Drug Regulatory Affairs – Xieon Life Sciences Pvt Ltd | Haryana
Company:
Xieon Life Sciences Pvt Ltd
Position:
Drug Regulatory Affairs Specialist
Qualifications Required:
- M.Pharm, B.Pharm, or Life Sciences degree
Experience:
- 1 to 2 years in Regulatory Affairs
Salary Package:
- ₹3.5 LPA – ₹4.6 LPA (₹3.8 LPA Average)
Location:
- Haryana, India
Job Overview
Xieon Life Sciences Pvt Ltd is hiring for the role of Drug Regulatory Affairs Specialist. If you have a background in pharmacy or life sciences and experience in regulatory compliance, this position offers a fantastic opportunity to grow in a company that prioritizes quality in pharmaceuticals, cosmetics, herbal products, and nutraceuticals.
Key Responsibilities
As a Drug Regulatory Affairs Specialist, your role will include:
- Regulatory Compliance:
Ensure that products comply with all relevant national and international regulations. - Dossier Preparation:
Prepare, review, and submit regulatory documents, dossiers, and reports as per compliance standards. - Documentation Management:
Maintain and update regulatory documentation, ensuring all records are accurate and complete. - Cross-functional Collaboration:
Work closely with manufacturing, research, and quality assurance teams to ensure compliance at all stages of product development. - Regulatory Submissions:
Assist in preparing submissions to regulatory authorities, including drug approvals and registrations. - Communication:
Liaise with internal teams and regulatory agencies to ensure timely approval of products and resolve any compliance issues.
Qualifications & Skills Required
To be successful in this role, candidates should meet the following criteria:
Qualification | Eligibility |
---|---|
Degree | M.Pharm, B.Pharm, or Life Sciences |
Experience | 1-2 Years in Regulatory Affairs |
Skills | Regulatory compliance, documentation, and strong communication skills |
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Skills to Succeed
- Attention to Detail:
Accuracy in dossier preparation and document management is crucial in this role. - Regulatory Knowledge:
Familiarity with pharmaceutical, cosmetic, or nutraceutical regulations is essential. - Communication Skills:
Strong verbal and written communication to liaise with various departments and regulatory authorities. - Team Collaboration:
Ability to work in cross-functional teams and contribute to projects that involve multiple departments.
Why Join Xieon Life Sciences?
Xieon Life Sciences is a leading player in the pharmaceutical, cosmetic, herbal, and nutraceutical sectors. The company is dedicated to producing high-quality products while maintaining strict compliance with regulatory standards. Working at Xieon Life Sciences means joining a team committed to innovation and excellence.
Key Benefits:
- Competitive salary package
- Exposure to global regulatory standards
- Professional growth opportunities in a supportive environment
- Access to cutting-edge research and product development
How to Apply
Interested candidates can apply by sending their CV to hr@xieon.com. Please ensure your email subject is “Drug Regulatory Affairs Application.” Tailor your resume to emphasize your regulatory experience, and include examples of dossier preparation and compliance work.