Global Regulatory Labeling Specialist - Medical Devices
ManpowerGroup Global, Inc.
ManpowerGroup Global, Inc. is seeking a Regulatory Specialist in Santa Clara, CA to lead international labeling initiatives and ensure regulatory compliance across product portfolios. The role involves coordinating with Regulatory, Quality, Supply Chain, and Manufacturing to implement labeling changes on schedule. The ideal candidate will have 6+ years in regulatory affairs or related fields, with strong knowledge of medical devices and labeling requirements, and excellent project management #J-18808-Ljbffr ManpowerGroup Global, Inc.
- ...Regulatory Specialist Our client, a leading organization in the medical device industry, is seeking a Regulatory Specialist to join their... ...supporting international labeling and compliance initiatives.... ...impactful projects within a global organization. Collaborate...Medical deviceWeekly payTemporary workFlexible hours
$55 - $60 per hour
...Regulatory Affairs Specialist Pay Range: $55hr - $60hr Requirement/Must Have... ...affairs experience working in a medical device company (can be in... ...and validation, and product labeling requirement. Ability to... ...changes. Influence and lead global regulatory strategies....Medical device$81.5k - $141.3k
Abbott Laboratories is looking for a dedicated Regulatory Affairs Specialist to join our Vascular Division team in Santa Clara, CA or Temecula... ...supporting EU and US regulatory activities for endovascular medical devices, requiring strong analytical and project management...Medical device- Abbott is hiring a Regulatory Affairs Specialist for their Vascular Division in Santa Clara, CA. This role focuses on supporting EU and US regulatory activities for endovascular medical devices used in treating peripheral artery disease. Ideal candidates should possess...Medical device
- ...Awaits You:The Principal Regulatory Affairs Specialist provides regulatory leadership... ...to the Senior Director of Global Regulatory Affairs.The... ...candidate would have had previous medical device experience and looking for... ..., manufacturing, and labeling changesRepresent RA...Medical deviceWork at office
- ...is hiring a Senior Regulatory Affairs Specialist to support Sports Medicine... ..., regional, and global levels by monitoring... .... Evaluate proposed device modifications to... ...regulatory input on product labeling and claims, ensuring... ...industry (e.g., medical devices, IVDs,...Medical deviceTemporary workLocal areaFlexible hours
$81.5k - $141.3k
...a passionate, experienced Regulatory Affairs Specialist to join our Vascular Division... ...and collaborate with the global regulatory organization to... ...portfolio of endovascular medical devices used in the treatment of... ...manufacturing, supplier, process, and labeling changes to determine...Medical deviceFor contractors$50 - $52 per hour
Akkodis is seeking a Sr Regulatory Specialist for a 12-month contract with a client... ...of international addendum labeling activities across Clients Vascular's medical device portfolio. This role will lead... ...successfully delivering results in global organizations. Experience...Medical deviceContract workTemporary workLocal area$55 - $60 per hour
Job Title: Regulatory Affairs Specialist IV Location: Sunnyvale, California Type... ...strategy and submissions for medical devices, supporting product... ...across the U.S., Canada, and global markets. Responsibilities... ...impact on design, materials, labeling, packaging, manufacturing...Medical deviceContract workLocal area- ...approach. Working with top medical professionals, they... .... Position Senior Regulatory Affairs Specialist (Contract Basis) -... ...design, materials, labeling, packaging,... ...Influence and lead global regulatory strategies... ...experience in a medical device environment. Strong...Medical deviceContract workFor contractorsRemote workWorldwide2 days per week
$90k - $180k
Abbott is a global healthcare leader that helps people live... ...products in diagnostics, medical devices, nutritionals and branded... ...peripheral stents. This Senior Regulatory Affairs Specialist position is an on-site... ...regulations. Assist with labeling development and review for...Medical deviceWork experience placementWorldwideShift work$100k - $200k
## Principal Regulatory Affairs Specialist - Vascular (on-site)Candidatar-selocations... ...id: 31155953Abbott is a global healthcare leader that... ...products in diagnostics, medical devices, nutritionals and branded... ...manufacturing, supplier, labeling, and process changes to determine...Medical deviceFor contractors- Ceribell, Inc in Sunnyvale, CA is seeking a Staff Supplier Industrialization Engineer to serve as the technical owner of our global vendor network. You will drive NPI, transfer manufacturing to international sites, and ensure supplier processes meet FDA and ISO requirements...Medical deviceContract work
- ...Sr. Regulatory Affairs Specialist We are searching for an experienced regulatory professional to work within the Companion... ...(CDx), the successful candidate must have global regulatory experience working in IVD, Medical Devices or Pharmaceutical, with a history of...Medical device
