Global Regulatory Affairs Specialist - Medical Devices
Abbott
Abbott's Electrophysiology business in Plymouth, Minnesota, seeks a regulatory affairs specialist to prepare documentation for regulatory submissions in heart disease treatment. The role involves collaborating with teams, ensuring compliance with FDA standards, and supporting product market entry. The ideal candidate will have a Bachelor’s Degree and strong communication and organizational skills. Abbott offers comprehensive career development and competitive benefits, including medical coverage and retirement plans. #J-18808-Ljbffr Abbott
- Abbott, a global healthcare leader, is hiring an International Regulatory Affairs Specialist I at its Plymouth, MN location. This key position involves regulatory submissions... ...to the successful market entry of medical devices. The ideal candidate will have a Bachelor’...Medical device
- Integer Holdings in Plymouth, Minnesota, is seeking a dedicated Regulatory Affairs Specialist to support compliance efforts for medical devices. You will work closely with the Regulatory Affairs team to prepare submissions and manage regulatory files while adhering to company...Medical device
- Integer Holdings Corporation in Plymouth, MN is looking for a Regulatory Affairs Specialist III to oversee compliance and regulatory submissions for medical devices. In this role, you'll support the Regulatory Affairs management team and ensure adherence to national and...Medical device
- ...Regulatory Affairs Specialist This role is ideal for a regulatory professional with strong experience in FDA, Health Canada, and EU medical device requirements. The Regulatory Affairs Specialist will maintain global registrations and technical documentation, support...Medical deviceWork at office
$110.18k - $120k
...Regulatory Affairs Specialist – Fridley Position Summary The Regulatory Affairs Specialist... ...responsible for initiating global regulatory strategies for... ...post-market changes for devices currently marketed to... ...cross functional peers on new medical device regulations, such as...Medical deviceFull time- ...center of product quality and regulatory excellence. In this role, you... ...regulatory teams, helping ensure their devices meet the highest standards and are ready for global markets. If you love variety,... ...Profile: * 1+ year in medical devices OR engineering/startup...Medical device
- ...Shift Type Job Title Regulatory Affairs Specialist II Education Bachelor's Degree Location... ...: Stereotaxis is the global leader in innovative robotic technologies... ...3-5 years' experience in regulated medical device industry highly preferred. • Knowledge...Medical deviceFull timeWork at officeShift work
$142.8k - $196.35k
...Principal Regulatory Affairs Specialist (Remote - United States) page is loaded## Principal Regulatory... ...the Dental Solutions business across global markets* Driving regulatory strategy... ...activities for assigned drug and medical device products* Leading or supporting regulatory...Medical deviceH1bRemote workRelocation packageFlexible hours- ...Join Stryker as a Regulatory Affairs Specialist in Bloomington, MN supporting Trauma & Extremities... ...activities, documentation, and global compliance across U.S. and international... ...S. FDA regulations or international medical device regulations Experience working with...Medical deviceTemporary workInternshipLocal areaFlexible hours
- ...Principal Regulatory Affairs Specialist At Boston Scientific, we'll give you the opportunity to harness... ...prepare submissions for Class II medical devices. Create innovative regulatory... ...product and project information to global regulatory teams and communicate international...Medical deviceWork at officeLocal areaWorldwide3 days per week
$102.1k - $194k
...week. Responsibilities Represent the Regulatory Affairs function on cross‑functional teams for... ...and prepare submissions for Class II medical devices. Create innovative regulatory pathways... ...timely product and project information to global regulatory teams and communicate...Medical deviceWork at officeLocal areaOverseas3 days per week$84.15k - $127.5k
...Regulatory Affairs Manager By living according to a common set of values, we create a culture... ...right Who are we? Integer is a global organization providing innovative, high... ...technologies and manufacturing to Medical Device OEM's (original equipment manufacturers...Medical deviceWork at officeImmediate startWorldwide$94k - $150k
...Senior Regulatory Affairs Specialist, Ultrasound The Senior Regulatory Affairs Specialist for Ultrasound collaborates with regulatory... ...Technical Files, Declarations of Conformity, and Medical Device Licenses—for various global markets. Support cross-functional teams with...Medical deviceFull timeWork at officeLocal areaWork visaRelocation package3 days per week$102.1k
...Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High... ...employees experience every day. This Regulatory Affairs Principal role supports the review and... ...sales support and training materials for medical devices used in interventional cardiology. The...Medical deviceHourly payWork at officeLocal areaShift work3 days per week$73.6k - $110.4k
