Quality Manager

Ashland

Columbus, OH, US
Not specified; not specified; comprehensive benefi...
Hybrid
5+ years medical device manufacturing experience
Iso 13485 and 21 cfr 820 knowledge
Experience with eu mdr regulations
This role supports the verification, enhancement, and improvement of processes for medical device design, manufacturing, testing, and release

Job Summary

  • This role supports the verification, enhancement, and improvement of processes for medical device design, manufacturing, testing, and release.
  • The position involves leading supplier quality activities, facility compliance, and conducting various customer, regulatory, and internal audits.
  • Ashland offers a comprehensive benefit package including medical, dental, and vision starting on Day 1, along with a 401(k) plan with company match.

Matching Summary

This role supports the verification, enhancement, and improvement of processes for medical device design, manufacturing, testing, and release.

Salary

Not specified; Not specified; Comprehensive Benefit package, Medical, Dental and Vision starting on Day 1; 401(k) plan with company match; Referral bonus plan

Skills & Requirements

Must-have

  • 5+ years medical device manufacturing experience
  • ISO 13485 and 21 CFR 820 knowledge
  • Experience with EU MDR regulations
  • Medical device design controls expertise
  • Lead internal and external quality audits

Nice-to-have

  • Project management abilities for continuous improvement
  • Strong verbal and written communication skills
  • Ability to translate technical information simply
  • Collaborative relationship building
  • Positive and constructive problem solving attitude

Key Requirements

  • Bachelor's degree in chemistry or chemical engineering
  • 5+ years experience in medical device manufacturing
  • Knowledge of global regulatory submissions (510k, CE mark)

Work Rights

Not specified

Tailored Resume

Cover Letter