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Sr Quality Compliance Specialist

Abbott

Healthcare Jobs

Sr Quality Compliance Specialist

full-timePosted: Jan 12, 2026

Job Description

Sr Quality Compliance Specialist
 

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to:

  • Career development with an international company where you can grow the career you dream of.
  • Free medical coverage for employees* via the Health Investment Plan (HIP) PPO
  • An excellent retirement savings plan with high employer contribution
  • Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
  • A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
  • A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

We are seeking a detail-oriented and proactive Sr. Quality Compliance Specialist to join our Compliance team. This role is critical in maintaining a state of continuous inspection readiness and ensuring compliance with applicable regulatory requirements, including ISO 13485 and MDSAP. The Compliance Specialist will lead and support internal and external audits readiness activities, manage audit-related documentation, and drive quality system improvements.

This position will be based out of our Abbott Diabetes Care in Alameda, CA and the individual will be expected to be onsite Monday-Friday.

What You'll Work On

  • Maintain and continuously improve the inspection readiness program to ensure the site is always prepared for regulatory and internal audits.
  • Coordinate and support internal audits, including planning, execution, reporting, and follow-up on corrective actions.
  • Serve as a support during external audits (e.g., Notified Bodies, FDA, Corporate), including logistics, documentation, and auditee coaching.
  • Monitor and ensure compliance with applicable regulatory standards applicable to ADC (ISO 13485, MDSAP, 21 CFR Part 820, etc.).
  • Maintain audit schedules, records, and metrics; track and trend audit findings to identify systemic issues.
  • Collaborate with cross-functional teams to ensure timely and effective CAPA implementation related to audit findings.
  • Support the development and delivery of training on audit readiness and compliance topics.
  • Participate in quality system improvement initiatives and support regulatory submissions as needed.

Required Qualifications

  • Bachelor’s degree in a scientific, engineering, or quality-related field.
  • 5+ years of experience in quality assurance or regulatory compliance in the medical device industry.
  • Strong knowledge of ISO 13485, MDSAP, and other applicable regulations.

Preferred Qualifications:

  • Experience supporting or leading audits (internal and external).
  • Excellent organizational, communication, and problem-solving skills.
  • Ability to work independently and collaboratively in a fast-paced environment

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:  www.abbottbenefits.com

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott, and on Twitter @AbbottNews.

Divisional Information

Medical Devices

General Medical Devices:

Our medical devices help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine fingersticks.

Diabetes

We’re focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions. We’re revolutionizing the way people monitor their glucose levels with our new sensing technology.



The base pay for this position is $90,000.00 – $180,000.00. In specific locations, the pay range may vary from the range posted.

Locations

  • Alameda, California, United States

Salary

Estimated Salary Rangemedium confidence

75,000 - 135,000 USD / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • inspection readiness program managementintermediate
  • audit coordination and supportintermediate
  • regulatory compliance (ISO 13485, MDSAP, 21 CFR Part 820)intermediate
  • CAPA implementationintermediate
  • training deliveryintermediate
  • organizational skillsintermediate
  • communication skillsintermediate
  • problem-solvingintermediate

Required Qualifications

  • Bachelor’s degree in scientific, engineering, or quality-related field (experience)
  • 5+ years experience in quality assurance or regulatory compliance in medical device industry (experience)
  • Strong knowledge of ISO 13485, MDSAP and other regulations (experience)

Responsibilities

  • Maintain and improve inspection readiness program
  • Coordinate and support internal audits (planning, execution, reporting, corrective actions)
  • Support external audits (Notified Bodies, FDA, Corporate) with logistics, documentation, coaching
  • Monitor compliance with regulatory standards
  • Maintain audit schedules, records, metrics; track trends
  • Collaborate on CAPA implementation for audit findings
  • Develop and deliver training on audit readiness and compliance
  • Participate in quality system improvements and regulatory submissions

Benefits

  • general: Career development with international company
  • general: Free medical coverage via Health Investment Plan (HIP) PPO
  • general: Excellent retirement savings plan with high employer contribution
  • general: Tuition reimbursement, Freedom 2 Save student debt program, FreeU education benefit

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Abbott logo

Sr Quality Compliance Specialist

Abbott

Healthcare Jobs

Sr Quality Compliance Specialist

full-timePosted: Jan 12, 2026

Job Description

Sr Quality Compliance Specialist
 

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to:

  • Career development with an international company where you can grow the career you dream of.
  • Free medical coverage for employees* via the Health Investment Plan (HIP) PPO
  • An excellent retirement savings plan with high employer contribution
  • Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
  • A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
  • A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

We are seeking a detail-oriented and proactive Sr. Quality Compliance Specialist to join our Compliance team. This role is critical in maintaining a state of continuous inspection readiness and ensuring compliance with applicable regulatory requirements, including ISO 13485 and MDSAP. The Compliance Specialist will lead and support internal and external audits readiness activities, manage audit-related documentation, and drive quality system improvements.

