• Regulatory Labeling Associate

    Integra LifeSciences (Princeton, NJ)
    …treatment pathways to advance patient outcomes and set new standards of care. The Labeling Associate - Design is responsible for creating, reviewing, ... perform each essential duty satisfactorily. + Assist in the design , development, and approval of product labeling ,...teams on all project execution + Assist the Senior Labeling Associate in integrating and implementing Integra's… more
    Integra LifeSciences (12/10/24)
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  • Associate Food Labeling Specialist

    Conagra (Omaha, NE)
    We are looking for an ** Associate Food Labeling Specialist** to join our R&D/Science & Regulatory Affairs team in Omaha, Nebraska. This is a great ... opportunity to begin or expand your career in Food Labeling . As an ** Associate Food Labeling...update, and approve label designs for Marketing and Brand Design . You will develop mandatory labeling information… more
    Conagra (12/06/24)
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  • Labeling Lead

    MicroVention, Inc. (Aliso Viejo, CA)
    labeling changes comply with company policies and procedures. + Collaborate with Labeling Design team to ensure labeling requests are completed ... Regulatory Affairs, and Legal. Job duties: + Support labeling activities for multiple projects from initiation to product...on pending and approved labels. 3. Ability to present labeling design and implementation strategies and obtain… more
    MicroVention, Inc. (11/24/24)
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  • Regulatory Associate I…

    LSI Solutions (Victor, NY)
    …with state-of-the-art devices. After all, our ultimate customer is the patient. POSITION TITLE: Regulatory Associate - Days 8am to 5pm SALARY RANGE: $85,000 - ... $95,000 JOB SUMMARY: The Regulatory Associate applies her/his experience, knowledge, organization...III - Labeling Area: + Accurately complete regulatory labeling checklist reviews for labeling more
    LSI Solutions (12/21/24)
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  • Associate Director Regulatory

    Ascendis Pharma (Princeton, NJ)
    …committed to working together as one team to achieve extraordinary results. The Associate Director Regulatory Affairs, Advertising and Promotion will be an ... the promotion of prescription drug and biologic products. The Associate Director Regulatory Affairs, Advertising and Promotion... impact of new campaign concepts, target, or product labeling , and to provide strategic regulatory guidance… more
    Ascendis Pharma (12/10/24)
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  • Regulatory Associate - Days - 8:00am…

    LSI Solutions (Victor, NY)
    …state-of-the-art devices. After all, our ultimate customer is the patient. POSITION TITLE: Regulatory Associate I, II SALARY RANGE: $85,000 - $104,000 POSITION ... in Victor, NY POSITION AT-A-GLANCE: Primary responsibilities of the clinically-focused Regulatory Associate will be collecting and collating relevant clinical… more
    LSI Solutions (11/01/24)
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  • Associate Director, Regulatory

    Bristol Myers Squibb (Princeton, NJ)
    …. **Position Responsibilities** + Leadership responsibility for global regulatory strategy to support the development of biomarkers, companion ... pharmaceutical products across therapeutic areas + Responsible for understanding the regulatory landscape, assessing regulatory risk, and developing global… more
    Bristol Myers Squibb (12/25/24)
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  • Associate Director, Patient Experience Data…

    AbbVie (Mettawa, IL)
    …HEOR Strategy and other functions (eg, Clinical Development & Operations, Regulatory , Commercial). The Associate Director, Patient-Centered Outcomes Research, ... consortiums, key opinion leaders, research organizations, patient advocacy groups). The Associate Director represents HEOR at global regulatory and payer… more
    AbbVie (10/30/24)
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  • Associate Medical Director, Clinical…

    Takeda Pharmaceuticals (Cambridge, MA)
    …will inspire you and empower you to shine? Join us as an Associate Medical Director, Clinical Science in our Gastrointestinal & Inflammation Therapeutic Area Unit-- ... vital contributor to our inspiring, bold mission ​ **​POSITION OBJECTIVES:** ​The Associate Medical Director leads and drives strategy for the overall global… more
    Takeda Pharmaceuticals (11/08/24)
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  • Associate Medical Director, Clinical…

    Takeda Pharmaceuticals (Cambridge, MA)
    …that will inspire you and empower you to shine? Join us as an Associate Medical Director Neurodegenerative Disorders in our Neuroscience Therapeutic Area Unit in our ... vital contributor to our inspiring, bold mission. ​ **​POSITION OBJECTIVES:** ​The Associate Medical Director leads and drives strategy for clinical studies focused… more
    Takeda Pharmaceuticals (12/25/24)
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  • Associate Director, WW Medical…

