STERIS Corporation

Quality Analyst

STERIS Corporation$76K — $86K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in a scientific or related technical field
  • Minimum 1 year of experience in Manufacturing/Quality Engineering or Quality Systems
  • Minimum 1 year in an ISO certified environment
  • Experience in the medical device or regulated industries preferred
  • Working knowledge of FDA QSR/EU GMP regulations strongly preferred

Responsibilities

  • Coordinate daily tasks and provide support for Quality Technicians
  • Oversee pre-reviews and releases of products and lab samples
  • Execute product releases for non-conforming processing runs
  • Initiate corrective actions and participate in continuous improvement activities
  • Conduct internal audits and manage remediation of findings
  • Manage the creation and revision of quality system policies and procedures
  • Analyze data and recommend process changes to enhance quality

Benefits

  • 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
  • Tuition Reimbursement and continuing education programs
  • Career advancement opportunities in a stable environment
Full Job Description
Position Summary

The Quality Analyst in the STERIS Applied Sterilization Technologies (AST) Chester, NY facility is responsible for assisting in administration of the quality management system at a site to assure adherence to ISO 9001, ISO 13485, FDA 21 CFR Part 820/211, EU GMPs, ISO 17025, ISO 11137 and/or ISO 11135 and other applicable regulatory standards. The Quality Analyst leads complaint/CAPA investigations, supplier quality improvement initiatives, continuous improvement initiatives and countermeasures with the use of statistical techniques and other accepted quality principles. The Quality Analyst executes activities concerned with the development, implementation, maintenance, and continuous improvement of STERIS quality systems. The Analyst also supports production and quality operations by coordinating and performing problem-solving investigations, pre-reviews and final acceptance/run release of processing runs that contain non-conformances.

The Quality Analyst is responsible for the activities related to quality and regulatory compliance to ensure all product processing requirements are met in accordance with Customer specifications including calibrations, dosimetry results, generation of test methods, audits, scheduling, validations, record keeping and reporting.

This position requires working onsite in our Chester, NY facility from 8:00 am to 5:00 pm (or 8:30m to 5:30pm).

What You'll do as a Quality Analyst

  • Coordinate day-to-day tasks and direction for Quality Technicians/Senior Quality Technicians by providing technical support, mentoring and oversight.
  • Responsible for oversight of all product and/or report pre-reviews and releases conducted by Quality Technicians/Senior Quality Technicians.
  • Responsible for executing product and/or report releases for all processing runs/lab samples containing a non-conformance, including management of Customer communication and leading the associated non-conformance investigations.
  • Initiate and/or participate in corrective actions, problem-solving and continuous improvement activities.
  • Perform internal audits at other AST facilities, including identification of non-compliances and report generation. Responsible for managing remediation of internal audit observations assigned by site Quality Manager.
  • Manage creation of new quality system policies and procedures and revisions to existing policies/procedures.
  • Review collected data to perform statistical analysis and recommend process 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.
  • Lead quality system programs (i.e. calibration, maintenance, training, CAPA, complaints, non-conformances, supplier quality, management review, operational qualifications, document control, change control, risk management, etc.).
  • Overall responsibilities include commitment to ensure external and internal requirements are met according to documented policies, procedures, standards and regulations.
  • Perform other duties as assigned.


The Experience, Skills and Abilities Needed

Required:
  • Bachelor's degree (Scientific or related technical field)
  • Minimum of 1 year of combined Manufacturing/Quality Engineering and/or Quality Systems experience.
  • Minimum of 1 year of experience working in an ISO certified environment required.


Preferred:
  • Minimum of 1 year experience with medical device or other regulated industries, preferred.
  • Working knowledge of FDA QSR/ EUGMP regulations strongly preferred.


Other:
  • Excellent problem-solving skills
  • Focus on identification of potential issues and continuous improvement.
  • Experience working on cross-functional teams and on own initiative.
  • Demonstrated excellent organizational, oral and written communications skills.
  • Must have PC experience, as well as working familiarity of desktop applications including Excel, Word, and PowerPoint.
  • Ability to work in a fast-paced, regulated environment with strict deadlines.
  • Mathematical skills including practical application of fractions, percentages, ratios, proportions and algebra.


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

#LI-MO1

#LI-Onsite

Pay range for this opportunity is $76,000 - $86,000. 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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