Senior QA Compliance Leader Medical Devices
$100k - $125kPulse Biosciences, Inc.
A bioelectric medicine company is seeking a Sr. QA Compliance Specialist to ensure all company quality standards are met. Responsibilities include managing quality assurance functions, supporting regulatory compliance, and conducting internal audits. The ideal candidate has over 5 years of relevant experience and a BA/BS degree in science. This full-time role is based in Hayward, California, offering a salary range of $100k-$125k, with comprehensive benefits and a commitment to diversity and inclusion. #J-18808-Ljbffr
- Bayside Solutions is looking for a Sr. QA Compliance Specialist in Hayward, California. This role includes ensuring quality standards... ...compliance. The ideal candidate has over five years of experience in medical devices, a BA/BS degree, and knowledge of FDA regulations. This...SeniorMedical device
- Exelixis Inc is looking for a Senior GCP/GVP QA Manager to oversee QA systems for GCP/GLP operations. Responsibilities include supporting vendor audits, compliance guidance, and working with clinical teams to ensure adherence to regulatory standards. The ideal candidate...Senior
$100k - $125k
...environment to our diverse workforce. About The Role The Sr. QA Compliance Specialist will be responsible for ensuring all company and... ...periodic safety update reports as required. Support vigilance and medical device reporting activities, including Advisory Notices, Field...SeniorMedical deviceWork at officeLocal areaFlexible hours- A leading medical device company in California is seeking an experienced professional to lead Quality Assurance and Regulatory Affairs teams... ...leadership skills. The successful candidate will manage compliance with FDA regulations and direct quality initiatives. Candidates...SeniorMedical device
$114k - $228k
...Risk Evaluations. Candidates should have a Bachelor’s degree and at least 8 years of relevant experience, particularly in the medical device sector. The position offers a salary range of $114,000 to $228,000 and is expected to be onsite from Monday to Friday. #J-18808...SeniorMedical deviceMonday to Friday- A leading medical device company in Fremont is seeking an experienced Senior Director of Quality Assurance and Regulatory Affairs to lead quality functions and regulatory... ..., and managing cross-functional teams to ensure compliance. The ideal candidate will have over 15 years in...SeniorMedical device
- A global healthcare company is seeking a Senior Quality Engineer to oversee QA processes for innovative medical devices. The ideal candidate will have at least 5 years of experience in quality assurance and a bachelor's degree in engineering. Responsibilities include leading...SeniorMedical device
$148.7k - $297.3k
...is a global healthcare leader that helps people live... ...in diagnostics, medical devices, nutritionals and branded... ...Manages subordinate QA management and experienced... ...external management and senior-level representatives... ...business goals and compliance requirements. • Resolves...SeniorMedical deviceWork experience placementWorldwide$160k - $175k
...professional to maintain the Quality Management System (QMS) and ensure compliance with cGMP regulations. The role involves assessing, improving,... ...initiatives. The ideal candidate will have over 10 years of QA experience in the Pharma/Biotech industry, a strong...Senior$110k - $115k
The Chronicle Of Higher Education, Inc. is seeking a Senior Investigator to operate as Deputy Title IX Coordinator at Cal State East... ...investigations related to discrimination and harassment, ensuring compliance with various regulations. Candidates should possess a Juris...Senior- ...studies. This role involves developing statistical methodologies and analyzing data to ensure device safety. The ideal candidate will hold a PhD with over 8 years of experience in medical device clinical trials, possessing strong knowledge of regulatory guidelines and...SeniorMedical device
- ...at least 5 years of experience in Quality Engineering, preferably in medical devices, and a degree in engineering or a related field. The role involves managing daily activities, ensuring compliance with regulations, and analyzing data for product improvement. Besides...SeniorMedical device
- The Senior Director of Quality Assurance and Regulatory... ...Affairs This leader oversees all aspects of... ..., regulatory affairs, compliance, and post-market surveillance... ...within the QA and RA department to help... ...registrations and listings, and Medical Device Reporting in...SeniorMedical device
$105k - $125k
Calyxo, Inc. is seeking a Senior Clinical Research Associate to provide operational leadership... ...management and ensuring regulatory compliance while developing resources and training... ...of clinical research experience in medical device trials, with strong communication and...SeniorMedical device$140k - $150k
