Quality Engineer II

Posted 2 Days Ago
Be an Early Applicant
07727, Wall, NJ, USA
In-Office
95K-105K Annually
Mid level
Healthtech • Defense • Industrial • Manufacturing
The Role
Supports quality and regulatory activities for sustaining products, including process improvements, risk management, complaint investigations, CAPA, design controls, validations, audits, nonconforming materials, and quality-system documentation. Serves as a quality representative and potential process owner while partnering with Engineering and cross-functional teams. Applies statistical analysis, root-cause investigation, FDA QSR, and ISO 13485 requirements to improve manufacturing processes and product quality.
Summary Generated by Built In

SUMMARY:
The Quality Engineer II is responsible for supporting process improvements, risk management activities, complaint process, design control activities, customer/ISO/FDA audits and non- conforming material as it relates to sustaining products.
The Quality Engineer II participates in review and approval of Quality System documents, resolves quality issues and ensure quality control of products and processes, in compliance with all applicable company policies and procedures.
The Quality Engineer II may be asked to be a quality system process owner in which this role will actively manage one or multiple key components of the quality system.
DUTIES AND RESPONSIBILITIES:
• Follows all Quality System requirements and company procedures ensuring regulatory requirements are met in an ethical manner.
• Meets commitments on time with accuracy and attention to detail.
• Maintains current knowledge base of existing and emerging regulations, standards, or guidance documents.
• Develop validation and/or verification protocols for changes related to process improvements; execute validations/verifications and report on the conclusions to support process improvements.
• Quality Representative for process and software validations (may require writing, reviewing, executing, analyzing and/or reporting on test protocols).
• Maintains a working knowledge of applicable statistical techniques for validation and process capability/performance purposes.
• Quality Representative for Risk Management Activities for existing products.
• Provide interpretive assistance, to all departments, regarding quality documents.
• Support training on Manufacturing and Quality System documents.
• Conduct customer complaint investigations, interface with customers to gather necessary details, determine root cause and implement corrective and preventive actions.
• Interface with Engineering to drive continual improvement on existing manufacturing processes.
• Quality Representative for Design Control Activities for existing product lines.
• Release documents via the change control process as necessary. Train others where required.
• Prepare quality related deliverables in a timely manner.
• Participate in CAPA root cause investigation and actions implementation.
• Implement ongoing quality improvement processes working with cross functional teams.
• Acts as a consultant for areas related to his/her expertise.
Performs other related duties as assigned by management.
• Quality Representative for contract review activities on existing products.
• Provides support as the primary Quality representative for Notices of Change (NOCs), Notices of Activity (NOAs), and Nonconforming Material Reports (NCRs) related to existing products.
• Potential Quality System Process Owner for the following (but not limited to):
o Non-conforming Reports (NCR)
o Customer Complaints
o Supplier Quality
o Environmental Monitoring
o Corrective and Preventive Actions (CAPA)
o Internal Audits
o Training
 

Qualifications

QUALIFICATIONS:
• 3 to 8 years of relatable experience in a regulated industry is required.
• A Bachelor's degree in engineering or related discipline is required; it may substitute for some of the years of required experience and knowledge.
• Well-rounded knowledge of ISO 13485:2016 and FDA QSR.
• Strong root-cause investigator and problem solver within a manufacturing environment.
• Mechanical aptitude with manufacturing experience.
• Well-developed written and verbal communication skills. Ability to write and comprehend instructions, short correspondence, and memos.
• Must possess the ability to work semi-independently with little daily input from a manager.
• Experienced in statistical analysis.
• Certified Lead Auditor
• Ability to solve practical problems and deal with a variety of concrete variables and ability to interpret a variety of instructions furnished in written and oral form.
• Well versed in data management and graphical presentation of data.
• Experienced with Microsoft Windows, Outlook, Word, Excel, Microsoft Project, etc. is required.
• Generate reports using data analysis, SPC analysis/tools, etc. and effectively communicate findings/proposals to various users in the organization.
COMPANY COMPETENCIES:
• Diversity - Demonstrates knowledge of EEO policy; Shows respect and sensitivity for cultural differences; Educates others on the value of diversity; Promotes a harassment- free environment; Builds a diverse workforce.
• Ethics - Treats people with respect; Keeps commitments; Inspires the trust of others; Works with integrity and ethically; Upholds organizational values.
• Professionalism - Approaches others in a tactful manner; Reacts well under pressure; Treats others with respect and consideration regardless of their status or position; Accepts responsibility for own actions; Follows through on commitments.
• Quality - Demonstrates accuracy and thoroughness; Looks for ways to improve and promote quality; Applies feedback to improve performance; Monitors own work to ensure quality.
• Safety and Security - Observes safety and security procedures; Determines appropriate action beyond guidelines; Reports potentially unsafe conditions; Uses equipment and materials properly.
SUPERVISORY RESPONSIBILITIES:
• This job has no supervisory responsibilities.

