Participate in innovative research and development programsBe respo
nsible for maintenance and preparation of the Pharmaceutical research equipment.In collaboration with the Regulatory Affairs, co
ntribute to the development and implementation of the pharmaceutical plan of R&D projects under her/his responsibilities.Helps design the clinical development plan of all R&D projects of the group in accordance with current regulatory guidelines.Helps manage the budget of R&D projects under his/her responsibilities.
Qualifications:
Graduate of BS in Pharmacy, Chemical engineering or any related course.At least 2 to 3 years experience in Pharmaceutical firm.with Strong working knowledge of cGMP principles.Strong working knowledge of technical and quality co
ncepts of the manufacturing and testing of pharmaceutical products.Experience in participating in deviation investigations, determining root cause, and developing corrective action ********** player with strong interpersonal, organizational, and communication skills.Willing to work in Barangay Bancal Carmona Cavite.-
A duly organized corporation establish in December 2011 addressed at Sta. Cruz, Manila. Our company is SEC, BIR and BFAD registered. Medicines are manufactured at ISO certified companies with Bio assay conducted at Cedres. We are one of the main suppliers of medicines in Metro Manila and provincesOur main goal is to provide holistic health care to people of different stages.