WE ARE HIRING
Manager -Product Development Department (Factory)
Job Responsibilities /Requirements
- Should have good knowledge and technical expertise of product development activities like licensing, pre-formulation studies, strategy design, formulation development, bio-equivalence study, manufacturing process development, technology transfer, and validation of various pharmaceutical dosages form
- Should have the capacity leading the Product Development team to achieve the business objective of the organization by providing necessary guidance to develop generic drugs for domestic and international markets.
- To be supervised the Product Development team by maintaining a standard workflow to maximize the operational efficiency of both formulation and analytical lab and rearranging the resource based on the requirements to meet organizational objectives.
- To be coordinated the formulation team for the new product development, Problem-solving of the existing product, Market complaints handling of the product, and Value addition by reformulation of all dosage forms (Oral Solid Dosage, Liquid, Semisolid, Sterile, and Oncology products)
- To be coordinated the analytical team for the analytical method development, validation, verification,compilation, evaluation, and interpretation of analytical data during product development of all dosage form (Oral Solid Dosage, Liquid, Semisolid, Sterile and Oncology products)
- Able to maintain all documentation as per GMP guidance.
- To be coordinated the product development activities like raising of requisition (Materials and machinery), sample submission in Drug Testing Laboratory (DTL), Analyzing the stability study & prepare reports, Development of specifications of raw materials, Development of new sources of raw materials by analyzing samples, Prepare the SOP, Troubleshoot, calibrate and maintain of analytical instruments.
- Should have knowledge for the evaluation of the proposal of new project feasibility in accordance with existing equipment & facility in the scope of R&D & production facility.
- Supervising the activities of technology transfer to the production and quality control department and Driving product development from concept to final launch.
- Cooperation for the buildup of the regulatory dossier for submission, addressing regulatory queries, and supporting the commercial launch.
- Participating in process improvement activities to optimize formulation cost, and development timelines, improve production efficiency, and improve the quality of product.
- Anticipating the market demand, planning, and developing products to meet consumer needs and remain competitive in the marketplace
- Review of project-related documents, protocols, reports, and records.
Educational Requirements
- Bachelor of Pharmacy (B.Pharm), Master of Pharmacy (M.Pharm) From Reputed Public University.
- Skills Required: Computer skills (MS Word, Excel), excellent communication skills.
Experience Requirements
- Having 6-8 years experience in similar positions in a reputed pharmaceutical company.
Additional Requirements
- Age 40 to 45 years
- Good analytical skills
- Self-management including the Ability to prioritize own workload, ability to work independently, commit to meeting deadlines, and maintaining confidentiality in all areas of work.
- Insightful knowledge of USP, NF, BP, IP, cGMP, cGLP, SOPs, ICH guidelines, FDA regulations, etc.
- Must have the ability to lead a Team.
Job Location:
Tongi BSCIC
Salary: Negotiable
Compensation & Other Benefits:
- Provident Fund
- Yearly Increment
- Festival Bonus: 2
- Yearly Bonus: 1
- Mobile Bill
- Other benefits as per company policy
Note: Job Advertisement published in bdjobs on 16th July 2023
Date Line: 26th July 2023
