Sorry, this job is no longer accepting applications. See below for more jobs that match what you’re looking for!

Quality Engineer (2015362)

Expired Job

Plastomer Technologies Deland , FL 32723

Posted 4 months ago

Technetics Group DeLand is a leading manufacturer of dynamic seal assemblies, noise attenuation material and pressure regulation products for critical applications in the global Aerospace market. As engineered solutions providers we have the opportunity to work on a variety of exciting applications for the commercial and military planes, rockets and spacecraft that you regularly hear about in the news.

We are looking for a dedicated Quality person to join our DeLand team in the role of Quality Engineer. In this position, you'll leads efforts of the organization to ensure compliance to the Quality Policy and industry standards, (AS9100/ISO9001). This exciting role will provide the opportunity to grow your career and leadership skills while being part of a dynamic, driven and growth oriented organisation.

What will you be doing in Quality?

  • Leadership: Manage multiple projects. Provide review to management on quality system and recommend corrective action as required.

  • Technical: Develop, communicate, and track quality standards and expectations to internal Technetics Group employees, external suppliers, and external customers as required. Conduct statistical analysis of data and communicate results.

  • Quality: Develop and implement corrective actions throughout the organization. Ensure compliance of organization to Quality Policy, standards, and requirements. Participate in both internal and external audits. Develop effective measurement systems.

  • Team Work: Assist cross functional teams to identify and verify quality requirements and take corrective/ preventive actions as necessary.

  • Safety: Promote safe practices in all activities.

  • Self Development: Personally committed to actively improving personal performance and knowledge.

  • Performs any other assigned duty as directed by management.

You'll have...

  • Bachelor of Science degree in mechanical/industrial engineering or equivalent engineering degree preferred.

  • 5+ years Quality Assurance experience in an aerospace manufacturing environment preferred.

  • Quality Engineer Certification or equivalent course work/experience required.

  • Quality Systems Auditor training or equivalent course work preferred.

  • Experience with Lean, Six Sigma, AS9100 and ISO 9000 required.

  • Machine shop inspection and CMM experience is a plus.

  • Proficiency in Microsoft Office required.

Technetics Group is part of EnPro Industries, a $2B global diversified manufacturer with more than 5,000 employees worldwide and over 50,000 customers in 100+ countries. We're widely known for our Dual Bottom Line culture where we seek to enable the full release of human possibility and individual development while achieving strong financial returns. We invest in our employees and provide opportunities for them to make a difference while building a culture that reflects our core values of safety, excellence and respect.

We offer generous benefits and competitive compensations packages that reward on target performance and profitable growth. Please apply to learn more about this exciting opportunity.

See if you are a match!

See how well your resume matches up to this job - upload your resume now.

Find your dream job anywhere
with the LiveCareer app.
Download the
LiveCareer app and find
your dream job anywhere

Boost your job search productivity with our
free Chrome Extension!

lc_apply_tool GET EXTENSION

Similar Jobs

Want to see jobs matched to your resume? Upload One Now! Remove
Quality Associate

Grifols Inc.

Posted 2 days ago

VIEW JOBS 11/16/2018 12:00:00 AM 2019-02-14T00:00 For more than 75 years, Grifols has worked to improve the health and well-being of people around the world. We are a global healthcare company that produces essential plasma-derived medicines for patients and provides hospitals and healthcare professionals with the tools, information and services they need to deliver expert medical care. Quality Associate Primary responsibilities ● Perform daily donor record file review. ● Perform equipment quality control review - daily, weekly, monthly, semi-annual and annual. ● Perform a review of donor center records. ● Perform weekly review of equipment incident logs. ● Verification and release of sample shipment. ● Perform Staging of plasma for shipment. ● Inspection and release of incoming supplies. ● Perform Weekly employee observations. ● Participate in the Quality Assurance meetings and be part of the Quality Assurance team. ● Assist the Center Quality Manager to ensure that cGMP regulations are followed. ● Assist the Center Quality Manager to ensure that SOPs are followed and regulatory requirements are met. ● Performs a review of the documentation of unsuitable test results and the disposition of the associated units. ● On an occasional basis, when the Center Quality Manager is absent, the Quality Associate may be required to perform the following duties: ● Performs all product release activities. ● Documents, investigates, and performs root cause analysis for deviations and customer complaints, specifically in how they relate to the safety of the donor and the quality of the product. ● Review of equipment records and DMS information if applicable to approve out of service machines for use. ● Review and approval of deferred donor reinstatement activities. ● Perform a review of lookback information ● Waste shipment review ● Initiates investigations and reports any supplies that have not met quality specifications and requirements prior to use. ● Perform a review of medical incident reports and the applicable related documentation. Primary Requirements Additional Responsibilities Is certified and maintains certification in the donor processing area. Education High school diploma or GED. Obtains state licensures or certifications if applicable. Experience Typically requires no previous related experience. Occupational Demands Occupational Demands Form # 70: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups. EEO Minorities/Females/Disability/Veterans CLK789 Location: NORTH AMERICA : USA : FL-DeLand:USDEL - DeLand FL-New York Ave-BIO Learn more about Grifols Grifols Inc. Deland FL

Quality Engineer (2015362)

Expired Job

Plastomer Technologies