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The Regulatory Affairs department is accountable for the direct management and guidance regarding the organization’s cGMP compliance and regulatory affairs for biologics, sterile injectables, cell and gene therapy, inhalation manufacturing and analytical services.
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Collaborate with cross-functional teams, including marketing, R&D, manufacturing, etc to ensure regulatory compliance and considerations throughout the product life cycle and across consumer touchpoints.
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Document Control – You will represent Regulatory Affairs as a standing member of the Change Control Board (CCB). Our future ambition is to become a leading consumer health technology company while continuing to develop solutions for serious health conditions.
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Wondercide, based in Austin, TX, is a privately held, high growth, and digitally native consumer packaged goods company that has an omni-channel presence and is expanding into specialty brick & mortar and beyond.
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Ensure effective execution for new innovative consumer-centric products and the life cycle management of products in the portfolio across the following regulatory classes (OTC monograph drugs, dietary supplements, cosmetics, foods, and medical devices.
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Successful agency advocacy results in policymakers that better understand the electric cooperative business model, the mitigation of any regulatory risk that drives up consumer-member costs without benefit, and the creation of workable new opportunities for electric cooperatives such as federal incentive programs that make sense for co-op communities and their consumer-members.
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Ranked No. 1 and widely recognized by US dermatologists and plastic surgeons for its clinical excellence and science-backed approach, Obagi remains a leader in the beauty space and operates as an innovative, global, omni-channel luxury consumer products business with sales distribution to physicians, wholesale partners, retail outlets, Amazon, and direct-to-consumer (DTC) channels.
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The Senior Manager, Regulatory Affairs will work closely with cross-functional leaders to develop and implement an effective and efficient regulatory strategy for domestic and international sales of skincare and cosmetic products through a deep understanding of the competitive market landscape, regulatory / legislative initiatives, and product marketing strategy.
$140,000 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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As our Regulatory Affairs Specialist, you will be joining our Health, Safety, Security, and Environment (HSSE) team and will be working closely with the Research and Development, Marketing, Operations and Sales groups.
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Founded in 1881, the Consumer Healthcare Products Association (CHPA) is the national trade association representing the leading manufacturers and marketers in the consumer healthcare industry with its core capabilities, including scientific and regulatory affairs, government affairs, and communications.
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Shell Energy and its affiliates is currently active in the western markets as a Power Generation Company (PGC), as a Retail Electric Provider (REP), as an Independent Power Marketer (IPM), as a Qualified Scheduling Entity (QSE) and as an end use consumer and participates extensively in market committees and groups towards helping strengthen market rules and competitiveness.
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To achieve its mission of improving people’s quality of life by acting responsibly towards society and the environment, the Group research, develops and markets innovative drugs in its three therapeutic areas: AIR (products and services that promote respiration, from new-born to adult populations), RARE (treatment for patients with rare and ultra-rare diseases) and CAR E (products and services that support special care and consumer-facing self-care.
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At least ten years of experience within Regulatory Affairs of which at least five in the global context. Knowledge of the drug development process, of drug regulations, regulatory procedures and drug development guidance.
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Liaise closely with colleagues (R&D, External Affairs, etc.) Coordinate and lead internal teams to develop Client responses and comments on draft legislation, regulations, guidelines and regulatory policies issues.
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Minimum of 8 years in Regulatory Affairs with experience in the consumer product (Rx/OTC, OTC Monograph, Nutritional, and/or Cosmetics) regulated environment. Responsible for the overall product strategy, reporting, administrative documentation, due diligence, market expansion, labeling content, regulatory compliance, regulatory intelligence and change management for consumer products (Rx/OTC, OTC Monograph, Nutritional, and Cosmetics.
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consumer job Title: regulatory affairs in Anoka, Minnesota
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