Quality Engineer II

The Quality Engineer II in our Conroe TX location is responsible for maintaining and improving the quality system in accordance with the requirements of as appropriate the following standards: IS0 9001 ISO 13485 MDSAP FDA 21 CFR Part 820/211 EU MDR and other applicable standards. This role supports complaint/CAPA investigations supplier quality improvement operations production and process controls and product and service quality improvement with the use of statistical techniques and other accepted quality principles. This role executes activities concerned with the development implementation maintenance and continuous improvement of STERIS quality systems.

This position requires working onsite in our Conroe TX location between the hours of 7:30am to 4:00pm or 8am to 5pm.

• Participate in cross-functional new product development teams with focus on product/ service quality and Quality System compliance.
• Develop and implement statistically valid sampling plans design experiments capability studies SPC and trend analysis.
• Initiate and/or participate in process and product corrective actions and problem-solving activities.
• Update/establish documented work instructions as needed.
• Review collected data to perform statistical analysis and recommend process/product changes to improve quality.
• Monitor and report on performance metrics.
• Instruct other STERIS employees in quality principles effective corrective actions and valid statistical techniques.
• Collaborate with other departments and facilities within the company on quality related issues.
• Maintain product integrity and quality through support of evaluation and disposition of nonconforming materials.
• Perform supplier audits and quality system audits; provide guidance on corrective actions.
• Perform other duties as assigned

Required:

• Bachelors Degree in Engineering.
• Minimum of 3 years of related experience (Manufacturing/Quality Engineering and/or Quality Systems) required.
• Minimum of 3 years of experience working in an ISO certified environment.
• Ability to travel domestically 10 %- 20%.

Preferred:

• ASQ QSR Certification or familiarity with QSR/GMP regulations preferred.
• Experience with statistical analysis software and Visio preferred.
• Knowledge of medical device industry standards ISO 13485 and FDA 21 CFR Part 820/211 preferred.
• QMS software(such as TrackWiseor other QMS software system) SAP or Oracle experience preferred.

We value our employees and are committed to providing a comprehensive benefits package that supports your health wellbeing and financial future.

Here is just a brief overview of what we offer:

• Market Competitive pay
• Extensive Paid Time Off and added Holidays
• Excellent Healthcare Dental and Vision benefits
• Long- and Short-Term Disability coverage
• 401(k) with a company match
• Maternity and Paternity Leave
• Additional add- on benefits / discounts for programs such as Pet Insurance
• Tuition Reimbursement and continuing education programs
• Excellent opportunities for advancement in a stable long-term career

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