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Saim Technologies

12 jobs near Columbus, OH

Saim Technologies

Mechanical Engineer

Gloucester, MA · On-site

Job Summary: We re seeking an experienced Mechanical Engineer to support design, engineering change control, and build activities for complex semiconductor capital equipment. The role demands hands ...

Saim Technologies

EquipmentEngineer

Los Angeles, CA · On-site

$93K - $119K/yr

Position : Equipment Engineer Location Northridge, CA-On Site Duration: Long Term Contract Key Responsibilities * Develop and execute Installation, Operational, and Performance Qualification (IQ/OQ ...

Saim Technologies

Mechanical Engineer

Gloucester, MA · On-site

Job Title: Mechanical Engineer Location: Gloucester, MA (Onsite) Job Summary: We re seeking an experienced Mechanical Engineer to support design, engineering change control, and build activities for ...

Saim Technologies

Salesforce Solution Architect

Washington, DC · On-site

$78 - $96.75/hr

Job Title: Salesforce Solution Architect Location: Washington, DC (Onsite) Experience: 9-11 Years Strong Salesforce platform knowledge: object model, security model, automation tools, and declarative ...

Supplier quality engineer

Saim Technologies

Salt Lake City, UT • On-site

Other

Posted 27 days ago

Job description

Position Summary:
Supplier Quality Engineer is responsible for ensuring suppliers deliver quality materials, components, and services in compliance with regulatory and organizational requirements within the medical device industry.

Key Responsibilities:
Ensure suppliers consistently deliver quality parts, materials, and services meeting client requirements.

  • Evaluate and onboard new suppliers into the Approved Supplier List (ASL).
  • Perform product and feature-level quality impact assessments and maintain necessary documentation.
  • Review and approve PPAP documentation including Control Plans, Process Flow Charts, Process Drawings, Capability Studies, DFMEA, and PFMEA.
  • Conduct supplier risk segmentation and maintain risk profiles.
  • Facilitate Supplier Quality Agreements and conduct supplier audits.
  • Coordinate supplier evaluation and selection activities for new suppliers or changes to existing products/processes.
  • Support and approve Process Validation activities (IQ, OQ, PQ), MSA/TMV, and Control Plans.
  • Route documentation in PLM systems and follow up for approvals and release.
  • Collaborate with Global Supplier Quality teams to implement Supplier Data Review (SDR) / Supplier Owned Quality (SOQ) activities.

Qualifications & Experience:
Bachelor s degree in engineering, Technical, or Scientific discipline.

  • Minimum 8 years of experience in Supplier Quality or related roles within the Medical Device industry.
  • Strong knowledge of regulatory standards, quality systems, and supplier quality processes.
  • Experience with PPAP, risk management, process validation, and quality tools (DFMEA, PFMEA, MSA).

Skills:
Strong analytical and problem-solving skills.

  • Excellent communication and stakeholder management abilities.
  • Ability to work collaboratively with cross-functional and global teams.
  • Proficiency in PLM systems and quality documentation tools.

Apply