Hetero’s strength lies in the talent and commitment of the 21,000+ employees, who have been playing a vital role in contributing to our business over the years. At Hetero, we provide you an environment for personal and professional growth. A healthy work-life balance is supported through a knowledge-driven work environment where ideas and skills are valued, where people can realize their full potential through dedicated training programs. Hetero strongly believes that each and every employee is the backbone of the organization and their contribution is respected, recognized, and rewarded.

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Numerous opportunities exist for qualified, talented, and passionate personnel from diverse backgrounds in various departments. No matter, if you are a fresher seeking a good break in the pharma industry or an experienced hand with an ability to make the difference, you are welcome to join our pursuit towards excellence while you enjoy a career that is exciting.

1. Designation: Executive/Jr Executive IPQA

Location: Jadcherla, Hyderabad, Telangana

Department: Quality Assurance – Bulk Drug – IPQA

Job Description:

  • Responsible for review of master and executed BMRs and BPRs.
  • Responsible for review of manufacturing department SOPs.
  • Responsible for giving line clearance between the startup of various manufacturing operations.
  • Responsible for performing in-process checks during manufacturing as per the respective SOPs & protocols.
  • Coordination and review of process validation and cleaning validation activities.
  • Responsible for review of all manufacturing logbooks.

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

Experience: 2-3 Years

Salary: Negotiable

2. Position: Officer/Jr Officer

Location: Jadcherla, Hyderabad, Telangana

Department: Quality Assurance – Finished Goods – IPQA

Job Description:

  • Responsible for IPQA activity during formulation& filling.
  • Responsible for giving Line clearance between Startup of various Manufacturing and Packing operations.
  • Responsible for performing in-process checks during manufacturing and packing operations as per the respective SOPs & protocols.
  • Responsible for Monitoring and Coordination of process validation, Hold time studies, media fill, and cleaning validation activities.
  • Responsible for review of manufacturing department SOPs.

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

Experience: 2-3 Years

Salary:  Negotiable

Contact Details:

edukondalu.m@heterodrugs.com

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