Piramal Enterprises Ltd. (PEL) is the flagship company of Piramal Group and has a leading position in the business verticals it is present in i.e. Healthcare and Financial Services.
We forayed into the health care space in 1988 with a move that was contrarian at that time, as most pharmaceutical players were exiting India due to the existing business climate. It has been 25 years, and we have established ourselves as one of the most recognizable and respected names in the pharmaceuticals industry.
Name of the Post : Executive – Quality Control (GC Section)
No.of.Posts : 02
Location : Zaheerabad
Experience : 4 – 7 Years
Salary : INR 4,00,000 – 6,00,000 P.A.
Job Description :
- Responsible for planning for GC analysis in GC section to meet the dispatch timeline as per the monthly schedule received from PPIC.
- Responsible for allotting the work to the chemist within the GC section.
- Responsible for performing the calibrations of all instruments in GC 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 GC 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 SOPs , 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 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 Lean lab activity.
- Responsible for coordination with QA/Production/PPIC/Warehouse/TSD for smooth dispatches
Qualifications:
- UG -B.Sc – Chemistry, Bio-Chemistry, B.Pharma – Pharmacy
- PG – M.Pharma – Pharmacy, MS/M.Sc(Science) – Chemistry, Bio-Chemistry
- Doctorate – Doctorate Not Required
