MSN Laboratories is amongst the world’s fastest-growing Pharmaceutical Company having 9 API Plants. MSN crated Benchmarks in Developing Complex drugs, Economically feasible, Making it No -1 in active DMF’s in the world.

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Key Achievement of MSN

  • Turnover above 600 Million USD
  • Asia’s Biggest State of Art R&D Center with 1400 Dedicated Scientists & 42 Scientific Labs
  • 9 API and 5 Finished Dosage formulation Facilities
  • World Class Manufacturing Facility in New Jersey, USA
  • No-1 Ranking in USA DMF Filings – 380 DMF’s & 100 ANDAs
  • Introduced 17 First’s in World of Generics

The Young and One of the Fastest Growing Pharmaceutical Company with Focus on 500 Cr Domestic Business in the near term through Suoer Specialty Business Focus, Expansions and New Launches in Oncology, Cardiology, CNS, Gastro, Pain Management, urology Nephrology, etc

Position: Executive/Sr Executive

Department: FR&D, Complex Injectables

Location: R&D Center, Hyderabad, Telangana, India

Job Description:

  • Design and Develop robust Injectable & Ophthalmic drug product for Global market requirement
  • Experience in designing & development of the product based on QbD & DOE for the generic products as needed.
  • Relevant experience in handling of development of Suspension, Emulsion, Microsphere, Nanoparticle, etc., based technology drug formulation
  • Author technical documents such as review of analytical data, the justification to an analytical variance if any, preparation of stability protocols, study plans, Product development report, and other relevant documents for dossier filing purpose.

  • Scale-up and technology transfer from R&D to production to meet timelines. Execution of pre-exhibit and exhibit batches
  • Involved in the preparation & review of batch records, process characterization reports, validation reports, and investigation reports.
  • Plan and contribute to project-related scientific/technical activities (e.g., interpret results, critical assessment of data, draw relevant conclusions, and write reports).
  • Work pro-actively with other cross-functional groups to execute all product-related activities such as Manufacturing and Packaging master records, SOPs and protocols, etc.
  • Review appropriate documentation and test results for accuracy and completeness and compliance with SOPs/GLP/GMP requirements.
  • Interaction with external testing laboratories as needed.
  • Co-ordination with other Dept. like analytical, Purchase, QC/QA, Regulatory, Production, Eng. etc. related to product development activity
  • Provide relevant documents to Regulatory Affairs in a timely manner for ANDA filings and Deficiency response

Qualification: M.Pharma

Experience: 1-6 Years

Salary: Negotiable

Contact Details:

simhachalam.piniminti@msnlabs.com

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