About the role
Position Summary
The Senior Quality Specialist is responsible for assisting in administration of the quality functions at a site to assure adherence to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable regulatory standards. This role manages document control transactions, site record retention, calibration and inspection activities. In addition, the Senior Quality Specialist will lead Customer complaint, CAPA and NCR investigations, manage site audit activities, support supplier quality and customer assessments and lead risk management activities where appropriate. This role may also track and trend Quality data and support a site’s Management Review process.
What You'll Do as a Senior Quality Systems Specialist
- Manage the document control processes for the site.
- Lead Customer complaint investigations and ensure complete complaint documentation.
- Lead CAPA and NCR investigations and ensure proper documentation.
- Manage the DHR and batch record release process.
- Manage record retention practices within the site.
- Coordinate site calibration activities and recordkeeping.
- Manage site audit activities and recordkeeping.
- Support supplier quality and Customer assessment activities.
- Track, trend and analyze Quality data.
- Support targeted Lean activities.
- Complete other duties as assigned.
Required Experience
- Bachelor’s degree required in related technical field (i.e. Engineering, Chemistry, Biology).
- Minimum five (5) years of experience in a regulated industry (i.e. FDA/ISO 13485)
- Knowledge of standard quality analysis tools (Problem Solving/Root Cause Analysis)
- PC experience and working familiarity of common desktop applications including Excel and Word.
- Takes ownership of task and projects and seeks clarification if unsure of direction.
- Understands and can interpret appropriate regulatory standards.
- Ability to analyze and interpret data and use as input to problem solving.
Preferred
- Certification: ASQ, QSR, or AAMI certification preferred.
What STERIS Offers
We value our employees and are committed to providing a comprehensive benefits package that supports your health, well-being and financial future.
Here Is a Brief Overview Of What We Offer
- Market Competitive Pay with shift differential
- Extensive Paid Time Off and (9) added Holidays
- Excellent Healthcare, Dental and Vision Benefits
- Long/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 continued education programs
- Excellent opportunities for advancement in a stable long-term career
Equal Opportunity Employer
STERIS is an Equal Opportunity Employer. We are committed to equal employment opportunity to ensure that persons are recruited, hired, trained, transferred and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law. We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity.
Millions of jobs, with real people getting hired every day
Questions, answered
Click "Apply with JobAssist" – we tailor your resume and application to this role and submit it for your approval.
Yes. This role at STERIS was screened before publishing – we confirmed the employer before listing it.
The employer didn't disclose a salary range for this listing. JobAssist shows pay whenever it's available.
This position can be done from anywhere, with no in-office requirement.
Yes – every application is tailored from your profile and this job's requirements, and you can review and edit before it's sent.