Title: Assistant Manager, Formulation Research and Development Department
Company Name: Popular Pharmaceuticals PLC.
Vacancy: --
Age: At least 30 years
Job Location: Anywhere in Bangladesh
Salary: --
Experience:
M. Pharm from any reputed institution
Experience: Minimum 10 years of experience in Research and Development
Skills:
Depth knowledge on formulation development of solid oral, liquid, sterile injectable, ophthalmic, and other dosage forms
Knowledge of FDA, EMA, WHO, and other regulatory requirements
Project planning and execution
Team leadership and mentoring
Decision-making and accountability
Excellent written and verbal communication skills
Ability to interpret complex data and create actionable recommendations
Proficient in Microsoft Office (Word, PowerPoint, Excel)
Job Context
Popular Pharmaceuticals PLC. is one of the top leading pharmaceutical companies in Bangladesh having state-of-the art manufacturing plant located in Tongi. Over the past twenty years we are maintaining very high growth rate in the pharmaceutical industry and today we are an organization of about 10000 employees. Popular Pharmaceuticals PLC. has already won the trust of the physicians and other stakeholders both in home and abroad. We export our medicines to 34 countries around the world.
To continue our success as a leading and innovative pharmaceutical company, we are looking for smart, talented and energetic candidates to join in our winning team.
Job Responsibilities
Lead formulation development activities for solid, liquid, sterile injectable, ophthalmic and other dosage forms
Design, develop, and optimize formulations in alignment with target product profiles (TPP), quality requirements, and applicable regulatory standards
Plan, supervise, and evaluate laboratory-scale formulation studies, while providing technical guidance for scale-up activities from pilot batches to commercial manufacturing
Investigate and resolve formulation, process, and manufacturing challenges encountered during product development, technology transfer, and and plant batches
Collaborate closely with Production, Quality Assurance (QA), Quality Control (QC), and cross-functional departments to ensure smooth product development and transfer
Support the preparation, review, and submission of regulatory documentation, including CTD dossiers, ensuring compliance with ICH, FDA, EMA, and other relevant international regulatory guidelines
Drive continuous improvement initiatives by identifying opportunities for formulation enhancement, process optimization, cost reduction, and operational efficiency
Ensure that all development activities are conducted in accordance with current Good Manufacturing Practices (cGMP), regulatory expectations, and organizational quality standards
Salary
Attractive compensation package will be offered to deserving candidates
Compensation & other benefits
Provident Fund
Gratuity
Festival Bonus: 3 (Yearly)
Leave Fare Assistance (LFA)
Soft Furnishing Allowance (SFA)
Mobile Phone Allowance (MSA)
Profit Bonus
Medical Facility
Earn Leave Encashment
Group Life Insurance
Subsidized Lunch Facility
Pick & Drop Facility
Weekly Holiday: 2 days