Cronus Pharma Hiring for Executive – Assistant Manager Positions

Cronus Pharma, a global leader in animal health pharmaceuticals, is conducting a walk-in interview for Executive to Assistant Manager positions in Solid Orals & Injectables (TTD). If you have 4-9 years of experience and hold an M.Pharm (Pharmaceutics/Pharm. Tech.), this is a great opportunity to join a rapidly growing company.
Job Details
- Position: Executive to Assistant Manager
- Department: Solid Orals & Injectables (TTD)
- Experience Required: 4-9 years (Independent contributory role)
- Qualification: M.Pharm (Pharmaceutics/Pharmaceutical Technology)
- Job Location: Hyderabad, Telangana
- Walk-in Date: 8th February 2025 (Saturday)
- Interview Location: Cronus Pharma Specialties India Pvt Ltd, Plot No: 1-98/5/78, Jubilee Enclave, Madhapur, Hitech City, Ranga Reddy (D), Hyderabad, Telangana – 500081
- HR Contact: 7337445157 / 7337445197
- Email for CV Submission: hr@cronuspharma.com, planthr@cronuspharma.com
About Cronus Pharma
Cronus Pharma is one of the top 5 largest animal health pharmaceutical companies globally. Headquartered in East Brunswick, NJ, USA, the company specializes in R&D, manufacturing, and marketing of veterinary pharmaceuticals. Cronus Pharma is dedicated to delivering high-quality, cost-effective medications to veterinarians and pet owners across the United States.
Key Highlights of Cronus Pharma:
- Fully integrated R&D and manufacturing company
- Extensive portfolio of 76 FDA-approved products, with 26 currently marketed
- Licensing in all 50 U.S. states for pharmaceutical distribution
- Innovative product development with multiple FDA approvals pending
- Commitment to Good Manufacturing Practices (GMP) for quality and safety

Job Responsibilities
- Conduct and oversee formulation development for Solid Orals & Injectables (TTD)
- Ensure adherence to GMP, quality standards, and regulatory guidelines
- Lead projects from concept to commercialization
- Work collaboratively with cross-functional teams in R&D, manufacturing, and regulatory affairs
- Perform troubleshooting and process optimization for formulations
- Maintain documentation and compliance as per FDA and industry standards