Senior Clinical Quality Associate

About Abbott 

For years, Abbott’s medical device businesses have offered technologies that are faster, more effective, and less invasive. Whether it’s glucose monitoring systems, innovative therapies for treating heart disease, or products that help people with chronic pain or movement disorders, our medical device technologies are designed to help people live their lives better and healthier. Every day, our technologies 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. 

Abbott Vascular provides innovative, minimally invasive and cost-effective products for treatment of vascular disease. Our extensive portfolio includes drug-eluting stents, bare metal stents, guide wires, balloon dilatation catheters, imaging catheters and software, vessel closure devices and peripheral stents 

Our location in Maple Grove, MN, currently has an opportunity for a Senior Clinical Quality Associate.  This position could also be based out of our Plano, TX site. 

THIS IS AN IN-HOUSE POSITION - NO REMOTE 

NO RELOCATION ASSISTANCE IS AVAILABLE FOR THIS POSITION. 

WHAT YOU'LL DO: 

Primary Job Function: 

Responsible for supporting Global Clinical Affairs personnel globally in ensuring compliance with medical device and GCP regulations and standards, as well as company policies and procedures and other applicable requirements. 

Core Job Responsibilities: 

Responsible for compliance with applicable regulations and standards, as well as Corporate and Divisional Policies and procedures. 

Study Support 

· Review study documents for compliance to applicable regulations, standards, and internal procedures 

· Act as a resource to clinical study teams regarding compliance to regulations, standards, and Abbott procedures 

· Support compliant execution of clinical research projects 

· Preferably has prior experience with GCP regulations and standards, including 21 CFR Parts 50, 54, 56, 812 and ISO 14155 

CAPA 

· Generate CAPA documentation, including investigations, resolution plans, and implementation reports 

· Ensure work complies with regulatory and compliance standards 

· Work cross-functionally to develop pragmatic and compliant solutions for CAPA activities 

· Drives continuous process improvement 

· Strong written communication skills 

Internal/External Audits 

· Key player in the preparation and overall support for internal and external audits, including responding to audit findings such as through the CAPA process 

· May perform internal compliance assessments and/or audits 

· Support project teams in preparation for regulatory authority inspection or audit, or corporate or divisional regulatory compliance audit 

May support other clinical quality tasks as requested and as need arises. 

Position Accountability / Scope: 

 Job/Technical Knowledge: 

· Strong understanding of Good Clinical Practice (GCP) including U.S. regulations and international standards, Quality Assurance/Control, as well as of relevant regulations and procedures 

· Cooperation/Teamwork: team player with autonomy capable of working independently under minimal supervision 

· Planning and organizational skills: organizes self in an efficient manner 

· Problem solving: gathers information before making decisions; weighs alternatives against objectives and arrives at reasonable decisions 

· Adaptability: remains open-minded; performs a wide variety of tasks and changes focus quickly as demands change 

· Initiative / Innovation: explores alternative successful ways of working and tools; able to challenge conventional practices; creates novel solutions to problems 

EDUCATION AND EXPERIENCE YOU’LL BRING: 

REQUIRED QUALIFICATIONS 

• Bachelors Degree (± 16 years), In related field OR an equivalent combination of education and work experience 

• Minimum 4 years, Related work experience with a solid understanding of specified functional area. 

• Broad knowledge and application of business concepts, procedures and practices.  

• Will perform this job in a quality system environment. Failure to adequately perform tasks can result in noncompliance with governmental regulations.  

• Learns to use professional concepts and company policies and procedures to solve routine problems.  

• Works on problems of limited scope.  

• Independent decision making required. 

PREFERRED QUALIFICATIONS  

Prefer at least 5 years of medical devices, clinical research experience, or related industry. Prefer at least 3 years of related work experience in Quality role in medical device area and/or clinical trial environment. Prefer GCP audit experience. 

WHAT WE OFFER : 

At Abbott, you can have a good job that can grow into a great career. We offer: 

A fast-paced work environment where your safety is our priority 

Training and career development, with onboarding programs for new employees and tuition assistance 

Financial security through competitive compensation, incentives and retirement plans 

Health care and well-being programs including medical, dental, vision, wellness and occupational health programs 

Paid time off 

401(k) retirement savings with a generous company match 

The stability of a company with a record of strong financial performance and history of being actively involved in local communities 

Learn more about our benefits that add real value to your life to help you live fully:  www.abbottbenefits.com 

Follow your career aspirations to Abbott for diverse opportunities with a company that provides the growth and strength to build your future. 

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.