R&D MDR Project Lead - Regulatory & LCM Leader
Creative Solutions Services, LLC
Creative Solutions Services, LLC is seeking a qualified candidate to provide R&D Lifecycle Management support for the MDR franchise initiative. This role involves engaging with cross-functional teams to ensure compliance and successful project execution in the medical device sector. The ideal candidate will hold a Bachelor's degree in Engineering or Life Sciences and have proven experience in leading projects relevant to medical device regulations. Strong communication and problem-solving skills are essential for success in this position. #J-18808-Ljbffr Creative Solutions Services, LLC
- ...Job Summary Provide R&D Lifecycle Management (LCM) support for the MDR franchise initiative to ensure... ...teams, and ensure regulatory documentation is developed... ...maintained in compliance with project requirements. Roles &... ...History Files (DHF) leading to the implementation of...Regulatory
$32 per hour
...Description Title: Quality Specialist - Project Lead Location: Bridgewater, NJ Company... ...compliance to quality, food safety, and regulatory requirements. What You'll Do: Be... ...Experience in food industry in quality, R&D, or manufacturing areas Demonstrated...RegulatoryHourly pay- Job title: Thought Leader Liaison, U.S. Hematologic Oncology... ...and Transplant Lead. Join the team transforming... ...About Sanofi We’re an R&D-driven, AI-powered... ...compliance, legal and regulatory guidelines. KOL Engagement... ...goal for each project. Speaker Bureau Operations...RegulatoryContract workWork experience placementWork at officeLocal areaHome office
$137k - $235.75k
...an Associate Director of AI Quality and Governance in Raritan, NJ. This role involves leading the AI governance framework to ensure responsible AI development and deployment across R&D. The ideal candidate has over 10 years' experience in AI/ML and data science within...Suggested- ...& Johnson is seeking a Portfolio & Consolidation Finance Manager to oversee financial planning and performance management across the R&D function. This pivotal role requires collaboration with FP&A and business leadership to ensure transparent financial performance and...Suggested
- ...Associate Director, Global Labeling Product Leader to drive their global labeling strategy.... ...role includes responsibilities like leading labeling development and ensuring high quality... ...experience, with a strong background in regulatory labeling for pharmaceutical products,...Regulatory
$160k - $228k
Job Title Thought Leader Liaison, Nephrology, Northeast Requisition JR000015847 Thought... ...reporting to the Thought Leader Liaison Lead, reporting through Specialty Brands Marketing... .... Strong understanding of legal and regulatory environment in pharmaceutical promotional...RegulatoryContract workWork at officeWeekend workAfternoon shift- ...cell‑based immunotherapy. From our three R&D sites around the world, we apply these innovative... ...is seeking a Global Viral Vector MSAT Lead as part of the Global Manufacturing &... ...Development, Manufacturing, Quality, Regulatory, and Supply Chain teams to enable reliable...RegulatoryPermanent employmentFull timeFor contractorsLocal areaWorldwide
$175k - $343k
Senior Global Medical Affairs Lead (GMAL), Prostate Hybrid - Raritan... ...management strategies. As the leader of the WWMAST (Worldwide... ...data reviews and analysis, and regulatory environment. Knowledge of study... ...business cases and working with R&D teams. Global mindset...RegulatoryLocal areaImmediate startWorldwide$124k - $174k
Colgate is seeking a Regulatory Affairs Project Manager in Piscataway, New Jersey. This hybrid position leads global regulatory submissions and ensures compliance with quality management systems. The ideal candidate has at least seven years of experience in regulatory...Regulatory$127.28k - $190.92k
Daiichi Sankyo US in Basking Ridge, NJ is seeking a Regulatory Affairs CMC project representative. The role involves managing developmental and post... ...-marketing projects, preparing submission documents, and leading FDA interactions with supervision. The ideal candidate...Regulatory- Colgate-Palmolive is looking for a Regulatory Affairs Project Manager in Piscataway, NJ, to oversee global regulatory submissions, ensuring compliance... ...device and pharmaceutical standards. The role involves leading cross-functional teams, coordinating quality management...Regulatory
- ...searching for a Principal Portfolio Lead, Statistical Programming -... ...role is a highly experienced project leader with expert understanding of... ...to delivery of the J&J IM R&D portfolio through effective... ...programming related aspects of regulatory agency inspections and J&J...RegulatoryFull timeTemporary workWork at officeLocal areaRemote work2 days per week
$58k
...Engineering, Technology & Telecom in Raritan, NJ is hiring an Executive Admin Assistant for a hybrid role to support senior leadership and the R&D team. This role emphasizes organizational and communication skills, requiring a high school diploma and at least 5 years of...- Johnson & Johnson MedTech is seeking a Biosurgery R&D Lab Operations Manager in Raritan, NJ, to lead multidisciplinary lab operations. The role involves oversight of daily lab activities, maintaining operational efficiency, ensuring compliance with health and safety standards...Full timeRemote work
- ...for a Portfolio & Consolidation Finance Manager responsible for financial planning, consolidation, and performance management within R&D. You'll partner closely with the finance team to drive transparency in financial performance and support strategic initiatives. The ideal...
