Regulatory Affairs Associate Hiring DDReg Pharma – Gurgaon
- B Pharm, M.Pharm Regulatory Affairs Associate | DDReg Pharma – Gurgaon
- Company Overview
- Job Role & Responsibilities
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Why Join DDReg Pharma?
- FAQs
- Summary Table
B Pharm, M.Pharm Regulatory Affairs Associate | DDReg Pharma – Gurgaon
Apply for Associate – Regulatory Affairs at DDReg Pharma, Gurgaon. Open for B Pharm, M.Pharm, Life Sciences graduates with 3+ years of experience.
Join DDReg Pharma, a reputed global regulatory consulting firm, as an Associate – Regulatory Affairs (India Market) in Gurgaon. This role offers an exciting opportunity for professionals passionate about pharmaceutical regulations, compliance, and ensuring the highest quality standards in drug, device, and cosmetic approvals. Candidates with strong understanding of CDSCO guidelines and experience with the Sugam Portal are especially encouraged to apply.
Company Overview
DDReg Pharma is a globally recognized regulatory consulting organization specializing in regulatory affairs, pharmacovigilance, and quality compliance solutions. With a strong presence across major pharmaceutical markets, DDReg partners with leading pharmaceutical, medical device, nutraceutical, and cosmetic companies to simplify complex global regulations. The company’s India operations focus on supporting CDSCO submissions, ensuring compliance, and enabling faster access of healthcare innovations to the Indian population.
At DDReg, employees thrive in a knowledge-driven, collaborative environment where regulatory excellence meets innovation. The company is committed to training and development, offering professionals the chance to work on high-impact projects and contribute to the advancement of public health.
Job Role & Responsibilities
As an Associate in Regulatory Affairs (India Market), you will play a key role in ensuring compliance with India’s regulatory framework across pharmaceuticals, medical devices, cosmetics, and nutraceuticals. Your day-to-day tasks will include:
- Preparing and managing CDSCO regulatory submissions for New Drugs, Generics, Biosimilars, Medical Devices, Nutraceuticals, and Cosmetics.
- Drafting and reviewing dossiers for registration and import licenses.
- Handling product lifecycle management including amendments, renewals, and license updates.
- Coordinating with CDSCO/DCGI for query resolution, deficiency responses, and timely approvals.
- Submitting applications via the Sugam Portal and tracking approval timelines.
- Managing multiple licenses and certificates such as CT-06/07/11/13/14/15/17/19/20/22/23/24/25/27, COS-2/4, MD-15/5/9, Form 41, etc.
- Ensuring regulatory compliance with applicable laws, guidance, and standards for import and registration of drugs, medical devices, and diagnostics.
- Interacting with FSSAI and Legal Metrology departments for Nutraceutical product registrations.
- Maintaining up-to-date knowledge of CDSCO regulations, GMP, and QMS practices.
Eligibility / Qualifications
Educational Requirements:
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or a related discipline (B Pharm, M.Pharm, MSc. in Life Sciences).
Experience:
- Minimum 3+ years of experience in Regulatory Affairs, preferably within the Drugs, Cosmetics, Nutraceuticals, and Medical Devices sectors.
- Proven track record in handling CDSCO submissions and using the Sugam Portal.
Technical Skills:
- Comprehensive understanding of India-specific regulatory frameworks.
- Experience in dossier compilation, registration documentation, and product lifecycle management.
- Familiarity with GMP and QMS systems.
Soft Skills:
- Strong communication and interpersonal skills.
- Analytical and problem-solving abilities.
- Excellent time management and multitasking.
- Proactive, detail-oriented, and adaptable mindset.
Location & Salary
Location: Gurgaon, Haryana, India.
Employment Type: Full-time.
Salary: Competitive, as per industry standards and experience.
Application Process
Interested and qualified candidates can apply online through the official DDReg Pharma careers page:
👉 Apply Here
Apply soon to secure your position at one of India’s most respected regulatory consulting firms.
Why Join DDReg Pharma?
- Work with a global regulatory leader that collaborates with top pharma and biotech organizations.
- Gain exposure to multi-category submissions – Drugs, Devices, Nutraceuticals, and Cosmetics.
- Be part of a knowledge-driven team focused on continuous learning and innovation.
- Opportunity to work on diverse regulatory projects and shape India’s healthcare compliance landscape.
FAQs
Q1. What qualifications are required for this role?
A Bachelor’s or Master’s degree in Pharmacy or Life Sciences (B Pharm, M.Pharm, MSc.) with at least 3 years of regulatory experience.
Q2. Is experience with the Sugam Portal necessary?
Yes, candidates must be proficient in managing submissions and approvals through the Sugam Portal.
Q3. What kind of regulatory submissions will I handle?
You will work on submissions for Drugs, Medical Devices, Biosimilars, Nutraceuticals, and Cosmetics with CDSCO and related agencies.
Q4. What is the work location?
The position is based in Gurgaon, Haryana, with opportunities to collaborate with national and international clients.
Q5. How can I apply?
Visit the official link and submit your updated resume: Apply Now
Summary Table
| Company | DDReg Pharma |
| Vacancies | Associate – Regulatory Affairs (India Market) |
| Required Education | B Pharm, M.Pharm, MSc. (Life Sciences) |
| Experience | Minimum 3+ years in Regulatory Affairs (Drugs/Cosmetics/Nutraceuticals/Medical Devices) |
To apply for this job please visit resource.ddregpharma.com.
