Piramal Enterprises Limited Recruitment 2021.Piramal Enterprises Limited Notification full detailes below.The Piramal Group is a diversified global business conglomerate, which has presence across various sectors such as healthcare, life sciences, drug discovery, healthcare information management, specialty glass packaging, financial services and real estate.
Important Vacancy details: Hiring For Senior Research Associate,Executive – Quality Assurance,Senior Research Scientist in Piramal Enterprises Limited!At India-GUJARAT,Maharashtra .intrested candidates Apply.
- Post Name: Senior Research Associate,Executive – Quality Assurance,Senior Research Scientist
- Qualifications : M.Pharm,M.sc
- Experience –01-3+ years
- Location: India-GUJARAT,Maharashtra
- Salary: NA
- Openings: NA
- To plan analytical activities and assign the related activities to subordinates.
- Review of all raw data in routine and address any unusual observation as per current quality system.
- Preparation/Review of technical documents like SOPs, specifications, COA, STP, Validation protocols/reports, Transfer protocol/reports for Solid oral dosage forms, Leachable evaluation method, Extractable & Leachable study protocols/reports etc.
- Follow GxP (GMP, GDP etc.) for all processes and train the subordinate to follow the same.
- Investigation of any unusual observation through suitable quality system.
- Training to subordinate for handling material safety.
- Co-ordination with engineering, vendor, supply chain etc.
Co-ordination with other manufacturing sites, contract laboratory etc
- Formulation development, process development, and manufacturing of GMP batches to the assigned product.
- Basic technical understanding about work done, rationale etc.
- Understanding about process selection and formulation (excipient) selection
- Knowledge about API Properties, preformation aspect
- Basic understanding about the process Roller compaction, wet granulation, compression, coating and equipments for the same
- Basic understanding about in process testing and instrument used for same (Blend flow properties, tablet characteristic)
- Blend uniformity and content uniformity testing and acceptance criteria
- Understanding on BCS classification
- Understanding about dissolution –basic and impurity
1.Knowledge of IPQA, Line Clearance for Manufacturing, Packing & Dispensing activity.
2.Sampling of Bulk and Finished goods, Review of production records and Finished Goods verification
3.On job training to the new people working in the production area
4.Statistical Process Monitoring, Online observation of process deviation and effective implementation of CAPA.
5.Reporting of daily non conformance.
6.Daily verification of weighing balance calibration activity.
7.Daily verification of environmental monitoring, verification and review of online Batch Manufacturing Records
8.Verification of production documents, Daily non conformance observation reported and maintained.
9.Knowledge of Change Control, Deviation, CAPA ,APQR, Stability study. Preparation of BMR/BPR.
10.Validation and Qualification
Selection Process: The selection will be on the basis of Interview.
How to Apply : Click here for full details and Apply Online