Therapiva Pharma | Walk-in interview for Production - QA | 27 July 2019 | Hyderabad

Join our WhatsApp Group



Like us on Facebook


Buy our Pharma Interview Q&A eBook


Date: 27th July 2019
Time: 9:30 AM to 4:00 PM 

Venue : 
Therapiva Private Limited 
Plot # 218 & 219, Phase II,
IDA Pashamylaram,Sangareddy,
Telangana.
Landmark: Beside Biocon Ltd.

Production Chemists 

Job Role: Production Chemists 
Experience: 1 to 4 yrs
Location: Hyderabad
Qualification: B.Sc/M.Sc

Key Responsibilities: 


• Responsible for day to day shift activities and report to Executive (or) Shift In charge.
• Responsible to maintain Good housekeeping in production block and surrounding areas of the production area.
• All documents like batch manufacturing and control records, cleaning records, equipment log books, housekeeping and weighing balance checklists etc to be maintained online.
• Manufacturing the drug products as per Batch Production and Control Records (BPCR) and performing process operations as per standard operation procedure.
• To check all the labels before batch charging.
• Any deviation (or) abnormality observed to be intimated to the executive (or) shift in charge.
• Responsible to follow safety instructions given in batch manufacturing and control records.
• Responsible to attend cGMP, Safety and other trainings conducted.
• Responsible to guide casual helpers to get the work in safe manner.

QA 

Job Role: QA Chemists
Experience: 2 to 6 years 
Location: Hyderabad
Qualification: M.Sc.(Chemistry)

Key Responsibilities :


• Review of BPCRs in line with technical package received for various projects from R&D centre.
• Review and approval of executed BPCRs received from manufacturing department related to various projects.
• Organizing and imparting trainings for various training programs.
• Checking online operations in concerned departments for ensuring GMP compliance.
• Handling and review of deviations and change controls related to concerned departments.
• Handling of customer complaints.
• Handling of OOS.
• Reviewing and approval of concerned department SOPs.
• Preparation, Review and approval of quality assurance SOPs.
• Preparation, Review and approval of Purified water system protocol, data and report.
• Online monitoring of purified water system for compliance.
• Review and approval of AHU protocols, data and report.
• Preparation, Reviewing and approval of cleaning validation protocols.
• Review and approval of process validation protocols and reports.
• Reviewing and approval of equipment qualification protocols and reports.
• Handling of internal audits.
• Identification of various procedures related to concerned departments for effective quality system implementation.
• Vendor qualification management.
• Facilitate during customer / regulatory audits by coordinating with Head-QA.
• Release of API / Intermediate.
Interested candidates can send their updated resume to ranjit.nalbothu@therapiva.net or hr@therapiva.net.