| Job alert | Jobs 1 - 10 of 1038 |
Medical Technologist
Wealth Recruitment, LLC
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Boston, MA
75000.00 - 105000.00
... JC, CAP, FDA, AABB) requirements. Requires the manual/visual dexterity necessary to prepare specimens, prepare solutions, screen specimens and operate a computer software system. Requires interpersonal and English verbal and written language skills ... - Mar 14
Principal Manufacturing Engineer
BlackTree Technical Group, Inc.
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Newton, MA
... All procedures and processes must comply with FDA and ISO standards. This is a working position in a start-up environment and will allow the individual to build a team as the business needs arise. BS in Engineering or Science required. Minimum of 7 ... - May 18
Senior Supplier Quality Engineer
InfraredX, Inc.
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Bedford, MA, 01730
... Maintains supplier quality records in accordance with FDA/GMP and EU MDR requirements. Coordinate review of supplier change requests with cross-functional team, including evaluation of change, implementation planning, and approval. Assist with ... - May 17
System Engineer (Verification & Validation)
Stellent IT LLC
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Waltham, MA
... through FDA submissions/audits would be a big plus FDA and (verification or validation or "V&V") and (medical or surgical or "medical device" or "medical equipment") and 60601 Best Regards Piyush Technical Recruiter Stellent IT Email: Call- Gtalk: - May 15
HCG - MES Engineer
Horizon Controls Group
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Boston, MA, 02108
... Compliance and Regulatory Support: Stay up to date with relevant regulatory guidelines and industry standards (e.g., FDA, GMP) pertaining to MES systems. Assist in ensuring compliance with these regulations through proper system configuration, data ... - May 09
Director of Clinical Operations
Global Life Science Hub
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Boston, MA
... Strong understanding of FDA, EMA, and PDMA regulations and guidelines. Exceptional written and verbal communication skills. Strong ethical values and ability to build and lead high-performing teams. Apply: The Global Life Science Hub are a niche ... - May 16
Senior Supplier Quality Engineer
InfraredX, Inc.
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Bedford, MA, 01730
... Maintains supplier quality records in accordance with FDA/GMP and EU MDR requirements. Coordinate review of supplier change requests with cross-functional team, including evaluation of change, implementation planning, and approval. Assist with ... - May 16
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
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
Regulatory Affairs Specialist II/Sr
Nova Biomedical
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Waltham, MA, 02454
... in our Waltham, MA facility (Hybrid) to focus on assuring company compliance to US 510k, Health Canada Licensing, International Device Submissions, Licensing and Registration requirements, ISO/FDA QSR, IVDD, ISO 13485, quality system auditing. ... - May 18