Regulatory Affairs Associate - Valencia, United States - 6 Degrees Collective
2 days ago
Description
Job Overview:
We are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to join our team. As a Regulatory Affairs Specialist, you will play a crucial role in ensuring compliance with FDA regulations and guidelines. You will be responsible for managing regulatory submissions, conducting research, and providing support for various regulatory activities.
Pay is based on experience. Willing to train the right team member
Responsibilities:
- Conduct research to stay updated on FDA regulations, guidelines, and industry best practices
- Prepare and submit regulatory documents like product registrations, and annual reports
- Assist in the development and implementation of quality assurance processes and procedures
- Participate in project management activities related to regulatory affairs, including timelines, milestones, and deliverables
- Provide guidance on compliance management activities, including labeling requirements and adverse event reporting
Skills:
- Proficiency in conducting research and analyzing scientific data
- Experience in quality assurance processes within a regulated industry
- Understanding oregulatory submissions
- Excellent project management skills with the ability to prioritize tasks and meet deadlines
- Strong attention to detail and accuracy in documentation
- Effective communication skills to collaborate with crossfunctional teams
Pay:
$ $26.00 per hour
Experience level:
- 1 year
- 2 years
- 3 years
- No experience needed
- Under 1 year
Schedule:
- 8 hour shift
- Day shift
- Monday to Friday
Ability to Commute:
- Valencia, CA required)
Work Location:
In person
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