Regulatory Affairs Specialist - Medical Devices (Onsite)
ManpowerGroup Global, Inc.
A staffing and workforce solutions company seeks a Regulatory Affairs Specialist to manage regulatory submissions and work with the FDA. The ideal candidate will have 5–8 years of experience in regulatory affairs specifically for medical devices, including knowledge of Class III devices. This role requires a Bachelor’s degree and offers a pay range of $41/hr to $46/hr for a 12-month contract, working onsite in Santa Clara, CA. #J-18808-Ljbffr ManpowerGroup Global, Inc.
$75k - $95k
A global medical device company is seeking Regulatory Affairs personnel for various levels (Associate/Specialist/Senior Specialist) in Mountain View, CA. Responsibilities include analyzing... ...skills. Work is conducted 100% onsite. #J-18808-Ljbffr Page Mechanical Group,...Medical deviceFull time- ...supporting teams, make sure the company's regulatory affairs activities are conducted in accordance... ...Skills and Experience Hybrid onsite weekly in Sunnyvale, CA or Peachtree... ...is required. Minimum 1 year of NMPA medical device regulatory requirement China GB/YY standards...Medical deviceFor contractorsLocal areaWorldwideFlexible hours
- ...Position Serve as the primary regulatory representative on project... ...core teams. The Regulatory Affairs Specialist works across the... ...relevant experience working in a medical device company (can be in combination... ...Schedule - This job will be onsite weekly, the percentage of onsite...Medical deviceLocal areaWorldwideShift work
- ...Regulatory Affairs Specialist (NMPA) This position will partner with the in-country RA team as well... ...skills and experience include hybrid onsite weekly in Sunnyvale, CA or Peachtree... ...is required, minimum 1 year of NMPA medical device regulatory requirement China GB/YY standards...Medical deviceFor contractorsLocal area
- ...and their patients. Primary Function of Position The Regulatory Post Market Surveillance Specialist investigates customer complaints, makes an initial... ...equivalent. Experience - 2+ years of experience in medical device field, with exposure in the following areas: Knowledge...Medical deviceContract workLocal area
- A medical device leader is seeking a Senior Supplier Quality Engineer to ensure suppliers meet quality, service, and delivery requirements.... ...improvements and supporting new product introductions in a fully onsite position. Candidates need a Master's degree in Mechanical or...Medical device
$42.74k - $72.7k
A leading medical device company in Santa Clara is seeking a Cardiac Monitoring Technician I. This onsite role involves interpreting EKG data to assist physicians, requiring 1 year of experience and a high school diploma. Preferred qualifications include formal EKG education...Medical deviceRelocation package- ...Job Title: Compliance Specialist 3 Duration: 6 months... ...Sunnyvale, CA (Min 3 days/week onsite) Primary Function of Position... ...retention based on company and regulatory standards.... ...combined experience) in the medical device or other regulated industry....Medical device3 days per week
- Intuitive in Sunnyvale, California is seeking a Regulatory Affairs Specialist to serve as the primary regulatory representative on projects. The... ...Ideal candidates will have a minimum of 5 years in the medical device industry. This position supports innovation in robotic-...Medical device
$90k - $180k
...Senior Regulatory Affairs Specialist Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio... ..., with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000...Medical deviceWork experience placementWorldwide- A global healthcare leader is seeking a Regulatory Affairs Associate in Santa Clara, CA. This role involves managing regulatory submissions and approvals for medical devices, particularly Class III products. Candidates should have a Bachelor's or Master's degree in a relevant...Medical device
$25 per hour
...Job Title: Compliance Specialist III Location: Sunnyvale, California Type... ...5/HOUR Contractor Work Model: Onsite Hours: 40.0 Overview This role supports quality and regulatory compliance activities within a medical device manufacturing environment. The...Medical deviceFull timeContract workFor contractorsWork at officeLocal area- We are searching for an experienced regulatory professional to work within the Companion... ...Reporting to the Sr. Director, Regulatory Affairs (CDx), the successful candidate must... ...regulatory experience working in IVD, Medical Devices, or Pharmaceuticals, with a history of...Medical device
- System One is seeking a Compliance Specialist III in Mountain View, California, for a 6-month contract position. The role involves supporting quality and regulatory compliance for medical device manufacturing, ensuring adherence to FDA regulations and ISO standards. Responsibilities...Medical deviceContract workWork at office
