Bridge Pharmaceuticals Ltd.
Executive / Sr. Executive, Regulatory — Join a Growing Pharmaceutical Company in Dhaka
Dhaka
Deadline: 2025-11-02
1 Positions
Job Overview
Company: Bridge Pharmaceuticals Ltd.
Location: Dhaka
Type: FullTime
Salary: Negotiable
Posted: 2025-10-04
Experience: 1 Years
Education Requirements
Master of Pharmacy (M.Pharm) or Bachelor of Pharmacy (B.Pharm)
Job Responsibilities
- Submission of new medicines and line extension dossiers according to DGDA requirements.
- Completion of timely registration and marketing authorization in line with business requirements in Bangladesh markets.
- Manage variations, renewals, and post-approval changes according to regulatory guidelines to ensure compliance.
- Obtain approval of new prices and price increases for registered products.
- Product sample submission to the DOF/DLS Lab and follow-up to complete required approval procedures.
- Assess and prepare documentation to obtain NOC for import of fish & livestock product/premix from DOF and DLS.
- Discuss and meet with officials to address NOC reviewing committee objections from DLS.
- Prepare and compile documents for license renewal from DLS & DOF and arrange/manage inspections for license renewal.
- Pursue DoE renewals and compliance procedures for various licenses and permits.
- Stay updated with changes in local drug and regulatory policies.
Required Skills
- Regulatory affairs (DGDA/DLS/DOF processes)
- Dossier preparation and submission
- License renewal and variation management
- Regulatory compliance and documentation
- MS Word
- MS Excel
- Stakeholder communication
- Inspection coordination
Benefits & Compensation
- T/A (Travel allowance)
- Mobile bill reimbursement
- Salary review: Yearly
- Lunch facilities: Fully subsidized
- Festival bonus: 2 per year
Job Description
Bridge Pharmaceuticals Ltd. is seeking a diligent and proactive Executive / Sr. Executive, Regulatory to join its regulatory affairs team in Dhaka. This job circular invites qualified candidates from pharmaceutical backgrounds to apply for a crucial role that ensures regulatory compliance, timely registrations, and license management for veterinary and related products in Bangladesh. The successful candidate will work closely with regulatory authorities (DGDA, DLS, DOF, DoE) and internal teams to prepare dossiers, manage renewals and variations, and support inspections and approvals. This job is ideal for professionals with 1–2 years of relevant experience in pharmaceutical/medicine companies, although freshers with strong academic credentials (M.Pharm or B.Pharm) are encouraged to apply. As a company committed to quality and compliance, Bridge Pharmaceuticals offers a dynamic workplace in Motijheel, Dhaka. What you will do (primary responsibilities) Prepare and submit registration dossiers for new medicines and line extensions as per DGDA requirements. Drive timely registration and marketing authorization processes to meet business requirements in Bangladesh markets. Manage regulatory post-approval activities: variations, renewals, and other post-market changes to ensure compliance. Obtain approvals for new product pricing and price increases for registered products. Coordinate product sample submission to DOF/DLS labs and follow up to completion of approval procedures. Prepare documentation and support to obtain NOC for import of fish & livestock products/premix from DOF and DLS, and address objections from review committees. Compile and submit necessary documents for license renewal with DLS & DOF; arrange and manage inspections related to renewals. Pursue Department of Environment (DoE) renewals and ensure compliance for required permits and licenses. Keep up-to-date with changes in local drug and regulatory policies and incorporate those changes into company processes. Required skills & qualifications Education: Master of Pharmacy (M.Pharm) or Bachelor of Pharmacy (B.Pharm). Experience: 1 to 2 years in pharmaceutical or medicine companies preferred; freshers may apply. Strong understanding of DGDA, DLS, DOF regulatory frameworks and registration processes in Bangladesh. Excellent documentation skills, attention to detail, and ability to prepare regulatory dossiers. Proficiency in MS Word and MS Excel; comfortable with standard office software for record keeping and reporting. Good communication and stakeholder management skills to liaise with regulators and internal teams. Ability to coordinate inspections, follow-up actions, and cross-functional compliance activities. Additional information Job type: Full Time, work at office (Motijheel, Dhaka). Gender: Male candidates preferred as indicated in the circular; Age: 28 to 40 years. Vacancies: 1 position. Salary: Negotiable (as per company policy). Benefits: Travel allowance (T/A), mobile bill reimbursement, yearly salary review, fully subsidized lunch, two festival bonuses per year. This job posting is published by Bridge Pharmaceuticals Ltd. on a public job circular platform. If you are interested to apply, please use the online apply option provided in the original job circular (Bdjobs listing) or contact the company for guidance. For queries related to this job posting, the company contact number listed is 01689932304. When you apply, ensure your CV highlights regulatory experience, dossier preparation, and familiarity with DGDA/DLS/DOF compliance procedures. Keywords for search engines and applicants: job, company, circular, bangladesh, apply — this posting is intended to help candidates find and apply for a regulatory affairs job in Bangladesh with a reputable pharmaceutical company. Apply promptly, as the deadline for applications is indicated in the circular.