Are you an experienced Quality Executive within the Medical Device Industry?
We have a great opportunity for you! The Director of Quality Management establishes, manages, coordinates, and evaluates the activities of Quality System and regulatory compliance programs. Oversees the development and field performance of medical products in compliance with corporate policies. Oversees quality metrics with a focus on root cause investigations and prevention of problems. Leads and monitors in achieving a culture of continuous improvement. Management of and participation in the Corporate Internal Audit program covering all domestic sites including planning, coordination and follow-up on global audits according to group directives and procedures. Continue reading Director of Quality Management – Waterbury, CT→
Do you have a proven track record in improving business in the Medical Device, Automotive or Aerospace industries?
We need you! Global Medical Device Manufacturer in New Jersey is seeking highly motivated engineers to join a new internal consulting team to support advanced manufacturing for their high-tech products and processes. You will focus on comprehensive system thinking, creative problem solving, and effective leadership to ensure continuous improvement and innovation while utilizing Lean Six Sigma. Continue reading Continuous Improvement Quality Engineer – New Jersey→
The Number 7 Line Extension Project is a two-track system that extends underground from the current terminus at the Port Authority Bus Terminal at Eighth Avenue/41st Street to new lay-up tracks at Eleventh Avenue/ 26th Street. The remaining work on the project includes fit out of the recently constructed tunnels, terminal station and ventilation buildings. Continue reading Assistant Quality Manager – NYC Subway Extension Project→
As our Senior Supervisor for Second shift, you will be hands on supervisor in our Operations area. Responsibilities include; ensuring effective operation by preparing work schedules, assigning tasks, coordinating the flow of work and assigned projects, oversee completion of work, and monitor performance of subordinates.
Attention to detail, inventory and warehousing processes, demonstrated supervisory abilities and proficiency in a manufacturing environment and in a lead supervisory role are the skills you will bring to the table for this position. Continue reading Senior Supervisor in York, PA→
For over 30 years VSC, an independent subsidiary of Verify, Inc., has been a trusted resource to over 200 companies in aerospace, defense, and high-technology industries. This partnership has created worldwide opportunities for contract Project Specialists to work with our customers and their suppliers. Together, we ensure quality in supply chain and supplier management programs. Continue reading Quality Source Inspection position (part-time)→
Job Purpose: Provide regulatory compliance expertise on quality systems for manufacturing and distribution of pharmaceuticals, medical devices and active medical devices, as well as compounding admixture pharmacies processes and related products. Ensure internal B. Braun compliance to applicable regulations and standards (FDA Drug/Medical Device regulations, ISO Standards, Medical Device Directives (MDD), Canadian Medical Device Regulations (CMDR), USP 797 and other applicable regulatory requirements), and the B. Braun quality systems and of B. Braun suppliers through periodic auditing. Establish guidelines and requirements from Quality Assurance perspective in supporting special projects. Continue reading Corporate Senior Regulatory Compliance Specialist→