Sr. Officer, R&D

Job Description

Title: Sr. Officer, R&D

Company Name: Healthcare Chemicals Limited

Vacancy: --

Age: Na

Job Location: Munshiganj (Gazaria)

Salary: --

Experience:

• 2 to 6 years
• The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies

B. Pharm/M. Pharm from any reputed university.

• 2 to 6 years
• The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies

• Maximum 6 years of experience in pharmaceuticals Solid Dosage Form R&D.

• Hands-on experience with tablets, capsules, and pellet formulations.

• Good understanding of excipients, process variables, and dissolution behavior.

• Familiarity with scale-up, validation, and technology transfer activities.

Skills & Competencies:

• Strong formulation and problem-solving skills

• Good technical documentation ability

• Cross-functional communication and teamwork

• Ability to handle multiple projects with deadlines

Healthcare Chemicals Limited (HCL), a sister concern of Healthcare Pharmaceuticals Limited, located in API Park, besides Dhaka-Chittagong Highway in Gazaria upazila of Munshiganj, envisions manufacturing world class pharmaceutical raw materials for the local and foreign markets. HCL would like to reduce dependency on foreign sourcing of raw materials for the pharmaceuticals industry and save valuable foreign currency of the country. HCL will manufacture Active Pharmaceutical Ingredients (APIs) and related key chemicals required for the pharmaceuticals industry.

We are looking for dynamic, self-motivated individuals for the mentioned position in HCL.

Job function: Research & Development

Location: API Industrial Park Gazaria, Munshiganj Bangladesh

Job Description/responsibilities:

• Develop and optimize formulations for solid dosage forms including tablets, capsules, and pellets.

• Conduct pre-formulation studies and excipient compatibility studies.

• Perform lab-scale and pilot-scale trials and support scale-up to production.

• Prepare and review development reports, SOPs, and technical documents.

• Support technology transfer from R&D to production and troubleshoot process issues.

• Coordinate with QA, QC, and Production for trial execution and validation batches.

• Ensure compliance with GMP, GLP, and regulatory guidelines.

• Participate in product improvement, cost optimization, and lifecycle management activities.

• Support regulatory documentation such as formulation summaries and process descriptions.