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At Zenovel, we are more than just a workplace, we are a thriving community where innovation meets impact. By joining us, you become part of a dynamic team that values creativity, collaboration, and continuous growth. We empower our employees with opportunities to work on groundbreaking projects, develop their skills, and make a meaningful difference in the industries we serve. With a culture rooted in inclusivity, integrity, and excellence, Zenovel is the perfect place to turn your ambitions into achievements. Together, let’s shape the future and redefine possibilities. If you’re interested in building your career with Zenovel, visit our Career Page or contact our HR team directly at +91 931-333-6390 (HR Desk)
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Business Development Executive
- (More Than 2 Years)
- Ahemdabad
- 3
Executive Regulatory Affairs
- (2-4 Years)
- Ahemdabad
- 4
Clinical Reseach Associate
- (2-4 Years)
- Ahemdabad
- 2
Quality Management System
- (5-7 Years)
- Ahemdabad
- 4
Clinical Project Management
- (5-8 Years)
- Ahemdabad
- 5
Senior Clinical Research Associate
- (4-7 Years)
- Ahemdabad
- 2
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In the pharmaceutical and biotechnology industries, obtaining regulatory approval is essential prior to introducing new drugs or biologics to the market. A pivotal aspect of this approval process is the FDA Pre-Approval Inspection (PAI), which involves a comprehensive assessment of manufacturing facilities, processes, and data integrity to ensure adherence to
Risk Based Monitoring (RBM) is a more efficient alternative to traditional clinical trials, focusing on high-risk areas through data-driven insights. It ensures patient safety, data integrity, and regulatory compliance while reducing costs and timelines. However, the success of RBM depends on the competency of monitors, who identify risks, analyze data,
Welcome to the Zenovel Blog! We are a leading provider of drug regulatory consulting and education, focusing on advancing pharmaceutical innovation while ensuring safety and compliance. This blog delves into the essentials of Drug Regulatory Affairs (DRA), covering its scope, career opportunities, and intricate processes involved in bringing new drugs
The international pharmaceutical landscape is inherently connected to the global economy and global trade, which is consisted with the quality and safety assurance , well-controlled quality and safety. Compliance with international pharmaceutical standards has changed from an optional step to a requirement. The Pharmaceutical Inspection Co-operation Scheme (PIC/S Certification) is
Lipinski’s Rule of 5 (Ro5) is a crucial guideline in pharmaceutical development, helping researchers evaluate a compound’s likelihood of becoming an effective oral drug. However, with the rapid evolution of therapeutic strategies, it’s worth considering the relevance of Ro5 in the current drug design landscape. Understanding Lipinski’s Rule of 5
Regulatory affairs (RA) play a crucial role in the pharmaceutical industry; ensuring products meet quality, safety, and efficacy. As the industry grow further the need for qualified professionals to bridge gaps between companies and regulators increases. This blog explores Zenovel regulatory affairs expertise, our various facets, and valuable contribution to
