ISO 13485 Jobs in USA

For further inquiries regarding the following opportunity please contact one of our Talent Specialists: Neha at Muskan at Title: Quality Engineer II Location: Kennebunk ME Duration: 9 Months Job Description : Must haves: Proficiency in Microsoft Office and Excel Ability More...

Role : Manufacturing EngineerUrgent Location : Mounds view MN need candidate from Medical domain side Keywords : Risk assessment Labeling TMVProduction control CAPA DFMEA PFMEA IQ/OQ/PQ QSR 21 CFR 820 ISO 13485 ISO 14971 Track wise Job Description: Review and approve the More...

For further information please contact our Talent Specialist: Infant at Title: Document Control Specialist Location: Oneonta NY Duration: 9 Months Working Hours: MF 8am 5pm Description Interview Process: Phone screen and then onsite interview Position could be extended but More...

The Quality Management System (QMS) Specialist will be responsible for developing implementing maintaining and improving the companys Quality Management System (QMS). This role ensures that the QMS is compliant with ISO 13485 ISO 9001 21 CFR 820 and 21 CFR 58. The QMS Specialist will More...

The Quality Management System (QMS) Specialist will be responsible for developing implementing maintaining and improving the companys Quality Management System (QMS). This role ensures that the QMS is compliant with ISO 13485 ISO 9001 21 CFR 820 and 21 CFR 58. The QMS Specialist will More...

Position: Quality Engineer Location: Walton KY Job Summary: Seeking an experienced Quality Engineer with at least 3 years of experience in food or medical device industries. Preferred candidates hold an ASQ CQE certification and have knowledge of FDA 21 CFR Part 820/821 and ISO 13 More...

For further information please contact one of our Talent Specialists: Meghna at Infant at Title: Quality Management Systems Specialist Location: Oneonta NY Duration: 9 Months Working Hours: MF 8am 5pm Description Interview Process: Phone screen and then onsite interview P More...

Job Title: Manufacturing Engineer Location: Mounds view MN Duration: 6 Month need candidate from Medical domain side Keywords : Risk assessment Labeling TMVProduction control CAPA DFMEA PFMEA IQ/OQ/PQ QSR 21 CFR 820 ISO 13485 ISO 14971 Track wise JD 1. Review and approve More...

RRD Plover WI is a medical device contract manufacturing facility.  The Quality/Regulatory Manager is responsible for directing planning organizing and controlling the processes procedures policies and activities for the assurance of the quality of the products according to spec More...

For further information please contact our Talent Specialist: Nagarajan Title: Document Control Specialist Location: Kennebunk ME Duration: 9 Months Description: Schedule: MF 8am 4:30pm Onsite 100% Responsible for administration of quality management system docume More...

Description: Job Title Eng Qua Assurance CtQ Summary In this contract role is under our Commitment to Quality Program. The Quality Engineer CtQ role is responsible for the implementation of materials master receiving inspection plans and regulatory compliance to ensure our prod More...

Description: Bill rate $65$70 depends on experience 100% onsite 5 days a week Job Summary Validation QE II and SR QE(Validation) : As directed by the Quality Engineering Leader the Quality Engineer II is accountable validation execution for manufacturing equipment and support in p More...

Job Title: GMP Operational Quality Specialist Location: Providence RI (onsite) Department: Operational Quality Assurance Vertex Biologics and Devices Reports To: Sr. Quality Engineering Manager 12 months with possibility of an extension Job Summary: We are seeking an experi More...

Eurofins Genomics is a global leader in providing highquality genomics services and solutions for academic clinical and industrial customers.  As a trusted partner Eurofins combines high quality product cuttingedge technology and exceptional turnaroundtimes to support customers i More...

Job PurposeThe QA Specialist I position will advance LGC Clinical Diagnostics purpose of understanding disease to  enable  precision  diagnostics  by supporting and contributing to LGC Clinical Diagnostics product quality and Quality Management System processes. LG More...

PurposeThe Sr. Manager Medical Device Quality Systems is responsible for supporting the sustainment improvement and globalization of the AbbVie quality management system in support of AbbVie medical devices and combination products.  The role serves as Deputy Person Responsible f More...

Job Title: Regulatory Affairs Senior Specialist Job Location: Boston MA USA Job Location Type: Remote Job Contract Type: Fulltime Job Seniority Level: As a Regulatory Affairs Senior Specialist youll be at the heart of our mission to enrich and save lives through technology and meani More...

As the Senior Medical Device Auditor you will perform thirdparty audits per SGS Certification procedures and the requirements for ISO 13485 MDSAP MDD and MDR standards. The Sr. Medical Device Auditor is responsible to make relevant decisions concerning the audit process More...

We are seeking a dedicated Manufacturing Quality Specialist to ensure the quality and compliance of products throughout the oligonucleotide manufacturing process per ISO 13485 ISO 9001 and 21 CFR 820. This role will focus on implementing process control systems conducting process audi More...

Role : Manufacturing Engineer Location : Mounds view MN Job Description: Review and approve the documents required to qualify through production process (Control Plan Flow Charts Process Drawings Capability studies Design Failure Mode Effect Analysis (DFMEA) and Process Failure Mod More...