Pharmaceutical Research and

A. Primary function

• Perform high quality research activities.

• Provide technical support to the pharmaceutical research and training teams.

• Responsible for maintenance and preparation of the pharmaceutical research equipment.

• Participate in innovative research and development programs.

• Maximize the academic research profile of the company by actively participating and organizing international conferences and workshops.

• In collaboration with the pharmaceutical development manager, contribute to the development and implementation of the pharmaceutical plan of R&D projects under his/her responsibilities.

• Design the clinical development plan of all R&D projects of the group in accordance with current regulatory guidelines.

• Monitor, create and manage of intellectual property.

• Coordinate project activities to ensure that new projects are delivered on time

• Project planning and communication of project status on a regular basis

• Meeting and Reports

1. Participate to monthly R&D meeting.

2. Provide weekly update on the status of the projects/ clinical studies.

•  Manage the budget of R&D projects under his/her responsibilities

1. For projects under his/her responsibilities, identify resources requirements and elaborate a budget plan including the pharmaceutical development budget (in collaboration with the pharmaceutical manager).

2. Elaborate clinical development plan budget including timelines and milestones.

3. Respect allocated budget.

• Organize, schedule and coordinate workloads for team members.

• Enforce safety procedures and reports safety incidences.

B. Perform other related duties that may be assigned from time to time.

Job qualifications

• A BS in Chemistry, Chemical Engineering, or a similar field is required
• Must be a Licensed Chemist or Chemical Engineer
• At least five (5) years of experience in a pharmaceutical company, with at least two (2) years in a supervisory role
• Comprehensive understanding of Good Clinical Practices and International Clinical Regulatory Requirements
• Strong knowledge of the drug development process
• Excellent problem-solving ability
• Ability to multitask
• Good moral character.
• Willing to be assigned in Bancal, Carmona, Cavite

Summary of role requirements:

• Looking for candidates available to work:
  • Monday: Morning, Afternoon
  • Tuesday: Morning, Afternoon
  • Wednesday: Morning, Afternoon
  • Thursday: Morning, Afternoon
  • Friday: Morning, Afternoon
• 2-3 years of relevant work experience required for this role
• Working rights required for this role
• Expected start date for role: 26 October 2024