Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms.
- Vacancy details:
- Department: Executive – Quality Assurance
- Qualification: B.Pharm or M. Pharm
- Salary: ₹Not Disclosed
Job Description: Greetings from Piramal Pharma Solutions (PPS) Ltd…!!
Important Details :
- Post of date:28/10/2024
- Location: Mahad, Maharashtra, India
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face To Face Interview
- Interview Rounds of Interview: HR
Job Description
Area and line clearance for Manufacturing, Packing & Dispensing activity in production area.
Inprocess checks in Manufacturing and Packing activity.
Inspection of dispensing activity intermediately.
Daily verification of weighing balance calibration activity.
Daily verification of environmental monitoring of raw material staging area and Manufacturing and Packing area.
Verification of each equipment cleanliness and area cleanliness during line clearance
Verification and review of online Batch Manufacturing Records.
Sampling of bulk stage and finished goods analysis and control sample.
Verification of production documents.
Daily non conformance observation reported and maintained.
In process quality checks in Tablet, Liquid, HNH, ANH manufacturing dept.
Line Clearance for Manufacturing, Packing & Dispensing activity.
Sampling of Bulk and Finished goods
Review of production records and Finished Goods verification
On job training to the new people working in the production area.
Statistical Process Monitoring.
Online observation of process deviation and effective implementation of CAPA.
Reporting of daily non conformance.
Execution of requirements for food/Dietary supplements regulations for export market (US)-21 CFR Part 111
Ensuring avoidance of breach of data integrity in area.
Implementation of effective sanitation program in area.
Imparting required training to shop floor personnel.
Adherence to the requirements of EHS norms.
