Job Summary The candidate will work as a Quality Engineer in the Medical Device Industry, focusing on process engineering validation and managing complaints through Corrective and Preventive Actions (CAPAs). They will be responsible for writing and executing protocols related to

IQ/OQ/PQ

processes and implementing process changes as needed.

Even Simpler:

The job is for someone who checks if medical devices are made correctly by writing plans and fixing problems when they arise. They make sure everything works well by following certain steps. Skill Requirements Must-Have 12+ years Experience in Process Engineering within the Medical Device Industry Proficiency in Validation processes including writing and executing protocols Knowledge of

IQ/OQ/PQ

procedures Experience in handling Complaint Management Expertise in managing CAPA's Disclaimer Equal Opportunity Employer/Veterans/Disabled Benefit offerings include medical, dental, vision, term life insurance, short-term disability insurance, additional voluntary benefits, commuter benefits and 401K plan. Our program provides employees the flexibility to choose the type of coverage that meets their individual needs. Available paid leave may include Paid Sick Leave, where required by law; any other paid leave required by Federal, State or local law; and Holiday pay upon meeting eligibility criteria.

Disclaimer:

These benefit offerings do not apply to client-recruited jobs and jobs which are direct hire to a client To read our Candidate Privacy Information Statement, which explains how we will use your information, please visit https://www.entegee.com/candidate-privacy-information-statement/ The Company will consider qualified applicants with arrest and conviction records. #

GRPA Pay:

$75.00 - $86.00 per hour Expected hours: 40.0 per week

Benefits:

401(k) Dental insurance Health insurance Vision insurance People with a criminal record are encouraged to apply

Work Location:

In person