Quality Engineer III
6901 Preston Road Plano, Texas 75024
Voca has an immediate opening available for a Quality Engineer III in Plano, TX! Interested candidates will email current resume to Chad Miller at email@example.com and call 612-324-0800.
Job Description:Responsible for compliance with applicable Corporate and Divisional policies and procedures.
Must be able to travel domestic and international.
Plans, executes, reports and follows-up on quality system audits (supplier and internal).
Actively participates in and supports departmental operations and responsibilities in accordance with existing internal procedures and external regulations and the ability to lead and/or facilitate group compliance activities associated with the AMO quality system (e.g. audit programs, personnel training).
Monitors compliance with company policies, procedures and applicable regulatory requirements.
Makes decisions that are aligned with management objectives regarding work processes, plans and schedules in order to achieve department objectives.
Tracks and reports progress across projects and departmental commitments by reviewing schedules and due dates, identifying risks, and assisting teams with contingency plans.
Resolves project issues by working with team members, project customers, and others as appropriate.
Assists department and project leaders in developing and reporting appropriate performance and quality metrics.
Demonstrates an ability to apply, recommend, create or innovate quality tools and apply them effectively to a variety of business situations related to work and team environments.
Demonstrates skill(s) or competency(s) that differentiate him/her from the peer group.
Auditor certification from an industry recognized organization desired.
Hands-on knowledge of computer applications including use of the Internet, Word and Excel applications and presentation software such as Power Point.
Excellent written and oral communication skills.
Good organizational skills.
Good presentation skills.
Works well in a team-oriented, cross-functional environment.
Ability to handle multiple tasks and operate in a fast-paced environment. A minimum of 7+ years? experience in an FDA regulated industry (Biotech, Pharma or Medical Device manufacturing).
Bachelor's Degree in Engineering, Chemistry, Biology or related science/technical field or an equivalent combination of education and work experience.
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