- Fantastic entry point into the world of sterile manufacturing! Join our team of technicians in Tuas who manufacture lifesaving cancer medications. The position is a 2 year WDA contract at company’s Biotech facility.
- Based in Singapore, the regional hub for Asia Pacific (AP) and top-ranked biopharmaceutical company on the Straits Times and Statista’s list of Best Employers in Singapore for two consecutive year (2021, 2022, 2023).
- Join the premier biopharmaceutical company that has been in Singapore for more than 25 years and in AP for over 60 years.
WHAT YOU WILL DO
Responsibilities include, but are not limited to:
WHAT YOU WILL DO
As a technician you will join one of the teams who manufacture our medicines. The environment that these teams work in is a clean room environment doing filling of sterile vials. Each team is approximately 10 people working on a 24x7 shift pattern. We are proud of being a diverse organisation with an even split of genders at a technician level within Biotech.
Routine Operation
- Setup and operate pharmaceutical production equipment including high-speed filling lines for sterile injectables, robotic technology, compounding panels and automatic CIP/SIP.
- Dispense, formulate and fill active biological product batches as required to meet the production schedule.
- Perform routine QC sampling and in-process testing of the product at various stages throughout manufacturing i.e bioburden sampling, water sampling
- Microbial sampling and swabbing of room and equipment.
- Perform cleaning and upkeep of the Grade C & D cleanrooms and production equipment.
- Perform filter integrity testing using an automatic filter integrity test unit.
- Preparation of equipment including loading and starting of sterilisation cycles in autoclaves.
- Complete batch documentation as required.
- Perform in-process sampling on semi-finished drug products
- Perform visual inspection, labeling and packaging on semi-finished drug products
- Perform all tasks in accordance with the standard operating procedures and maintain strict compliance to GMP at all times.
Event, Atypical Investigations
- Report QN/deviations if any.
- Participate in SHE, Business Compliance, cGMP and compliance matters, where applicable.
- Responsible to escalate Operations issues to Lead Tech or Shift Manager when required
Continuous Improvement
- Responsible to participant in Kaizen events in pharm operations in accordance with Kaizen plans when assigned
WHAT YOU MUST HAVE
To be successful in this role, you will have:
- A Diploma or Technical School graduate with background in operations and maintenance or any relevant studies
- Must be willing to work in 24x7 rotating shift pattern
- Min 2 years of working experience preferably in manufacturing industry preferred
- Good understanding of safety procedures/practices.
We are proud to be a company that embraces the value of bringing diverse, talented, and committed people together. The fastest way to breakthrough innovation is when diverse ideas come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. We are an equal opportunity employer, committed to fostering an inclusive and diverse workplace
