| Job alert | Jobs 1 - 10 of 286 |
Maintenance Manager
Nationwide Food Recruiters
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Anaheim, CA, 92808
... Position: Maintenance Manager Location: Anaheim, CA (Relocation Available) Type: Onsite Company Quick Facts: Privately owned contract manufacturer Reports to: VP Operations Direct Reports: <10 Size of Team: <30 FDA, SQF, HACCP, USDA-Organic, Kosher ... - Sep 15
Electrical Engineer (Medical Device)
Intellectt Inc
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Irvine, CA
... Ensure compliance with quality management systems (ISO, FDA, etc.). Maintain professional behavior with internal/external associates. Education/Experience: Degree: BS in Electrical Engineering; MS preferred Experience: 3+ years in medical device ... - Sep 22
Regulatory Affairs Specialist II
QuinTalent Inc
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Irvine, CA
... Knowledge of FDA, and CE marking requirements for IVD products is a plus Able to work independently and with others Communication skills, including negotiation and persuasion. Analytical, problem solving, computer, and critical thinking skills. ... - Sep 19
Quality Control Inspector
Aerotek
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Irvine, CA, 92602
... Food and Drug Administration (FDA) regulations, other regulatory requirements, company policies, operating procedures, processes, and task assignments. 9. Maintain positive and cooperative communications and collaboration with all levels of ... - Sep 05
Staff Quality Engineer
BioTalent
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Irvine, CA
... Knowledge of industry standards and regulations (e.g., FDA, ISO, etc.). Strong manufacturing background with a proven track record in supporting FMEA, NCMRs, CAPAs, and validation activities. This is a challenging and rewarding opportunity for a ... - Sep 01
Complaint Specialist (Medical Device)
Talent Elite Group
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Irvine, CA
... Regulatory Compliance: - Ensure complaint handling processes and investigations comply with regulatory requirements (e.g., FDA, ISO 13485, EU MDR). - Prepare and submit regulatory reports, as needed, including Medical Device Reporting (MDR) and ... - Sep 14
Design Assurance Engineer
Oxenham Group
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Irvine, CA
... Participate in FDA inspections, ISO Certification and surveillance audits and customer audits as an NPD subject matter expert. Writing & coordinating efforts for the development and implementation of new and updated Design Control processes, ... - Sep 22
Director of Regulatory Affairs
Skills Alliance
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Irvine, CA
... Responsibilities: Develop and execute global regulatory strategies for new and existing medical devices Lead the submission process for regulatory approvals, including FDA, CE Mark, and other international regulatory bodies: US FDA IDE, 510(k), CE ... - Sep 12
Senior Analytical Chemist
Kelly Science, Engineering, Technology & Telecom
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Irvine, CA
... Understand and apply cGMP principles and FDA regulations for pharmaceuticals. Must be a self-starter, work under limited supervision, and be capable of taking initiative in prioritization and implementation of work. Able to read and interpret ... - Sep 22
Sr Analyst, Supply Chain
Planet Pharma
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Irvine, CA
... knowledge and understanding of policies, procedures and guidelines relevant to local and/or global supply chain including FDA and ISO laws and regulations applicable to medical device industry Good problem-solving skills Strict attention to detail ... - Aug 29