Responsible for all Qualification and Validation activities for Oral Solid Dosage facility
Representing Qualification and Validation function in Regulatory audits (USFDA )
Representing Oral Solid Dosage Facility in External/ Internal Audits.
Monitoring departmental compliance with company SOPs / Global regulatory procedures for Oral Solid Dosage Facility
Validation and GMP co-ordinator for all Qualification -Validation activities
Actively involved in scale up and validation batches along with Process Development department.
Candidates must be currently working with company from USFDA, MHRA approved OSD (Tablet, Capsules) Plant.
Must be knowledge of Process Validation & Qualification in QA.
Qualification must be B.Pharm / M.Pharm.
Willingness to relocate to Ahmedabad