Hetero Drugs Immediate joiners in Formulation – DQA

Hetero is a research based global pharmaceutical company focused on development, manufacturing and marketing of Active Pharmaceutical Ingredients (APIs), Intermediate Chemicals & Finished Dosages. Ever since its establishment in 1993, Hetero showed a tradition of excellence and deep sense of commitment in developing cost effective processes to offer wide range of affordable drugs.

Vacancy details:

  • Department:Formulation – DQA
  • Qualification: M.Pharmacy ,Any Postgraduate
  • Experience:4 to 9 year(s) 
  • Salary: Not Disclosed

Job Description : Greeting from Hetero Drugs Ltd  !!!!

Important Details :

  • Location: Hyderabad
  • Post of date:01/06/2024
  • Selection Process: The selection will be on the basis of Interview.
  • Mode of Interview: Face to face
  • Interview Rounds of Interview: HR

Dear All,

Greeting from Hetero.

We are looking for Immediate joiners in DQA- Department.

Department: DQA

Experience: Freshers

Education Qualification: M.Pharmacy (Ceutics)

Department: DQA

Designation: Dy Manger/ Manager – DQA (Research & Development)

Experience: 8-12 Yrs

Job Description

  • Must have knowledge on review of Product development documents review.
  • Review / Approval of FRD and ARD documents, System.
  • Expertise in review of PDR, MFC, MPC, Scale up documents, Specification/STP etc.
  • Review / Approval of Regulatory query protocol and Reports.
  • Quality compliance in R&D. Review of product development documents.
  • Knowledge on review of Scale up activities / Pkg development activities review.
  • Exp in Technology Transfer and Plant QA activities.
  • Should be able to lead the team

Department: DQA-(FRD)

Designation: Executive

Experience: 4-6 Yrs

Job Description

  • Review / Approval of Formulation development documents and activities.
  • Knowledge on PDR, MFC/MPC, scale up documents review.
  • Formulation development document review.
  • GMP and Quality system

Department: DQA (ARD)

Designation: Executive

Experience: 4-6 Yrs

Job Description

  • Review / Approval of Analytical development documents and activities.
  • exposure on analysis and GLP compliance.
  • Knowledge on Specification / STP review.
  • Analytical development document review.
  • Quality system.

Job Location: Hyderabad

Interested candidates please share profiles to edukondalu.m@heterodrugs.com