DD NUTRITIONS INDIA

Job Description: Position: Regulatory Affairs Executive – Pharmaceuticals Location: New Delhi, India Department: Regulatory Affairs Reports To: Head of Regulatory Affairs / Managing Director Role Summary: As a Regulatory Affairs Specialist, you will play a vital role in managing the preparation and submission of high-quality regulatory documentation to health authorities to support the development, approval, and maintenance of pharmaceutical products. You will ensure that all products meet national and international regulatory requirements throughout their lifecycle. Key Responsibilities: Prepare, compile, and submit regulatory dossiers (e.g., CTD, eCTD) for new product approvals, renewals, and variations. Ensure timely submissions to regulatory agencies (e.g., FDA, EMA, CDSCO, MHRA). Manage communication and correspondence with health authorities. Track and interpret changes in pharmaceutical regulations and provide regulatory guidance to internal stakeholders. Review and approve product Labelling, packaging, and promotional materials for compliance with regulatory requirements. Support clinical trials by submitting and maintaining INDs or clinical trial applications (CTA). Maintain regulatory databases and documentation for inspections and audits. Liaise with cross-functional teams such as R&D, QA/QC, Medical Affairs, and Manufacturing to ensure compliance and regulatory readiness. Contribute to regulatory strategy and risk assessments during drug development and post-marketing phases. Required Qualifications: Bachelor’s or Master’s degree in Pharmacy, Pharmaceutical Sciences, Life Sciences, or related field. 4–5 years of experience in pharmaceutical regulatory affairs. Strong knowledge of global regulatory requirements (FDA, EMA, ICH, CDSCO, etc.). Experience with CTD/eCTD formats and regulatory submission processes. Attention to detail, critical thinking, and strong organizational skills. Excellent communication skills, both written and verbal. Preferred Qualifications: Regulatory Affairs Certification (RAC) or equivalent is a plus. Familiarity with global submission platforms (e.g., ESG, CESP, EU Portal). Experience in new drug applications (NDA), abbreviated NDAs (ANDA), and post-marketing surveillance. TANVEER KAUR, HR, +91 97738 06363 Job Type: Full-time Pay: ₹30,000.00 - ₹50,000.00 per month Benefits: Cell phone reimbursement Schedule: Day shift Supplemental Pay: Performance bonus Work Location: In person

Job Description: Position: Regulatory Affairs Executive – Pharmaceuticals Location: New Delhi, India Department: Regulatory Affairs Reports To: Head of Regulatory Affairs / Managing Director Role Summary: As a Regulatory Affairs Specialist, you will play a vital role in managing the preparation and submission of high-quality regulatory documentation to health authorities to support the development, approval, and maintenance of pharmaceutical products. You will ensure that all products meet national and international regulatory requirements throughout their lifecycle. Key Responsibilities: Prepare, compile, and submit regulatory dossiers (e.g., CTD, eCTD) for new product approvals, renewals, and variations. Ensure timely submissions to regulatory agencies (e.g., FDA, EMA, CDSCO, MHRA). Manage communication and correspondence with health authorities. Track and interpret changes in pharmaceutical regulations and provide regulatory guidance to internal stakeholders. Review and approve product Labelling, packaging, and promotional materials for compliance with regulatory requirements. Support clinical trials by submitting and maintaining INDs or clinical trial applications (CTA). Maintain regulatory databases and documentation for inspections and audits. Liaise with cross-functional teams such as R&D, QA/QC, Medical Affairs, and Manufacturing to ensure compliance and regulatory readiness. Contribute to regulatory strategy and risk assessments during drug development and post-marketing phases. Required Qualifications: Bachelor’s or Master’s degree in Pharmacy, Pharmaceutical Sciences, Life Sciences, or related field. 4–5 years of experience in pharmaceutical regulatory affairs. Strong knowledge of global regulatory requirements (FDA, EMA, ICH, CDSCO, etc.). Experience with CTD/eCTD formats and regulatory submission processes. Attention to detail, critical thinking, and strong organizational skills. Excellent communication skills, both written and verbal. Preferred Qualifications: Regulatory Affairs Certification (RAC) or equivalent is a plus. Familiarity with global submission platforms (e.g., ESG, CESP, EU Portal). Experience in new drug applications (NDA), abbreviated NDAs (ANDA), and post-marketing surveillance. TANVEER KAUR, HR, +91 97738 06363 Job Type: Full-time Pay: ₹30,000.00 - ₹50,000.00 per month Benefits: Cell phone reimbursement Schedule: Day shift Supplemental Pay: Performance bonus Work Location: In person

Urgent Requirement for Business Development executive. candidate having knowledge of amazon, flipkart and other online platform where he can sell company product and handle full account of online platform. Candidate having experience in export BDM. candidate having affiliate marketing work experience. Candidate will comfortable to work from office. pharma background candidate is preferred . Interested candidate will share their resume. Job Type: Full-time Pay: ₹25,000.00 - ₹50,000.00 per month Benefits: Cell phone reimbursement Paid sick time Paid time off Ability to commute/relocate: Rohini Sub City, New Delhi - 110085, Delhi: Reliably commute or planning to relocate before starting work (Required) Education: Bachelor's (Preferred) Experience: Business development: 1 year (Preferred) total work: 1 year (Preferred) Language: Hindi (Preferred) Work Location: In person

Urgent Requirement for Business Development executive. candidate having knowledge of amazon, flipkart and other online platform where he can sell company product and handle full account of online platform. Candidate having experience in export BDM. candidate having affiliate marketing work experience. Candidate will comfortable to work from office. pharma background candidate is preferred . Interested candidate will share their resume. Job Type: Full-time Pay: ₹25,000.00 - ₹50,000.00 per month Benefits: Cell phone reimbursement Paid sick time Paid time off Ability to commute/relocate: Rohini Sub City, New Delhi - 110085, Delhi: Reliably commute or planning to relocate before starting work (Required) Education: Bachelor's (Preferred) Experience: Business development: 1 year (Preferred) total work: 1 year (Preferred) Language: Hindi (Preferred) Work Location: In person

looking for experienced candidate for health supplement/pharmaceutical company for managing business development for supplements product globally Job Types: Full-time, Permanent Pay: ₹19,233.22 - ₹80,487.67 per month Benefits: Cell phone reimbursement Health insurance Life insurance Paid time off Work Location: In person

Urgent Requirement for Business Development executive. candidate having knowledge of amazon, flipkart and other online platform where he can sell company product and handle full account of online platform. Candidate having experience in export BDM. candidate having affiliate marketing work experience. Candidate will comfortable to work from office. pharma background candidate is preferred . Interested candidate will share their resume. Job Type: Full-time Pay: ₹40,000.00 - ₹70,000.00 per month Benefits: Cell phone reimbursement Paid sick time Paid time off Work Location: In person

looking for experienced manager for export specially from pharmaceuticals or nutritions field only having a good knowledge: sales and lead generation product selection good knowledge of distributors registration guidelines market research analysis contract and proposal management Job Type: Full-time Pay: ₹50,000.00 - ₹100,000.00 per month Benefits: Health insurance Paid sick time Work Location: In person