Responsible for documentation and implementation of all QA & QC activities
Verification and technical support for all technical documents master formula,standard operating procedure,raw material,finished product specifications.
Responsible for handling various quality management systems like deviation,change control and market complaints.
Responsible for providing quality assurance support to the manufacturing operations.
Internal auditing of QA/QC and other departments .
Review of all QC/QA activities .
Art work control of labels,leaflets,visual aids,promotional materials of domestic and export.
Verification and implementation of new label matter design and promotional materials as per regulatory compliances,
Export related technical support-material safety data sheet,ingredient report etc.
Coordination with R&D and technology transfer group during Trial/Validation of batches.
Review and approval of records(ie: SOP,Batch record,master formulation,specification certificate of analysis,stability studies,labeling etc.
Imparting training to quality control and quality assurance executives as required
Partner with third party laboratories for out sourcing of testing.
Control of all records & documents relating to quality control & assurance.
candidate must have at least 4 years of experience in QA in pharma sector.
ARBRO PHARMACEUTICALS LIMITED, a tested & trusted name in Indian pharmaceutical... Industry having more than 25 years of experience in manufacturing and exporting of pharmaceutical formulations , trading of raw materials and Research & Development for pharmaceutical Industry Dedicated to provide best quality products in pharmaceutical, bio-technology & healthcare Industry, Arbro is at paramount & has strong presence in exports, generic formulations, ethical range of products, institutional & government supplies as well as recognized as Government approved R & D facility by Department of Science and technology, Government of India. Read full description