About the role
AI summarisedJoin the Quality Control team in Singapore as a QC Associate 1. You will perform routine laboratory testing, sample handling, and data recording to ensure materials and products meet stringent regulatory and company standards. This role offers hands-on learning and the chance to contribute to meaningful advancements in healthcare.
BiopharmaOnsiteQuality
Key Responsibilities
- Perform routine and adhoc/non-routine biological testing of raw materials, intermediates, product, and utilities samples in adherence to GMP requirements.
- Conduct routine environmental monitoring of classified environments.
- Initiate and participate in laboratory investigations regarding OOS, deviations, atypical, or invalid results, assisting with timely closure and CAPA.
- Perform equipment maintenance and validation tasks.
- Participate in method transfer, verification, or validation projects.
- Assist in the writing of Standard Operating Procedures (SOPs).
- Maintain good housekeeping and proper inventory management for QC materials, ensuring appropriate waste disposal.
- Adhere strictly to all safety and security policies and practices.
Requirements
- Minimum Diploma in Microbiology, Biotechnology, Life Sciences, Chemistry, or Biochemistry.
- Basic laboratory experience or coursework in chemistry, biology, pharmaceutical, or a related field.
- Ability to follow instructions precisely and document all work clearly.
- Willingness to safely handle reagents and operate laboratory equipment.
- Proficiency in written and spoken English.
- Comfortable working on-site in Singapore.