Iso 13485 Jobs in Others

Please share your resumes at Job Role: Manufacturing Engineer Location: Foxborough MA Contract: W2 Responsibilities: Design processes specify equipment develop work instructions conduct validation (IQ OQ PQ) and train production staff. Create validate and deploy More...

Role: Senior Quality Systems Specialist Location: Illinois Duration: Permanent Salary: $110000$115000K Job Description: We are establishing a new department and seeking an individual to join our team as a Senior Quality Systems Specialist in a manufacturing company specializing i More...

Job Title: Quality Systems Program Manager Client: Medical Device Manufacturing Company Duration: 7 months contract with possible extension Location: Northridge CA 91325 Shift: 1st Shift Job Description: Experienced project manager in the medical device industry responsible for inspec More...

Job Title: Quality Systems Program Manager Client: Medical Device Manufacturing Company Duration: 7 months contract with possible extension Location: Northridge CA 91325 Shift: 1st Shift Job Description: Experienced project manager in the medical device industry responsible for inspec More...

Job Title: Packaging Engineer Location: On site Grand Rapids MI (Must be local) Length: 12 year contract Musthaves Minimum 5 YOE in packaging Experience in packaging FFS equipment process development and validation IQ/OQ/PQ Experience in manufacturing environment process or man More...

Position Responsibilities Support the Vice President RAQA to develop best practices for Enlitic regulatory and standards compliance.Assess procedures processes and organizations for compliance with GMP ISO 13485 EU MDR (2017/745) MDSAP Canadian MDR etc. standards and regulations.Work More...

Job Title: Sr Packaging Engineer Exempt 13811 Location: Grand Rapids MI 49504 Duration: 4/15/2024 4/14/2025 Education Required: Bachelor of Science Degree in Packaging Science Mechanical Engineering or similar discipline Years Experience Required: Minimum of 5 years in med More...

Role: Sr System Engineer Location: Pittsburg PA Onsite Duration: Fulltime / Contract 2 POSITIONS Job Description: Mandatory Skills: Systems Engineering for Electromechanical Medical Devices InCose certification ISO 13485 ISO 14971 IEC 62304 Usability for Medical devices Re More...

Please share your resumes at Job Role: Senior QA Specialist Location: Concord CA Contarct: W2 RESPONSIBILITIES Overseeing and ensuring timely completion of quality system deliverables including nonconformance (NC) and corrective/preventive actions (CAPA) interna More...

This is a remote position. Stand out in the crowd! Create a short 90 second cell phone quality video explaining why you are the ideal candidate for this role. Submit your video to Please include Inside Sales Specialist in the subject line. Position Responsibilities More...

Title : Software Verification Engineer (Non Clinical) Must to have : Python C# 3 Positions Customer : Siemens Location Palo Alto CA Rate : $60/hr.. Max Job Summary We are seeking a meticulous and detailoriented Medical Device Software Verification Tester to join our team. The su More...

Position: Project Manager Location: Danvers MA Position Description: The Project Manager will play a key role in leading crossfunctional teams with the global IZiel support ensuring the seamless integration of MES (Manufacturing Execution System) software solutions. The aim is to fost More...

Project Manager Our client is seeking a Project Manager to lead internal company projects. This role is designed for an individual with experience in project management ideally within clinical diagnostics medical devices or pharmaceuticals. The ideal candidate will have a proven trac More...

Job Title: Manufacturing Supervisor Synthesis and Production Microbiology Duration: 12 Month Shift: 7:00 am 3:00 pm PST Work Location: San Diego CA 92127 SUMMARY: The main responsibility for the Synthesis and Production Microbiology Supervisor is to lead and oversee all p More...

We are seeking a Regulatory Affairs Specialist to support a leading medical device company in Ithaca NY. This is an onsite role open to local candidates. Job Summary: This position will support worldwide regulatory registrations for our current and future medical devices as More...

As the Quality Engineer you are responsible for product quality assurance and quality engineering. You will provide technical oversight and maintain quality systems that are effective and comply with federal state local and other applicable international regulations and standards. You More...

As the Quality Engineer you are responsible for product quality assurance and quality engineering. You will provide technical oversight and maintain quality systems that are effective and comply with federal state local and other applicable international regulations and standards. You More...

As the Quality Engineer you are responsible for product quality assurance and quality engineering. You will provide technical oversight and maintain quality systems that are effective and comply with federal state local and other applicable international regulations and standards. You More...

As the Quality Engineer you are responsible for product quality assurance and quality engineering. You will provide technical oversight and maintain quality systems that are effective and comply with federal state local and other applicable international regulations and standards. You More...

As the Quality Engineer you are responsible for product quality assurance and quality engineering. You will provide technical oversight and maintain quality systems that are effective and comply with federal state local and other applicable international regulations and standards. You More...