Regulatory eXVMPD Coordinator Job at Kenvue Apply Online
Are you an experienced regulatory professional looking for a challenging role in a global consumer healthcare company? Kenvue, a renowned name in the healthcare industry, is currently hiring for the position of Regulatory eXVMPD Coordinator in Mumbai. This opportunity offers a dynamic work environment and the chance to contribute to data compliance activities at a global level. Regulatory eXVMPD Coordinator Job
If you hold a background in Pharmacy, Life Sciences, or a related technical field, and have experience in regulatory operations, this position could be the perfect step forward in your career.
About Kenvue
Kenvue is a global leader in consumer health with a heritage that spans over a century. It is home to iconic brands such as NEUTROGENA®, LISTERINE®, TYLENOL®, AVEENO®, BAND-AID®, and JOHNSON’S®, all trusted by millions worldwide. Regulatory eXVMPD Coordinator Job
With a global workforce of over 22,000 professionals, Kenvue focuses on delivering innovative, science-backed solutions to improve everyday health. The organization fosters a culture built on trust, empathy, scientific excellence, and diversity, ensuring both employee growth and customer satisfaction.
Job Overview – Regulatory eXVMPD Coordinator
Position: Regulatory eXVMPD Coordinator
Location: Mumbai
Experience Required: 1–3 Years
Qualification: B.Pharm, M.Pharm, MSc, M.Tech
Job Type: Full-time
Application Mode: Online
Posted On: June 11, 2025
Industry: Consumer Health / Regulatory Affairs
Kenvue is looking for a skilled regulatory coordinator who will support data management and ensure compliance with European regulations, especially Article 57(2) of the EMA regarding the Extended EudraVigilance Medicinal Product Dictionary (xEVMPD). Regulatory eXVMPD Coordinator Job
Key Responsibilities
As a Regulatory eXVMPD Coordinator, your core duties will include: Regulatory eXVMPD Coordinator Job
- Data Management Support: Provide tactical and strategic support for the implementation and maintenance of IDMP and ISO SPOR programs.
- Regulatory Data Entry: Create, validate, and update medicinal product data in compliance with EMA’s Article 57(2) regulations.
- Process Documentation: Develop and maintain standard operating procedures and regulatory data management documentation.
- Audit Readiness: Support internal audits and Health Authority inspections by ensuring data accuracy and documentation compliance.
- Issue Resolution: Identify and address data discrepancies that could impact regulatory compliance or delay submissions.
- System Compliance: Ensure alignment with Good Manufacturing Practices (GMP), system validation principles, and electronic record requirements.
- Cross-functional Collaboration: Work closely with internal stakeholders, regulatory teams, and external vendors to execute projects efficiently.
- Continuous Improvement: Contribute to enhancements in operational processes and data quality through regular reviews and training initiatives.
Required Qualifications
To qualify for this role, candidates must have:
- A Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Biotechnology, M.Tech, or related disciplines.
- 1 to 3 years of experience in regulatory affairs, preferably with xEVMPD data submission exposure.
- Solid understanding of European medicinal product regulations, including EMA’s Article 57(2).
- Familiarity with GMP, electronic system validation, and compliance documentation.
- Hands-on experience with Microsoft Office tools, especially Excel, Word, and PowerPoint.
Desired Skills
- Strong communication skills in English (both written and verbal).
- Analytical thinking and strong problem-solving abilities.
- Ability to work under pressure and meet tight deadlines in a fast-paced environment.
- Prior experience working in matrixed, multicultural organizations is a plus.
- Knowledge of regulatory systems and global databases will be an added advantage.
Why Join Kenvue?
Kenvue is more than just a workplace—it’s a global community of professionals dedicated to advancing health for humanity. Here’s what makes working at Kenvue a rewarding experience: Regulatory eXVMPD Coordinator Job
- Competitive Salary and industry-leading employee benefits.
- Paid time off, including holidays, vacation days, and community volunteering days.
- Access to learning & development programs designed to enhance your professional growth.
- Active Employee Resource Groups (ERGs) promoting diversity, equity, and inclusion.
- Opportunity to work on projects related to globally recognized healthcare brands.
How to Apply
Interested candidates can apply online via the official Kenvue Careers Portal or through verified pharma job platforms like Pharmabharat. Make sure your CV is updated with relevant experience in regulatory affairs, especially xEVMPD compliance, and clearly highlights your technical skills and regulatory knowledge.
Additional Opportunities for Freshers
If you’re a fresher looking to begin your career in regulatory affairs or R&D, SERIGEN is currently offering internships in Regulatory Affairs, R&D, Market Research, and Digital Marketing. It’s a great opportunity to build foundational knowledge and gain practical experience in the pharmaceutical industry. Regulatory eXVMPD Coordinator Job
Final Thoughts
The Regulatory eXVMPD Coordinator position at Kenvue Mumbai is an excellent opportunity for early to mid-career professionals in regulatory affairs to expand their expertise in European compliance and data governance. With Kenvue’s strong brand presence and culture of innovation, you’ll not only grow your career but also contribute to advancing global health standards. Regulatory eXVMPD Coordinator Job
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