Vacancy caducado!
Get excited to join a global leader in drug and consumer product dosing, dispensing, and protection technologies!Description: develop and implement systems that will ensure product conformance to specifications execute changes and improvements to the quality process review and approve specifications for manufactured products own one or more Quality Management System Processes (i.e. Complaints, NCR, CAPA, Training etc.) will be the local point person for external complaints which may include conducting/leading investigations and executing corrective and preventive actionsSkills:iso 13485, investigation and analysis, complaint handling, quality engineering, Root cause analysis, Capa, quality management systemAdditional Skills & Qualifications:1+ year of experience working in an ISO 9001 and / or ISO 13485 environment 1+ year of experience running the investigations ( not just being involved )Experience Level:Entry LevelDiversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
Hiring diverse talent
Maintaining an inclusive environment through persistent self-reflection
Building a culture of care, engagement, and recognition with clear outcomes
Ensuring growth opportunities for our people
Actalent is an equal opportunity employer.About Actalent Actalent connects passion with purpose. We help visionary companies advance their engineering and science initiatives through access to specialized experts that drive scale, innovation, and speed to market. With a network of almost 30,000 engineering and sciences consultants and more than 4,500 clients across the U.S., Canada, Asia, and Europe, Actalent serves many of the Fortune 500. An operating company of Allegis Group, the global leader in talent solutions, Actalent launched as a new specialized engineering and sciences services and workforce solutions brand in 2021.
Vacancy caducado!