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Regulatory Affairs Scientist – Nutritional Supplements
Company | Wellington Executive Search |
Address | Denver, CO, United States |
Employment type | FULL_TIME |
Salary | |
Category | Chemical Manufacturing,Wellness and Fitness Services,Pharmaceutical Manufacturing |
Expires | 2023-08-19 |
Posted at | 9 months ago |
Overview
Our client specializes in producing exceptional products and solutions for the dietary supplement, food, and beverage industries. We offer a complete vertical to bring a product to market:
- An in-house microbiological laboratory
- Sustainable farming relationships
- Manufacturing ability for a diverse range of products: liquids, capsules, pouches, and more
- An experienced formulation and applications team
- On-staff regulatory and claims experts
We are looking to hire a scientist who has at least 2 years of experience in in Regulatory Affairs, Quality Assurance, Compliance, Labelling, Documentation, and Regulatory Requirements to join our team.
The Job
The ideal candidate should have an understanding of SQF or other GFSI quality systems, food labelling regulatory requirements, Organic, Non-GMO Project Verified, and other identity preserved foods systems. Must be familiar with 21 CFR Compliance. Must be a self-starter, with a strong attention to detail, and organized.
Qualifications
- Can relocate to the Denver CO area or already live within commuting distance of the laboratory
- Bachelors degree in Chemistry, Nutrition, Biology, or other scientific discipline
- Experience with 21 CFR
- Good analytical problem-solving skills. Meticulous with follow-up
- 2 years minimum working in a Scientific role, in Regulatory or Quality in the nutritional space
- Good communication skills. Able to give clear directions to others.
- Prior experience working with documentation pertaining to nutritional supplements and ingredients
Essential Functions:
- Work closely with the operations team to modify, implement, and review all existing and new procedures in accordance with 21 CFR and company requirements.
- Develop, implement, and maintain regulatory standards for the company
- Must have the ability to identify and define problems, collect data, establish facts, and draw conclusions.
- Communicate to the Operations Manager, Director of Quality, or other Senior Management as appropriate any potential issue.
- Maintain all technical documentation and send to customers as needed
For the successful candidate we offer a competitive base salary, 401K, health / dental insurance, generous paid time off, and much more. Room for professional growth. Candidates must currently be living and working in the USA to be qualified for this job.
If you are interested and qualified please apply today!
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