- Medtronic (Irvine, CA)
- …of medical device experience, including knowledge of the US and International regulatory requirements for Advertising & Promotional labeling , or an advanced ... to ensure that it meets all medical, legal, and regulatory (MLR) process requirements. + Facilitate review meetings online...+ Support the preparation of US and International promotional labeling material, including the creation of a claims matrix… more
- Organon & Co. (Plymouth Meeting, PA)
- …success with cross-geographically based cultural collaborations. + Knowledgeable about key labeling regulatory requirements worldwide, with a key strength in ... the core labeling documents (CCDS) and US labeling for marketed products; and supporting country Regulatory... labeling for marketed products; and supporting country Regulatory Affairs in the development and maintenance of the… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …components, randomization file and label text). + Oversee the internal packaging and labeling production orders in accordance with the clinical trial design and all ... relevant regulatory requirements for assigned projects. + Ensure the creation...teams in various areas. + Manage external packaging and labeling activities + Responsible for improving business processes and… more
- Bausch + Lomb (Juneau, AK)
- …business outcomes. **Responsibilities:** + Formulate, lead, and drive integrated regulatory strategies across CMC and clinical/non-clinical, labeling , adpromo ... operational excellence, compliance, and timely execution of deliverables. + Drive regulatory strategies for clinical, non-clinical, CMC and labeling development… more
- J&J Family of Companies (Danvers, MA)
- …more at https://www.jnj.com/medtech We are searching for the best talent for a ** Senior Regulatory Affairs Specialist ** to support our Abiomed business. ... and relocation assistance is not provided. **Purpose** : The Senior Regulatory Affairs Specialist is...). + Experience in reviews of engineering, manufacturing, marketing, labeling and clinical documents for regulatory compliance.… more
- Abbott (Plymouth, MN)
- …get on with their lives. **The Opportunity** Abbott is seeking a passionate, experienced ** Senior Regulatory Affairs Specialist ** to join our team on-site in ... Plymouth, MN. In this role, you will lead the preparation and submission for regulatory approvals and identify and resolve problems. You will provide regulatory … more
- Stryker (Fremont, CA)
- **Join Stryker's Neurovascular Division in Fremont, CA as a Senior Regulatory Affairs Specialist .** At Stryker, we're driven by a mission to "Make Stroke ... + Support the Neurovascular product portfolio by assessing design, manufacturing, and labeling changes to ensure regulatory compliance throughout the product… more
- Stryker (Redmond, WA)
- We are currently seeking a ** Senior Regulatory Affairs Specialist ** to join our **Medical** **Division** to be based **Hybrid** Monday through Wednesday in ... **What you will do** As part of the Medical Regulatory Affairs team, you will work with the team... guidance throughout the product lifecycle, including development, planning, labeling , and claims, while maintaining current product registrations +… more
- Bausch + Lomb (Juneau, AK)
- …product strategy, reporting, administrative documentation, due diligence, market expansion, labeling content, regulatory compliance, regulatory intelligence ... products in the US and/or Canada + Formulate, lead, and drive integrated regulatory strategies across CMC and clinical/non-clinical, labeling , adpromo domains +… more
- Edwards Lifesciences (Irvine, CA)
- …on utilizing regulatory updates to expedite approval process + Review labeling content product and process changes, and product documentation to assure ... difference to patients around the world. From design to production, our Regulatory Affairs teams help guide our innovative technologies through complex domestic and… more
- Cardinal Health (Cheyenne, WY)
- …and services are properly reviewed for quality and documented. **_Job Summary_** The Senior Specialist , Quality Assurance - Labeling Team is responsible ... ** Senior Specialist , Quality Assurance - Pharmaceutical...documentation and compliance standards for pharmaceutical and medical device labeling . + Ability to interpret and apply regulatory… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …self. Become a **maker of possible** with us. **Job Overview** As a Staff Regulatory Affairs Specialist , you will play a crucial role in supporting Medication ... Directive, EU Electromagnetic Compatibility Directive, etc.). + Problem-solve and escalate regulatory and compliance issues to senior management as necessary.… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- **Job Description Summary** As Staff Regulatory Affairs Specialist , you will be responsible for supporting MMS Dispensing products consisting of Medical Devices ... regulations (eg, FDA Medical Device Regulations, EU-MDR) + Problem solve and escalate regulatory and compliance issues to senior management as necessary + Drive… more
- Curia (Rensselaer, NY)
- Senior QA Validation Specialist - CSV Systems Engineer Summary: The Senior Validation Specialist , assists with the validation activities throughout the ... and approval, investigations for deviations and champion local, corporate and regulatory standards + Present and support validation concepts and approaches with… more
- Caterpillar, Inc. (Griffin, GA)
- …**Job summary:** The Large Power System Division currently seeking an EHS Specialist to serve as an individual contributor on the Environmental, Health and/or ... and complaints. + Ensure environmental training is completed to comply with regulatory requirements or in support of facility, division, or enterprise objectives. +… more
- Bristol Myers Squibb (Bothell, WA)
- …commercial lot file review, testing of incoming raw materials, sampling, labeling tracking and shipping of samples. **Duties/Responsibilities** + Perform review of ... to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements. + Apply scientific principles to analytical testing… more
- Kelly Services (Winston Salem, NC)
- **Job Title:** QA Specialist II - Contract **Location:** Winston Salem, NC **Schedule:** Monday-Friday, 8:00 AM - 5:00 PM **Employment Type:** Contract **Pay Rate:** ... $30-$33/hour **Position Summary:** The QA Specialist II provides critical Quality Assurance (QA) support to Quality Operations, with a strong emphasis on material… more
- Stanley Black and Decker (Elyria, OH)
- EH&S Specialist - Onsite Elyria, OH, US **Come build something that matters.** It takes great people to achieve greatness. People with a sense of purpose and ... CUB CADET(R), and HUSTLER(R). **The Job:** As an EH&S Specialist you'll be part of our Elyria, OH team...onsite for hazard communication, and to assist in chemical labeling , waste management, spill response, and annual reporting under… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …Life at Olympus (https://www.olympusamerica.com/careers) . **Job Description** As a Medical Safety Specialist II (MSSII) you will have an integral role in the ... Olympus therapeutic areas. You will report directly to the Senior Director Medical Safety as a member of the...well as Infection Prevention & Control, Quality Affairs & Regulatory Affairs, Research & Development, Legal, and Health Care… more
- Lenovo (Morrisville, NC)
- …ourStoryHub (https://news.lenovo.com/) . **Description and Requirements** Lenovo is currently seeking a Senior Trade Compliance Specialist for NA trade. The NA ... Senior NA Trade Compliance Analyst **General Information** Req...of Lenovo's Global Trade Compliance team. The trade compliance specialist is responsible for ensuring regulatory legal… more