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Responsible for representing the department in cross functional meetings Participate in projects involving Quality Control which include new test methods Ensure compliance with all company policies and procedures and…
· The Quality Leader is responsible for providing manufacturing support in accordance with documented procedures and practices. · This is a key technical role responsible for the development, implementation,…
Preffered Knowledge: Appropriate safety precautions, procedures, practices and regulations External Standards including; ISO10012, ISO 13485, ISO17025 and others Installation, repair and maintenance of a wide range of…
Job Title: Quality Systems Specialist Location: Columbia Heights, MN Duration: 12+months (Possibility of extension) POSITION DESCRIPTION: · This position has primary responsibility for supporting and providing…
Job title: Regulatory Affairs Specialist Location: Mansfield, MA Duration: 5+ months (possibility of extension) ROLES& RESPONSIBILITY: · The skills required include a Regulatory Affairs contracted professional with…
Design and deliver the medical device and supplies breakthroughs that make a difference in the lives of millions of patients. Responsible for ensuring that software used in the development, manufacturing and as part of…
Work with a senior design quality engineer to oversee the quality of a number of products in the Health Informatics and Monitoring product line. • Create risk management plans, perform product risk assessment,…
• At least 6 years of experience in technology consulting, enterprise and solutions architecture and architectural frameworks • At least 8 years of experience in design and development of Medical Devices Software…
Description: This Senior Software Consultant will work within the R&D engineering team to develop and support the next-generation minimally invasive platform. This Senior Software Consultant will develop embedded…
• The Quality Engineer will be responsible for Consistent application of Quality system standards to assigned Quality system area • Developing solutions to routine assigned activities of moderate scope &…
Client: Direct Client Location: West Chester, PA Job Title: Senior Regulatory Affairs Specialist Duration: 1 year + (Possible Extension) Job Summary: The Recall Regulatory Specialist III will be responsible for leading…
• Support R&D, Manufacturing Department to ensure compliance with quality system policies and procedures, FDA and international requirements, and ISO Standards for Medical Devices DUTIES & RESPONSIBILITIES: •…
JOB RESPONSIBILITIES: • Develop novel diagnostic assays blood or cell based applications on flow cytometry platforms using cutting edge, strategies, reagents and instruments. • Become subject matter expert in disease…
Position Details: Job Summary The Associate Director Project Management will provide project management support to medical device (MD) and combination product (CP) compliance efforts for the creation of an efficient…
PERMANENT FULL TIME POSITION Overview: Under very limited supervision, responsible for selection, management and development of a professional team, design and set up of development facilities, and design, performance…
Overview: This position is responsible for carrying out T-SPOT® assays and other processes during validation of procedures, QC of finished product and raw materials, and to support the Quality Manager in the running of…
Company: SystemCanada | www.systemcanada.com World wide office: Canada - USA - Australia - UK - South Africa - New Zealand - Ireland - Japan Job Description Extensive experience in Product Development, Sustaining,…
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