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Lief Labs is a premier formulation and product development innovator and manufacturer of dietary supplements. Previous experience in a packaging development or quality control role, preferably in the pharmaceutical or dietary supplements industry.
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Seeking a Vice President of Product Development, R&D, and Scientific Affairs for a direct hire opportunity in Valencia, CA. Our client is a premier formulation and product development innovator and manufacturer of dietary supplements and has formulated over 1,000 products for a multitude of dietary supplement categories.
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Your responsibilities include: Support the preparation of submissions (i.e. PMA, PMA supplements, CE marking applications, etc.) to obtain various worldwide approvals to commercially distribute products In conjunction with Clinical Research, support the preparation of applications (i.e., IDE, IDE supplements, Investigator Brochure) for conducting clinical investigations in U.S., Canada, Australia and EU countries.
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Partner programs: Access to discounts to your favorite lifestyle brands (Meal Prep, Supplements, etc) The Certified Personal Trainer will be responsible for providing one-on-one and couples personalized fitness instruction in person to clients at their home, apartment gym or outside while encouraging them to reach their fitness goals.
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Pharmavite is committed to meeting the needs of our employees and their families with a Total Rewards package that's as comprehensive as the vitamins and supplements we deliver to consumers. You'll have the opportunity to work on the #1 selling national vitamin and supplement brand, Nature Made, as well as an exciting portfolio of other products that are shaping the future of the healthy living industry.
$128,228 - $192,290 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Years of experience in formulation development within the pharmaceutical or dietary supplement industry. Support technology transfer activities, guiding product and process development efforts in coordination with Strategic Sourcing, Analytical Research Services, Quality Control, Quality Standards, and Plant Operations teams.
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Experience with either 510(k) applications, PMA supplements and US device regulations or with EU and other international medical device regulations and submissions. We are presently hiring for a Regulatory Affairs Specialist II at our Cardiac Rhythm Management (CRM) location in Sylmar, CA. As an individual contributor, this position performs specialized level work assignments and/or analyses, evaluation, preparation, and submission of documentation for the worldwide regulatory registration, ensuring products and procedures comply with regulatory agency specifications.
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