Licensed Pharmacist

Delta Kappa Commerce Corporation; Makati; On-site; PHP 446,400 - 669,600; Full time

Job summary

A pharmaceutical company in Metro Manila is seeking a Production Pharmacist to oversee compliance with GMP regulations in manufacturing. Responsibilities include monitoring production processes, approving batch records, and coordinating across departments. The ideal candidate has a Bachelor's degree in Pharmacy and 2-3 years of experience in the pharmaceutical industry. Strong scientific knowledge and project management skills are essential for success in this role.

Qualifications

• 2-3 years of experience in Pharma (Biological) Industry.
• Competent in planning and organizing tasks.

Responsibilities

• Monitor the manufacturing process and approve batch production records.
• Check adherence to GMP compliance.
• Coordinate with other departments for production activities.
• Report any incidents, accidents, or violations to the supervisor.

Skills

Strong scientific background

Project management skills

Good communication skills

Planning and organizing

Decision making

Negotiation skills

Conflict management

Fluent in English

Knowledge of GMPs/GLPs

Education

B.S. Pharmacy / Licensed Chemist or Biologist

Job description

The role of Production Pharmacist is to monitor that the routine production activities in primary and secondary manufacturing comply with GMP regulations and requirements and approve the batch manufacturing records accordingly. To ensure strict compliance with Pharmaceutical Good Manufacturing Practices according to Philippine law.

Responsibilities

• Monitoring the manufacturing process (primary and secondary) and approval of batch production records
• Check adherence to GMP compliance as per regulatory requirements
• Responsible for shop floor level working program implementation; hands-on working, monitoring, supervision and control of various production activities and reporting of the events to the department Manager
• Monitoring for the compliance to gowning, health and safety practices, biosafety practices as per the regulatory or law requirements
• Preparation and review of batch production records, SOP, protocols, lab notebooks, SOPs, log books and other documents as per the regulatory requirements
• Coordination with the other departments for routine production activities
• Handling of equipment, supervision and maintenance follow up with complete documentation
• Facility commissioning, validation and monitoring
• Managing workload and time to perform multiple projects or activities effectively
• Periodic participation to internal audits, training programs, departmental reviews, meetings etc.
• Perform other related duties as may be reasonably assigned in the course of business
• Other jobs assigned by superiors to support the organization achievement as well as cooperation in company rule and regulations, safety policy and all activities according to company policy
• Report any incident, accident, near miss and any violations of the HSE or safe work practices including malfunctioning of the equipment or workplace hazards that he/she is aware of to the direct supervisor
• Follow the health and safety procedures related to the job functions, which includes the use of Personal Protective Equipment (PPE), safe operation of equipment, machinery, tools and handling of hazardous substances

Qualifications

• Must be a Graduate of B.S. Pharmacy / Licensed Chemist or Biologist
• 2–3 years of experience in Pharma (Biological) Industry
• Strong scientific background and technical skills
• Possess project management skill and knowledge
• Good communication skills
• Competent in planning and organizing, people management, decision making, negotiation and conflict management
• Fluent in both written and spoken English
• Good knowledge of GMPs/GLPs