    Bristol Myers Squibb (Princeton, NJ)
    …their personal lives. Read more: careers.bms.com/working-with-us . **Position: Associate Director, WW Medical Neuropsychiatry Strategy, Schizophrenia** **Location: ... Princeton Pike or Madison, NJ** The Associate Director of Medical Strategy, Schizophrenia will partner with key medical team to support development, implement, and… more
    Bristol Myers Squibb (12/25/24)
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  • Associate Director - QA Packaging

    Lilly (Durham, NC)
    …who are determined to make life better for people around the world. Associate Director - Quality Assurance (QA) Packaging is responsible for the staffing, training, ... and Packaging (DAP) production area at Lilly RTP. The Associate Director will help build a strong quality culture...and ensure compliance with area procedures and controls for labeling and packaging operations + Foster a strong quality… more
    Lilly (12/24/24)
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  • Instrument Documentation Writer

    Grifols Shared Services North America, Inc (San Diego, CA)
    …European Union (EU Medical Device Regulation). + Deliver supporting documentation to the labeling product, including labeling design plans, trace documents, ... for documentation and software development. + Ensure compliance of labeling with all applicable regulatory /QSR requirements. +...an equivalency could include 8 years of experience, an Associate 's degree with 6 years of experience, or a… more
    Grifols Shared Services North America, Inc (11/26/24)
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  • QO Manager Compliance/TL

    Pfizer (Rochester, MI)
    …Integrity Program + Medical Device and Combination product program - conduct regulatory assessments, create/maintain design history file, participate and develop ... standards, policies and procedures are aligned with global Pfizer Quality Standards, regulatory agency's guidance's and are operating in a state of compliance.… more
    Pfizer (12/22/24)
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  • OncoImmuno Cross Functional Area Intern

    J&J Family of Companies (Spring House, PA)
    …strategy, study design and protocols for clinical trials that support regulatory submissions and product labeling + Engage in clinical trial execution ... + Work effectively with team members to optimize study design , dose selection and dosage regimens in accordance with...in data management to enable system level software designs Regulatory Affairs Associate : + Conducting a research… more
    J&J Family of Companies (11/23/24)
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  • Senior Engineer, Quality Operations

    Catalent Pharma Solutions (Philadelphia, PA)
    …for Clinical Supply Packaging. Catalent offers GMP secondary packaging and clinical labeling services throughout our global network. Packaging can be configured to ... depending upon your project needs. Using our Clinicopia global labeling system with its multi-lingual label phrase library we...system with its multi-lingual label phrase library we can design single panel, booklet labels or our unique Peel-ID… more
    Catalent Pharma Solutions (12/03/24)
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  • Lab Section Head - $10,000 sign on bonus

    Munson Healthcare (Manistee, MI)
    …discussedwith the manager.2. Ensures compliance with section standards for regulatory and accreditingagencies.3. Drafts, reviews, tests, develops, and implements new ... requests (when necessary) and checks specimen for propercollection and labeling .5. Processes specimen into desired testing form; centrifuges blood, preparesslides,… more
    Munson Healthcare (10/24/24)
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  • Quality Assurance Manager

    Catalent Pharma Solutions (Philadelphia, PA)
    …for Clinical Supply Packaging. Catalent offers GMP secondary packaging and clinical labeling services throughout our global network. Packaging can be configured to ... depending upon your project needs. Using our Clinicopia global labeling system with its multi-lingual label phrase library we...system with its multi-lingual label phrase library we can design single panel, booklet labels or our unique Peel-ID… more
    Catalent Pharma Solutions (12/03/24)
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  • Quality Inspector II

    Integra LifeSciences (Plainsboro, NJ)
    …in ensuring that products meet the required safety, performance, and regulatory standards before they reach the market. Their responsibilities typically include: ... visual, mechanical, and sometimes functional tests to ensure products meet regulatory requirements (such as FDA or ISO standards). Documentation and Reporting:… more
    Integra LifeSciences (12/14/24)
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  • Software Engineer

    Rapid Cycle Solutions (Reston, VA)
    …have unique strengths in complex, cross-organizational solution analysis, design , development, implementation, and change management supporting enterprise ... of the software engineering life cycle including scope and work estimation, design , documentation, implementation, testing and integration. + Design and develop… more
    Rapid Cycle Solutions (11/08/24)
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