
Senior Regulatory Affairs Specialist
3 days ago
Job Title: Senior Regulatory Affairs Specialist
OverviewKamet Consulting Group is a leading management consulting firm serving the life sciences industry. We are currently seeking an experienced Senior Regulatory Affairs Specialist to join our team.
Key Responsibilities- Monitor and analyze regulatory changes, trends, and developments in the pharmaceutical and medical device industries.
- Conduct research and provide insights on regulatory requirements, guidelines, and policies issued by regulatory authorities.
- Evaluate the potential impact of regulatory changes on product development, manufacturing, distribution, labeling, and marketing practices.
- Collaborate with cross-functional teams to ensure compliance with applicable regulations and requirements governing pharmaceutical and medical device products.
- Identify and assess regulatory risks and vulnerabilities related to product development, manufacturing processes, and post-market surveillance.
- Bachelor's degree in Pharmacy, Life Sciences, or a related field; advanced degree or professional certification preferred.
- Minimum 4-6 years of experience in regulatory affairs, compliance, or a related role within the pharmaceutical or medical device industry.
- Proven track record of staying up-to-date on regulatory changes and developments.
- Strong understanding of regulatory frameworks, laws, and compliance requirements governing pharmaceuticals and medical devices.
- Competitive salary and benefits package.
- Opportunity to work on groundbreaking projects with top organizations.
- Professional development and growth opportunities.
- Hybrid work options.
We thank all applicants for their interest; however, only those selected for an interview will be contacted.
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