- Abbott (Alameda, CA)
- …to work for diversity, working mothers, female executives, and scientists. **The Opportunity** This ** Regulatory Affairs Specialist II - APAC** will work ... team goals and division regulatory priorities. + Provides support to Regulatory Affairs management when working towards resolution of compliance issues,… more
- Abbott (Pleasanton, CA)
- …a best place to work for diversity, working mothers, female executives, and scientists. This ** Regulatory Affairs Specialist ** ** II ** will work out of ... + Experience working in the Medical Device industry. + Regulatory Affairs Professionals Society Certification is a...in the Medical Device industry. + Regulatory Affairs Professionals Society Certification is a plus. Apply Now… more
- BD (Becton, Dickinson and Company) (Covington, GA)
- **Job Description Summary** As Regulatory Affairs Specialist II , you will be responsible for the implementation of strategies including domestic and ... compliance or quality systems; or a combination of equivalent.education and experience + Regulatory Affairs Certification (RAC) desired For certain roles at BD,… more
- Abbott (Plymouth, MN)
- …and get on with their lives. **The Opportunity** Abbott is seeking a passionate, experienced ** Regulatory Affairs Specialist II ** to join our team ... is preferred. + Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society.) + Proficient with MS Office suite (Word, Excel, Outlook)… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …diversity and excellence of our academic community. **Description** JOB DESCRIPTION: + The Regulatory Specialist II is an intermediate level position ... supporting regulatory affairs in clinical trial research. + Incumbents are responsible...research. + Incumbents are responsible for coordinating and supporting regulatory affairs activities for non-interventional and interventional… more
- Teva Pharmaceuticals (Weston, FL)
- Quality Specialist II Date: Apr 26, 2024 Location: Weston, United States, Florida, 33331 Company: Teva Pharmaceuticals Job Id: 55617 **Who we are** Teva is a ... work experience related to pharmaceutical industry, supply chain management (distribution), regulatory affairs or equivalent education and experience. *… more
- Methodist Health System (Dallas, TX)
- …addressing and resolving no response claims, denied claims, and correspondence. As an AR II Specialist , you will play a crucial role in optimizing revenue flow ... :** **Job Description :** **Your Job:** We are seeking an experienced Accounts Receivable II (AR II ) Specialist specializing in Professional Billing for… more
- Actalent (Alameda, CA)
- …day to day activities for change control. + Provides consultation/advice to regulatory specialist for change control and product development. + Provides ... knowledge of site and division level policies and procedures. Skills: regulatory affairs , medical device, regulatory submission, fda Additional Skills &… more
- Bausch Health (Bridgewater, NJ)
- …of improving people's lives with our health care products. The Quality Specialist provides support for the business' product development portfolio and ensures ... to Quality-by-Design principles as well as compliance with relevant regulatory requirements and corporate standards. Experience: + Partner with cross-functional… more
- Gilead Sciences, Inc. (Foster City, CA)
- …such as Formulation and Process Development, Manufacturing, Engineering, Packaging, and Regulatory Affairs to ensure that Clinical/Commercial Drug Products are ... a wide variety of activities to ensure compliance with applicable regulatory requirements. + Participates in developing Standard Operating Procedures (SOPs) to… more
- ThermoFisher Scientific (Florence, SC)
- …years meaningful experience. **Experience:** Prefer 2 years direct experience in regulatory affairs /Quality Assurance, analytical r&D, or quality control ... document and maintain the company's Quality Systems conformance to regulatory requirements and company policies where appropriate through effective utilization… more
- Kelly Services (Irvine, CA)
- ** Regulatory Affairs Specialist ** The Regulatory Affairs Specialist II , will provide administrative and technical support to regulatory ... with US and international regulatory requirements. The Regulatory Affairs Specialist provides direct...new product development/new product introduction international product registrations., The Regulatory Specialist II , will: +… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …a relatively small trial portfolio. + Duties include: + Assists regulatory team ( Regulatory Specialist II and III) in research efforts by facilitating ... Specialist I is an entry-level position supporting regulatory affairs in clinical trial research. +...entities. + Supports the Assistant Director, Operations Manager, and Regulatory Coordinators II /III in Program Research in… more
- Medtronic (Santa Rosa, CA)
- Principal Regulatory Affairs Specialist -...a view through the full product lifecycle. The Prin. RA Specialist will execute regulatory ... Affairs team and looking to hire a Principal Regulatory Affairs Specialist to make...life cycle. + Medical device industry experience with Class II /III/IV products. + Experience supporting software device development (for… more
- Medtronic (Plymouth, MN)
- Senior Regulatory Affairs Specialist -...every day. In this role, you will have primary RA responsibility for multiple Class II products, ... and your career. Career That Change Lives The Senior Regulatory Affairs Specialist (Sr. RAS)...process to ensure submission approval. May be included as RA Representative on project teams with members of development… more
- Medtronic (Northridge, CA)
- …90,000+ employees in more than 160 countries. **A Day in the Life** As Principal Regulatory Affairs Specialist , you will develop and implement medical device ... external networks. In this role, you will have primary RA responsibility for multiple Class II (IIa/IIb)... agencies. + As an individual contributor, the Principal Regulatory Affairs Specialist is responsible… more
- Bausch + Lomb (O'Fallon, MO)
- …advancement of eye health in the future. **Objectives:** Responsible for providing Regulatory Affairs support under direct supervision supporting regulatory ... (new registrations, renewals, technical files) based on input from RA Managers and Regional Regulatory groups. +...biology, chemistry, physiology, engineering, medical or law or related regulatory affairs experience with medical devices or… more
- Medtronic (Minneapolis, MN)
- Position Description: Sr. Regulatory Affairs Specialist for Medtronic, Inc. Minneapolis, MN. Multiple positions available. Responsible for developing ... or 510(k) submissions for US Class III or Class II medical devices. Work on MDD (Medical Device Directive)...closely related field and 2 years' experience as a Regulatory Affairs Specialist , R&D Engineer… more
- Abbott (Pleasanton, CA)
- …mothers, female executives, and scientists **The Opportunity** We are seeking a **Principal Regulatory Affairs Specialist ** to join Abbott's Heart Failure ... Pleasanton, CA. As an experienced individual contributor, a Principal Regulatory Affairs Specialist is to...Class II and/or Class III medical devices. Regulatory Affairs Certification (RAC) is a plus.… more
- Abbott (Alameda, CA)
- …help Abbott shape the future of healthcare. As an individual contributor, the **Senior Regulatory Affairs Specialist ** will support product development and ... opportunity at Lingo. **What You'll Work On** + Represent Regulatory Affairs on cross functional project teams...input and technical guidance on product lifecycle planning and regulatory requirements for Class II software medical… more