STERIS Corporation

Senior Quality Engineer

STERIS Corporation$95K — $118K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in Engineering
  • 5+ years in Manufacturing/Quality Engineering or Quality Systems
  • Experience in an ISO certified environment
  • Familiarity with medical device and regulated industry standards
  • Knowledge of FDA QMSR and GMP regulations
  • Willingness to travel to local suppliers up to 10%-20%

Responsibilities

  • Serve as a Core Team Member in cross-functional development teams focusing on quality plans
  • Develop and implement statistically valid sampling plans and designs
  • Lead corrective actions and problem-solving activities
  • Review and recommend improvements to the quality system
  • Use data for statistical analysis and suggest process/product enhancements
  • Lead projects aimed at quality system and product improvements
  • Collaborate with other departments on quality issues

Benefits

  • Market Competitive pay
  • Extensive Paid Time Off and Holidays
  • Healthcare, Dental, and Vision benefits
  • Long- and Short-Term Disability coverage
  • 401(k) with company match
  • Maternity and Paternity Leave
  • Tuition Reimbursement and continuing education opportunities
  • Excellent advancement opportunities in a stable career
Full Job Description
Position Summary

The Senior Quality Engineer is responsible for managing processes and leading projects to maintain and improve the quality system in accordance with the requirements of, as appropriate, the following standards: IS0 9001, ISO 13485, MDSAP and FDA 21 CFR Part 820/211, EU MDR and other applicable standards. This role leads complaint/CAPA investigations, supplier quality improvement actions, operations production and process control improvements, and product and service quality improvements with the use of statistical techniques and other accepted quality principles. This role plans and executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems.

This position requires working onsite in our Conroe, TX facility Monday through Friday during core business hours 7:30 am to 4:30pm or 8:00am to 5:00pm.

What You'll do as a Senior Quality Engineer

  • Serves as the Core Team Member on cross-functional new product/service development teams with focus on the execution of quality plans and design/service transfer.
  • Develops and implements statistically valid sampling plans, designed experiments, capability studies, SPC and trend analysis in support of products and service improvements.
  • Leads process and product corrective actions and problem-solving activities.
  • Reviews the current quality system and recommend / implement improvements as needed.
  • Uses data to perform statistical analysis and recommend process / product changes to improve product and service quality.
  • Leads projects focused on quality system, product quality and service quality improvements.
  • Develops analyses and reports on the performance of the quality system.
  • Leads supplier audits and corrective actions.
  • Leads and supports internal and external quality system audits.
  • Instructs other STERIS employees in quality principles, effective corrective actions, and valid statistical techniques.
  • Collaborates with other departments and facilities within the company on quality related issues.
  • Supervises Quality Engineers and other Quality staff in the execution of their assigned duties and objectives.
  • Maintains product integrity and quality through the evaluation and disposition of nonconforming materials and processes.


The Experience, Skills and Abilities Needed

Required:

  • Bachelor's Degree in Engineering.
  • Minimum of 5 years of related experience required. (Manufacturing/Quality Engineering and/or Quality Systems).
  • 5+ years of experience working in an ISO certified environment.
  • Experience with medical device or other regulated industries.
  • Quality Management System Regulation FDA (QMSR) Certification or familiarity with QMSR/GMP regulations.
  • Ability to travel to local supplier sites up to 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 regulations such as ISO13485 and 21 CFR 820, preferred.
  • QMS software (such as TrackWise or other QMS software system), SAP or Oracle experience, preferred.


Other:

  • Shares technical knowledge with others in the team.
  • Identifies technical problems and provides innovative solutions.
  • Generates alternatives and takes reasonable risks while solving technical problems.
  • Generates detailed, high quality technical documentation to capture and communicate designs.
  • Completes tasks on time with minimal supervision while identifying potential risks.
  • Drives improvements in processes for better efficiency.
  • Utilizes advanced tools and best practices to track product and process metrics.
  • Mentors team members on timely task completion and actively participates in brainstorming sessions.


What STERIS Offers

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


Pay range for this opportunity is $95,000 - $118,000. This position is eligible for bonus participation.

Minimum pay rates offered will comply with county/city minimums, if higher than range listed. Pay rates are based on a number of factors, including but not limited to local labor market costs, years of relevant experience, education, professional certifications, foreign language fluency, etc.

STERIS offers a comprehensive and competitive benefits portfolio. Click here for a complete list of benefits: STERIS Benefits

Open until position is filled.

About STERIS Corporation

STERIS Corporation is a leading provider of infection prevention and other procedural products and services. The company was founded in 1985 and is headquartered in Mentor, Ohio. STERIS offers a wide range of products and services, including sterilization systems, surgical tables, and cleaning and disinfection products. The company has operations in over 100 countries and serves customers in the healthcare, pharmaceutical, and research industries. STERIS has been recognized for its commitment to sustainability and has received several awards for its environmental initiatives.
Learn more about STERIS Corporation
Size
16,422 employees
Market Cap
$18.2 billion
Industry
Net Income
$431.8 million
Founded
1985
5 Year Trend
+11.9%
Revenue
$3 billion
NASDAQ

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