Company Name: SMC Enterprise Ltd.
Roles & Responsibilities:
- Carryout pre-formulation study, prepare technical data, annexure and recipe to submit drugs administration of all dosage form (Oral solid dosage, Liquid, Semisolid, Sterile and Oncology Products).
- Raise requisition for required raw and packaging materials for developing lab batch/pilot batch.
- Perform lab batch and pilot batch considering critical attributes.
- Prepare Drug Testing Laboratory (DTL) sampling in case of INN products.
- Develop raw & packaging materials specification.
- Prepare BMR, BPR and process validation protocol.
- Perform the validation of first three commercial batches to evaluate the process and prepare report.
- Compile the product master file with approved documents.
- Prepare the SOP for related activities of product development.
- Review formulation of existing products based on product or market complaints, stability related problems or cost saving need.
- Perform other related activities assigned by the supervisor.
Educational Qualification:
- Master of Pharmacy (M.Pharm)
- M.Sc. in Chemistry/Applied Chemistry/Bio Chemistry from any recognized University with excellent academic record.
Work Experience:
- At least 3 year(s)
Others Requirements:
- Experience in product development activity (Especially in formulation development of Oral Solid Dosage, Sterile Products & Oncology products in any reputed pharmaceutical company).
- Should have excellent communication skills both in Bangla and English.
- Should have sufficient knowledge on cGMP and GLP rules and regulation.
- Should have good documentation practice.
- Hard working and ability to work under pressure
Others Benefit:
As per company rules.