Regulatory Affairs Associate
$35 - $40 per hourObagi
Salary range: $35.00 - $40.00/hour Who We Are: Obagi Cosmeceuticals is an industry leading dermo-cosmetic brand that provides transformational skin care products, with a 35+ year legacy backed by science and innovation to protect and enhance skin tone and texture. Obagi is widely recognized by US dermatologists and plastic surgeons for its clinical excellence and science-backed approach, remaining 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. On a mission to create a global, best-in-class multi-brand, multicategory portfolio, Obagi will continue to redefine the future of skincare. We are Obagi. Fearless. Together. What We Need: Obagi is seeking a reliable and meticulous Regulatory Affairs Associate to help the Regulatory team ensure global compliance across its collection of skincare products. This individual will help organize, manage, and maintain files across our databases and platforms, along with ensuring that all files adhere to regulatory and compliance requirements across the jurisdictions where our operations extend. What You’ll Do: Reviewing ingredients for regulatory compliance for different markets and product categories. Partner with manufacturers and ingredient suppliers to acquire all necessary documentation to maintain an accurate library of robust products and raw materials. Prepare, compile, and organize all relevant documentation for product registrations and listings. Ensure renewals for state licenses. Maintain business systems, databases, and knowledge sharing systems as appropriate. Coordinate FDA Drug Listing submissions for Rx and OTC products under supervision from Regulatory Leadership Ensure appropriate follow-up correspondence, such as re-submissions, re-certifications, renewals as required. Other duties as assigned by the Supervisor. What You’ll Need: A bachelor’s degree from an accredited university is required. A focus in Life Sciences or Chemistry is highly preferred. At least 3-4+ years of relevant experience within regulatory affairs; familiarity with regulatory frameworks across various jurisdictions and a keen ability to accurately interpret and apply them real time. Exceptional organizational and prioritization/time management skills; demonstrated ability to work under pressure to meet deadlines. Comfortable operating in a fast paced, ever-changing environment; someone who thrives in ambiguity and adapts quickly. Proficiency in Microsoft Office and other technologies. An energetic, positive attitude that encourages a team and supports the growth and professional development of others. Physical Requirements: These demands document the physical requirements of a specific job. Criteria may include: Lifting, Carrying, Push/Pull, Sitting/Standing (In Place); On Feet, Walking, Bending, Turn/Twist; Kneeling; Squatting; Crawling; Climbing; Reaching (Out)/Reaching (Up), Grasping, Wrist Turning; Pinching; Finger Manipulation, Hearing, Talking, Working with a computer for eight hours, Working in close quarters. Communicating over the telephone for eight hours. #J-18808-Ljbffr Obagi
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## Sr. Regulatory Affairs Specialist, Medical Devices (Long Beach, CA)Bewerbenlocations: USA, California - Long Beachtime type: Full timeposted on: Vor 7 Tagen ausgeschriebenjob requisition id: JR101558**Wir über uns**Hydrafacial is a global category-creating company focused...Temporary workLocal area- ...Hydrafacial is seeking a Senior Regulatory Affairs Specialist for Medical Devices to lead regulatory planning and submissions across the product lifecycle, supporting new launches and ongoing compliance in the U.S. and international markets. You will draft technical documentation...
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...Compliance, this leader will stand up and scale the control environment that lets these businesses grow quickly without taking on undue regulatory, financial, or reputational risk. This is a builder role. The successful candidate will design the compliance management system...Odd jobFull timeRemote workWorldwideFlexible hoursShift work- ...excellence Mentor and develop nursing leaders and frontline teams Ensure compliance with the Joint Commission (TJC), CMS, and state regulatory standards Oversee staffing models, budgets, and workforce planning Collaborate closely with physicians and interdisciplinary...Local areaRelocation package
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$26 - $32 per hour
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FNS, Inc. seeks a Customs Entry Writer in Carson, CA, responsible for processing customs clearances and ensuring compliance with regulations. The role involves developing documentation, tracking shipments, and communicating with clients. Preferred qualifications include...Work at office$130k - $150k
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The future you want is within reach. Let’s build it together. At PCL Construction, Inc., part of the PCL Family of Companies (PCL), we don’t just build projects—we build opportunities, careers and communities. We are 100% employee-owned, every employee has a stake in...Contract workWork at office- ...Ongoing governance and oversight of covered business areas, and works closely with the business units to ensure full compliance with regulatory requirements Assessing, developing and providing compliance training on relevant topics Identifying training requirements needed...Contract workWork experience placementBank staffImmediate startRemote workFlexible hours
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