Full-Time Bengaluru
Key Accountabilities: Review documentation related to packing activity and monitor standard packing parameters as per BPR to meet regulatory requirement
Perform qualification and calibration of equipment as per schedule and update output of all activities in the system
Prepare manufacturing records and update online documentation to meet production and cGMP requirement
Prepare new documents and update existing documents as per GMP requirement
Monitor adherence to safety guidelines in the block during a shift for packing activities to create safe working environment
Ensure compliances to safety training targets by monthly reconciling attendance records
Provide training to staff & workmen for packing activity by regular interactions with them to get quality product
Conduct training related to equipment handling, cGMP, documentation and unit operations
Provide new ideas and simplify processes to reduce process cycle time and achieve new targets
B. Pharm. / B. Sc. (Chemistry)
Relevant Work Experience 1-5 years of experience in packing with knowledge of handling of QMS activity, qualification and other related document