This position will be based out of our Abbott Diabetes Care in Alameda, CA and the individual will be expected to be onsite Monday-Friday.

What You'll Work On

  • Maintain and continuously improve the inspection readiness program to ensure the site is always prepared for regulatory and internal audits.
  • Coordinate and support internal audits, including planning, execution, reporting, and follow-up on corrective actions.
  • Serve as a support during external audits (e.g., Notified Bodies, FDA, Corporate), including logistics, documentation, and auditee coaching.
  • Monitor and ensure compliance with applicable regulatory standards applicable to ADC (ISO 13485, MDSAP, 21 CFR Part 820, etc.).
  • Maintain audit schedules, records, and metrics; track and trend audit findings to identify systemic issues.
  • Collaborate with cross-functional teams to ensure timely and effective CAPA implementation related to audit findings.
  • Support the development and delivery of training on audit readiness and compliance topics.
  • Participate in quality system improvement initiatives and support regulatory submissions as needed.

Required Qualifications

  • Bachelor’s degree in a scientific, engineering, or quality-related field.
  • 5+ years of experience in quality assurance or regulatory compliance in the medical device industry.
  • Strong knowledge of ISO 13485, MDSAP, and other applicable regulations.

Preferred Qualifications:

  • Experience supporting or leading audits (internal and external).
  • Excellent organizational, communication, and problem-solving skills.
  • Ability to work independently and collaboratively in a fast-paced environment

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives:  www.abbottbenefits.com

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott, and on Twitter @AbbottNews.

Divisional Information

Medical Devices

General Medical Devices:

Our medical devices help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with chronic pain and movement disorders, and liberate more than 500,000 people with diabetes from routine fingersticks.

Diabetes

We’re focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions. We’re revolutionizing the way people monitor their glucose levels with our new sensing technology.



The base pay for this position is $90,000.00 – $180,000.00. In specific locations, the pay range may vary from the range posted.

Locations

  • Alameda, California, United States

Salary

Estimated Salary Rangemedium confidence

75,000 - 135,000 USD / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • inspection readiness program managementintermediate
  • audit coordination and supportintermediate
  • regulatory compliance (ISO 13485, MDSAP, 21 CFR Part 820)intermediate
  • CAPA implementationintermediate
  • training deliveryintermediate
  • organizational skillsintermediate
  • communication skillsintermediate
  • problem-solvingintermediate

Required Qualifications

  • Bachelor’s degree in scientific, engineering, or quality-related field (experience)
  • 5+ years experience in quality assurance or regulatory compliance in medical device industry (experience)
  • Strong knowledge of ISO 13485, MDSAP and other regulations (experience)

Responsibilities

  • Maintain and improve inspection readiness program
  • Coordinate and support internal audits (planning, execution, reporting, corrective actions)
  • Support external audits (Notified Bodies, FDA, Corporate) with logistics, documentation, coaching
  • Monitor compliance with regulatory standards
  • Maintain audit schedules, records, metrics; track trends
  • Collaborate on CAPA implementation for audit findings
  • Develop and deliver training on audit readiness and compliance
  • Participate in quality system improvements and regulatory submissions

Benefits

  • general: Career development with international company
  • general: Free medical coverage via Health Investment Plan (HIP) PPO
  • general: Excellent retirement savings plan with high employer contribution
  • general: Tuition reimbursement, Freedom 2 Save student debt program, FreeU education benefit

Target Your Resume for "Sr Quality Compliance Specialist" , Abbott

Get personalized recommendations to optimize your resume specifically for Sr Quality Compliance Specialist. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Sr Quality Compliance Specialist" , Abbott

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Answer 10 quick questions to check your fit for Sr Quality Compliance Specialist @ Abbott.

Quiz Challenge
10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.