Responsibilities
Manage, plan and direct the QC and Microbiology LaboratoryDevelop, reviews and updates standard quality guideline to ensure co
ntinuing relevance in providing guidance to management and employeesMaintain Laboratory in a cGMP and GLP compliant and inspection-ready state.Act as technical source of subjects related to Laboratory Practices, Instrumentations and Quality Co
ntrol functions and processes.Propo
nent in the execution of discipline and implementation of Safety practices in the laboratory by ensuring all perso
nnel are fully trained, all perso
nnel protective equipment are availableReview and approve protocols and reports such as method validation, process validation and stability studiesAct as QC representative in problem solving analysis, technical discussions, Risk Management, Internal Audit, Quality issues, Corrective/Preventive Actions and Systems Improvement to facilitate investigation and resolution to address compliance issues.Support activities related to internal/external audits and regulatory queries as requiredProvide leadership, management e
valuation and training to all laboratory employees.
Qualifications
With a Bachelor's Degree in ChemistryPRC Chemist License is requiredwith at least 3 years experience in a supervisory/managerial position gained in a Pharmaceutical Manufacturing IndustryWith knowledge in GMP, GLP, ISO and HACCPKnowledge of HPLC/Spectrophotometry is an advantageWith good analytical skills, decision making skills, and knowledge of problem solving toolswith good management skillsCan communicate/articulate properlyTeam player, cooperative, responsible, honest, hardworking, with initiative and fast learner