Participate in innovative research and development programs
Be responsible for maintenance and preparation of the Pharmaceutical research equipment.
In collaboration with the Regulatory Affairs, contribute 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 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 Barangay Bancal Carmona Cavite.
Job Type: Full-timeSchedule:
8 hour shift
Ability to commute/relocate:
Carmona, Cavite: Reliably commute or planning to relocate before starting work (Required)
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