REGULATORY AFFAIRS SR. EXECUTIVE

Company Description Vickro Biopharma Private Limited (VBPL) is a science-driven biopharmaceutical company established in 2016, specializing in nutraceuticals, pharmaceuticals, probiotics, enzymes, antioxidant pigments, and semisynthetic biomolecules. The company operates state-of-the-art manufacturing facilities in Karkapatla Biotech Park, Hyderabad, with a DSIR-recognized R&D center in Kukatpally, Hyderabad. VBPL focuses on fermentation, purification, and formulation across multiple dosage forms, and also produces specialized feed supplements for poultry, large animals, and aquaculture. Certified under ISO 9001:2008, GMP, FSSC 22000, and FSSAI, VBPL emphasizes quality, scientifically validated processes, and robust R&D. With a strong focus on innovation and customer satisfaction, VBPL is committed to advancing biotechnology solutions for a healthier future.
Role Description The Regulatory Affairs Sr. Executive is responsible for managing regulatory activities to support product registrations, approvals, and compliance in nutraceuticals, pharmaceuticals, probiotics, enzymes, and related product lines. This full-time, on-site role based in Hyderabad involves preparing, reviewing, and submitting regulatory dossiers, maintaining up-to-date knowledge of relevant regulations and guidelines, and ensuring that all documentation meets local and international regulatory standards. The role includes coordinating with R&D, quality, manufacturing, and commercial teams to gather data, align on regulatory strategies, and respond to regulatory authority queries in a timely manner. The Sr. Executive will monitor regulatory changes, help implement necessary updates in processes and documentation, and contribute to audit readiness and continuous improvement of the regulatory framework. The position requires meticulous attention to detail, strong organizational skills, and effective communication with internal stakeholders and external regulatory bodies.
Qualifications
Candidates should possess strong skills in Regulatory Affairs and understanding of Regulatory Requirements in the biopharmaceutical or related industry.
Candidates should possess skills in Regulatory Documentation and Dossier Preparation for product registrations and approvals.
Candidates should possess expertise in Regulatory Compliance, ensuring adherence to national and international standards and guidelines.
Relevant academic background such as a bachelor’s or master’s degree in Pharmacy, Biotechnology, Life Sciences, or a related field.
Experience in nutraceuticals, pharmaceuticals, probiotics, or enzymes, preferably in a GMP- and ISO-certified environment.
Strong analytical, documentation, and data interpretation skills, with proficiency in standard office and documentation tools.
Ability to work collaboratively with cross-functional teams, manage multiple projects, and meet regulatory timelines.
Good written and verbal communication skills in English; familiarity with local regulatory frameworks and international guidelines (e.g., WHO, ICH) is an advantage

Work arrangement
No