Senior Manager Quality
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Job Location:
Des Plaines, IL - USA
Monthly Salary:
$ 127300 - 254700
Posted on:
Yesterday
Vacancies:
1 Vacancy
Job Summary
JOB DESCRIPTION:
Senior Manager Quality
Working at Abbott
At Abbott you can do work that matters grow and learn care for yourself and your 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.
- Employees can qualify forfree medical coverage in ourHealth Investment Plan (HIP) PPOmedical plan in the next calendar year.
- An excellent retirement savings plan with a 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 worldwide 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 the best place to work for diversity working mothers female executives and scientists.
The Opportunity
At Molecular Diagnostics we realize the potential of personalized care as the laboratorys most trusted and preferred source for molecular diagnostic solutions. We are a division of Abbott Laboratories a global diversified healthcare innovator with a legacy of pioneering work in medical diagnostics.
The position of Senior Manager Quality within our Molecular Diagnostics Business Unit located in Des Plaines Illinois. This position provides leadership and guidance for the quality department with overall responsibility to maintain high quality levels on all products while achieving high efficiency. Responsible for Nonconformance/CAPA process management and oversight including Material Review Board CAPA Review Board process metrics quality record approvals and partnering with cross-functional areas on strategic initiatives. Responsible to lead Global QA initiatives to implement quality systems/processes across the organization and Division achieving quality improvements cross plant consistency and regulatory compliance. Responsible for developing goals objectives procedures policies and systems that are in line with company goals and objectives mission and vision and FDA/ISO regulations. Daily responsibilities include ensuring that the manufacturing quality system requirements are effectively established and maintained reports on the performance of the quality system to management with executive responsibility for review. Assures the overall quality of products and services meet internal and external customer requirements.
What Youll Work On
- Oversee and execute the Nonconformance and CAPA subsystems including Material Review Board (MRB) and CAPA Review Board activities Material control processes Investigations and root cause analysis development and implementation of resolution plans and effectiveness checks to verify corrective actions.
- Apply Statistical Process Control (SPC) and process monitoring techniques to ensure product and process stability.
- Utilize statistical analysis to interpret data identify trends and drive continuous improvement initiatives.
- Implement and maintain risk management strategies to mitigate potential issues and ensure compliance with regulatory standards.
- Demonstrate strong critical thinking and problem-solving skills to support decision-making and process improvements.
- Interacts frequently with internal and external management and senior-level representatives concerning projects operational decisions scheduling requirements and or contractual clarifications.
- Provides direction and guidance to exempt specialists and/or supervisory staff who exercise significant latitude and independence in their assignments.
- May supervise non-exempt employees.
- Keeps the organizations vision and values at the forefront of decision making and action.
- Demonstrates effective change leadership.
- Builds strategic partnerships to further departmental and organizational objectives.
- Develops and executes organizational and operational policies that affect one or more groups by utilizing technical/professional knowledge and skills.
- Monitors compliance with company policies and procedures (e.g. compliance with FDA BSI EEO regulations etc.).
- Makes decisions regarding work processes or operational plans and schedules to achieve department objectives.
Required Qualifications
- Bachelors degree in a scientific or technical discipline or related field or an equivalent combination of education and work experience.
- 9 years related work experience.
- Proven performance in nonconformance management and reduction value improvement risk reduction and cost containment.
- Strong project management and people leadership skills.
- Ability to work in a highly matrixed and geographically diverse business environment.
- Strong leadership skills including goal setting and providing positive and constructive feedback to build relationships and improve business results.
- Effective team collaboration in a fast-paced changing environment.
- Excellent verbal and written communication skills with the ability to communicate effectively at multiple levels within the organization.
Preferred
- Masters Degree in related field
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.
The base pay for this position is
$127300.00 $254700.00In specific locations the pay range may vary from the range posted.
JOB FAMILY:
Operations Quality
DIVISION:
AMD Molecular
LOCATION:
United States > Des Plaines : DP01
ADDITIONAL LOCATIONS:
WORK SHIFT:
Standard
TRAVEL:
Yes 10 % of the Time
MEDICAL SURVEILLANCE:
Not Applicable
SIGNIFICANT WORK ACTIVITIES:
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day) Keyboard use (greater or equal to 50% of the workday) Work in a clean room environmentAbbott 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 Manager
Key Skills
- Continuous Integration
- Quality Assurance
- FDA Regulations
- Root cause Analysis
- TFS
- Food Processing
- ICH Q10
- Jira
- Software Testing
- Quality Management
- Selenium
- Github
About Company
WHO WE ARE CREATING LIFE-CHANGING TECHNOLOGY From removing the regular pain of fingersticks as people manage their diabetes to connecting patients to doctors with real-time information monitoring their hearts, from easing chronic pain and movement disorders to testing half the world’s ... View more
