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 [email protected]
