Posted:
12/3/2024, 10:21:14 AM
Location(s):
Plano, Texas, United States ⋅ California, United States ⋅ Texas, United States ⋅ Maple Grove, Minnesota, United States ⋅ Minnesota, United States ⋅ Los Angeles, California, United States
Experience Level(s):
Junior
Field(s):
Medical, Clinical & Veterinary
Workplace Type:
On-site
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:
For years, Abbott’s medical device businesses have offered technologies that are faster, more effective, and less invasive. Whether it’s glucose monitoring system, 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.
The Opportunity
Our team currently has an opportunity for a Clinical Quality Associate. This new team member will be 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. Responsible for compliance with applicable regulations and standards, as well as Corporate and Divisional Policies and procedures.
This position is onsite at our Maple Grove, MN; Plano, TX; or Sylmar, CA sites.
What You’ll Work On
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.
Responsible for compliance with applicable regulations and standards, as well as Corporate and Divisional Policies and procedures.
Study Support
Review study documents; identify compliance concerns to applicable regulations, standards, and internal procedures
With oversight and mentorship, act as a resource to clinical study teams regarding compliance solutions to meet requirements of regulations, standards, and Abbott procedures
Contribute to WI/procedure development related to execution of clinical research projects
Understanding of principles of GCP regulations and standards, including 21 CFR Parts 50, 54, 56, 812 and ISO 14155
Internal/External Audits
Support preparation for internal and external audits
May perform internal assessments and quality checks as assigned
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.
CAPA & General
May support CAPA related tasks, including review of documentation for accuracy and completeness
May support other areas of the clinical quality system as needed: training, document control, etc.
Job/Technical Knowledge
Understanding of Good Clinical Practice (GCP) including U.S. regulations and international standards, as well as other relevant regulations and procedures is an asset
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
Required
Preferred
* 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.
The base pay for this position is
$57,300.00 – $114,700.00In 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
Website: https://abbott.com/
Headquarter Location: Illinois City, Illinois, United States
Employee Count: 1001-5000
Year Founded: 1944
IPO Status: Public
Last Funding Type: Post-IPO Debt
Industries: Biotechnology ⋅ Emergency Medicine ⋅ Genetics ⋅ Health Care ⋅ Health Diagnostics ⋅ Manufacturing ⋅ Medical ⋅ Medical Device ⋅ Nutrition ⋅ Pharmaceutical