5 Ayush Jobs

As a Product Compliance & Quality Specialist in the Hygiene & Personal Care industry, you will be responsible for leading compliance, product claims, and quality systems for impactful categories including Handwash, Sanitizers, Toilet Cleaners, Detergents, Baby Products, Cosmetics, AYUSH, Medical Devices, and Wellness Products. Your role will involve ensuring compliance with regulatory bodies such as BIS, LM, CDSCO, AYUSH, and EPR rules. You will define test protocols, verify claims, drive audits, manage product documentation, artwork, risk assessments, and CAPA processes. Collaboration with cross-functional teams including R&D, Legal, Marketing, and Vendors will be key to success in this role. To excel in this position, you must possess 6-10 years of experience in QA/Compliance within industries such as FMCG, E-commerce, Laboratories, or Retail. Skills in claims management, regulatory documentation, and experience with private label products are highly desirable. This is a contractual/temporary position with a duration of 12 months. As part of the benefits package, you will have access to health insurance, paid sick time, paid time off, and Provident Fund. The work schedule is during day shifts with additional perks such as performance bonuses and yearly bonuses. Additionally, interested candidates will be required to specify their notice period in days as part of the application process. The work location is in person in Bangalore for the specified contract duration.,

Join us to transform global healthcare at our organization located in New Delhi, India. We are currently hiring Project Associates with qualifications such as MBBS, AYUSH, Pharmacist, Nurse, Management Graduates, and AI-ML Professionals, each with 1-3 years of experience in the relevant domain. There are 2 vacancies available per position. At the forefront of global healthcare transformation, our group of Strategic Business Units (SBUs) are redefining how health is designed, delivered, governed, and experienced. Our SBUs include: - Health Parliament: A global health policy think tank connecting professionals, policymakers, researchers, and citizens across 67+ countries. - Academy of Digital Health Sciences (ADHS): A pioneering academy skilling clinicians and health professionals in digital health. - International Patients Union (IPU): A platform advocating for patients" rights, access, and dignity in healthcare. - The Global Digital Health Summit (GDHS): The world's largest marketplace for digital health leaders, innovators, and policymakers. Join us to be part of global impact initiatives, work alongside visionary leaders, contribute to meaningful projects, and build your career in a mission-driven environment. We are looking for dynamic professionals with strong domain knowledge, a passion for healthcare transformation, and the ability to work in multi-disciplinary teams with excellence. Strong analytical, communication, and execution skills are required, along with a mindset to create real impact. A flair for marketing would be an added advantage. Your role will involve contributing to research, policy papers, and strategic initiatives, leading or supporting projects, engaging with global experts and stakeholders, supporting training programs and events, and innovating solutions for digital health adoption, policy reforms, or patient advocacy. If you are ready to reshape the future of healthcare, please send your CV and a brief note on Why You Want to Join Us to director@digitalassociates.health / contact@parliament.health. Please note, do not inbox, just send the email to the above email addresses.,

You will be responsible for reviewing and conducting chemical testing of raw materials, finished products, cosmetics, Ayurveda, Sidha & Unani products. You will need to accurately enter the test results into the LIMS software. Additionally, you will be required to handle instruments like HPLC, GC, FTIR, Dissolution, etc. Technical documentation in compliance with FDA, CDSCO & Ayush standards for audits will also be part of your responsibilities. The position is based in Gurugram and requires a minimum qualification of B.Pharma, M.Pharma, MSc. Chemistry or a related field. The ideal candidate should have 2 to 15 years of relevant experience.,

Program Duration: 1-Year Apprentice Program Post-Apprenticeship Role: RA Associate Role Outline: The Regulatory Affairs (RA) Apprentice will support the maintenance of regulatory compliance mandates, including FSSAI, Legal Metrology, and other applicable standards. The role involves statement preparation for new product endorsements, license renewals/modifications, and submission of annual and quarterly returns. This program provides hands-on training and exposure to regulatory frameworks and compliance procedures, equipping you with the skills to transition to an RA Associate role after one year. Key Deliverables: 1. Operational Support FSSAI Compliance Review and ensure compliance of formulations as per FSSAI guidelines, including pack size checks and client license reviews. Identify gaps in compliance and recommend necessary modifications to align with regulatory mandates. Validate and review LCs (Label Claims) and artworks for new product prototypes and existing products. Coordinate with stakeholders to implement required changes based on FSSAI, ICMR RDA mandates. Validate shade cards and coordinate with QC and packaging vendors for necessary adjustments. Collaborate with departments to update BOM (Bill of Materials) based on recommended formula or artwork changes to maintain compliance. Address client queries related to product or artwork compliance mandates. 2. Operational Support AYUSH Compliance Arrange and compile MFR (Master Formula Report) data from R&D, finished goods testing reports, and PMT (Product Management Team) comments for health claims to prepare Product Approval Copies for submission to AYUSH Licensing Authority. Review and finalize artwork compliance as per the Drugs & Cosmetics Act (D&C Act). File Schedule TA with the National Medicinal Plant Board and AYUSH Authority within the required timelines. What You Will Learn: Comprehensive understanding of FSSAI, AYUSH, and Legal Metrology compliance requirements. Skills in reviewing and validating formulations, labels, and artworks against regulatory standards. Hands-on experience in managing regulatory filings, license modifications, and client queries. Coordination with cross-functional teams such as R&D, QC, and packaging for compliance-related tasks. Knowledge of regulatory documentation and filing procedures for AYUSH and FSSAI. Eligibility Criteria: Qualification: MSc. in Food / B.Tech in Food Passion for understanding and applying regulatory standards. Strong communication and coordination skills. Program Benefits: 1-year intensive training program with structured learning opportunities. Placement as an RA Associate upon successful completion. Exposure to real-world regulatory challenges and solutions. If you are eager to build a career in Regulatory Affairs and learn through hands-on experience, this is the perfect opportunity for you!

JOB DESCRIPTION OF SENIOR RESEARCH SCIENTIST QUALITY Qualification - M. Sc. /M. Phil. /Ph. D in Chemistry Experience - 15 years in Quality Control/Assurance Industry -Toiletries/Cosmetics/Personal Care/Pharma Technical requisites : Hands-on experience in the following areas : 1. Ability to handle independently instrumental and chemical analytical laboratory 2. Analytical method development and validation 3. Stability study evaluation of products 4. Quality Management system and audits 5. Document and data control 6. Preparation of documents for drug/product licensing 7. Ensuring compliance to Drug & Cosmetics Act & Rules, GMP/GLP and regulations of Weights and measures act and rules 8. Product dossier preparation 9. Training Quality personnel in laboratory quality systems and management 10. Exposure in handling market complaints and root cause analysis 11. Exposure in handling Export regulations and documentation 12. Exposure in handling Halal/ISO/AYUSH License documentation