Changing lives. Building Careers.

Joining us is a chance for you to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, more than 4,000 of us are challenging what's possible and making headway to help improve outcomes.

Primary responsibilities are to:

* Inspect raw materials, manufacturing materials, packaging, WIP and finished goods per standard operating procedures

* Sample and perform chemical assay of solutions per standard operating procedures

* Assesses inspection and test results against acceptance criteria

* Documents activities in device history records

* General laboratory maintenance

* Complies with current Good Manufacturing Practices and all applicable standards and regulations

* Maintains a working inventory of all components, materials and solutions

* May assist as needed in execution of test method validations

* May assist with document review and revision

* Assist in Out of Specification (OOS) and nonconformance investigations

* Escalates nonconformances to supervisor

* Perform other duties as required

Minimum Qualifications:

* High School Diploma or equivalent

* 0-2 years' experience in Quality Inspection, Quality Control or Quality Assurance. Experience in medical device, pharmaceuticals, or other regulated industry preferred.

* Ability to assess results against acceptance criteria.

* Ability to follow instructions precisely, recognize deviations, and recommend corrective action.

* Working knowledge of current Good Manufacturing Practices and familiarity with application of FDA and ISO quality standards in a government regulated industry is a plus.

* Familiarity with application of FDA and ISO quality standards in a government regulated industry.

* Proficient computer skills, including experience with database applications and Microsoft Office.

* Working knowledge of standard laboratory practices and safety.

* Detail-oriented.

* Excellent organizational and time management skills.

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 | EOE including Disability/Protected Veterans

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. 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.

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