- Monster (Boston, MA)
- …and application of quality assurance and compliance. The Sr . Quality Specialist coordinates GMP activities in support of clinical and commercial Drug ... Job Title: QA Sr . Specialist Location: Boston, MA Shifts...o Cell and gene therapy cGMP's and associated CMC regulatory considerations o Aseptic processing . Experience successfully leading… more
- Monster (Naples, FL)
- …development and medical education in orthopedics. Arthrex is actively searching for a Sr . Biocompatibility Specialist for our Global Headquarters in Naples, FL ... vivo testing methodologies in accordance with ISO 10993, FDA Guidance, and global regulatory requirement; Participate in design review meetings as a key member of… more
- Beth Israel Lahey Health (Boston, MA)
- …you're making a difference in people's lives.** The Sr . Regulatory Specialist supports regulatory compliance for clinical research at Beth Israel ... submit applications, including preparation of consent forms to the IRB on all clinical trials (industry, cooperative groups and PI initiated studies), and respond to… more
- Houston Methodist (Houston, TX)
- …protocols/plans and processes. The Sr Regulatory Compliance Specialist position maintains documentation for clinical research studies, case report ... At Houston Methodist, the Senior ( Sr .) Regulatory Compliance Specialist ...Regulatory Affairs Certifications (RAPS) or CCRC - Certified Clinical Research Coordinator (ACRP) or CCRP - Certified … more
- West Pharmaceutical Services (Exton, PA)
- Sr . Specialist , Regulatory Affairs, Product Stewardship Requisition ID: 69466 Date: Sep 7, 2025 Location: Exton, Pennsylvania, US Department: Regulatory ... healthier environment and planet through our sustainability efforts. **Job Summary** The Sr . Specialist , Regulatory Affairs evaluates supplier regulatory… more
- Caldera Medical (Westlake Village, CA)
- …Quality of Life for Women! Message from the Hiring Manager: In your role as a Sr . Regulatory specialist , you will develop and implement medical device ... Sr . Regulatory Affairs Specialist ... Sr . Regulatory Affairs Specialist 100% ONSITE in...licensing by jurisdictions. * Work cross-functionally with R&D, Quality, Clinical , and Marketing teams to ensure regulatory … more
- Terumo Neuro (Aliso Viejo, CA)
- **12870BR** **Title:** Sr Specialist , Clinical Trial Quality Assurance **Job Description:** Provide support to all aspects of the Clinical Quality ... on technology for communication and handling confidential information. **External-Facing Title:** Sr Specialist , Clinical Trial Quality Assurance **Posting… more
- Children's Hospital Los Angeles (Los Angeles, CA)
- …Matters.** **Overview** **Purpose Statement/Position Summary:** The Clinical Research Training Specialist Sr serves as a senior -level contributor within ... goals and evolving industry practices. Additionally, the CR Training Specialist , Sr . remains current on emerging trends...us to better serve our patients and create a strong community at CHLA. Clinical Research Regulatory … more
- J&J Family of Companies (Irvine, CA)
- …Learn more at https://www.jnj.com/medtech **Key Responsibilities:** Under general direction, this Senior Clinical Research Specialist will be responsible ... States of America **Job Description:** Our J&J MedTech Electrophysiology clinical team is currently recruiting for two ** Sr...procedures and guidelines, this position: + Serves as a Senior Clinical Research Specialist within… more
- Medtronic (Minneapolis, MN)
- …to innovation in a more connected, compassionate world. **A Day in the Life** ** SENIOR REGULATORY AFFAIRS SPECIALIST ** _Location: Minnesota Rice Creek East ... we provide. Therefore, we are looking for a passionate Senior Regulatory Affairs Specialist who...of industry experience, with at least 2-3 years in regulatory , clinical , or quality roles. + Advanced… more
- BD (Becton, Dickinson and Company) (Durham, NC)
- …Washington, DC. **This position does not offer relocation assistance** **About the role:** The Senior Regulatory Affairs Strategy Specialist will work in BD ... best self. Become a **maker** **of possible** with us. Our vision for Central Regulatory Affairs at BD Explore innovative solutions in BD Central Regulatory … more
- GE HealthCare (Madison, WI)
- …GE HealthCare establishes best practices in compliance with regulatory requirements. The Senior Regulatory Affairs Specialist will be involved with ... to help guide regulatory submission pathways, taking into consideration regulatory requirements (including product testing, clinical data, etc.), product… more
- Johns Hopkins University (Fort Defiance, AZ)
- …Boards (IRBs) that we report to and interact with to conduct our work. The Sr . Compliance Monitoring Specialist is an integral member of the research team and ... individual serves as the Center's expert on IRB and regulatory requirements and will lead all IRB related activities...lead all IRB related activities at the Center. The Sr . Compliance Monitoring Specialist will help prepare… more
- Globus Medical, Inc. (Audubon, PA)
- …and annual registrations. Recommends changes for labeling, manufacturing, marketing and clinical protocol for regulatory compliance. Monitors and improves ... of exceptional response by partnering with researchers and educators to transform clinical insights into tangible solutions. Our solutions improve the techniques and… more
- J&J Family of Companies (Irvine, CA)
- …ensuring the delivery of key regulatory and medical documents. Specifically, the Sr . Specialist will lead the review of Clinical Evaluations (CERs), ... a member of Johnson & Johnson family of companies, is recruiting for a ** Sr ** . ** Specialist , Scientific Operations** to join the team in Irvine, CA.… more
- J&J Family of Companies (Santa Clara, CA)
- …information while adhering to legal, compliance and regulatory requirements. The Sr . Medical Sciences Specialist will be hands-on and is expected to ... **Job Description:** Johnson & Johnson is hiring for a ** Sr . Medical Sciences Specialist ** **- Shockwave Medica**...including study protocols, case report forms, instructions for use, clinical study reports, and regulatory submissions. +… more
- Guthrie (Sayre, PA)
- …various departments, and ensuring compliance with regulatory standards. The Sr . Provider Onboarding Specialist is responsible for submitting employment ... Summary The Senior Provider Onboarding Specialist oversees the...team members. Thorough understanding of provider credentialing, licensing, and regulatory compliance Education A high school diploma is required.… more
- Fluor (North Charleston, SC)
- Sr . Manufacturing Specialist Job Overview **Location** **:** United States, North Charleston, South Carolina 1. **Job skills** QA/QC 2. **Type** Permanent **Job ... subscribed to receive alerts for jobs similar to this one. **Position:** Sr . Manufacturing Specialist **Location:** Charleston, South Carolina **Shift:** 2nd… more
- Terumo Medical Corporation (Elkton, MD)
- Sr . Quality Systems Documentation Specialist Date: Aug 18, 2025 Req ID: 5082 Location: Elkton, MD, US Company: Terumo Medical Corporation Department: Quality ... wherever we go next!** **_Advancing healthcare with heart_** **Job Summary** The Senior Quality Systems Documentation Specialist will be responsible for… more
- Charles River Laboratories (Horsham, PA)
- …build a career that you can feel passionate about. **Job Summary** The Specialist / Sr . Specialist supports departmental operations by contributing to ... Specialist : 9-12 years of contract lab or scientific monitoring experience; Sr . Specialist : minimum of 12+ years of contract laboratory (operational and/or… more
