Regulatory Affairs Coordinator Salary in Louisiana

Job Title: Regulatory Affairs Coordinator/Regulatory Windchill Coordinator Location: 91342, Los Angeles, California, United States Duration: 06 Month Job Description: This position is a shared role providing business support to the Medical Device division and collaborating with the Supply Chain Group, Regulatory Affairs, Clinical, and Customer Service. Person will help in getting products to market through the use of SAP/PLM system to create shipping licenses, will conduct clean-up work and release products. Preferred or nice to have understanding of EUMDR (European Medical Device Regulations) for an understanding of compliance. Conducts Compliance checks, and works with Logistics partners and customers. Must feel comfortable with verbal and written communication as they will be communicating and working with others. Will be gathering data and executing such by conducting Data Analysis through the use of Excel pivot tables and vlookups - EXCEL IS A MUST HAVE. Will be pulling inventory

Regulatory Coordinator I Sewickley, PA 15143 6 Months Contract Job Description Candidate will review internal and external products and raw materials to evaluate hazards and assign transportation classifications and maintain regulatory compliance in this entry-level scientific, non-laboratory position. We are looking for a team player who is self-motivated, able to maintain high quality while handling repetitive tasks, and manage multiple projects. RESPONSIBILITIES Work as part of team that provides support to all SW business units Apply GHS and Transportation regulations to assess product hazards Use outside vendor SDS to assess transport hazards Use in-house computer systems to assign transport classifications Assist with overflow regulatory compliance projects as requested QUALIFICATIONS Bachelors degree in Chemistry, Biochemistry, Biology, or related science Familiarity with regulatory programs - DOT/Transport preferred Working knowledge of Safety Data Sheets (SDS) preferred Experi

Overview: Rocky Mountain Cancer Centers, Colorado's largest and most comprehensive provider of cancer care has an exciting opportunity for an experienced Regulatory Affairs Coordinator in Denver. We realize that it sounds clich but it is true - taking care of cancer patients is a calling. Its much more than a job. Each of us has a unique story that brought us to Rocky Mountain Cancer Centers (RMCC), but those stories usually share common themes of care, compassion, and commitment. No matter the role each RMCC team member serves in, the goal is the same: to provide the best care possible for each and every one of our patients. Whether we are a nurse holding our patients hand, or a scheduler on the phone finding an appointment that fits into a patients schedule, we are deeply connected to our patients and do what we can to help. If this sounds like you, wed love to have you join our team. Under minimal supervision is responsible for the research regulatory and administrative activities o

JOSIE MARAN REGULATORY AFFAIRS COORDINATOR WHO WE ARE Josie Maran is the pioneer of clean, Argan oil-powered beauty. The first to champion the natural potency of pure oils, we are now the leading innovator in clean beauty. Sourced from a UNESCO-protected region in Morocco, 100% Pure Argan Oil is the center of everything we dofrom our skin-transforming products to our collaboration with womens co-ops and Earth-first sustainability platform. Our cruelty-free formulations honor inclusivity from soil to seed to bottle and are safe and effective for every skin type and lifestyle. We believe in the vibrational energy of conscious skincare.It is a community-centered effort, with a responsibility to support the environment, nurture the self, and cultivate joyful human connection. We celebrate the radical courage behind bare skin, and the reverberating effects of nourishing yourself from the inside out. We are an equal opportunity employer. We value diversity and prohibit discrimination and har

Regulatory Affairs Expert-Medical Devices 1 Year (Temp to perm) St Louis, MO (Hybrid 2-3 days onsite) Pay: $33.00/hr Your Role: With minimal supervision, the Regulatory Affairs Expert-Medical Devices manages assigned regulatory tasks related to health authority notifications, submissions, and registrations regarding renewals and new products, and changes to products or sale of products ensuring continual compliance to all applicable regulations and ensuring that site regulatory strategy aligns with overall corporate regulatory strategy, goals, and objectives. Responsibilities Independently assemble and maintain technical files and other regulatory documentation to ensure timely registrations and renewals Maintain library/database of technical documentation Monitor the status of standards and regulations. Conduct a review and analysis in case if requested. Assist and advise in activities related to regulatory registrations, listing, and regulatory compliance, with particular focus on In

Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas immunology, oncology, neuroscience, and eye care and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description We're seeking a Quality Assurance Manager to ensure compliance and efficiency in our quality system for drug, biologics, device, and/or combination products. You'll lead cross-functional teams, design effective quality systems, and coordinate interrelated function activities. You'll support the introduction of new products, identify potential gaps, and oversee training programs. If you're a detail-oriented professional with a strong background in q