Job Context
Full time permanent position

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 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 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 complain handling of the product  and Value addition by reformulation  of all dosage form (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 documentations as per GMP guidance .
• To be coordinated  the product development activities like raise of requisition (Materials and machineries ), sample submission in Drug Testing Laboratory (DTL), Analyze the stability study & prepare of 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 production and quality control department and Drive 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, 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 skill (MS Word, Excel), excellent communication skill.

Experience Requirements

• Having 6-8 years’ experience in the similar positions in a reputed pharmaceutical company.

Additional Requirements

• Age 40 to 45 years
• Good analytical skills
• Self-management including: Ability to prioritize own work load, able to work independently, committed to meet deadlines and maintain 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