JOB COMPETENCIES:
• Problem Solving - Identifies and resolves problems in a timely manner; Gathers and analyzes information skillfully; Develops alternative solutions; Works well in group problem solving situations; Uses reason even when dealing with emotional topics.
• Written Communication - Writes clearly and informatively; Edits work for spelling and grammar; Varies writing style to meet needs; Presents numerical data effectively; Able to read and interpret written information.
• Validation / Verification – Has a clear understanding of how to design and execute validation and verification activities as they pertain to new product development, process improvements and/or changes.
• Analytical - Synthesizes complex or diverse information; Collects and researches data; Uses intuition and experience to complement data; Utilizes data analysis to justify process changes.
• Dependability - Follows instructions, responds to management direction; Takes responsibility for own actions; Keeps commitments; Commits to long hours of work when necessary to reach goals; Completes tasks on time or notifies appropriate person with an alternate plan.
PHYSICAL DEMANDS AND WORK ENVIORNMENT:
• Occasionally required to stand
• Occasionally required to walk
• Frequently required to sit
• Occasionally required to climb, balance, bend, stoop, kneel or crawl
• Frequently required to talk or hear
• Occasionally work near moving mechanical parts
 

Skills Required

  • 3 to 8 years of experience in a regulated industry
  • Bachelor's degree in engineering or a related discipline
  • Working knowledge of ISO 13485:2016 and FDA QSR
  • Root-cause investigation and problem-solving experience in a manufacturing environment
  • Mechanical aptitude with manufacturing experience
  • Strong written and verbal communication skills
  • Ability to work semi-independently with limited daily management input
  • Experience with statistical analysis
  • Certified Lead Auditor
  • Data management and graphical data presentation experience
  • Experience with Microsoft Windows, Outlook, Word, Excel, and Microsoft Project
  • Experience generating reports using data analysis and SPC tools
  • Understanding of validation and verification activities

Spectrum Plastics Group Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Spectrum Plastics Group and has not been reviewed or approved by Spectrum Plastics Group.

  • Retirement Support — A 401(k) match is included in the core package for full-time employees. This provides employer-backed retirement savings support beyond base pay.
  • Wellbeing & Lifestyle Benefits — Paid Volunteer Time Off, wellness resources, an Employee Assistance Program, and employer‑paid life/short‑term/long‑term disability are part of the offering. These programs extend support for personal wellbeing and community involvement.
  • Healthcare Strength — Health and dental coverage are available, with HSA options noted. The overall package is characterized as solid in multiple descriptions.

Spectrum Plastics Group Insights

Am I A Good Fit?
beta
Get Personalized Job Insights.
Our AI-powered fit analysis compares your resume with a job listing so you know if your skills & experience align.

The Company
HQ: Atlanta, GA
2,200 Employees
Year Founded: 1949

What We Do

Spectrum Plastics Group is a global leader in the design, development, and manufacturing of specialty medical components and devices, providing solutions from development through scaled manufacturing for medical and other demanding markets.

Similar Jobs

RELX Logo RELX

Test Engineer

Information Technology • Legal Tech • Analytics
In-Office
2 Locations
10001 Employees

Elsevier Logo Elsevier

Test Engineer

Artificial Intelligence • Healthtech • Information Technology • Other • Analytics
In-Office
2 Locations
In-Office
2 Locations
3489 Employees
71K-98K Annually
In-Office
Plainsboro, NJ, USA
3489 Employees
71K-98K Annually

Similar Companies Hiring

Amalgamated Sugar Thumbnail
Food • Greentech • Agriculture • Industrial • Manufacturing
Boise, Idaho
768 Employees
Outpost Space Thumbnail
Aerospace • Defense
Los Angeles, California
38 Employees
Vitalize Thumbnail
Artificial Intelligence • Healthtech • Software
US
50 Employees

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account