Regulatory Affairs Associate
Lakeside, California, United States
Job Description
Title: Regulatory Affairs Associate
Location: Santa Clara, California
Duration: 12 Months
100% Onsite
Qualifications:
Preferred Qualifications:
Consultants Eligible Benefits Upon Waiting Period:
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines.
Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives. Abbott believes all employees are essential to creating life-changing breakthroughs, performing key duties to create life-changing breakthroughs.
Location: Santa Clara, California
Duration: 12 Months
100% Onsite
Qualifications:
- Bachelor's degree in Regulatory Affairs, Biomedical Engineering, or a related field.
- Minimum 4 years of experience in a regulated industry and experience in related operations areas such as quality control, quality engineering, document control, regulatory compliance, engineering and/or regulatory.
- Experience working with policies and procedures impacting documentation and documentation practices.
- Proven experience in labeling design and development from a regulatory perspective.
- Strong knowledge of regulatory requirements for medical device labeling.
- Proficiency in SAP MD and other relevant software systems.
- Excellent communication and collaboration skills.
- Detail-oriented with strong organizational skills.
- Good people relations, able to work independently with good administrative and time management skills. PC and Microsoft Office experience.
Preferred Qualifications:
- Experience with medical device labeling or labeling for highly regulated industry and international regulatory requirements.
- Familiarity with Adobe Acrobat Pro, SAP, and other content management systems.
- Substantial experience coordinating and executing project activities in a highly regulated industry.
Consultants Eligible Benefits Upon Waiting Period:
- Medical and Prescription Drug Plans
- Dental Plan
- Vision Plan
- Health Savings Account (for High-Deductible Health Plans)
- Flexible Spending Accounts (Health, Limited Purpose, Dependent Care, Commuter Parking and Commuter Transit)
- Supplemental Life Insurance
- Short Term Disability (coverage varies by state)
- Long Term Disability
- Critical Illness, Hospital coverage, Accident Insurance
- MetLife Legal, MetLife ID Fraud, and MetLife Pet Insurance
- 401(k)
Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines.
Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives. Abbott believes all employees are essential to creating life-changing breakthroughs, performing key duties to create life-changing breakthroughs.
- Published on 14 Oct 2026, 1:19 PM
Apply
Career Focus: Regulatory/Compliance
This role is part of a curated selection of life science opportunities featured on Xtalks. Employers may request edits or removal here.
Similar Jobs
Regulatory Affairs Intern
At Johnson & Johnson, we believe health is everything. Our strength...
Manager of Regulatory Affairs
Remote | Approximately 20% travel to sites across the South, Southeast, ...
Director of Global Privacy and...
We are seeking an experienced Director of Global Privacy and Compliance ...
Senior Regulatory Affairs Specialist (Wound...
At Johnson & Johnson, we believe health is everything. Our strength...