Sr. Quality Compliance Specialist
Sr. Quality Compliance Specialist
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$ 86700 - 173300
1 Vacancy
Job Description
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. Youll 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 bachelors 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 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.
What Youll 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
- Bachelors 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:
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 on Facebook at and on Twitter @AbbottNews.
Divisional Information
Medical Devices
General Medical Devices:
Our medical devices help more than 10000 people have healthier hearts improve quality of life for thousands of people living with chronic pain and movement disorders and liberate more than 500000 people with diabetes from routine ngersticks.
Diabetes
Were focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions. Were revolutionizing the way people monitor their glucose levels with our new sensing technology.
The base pay for this position is
$86700.00 $173300.00In specific locations the pay range may vary from the range posted.
JOB FAMILY:
Operations Quality
DIVISION:
ADC Diabetes Care
LOCATION:
United States > Alameda : 1360-1380 South Loop Road
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
No
MEDICAL SURVEILLANCE:
No
SIGNIFICANT WORK ACTIVITIES:
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day) Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day) Keyboard use (greater or equal to 50% of the workday)Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
EEO is the Law link - English: EEO is the Law link - Espanol: Experience:
Senior IC
Employment Type
Full-Time
Key Skills
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