- Envista Holdings Corporation (Pomona, CA)
- **Job Description:** Under the direction of the Senior QA Manager, this position is responsible for ensuring that core functions of Quality Assurance are ... consistently in compliance with regulatory requirements and corporate standards. This involves assuring quality standards (FDA, ISO, CMDCAS, MDD, MDR, MDSAP and Canadian Medical Device requirements) are with respect to such process as CAPA, and Internal… more
- Merck (Rahway, NJ)
- …and our Research and Development Division's IT) to serve company patients. The Sr . Specialist , Global Clinical Supply Compliance is a support role for ... adheres to compliance standards set forth in the overarching Quality Management System ( QMS ). This role is critical in supporting a culture of compliance throughout… more
- Medtronic (Minneapolis, MN)
- …and efficiently, with more predictable procedure times and outcomes. The ** Senior Regulatory Affairs Specialist ** develops strategies for worldwide product ... requirements, prepares worldwide submissions and negotiates their approval. The specialist also assists with the license maintenance including renewals,… more
- West Pharmaceutical Services (Exton, PA)
- …US Department: Regulatory Affairs Description: **Thank you for your interest in our Sr Specialist , Regulatory PM (Evergreen) position. Applicants of this role ... Sr . Specialist , Regulatory Project Management (Evergreen...and planet through our sustainability efforts. **Job Summary:** This Senior Specialist , Regulatory Project Management (RPM) role… more
- RES (Denver, CO)
- …feel valued for your contributions and the perspectives you bring. **Summary:** The Sr . Procurement Specialist position is a member of the center-led Procurement ... best practices in supply management and driving overall business profitability. The Sr . Procurement Specialist will collaborate with construction project teams,… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- **Job Description Summary** As Sr . Specialist of Regulatory Affairs you will be responsible for supporting MMS Dispensing products consisting of Medical Devices ... Support will consist of new product development, sustaining, and end of life activities. This hybrid role requires that candidates be onsite 4 days a week in our San… more
- Stryker (Mahwah, NJ)
- …comprehensive upgrades to prevent future issues. **What you will do** As the ** Senior ** **Re** **gulatory Affairs Specialist ** for Market Continuity, you will ... technical files, and interact with regulatory agencies and notified bodies. The Senior Regulatory Affairs Specialist is the Regulatory SME on cross-functional… more
- Kelly Services (Cambridge, MA)
- Kelly Science is seeking a Senior Quality Assurance Specialist to join a document control & quality systems department of a growing client located in Cambridge, ... MA. ** This is a hybrid position will the requirement to report on-site 1-2...periodic metric analysis and reporting to end users and senior management. + Performing periodic quality system assessments. Qualifications:… more
- Kelly Services (Brea, CA)
- **Position Overview:** The Senior Regulatory Affairs Specialist creates, evaluates, and completes regulatory tasks related to the following: worldwide product ... activities. **Location:** Brea, CA **Shift** : M-F, standard working hours ** Hybrid Role** **Pay:** 45/hr **6-8 month contract role** **RESPONSIBILITIES:** + Assist… more
- GE HealthCare (Wauwatosa, WI)
- …during internal and external audits of GE Healthcare's Quality Management System ( QMS ). + Develops knowledge of GE HealthCare's Quality Management System and Product ... + Resolves issues using established procedures. + Consults People Leader or more senior team members for issues outside of defined parameters. + Collaborates with… more