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Integra LifeSciences Calibration Compliance Technician in Billerica, Massachusetts

Calibration Compliance Technician

US–MA–Billerica, Vacancy ID2021-38328

Career Home › Job Search Results ›Calibration Compliance Technician

Changing lives. Building careers.

Integra LifeSciences, a world leader in medical technology, is dedicated to limiting uncertainty for surgeons, so they can concentrate on providing the best patient care. Integra offers innovative solutions in orthopedic extremity surgery, neurosurgery, reconstructive and general surgery, and regenerative wound care.

Founded in 1989 Integra is headquartered in Plainsboro, New Jersey and has more than 4,000 employees worldwide. Integra’s common stock is listed on The NASDAQ Stock Market under the symbol “IART.”

RESPONSIBILITIES

Responsibilities

SUMMARY DESCRIPTION

The Quality Control Technician will be responsible for performing quality inspections and testing according to established procedures. Inspection and testing activities will cover incoming, work-in-process, and finished goods. Assist in the daily operations of the Quality Control Laboratory

SUPERVISION RECEIVED

Manager or Director of Quality Assurance and Regulatory Affairs or Designated Quality Engineer

Oversee all functions and activities of the Quality Control Laboratory Area

Set priorities for departmental workloads and special requests

Maintain the calibration of all equipment and the calibration documentation system

General Inspection to Include:

o Mechanical testing of incoming components, WIP, finished devices, and repair/loaner devices using measuring equipment (i.e.,micrometers, and calipers)

o Electrical testing of incomingcomponents, WIP, finished devices, and repair/loaner devices using test equipment (i.e. Hipot tester and oscilloscope)

o Visual inspection, with or without magnification (i.e.,microscope)

o Operating automated inspection equipment; namely the CMM and Optical Vision Systems

Accurate completion of inspection records to be retained at Integra Burlington as the Device History Records and documentation of all transactions using current MRP system.

QUALIFICATIONS

What are we looking for?

Qualifications

The requirements listed below are representative of the knowledge, skill and/or ability required for his position.

  • Education: High School Graduate (or GED)

  • Certifications

None required

  • Experience:

  • Experience working within a formalized FDA or ISO quality system is required

  • Ability to follow established procedures, organization skills, and attention to detail are essential

  • Working knowledge of inspection equipment and blueprint reading (GD&T) preferred

  • Proficient with an MRP database

  • Strong knowledge of Good Manufacturing Practices and Good Laboratory Practice’s

  • Proficient in all aspects of Quality Control in an FDA regulated industry such as medical devices or pharmaceuticals is desired

  • Time as QC professional 5-10 years in medical device or technologically related environment

TOOLS AND EQUIPMENT USED

  • CMM Measurement Equipment

  • Optical Comparator

  • Height Gage

  • Various hand held measurement devices

Ability to utilize a computer, telephone, fax and copy machine as well as other general office equipment. Strong computer skills are required.

PHYSICAL REQUIREMENTS

Product inspection and computer data entry requires eyesight that can be correct to 20/20.

The physical requirements listed in this section include, but are not limited, to the motor/physical abilities and skills require of position in order to successfully undertake the essential duties and responsibilities of this position. In accordance with the Americans with Disabilities Act (ADA), reasonable accommodations may be made to empower individuals with disabilities to undertake the essential duties and responsibilities of the position.

While undertaking the essential duties and responsibilities of the position, the employee must repeatedly sit, listen, speak, type and move throughout the facility. Must be capable of using a keyboard for computer purposes.

ADVERSE WORKING CONDITIONS

There are no adverse working conditions associated with this position

SELECTION GUIDELINES

Formal application, rating of education and experience; oral interview and reference check; job related tests may be required

DISCLAIMER

The duties listed above are intended only as illustrations of the various types of work that may be performed. The omission of specific statements of duties does not exclude them from the position if the work is similar, related, or a logical assignment to the position.

The job description does not constitute and employment agreement between the employer and employee and is subject to change by the employer as the needs of the employer and requirements of the job change.

OUR PRODUCTS

We are proud of our 25 year heritage as a leader in regenerative medicine. Today, our scientific innovation and diverse product portfolio continue to help patients and surgeons around the world.

OUR CULTURE

We have an entrepreneurial, small company feel, yet deliver big company results. Your ideas – big and small – are welcome here. We embrace change and reward our people who are committed to making Integra a stronger company.

OUR VALUES

We believe how we do things is as important as what we do. Our Values guide how we work and how we act towards our customers, patients and each other every day. We value Our People, Integrity, Excellence, Embracing Change, Decisiveness and Teamwork.

Integra LifeSciences is an equal opportunity employer, and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status.

This site is governed solely by applicable U.S. laws and governmental regulations. If you'd like more information on your rights under the law, please see the following notices:

EEO Is the Law (https://www.eeoc.gov/laws/index.cfm) |EOE including Disability/Protected Veterans (https://www.eeoc.gov/eeoc/publications/ada_veterans_employers.cfm) Integra LifeSciences is committed to provide qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the ADA (https://www.eeoc.gov/eeoc/publications/fs-ada.cfm) . If you have difficulty using our online system due to a disability and need an accommodation, please email us at careers@integralife.com or call us at 855-936-2666.

Please see our Privacy Policy (https://www.integralife.com/privacy) . Use of this site constitutes your consent to application of such laws and regulations and to our Privacy Policy. Your use of the information on this site is subject to our Terms of Use (https://www.integralife.com/terms) . You should view the News section and the most recent SEC Filings in the Investor section in order to receive the most current information made available by Integra Life Sciences. Contact Us (https://www.integralife.com/contact) with any questions or search this site for more information.

© Copyright 2020 Integra LifeSciences Corporation. All Rights Reserved.

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