Quality Engineer, Manufacturing Operations
Job Location:
Mahwah, NJ - USA
Monthly Salary:
Posted on:
Vacancies:
Job Summary
As a Quality Engineer Manufacturing Operations in Mahwah NJ you will support quality assurance quality control and continuous improvement activities across operations and other business functions. This role focuses on maintaining product and process quality driving preventive quality initiatives and supporting compliance with applicable regulations standards and internal quality requirements. You will work cross-functionally to promote quality throughout the product lifecycle and contribute to ongoing process improvements.
What You Will Do
Support quality assurance and quality control activities for products processes and manufacturing operations.
Lead and participate in quality improvement initiatives focused on reducing defects improving compliance and enhancing process performance.
Review analyze and investigate quality data to identify trends risks and opportunities for improvement.
Apply quality engineering principles risk-based methodologies and statistical techniques to support decision-making and process optimization.
Collaborate with cross-functional teams to address quality issues implement corrective actions and prevent recurrence.
Ensure compliance with applicable regulatory requirements quality standards and internal procedures.
Create review and maintain quality documentation reports and records in accordance with established requirements.
Represent the Quality function in cross-functional discussions audits projects and operational activities.
What You Will Need
Required Qualifications
Bachelors degree in Biomedical Engineering Mechanical Engineering or a related engineering discipline.
Minimum 0 years of experience
Preferred Qualifications
Internship experience in quality engineering manufacturing or related technical functions within regulated industries is strongly preferred.
Experience within the medical device industry.
Familiarity with ISO 13485 Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).
Knowledge of risk management methodologies and statistical analysis tools.
Experience supporting quality systems manufacturing quality or process improvement activities.
US20: $83400 - $133100 USD Annual
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Travel Percentage: 10%Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race ethnicity color religion sex gender identity sexual orientation national origin disability or protected veteran status. Stryker is an EO employer M/F/Veteran/Disability.Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about discussed or disclosed their own pay or the pay of another employee or applicant. However employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information unless the disclosure is (a) in response to a formal complaint or charge (b) in furtherance of an investigation proceeding hearing or action including an investigation conducted by the employer or (c) consistent with the contractors legal duty to furnish information.Required Experience:
IC
About Company
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongsid ... View more
