Skip to main content
Tallo logoTallo logo

Find Jobs

Find Jobs Near You – Available Work in Your Location

Engineering
Validation Engineer
Airmont, NY

Find & Apply For Validation Engineer Jobs in Airmont, New York

Browse jobs from a variety of sources below, sorted with the most recently published, nearest to the top. Click the title to view more information and apply online.

Skip to job details
Now viewing: Quality Engineer - 27693
Apply for this opportunity

To apply for this job, you'll continue to an external website or email application.

iMPact Business Group

Quality Engineer - 27693

Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
73
out of 100
Average of individual scores

Were these scores useful?

Job Description

Quality Engineer - 27693 at iMPact Business Group Quality Engineer - 27693 at iMPact Business Group in Tallman, New York Posted in 11 days ago.

Type:

full-time Quality Engineer | Medical Device Industry 12-Month+ Contract | 1st Shift | Monday-Friday, 8:00 AM-5:00 PM ET | Hybrid | 3 Days Onsite Our client, a global leader in the medical device industry , is seeking a Quality Engineer to support quality assurance, process control, validation, and continuous improvement within a highly collaborative manufacturing environment. This is a great opportunity for a quality professional who enjoys working cross-functionally and making a direct impact on product quality, process performance, and regulatory compliance . Key Focus Quality Engineering Process Control & Improvement Validation & Change Control PPAP & First Article Inspection Quality Management Systems SOPs & Inspection Plans What You'll Do Provide quality engineering support across quality assurance, quality control, and preventative activities Develop and implement methods for process control, improvement, testing, and inspection Lead quality initiatives and projects while maintaining compliance with applicable regulations and standards Support product transfers and supplier change requests Manage PPAP activities for new and modified parts Lead validation projects for new equipment and processes Develop and execute First Article Inspection (FAI) strategies Create and update SOPs and inspection plans through the change management system Partner with cross-functional teams and stakeholders to identify and resolve quality issues What We're Looking For Bachelor's degree in Biomedical Engineering, Mechanical Engineering, or a related field 1+ year of quality engineering or related industry experience Experience in medical device manufacturing or another regulated environment Strong understanding of Quality Management Systems (QMS) and change management Experience with validation activities and change control Strong analytical and problem-solving skills Excellent written and verbal communication Proficiency with Microsoft Word, Excel, and PowerPoint Ability to manage multiple priorities in a fast-paced environment Interested in learning more? Send me a message or apply today!