- Title: Regulatory Affairs Associate Location: Santa Clara, CA Duration: 12Months 100% Onsite Summary: We are looking for an experienced Regulatory Affairs professional to... ...regulatory submissions and approvals for medical devices, including high-risk (Class III) implantable...Medical deviceTemporary workFlexible hours
- ...Regulatory Affairs Associate Location: Santa Clara, CA Mode: 12 Months Contract / 100% Onsite Pay Range: $42 to $46/hr on W2 What's the Job? Manage regulatory labeling... ...approvals for Class III implantable medical devices Maintain compliance with FDA...Medical deviceWeekly payContract workTemporary workFlexible hours
$24.5 per hour
...Hiring Medical Device Assemblers for a Catheter Medical Device Company in Santa Clara, CA! Description: Working in a clean room environment... ..., Vacation or Sick Leave) Workplace Type This is a fully onsite position in Santa Clara,CA. Application Deadline This...Medical deviceWeekly payContract workTemporary workWork at office- ...Description Lead Project Engineer for Onsite Project co-ordination and execution... ...adherence to international standards and regulatory requirements. Mentor and coach engineering... ..., energy, hi-tech, healthcare, medical devices, rail and semiconductor industries....Medical device
- ...stage risk evaluations, and collaborating with engineering teams. Candidates should have 8+ years in medical device development and strong analytical skills. An onsite position with potential travel is offered within a diverse and inclusive work environment. #J-18808-Ljbffr...Medical device
$20 - $25 per hour
...Overview: Pay Range: $20hr - $25hr Responsible for supporting regulatory compliance and quality management activities, including... ...timely resolution of issues. Should Have: Knowledge of medical device regulations and international quality standards....Medical device$136.1k - $195.9k
...and construct manufacturing equipment for minimally invasive medical devices. Responsibilities include prototyping, ensuring safety and validation... ...mechatronics and mechanical design. This position is fully onsite and offers competitive compensation ranging from $136,100 to...Medical device$45 - $65 per hour
...tangible advancements and are poised to advance your career, join us as we pioneer progress in the biotechnology and medical device industries. Workplace: Onsite in San Francisco CA Position Title: Scientist, iPSC Models Position Type: contract-to-hire...Medical deviceHourly payContract work- ...Position : Phlebotomist (5 days per week, approximately 3 hrs/day (15hrs/week) Onsite Location : San Jose, CA Duration : 12 Months Total Hours/week : 40.00 1st Shift Client: Medical Device Company Job Category: Healthcare Level Of Experience: Entry Level...Medical deviceContract workPart timeDay shift3 days per week
- A leading medical technology company is seeking a Complaints Specialist II in Santa Clara, CA. The role requires ensuring compliance with regulatory standards for medical devices. Responsibilities include initiating complaints, collaborating with teams, and reporting regulatory...Medical device
$110k - $130k
...Overview: Ampa is seeking a highly detail-oriented Regulatory Affairs Specialist to support our post-market regulatory activities and... ...Experience in quality systems is a strong plus, especially in a medical device startup environment where regulatory and quality work...Medical devicePermanent employmentH1bVisa sponsorship- Ampa Inc. in Palo Alto is seeking a Regulatory Affairs Specialist to ensure compliance in post-market activities for its neurostimulation systems... ...ideal candidate will have over 5 years of experience in medical device regulatory affairs, strong documentation skills, and...Medical device
- ...Regulatory Intelligence Specialist It started with a simple idea: what if surgery could be less invasive... ...years of experience in regulatory affairs and bachelor's degree in a relevant... ..., digital health, or complex medical devices. Familiarity with global regulatory...Medical deviceWork at officeLocal areaWorldwideFlexible hours
- ...Position: Regulatory Affairs Specialist Location: San Jose, CA Duration: 12+ Months Contract Total Hours/week: 40.00 1st Shift: Work hours: 8AM – 5PM Client: Medical Device Company Job Category: Regulatory Affairs / Compliance Level Of Experience: Seniority...Medical devicePermanent employmentContract workTemporary workH1bLocal areaRemote workShift workDay shift
$145k - $175k
A medical device innovation hub located in Los Gatos, CA is seeking a Sr. Software Engineer to contribute to software development for embedded... ...teams to deliver compliant software solutions and support regulatory submissions. Candidates should have extensive software...Medical device- ...Function of Position The Compliance Specialist 3 - Supply Chain Audits executes audit... ...in conformance with applicable regulatory standards (21 CFR Part 820, ISO 13485,... ...Experience working in a regulated medical device or life sciences manufacturing environment...Medical deviceContract workLocal areaWorldwideFlexible hours
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