Senior Production Pharmacist: cGMP & Compliance Lead

DYNAPHARM (M) SDN BHD; Seberang Perai; On-site; MYR 67,000 - 112,000; Full time

Benefits offered by this job

Competitive remuneration packages

Career development opportunities

Job summary

DYNAPHARM (M) SDN BHD is seeking a Production Pharmacist Executive to oversee non-sterile manufacturing operations. The role ensures safe, efficient production, strict cGMP compliance, and alignment with local regulatory guidelines and internal quality targets.

You will review batch records, manage deviations, and provide technical guidance to staff while collaborating with QA and regulatory bodies to sustain product quality and regulatory compliance.

Qualifications

• Bachelor’s degree in Pharmacy or related pharmaceutical field.
• Valid pharmaceutical license/registration with the regulatory body.
• 3–5 years of experience in pharmaceutical production/manufacturing.
• Solid knowledge of cGMP and pharmaceutical regulations.
• Strong understanding of formulation, QC principles and batch records.

Responsibilities

• Oversee and monitor all production processes for cGMP compliance.
• Review and approve batch records, procedures and documentation.
• Investigate deviations and implement CAPA actions.
• Coordinate with QA to meet regulatory standards.
• Maintain accurate records of production activities and QA data.
• Provide technical guidance to production staff on procedures.
• Ensure compliance with pharmaceutical regulations and authority requirements.
• Participate in continuous improvement initiatives for efficiency and quality.
• Assist in training and mentoring production personnel.

Skills

Communication skills

Problem-solving

Teamwork

Attention to detail

Regulatory knowledge

Education

Bachelor’s degree in Pharmacy or related field

Tools

Pharmaceutical manufacturing software

Job description

DYNAPHARM (M) SDN BHD is seeking a Production Pharmacist Executive to oversee non-sterile manufacturing operations. The role ensures safe, efficient production, strict cGMP compliance, and alignment with local regulatory guidelines and internal quality targets.

You will review batch records, manage deviations, and provide technical guidance to staff while collaborating with QA and regulatory bodies to sustain product quality and regulatory compliance.