Pharmacist (Active Pooling)

Product Development Officer — Responsibilities

• Develop new products compliant to client and regulatory requirements at the shortest time, quality, and competitive price in the market.
• Conduct trials on existing products with or without modifications as required by clients.
• Conduct physicochemical analyses and stability studies on the results of trials.
• Conduct research to support modification of existing products.
• Coordinate closely with Product Introduction officer/Production for the scheduling of products for compression, encapsulation, capping, blistering, stripping, and other works related to the pilot batch of a particular product.
• Assist in the request of materials needed in the development and help in follow-up purchasing.
• Participate in the conduct of problem solving analysis and design of experiments during product development.
• Conduct inventory of materials, finished products, glass wares, fixtures and books of the department.
• Submit weekly reports to superior on accomplishments, plants, issues and concerns.
• Perform other duties assigned by Supervisor from time to time.

Dispensing Pharmacist — Responsibilities

• Coordinate with the Production Planner regarding production schedule and priorities for dispensing.
• Ensure that all computations are equivalent to the weight indicated from the BMR versus the actual weighing.
• Validate that the Control Number of the Actual Raw Material used matches the Control Number indicated in the Batch Monitoring Record (BMR) and ensure all tags are properly signed and attached to its designated Raw Material to avoid mix-ups.
• Ensure the expiration of each Raw Material is not out of date.
• Conduct line clearance before and after dispensing of every batch and calibrate all weighing balances prior to the start of dispensing.
• Submit weekly reports to superior on accomplishments, plans, problems, issues and concerns.
• Ensure compliance to SOP, cGMP and ISO.

Regulatory Affairs Pharmacist — Responsibilities

• Ensure timely application and finalize preparation of documents for initial, renewal, amendment, PCPR and CLIDP product registration to FDA and all necessary compliances associated with it during the application process (if applicable), ensuring completeness and correctness of documents prior to checking and approval of Supervisors and Managers.
• Prepare documents needed for application of licenses and/or legal compliances such as CPRs and permits from FDA, PDEA or any government agencies.
• Prepare and submit batch notification documents to FDA for antibiotic products upon full completion of the batch as endorsed by QA Unit; update reports upon receipt of batch notification approval from FDA.
• Prepare and route memo for the CPR whether initial, renewal, amendment, PCPR, CLIDP and ensure that notification of change is attached for any changes made.
• Regularly update the database for CPR application tracking and CPR master list.
• Perform daily monitoring of FDA website for latest advisories and report to Supervisor; evaluate and assess the impact of FDA or regulatory memos, circulars or notices to the organization through a written memo or email.
• Provide assistance to Regulatory Affairs/pharmacists of clients when required.
• Practice integrity in all business transactions, especially when representing the organization to regulatory agencies.

Qualifications

• Candidate must possess a Bachelor's/College Degree in Pharmacy and must have a valid PRC license.
• Possess good planning/decision making and negotiation skills.
• Experience either in Regulatory, Research and Development and Dispensing is an advantage.
• Analytical and proactive.

Note: This job posting is for the active pooling of candidates, and selected candidates will be contacted as positions become available.

Job Type

Pay: Php20, Php25,000.00 per month

Benefits

• Company Christmas gift
• Company events
• Employee discount
• Health insurance
• Life insurance

Work Location

In person

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