Quality Engineer II

Ultralife Corporation; Raynham (MA); On-site; USD 100,000 - 120,000; Full time

Job summary

Ultralife Corporation in Raynham, MA is seeking a Quality Engineer II to support Operations and ensure compliance with QMS/EMS and regulatory standards. This full-time role oversees 1-3 technicians and drives process improvements and product quality.

You will review BOMs, lead test method validation, support audits, manage deviations and CAPA, and mentor inspectors. A bachelor’s degree in engineering and 2–5 years in quality engineering are required, with proficiency in Minitab and Microsoft

Qualifications

• 2–5 years Quality Engineering experience, preferably in manufacturing.
• Bachelor's degree in engineering or related field.
• Competence in Quality Engineering Tools and Techniques.
• Good knowledge of relevant Domestic and International Regulations and Industry Standards (e.g. ISO, QSR, UL, MDD, TGA).
• Proficient in Microsoft Office and Minitab.

Responsibilities

• Ensure QMS/EMS compliance for manufactured components and products.
• Support regulatory inspections, audits, investigations, and inquiries.
• Monitor manufacturing and provide deviation/waiver guidance with proper records.
• Review BOM changes, assembly procedures, drawings, and specifications.
• Lead test method validations and protocol completion.
• Coordinate with Design/Manufacturing for process validations and CAPA.

Skills

Quality engineering

Statistical QC

Communication

Education

Bachelor's degree in engineering or related field

Tools

Minitab

Microsoft Office

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Quality Engineer II

Full-time Regular Raynham, MA, US

4 days ago Requisition ID: 1503

Salary Range: $100,000.00 To $120,000.00 Annually

Job Summary:

The primary purpose of this job is to provide Quality Engineering support for Operations to ensure that the Quality System requirements are adhered to for manufactured components and products in accordance with applicable Regulatory and Standards requirements for compliance. Provide work direction for 1-3 Technicians/Inspectors.

Essential Functions*:

• Adheres to Core Beliefs and all safety and quality requirements including but not limited to: Quality Management Systems (QMS), Environmental Management Systems (EMS), Company policies and operating procedures, and other regulatory requirements.
• Support regulatory and agency inspections, audits, investigations, and inquiries regarding the control and assessment of product design and manufacturing quality.
• Monitor manufacturing of assigned products, assuring compliance while providing deviation/waiver guidance, and assuring complete and correct Device History Records are maintained.
• Review the adequacy and correctness of changes to Bill of Materials (BOM’s), Assembly Procedures, Drawings, Component Specification, FMEAs, Control Plans, etc.
• Lead generation and completion of protocols and reports for test method validations.
• Interfaces with Design and Manufacturing Engineers to review processes for new and existing products and coordinate process validations and capability studies. Recommends process monitoring devices where applicable.
• Develops various inspection techniques and procedures to ensure product integrity to design specifications.
• Responsible for the writing, approval, and implementation of Incoming, In-Process, and Final Inspection procedures.
• Ensure that the disposition of non-conforming materials meets all necessary regulatory requirements and assure adequacy of corrective actions to prevent recurrence.
• Lead and manage customer complaint investigations.
• Participate in plant CAPA activities, including analysis of data and trends in complaints, supplier quality, nonconforming material, training effectiveness, and root causes analysis.
• Participate in continuous improvement projects.
• Assist with product transfers.
• Works with suppliers, management, Engineers and Manufacturing associates in the resolution of quality problems. Also, assist each of these groups with capability studies and the application of statistical quality control which include Cpk, DOE, Hypotheses Testing, etc.
• Mentor and support quality inspectors and technicians.
• Performs other functions as required
• Other duties as assigned.

Education / Training / Skills / Experience:

• Minimum 2-5 years Quality Engineering experience, preferably in manufacturing
• Bachelor's degree in engineering or related field required
• Competence in the selection and use of Quality Engineering Tools and Techniques.
• Good knowledge in the interpretation and application of relevant Domestic and International Regulations and Industry Standards (e.g. ISO, QSR, UL, MDD, TGA, etc.)
• Proficient in Microsoft Office and Minitab
• Ability to work independently and in a team environment.
• Ability to effectively communicate written and verbally.
• Ability to manage time effectively to ensure timely completion of tasks.
• High level of initiative and strong work ethic.

Physical Requirements:

• Not applicable

Preferred Certifications

Certified Quality Engineering (CQE), Certified Software Quality Engineer (CSQE),

Certified Reliability Engineer (CRE), Certified Quality Auditor (CQA),

*Employees must be able to perform the essential functions of the job with or without reasonable accommodation.

This job description is intended to convey information essential to understanding the scope of the position described above, and it is not intended to be an exhaustive list of skills, efforts, duties, responsibilities or working conditions associated with the position.