Company Description At Zenovel, we specialize in delivering high-impact solutions across three critical areas of the pharmaceutical industry: Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), and Regulatory Affairs. With over 20 years of global experience, we help pharma and biotech companies ensure their trials, facilities, and products meet international regulatory standards efficiently and effectively. Our core services include risk-based monitoring, audits, facility setup, strategic regulatory planning, and dossier submission. Zenovel is committed to turning regulatory complexity into competitive advantage, aiding partners in scaling safely, compliantly, and globally. Role Description This is a full-time on-site role for a Head of Regulatory Affairs, located in Ahmedabad. The Head of Regulatory Affairs will oversee and manage regulatory compliance, develop and implement regulatory strategies, ensure adherence to regulatory requirements, and lead the submission of regulatory dossiers. Responsibilities include strategic regulatory planning, compliance audits, facilitating product registrations with various international regulatory bodies, team leadership, and maintaining up-to-date knowledge of relevant laws and regulations. Qualifications Experience in Regulatory Compliance and Regulatory Requirements Proficiency in Regulatory Strategy and Regulatory Affairs Skills in Regulatory Submissions and Dossier Compilation Excellent leadership and team management abilities Strong communication and interpersonal skills Proven ability to work effectively in a fast-paced environment Bachelor's or Master's degree in Pharmacy, Life Sciences, or related field Advanced knowledge of global regulatory standards and procedures Experience in the pharmaceutical or biotech industry is highly desirable
Company Description ZENOVEL is a global leader in the pharmaceutical industry, specializing in providing comprehensive solutions for Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), and Regulatory Affairs. Our experienced team has over 17 years of expertise in GCP, GMP, and regulatory affairs, and we are dedicated to helping organizations in the pharmaceutical industry achieve success. Role Description This is a full-time on-site role for a Senior Clinical Research Associate at our Ahmedabad location. The Senior Clinical Research Associate will be responsible for Monitoring BA-BE (Healthy Volunteer), overseeing clinical operations, and ensuring protocol compliance. They will also be involved in research activities and collaborate with cross-functional teams. Qualifications Clinical Research Associates and Clinical Trials skills Experience in clinical operations and protocol adherence Strong research skills Monitoring/Auditing Experience into BA-BE. Excellent written and verbal communication skills Attention to detail and ability to work independently and efficiently Bachelor's degree in a relevant field