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 pharmaceutical industry.

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Today, we have manufacturing bases across India, UK, Scotland, the USA, and Canada through subsidiaries. Our critical care products are available in the emergency rooms of hospitals across the globe and our products are available in over 100 countries. We are presently the third-largest player in the global Inhalation Anesthesia (IA) market and the only company in the world with a complete product portfolio of Inhalation Anesthetics drugs.

Our manufacturing capabilities make us one of the largest custom manufacturing companies in the world. The ‘UN Conference on Trade and Development’s World Investment Report 2011’ ranks us among the top 5 in the world.

Through the years, we at Piramal Healthcare have partnered with the largest and most reputed organizations in the global pharmaceutical industry to expand our product offering and deliver the best innovations to our customers.

Position: Executive – Quality Control

Location: Medak, Telangana

Job Description:

  • Responsible for performing the chemical and instrumentation analysis for in-process, raw materials, intermediates and finished products to meet the dispatch timeline as per the monthly schedule received from PPIC.

  • Performing of analytical, calibration, and qualification data (if, required) and keeping all instruments within the calibration schedule.

  • Responsible for maintaining all the documentation and documenting the data in logbooks and hard books online.

  • Maintaining GLP & GDP across the lab.

  • 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, glassware, and solvents required for analysis.

  • Responsible for keeping instruments neat and clean and overall responsibility of Internal & External calibrations follow-ups and completions within the timelines.

  • Performing and maintenance of all the calibration certificates, qualification certificates, standard weight certificates, and working/reference standard certificates.

  • Responsible for review of analytical data, calibration data, qualification data.

  • Maintaining online documentation and real-time data monitoring.

  • Responsible for maintaining the consumption records and traceability of working/reference standards.

  • Responsible for review of SOP’s, test procedures, and specifications.

  • Responsible for Controlling the cost and operate within the approved budget.

  • Responsible for following 21 CFR Part-11 compliance and maintaining data integrity in the lab.

  • Responsible for maintaining the instruments in working condition and reduce the breakdown time of instruments.

  • Responsible for performing method transfer analysis.

  • Filing the ATR`s  and other documents with proper labeling and to be handed over to QA within the given timelines

  • Communicating any abnormalities, deviations, laboratory Incidents happening during analysis to the section in-charge or manager for further plan.

  • Responsible for safe working conditions and clean environmental practices.

  • Responsible for training the contract persons and helpers on glassware cleaning.

  • Responsible to sign all the documents connected with the activities under her control.

  • In the absence of superior, she/he is responsible for his activity/responsibilities.

Qualification: B.Sc/M.Sc

Experience: Fresher/Experienced

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