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Sydenham Laboratories, Inc. in Dasmariñas, Cavite, seeks a QC Analyst to perform laboratory testing and ensure product safety and regulatory compliance through GLP-guided protocols.
The role involves sampling materials, sterility testing, environmental monitoring, and accurate logging of equipment usage while maintaining high attention to detail and teamwork. Shift work flexibility is required.
About the role
This role involves laboratory testing and quality control work in a pharmaceutical or manufacturing environment, ensuring product safety and regulatory compliance through rigorous testing and monitoring protocols.
Key responsibilities
Strictly adhere to Good Laboratory Practices (GLP), safety protocols, and "Clean as You Go" rules, including wearing appropriate PPE and maintaining the micro-sterile lab
Sample raw materials and products to detect contaminants, perform sterility testing for market release, conduct growth promotion tests, and validate testing methods
Prepare required culture media/reagents and monitor chemical inventory levels to request timely stock replenishments
Implement environmental, water, and personnel monitoring programs to uphold hygiene standards across the plant facility
Accurately log equipment usage and calibration, maintain analyst journals, and timely submit laboratory reports to the supervisor
Investigate Out-of-Specification (OOS) results, proactively report regulatory non-compliance, and immediately escalate equipment breakdowns or potential problems
Follow the QC Manual, participate in company audits/validations, and carry out additional tasks as assigned
About you
Bachelor's/College Degree in Chemistry, Microbiology, Biochemistry or other related courses
Licensed Chemist, Chemical technician and/or Registered Microbiologist
At least 1 to 2 years laboratory experience
Works systematically and has good attention to details
Team player, results-oriented
Amenable with a shifting schedule