Fabrication Record Book Coordinator

Newport News, VA 23601

Must be a US Citizen or Green Card holder.

This role is onsite from Day 1 !

Overview:

Are you interested in growing your career with one of the top tier manufacturing companies in the world? We are ready to hire a motivated and hardworking supervisor to join our Family! In this role, you will supervise and coordinate activities for quality system members and members performing inspections to support the Medical Products Group.

Responsibilities:

• Responsible for performance and activities of direct reports to include allocation of workload, goal setting, coaching, training and providing continuous feedback. Oversees and provides clear direction on assigned work.
  
• Develops personnel to ensure efficient and highly skilled workforce to meet the department and organizational goals/activities; recommends training, assigns projects, and provides other avenues for employee development opportunities; provides constructive feedback and coaching to members when necessary to encourage professional development.
  
• Assigns or delegates responsibility for specific projects, tasks or assignments; provides clear direction and continuous feedback, resolves problems, prepares work schedules, establishes objectives and sets deadlines to ensure completion of operational functions.
  
• Promotes teamwork and collaboration between subordinate employees to promote knowledge sharing and increase department morale.
  
• Conducts performance management activities, counsels, and advises subordinates concerning performance. Monitors and documents employee performance for annual performance review.
  
• Initiates, recommends, and approves personnel actions such as hires, promotions, transfers, and discharges for area of responsibility based on departmental/organizational needs.
  
• Works with recruiting during the hiring process (i.e. reviewing resumes, participating in interviews, providing timely feedback, etc.);
  
• Participate and lead cross-functional and departmental teams to ensure timely completion of FDA, other regulatory authority and internal audit commitments as well as commitments arising from any CVIMPG Quality Improvement initiatives.
  
• Perform and or facilitate completion of gap analyses and implementation plans for standard operating procedures.
  
• Coordinates inspection activities (incoming, in-process and final product testing).
  
• Verifies that the INQI team has appropriate equipment and materials to support inspection activities.
  
• Provides direction and oversight for the quality system members who are responsible for MasterControl, Blue Mountain and other electronic systems as applicable.
  
• Works with Quality Engineering/Purchasing for supplier qualification and supplier maintenance.
  
• Ensures compliance with all safety regulations.
  
• Develops work instructions/procedures to perform inspection activities. Drives first article inspections.
  
• Performs inspections as needed.
  
• Performs routine audits to ensure compliance to inspection plans/procedures.
  

Requirements

1. Bachelor s degree; or equivalent combination of education and experience

2. 5-8 years Quality Assurance, in a manufacturing environment

3. 1-3 years experience in a lead or supervisory position.

4. Experience in FDA

5. Experience with compliance and safety regulations.

6. Ability to read Blue Prints, assist with fixture design and set up measurement equipment/machines.

7. Must be a US Citizen or Green Card holder.

Benefits