Dy. Manager/ Manager- R & D and Product Development

Job Description

Title: Dy. Manager/ Manager- R & D and Product Development

Company Name: GET WELL LIMITED ( A Concern of RFL Group)

Vacancy: 2

Age: Na

Job Location: Habiganj

Salary: Negotiable

Experience:

  • At least 6 years
  • The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies, Medical Equipment


Published: 2026-04-20

Application Deadline: 2026-05-20

Education:
  • Master’s or Bachelor’s degree in: Pharmacy, Chemistry, Applied Chemistry, Biochemistry, biotechnology & Biomedical Engineering.

  • Candidates from reputed universities will get preference



Requirements:
  • At least 6 years
  • The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies, Medical Equipment


Skills Required: Product Development,Production,Research and Development

Additional Requirements:
  • Strong knowledge of pharmaceutical formulation and process development

  • Hands-on experience in technology transfer & scale-up

  • In-depth understanding of GMP, GLP, WHO guidelines

  • Strong analytical, problem-solving, and decision-making skills

  • Excellent leadership and team management capability

  • Good communication and documentation skills.



Responsibilities & Context:

GET WELL LIMITED, a concern of RFL Group is hiring

Position: Dy. Manager/ Manager- R & D and PD

Job Location: Habigonj

Why Join RFL Group?

RFL Group is one of the largest and fastest-growing conglomerates in Bangladesh with diversified businesses in manufacturing, consumer goods, plastics, building materials, electronics, retail & medical devices. It is a growing and dynamic pharmaceutical & medical device company in Bangladesh & here there is an opportunity to work with modern manufacturing and quality systems

Position Overview

We are seeking a highly skilled and innovative Dy. Manager/ Manager – R & D and Product Development to lead formulation development, technology transfer, and product lifecycle management for pharmaceutical & Medical Devices.

Key Responsibilities:

  • Develop new formulations (solid, liquid, semi-solid dosage forms)

  • Conduct pre-formulation and compatibility studies

  • Optimize formulations for stability, efficacy, and cost-effectiveness

  • Execute lab-scale to pilot-scale development

  • Prepare and review BMR, BPR, and development reports.

  • Coordinate with Production, QA & QC for smooth commercialization.

  • Troubleshoot process and formulation issues

  • Prepare CTD/ACTD dossiers for regulatory submission

  • Ensure compliance with GMP, WHO, and regulatory guidelines

  • Handle documentation for product registration (local & export)

  • Support regulatory audits and inspections

  • Design and monitor stability studies (accelerated & long-term)

  • Work closely with QC for method development and validation

  • Interpret analytical data and ensure product quality standards

  • Lead and mentor R&D team members



Job Other Benifits:
  • Provident fund,Mobile bill,Performance bonus
  • Lunch Facilities: Partially Subsidize
  • Salary Review: Yearly
  • Festival Bonus: 2
    • Attractive Salary Package.

    • Leave Encashment

    • Promising career path with promotion opportunity after 6 months of a successful probation period.

    • Credit purchase facilities with discounts at PRAN-RFL outlets.



Employment Status: Full Time

Job Work Place: Work at office

Company Information:

Gender: Male and Female can apply

Read Before Apply: Please apply only who are fulfilling all the requirements of this job

Category: Production/Operation

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