About Abbott
Abbott is a global healthcare leader, creating breakthrough science to improve people’s health. We’re always looking towards the future, anticipating changes in medical science and technology.
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:
The Opportunity
This position works out of our Alameda, CA location in the Diabetes Care division where 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.
As the Quality Engineer II you will be responsible for activities related to design control; qualification; specification and corrective and preventative action of medical devices, including software as a medical device (SaMD), in-vitro, diagnostic devices, consumer devices, and accessories. You will lead/support design planning efforts to include heading CFTs; establishing deliverables and tracking completion for complex projects. You will lead/support complex investigations and CAPA activities.
What You’ll Work On
• Drives alignment in cross functional meetings acting as QA representative on new and on market product design projects to ensure compliance with the design control process.
• Reviews and approves engineering changes in a timely manner
• Collaborates with R&D and Marketing to support mobile app deployment activities (for Software as a Medical Device projects)
• Drives alignment during cross functional review and approval of impact assessments, root-cause analysis investigation and resolution activities
• Reviews and approves batch records for products used in design verification/validation testing and clinical investigations
• Ensures Device History File (DHF) and Device Master Record (DMR) are in compliance with regulatory standards and quality management policies and procedures
• Collects, organizes, and monitors information related to quality and process improvement
• Participates in internal & external audits and ensures audit responses are submitted in a timely manner
Required Qualifications
Minimum 5 years applicable technical/engineering experience and demonstrated use of Quality tools/methodologies.
Minimum 2 years regulated environment such as medical devices, pharmaceutical products, food manufacturing, aerospace, or automotive.
* Participants who complete a short wellness assessment qualify for FREE coverage in our HIP PPO medical plan. Free coverage applies in the next calendar year.
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 and @AbbottGlobal.
The base pay for this position is
$90,000.00 – $180,000.00In specific locations, the pay range may vary from the range posted.
Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf
EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf