Aptar Group

Quality Engineer

Aptar Group$75K — $95K *
Manufacturing & Automotive
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Quality Engineering or related field required; equivalent experience may be considered
  • Minimum of 4 years in quality roles, preferably in a regulated industry
  • At least 2 years' experience with ISO 9001 or comparable standards
  • Proficiency in quality analysis tools such as 8D, DOE, and FMEA; six sigma experience is advantageous
  • Strong analytical skills and problem-solving abilities in team environments

Responsibilities

  • Lead investigations into internal non-conformances; identify root causes
  • Support production by troubleshooting non-conforming materials
  • Develop systems to ensure product conformance to specifications
  • Execute changes to quality processes within the organization
  • Review and approve product specifications
  • Support root cause analysis for customer complaints
  • Facilitate cross-functional teams to resolve quality issues

Benefits

  • Diverse and values-driven work environment
  • Award-winning corporate university for personal development
  • Innovative benefits including 401k, medical, dental, and vision
  • Community contribution initiatives
  • Generous paid maternity and paternity leave
Full Job Description
Job Opportunity - Quality Engineer

What's new with Aptar

We have an exciting position open: Quality Engineer, reporting to the Quality Manager and be based in Eatontown, NJ. The position of the Quality Engineer requires a results driven individual who will be responsible for executing quality initiatives for our manufactured products and drives quality system improvements to achieve department objectives. With a sense of urgency, handles all internal and external quality issues related to the quality of manufactured product. Works closely with the Support team and provides leadership pertaining to product quality.

This is how your journey begins
  • You will lead cross-functional teams to investigate internal non-conformances to identify root cause, obtain containment and implement corrective actions.
  • You will support daily production goals by supporting trouble-shooting efforts related to non-conforming material.
  • You will develop and implement systems that will ensure product conformance to specifications
  • You will work within the organization to execute changes and improvements to the quality process
  • You will review and approve specifications for manufactured products
  • You will support Root Cause Analysis efforts related to customer complaints.
  • You will be the key Quality Representative on corrective and preventive actions that result from customer complaint, CAPA and/or non-conforming material report investigations.
  • You will support the on-going evaluation of inspection techniques, methods and frequencies. From the evaluations, you will make any changes within the Inspection Plan that may be required.
  • You will support the qualification of new mold, assemblies and equipment by conducting capabilities studies and validations.
  • You will provide AQP support for new products and processes, including planning, development, validation and verification activities
  • You will use statistics, metrology, and a problem solving skills to troubleshoot internal and external manufacturing problems
  • You will demonstrate proficiency in root cause analysis and permanent corrective action implementation
  • You will facilitate cross-functional teams in order to address and resolve isolated or recurring internal and external quality issues
  • You will have excellent communication skills. Possess the ability to persuasively present information both orally and in writing and an ability to make presentations to executive team members as well as to key contacts at major customers
  • You will communicate directly with customers regarding technical support, manufacturing issues, and quality non-conformances
  • You will help develop, track, and drive continuous improvement activities in order to meet or exceed the facility quality goals and objectives (KPI's)
  • You will have active involvement and leadership in the Quality Improvement Process
  • You will participate and lead in internal, customer, and Aptar certification audits
  • You will support and adhere to all system procedures and company policies/procedures
  • You will maintain a clean and safe work environment. Follow all safety regulations
  • You will perform other related duties assigned

What you will bring on the journey

Education
  • Bachelor's degree in Quality Engineering or a related technical discipline is required. Adequate experience in Quality in lieu of a degree may be considered


Experience:
  • Minimum of 4 years of experience directly related training and/or experience is required Experience building and maintaining external customer relationships.
  • Minimum of 2 years' experience within a regulated industry (preferably med device, automotive or pharmaceutical); working knowledge of ISO 9001 (or similar regulation like ISO 13485)
  • Must demonstrate analytical abilities to facilitate problem resolution in a team environment
  • Working knowledge and proficiency using quality analysis and tools such as root cause analysis, 8D, DOE, FMEA (six sigma and design controls experience is a plus)

Skills
  • Excellent written and verbal communication skills
  • Ability to work independently with customers, resolve conflicts and drive customer satisfaction
  • Ability to work in a team environment
  • Knowledge of injection molding and assembly processes
  • Knowledge of packaging applications (closures, bottles & tubes)

What we offer:
  • An exciting, diverse and value based working environment
  • Award-winning corporate university offering personal development and training opportunities.
  • Competitive base salary and performance-based bonus plan.
  • Contribute to the communities where we reside.
  • Innovative benefits plan, which includes: 401k plan, vacation, medical, dental, vision, life, disability, pet insurance, wellness plan, and generous paid maternity/paternity leave].

Location Statement

For additional information about location requirements, please discuss with the recruiter following submission of your application.

About Aptar Group

AptarGroup, Inc. is a global leader in the design and manufacturing of a broad range of drug delivery, consumer product dispensing and active packaging solutions. Aptar's headquarters are located in Crystal Lake, Illinois. The company was founded in 1992 as a spin-off from the Illinois Tool Works (ITW) company. Aptar's mission is to be the global leader in innovative dispensing, drug delivery and active packaging solutions. The company's vision is to be the recognized global leader in the markets it serves, providing innovative solutions that enhance the lives of its customers.
Learn more about Aptar Group
Size
13,000 employees
Market Cap
$7.1 billion
Industry
Net Income
$214 million
Founded
1992
5 Year Trend
+6.7%
Revenue
$2.9 billion
NASDAQ

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