Glenmark Pharmaceuticals Limited [Glenmark] is an India-based growing pharmaceutical company headquartered at Mumbai [formerly, Bombay]. Incorporated in 1977, the Company is focused on the manufacture and marketing of formulation products and active pharmaceutical ingredients [API] in India as well as globally and enjoys a diversified and growing presence in regulated and developing international markets. Over the past five years, the Company has also catalyzed its growth through investment in dedicated research and development including cutting-edge New Chemical Entity [NCE] research.

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At Glenmark, our people are encouraged to discover and follow their own unique path of career development.

Aligning individual aspirations to business goals, we offer a range of opportunities that allows our talent to develop both breadth and depth of experience. This includes cross-functional movements, stretch assignments, and international stints.

We recognize high performance & drive for results through fast track career paths & other developmental opportunities. Each team member is supported on their growth journey through continuous learning interventions.

Position: Research Associate – Pharmacokinetics – Bioanalytical

Location: Navi Mumbai, Maharashtra

Job Description:

Job Purpose: To support method development, method validation & bio-study activities by analysis and related documentation in coordination with Senior Analyst and Group Leader on LC-MS/MS instrument. To calibrate and maintain the laboratory equipment.

Role & Responsibilities:

  • To support the day to day planning by analyzing samples of method development, method validation, study sample analysis as per study plan on LC-MS/MS systems.
  • To analyze samples for developing the rugged, reproducible, time saving and cost-effective bio-analytical methods.
  • Documentation of method development activity.
  • To analyze samples of method validation activity as per plan in accordance with the in-house SOP.
  • Documentation of validation experiments as per standard procedures
  • Follow the GLP system by strictly following the in-house SOPs. Real-time documentation of each activity of analysis, calibration, and maintenance.
  • To actively participate in the review procedure of data to be audited.
  • To support the planned activity for the preparation of audits.
  • Do necessary correction and preventive actions for the QA/QC observations.
  • Coordinate with QA/QC personnel during the audit.
  • Ensure a sufficient quantity of chemicals, working standards, SPE cartridges, HPLC columns, and other accessories are available for upcoming projects. Recording of consumption of chemicals, solvents, working standards.
  • To handle all the activities related to biological samples as per bio-safety SOPs.

Desired Knowledge & Skills:

  • Understanding of basic chemistry, analytical chemistry,
  • Sound Knowledge of bioanalytical field
  • Knowledge of GLP.
  • Knowledge of analytical instrumentation such as LC-MS/MS, HPLC, etc.

Qualification: B.Pharma/M.Pharma/MS/M.Sc

Experience: 1-3 Years

Salary: 2,00,000 to 3,00,000 INR CTC/PA

Contact Details:

Mr Varun Jain

varun.jain@glenmarkpharma.com

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