- Johnson & Johnson is seeking a Senior Manager in MedTech R&D Procurement. This position will be responsible for developing category strategies and managing supplier relationships across a complex global category exceeding $85MM in annual spend. The ideal candidate will...
- DePuy Synthes is seeking a Sr. Manager, Procurement R&D Category located in New Brunswick, NJ. This role involves leading procurement activities across various spend categories and driving alignment between business strategies. The ideal candidate will have at least 8 years...
- Johnson & Johnson Innovative Medicine is seeking a Sr. Manager, MedTech Technology Product Lifecycle Management Platform in Raritan, NJ. This role involves owning the strategy and vision for the PLM platform, ensuring cross-functional teamwork to meet technical needs while...
$137k - $235.75k
...Associate Director, Global Labeling Product Leader (Regulatory Affairs) Location: Hybrid - Raritan, NJ... ...and partner with Global Regulatory Leads and functional partners (clinical,... ...labeling guidance. Experience leading project teams in a matrix environment. Experience...RegulatoryTemporary workWork experience placementLocal areaWorldwide$84.6k - $157.2k
...love. That's what makes us Roche. As a Regulatory Affairs Project Manager you will have the opportunity to... ...and live in the spirit of "We all lead" using VACC principles. You foster an exchange... ...(5-10 years preferred), in Regulatory, R&D, Quality, Operations and/or Clinical...RegulatoryLive inLocal areaRelocation packageShift work- A leading regulatory affairs company in Raritan, New Jersey, is looking for a Customer Quality Specialist. This role focuses on supporting... ...investigations. This position offers opportunities to engage in projects and achieve productivity and accuracy targets. #J-18808-...Regulatory
- Humanscale is seeking a Site Quality Manager in Piscataway Township, NJ. This role is responsible for leading quality functions and ensuring compliance with customer and regulatory requirements while driving continuous improvement in operational efficiency. The position...Regulatory
- ...supplier lifecycle and compliance auditing in Raritan, NJ. You will lead supplier performance, engage with cross-functional teams, and... ...management, a Bachelor's degree, and a strong understanding of regulatory standards in Biotherapeutics. This role offers a competitive...Regulatory
- ...You will work closely with team members and assist in training, regulatory audits, and process improvements. The successful candidate will... ...or Science and at least three years of experience as a Lead Engineer. Benefits include medical, dental, and vision insurance...Regulatory
- ...Executive Director for Oncology R&D, responsible for overseeing multiple programs and leading clinical development strategies... ...management, ensuring effective project execution. The successful... ...group, while being proficient in regulatory strategies and collaboration with...Regulatory
$102k - $177.1k
...following legal requirements and regulatory approvals. If accepted, the... ...performance management across the R&D function. The role partners... ...analytics. Responsibilities Lead financial planning, budgeting,... ...Partner with Finance and R&D leaders to lead the Long‑Range Innovation...RegulatoryLocal areaImmediate start- ...displayed at the store to support accurate pricing of products. Ensures any additional pricing tasks related to local regulations and/or regulatory compliance programs are completed accurately and within the required time frame. Assist with bookkeeping activities, including...RegulatoryWork experience placementSeasonal workLocal areaShift work
- ...Pest Management (IPM) in Readington Township, NJ. This role involves leading a high-performing IPM team to ensure the effective treatment of pests and pathogens while adhering to safety and regulatory standards. The ideal candidate will have significant experience in cannabis...Regulatory
- ...biotechnology company in Raritan, NJ, is seeking a QA Investigations Lead I to provide quality oversight during investigations in a GMP... ...will ensure timely investigations, develop CAPAs, and support regulatory audits. Applicants should have a Bachelor's degree and relevant...Regulatory
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