| Job alert | Jobs 1 - 10 of 625 |
Sr. Project Manager (Must Have Medical device/ FDA regulated
MILLENNIUMSOFT
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Andover, MA
... Project Manager (Must Have Medical device/ FDA regulated experience) Location : Andover, MA Duration : 12+ Months contract Total Hours/week: 40.00 1st Shift: Mon. - Fri. 8AM - 5PM Client: Medical Device Company Level Of Experience: Senior Level ... - Apr 03
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
Quality Director
Connect Life Science
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Boston, MA, 02298
... You’ll ensure compliance to ISO13485 and FDA Quality Systems Regulations. You’ll be the main points of contact for FDA and other regulatory agencies for all Quality Management Systems aspects of the business. Job Responsibilities: direct and control ... - Apr 22
Design Assurance Engineer- Medical Device
CEI Group
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Woburn, MA, 01801
Design Assurance Engineer Responsibilities: Ensuring that the design process complies with relevant regulations and standards such as FDA guidelines, ISO standards, and other applicable regulatory requirements. Working with the verification and ... - Apr 23
Design Assurance Engineer- Medical Device
CEI Group
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Woburn, MA, 01801
Design Assurance Engineer Responsibilities: Ensuring that the design process complies with relevant regulations and standards such as FDA guidelines, ISO standards, and other applicable regulatory ; Working with the verification and valida Permanent - Apr 29
Senior Quality Engineer
Infotree Global Solutions
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Danvers, MA, 01923
... Danvers Massachusetts (Hybrid) Job Duration: Long Term Contract Top 3 technical skills that are required for this role: Assist with writing and exectuing process validation procedures in accordance with QSR, FDA and international guidelines. ... - Apr 26
Sr Production Engineer
Whitridge Associates
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Burlington, MA, 01805
... • Support and enforce company goals and objectives, policies and procedures, Good Manufacturing Practices, Good Documentation Practices, FDA QSR and ISO regulations. Knowledge of FDA QSR and ISO regulations required. • Identify and execute process ... - Apr 14
Medical Device Product Manager
Exergen Corporation
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Watertown, MA, 02472
... Required Education and Experience: · 8+ years of experience working in an FDA/ISO regulated medical device/medical equipment environment. · 5+ years of experience preferred managing technical teams and programs. · Detail oriented with strong ... - Apr 28
Cleanroom Production Associate
Monroe Staffing
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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 • ... - Apr 16
Director, Clinical Scientist
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 the time. The base range is $207,255- $250,000 per year. Individual pay may vary based on additional factors, including, and ... - Apr 30