Work Schedule

Flex 12 hr shift/nights

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Cold Room/Freezers -22degreesF/-6degrees C, No contact lens allowed; prescriptive glasses will be provided, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products etc.), Warehouse, Will work with hazardous/toxic materials

Job Description

Join us at Thermo Fisher Scientific Inc. in Singapore for an outstanding opportunity in the Manufacturing sector! Our world-class team is dedicated to making a positive impact on global health, and we are looking for ambitious individuals to contribute to our success.

Responsibilities

Operate pharmaceutical manufacturing machinery, such as high-speed filling lines and fully automatic Lyophilizer, following SOPs and Batch Record guidelines.Perform formulation tasks for production batches, guaranteeing seamless implementation and adherence to SOPs and Batch Record.Perform parts preparation, washing, and sterilization of materials with strict adherence to safety protocols.Coordinate the packaging and transfer of the final product to the freezer, ensuring accuracy and quality standards are upheld.Complete relevant training and maintain compliance with all safety and GMP regulations.Complete materials and process (SAP) transactions at each manufacturing step, ensuring data integrity.Adhere to aseptic techniques and practices during aseptic operations.Preserve the cleanliness and maintenance of production equipment and designated areas.Conduct routine QC sampling and in-process testing of products throughout manufacturing.Ensure timely completion of batch records and logbooks, adhering to Good Documentation Practice (GDP).Manage material transfers and prepare filters for testing, following established protocols.Arrange the loading/unloading process of production equipment and carry out stock verifications of consumables.Align with safety and quality standards, promptly reporting any anomalies to supervisors.Participate in EHS, Business Compliance, cGMP, and other compliance-related activities.Perform additional duties as assigned and liaise with external vendors for instrument calibration and maintenance.

How will you get here?

Education

Minimum “O” Level, NITEC/ITE education, or Diploma in a relevant field.

Experience

3 to 5 years of pertinent experience within the pharmaceutical sector.

Knowledge, Skills, Abilities

Solid understanding of safe working practices and cGMP.Eager to thrive in the pharmaceutical sector.Excellent teammate with the ability to work rotating shifts.