A medical device company based in Pleasanton, CA seeks a Clinical Project Manager to lead clinical trials from initiation to completion. This role collaborates with various stakeholders to ensure compliance with regulatory standards while overseeing the management of clinical...SeniorMedical device- ...a Staff Regulatory Affairs Specialist in Pleasanton, California. This senior role requires 12+ years in regulatory affairs, focusing on leading complex submissions and ensuring regulatory compliance throughout product development. The ideal candidate has extensive FDA...SeniorMedical device
- A global healthcare leader is seeking a Senior Regulatory Affairs Specialist in Pleasanton, CA. The role involves supporting product development... ...experience, including 4 years in regulatory within the medical device industry. A Bachelor’s Degree in a technical field is...SeniorMedical device
- ...complex agreements in the healthcare sector, and ensuring compliance with various regulations. Candidates should have a Juris Doctor... ...opportunity offers competitive compensation and benefits as part of a global leader in medical devices. #J-18808-Ljbffr Abbott LaboratoriesSeniorMedical device
- ...We are partnering with a growing, innovative medical device organization seeking a Senior Regulatory Affairs Specialist to support global regulatory strategy, submissions, and product lifecycle activities. This is a high-impact opportunity to work cross-functionally...SeniorMedical deviceLocal area
$100k - $150k
...We are partnering with a growing, innovative medical device organization seeking a Senior Regulatory Affairs Specialist to support global regulatory strategy, submissions, and product lifecycle activities. This is a high-impact opportunity to work cross-functionally...SeniorMedical deviceLocal area$140k - $160k
A medical device company in Pleasanton, CA, is seeking an experienced Senior NetSuite System Administrator to oversee and optimize the NetSuite ERP platform. The candidate will work collaboratively with Finance, Supply Chain, and other teams to enhance operational efficiency...SeniorMedical deviceRemote work- ...industry player is seeking a Regulatory Affairs Specialist with extensive experience in medical devices. This pivotal role involves overseeing complaint handling processes, ensuring compliance with regulatory standards, and actively participating in the development of...SeniorMedical device
- ...Senior Regulatory Affairs Specialist The Senior Regulatory Affairs Specialist supports... ...and executes regulatory activities for medical devices across the product lifecycle, with... ...evaluate current product and quality system compliance against new or evolving regulatory...SeniorMedical deviceWork experience placementWork at officeLocal area
$130k - $150k
Mizuho OSI is looking for a Systems Engineer in Union City, California. In this role, you'll be integral to the development of medical devices, from initial exploration to product testing. The ideal candidate will have a Bachelor's degree in engineering and 5-8 years of...SeniorMedical device- A public university in California is seeking a Senior Investigator to oversee Title IX investigations and ensure compliance with related laws. The role involves conducting investigations, providing leadership for educational programming, and working with various stakeholders...Senior
$25.96 - $29.81 per hour
...Quality Control (QC) Inspector in Union City, California. This role focuses on examining incoming and in-process products to ensure compliance with standards. Candidates should have a high school diploma and 2-5 years of relevant experience. Responsibilities include...Medical deviceHourly pay$155k - $200k
...Manager/AD/Director of QC to oversee Quality Control Operations in Fremont. This role involves leading all QC functions, ensuring compliance with regulatory standards, and optimizing laboratory IT systems. The ideal candidate has over 6 years of experience, strong...Senior$78k - $156k
...Senior Auditor, Global Compliance Audit Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing... ...leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines....SeniorMedical deviceRotational programWork experience placementLocal areaWorldwide$165k - $185k
...Apartments project in Fremont, CA. You will oversee daily construction operations, manage subcontractors, ensure safety and quality compliance. The ideal candidate has at least 7 years of construction experience, with 3 years in a leadership role, ideally in multifamily...SeniorFor subcontractor$225k
...managing complex family law cases, mentoring attorneys, and ensuring compliance with laws. Candidates should have at least 10 years of Family... ...of $225,000 per year and benefits including a 401K match, medical insurance, and vacation time are offered. #J-18808-Ljbffr...Senior
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