- ...The client seeks a Principal Regulatory Affairs Specialist to lead complex regulatory... ...for Class III implantable devices and software-driven technologies... ...compliance for Class III medical devices, including software... ...-functionally to support global market access and...Medical device
$148.55k - $174.77k
...treated? Join us as a Senior Regulatory Affairs Specialist and be at the forefront of regulatory science for medical robotics. Your mission? To... ...partners, developing global regulatory strategies for new... ...modified Class II and III devices and preparing and submitting...Medical device- System One is seeking a Regulatory Affairs Specialist IV in Sunnyvale, California to lead regulatory strategy and submissions for medical devices across the U.S., Canada, and global markets. You will support product development, design changes, lifecycle management, and...Medical device
- ...Position: Regulatory Affairs Specialist Location: San Jose, CA Duration: 12+ Months Contract... ...Work hours: 8AM – 5PM Client: Medical Device Company Job Category: Regulatory... ...other corporate groups. 3. Track global registration status for project...Medical devicePermanent employmentContract workTemporary workH1bLocal areaRemote workShift workDay shift
$145k - $167k
...Senior Regulatory Affairs Specialist Palo Alto, CA - Hybrid Hyperfine,... ...revolutionize patient care globally through transformational... ...for the company's devices and ensures compliance to... ...Strong knowledge of medical device labeling requirements. Effective...Medical deviceWork experience placementWork at officeWorldwideWork visaNight shiftWeekend work3 days per week- ...Employee Min. Salary Region 1: 125900 USD Global Job Level (HCM): Professional 3 (9) Min... ...teams, make sure the company's regulatory affairs activities are conducted in accordance... ...is required. Minimum 1 year of NMPA medical device regulatory requirement China GB/YY standards...Medical deviceFor contractorsLocal areaWorldwideFlexible hours
$60 per hour
...Job Title: Regulatory Affairs Specialist IV Location: Sunnyvale, California... ...strategy and submissions for medical devices, supporting product development... ...the U.S., Canada, and global markets. Responsibilities... ...impact on design, materials, labeling, packaging, manufacturing...Medical deviceContract workLocal area- ...partner Raise, are hiring. We’re a global technology leader in minimally... ...Primary Function of Position The Regulatory Post Market Surveillance Specialist investigates customer complaints,... ...Experience - 2+ years of experience in medical device field, with exposure in the...Medical deviceContract workLocal area
$114k - $228k
Abbott is seeking a Global Product Manager in Santa Clara, CA, to join the Global Strategic Marketing team. In this onsite role, you... ...drive better patient outcomes. Candidates need 5+ years in a medical device company and strong leadership skills, with a competitive salary...Medical device$197.3k - $394.7k
A leading healthcare company is seeking a Global Endovascular Franchise Director to manage marketing strategies for its expanding... ...This role requires over 10 years of B2B marketing experience in medical devices or pharmaceuticals and a proven ability to influence...Medical device- ...Executive Director, Global Market Access About the Company Innovative pharmaceutical company specializing in metabolic & fatty... ...& Research Healthcare Biopharma Biotechnology Medical Device Pharmaceutical Specialties liver disease nash...Medical device
$148.7k - $297.3k
Abbott Laboratories is looking for an Associate Director, Global Data Science & Analytics to join our Medical Devices team on-site in Santa Clara, CA. In this role, you will lead data analytics projects aimed at generating impactful insights for healthcare decisions. The...Medical device- ...Cupertino, CA is seeking an International Regulatory Affairs Lead to head a team responsible... ...expansion of Apple Health’s regulated medical device features. This strategic role focuses... ...leading regulatory programs, developing global submissions, and guiding quality...Medical device
- Intuitive in Sunnyvale, CA seeks an experienced Regulatory Affairs professional to provide expert leadership in global submissions and compliance strategy. The role focuses on cross-functional coordination, technical documentation, and agency interactions to support product...Medical deviceWorldwide
$106k - $197k
Roche is seeking a Regulatory Affairs Specialist based in Santa Clara, California, to oversee regulatory... ...and manage comprehensive global regulatory strategies. You will utilize... ...3-8 years of experience in IVDs or Medical devices, demonstrating solid stakeholder management...Medical device- ...Surgical is seeking a Vice President of Trade Compliance to lead its global program for medical devices and compliant supply chains. This executive will define strategy, govern policy, and partner with Regulatory Affairs to ensure FDA and international requirements are met...Medical device
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