| Job alert | Jobs 21 - 30 of 996 |
Principal Supplier Quality Engineer
InfraredX, Inc.
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Bedford, MA, 01730
... Maintain supplier quality records in accordance with FDA/GMP and EU MDR requirements. Lead the review of supplier change requests with cross-functional team, including evaluation of change, implementation planning, and approval. Generate KPI’s and ... - May 15
Principal Supplier Quality Engineer
InfraredX, Inc.
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Bedford, MA, 01730
... Maintain supplier quality records in accordance with FDA/GMP and EU MDR requirements. Lead the review of supplier change requests with cross-functional team, including evaluation of change, implementation planning, and approval. Generate KPI’s and ... - May 18
Hybrid Regulatory Intern
Withings
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Boston, MA
The Regulatory Affairs Intern will support the Regulatory Affairs team in daily tasks, projects, and FDA submission activities including: Assist in drafting, organizing, and editing regulatory documents for 510(k) submissions. Coordinate workflow ... - May 09
Product Security Analyst
VBeyond Corporation
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Boston, MA, 02298
... Experience working in a regulated environment, FDA-regulated preferred. - May 19
Automation Engineer (DeltaV)
LVI Associates
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Boston, MA, 02298
... With extensive experience in cGMP and FDA regulated industries, our team of engineers delivers innovative automation solutions aligned with industry standards. We provide professional support and expertise in Automation, Manufacturing Systems, and ... - May 13
Senior Quality Auditor
RBW Consulting
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Boston, MA, 02298
... Reporting to the Head of Quality, our client seeks a candidate with several years of experience as a qualified auditor (cGMP, QSR, ICH) in life sciences, with a strong knowledge of FDA and global regulations/guidelines. A successful candidate needs ... - May 02
Senior Clinical Trial Leader
Kura Oncology
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Boston, MA
... Detailed knowledge of GCP, ICH Guidelines and current US FDA regulations. Ability to travel up to approximately 30% of time. Hybrid on-site in Boston two days per week. WORK ENVIRONMENT: Employee frequently works in a professional office environment ... - Apr 30
Head of Regulatory Affairs
Discera Search
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Boston, MA, 02298
... Demonstrate resilience and assertiveness in interactions with the FDA, advocating for our innovative therapies and proactively addressing regulatory challenges to ensure timely approval and market access. Facilitate communication with the FDA, ... - May 01
Director Quality Operations
EPM Scientific
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Cambridge, MA, 02140
... Oversee implementation and adherence to cGMP, ICH, FDA, and ISO quality standards. Maintain and oversee a robust quality management system. Collaborate effectively with cross-functional teams to ensure seamless product launches. Proactively identify ... - May 11
Principal Supplier Quality Engineer
InfraredX, Inc.
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Bedford, MA, 01730
... Maintain supplier quality records in accordance with FDA/GMP and EU MDR requirements. Lead the review of supplier change requests with cross-functional team, including evaluation of change, implementation planning, and approval. Generate KPI’s and ... - May 16