Maetrics Jobs in Fremont

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Here are some related jobs:
Maetrics Atlanta, GA
Role: Daily Complaint Volume Specialist Location: West Chester, PA Duration: 9 month contract Daily Complaint Volume Specialists Receives daily product complaints (intake), works phones, distributing necessary forms for request for information and entering complaints into client Complaint Handling System (CatsWeb). Understands and has been part of the Complaint Handling process within a Medical De...
Maetrics Dover, OH
Founded in 1984, Maetrics® is a professional services firm that offers Compliance and Quality consulting services to the Medical Device, Pharmaceutical, Nutritionals, and Biotech industries. Maetrics brings a wealth of best practices, experience, knowledge, tools, and methods to design compliance and quality solutions that will with stand regulatory scrutiny and improve product quality. Headquarte...
Maetrics Elyria, OH
Founded in 1984, Maetrics® is a professional services firm that offers Compliance and Quality consulting services to the Medical Device, Pharmaceutical, Nutritionals, and Biotech industries. Maetrics brings a wealth of best practices, experience, knowledge, tools, and methods to design compliance and quality solutions that will with stand regulatory scrutiny and improve product quality. Headquarte...
Maetrics Monument, CO
As an experienced Manufacturing Engineer within the Medical Device industry, the engineer will be providing guidance and conduct remediation activities related to Process Validation. 5+ years validation experience Test Method, Equipment, and Process Validation experience Experience writing and executing protocols including IQ,OQ,PQ,PPQ FDA regulated experience Has a good holistic understanding of...
Role: Medical Device Reporting SME Location: West Chester, PA Duration: 6 months MDR SME - responsible for managing / running clients internal complaint system / process and responsible for training internal personnel Responsible for "Containment Planning & Implementation" until new CHU system is in place. 7+ as a Complaints Manager for a Medical Device company Must have a Medical background (RN o...
As an experienced Manufacturing Engineer within the Medical Device industry, the engineer will be providing guidance and conduct remediation activities related to Process Validation. 5+ years validation experience Test Method, Equipment, and Process Validation experience Experience writing and executing protocols including IQ,OQ,PQ,PPQ FDA regulated experience Has a good holistic understanding of...
Maetrics Bridgeport, MI
Assures compliance and progress toward company established goals of the organization as the quality department head and designated management representative through developing and enforcing quality management systems and procedures; good business practices; understanding, communicating and assuring customer expectations; building in quality to assure consistent quality products in a timely manner;...
· 5+ yrs. of experience within the Medical Device as a Supplier Quality Engineer with the following skills: · Process Validation · Project Management Skills · The level of resource will determine the managerial skill sets and ability to direct others. · Should have a strong work ethic, be able to work independently, be self-motivated and attentive to detail and deliverables. · The resource will be...
Compliance Auditors will be part of the Regulatory Compliance Work Stream. Responsible for conducting audits with focus on both standard compliance (21 CFR 820) as well as Process Compliance. 5+ yrs. experience Experience with conducting audits with focus on both standard compliance as well as process compliance Support back and front room activities during notified body audits Conduct internal au...
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