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We develop, manufacture and market a range of products, primarily in gastroenterology, hepatology, neurology, dermatology, medical aesthetic devices, international pharmaceuticals. To learn more please read Bausch Health's Job Offer Fraud Statement.
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We are seeking a highly motivated Vice President of Operations who will be responsible for the launch, ramp-up, and oversight of cGMP Operations within a state-of-the-art multi-product cell therapy manufacturing facility that will be utilized to manufacture autologous and allogeneic cell therapy products.
$300,000 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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The Team Lead for Authoring Support Group will be part of the Global Regulatory Operations group and will develop and manage the authoring support group within Regulatory Affairs (RA) to ensure timely and high-quality document delivery to the Regulatory Publishing Group.
$142,500 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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As an AbbVie Operations intern, you will participate in a paid, ten-to-twelve-week summer program working on meaningful assignments that have a real impact on our business and patients worldwide.
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Sunglass Hut is a part of Luxottica, N.A. Luxottica is a leader in the design, manufacture and distribution of fashion, luxury and sports eyewear. Sunglass Hut is a part of Luxottica, N.A. Luxottica is a leader in the design, manufacture and distribution of fashion, luxury and sports eyewear.
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He/she/they manages the writing of response to CMC questions from Health Authorities with support from Quality, Global Regulatory Affairs (GRA), technical experts or CMOs. He/she/they defines and manages the compilation of the documentation, required for the authoring by reaching out to appropriate internal/external functions such as quality, manufacturing, Global Regulatory Affairs (GRA), technical experts from global Client locations or contract manufacturing organizations (CMOs), or alliance partners.
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Statistical SAS Programmer Intern Statistical SAS Programmer in Bridgewater, NJ Office Or Waltham, MA Office : Provide statistical programming, data analysis, and data mapping to support clinical trials and FDA submission for new drug development.
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2+ years in Regulatory Affairs or Policy. Johnson and Johnson is currently seeking a Director, Regulatory Policy and Intelligence Research Coordinator located in Raritan, NJ, Titusville, NJ, or Spring House, PA. Remote work options in the United States may be considered on a case-by-case basis and if approved by the company.
$281,750 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Location: Whippany, New Jersey Type: Contract Job #80210 Our client, a leading financial services company is hiring an AVP Broker Dealer Regulatory on a long-term contract basis. Responsibilities: Contribute to the preparation and oversee aspects of various regulatory reporting requirements for the broker-dealer including SEC Rule 15c3-1, 15c3-3, and the required filing submissions.
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Regulatory affairs (RA) is a profession developed from the desire of governments to protect public health by controlling the safety and efficacy of products in areas including pharmaceuticals, medical devices and consumer products among others, and by the companies responsible for the discovery, testing, manufacture and marketing of these products wanting to ensure that they supply products that are safe and make a worthwhile contribution to public health and welfare.
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The successful candidate will perform duties that will assist the Economic Transformation Division /Product Operations Department in reviewing applica tion s to various Clean Energy programs , as well as to other Economic Transformation and Commission on Science, Innovation and Technology ( CSIT ) programs , as needed.
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Manager, Regulatory Affairs: Base Salary Range $90,000 - $120,000. Regulatory, Legal/Compliance, Medical, Marketing, Creative Agencies. Perform other regulatory tasks as assigned.
$120,000 a yearFull-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Kelly® Science & Clinical is seeking a Regulatory Affairs Associate for 1 year contract position (with possibility of extension) position at a premier client in Skillman, NJ. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.
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As a member of Chubb's Actuarial Team, you will help evaluate business opportunities in a given market by analyzing data to identify the potential profitability and possible pitfalls.
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On-Board Scientific is hiring a Regulatory Affairs Assistant! 5+ years of related pharmaceutical or biopharmaceutical industry experience with a previous regulatory submissions experience.
$35 an hourFull-timeExpandApply NowActive JobUpdated Today
manufacture job Title: regulatory affairs intern in Raritan, NJ
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