Our Medical Device client in Pano Texas is urgently hiring for a Manufacturing Engineer III. Candidates will be required to work onsite on the production floor at:
901 Preston Road Plano, Texas USA 75024
Here is the Job Description for the opening:
WHAT YOU’LL DO
- Support on-market products, work with design engineers and suppliers to optimize product design.
- Work with Senior Engineers to provide support and consultancy to suppliers on process validations and process development.
- Manage Design Change Package activities to implement a variety of updates including process improvements, product enhancements, and supply continuity updates.
- Contribute to the technical aspects of Problem Solving, Failure Analysis, and Corrective and Preventative Actions.
- Work with internal departments and external vendors to obtain prototype parts and to understand their capabilities and limitations.
- Gain a detailed understanding of the quality and regulatory requirements of Abbott, FDA and ISO regulations, managing projects within these requirements.
- Gain a detailed understanding of overall scheduling, managing time and tasks within a defined schedule.
- Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.
- Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, company policies, operating procedures, processes, and task assignments
- Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.
EDUCATION AND EXPERIENCE YOU’LL BRING
Required
- Bachelor's degree in Engineering Field (Biomedical, Electrical, Mechanical preferred).
- Experience in fast paced operations engineering environment, medical device experience preferred.
- Must be capable of coordinating cross functionally with groups such as R&D, Supply Chain, GP (Global Procurement), Design and Supplier Quality to drive design change packages and nonconformances.
- Ability to work within a team and as an individual contributor in a fast paced changing environment.
- Ability to leverage and/or engage others to accomplish projects.
- Strong verbal and written communications with ability to effectively communicate at multiple levels in the organization.
- Multitasks, prioritizes and meets deadlines in a timely manner. Strong organizational and follow-up skills, as well as an attention to detail.
- Ability to work in a highly matrixed business environment.
Preferred
- 1+ years of engineering experience in Medical Device Industry
NOTE: This position summary is not intended to be all-inclusive. Employee may perform other related duties as negotiated to meet the ongoing needs of the organization.
The Company complies with all laws respecting equal employment opportunity and does not discriminate against applicants with regard to any protected characteristic as defined by federal, state, and local law, including disability/veteran status. This position may require you to work onsite or interact in person with customers of the Company and/or work onsite from time to time at the Company’s facilities.