QC / QA MANAGER

Process validation
Technology transfer from one manufacturing location to other
Transfer from development lab/pilot plant to commercial locations
Handling changes like batch size, Equipment, Alternate Vendors, Material Vendors, specifications etc
Preparation of master batch documents, validation protocols and reports
Trouble shooting
Process improvements, cycle time reduction
Quality improvement
Data collection, review & analysis of data
Desired Skills:
2 - 8 years of experience in Process development/Tech transfer areas.
Having good knowledge and hands of experience on the equipment, process and materials of Oral dosage forms.
Additional exposure in other dosage forms is desirable. Knowledge on Formulation development, GMP & regulatory requirements will be an added advantage.
Key personal attributes:
Should have good communication & interpersonal relationships.
Ability to work with cross functional teams
Should have positive attitude and problem solving ability
Willing to travel frequently to other manufacturing sites