...Job Overview Regulatory Affairs Specialist – Onsite (4 days per week). Application window closes 30 Mar... ...Medtronic’s regulatory partners and global agencies, assisting product... ...agencies at reviewer level. Qualifications Medical device experience, particularly with Class...Medical deviceTemporary workWorldwideFlexible hours$110k - $160k
...ABOUT INSPIRE MEDICAL SYSTEMS Inspire is the first of its kind medical device designed to make a difference in the... ...team! The Senior Regulatory Affairs Specialist will lead and execute regulatory... ...apnea. This role supports global regulatory activities with...Medical deviceWork experience placementLocal areaFlexible hours$50.7k - $101.3k
Abbott is a global healthcare leader that helps people live more fully at all stages... ...and products in diagnostics, medical devices, nutritionals and branded generic medicines... ...contributor, the International Regulatory Affairs Specialist I performs specialized level work assignments...Medical deviceFor contractorsWork experience placementWorldwide$50.7k - $101.3k
## Regulatory Affairs Specialist - Electrophysiology (on-site)Applylocations: United States - Minnesota... ...requisition id: 31154127Abbott is a global healthcare leader that helps people... ...businesses and products in diagnostics, medical devices, nutritionals and branded generic...Medical deviceFor contractorsWork experience placementWorldwideShift work$60k - $120k
...Regulatory Operations Specialist I Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-... ...leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our...Medical deviceFor contractorsWork experience placementWorldwideShift work- ...Plymouth, Minnesota, to guide cross-functional teams in developing medical devices. The successful candidate will lead new product development... ...skills. The position offers a competitive salary and growth opportunities in a global healthcare company. #J-18808-Ljbffr AbbottMedical device
- ...Electrophysiology Division in Plymouth, MN. This role involves driving global marketing strategy and leading product launches for the Left... ...over 7 years of experience in product marketing within the medical device sector. We're looking for someone with leadership capabilities...Medical device
- A global healthcare company in Plymouth, MN is seeking a Senior Regulatory Affairs Specialist to lead regulatory submissions and ensure compliance with FDA and international... ...2 years of regulatory experience in medical devices or pharmaceuticals. This role offers competitive...Medical device
- ...its LAA Management franchise. This role involves overseeing the global marketing strategies, managing product launches like Amulet360... ...will have a strong background in product marketing within the medical device sector, preferably cardiovascular or electrophysiology. The...Medical device
$61.3k - $122.7k
Abbott is a global healthcare leader that helps people live more fully at all stages... ...and products in diagnostics, medical devices, nutritionals and branded generic medicines... ...seeking a passionate, experienced Regulatory Affairs Specialist II to join our team on-site in...Medical deviceFull timeWork at officeShift work- Abbott Laboratories in Plymouth, MN is looking for a Regulatory Affairs Specialist I to handle regulatory submissions and ensure compliance for product market entry. You will work in a global healthcare leader dedicated to advancing technology for heart disease treatment...
$171k - $234k
A leading medical device company in Eden Prairie, MN, is seeking a Global Controller to lead financial operations. This role involves overseeing accounting functions, ensuring global compliance with financial regulations, and managing teams across locations. The preferred...Medical device- ...Senior Regulatory Affairs Associate – Medical Device We are partnering with an innovative medical device company seeking a Senior Regulatory Affairs Associate... .... Coordinate international regulatory submissions and global product registrations. Interpret and apply EU MDR...Medical device
- Elucent Medical, Inc. is hiring a Principal Regulatory Affairs Specialist in Eden Prairie, MN. This role requires advanced knowledge of U.S. FDA regulations to oversee... ..., submissions, and compliance for medical devices. The position emphasizes hands-on execution and collaboration...Medical device
$50.7k - $101.3k
Abbott Laboratories in Plymouth, Minnesota is looking for a Regulatory Affairs Specialist to support regulatory activities and ensure compliance... ...prepare regulatory applications and maintain current medical device regulations. Required qualifications include a Bachelor'...Medical deviceFull time$113.03k - $165.77k
...job is to strategically plan, execute and provide oversight to regulatory activities necessary to obtain and maintain regulatory... ...field. Minimum Experience: 7+ years of US and International medical device regulatory submission/approval experience, to include FDA,...Medical deviceImmediate start
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