Dietary Supplement Factory- Regulatory Affairs Specialist Dietary Supplement Factory- Regulatory Aff

Dietary Supplement Factory

• Regulatory Affairs Specialist Dietary Supplement Factory
• Regulatory Aff AMF Pharma LLC Ontario, CA Job Details Full-time $22
• $26 a year 1 hour ago Benefits Health insurance Qualifications Teamwork GMP Attention to detail Chemistry, manufacturing & controls Training & development Full Job Description Company Overview AMF Pharma LLC is a fully licensed contract manufacturer specializing in dietary supplements, committed to product excellence and promoting good health.

Our mission is to serve our clients with integrity, knowledge, and value by providing superior quality products under strict compliance standards at competitive prices. Job Overview We are seeking a dedicated and detail-oriented Regulatory Affairs Specialist to oversee compliance and regulatory processes within our dietary supplement manufacturing facility. The ideal candidate will possess a strong understanding of FDA regulations, quality assurance, and research practices related to dietary supplements. This role offers an exciting opportunity to ensure our products meet all regulatory requirements while supporting the company's growth and commitment to quality. Duties Ensure all dietary supplement products comply with FDA regulations, including labeling, ingredient safety, and manufacturing practices. Prepare and submit necessary documentation for regulatory approvals, notifications, and registrations related to dietary supplements. Monitor changes in regulations and industry standards to maintain ongoing compliance across all manufacturing processes. Collaborate with research and development teams to review product formulations for regulatory adherence and safety. Manage documentation related to clinical trials, stability testing, and quality assurance activities. Conduct internal audits to verify compliance with cGMP (current Good Manufacturing Practices) and other regulatory standards. Provide training to staff on regulatory requirements, compliance procedures, and quality assurance protocols. Skills In-depth knowledge of FDA regulations governing dietary supplements, including labeling, manufacturing, and marketing standards. Strong understanding of chemistry, manufacturing & controls (CMC), clinical trials, and quality assurance processes. Proven experience in compliance management within the dietary supplement or pharmaceutical industry. Excellent project management skills with the ability to coordinate multiple tasks efficiently. Research-oriented mindset with the capability to interpret complex regulatory documents and guidelines. Effective communication skills for cross-departmental collaboration and training purposes. Familiarity with industry standards such as cGMP is highly desirable. Join our team as a Regulatory Affairs Specialist and play a vital role in ensuring that our dietary supplements meet the highest standards of safety, efficacy, and compliance—contributing directly to the health and well-being of consumers worldwide!

Pay:

$22.00

• $26.

00 per year

Benefits:

Health insurance

Work Location:

In person