7-10 years of relevant experience or equivalent education
Experience with QS / ISO Systems
Knowledge of ISO13485 and FDA 21 CFR Part 820 and 11
Previous auditing experience
Familiarity with ISO class 8 cleanroom requirements
Ability to drive change and influence team culture
Responsibilities
Monitor and improve Quality System Elements
Ensure compliance with safety and standard operating procedures
Conduct batch record reviews to approve product releases
Develop and analyze validation protocols and reports
Facilitate audit findings and complaint investigations
Mentor junior Quality Engineers in daily tasks
Act as liaison between customers and the company
Benefits
Medical, dental, and vision insurance
Company-paid life and disability insurance
Paid time off
Generous 401(k) match
Full Job Description
Job Description Summary
The Senior Quality Engineer is responsible to monitor and continuously improve upon the Quality System Elements.
Essential Functions
Qualification for this position is predicated not only on satisfactory performance of essential duties as outlined below, but also on compliance with general company policies and procedures and any other duties as assigned. Strict compliance with Company's Attendance Policy is considered an essential duty and responsibility. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Know and follow all of the Company's safety rules, such as safe work practices and standard operating procedures.
Serve as a good role model to employees for safe work practices and behavior by conducting yourself professionally, keeping in mind your own safety and the safety of others.
Learn and master all necessary areas of the quality system.
Follow Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).
Perform batch record review to release products.
Develop, review and approve validation protocols and final reports. Analyze the validation data. Assist in deviation resolution and corrective actions.
Facilitate audit finding and complaint investigation meeting.
Review and approve complaint, CAR and exception report.
Act as a liaison between customer and MGS.
Act as subject matter experts on quality system processes.
Assist in development of control plan, PFMEA, visual criteria, manufacturing work instruction, incoming inspection plan and in process inspection report for new products.
Provide disposition of nonconforming products.
Review and approve engineering change package.
Update manufacturing related procedures and quality system procedures to address gaps.
Mentor QEs in their daily tasks.
Continuously improve the quality system.
Acts as backup for the quality manager during 2nd and 3rd party audits.
Perform internal audit.
Any other duties as assigned.
Competencies
Positive Attitude
Teamwork and Cooperation
Flexibility
Initiative
Judgement
Customer Focused
Organization
Attention to Detail
Ability to multi-task
Critical thinking
Communication skills
Experience and Skills A qualified Senior Quality Engineer candidate would fulfill these requirements:
High School Diploma or equivalent is required.
Seven to ten years of experience and/or training, or equivalent combination of education and experience.
QS / ISO System experience.
Understanding/working knowledge of ISO13485 and FDA 21 CFR Part 820 and 11.
Previous auditing experience.
Experience with ISO class 8 cleanroom.
Experience in working with team, ability to drive change and influence cultural change.
Job Benefits To learn more about MGS Mfg. Group, go to www.mgsmfg.com. We offer a competitive benefits package including medical, dental and vision insurance, company paid life and disability insurance, paid time off, and a generous 401(k) match.