Home Production Executive QC AMV & AMT | Alembic Pharmaceuticals | Vadodara

Executive QC AMV & AMT | Alembic Pharmaceuticals | Vadodara


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 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 a part of Quality Control for our New Formulations (OSD) plant-based at Jarod Vadodara– Gujarat.

Positions: Executive QC

Location: Vadodara, Gujarat, India

Job Description:

  • To perform Analytical Method Validation, Method Transfer, and Verification activities as per SOPs and STPs.
  • To prepare protocols and reports of Method Validation & Transfer.
  • Handling QC instruments like HPLC, GC, GC-MS, ICP-MS, UV, FTIR, pH Meter, etc.
  • To perform calibration of QC instruments and review their documents.
  • To perform cleaning validation and swab sampling.
  • Exposure of Labware LIMS software.

Qualification: B.Pharma, MS/M.Sc

Experience: 2-6 Years

Salary: Negotiable

Contact Details:


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