Manager jobs in the Quality Assurance & Safety category and Medical Devices and Supplies industry

The Colonial Group specializes in the placement of outstanding talent in regulated Manufacturing environments (Pharma, Food, Device) and organizations that sell to those industries (Specialty Chemical, Packaging, Equipment, and affiliated industries). Our clients understand that our decades of industry experience give us unique insight and access to top talent at all levels. The Colonial Group is ...
full job description

TE Connectivity is an industry leader with an entrepreneurial spirit, fueled by innovation and collaboration. Our emphasis on forward thinking has attracted the brightest industry minds, allowing them to thrive and create breakthrough solutions that deliver a competitive advantage to our customers. TE Connectivity is a global, $12.1 billion company that designs and manufactures over 500,000 produc...
full job description

Current Need Mckesson is hiring for a Process Manager of Distribution Operations in our Memphis, TN. Position Description Map processes at both high and detailed level. Conduct data analysis, process analysis, and root cause analysis. Select most appropriate type of control method for each project; create and sustain a Response Plan. Create buy-in for operational excellence; specifically, diagnose...
full job description

Function: Manage and maintain an effective quality assurance program for the plant. Ensure that the requirements of the International Standard are implemented and maintained. Responsibilities: ? Manage and maintain an effective quality assurance program for the plant in alignment with Global Operating Procedures, and capable of maintaining Site ISO 9001 certification status. ? Review, approve and ...
full job description

Regulatory Affairs Medical Devices There is an immediate need for a Regulatory Affairs Associate or Regulatory Affairs Specialist with experience in medical devices in the Encinitas, CA area. This is an opportunity to join a fast growing company in the class I and class II business. They need someone that understands regulatory reporting, has knowledge of the 510k process and audits either through...
full job description

SENIOR QUALITY ENGINEER Medical Device Manufacturing An opportunity exists for a Senior Quality Engineer with experience in medical device project management, process improvement, and new product development in the Encinitas, CA area. The right candidate will have 8+ years in quality assurance with at least 5 of those years in medical device design and/or operations. An extensive knowledge of NPD,...
full job description

Description Medline Industries has an immediate opening for Associate QA Specialist-Supplier Quality position, located in Mundelein, IL headquarters. The Associate QA Specialist will be responsible for quality assurance activities related to the Supplier Quality group within the QA/RA Division. The position will be responsible for maintaining design control files and device master records for FDA ...
full job description

QUALITY ENGINEER Medical Device Manufacturing There is an excellent opportunity for a Quality Engineer with experience in medical device CAPA and Design Quality in the Encinitas, CA area. The right candidate will have extensive knowledge of CAPA, design controls, and risk assessment. This is an automated high speed manufacturing environment with injection molding, extrusion, and assembly operation...
full job description