Experience
- 2 to 5 years
- The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies
Requirements
- 2 to 5 years
- The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies
Additional Requirements
- Age At most 32 years
- Only Male
B. Pharm/M. Pharm from any reputed University.
At least 2 - 5 years’ experience in Pharmaceuticals.
Practical experience in PD (Formulation & Analytical).
Must have computer knowledge.
Responsibilities & Context
Context:
One Pharma Ltd. embarked on its pioneering journey in November 2015 with a focus on incorporating cutting-edge manufacturing technology and producing globally acclaimed pharmaceutical products for the patients of Bangladesh and beyond. One Pharma Limited is looking for some experienced, reliable, honest & dedicated candidate for the position of Executive/ Senior Executive, Product Development (PD) department for its factory (BSCIC, Bogura).
Job Responsibilities:
To undertake the development and manufacturing of laboratory, pilot, stability, trial, and scale-up batches of new pharmaceutical products.
To provide technical and product-related documentation and support for regulatory dossier preparation, submission, and responses to regulatory queries for national & International Market
To develop product formulations, prepare manufacturing recipes, and conduct stability studies for new products.
To prepare, review, and update product development documents, including specifications, manufacturing process sheets, analytical test methods, product manuals, SOPs, Batch Manufacturing Records (BMRs), Batch Packaging Records (BPRs), and process validation protocols and reports in compliance with cGMP and applicable ISO requirements.
To coordinate with Quality Control (QC), Production, Quality Assurance (QA), and other relevant departments to resolve formulation, analytical, and manufacturing-related problems.
To develop, implement, and maintain approved procedures, policies, and protocols for operations at contract manufacturing facilities.
To perform or coordinate the physical and chemical evaluation of raw materials and packaging materials in collaboration with QC, as applicable.
To monitor and review in-process, intermediate, and finished product quality data and maintain relevant records.
To minimize product rejection, manufacturing defects, and process-related deviations by implementing quality-by-design principles and appropriate process controls during product development and scale-up.
To maintain up-to-date knowledge of applicable regulatory requirements, guidelines, and documentation requirements issued by the Directorate General of Drug Administration (DGDA), Drug Testing Laboratories (DTL), and other relevant regulatory authorities.
Job Other Benifits
- Provident fund,Tour allowance,Mobile bill,T/A
- Festival Bonus: 2
- Salary Review: Yearly
Competitive Career Growth
Other Financial/Non-financial Benefits