Collect information about the composition of chemical substances, and process and communicate this information through the principles of science, engineering, and mathematics. Develop and improve processes, equipment, and formulas, and prepare compounds and solutions to conduct tests.
- Sampling and testing of raw materials, intermediates, and finished products
- Preparing Quality reports, including analytical reports (for raw materials and finished products)
- Calibrating analytical equipment when required.
- Creating and executing method development and validation test protocols for finished products and generating the appropriate analytical methods.
- Perform routine and non-routine chemical analysis of products using standard operating procedures.
- Write and execute chemical testing procedures.
- Maintain up-to-date documents for chemical testing methods and activities.
- Operate laboratory equipment safely and effectively to conduct testing.
- Record, analyse and report test results to Managers.
- Maintain inventory of chemicals and supplies in the laboratory.
- Supporting all Quality Control activities.
- Ensuring good relations and communications with all members of the team and responding politely and in a timely fashion to internal and external customers.
- Perform various techniques like HPLC.
- Observing and complying with Good Manufacturing Practices (GMP) and Good Distribution Practices (GDP).
- Perform other related duties that may be assigned from time to time.
Job Qualifications:
- BS degree in Chemistry, Chemical Engineering, or Chemical Technology/Pharmacist
- At least two (2) years of direct lab experience in an FDA-regulated pharmaceutical firm as an advanced but not required.
- Must be a Registered Chemical Engineer or Registered Chemical Technician.
- Strong knowledge of Standard Operating Procedures and compliance with Good Laboratory Practices, Good Documentation Practices, and Current Good Manufacturing Practices.
- Strong working knowledge of technical and quality concepts of the manufacturing and testing of pharmaceutical products.
- Experience in participating in deviation investigations, determining root cause, and developing corrective action plans.
- Team player with strong interpersonal, organizational, and communication skills.
- Willing to work in Bancal, Carmona Cavite
- Working schedule will be from Mondays to Fridays
Job Type: Full-time
Benefits:
- Company Christmas gift
- Employee discount
- Free parking
Schedule:
- 8 hour shift
Supplemental Pay:
- 13th month salary
- Overtime pay
- Performance bonus
Ability to commute/relocate:
- Carmona, Cavite: Reliably commute or planning to relocate before starting work (Preferred)
Experience:
- Manufacturing: 2 years (Preferred)
License/Certification:
- Licensed Chemist (Preferred)
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