0 years
0 Lacs
Posted:3 weeks ago|
Platform:
On-site
Full Time
Role & responsibilities Supervising the activities as per the assignment by Executive/Assistant Manager Maintaining proper storage conditions and documentation as per the statutory and customer requirements. Adherence to cGMP requirements in the assigned section. Check in process done in log books. Handling rejections on line. Daily Line clearance, Batch change over & product change over on decartoning / filling /packing area. Handling deviation/ change parts / stereos/SAP functions. Coordinate with engineering Dept. for machine breakdowns Daily status report to HOD or production head Timely completion of batch records and other documents in assigned section. Organize for proper maintenance of the equipment in assigned section. Organize for proper disposal of rejected material or waste generated during the processing. Optimize the utilization of manpower and equipment in the assigned section. Review and update the GMP documentation in assigned section. Preferred Candidate Profile: Qualification: B. Pharm Basic knowledge of cGMP and production processes Good communication, documentation, and coordination skills Willingness to work in shifts as per operational requirements Should possess good communication skills, theoretical and pharma knowledge Interested candidate can apply on ashwini.b@encubeethicals.com Show more Show less
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Ponda, Goa, India
Experience: Not specified
Salary: Not disclosed
Ponda, Goa, India
Experience: Not specified
Salary: Not disclosed