Regulatory Affairs Specialist (Contract Manufacturing & Export)

Expired

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Contract Manufacturing, Export Operations

Anywhere in Bangladesh

Full Time

Any

Salary Negotiable

Vacancy 5 positions

Experience (years) 2 – 4

Salary & vacancy

Salary: Negotiable

5 vacancies

Application

Deadline:

April 3, 2026 (Expired)

Job Description

Eagle Eye Limited BD offers an exciting opportunity for a Regulatory Affairs Specialist to join their pharmaceutical export operations team in Bangladesh. This full-time position involves managing contract manufacturing and export processes, requiring expertise in Bangladesh’s pharmaceutical regulatory framework and experience with DGDA registration procedures. The role provides a chance to work with international pharmaceutical supply chains and contribute to the company’s mission of delivering high-quality generic drugs to global markets.

The successful candidate will enjoy a competitive salary package with performance bonuses, comprehensive benefits including social and medical insurance, and professional development opportunities. Working in a modern office environment with flexible arrangements, you’ll collaborate with both local manufacturing partners and the Hong Kong headquarters team. This position is ideal for professionals passionate about pharmaceutical regulatory affairs who want to make an impact in the growing generic drug export industry while building expertise in international pharmaceutical supply chain management.

Requirements

• Experience: 2 – 4 years

Education Requirements

Required educational qualifications for this role:

Bachelor of Pharmacy (B.Pharm) or equivalent degree
Bachelor’s degree or above in Pharmacy, Pharmaceutical Sciences, Chemistry, Biotechnology, or related field
M.Pharm degree preferred but not mandatory

Experience Requirements

Experience requirements for this Regulatory Affairs Specialist position:

2-4 years of experience in pharmaceutical regulatory affairs
At least 2 years of hands-on DGDA new drug registration experience
Experience with variation applications, renewals, and dossier submissions
Prior experience with export permits, contract manufacturing, or toll manufacturing projects

Qualifications

Key qualifications for success in this role:

Strong familiarity with Bangladesh pharmaceutical regulations and international standards
Proven track record of direct interaction with DGDA on export-related applications
Excellent document management and timeline control abilities
Ability to work independently while collaborating with Hong Kong team and local manufacturers

Skill Requirements

Pharmaceutical Regulatory Affairs
DGDA Registration Process
Contract Manufacturing Management
Export Documentation
Technical File Preparation
Cross-functional Coordination
Document Management
Regulatory Compliance

Incentive & compensation

The position offers competitive compensation and benefits including:

Performance-based bonus
Year-end bonus and festival allowances
Comprehensive social and medical insurance
Professional training opportunities
Modern office environment with flexible work atmosphere

How to apply for Eagle Eye Limited BD jobs

Follow these steps to apply for the Regulatory Affairs Specialist position:

Prepare your updated CV and relevant documents
Visit the external application URL: https://bdjobs.com/h/details/1465736
Submit your application before the deadline of April 3, 2026
Ensure all required information is complete and accurate
Include details of your relevant experience in pharmaceutical regulatory affairs

About Eagle Eye Limited BD

Eagle Eye Limited BD is a Hong Kong-headquartered professional pharmaceutical wholesale and trading company specializing in global generic drug supply chain management. The company focuses on connecting high-quality pharmaceutical manufacturing partners in Bangladesh with international markets across Asia, Africa, and other regions, ensuring compliance with global regulatory standards and quality requirements.