STERIS · 11 hours ago
Advanced Process Manufacturing Engineer
STERIS is a company that helps create a healthier and safer world by providing innovative healthcare and life science solutions. The Advanced Process Manufacturing Engineer will provide engineering and manufacturing technical expertise to support operations, establish and maintain manufacturing processes, and mentor engineering teams.
BiotechnologyHealth CareMedical Device
Responsibilities
Support all Company Quality Policies including ISO 13485, MDD, and FDA
Develops methods, standards, procedures, plans, processes, programs, and schedules to meet operational needs
Designs tooling, current products, fixturing, facilities and systems
Maintains the integrity of the above listing based on changing requirements and needs
Identifies and analyzes engineering related problems and/or opportunities
Determines and implements economical solutions to problems and opportunities which consistently continue to meet our customers’ needs and requirements
Conducts cost analysis, cost justification, and feasibility studies for product and process changes including investigation of innovative technologies
Performs training of operators and other personnel, as needed
Participates in cost reduction programs
Ensures operations and practices conform to safety regulations
Coordinate tests to verify performance and/or conformance to manufacturing standards
Audits/maintains systems to ensure integrity of Company and customer quality standards and requirements
Effectively evaluates and own commination with new vendors. Give guidance to peers and customers on current and future manufacturing capabilities
When needed, act as representative for operations in audit settings
Give feedback on division level decisions and initiatives
Lead smaller teams of Engineers or manufacturing personnel to support department goals and enhance manufacturing experience competency
Qualification
Required
Bachelor of Science degree required in Engineering or related technical field
Minimum of 10 years of manufacturing engineering experience
Minimum of 7 years' experience in medical device manufacturing or equivalent field
Lean manufacturing experience required; Six Sigma experience is a plus
Understanding of the medical device regulatory, document, and quality control issues
Proficiency in AutoCAD, SolidWorks, or equivalent drawing program
Familiarity with 3-D Programming & Analysis Package required—SolidWorks preferred
Strong interpersonal skills and verbal and written communication skills
Ability to lead and facilitate cross functional teams
Experience with tools such as SPC, PFMEA, and IQ/OQ/PQ Required
Preferred
MiniTab experience is a plus
Supplier audit experience is preferred
Benefits
Extensive paid time off and (9) added holidays
Excellent healthcare, dental, and vision benefits
Long/short term disability coverage
401(K) with company match
Maternity and parental leave
Additional add on benefits/discounts for programs such as pet insurance
Tuition reimbursement and continued educational programs
Excellent opportunities for advancement in a stable long-term career
Company
STERIS
STERIS is a leading provider of infection prevention and other procedural products and services, focused primarily on healthcare, pharmaceutical and medical device Customers.
H1B Sponsorship
STERIS has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (26)
2024 (28)
2023 (15)
2022 (33)
2021 (18)
2020 (19)
Funding
Current Stage
Public CompanyTotal Funding
$0.28M2010-05-21Post Ipo Debt· $0.28M
1998-12-01IPO
Leadership Team
Recent News
GlobeNewswire
2026-01-22
2025-11-05
Company data provided by crunchbase