Key Responsibilities :
1. Manufacturing & Technical Excellence
Act as the Subject Matter Expert (SME) for Ayurvedic formulations, production processes, and quality standards, with a strong emphasis on documentation.
Ensure compliance with GMP, AYUSH guidelines, the Drugs & Cosmetics Act, and state FDA regulations.
Review, standardize, and continuously improve SOPs for manufacturing, quality control, and packaging.
Oversee batch records, raw material authentication, and ensure adherence to pharmacopeial standards.
Work closely with QA / QC teams to implement process improvements and validate manufacturing processes.
2. Regulatory & Compliance
Serve as the authorized technical person for product licensing, renewals, and approvals in Haryana.
Ensure product claims, labels, and advertisements align with AYUSH, FSSAI, and Drug Controller regulations.
Maintain relationships with regulatory bodies for inspections, audits, and licensing activities.
3. Center of Excellence (COE) Contributions
Lead innovation in Ayurvedic product formulations and manufacturing processes to continuously improve efficiency, quality, and compliance.
Act as a key driver for process excellence, setting high standards in operational performance across the organization.
Key Skills & Competencies :
Deep understanding of Ayurvedic formulations, manufacturing processes, and pharmacology.
Expertise in GMP and regulatory compliance (AYUSH, FSSAI, Drugs & Cosmetics Act).
Strong technical writing skills (SOPs, batch records, product dossiers).
Excellent communication and training abilities to lead teams and foster collaboration.
Analytical mindset focused on process optimization, compliance, and continuous improvement.
License Requirement :
Must hold a valid BAMS (Bachelor of Ayurvedic Medicine and Surgery) registration / license to practice in Haryana.
Skills Required
Technical Writing, batch records , Sops, Gmp, Regulatory Compliance
Bams • India, Faridabad