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. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products.
- Vacancy details:
- Department: Executive-QC
- Qualification: B.Sc / M.Sc / B.Pharmacy / M.Pharmacy
- Salary:₹Not Disclosed
Job Description: Greeting from Piramal Pharma Solutions (PPS) . .!!!!!
- Important Details :
- Location:Medak, Telangana, India
- Post of date :05/08/2024
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to face
- Interview Rounds of Interview: HR
Job Description
- Responsible for performing the chemical and instrumentation analysis for In-process, raw materials, packing materials, intermediates and finished products to meet the dispatch timeline as per the monthly schedule received from PPIC.
- Responsible for allotting the work to the chemist within the raw material section.
- Responsible for performing the calibrations of all instruments in raw material section as per the schedule.
- Responsible for maintaining all the documentation online.
- Responsible for maintaining the minimum stock for working standards, reference standards and impurity standards and ordering as and when required.
- Responsible for maintaining the minimum stocks for chemicals, reagents, glass wares and solvents required for analysis.
- Responsible for keeping instruments neat and clean and overall housekeeping in the FP section.
- Responsible for review of analytical data, calibration data, qualification data
- Responsible for keeping all instruments within the calibrated status.
- Responsible to do the analysis, review and release on time to support the production
- Responsible for reducing the lab incidences, repeat analysis and no Data Integrity issues.
- Responsible for real time data monitoring.
- Responsible for reviewing the analytical data received from external laboratory.
- Responsible for maintaining all the calibration certificates, qualification certificates, standard weight certificates and working/reference standard certificates.
- Responsible for maintaining the consumption records and traceability of working/reference standards.
- Responsible for OOS investigations, deviations and CAPA implementations
- Responsible for review of SOP’s , test procedures and specifications
- Responsible for providing the training on GLP/GMP to the employees working the section.
- Responsible for releasing the batches timely manner to achieve the site requirement.
- Responsible for preparing the COA’s as per the customer requirement
- Responsible for approving/rejecting the batches in SAP
- Responsible for Controlling the cost and operate within the approved budget.
- Responsible for maintaining the instruments in working condition and reduce the breakdown time of instruments.
- Responsible for carrying out the analytical method transfers.
- Responsible for keeping the critical spare parts of the instruments.
- Responsible for Safe working conditions and clean environmental practices.
- Responsible for usages of required safety appliances in the section.
- Responsible for SFTI.
- Responsible for coordination with QA/Production/PPIC/Warehouse/TSD for smooth dispatches
- Responsible for training the contract persons and helpers on glassware cleaning.
Qualifications
B.Sc / M.Sc / B.Pharmacy / M.Pharmacy

