Closed listing
Director Global PQA
- Alameda, CA, United States
The base pay for this position is $172,000.00 – $344,000.00.
This opening has closed.
The original listing is kept below for reference.
Job details
- Pay
- The base pay for this position is $172,000.00 – $344,000.00.
- Experience
- Minimum 6 years of experience in the Medical Device industry or other FDA regulated industry.
- Posting language
- English
- Posted
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Search current openingsOriginal job description
Archived listing. The details below describe a past opening.
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, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries.
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.
- Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
- 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.
Job Title Director, Global Product Quality Assurance
The Opportunity
The Director, Global Product Quality Assurance directs and coordinates the on-market Quality Assurance activities for complaint handling, risk management, and product monitoring for Abbott Diabetes Care (ADC). Responsibilities include ensuring assigned Quality System responsibilities are completed efficiently and support outputs that improve customer satisfaction while maintaining compliance. Responsibilities include advising senior management regarding action plans for critical events related to product quality and product safety. The position also has direct interface and activity/strategy coordination with leadership teams in Global manufacturing, Commercial, Regulatory Affairs and Legal and extends to external business partners (TPMs) and regulators.
What You’ll Work On
- Responsible for implementing and maintaining the effectiveness of the quality system.
- Develop the product quality strategy to achieve business objectives while ensuring compliance with global regulatory requirements, making key decisions on product quality issues.
- Assure line of communication with DVP Quality Assurance and Senior Leaders on critical quality issues.
- Lead the Plant & Division Product Quality Assurance organizations. Assure business continuity in leadership positions and critical roles through talent management planning and development. Create a diverse organization and encourage diversity within the organization.
- Direct and implement programs across the Division to ensure improved customer satisfaction and compliance with regulatory requirements. Monitor customer complaint trends, identifies, communicates, and addresses adverse trends that may impact the business / customer.
- Provide feedback into product improvement initiatives using customer data.
- Provide oversight to disposition high-risk product non-conformance situations, assure adequate investigation and corrective actions are in place to prevent future occurrences.
- Support cost controls of both plant Quality Operations and Division staff. Authorizes cost efficiency projects that contributes to Division margin improvement initiatives.
- Directly responsible with interface with outside regulators (FDA, Ministries of Health, Notified Bodies) and other government regulatory bodies.
Required Qualifications
- Bachelor’s degree in a scientific or technical field.
- Minimum 6 years of experience in the Medical Device industry or other FDA regulated industry.
- Experience in a role in Quality/Compliance discipline while holding positions of leadership responsibility.
The base pay for this position is $172,000.00 – $344,000.00. In specific locations, the pay range may vary from the range posted.