Job Description

• Coordinates, motivates and monitors the proper functioning of the Quality Control Section.
• Responsible for the compliance of the quality management of raw materials, in-process and finished products testing to the established Standard Operating Procedures (SOP) and Testing Procedures.
• Develops & monitors programs/systems/ test procedures to control the quality check and verification of all items under physical & chemical analysis in the most cost-effective and efficient manner.
• Evaluates measurement and analysis of data & results of all conducted testing on materials, bulk products, in-process goods and finished products prior to its approval and releasing for production use.
• Ensures the manufacturing and distribution of only Quality products as defined by the company's specification and requirements indicated in the official monograph or compendium and/or by the individual customer/client.
• Conducts investigation for any identified non-conformity related to the evaluated results eventually, provide corrective action appropriate to the case.
• Conducts researches and related studies on new developments pertinent to Quality Control activities.
• Participates in qualification assessment for the laboratory instruments on its Installation Qualification (IQ), Operational Qualification (OQ) and Performance Qualification (PQ) in coordination with the Engineering & Maintenance Department (EMD).
• Provides technical assistance to the Laboratory Analyst/s whenever problems occur in the analyses being conducted.
• Facilitates the conduct of the physical-chemical analyses of the Concurrent Stability Studies Program for our Finished Product and report to the Product Development; related results that need to be address in comparison with the Accelerated Stability Studies conducted by the Product Development Team.
• Maintain cost containment program of the company by maximizing skills and proper control of supplies, e.g. chemical reagents, glass wares and other laboratory supplies.
• Assists/ supports in the conduct of internal workshops/seminars/lectures on GMP & GLP and other technical-related topics to QMD Personnel.
• Closely coordinates with the Quality Assurance Supervisor for any quality related issues pertinent to materials and method of analysis and in the performance management of the entire Quality Management functions.
• Ensures supplier's management through evaluation of chemical reagents, laboratory equipment & gadgets and reference books & materials used in the performance of quality controlling of product & laboratory services to our valued clients.
• Performs other function as that may be assigned from time to time.
• Qualifications

EDUCATION : Preferably a graduate of B.S. Chemistry, B. S. Chemical Engineer, B.S. Pharmacy; Industrial Pharmacy or any other science-related courses. A professional board license would be an advantage.

• RELATED EXPERIENCE : With at least five (5) years of relevant work experience in managing a laboratory in a Supervisory level and/or second (2nd) line management level.

Job Type: Full-timeBenefits:

• Company Christmas gift
• Company events
• Free parking
• Life insurance
• Staff meals provided

Schedule:

• Monday to Friday

Supplemental Pay:

• 13th month salary
• Performance bonus

Ability to commute/relocate:

• Carmona, Cavite: Reliably commute or planning to relocate before starting work (Required)