R&D Technical Services

MAC Incorporated

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R&D Technical Services Long Beach, California
Job Ref:
37883

$24/hr – $26/hr – Monday to Friday, Saturdays as needed. 6:30 am to 3:30 pm or to be determined (1 hour lunch)

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*This is more of an entry level role, someone who’s out of college in the last 2 years, working with documentation all of the time, won’t be working in the lab though, ingredient labels, SQF documentation, looking for a couple years of experience.

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nJob Summary:

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This position is responsible for maintaining existing formulas and assisting in developing new products, including ensuring compliance with government regulations which address food safety, label claims for dietary supplements, and customer requirements. 

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Responsibilities

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  • Develops and publishes Material Requirement Plans (MRPs) associated with Pos received, reviews and updates existing formulas as needed and communicates ingredient ordering requirements to the purchasing department.
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  • Develops and publishes QC Release (QCR) forms and master manufacturing batch records for production.
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  • Develops finished product specification sheets that meet customer and dietary supplemental requirements.
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  • Performs documentation project tasks including requesting current documents for raw materials and reviewing for label claim requirements.
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  • Assists in sourcing and qualifying raw materials within the firm's Approved Supplier Program.
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  • Performs sensory, organoleptic, short- and long-term shelf-life testing on the items. Use third party laboratories for validation as necessary.
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  • Research and studies different ingredients and their functionalities to assist formulators in developing new product and planning of laboratory trials.
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  • Reviews labels and packaging against current FDA regulations and checks documentation to support label claims.
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  • Formulate new products
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  • Attends yearly tradeshows including SSW, IFT and Expo West (When shows reopen)
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  • Creates, develops, and publishes compliant Nutrition Facts Panels.  Includes domestic compliance with 21 CFR Parts 100 to 169, & Part 111 referring to the cGMPs for Dietary Supplements, NLEA, & DSHEA.
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  • Develops new items designed for commercialization.
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  • Attends yearly tradeshows including SSW, IFT and Expo West.
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  • Other duties as assigned
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Qualifications (Minimum education requirements, training or experience)

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  • BS Degree in Food Science, Engineering, Chemistry, or related fields
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  • Minimum 1-2 year’s work experience in related fields
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  • Experience working with Genesis Program, a plus
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  • Proficient with Microsoft Office Suite (Outlook, Excel, Word)
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  • Strong analytical and problem-solving skills
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  • Excellent verbal and written communication abilities
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  • Bi-lingual in English and Spanish, a plus
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Reporting Structure

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  • Direct Report – R&D Manager
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