QA Regulatory Affairs Job at NaturMed Scientific – BSc Life Sciences, Biotech Apply at Biotecnika
Job Title: Quality Assurance & Regulatory Affairs Associate
Company Name: NaturMed Scientific
Location: Mayur Vihar Phase 1, Delhi
Salary: ₹20,000 – ₹24,000/month
Experience: 1-2 Years
About NaturMed Scientific:
NaturMed Scientific is a leader in the development, manufacturing, and supply of high-quality, natural, plant-based ingredients and extracts for the dietary supplement, pharmaceutical, food, beverage, and sports nutrition industries. Our diverse product range includes plant extracts, carotenoids, CO2 extracts, essential oils, oil powders, and fruit powders.
Driven by innovation and a commitment to sustainability, we develop research-based natural ingredients that enhance quality of life. We value ethical sourcing and sustainable processes, forging long-term partnerships across the supply chain to deliver premium-quality ingredients to global markets.
Position Overview:
We are seeking a motivated and detail-oriented Quality Assurance & Regulatory Affairs Associate to support our QA and RA functions. This is an exciting opportunity for a fresh graduate or a professional with up to 1 year of experience who is passionate about regulatory compliance, quality systems, and contributing to the natural health industry.
Qualifications:
• Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Chemistry, Biology, or Food Science.
• Minimum 1 year of experience preferred in Quality Assurance and Regulatory Affairs, ideally within the herbal, nutraceutical, or food industry.
Skills & Competencies:
• Foundational understanding of QA/RA functions, audit processes, and regulatory documentation.
• Exposure to industry-specific certifications and standards (e.g., ISO, HACCP, GMP, FSSAI).
• Familiarity with EU and US Pharmacopoeia (USP) standards is an advantage.
• Proficiency in Microsoft Outlook, Word, and Excel.
• Excellent analytical thinking and problem-solving skills.
• Strong interpersonal and communication abilities.
• Ability to manage tasks independently and work collaboratively with cross-functional teams.
Roles & Responsibilities:
• Monitor and implement updates related to regulatory certifications and quality standards.
• Coordinate internal and external audits; support documentation and corrective actions.
• Prepare regulatory-compliant documentation such as TDS, COA, MSDS, and product specifications.
• Assist in the preparation of export-related regulatory documentation.
• Provide quality-related documentation support to the sales and customer service teams.
• Manage product sample preparation and coordinate with external laboratories.
• Assist in developing country-specific regulatory dossiers.
• Support the creation and maintenance of SOPs, HACCP plans, CAPA reports, and related quality system documentation.
• Identify and assess regulatory risks; assist in mitigation planning.
• Collaborate with cross-functional teams to ensure alignment on quality and regulatory goals.
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