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.

Positions: Executive – Quality Assurance – IPQA (Sterile injection)

Location: Vadodara, Gujarat, India

Job Description:

  • Responsible for the IPQA related activity like line clearance at different stages of batch manufacturing and packing.
  • Perform in-process checks and sampling of swab samples, controlled samples, stability samples.
  • Responsible for issuance and review of BMR and BPR.
  • Responsible for the preparation and review of SOPs, specifications, and other necessary master documents.
  • Calibration and verification of D.T., Friability, and Analytical weighing balance.
  • Responsible for execution of validation related activities like process validation and cleaning validation.
  • Exposure to working in an oncology facility will be preferable.

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

Experience: 1-2 Years

Salary: Negotiable

Contact Details:

Ms. Bhavna Kadam

bhavna.kadam@alembic.co.in, qualityform@alembic.co.in

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