Job Description:

  • All Procedures shall be carried in accordance with GMP & GLP on a Daily basis
  • Approving SOP, STP, Validation protocols, specifications, recording results related to QC dept
  • Managing stocks of Chemicals, Reagents, media, etc for smooth QC Functioning.
  • Responsible for complying with the customer and internal audit observations.
  • Responsible for overall compliance of the microbiological section as per GMP and GLP.
  • Responsible for timely execution of method transfer/method verification activities for new products and drug substances in coordination with ARD and project management team.
  • Only Formulation Experienced, Candidates with API experience are not eligible
  • Good Communication & Leadership skills

Location: Mirza, Guwahati

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

Experience: 16-20 Years

Salary: Negotiable

Contact Details:

gwhr@natcopharma.co.in, usharani@natcopharma.co.in

 

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