- Insmed Incorporated (NJ)
- …for the future of science, we're in. Are you?About the Role:We're looking for an Associate , Regulatory Operations on the Regulatory team to help us expand ... multiple projects with competing priorities.High technical aptitude for regulatory publishing and document management systems.Detail-oriented with strong focus on… more
- Insmed Incorporated (NJ)
- …expand what's possible for patients with serious diseases. Reporting to the Associate Director, Regulatory Affairs, Tactical Implementation, you'll have a ... and consistency Lead document workflows throughout document lifecycles for regulatory documents, including creation, review , approval, revision, distribution,… more
- Merck & Co. (Rahway, NJ)
- …our center of excellence.Description:-Under the direction of the GTD Director, the Associate Director will be responsible for developing multiple global brand ... accordance with health authority and governmental trademark office requirements. The Associate Director will manage individual projects within multiple … more
- Merck & Co. (Rahway, NJ)
- …promote best practices.Prepare materials for program presentations for management review and regulatory submissions, ensuring clarity and thoroughness.Contribute ... Job DescriptionThe Associate Principal Scientist, Device Risk Management Lead, is...Device Development team and with external partners.Understand and apply regulatory and compliance requirements relevant to device risk management… more
- Eisai, Inc (Nutley, NJ)
- …If this is your profile, we want to hear from you. The Associate Senior Counsel, Privacy, is a strategic, business-minded, and hands-on attorney role whose ... In expanding and managing Eisai's US Privacy Program, the responsibilities of the Associate Senior Counsel, Privacy, include, but are not limited to, practical and… more
- Insmed Incorporated (NJ)
- …the future of science, we're in. Are you?About the Role:The Associate Director, Programming provides technical leadership and ensures adequate programming support ... Collaborates with cross-functional team members within Biometrics, Clinical Operations, Regulatory , and Clinical Development, as well as with external vendors.… more
- Merck & Co. (Rahway, NJ)
- …milestones, and risks within our Company and with external suppliersAuthor and review relevant portions of the regulatory submissions (INDs, IMPDs, NDAs, ... DescriptionAssociate Principal Scientist - Device Technical and Engineering Lead ( Associate Director Equivalent) Our company's Device Product & Process Development… more
- Insmed Incorporated (NJ)
- …patches; review system releases and patches for impact across multiple systemsEnsure that System Administration and Maintenance SOPs are created/updated as ... requires a blend of technical expertise and business acumen to ensure regulatory compliance, system integrity, and alignment with business objectives across … more
- Merck & Co. (Montgomery County, PA)
- …of Record (AOR) on our creative campaign(s) and collaborating across multiple stakeholders (including sales, marketing operations, Legal, Regulatory , Medicals, ... in the Pipeline Advertisemen We are currently recruiting for several Associate Director positions within US Marketing, covering Physician (HCP), Consumer (HCC),… more
- Merck & Co. (North Wales, PA)
- …(nAMD), and retinal vein occlusion (RVO)).-We are currently recruiting for an Associate Director US Marketing, HCP Strategy - Ophthalmology. This is an exciting ... of Record (AOR) to develop creative campaigns and collaborate across multiple stakeholders including sales, marketing operations, Learning and Development, Legal, … more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …and complexity. The individual will be responsible for leveraging data from multiple sources to understand business complexities to develop the positioning and ... at Pricing Committee and Pre-PC for aligned accounts/channels and leads review of business case and financial impact scenarios. Ensures appropriate stakeholder… more
- Merck & Co. (Durham, NC)
- Job DescriptionThe Quality Associate Director/GMP Lead Site Auditor will have leadership responsibility for the site internal audit program, encompassing the full ... execution (audit pre-work, conducting audit, issuance of audit report, CAPA review and verification) meet established expectations. Perform, lead, and mentor other… more
- Cipla (Fall River, MA)
- …to the following : Works with Manufacturing/Packaging to deliver timely batch record review across all shifts. Reviews and approval of master batch records. Develops ... Creates training materials for subject matter input. Track and manage periodic review of approved procedures. Develop strategies and documents for cleaning and… more
- Cipla (Fall River, MA)
- …Creates training materials for subject matter input. Track and manage periodic review . Develop strategies and documents for cleaning and process validation of API ... equipment and products in compliance with site SOPs and regulatory guidance. Autonomously leads and manages projects to implement continuous improvement… more
- University of California Agriculture and Natural Resources (Yuba City, CA)
- …Posting Close Date: This job is open until filled. The first application review date will be 3/17/2025. Key Responsibilities: 0% Program Liaison and Coordination: ... diverse volunteer management system. Effectively resolve conflict. Provide oversight, review complaints, and follow 4-H Conflict Resolution Policy. Effectively and… more
- University of California Agriculture and Natural Resources (Davis, CA)
- …departments, and develop resources to assist California cottage foods operators with regulatory compliance and food safety best practices. This position will work ... Manager and will collaborate closely with the UC SAREP Associate Director for Sustainable Food Economies to integrate cottage...This job is open until filled. The first application review date will be 10/27/2025. Key Responsibilities: 60% Develop… more
- Cipla (Hauppauge, NY)
- …physically carrying ability of 100 kg (25 Kg x 4 No's) weights for multiple balances. Ensure the proper isolation of rejected material generated during batch process ... in the batch record. Monitor facility and product environmental operating conditions. Review of engineering records (temperature and humidity data calibration and PM… more
- GreenState Credit Union (North Liberty, IA)
- …are always available, always relevant, and always scalable. POSITION SUMMARY: The Associate Enterprise System Administrator will maintain the core platform to ensure ... custom work and writes reports as needed. Ensures departmental systems meet regulatory compliance and internal policies. Track and document changes as system… more
- Rock Springs (Georgetown, TX)
- …Provide support to the intake department as necessary. Maintain knowledge of regulatory standards (TJC, Medicaid, state and federal laws) and ensure compliance. ... In addition to your base compensation, this position also offers: Comprehensive Benefits: Multiple levels of medical, dental and vision coverage - with medical plans… more
- Fox Rothschild LLP (Dallas, TX)
- Corporate (Health Care Regulatory ) Associate - Multiple Offices **Atlanta, GA; Dallas, TX; Miami, FL; Sarasota, FL; West Palm Beach, FL** **Description:** ... their career development. Fox Rothschild has an opening in multiple offices for a Corporate Associate to...six years of corporate transactions, M&A, health law and regulatory experience. We are not currently accepting resumes from… more
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