Senior Officer, Production (Insulin)

Job Description

Title: Senior Officer, Production (Insulin)

Company Name: Healthcare Formulations Limited

Vacancy: --

Age: Na

Job Location: Gazipur (Sreepur)

Salary: --

Experience:

• 2 to 5 years
• The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies, Herbal Medicine

• Bachelor of Pharmacy (B.Pharm)
• Master of Pharmacy (M.Pharm)

• 2 to 5 years
• The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies, Herbal Medicine

• 2 to 5 years of experience in sterile production in pharmaceutical company

• Strong organizational and planning skills

• Attention to detail and a commitment to quality

• Good interpersonal and communication skills

Healthcare Formulations Limited, Sreepur, Gazipur is a sister concern of Healthcare Pharmaceuticals Limited. The state-of-the-art manufacturing facilities intend to produce vaccines, injectables, solid, liquid, powder, biological and non-biological range of products.

We are looking for candidates for the following position:

Job Responsibilities

• Assisting with the execution, review, and tracking of IQ/OQ/PQ documents. qualification protocols, reports, and related GMP records in collaboration with QA, Engineering, Validation, and project teams.

• Participating in equipment commissioning, qualification execution, and vendor coordination to ensure alignment among equipment operation, process requirements, and approved design specifications.

• Preparing, reviewing, and implementing production documents, including SOPs, BMRs/BPRs, equipment logbooks, process documents, and other GMP records required for qualification and routine production activities.

• Supporting technology transfer, process validation, and production readiness in coordination with Production, QA, QC, and R&D teams.

• Assisting in developing and executing personnel training plans, including GMP, equipment operation, manufacturing procedures, and process-specific training requirements.

• Maintaining tracking sheets for equipment qualification status, production documents, training completion, validation activities, and project milestones in collaboration with QA and relevant departments.

• Participating in risk assessments, deviation investigations, CAPA implementation, and continuous improvement activities related to production processes and GMP compliance.

• Ensuring proper documentation practices, archiving, and version control of qualification and production records while supporting the establishment of compliant commercial manufacturing operations.