Archive Log creation.
- Labeling and boxing of binders
- Palletizing of boxes and Coordinate shipment of documents and/or retained samples.
- Writing GMP decommissioning/retirement documents according to specific standard operating procedures.
- Reporting to the project lead and, if required, to other stakeholders.
- Perform all duties in accordance with company guidelines and regulatory requirements
Requirements
- Background in Life Science or equivalent discipline
- Excellent organizational and interpersonal skills
- Ability to work independently or as part of a team. Skills for working into a team and following project manager guidelines, and capable to report progress and issues in order to find the best solution.
- Experience in Record Management, Inventory-ing and archiving.
- Experience with validation/qualification in the pharmaceutical industry.
- Experience with GMP decommissioning process.
- Working experience in the GMP-regulated environment of the pharmaceutical industry will be an advantage (Former pharmaceutical industry experience or API plant experience. Production, Quality, and Technical Support will be considered)
Interested candidate please click "APPLY" to begin your job search journey and submit your CV directly through the official PERSOLKELLY job application platform - GO Mobile.
We regret to inform that only shortlisted candidates will be notified.
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PERSOLKELLY Singapore Pte Ltd • RCB No. 200007268E • EA License No. 01C4394 • Reg No: R23117066 (CHEW KIA ZHENG)
