Engineer, Quality Assurance – Onsite

Ledgent Technology; Mahwah (NJ); On-site; USD 52,000 - 59,000; Full time

Job summary

Ledgent Technology in Mahwah, NJ is seeking an Engineer, Quality Assurance – Onsite. This role requires providing quality engineering support in QA, control and preventative activities across operations and other functions.

You will develop and implement methods for process control, testing and inspection to ensure products are free of flaws and function as designed. The position demands a degree and the ability to work independently, applying procedures and professional judgment.

Qualifications

• Bachelor’s degree in Biomedical or Mechanical Engineering or related field.
• 2 years of industry experience.
• Familiar with QMS principles and change management.
• Understanding of Med Device concepts is desirable.
• ISO 13485 and EU regulations familiarity desirable.
• Excellent written and verbal communication.
• Strong engineering and quality knowledge; good PC skills.

Responsibilities

• Develop and implement methods for process control, testing and inspection.
• Lead First Article Inspection (FAI) strategy and PPAP activities.
• Manage change control processes and assess impact of changes.
• Validate equipment and processes; support SOP and risk management updates.
• Collaborate across sites to drive quality improvements.

Skills

Quality mindset

Communication

Problem solving

Team player

Self-starter

Education

Bachelor’s Degree – Biomedical Engineering

Bachelor’s Degree – Mechanical Engineering

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Job description

Engineer, Quality Assurance – Onsite

Location: Mahwah, NJ

Pay Rate: $38.00 – $43.00/hr.

Job Description

As a Quality Engineer you will provide quality engineering support in quality assurance, control and preventative activities within operations and other business functions.

You will be tasked with developing and implementing methods and procedures for process control, process improvement, testing and inspection to ensure that the products are free of flaws and function as designed.

You will be expected to support:

• First Article Inspection (FAI) strategy development, execution, and approvals.
• Production Part Approval Process (PPAP)
• Change control processes and change impact assessments
• Equipment and Process validations
• SOP and Risk Management documentation updates and reviews
• And more

This is an individual contributor role that requires the use of judgement in applying professional expertise and is expected to work independently with minimal supervision. Roles typically require a university degree or an extensive amount of practical knowledge gained through experience. Job requires an understanding and application of procedures and concepts of own discipline. The job requires the ability to make judgements based on practice and previous experience.

You will advocate and lead the execution of initiatives & projects to enhance quality performance within the business and ensure compliance to regulations and standards.

Expected Qualifications:

• * Bachelor’s Degree – Biomedical Engineering, Mechanical Engineering or related field
• * 2 years of experience in industry required
• Knowledge of Change Management and Quality Management Systems (QMS) principles.
• * Firm understanding of Med Device concepts highly desirable.
• * Familiarity with ISO 13485 and EU Regulations, GDP, GMP concept highly desirable.
• * Excellent communication skills and attention to detail.
• * Good understanding of engineering and quality concepts / theories.
• * High level of PC skills. Must be proficient with Microsoft Word, Microsoft Excel and PowerPoint packages.
• * Self-starter with efficient work style and ability to handle multiple tasks in a fast-paced environment.
• * Be willing to work as part of a multi-site team.
• * Have knowledge of Risk Based and statistical concepts is desirable.
• * Problem solving and analytical skills.
• * Be able to build strong relationships by fostering open communications, respect and trust. Strong team player and acts with a customer service/stakeholder focused approach.
• * Ability to be the voice of Quality when dealing cross functionally.
• * Excellent English (both oral and written).

All qualified applicants will receive consideration for employment without regard to race, color, national origin, age, ancestry, religion, sex, sexual orientation, gender identity, gender expression, marital status, disability, medical condition, genetic information, pregnancy, or military or veteran status. We consider all qualified applicants, including those with criminal histories, in a manner consistent with state and local laws, including the California Fair Chance Act, City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance, Los Angeles County Fair Chance Ordinance, and San Francisco Fair Chance Ordinance.