Quality Assurance Specialist

Nordic Naturals has been revolutionizing omega-3s since 1995, pioneering a new definition of fish oil as it relates to purity, freshness, taste, and dosage. Headquartered in Watsonville, CA, the company has expanded beyond solely omega-3s and offers complementary, foundational nutrients essential to health. Our portfolio, which is distributed to over 35 countries, includes more than 200 products in a variety of flavors and formulations for adults, kids, athletes, and pets. Family owned, Nordic Naturals works passionately to see generations of healthier, happier people around the world.

Nordic Naturals offers a great work environment, support for a healthy lifestyle, and an opportunity to be part of a company that?s making a positive difference. We are committed to the shared goal of promoting health and wellness by delivering the world?s safest, most effective omega oils. We see a growing worldwide market and need a great team of people to enable our company to continue to fulfill its mission.

The Quality Assurance Specialist will work across departments and with consultants to manage and assist the development, compliance and release of QA regulated product documentation such as product labels and boxes.

In this role you will:

• Coordinate creation, review and approval of Label Specifications including supplement facts panels, ingredient/allergen statements and required warnings/disclosures; initiate documents and gain approvals from Product Development and Quality Assurance.
• Ensure that product labels and boxes for accurate, complaint to current regulations and for format consistency in a timely manner.
• Uphold a strong familiarity with all current supplement labeling regulations and best practices to assure compliance.
• Review raw material documentation for specifications and compliance.
• Coordinate and track third party and internal laboratory testing.
• Coordinate testing Investigations (OOS) and Resolutions. Inform vendors; collaborate with laboratories, third parties, and suppliers to facilitate a resolution.
• Perform internal documentation audits, providing feedback and training when necessary.
• Perform product inspections according to Standard Operating Procedures.
• Prepare revisions to Standard Operating Procedures, attachments and forms.
• Ensuring printed material archives are well maintained.
• Organize and file paperwork.
• Provide support in ensuring cGMP compliance.
• Assist with product research and development.

Qualifications

• Education: Bachelor degree preferred.
• Experience: 3-10 Years in a document control position. Experience with Dietary Supplement Health and Education Act (DSHEA), Non-GMO Project certification, familiar with cGMP regulations for dietary supplements, food or pharmaceutical, change control management and associated systems.
• Computer Skills: Proficient in Office- Word, Excel, familiar with FileMaker or similar database software. Ability to navigate and interact with online certification systems

If you are qualified and interested in this job opportunity, please submit a cover letter and resume to nordichr@nordicnaturals.com for consideration.

Nordic Naturals is an equal opportunity employer. A pre-employment drug screening and background check are part of the hiring process.

Download a printable PDF application.