Goodman Pharmaceuticals Ltd
Requirements
Education
Master of Pharmacy (M.Pharm) in Pharmacy
Master of Science (MSc) in Chemistry
Experience
At least 3 years
The applicants should have experience in the following business area(s): Pharmaceutical/Medicine Companies
Additional Requirements
Age 23 to 32 years
Responsibilities & Context
To prepare, review and regular updating of SOPs, manufacturing processes, specifications &method of analysis and other relevant documents.
To prepare process validation protocol and work closely with the Production, Product Developmentand Engineering Department for validation of equipment, processes, control procedure, criticalsystems.
To conduct self-inspection audit.
To prepare & review Annual Product Review related document and records.
Management of market returned products & other non-conforming materials and submit report asinstructed by the reporting supervisor.
To prepare & review the qualification documents and take approval.
To conduct training on GMP & SOPs.
To conduct Qualification and validation.
To perform of Quality Management System activities eg. Change Controls, deviations, Out ofSpecification, Market complain.
To perform Quality Risk Management.
To review the batch documents and Batch release.
Skills & Expertise
cGMP Compliance
Process Validation
SOP
Other Relevant Skills
Quality Assurance
SOP writing
Document Control
Quality Management System
Compensation & Other Benefits
Over time allowance
Lunch Facilities: Full Subsidize
Salary Review: Yearly
Festival Bonus: 2
Workplace
Work at office
Employment Status
Full Time
Job Location
Gazipur
To apply for this job email your details to apply@chakricircular.com