Mankind Pharma

Delhi, Delhi-NCR

Company details

Industry:
Biotechnology/Chemical/Pharmaceutical
Number of workers:
1000
Website:
http://www.mankindpharma.com/

Company Description

Mankind Pharma, the 8th largest Pharmaceutical Company of India, was incepted in 1995 with a meagre capital of 50 lakhs and 20 employees. Today, we are amongst the top 5 fastest growing Pharmaceutical companies of India with an employee base of more than 10000 and heading towards a turnover of INR 3000 crores. We aspire to aid the community in leading a healthy life through two parallel objectives: formulating, developing & commercializing medicines and delivering affordable & accessible medication that satisfies urgent medical needs.

Mankind Pharma

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job postings

  • Position will be responsible for Development of nanoparticles, liposomes or nanotechnology products To design & execute Lab scale Formulation development and stability batches of nanoparticles, liposomes or nanotechnology products Execution of Formula Optimization & Process Optimization batches at R & D and pilot plant scale. Execution of Pilot batches for bio-studies. Execution of Process Optimization ...

  • Position will be responsible for Development of nanoparticles, liposomes or nanotechnology products To design & execute Lab scale Formulation development and stability batches of nanoparticles, liposomes or nanotechnology products Execution of Formula Optimization & Process Optimization batches at R & D and pilot plant scale. Execution of Pilot batches for bio-studies. Execution of Process Optimization ...

  • Position will be responsible for 1. Review and finalizing of regulatory strategy related to product filing (White paper/Controlled correspondence/Filling pathways/Query response), Change control, Deviations and other R&D/Plant documents* for Regulatory Submission or cGMP Compliance throughout Products life cycle management in coordinating with Cross Functional Team, Contract Manufacturer, Contract ...

  • Agm/dgm - Regulatory Affairs

    Paonta Sahib, Himachal Pradesh

    Position will be responsible for 1. Review and finalizing of regulatory strategy related to product filing (White paper/Controlled correspondence/Filling pathways/Query response), Change control, Deviations and other R&D/Plant documents* for Regulatory Submission or cGMP Compliance throughout Products life cycle management in coordinating with Cross Functional Team, Contract Manufacturer, Contract ...

  • Design and Execute marketing strategy. Studying, analyze and identifying Gynae market situation, Prepare business strategy and execute the same Risk analysis and Business Advisory To Launch Gynae products and develop market, Responsible for Design Promotional Campaign, Develop and improve efficiency and business growth, Strategic planning, Competitive Insights, Pricing. Efficient in utilization of digital ...

  • Design and Execute marketing strategy. Studying, analyze and identifying Gynae market situation, Prepare business strategy and execute the same Risk analysis and Business Advisory To Launch Gynae products and develop market, Responsible for Design Promotional Campaign, Develop and improve efficiency and business growth, Strategic planning, Competitive Insights, Pricing. Efficient in utilization of digital ...

  • Design and Execute marketing strategy. Studying, analyze and identifying Gynae market situation, Prepare business strategy and execute the same Risk analysis and Business Advisory To Launch Gynae products and develop market, Responsible for Design Promotional Campaign, Develop and improve efficiency and business growth, Strategic planning, Competitive Insights, Pricing. Efficient in utilization of digital ...

  • Position will be responsible for Development of nanoparticles, liposomes or nanotechnology products To design & execute Lab scale Formulation development and stability batches of nanoparticles, liposomes or nanotechnology products Execution of Formula Optimization & Process Optimization batches at R & D and pilot plant scale. Execution of Pilot batches for bio-studies. Execution of Process Optimization ...

  • > Environment monitoring. > Surface monitoring of equipments >Water sampling and analysis >Sterlity analysis, BET > Candidate should be from Pharma background. > Injectable experience > Ready to work in shifts ...

  • > Environment monitoring. > Surface monitoring of equipments >Water sampling and analysis >Sterlity analysis, BET > Candidate should be from Pharma background. > Injectable experience > Ready to work in shifts ...

  • Microbiologist,pharmaceuticals, Injectable

    Paonta Sahib, Himachal Pradesh

    > Environment monitoring. > Surface monitoring of equipments >Water sampling and analysis >Sterlity analysis, BET > Candidate should be from Pharma background. > Injectable experience > Ready to work in shifts ...

  • Position will be responsible for 1. Review and finalizing of regulatory strategy related to product filing (White paper/Controlled correspondence/Filling pathways/Query response), Change control, Deviations and other R&D/Plant documents* for Regulatory Submission or cGMP Compliance throughout Products life cycle management in coordinating with Cross Functional Team, Contract Manufacturer, Contract ...

  • >Finished Good and Semi-finished good sample allotment to chemists. >Responsible for to investigate the lab variation,OOS,OOT and deviation in laboratory. >To approve and release In-Process and semi-finished good sample. >To review the analytical data. >To ensure good documentation for analytical data being maintained as per cGMP. >To ensure STP and specification are updated as per current pharmacopeia ...

  • >Finished Good and Semi-finished good sample allotment to chemists. >Responsible for to investigate the lab variation,OOS,OOT and deviation in laboratory. >To approve and release In-Process and semi-finished good sample. >To review the analytical data. >To ensure good documentation for analytical data being maintained as per cGMP. >To ensure STP and specification are updated as per current pharmacopeia ...

  • >Finished Good and Semi-finished good sample allotment to chemists. >Responsible for to investigate the lab variation,OOS,OOT and deviation in laboratory. >To approve and release In-Process and semi-finished good sample. >To review the analytical data. >To ensure good documentation for analytical data being maintained as per cGMP. >To ensure STP and specification are updated as per current pharmacopeia ...

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