Job Description / Responsibility
Process validation and analytical method validation.
Conducting stability studies as per ICH guideline.
Technology (Process and analytical) Transfer
Perform and Maintain all activities and documents in line with GMP requirement.
Archiving of documents of all formulation and laboratory activities.
Establishment of test methods for new products.
BMR & Batch costing sheet preparation.
Process validation & verification.

Job Nature
Full-time

Educational Requirements
Minimum B.Sc. Hon`s in Chemistry/ Bio Chemistry from any reputed University

Experience Requirements
1 to 2 year(s)
The applicants should have experience in the following area(s):
Bio-Chemist/Chemist
The applicants should have experience in the following business area(s):
Pharmaceutical/Medicine Companies

Additional Job Requirements
Age 22 to 30 year(s)
Hands on experience in manufacturing table, capsule, bolus, suspension & injection in pharmaceuticals & veterinary division.
QC knowledge will be additional advantages.
Work as Team Member
Pleasant personality with self motivated.
Positive attitude with hard working, honest & sincere

Salary Range
Negotiable

Other Benefits
Provident Fund
Gratuity
Health Insurance
Life Insurance
Others benefit as per company rules

Send your CV to jobs@eongroup.net.bd