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SourcePro Search is conducting a search for a highly motivated and hands-on 2nd and 3rd Shift Trade Support & Quality Assurance Analyst to join a Trading Operations Futures Team. Must have the capacity to thoroughly understand the Software Quality Assurance testing process and best practices.
$90,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Knowledge of key concepts including unit operations, processes, quality by design (QbD), tech transfer, process validation, quality attributes, and regulatory milestones across pharma development.
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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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ZS is looking for a Decision Analytics Consultant in the ZS Supply Chain and Manufacturing practice with an experience in pharmaceutical drug development and tech transfer. Hands on experience with at least one of the functions in CMC development such as Process Chemistry, Process Engineering, Formulation, and Analytical Chemistry.
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Provide recommendations on whether to invest in proactive mitigation plans and regularly present investment plan to senior leaders including CEO, CFO, EVP's in quality and R&D, and all supply chain ELT.
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Providing quality care as an RN in post-acute care facilities. Submit your application for an RN job and learn how you can achieve balance as an RN and join the team of nursing professionals ranked #1 in quality.
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At least three (3) years of experience and demonstrated leadership in Health Care Compliance, Regulatory Advertising & Promotion, Communications, Sales Learning & Development, Data Science, Data Analytics or Quality & Compliance area.
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We are a full-service, multi-doctor hospital that provides quality veterinary care for dogs, cats, and exotic pets. West Trenton is a great place to live and work, ideally located in Ewing Township which is right between Philadelphia and New York as well as close to Princeton, Point Pleasant, Asbury Park, and other Jersey Shore points.
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The Deputy General Counsel, Codman Specialty Surgical will report to the General Counsel, U.S. and will have primary responsibility for handling or managing a variety of general corporate and commercial contracting matters and will provide advisory services to CSS leaders, including the division president as well as sales, marketing, regulatory, quality, clinical and product development leaders.
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Your Responsibilities as an Appliance TechnicianAs an Appliance Repair Technician, you are the key component in providing excellent customer service by providing high-quality maintenance services for our customer's appliances.
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This position will report to Senior Director Safety Surveillance, U.S. East Coast Development Hub. Key internal stakeholders include Medical & Science, Clinical Operations, Regulatory Affairs, Data Management, Biostatistics, Non-clinical, Medical Affairs, Marketing, Legal, Quality, and other affiliates.
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Researches design options and documents findings for Project Designer/Engineer. Selects equipment based on recommendations of the Project Designer/Engineer and fills out equipment schedules.
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Take samples from raw materials and finished product for testing, while adhering to Quality Control requirements. You’ll be supported by your team with possibilities to grow into a Manufacturing Professional and directly impact the quality of our products – helping to improve real lives.
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With over 7,000 therapists in 28 states and growing, we provide quality rehabilitation services to homecare, sub-acute, long-term care, outpatient, hospital, and assisted living facilities throughout the nation.
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Ensures that appropriate CMC regulatory activities occur in support of both pre and post-approval submissions while meeting aggressive timelines and adhering to the highest quality standards. Collaborates with functional groups to plan, author, compile and submit high-quality original applications, amendments, supplements and responses to inquiries from FDA.ORGANIZATION STRUCTUREThe Director, Regulatory Affairs reports into the VP, Regulatory Affairs and is based in Pine Brook, New Jersey.
$180,000 a yearFull-timeExpandApply NowActive JobUpdated Today
qa quality jobs Title: engineer in Hopewell, NJ
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