Quality Control Technician II (Wayne, NJ)

With a passion for life

Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers – and to save more lives, we need team players, forward thinkers, and game changers.

Are you looking for an inspiring career? You just found it.

Position Summary

The Quality Control Technician II performs acceptance testing and inspection activities on in-process and finished goods to ensure products meet established requirements. This role is responsible for executing testing and inspection tasks accurately, documenting results in a timely manner, and supporting quality system compliance in a regulated manufacturing environment.

The position is onsite 5 days a week. This is a first shift position with hours from 6am-2:30pm. There may be a possibility for overtime via extended hours or weekends.

Job Responsibilities and Essential Duties

• Perform functional acceptance testing, destructive, non-des and inspections on products assembled on the manufacturing floor in accordance with approved procedures and test methods.

• Perform destructive and non-destructive testing on in-process and finished goods (e.g., Visual Inspection, Seal Width, Length, Water Entry Pressure, Instron Testing, Radial Burst, Borescope, Spectrophotometry).

• Conduct independent review of Shop Floor Paperwork (SFP) to verify completeness and accuracy prior to product release or further processing.

• Identify and subject non-conforming materials to the NCMR process in accordance with established quality procedures.

• Ensure all testing is performed according to established procedures, protocols, quality standards, and regulatory requirements.

• Read, comprehend, and follow job instructions, procedures, protocols, and work-related documents, including verbal and written directions.

• Train Inspectors on acceptance testing methods, applicable procedures, and newly implemented policies, as assigned.

• Assess daily priorities and adjust own work schedule as needed to support operational requirements.

• Perform additional duties as assigned; responsibilities listed are not exhaustive.

Minimum Requirements

• High school diploma or equivalent required; Associate or Bachelor’s degree in science, Math, Business, or a related field preferred.

• Minimum of 2 years of experience in a quality function or regulated environment, or a bachelor’s degree or Certified Quality Technician (CQT) certification.

• Experience in an FDA-regulated environment preferred; medical device experience strongly preferred.

Required Knowledge, Skills and Abilities

• Ability to perform functional testing, inspections, and basic measurements accurately.

• Prior Instron testing experience or prior training in one of the following Instron operator courses—Series IX, Merlin, or Blue Hill—is preferred.

• Competence in reviewing documentation for completeness and compliance.

• Ability to perform basic math across multiple units of measure.

• Ability to use electronic quality systems and databases (e.g., SAP) for data entry and record maintenance.

• Strong attention to detail and commitment to data integrity.

• Effective verbal and written communication skills.

• Ability to work collaboratively in a team environment.

• Demonstrated flexibility and willingness to learn new tasks and procedures.

• Ability to work independently, manage multiple priorities, and adapt to changing workflows.
• Proficiency with Microsoft Office Products or equivalent software applications.

Internal and External Contacts/Relationships

• Works cross-functionally with internal teams and external stakeholders, as required, to support quality activities.

Environmental/Safety/Physical Work Conditions

• Ability to lift up to 40 pounds occasionally and handle materials, test fixtures, and equipment.

• Ensures environmental consciousness and safe practices are exhibited in decisions

• Use of computer and telephone equipment and other related office accessories/devices to complete assignments

• May work extended hours during peak business cycles

• Must be able to perform repetitive motions, including frequent use of hands, wrists, and fingers for sample preparation, testing, and instrument operation.

• Must be able to remain in a stationary or standing position for extended periods during testing.

• Close visual acuity required for sample preparation, reading measurements, and data verification.
• Must follow all safety and environmental requirements of the QC laboratory environment

The base salary for this position is a minimum of $27/hour and a maximum of $29/hour plus overtime

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About us 

With a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the products are sold in more than 135 countries.  

Benefits at Getinge:

At Getinge, we offer a comprehensive benefits package, which includes:

• Health, Dental, and Vision insurance benefits
• 401k plan with company match
• Paid Time Off
• Wellness initiative & Health Assistance Resources
• Life Insurance
• Short and Long Term Disability Benefits
• Health and Dependent Care Flexible Spending Accounts
• Commuter Benefits
• Parental and Caregiver Leave
• Tuition Reimbursement

Getinge is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, pregnancy, genetic information, national origin, disability, protected veteran status or any other characteristic protected by law. Reasonable accommodations are available upon request for candidates taking part in all aspects of the selection process.