| Job alert | Jobs 1 - 10 of 846 |
Medical Technologist
Wealth Recruitment, LLC
–
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
Senior Supplier Quality Engineer
InfraredX, Inc.
–
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 24
Cleanroom Production Associate
Monroe Staffing
–
Danvers, MA
... in daily activities • Adhere to general safety rules, manufacturing procedures, company policies and procedures, QSR, and FDA regulations Job Qualifications (minimum requirements): • High School Graduate or equivalent manufacturing experience • ... - May 16
Supply Chain Engineer
InfraredX, Inc.
–
Bedford, MA, 01730
... Knowledge of regulatory requirements and quality standards applicable to medical device manufacturing (e.g., FDA regulations, ISO standards) is a plus. Six Sigma, Lean, or other process improvement certifications are desirable. Advanced computer ... - May 24
Project Manager- must have med device & quality engineer experience
Diverse Lynx
–
Danvers, MA, 01923
... • Knowledge on Quality Management and its tools & techniques • Knowledge about FDA, ISO 13485 and compliance regulations • Knowledge on Medical Device Regulatory Standards, MDD and MDR • Knowledge on NC, CAPA, Audit processes • Knowledge in ... - May 29
Principal Supplier Quality Engineer
InfraredX, Inc.
–
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
Sr. Manager, Quality Assurance
EPM Scientific
–
Billerica, MA, 01821
... 8-10 years of Quality experience in medical device, combination product experience preferred Direct experience with medical device complaints investigations and inspection readiness Experience working directly with FDA/notified bodies Must be ... - May 26
Software Engineer
Engtal
–
Andover, MA
... Formulate and uphold software development protocols in compliance with regulatory standards, including FDA guidance and IEC 62304. Oversee procedures and deliverables for software verification. Investigate field complaints to ascertain root cause ... - May 15
Food Safety and Quality Manager
The Judge Group
–
Haverhill, MA, 01832
... of Quality Management experience in food manufacturing Experience with sanitation oversight Strong knowledge of FDA/USDA/PCQI/SQF or BRC HACCP certification Strong leadership skills, excellent communication skills Experience managing a large team - May 31
Clinical Research Coordinator
Alcanza Clinical Research
–
Methuen, MA
... The Clinical Research Coordinator under the direction of the Site Manager/Director and the Principal/Sub Investigators conducts the following according to the study protocol, company processes & procedures, and in compliance with FDA, GCP, and ICH ... - May 15