Healthcare Formulations Limited, located in Sreepur, Gazipur, is a prominent sister concern of Healthcare Pharmaceuticals Limited. Our state-of-the-art manufacturing facilities are dedicated to producing vaccines, injectables, solid, liquid, powder, biological, and non-biological ranges of products to meet the highest standards of healthcare excellence. We are currently seeking a dynamic and qualified professional to join our team as a Senior Officer, Production (Insulin).

In this role, you will play a crucial part in overseeing production activities, ensuring strict adherence to GMP compliance, and collaborating with cross-functional teams including QA, Engineering, and Validation. You will be responsible for equipment commissioning, documentation, technology transfer, and process validation within our advanced insulin manufacturing units.

Interested candidates who meet the qualifications are encouraged to apply directly through our official company career portal using the provided application link before the deadline of October 19, 2026. Please ensure all your academic and professional details are updated prior to submission.

• Education: Bachelor of Pharmacy (B.Pharm) or Master of Pharmacy (M.Pharm).

• Experience: 2 to 5 years of relevant experience in sterile production within a pharmaceutical company.

• Specific Industry Experience: Experience in Pharmaceutical/Medicine Companies or Herbal Medicine business areas.

• Technical Skills: Strong knowledge of GMP records, IQ/OQ/PQ documents, SOPs, BMRs/BPRs, and equipment commissioning.

• Soft Skills: Strong organizational and planning skills, attention to detail, and a commitment to quality.

• Communication Skills: Good interpersonal and communication skills for effective collaboration with cross-functional teams.

• 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.

Healthcare Formulations Limited, located in Sreepur, Gazipur, is a prominent sister concern of Healthcare Pharmaceuticals Limited. Our state-of-the-art manufacturing facilities are dedicated to producing vaccines, injectables, solid, liquid, powder, biological, and non-biological ranges of products to meet the highest standards of healthcare excellence. We are currently seeking a dynamic and qualified professional to join our team as a Senior Officer, Production (Insulin).

In this role, you will play a crucial part in overseeing production activities, ensuring strict adherence to GMP compliance, and collaborating with cross-functional teams including QA, Engineering, and Validation. You will be responsible for equipment commissioning, documentation, technology transfer, and process validation within our advanced insulin manufacturing units.

Interested candidates who meet the qualifications are encouraged to apply directly through our official company career portal using the provided application link before the deadline of October 19, 2026. Please ensure all your academic and professional details are updated prior to submission.

• Education: Bachelor of Pharmacy (B.Pharm) or Master of Pharmacy (M.Pharm).

• Experience: 2 to 5 years of relevant experience in sterile production within a pharmaceutical company.

• Specific Industry Experience: Experience in Pharmaceutical/Medicine Companies or Herbal Medicine business areas.

• Technical Skills: Strong knowledge of GMP records, IQ/OQ/PQ documents, SOPs, BMRs/BPRs, and equipment commissioning.

• Soft Skills: Strong organizational and planning skills, attention to detail, and a commitment to quality.

• Communication Skills: Good interpersonal and communication skills for effective collaboration with cross-functional teams.

• 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.