Fabrication Record Book Coordinator

2 weeks ago


Doha, Qatar Brunel Qatar Full time
Supervisor, QualitySystems - Medical

Newport News, VA23601

Must be a US Citizen or Green Cardholder.

This role isonsite from Day 1

Overview:

Areyou interested in growing your career with one of the top tiermanufacturing companies in the world? We are ready to hire amotivated and hardworking supervisor to join our Family In thisrole, you will supervise and coordinate activities for qualitysystem members and members performing inspections to support theMedical ProductsGroup.

Responsibilities:

  • Responsiblefor performance and activities of direct reports to includeallocation of workload, goal setting, coaching, training andproviding continuous feedback. Oversees and provides cleardirection on assignedwork.
  • Developspersonnel to ensure efficient and highly skilled workforce to meetthe department and organizational goals/activities; recommendstraining, assigns projects, and provides other avenues for employeedevelopment opportunities; provides constructive feedback andcoaching to members when necessary to encourage professionaldevelopment.
  • Assignsor delegates responsibility for specific projects, tasks orassignments; provides clear direction and continuous feedback,resolves problems, prepares work schedules, establishes objectivesand sets deadlines to ensure completion of operationalfunctions.
  • Promotesteamwork and collaboration between subordinate employees to promoteknowledge sharing and increase departmentmorale.
  • Conductsperformance management activities, counsels, and advisessubordinates concerning performance. Monitors and documentsemployee performance for annual performancereview.
  • Initiates, recommends, and approves personnel actions such ashires, promotions, transfers, and discharges for area ofresponsibility based on departmental/organizationalneeds.
  • Workswith recruiting during the hiring process (i.e. reviewing resumes,participating in interviews, providing timely feedback,etc.);
  • Participateand lead cross-functional and departmental teams to ensure timelycompletion of FDA, other regulatory authority and internal auditcommitments as well as commitments arising from any CVIMPG QualityImprovementinitiatives.
  • Performand or facilitate completion of gap analyses and implementationplans for standard operatingprocedures.
  • Coordinatesinspection activities (incoming, in-process and final producttesting).
  • Verifiesthat the INQI team has appropriate equipment and materials tosupport inspectionactivities.
  • Providesdirection and oversight for the quality system members who areresponsible for MasterControl, Blue Mountain and other electronicsystems asapplicable.
  • Workswith Quality Engineering/Purchasing for supplier qualification andsuppliermaintenance.
  • Ensurescompliance with all safetyregulations.
  • Developswork instructions/procedures to perform inspection activities.Drives first articleinspections.
  • Performsinspections asneeded.
  • Performsroutine audits to ensure compliance to inspectionplans/procedures.


Requirements

1.Bachelor s degree; or equivalent combination of education andexperience

2.5-8 years Quality Assurance, in a manufacturingenvironment

3.1-3 years experience in a lead or supervisoryposition.

4.Experience inFDA

5.Experience with compliance and safetyregulations.

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

7.Must be a US Citizen or Green Cardholder.



BenefitsFull
1. Bachelor s degree; or equivalent combination of education andexperience 2. 5-8 years Quality Assurance, in a manufacturingenvironment 3. 1-3 years experience in a lead or supervisoryposition. 4. Experience in FDA 5. Experience with compliance andsafety regulations 6. Ability to read Blue Prints, assist withfixture design and set up measurement equipment/machines. 7. Mustbe a US Citizen or Green Card holder.

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