Quality Control Pharmacist

Ambica International Corporation.; Pasay; On-site; PHP 520,000 - 760,000; Full time

Job summary

Ambica International Corporation is seeking a Quality Control Pharmacist to verify activities during in-house inspection of finished products and ensure FDA and GMP compliance. You will sign Batch Inspection Records, monitor staff adherence to SOPs, and coordinate with Production, Warehouse, Sales, and Regulatory departments.

The role requires a licensed pharmacist, proficiency in MS Office, and the ability to work 100% on-site in Pasay.

Qualifications

• Licensed Pharmacist with active license.
• Knowledge of GMP and FDA guidelines.
• Proficient in Microsoft Office Applications.
• Self-motivated, goal-oriented, and committed to a long-term career.
• Can work under minimal supervision.
• Must be amenable to work 100% on-site.

Responsibilities

• Verify activities during in-house inspection of finished products and ensure FDA requirements are met.
• Monitor staff compliance with GMP requirements.
• Ensure products meet specifications per finished product specs or approved artwork.
• Sign Batch Inspection Records after activities.
• Coordinate with Production, Warehouse, Sales, and Regulatory Departments on quality issues.
• Calibrate measuring devices and maintain calibration master plan.
• Prepare and review inspection reports and quality system documentation.
• Train QC staff and ensure adherence to SOPs.

Skills

Self-motivated

Goal-oriented

Committed

Independent worker

On-site work

Education

Licensed Pharmacist with active license

Tools

MS Office

Job description

QUALITY CONTROL PHARMACIST is responsible for verifying the activities done during the In-house inspection of finished products and ensuring FDA requirements and company objectives are met.

• Monitors compliance of all staff with the requirements of GMP


• Ensures that the products comply with the specifications as per approved artwork or finished product specifications


• Signs Batch Inspection Records after every activity is done


• Counterchecks damages and non-conformances


• Ensures that the products are inspected and stored accordingly, to obtain the required quality


• Ensures strict implementation of instructions (SOPs) to QC procedures.


• Makes new SOPs, revises or updates existing SOPs


• Performs activities related to Pharmaceutical Quality System (such as Product Quality Review, Quality Risk Management, Change Control, Deviations, OOS and CAPA)


• Ensures initial and continuing training of QC staff is carried out and adapted according to need


• Ensures communication with the concerned departments to raise quality issues to the appropriate levels of management


• Coordinates with the Production, Warehouse, Sales, and Regulatory Departments regarding quality issues


• Generates inspection reports, or other reports, as needed


• Ensures that all measuring and monitoring devices (weighing balances, thermohydrometers, data loggers, bio ref, thermal gun, etc.) used by the company are calibrated; ensures proper coordination with other concerned departments (ex. Production and Warehouse) regarding calibration schedules and maintains an updated calibration master plan as needed


• Performs and/or supervises daily and monthly internal calibration of weighing balances in the Production/QC Area


• Other responsibilities that are deemed necessary by the Management

Job Qualification

• A Licensed Pharmacist with active license


• Knows how to operate Microsoft Office Applications


• Knowledge of the Good Manufacturing Practices and FDA guidelines


• Highly self-motivated, goal-oriented, and committed to pursuing a long-term career


• Can work under minimal supervision


• Must be amenable to work 100% on-site