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This is where you make a difference in our patients’ safety. As a member of the Baxter Quality team, you will play an essential part in our mission of saving and sustaining lives. Quality is important throughout the entire product lifecycle and works collaboratively with all areas of the organization. Because Quality touches everything Baxter does, a role in Quality provides many opportunities for growth, learning and a successful career that has a daily impact on people’s lives.
Job Responsibility
Conduct inspections to ensure compliance with quality and regulatory requirements
Perform measurements to ensure compliance to the drawing
Conduct floor audits and inspections of manufacturing processes and equipment to ensure compliance with quality and regulatory requirements
Create non-conforming material reports and perform containments as needed
Maintain accurate and detailed records of inspections
Develop and implement corrective actions to address quality issues
Participate in investigations and root cause analysis of quality issues
Collaborate with cross-functional teams to resolve quality issues
Provide training and guidance to production staff on quality procedures and regulatory requirements
Work closely with cross-functional teams, including production, engineering, and quality assurance, to ensure effective communication and collaboration on quality-related matters
Participate in team meetings and contribute to discussions on quality improvement and best practices
Contribute to continuous improvement initiatives by providing feedback on inspection processes and suggesting enhancements to quality control procedures
Proactively contributes to zero harm in the workplace for all employees by complying with legal and corporate (EHS) Environmental Health & Safety requirements, safe work practices, and EHS policies and procedures consistently
Report all hazards, near misses and incidents as soon as practicable and participate in identifying actions to prevent harm from occurring to our people and/or our environment
Employees at every level are responsible for quality (GMP) Good Manufacturing Processes and regulatory performance in the department to ensure quality program is met
Ensure compliance with FDA, ISO and other government regulations, legal documents and safety and ethical standards, obtaining legal compliance training
Requirements
High school diploma or equivalent required
1-3 years of experience in a quality control environment
Experience with quality management systems, including experience in implementing and maintaining QMS
Experience with measuring tools and reading drawings (GD&T)
IPC certification, such as IPC-A-600 or IPC-J-STD-001 required within 30 days
Intermediate knowledge of quality control principles and medical device manufacturing processes
Experience measuring tooling and equipment
What we offer
Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer
medical and dental coverage that start on day one
insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
Flexible Spending Accounts
educational assistance programs
time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service