Regulatory Specialist

4 weeks ago


Santa Monica, United States alphapro technology, a.p.r., inc. Full time

Overview:
**Duties**:

- Develop and implement regulatory strategies for product approvals and compliance
- Ensure adherence to FDA regulations and guidelines
- Coordinate and support regulatory submissions for new products or changes to existing products
- Conduct regulatory research and stay current on industry regulations
- Collaborate with cross-functional teams to ensure regulatory requirements are met
- Assist in the preparation of documentation for regulatory authorities
- Participate in audits and inspections as needed

**Requirements**:

- Bachelor's degree in a related field; advanced degree preferred
- Proven experience in regulatory affairs within the pharmaceutical or healthcare industry
- Strong knowledge of FDA regulations and guidelines
- Ability to manage multiple projects simultaneously
- Excellent communication and organizational skills
- Detail-oriented with strong analytical skills
- Certification in Regulatory Affairs is a plus

Join our team as a Regulatory Specialist and contribute to ensuring compliance with regulatory standards while supporting the development of innovative products.

**Job Types**: Contract, Temporary

Pay: $42.68 - $54.00 per hour

**Experience**:

- FDA regulations: 1 year (preferred)
- commercial/central IRB: 3 years (preferred)
- authority logging: 2 years (preferred)
- field of clinic research: 4 years (preferred)
- Regulatory Specialist: 3 years (preferred)

Work Location: On the road


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