Associate Specialist Quality-Document Control

Responsibilities

• Implement and maintain the effectiveness of the Quality System
• Manage document versioning, approvals, and distribution
• Participate in Quality System processes including training, CAPA activities, and quality audits
• Maintain life cycle management systems and databases
• Complete documentation in a timely manner in accordance with business standards
• Assist in determining quality attributes and requirements
• Participate in cross-functional teams to drive functional performance

Requirements

• Bachelor's degree or an equivalent combination of education and work experience
• 0-2 years of experience (entry-level position)

Preferred Qualifications

• Knowledge of FDA Quality System Requirements and US Code of Federal Regulations for Devices
• Knowledge of ISO 13485 standards
• Knowledge of document lifecycle and version control
• Strong attention to detail and ability to manage multiple priorities in a fast-paced environment
• Demonstrated problem-solving, critical-thinking, and organizational skills
• Proficiency in using various databases and computer software

Benefits

• Career development opportunities within an international company
• Eligibility for free medical coverage via the Health Investment Plan (HIP) PPO plan
• Retirement savings plan with high employer contribution
• Tuition reimbursement and student debt programs
• Access to FreeU education benefits

About the Company

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.