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LCMS/GCMS Analyst – Central Validation Lab | Alembic Pharmaceuticals | Vadodara | 2.35-5.50 L

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The legacy of Alembic Pharmaceuticals Limited (APL) dates back to over 100 years. Established in 1907 with an objective to develop and revolutionize the Pharmaceutical and Drug industry in the Indian subcontinent, Alembic Pharmaceuticals Limited today is one of the leading pharmaceutical companies in India.

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The publicly listed entity that manufactures and markets generic pharmaceutical products across the globe has grown by leaps and bounds over the last century.

With an emphasis on innovation and technology, the company has established a state-of-the-art research facility – Alembic Research Centre (ARC)-including formulation research, and a 150-bed bioequivalence facility at Vadodara, Gujarat. Additionally, APL has recently invested in an ultra-modern R&D center at Hyderabad. APL is one of the leading players in the industry to have invested about 11% of its turnover in R&D.

As a growth strategy, the company has aggressively started investing in the international generics market with successful ANDA and DMF filings. APL has also filings across Canada, Europe, Australia, South Africa & Brazil. The company caters to the rest of the world markets through branded formulation sales.

The company aims to explore opportunities in therapeutic areas such as Dermatology, Oncology, and Injectable Formulations. APL also has also co-promoted a company focused on the discovery and development of innovative, small molecule drugs that target signal transduction networks and ion channels for the treatment of cancer, inflammation, autoimmune diseases, and metabolic disorders.

Alembic Pharmaceuticals is looking for competent personnel to be an integral part of our Central Validation Lab Dept. for our API plant-based at Karakhadi, Vadodara-Gujarat.

Positions: LCMS/GCMS Analyst – Central Validation Lab

Location: Vadodara, Gujarat, India

Job Description:

  • Performing analytical method validation/verification/transfer activities and method feasibility studies.
  • Hands-on experience on QC instruments like LCMS, GC-MS.
  • Performing related substance, residual solvent, assay, and PSD method validation test as per ICH guidelines.Preparation of AMV/AMT protocols & reports.
  • Hands-on experience in major analytical instruments like LCMS GC-MS.
  • Exposure to software like Empower 3 and Labware LIMS.
  • Good understanding of GLP and GDP.

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

Experience: 3-6 Year

Salary: 2,25,000 – 5,50,000 INR CTC/PA

Contact Details:

Ms. Sameeksha Upadhyay

samiksha.upadhyay@alembic.co.in, researchcareers@alembic.co.in

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