- Merck & Co. (Rahway, NJ)
- …years of labeling experience or relevant experience in the pharmaceutical industry (eg, Medical Affairs, Regulatory Affairs, Clinical, Pharmacovigilance).- - ... expertise and guidance to teams while ensuring compliance with applicable regulatory requirements- Serving as regulatory labeling point of contact on global … more
- Merck (Rahway, NJ)
- …years of labeling experience or relevant experience in the pharmaceutical industry (eg, Medical Affairs, Regulatory Affairs, Clinical, Pharmacovigilance). ... ensuring compliance with applicable regulatory requirements + Serving as regulatory labeling point of contact on global Regulatory Affairs sub-teams to… more
- MicroVention, Inc. (Aliso Viejo, CA)
- **11890BR** **Title:** Sr Specialist , Labeling Design **Job Description:** Design, develop, and update global labeling documents to include product labels, ... optimized label templates and identify issues associated with design. + Ensure labeling compliance with quality management system (QMS), regulatory requirements… more
- AbbVie (Irvine, CA)
- …both internal and external to AbbVie. + Scope of label changes includes Regulatory Affairs for labeling submissions, AbbVie manufacturing sites, third party ... for guidance). + Minimum of 2 - 4 years combined experience from totals: Quality/ Regulatory - 2 years, Operations - 2 years, Pharmaceutical /Device Regulations - 2… more
- Mallinckrodt Pharmaceuticals (St. Louis, MO)
- Job Title Senior Regulatory Affairs Product Specialist Requisition JR000013781 Senior Regulatory Affairs Product Specialist (Open) Location Webster ... (Pharma) - USA038 Additional Locations St. Louis, MO Job Description The Senior Regulatory Affairs Product Specialist (RAPS) is responsible for developing and… more
- Bausch + Lomb (Bridgewater, NJ)
- …products. **Key Activities/Responsibilities:** + Provide support for the execution of the pharmaceutical regulatory strategy for assigned products. + Support ... health in the future. **Objectives/Purpose of Job:** + The Regulatory Affairs Senior Specialist handles US ...development team for agency filing. + Work with the Pharmaceutical Regulatory Management to make certain all… more
- Abbott (Temecula, CA)
- …to work for diversity, working mothers, female executives, and scientists. This ** Regulatory Affairs Operations Specialist ** will work on-site at our Temecula, ... ethical standards. **Preferred** **Qualifications** + 4+ years of related regulatory submission experience from medical device, pharmaceutical , or healthcare… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- **Job Description Summary** The Staff Regulatory Affairs Specialist will work in BD Medical - Pharmaceutical Systems Business Unit taking on a lead role at ... and/or approves product marketing claims and communication, Advertising/promotional materials, and labeling + Conduct trainings on regulatory issues for staff… more
- ThermoFisher Scientific (Asheville, NC)
- …need to take science a step beyond. **Discover Impactful Work:** The Regulatory Specialist is responsible for product compliance, design consultation, testing, ... impact of product changes in markets. + Recommends changes for design, labeling , manufacturing, and marketing for regulatory compliance. + Reviews, approves,… more
- Abbott (Plymouth, MN)
- …with their lives. **The Opportunity** Abbott is seeking a passionate, experienced **Senior Regulatory Affairs Specialist ** to join our team on-site in Plymouth, ... scientific affairs function. **Preferred** **Qualifications** + 4+ years of related regulatory submission experience from medical device, pharmaceutical , or… more
- ManpowerGroup (Alameda, CA)
- Our client is seeking a Regulatory Specialist II to join their team. **Job Title:** Regulatory Specialist II **Location:** Alameda, CA **Job Type:** 1 ... or Chinese) **Job Description:** Experience Background (Any): Medical Device, Pharmaceutical , Regulatory Affairs, Quality Assurance, SW Engineering, APAC… more
- Bausch + Lomb (Bridgewater, NJ)
- …+ Knowledge of pharmaceutical , consumer or medical device industry product labeling processes for review and obtaining regulatory approvals. + Knowledge of ... labeling changes. + Responsible for post approval lifecycle management of labeling . + Coordinate with Regulatory Affairs members and other cross-functional… more
- Merck (Wilson, NC)
- …with our incredibly high standards of quality and meets all regulatory requirements. Partnering across our internal manufacturing facilities, external contract ... supply to customers and patients on time, every time, across the globe. The Specialist , Digital and Data Quality will be responsible for the quality aspects of GMP… more
- Gilead Sciences, Inc. (Foster City, CA)
- …+ Prepares global resources in collaboration with local affiliate teams (TA specialist team). + Identifies, reports, and records adverse events and product ... collaborates with cross-functional colleagues to respond to complex requests. TA specialist responds to complex requests from affiliate MI and internal colleagues… more
- Regeneron Pharmaceuticals (East Greenbush, NY)
- …experience in GMP environment, specifically one or more of the following: pharmaceutical filling, packaging/ labeling , assembly, and/or visual inspection. To be ... in Life Sciences or Engineering with the following amount of experience in Pharmaceutical Filling, packaging/ labeling and/or visual inspection for each level: +… more
- Bausch Health (Bridgewater, NJ)
- …for production artwork development and color management, is a crucial role for the Regulatory Labeling and Graphics group. This role will be the primary graphic ... and maintaining artwork files with the digital workflow system. The Graphics Project Specialist will work closely with the packagers to ensure the artwork is built… more
- Kelly Services (Rahway, NJ)
- …Commerce, FDA, USDA, etc.). + Experience working with international customers and regulatory agencies. + Experience in the pharmaceutical or chemical industry. ... and Clinical FSP is currently seeking a Distribution Planning Specialist for a long-term engagement in Rahway, NJ or...or West Point, PA with one of our Global Pharmaceutical clients. This is a hybrid position. This person… more
- Boehringer Ingelheim (Athens, GA)
- **Description** The Principal Specialist , Packaging Training & Compliance will lead the Packaging (PKG) documentation team to support the production line as required ... and document creation / revision in compliance with procedures and regulatory requirements.This role develops, reviews, and maintains an up-to-date training program… more
- Kedrion Biopharma, Inc. (Melville, NY)
- …in hematology, immunology, neurology, and transfusion medicine. The Quality Operations Specialist has a robust understanding of applicable CGMP regulations and ... quality and appropriate corrective actions. **Main Responsibilities:** The Quality Operations Specialist in this role is responsible for performing various and… more
- Medtronic (Northridge, CA)
- …90,000+ employees in more than 160 countries. **A Day in the Life** As Sr Regulatory Affairs Specialist , you will support on the implementation of the medical ... agencies. + As an individual contributor, the Sr. Regulatory Affairs Specialist is responsible for providing...regulatory experience within the medical device, biotech, or pharmaceutical industries + Or advanced degree and a minimum… more