What are the responsibilities and job description for the Quality Inspector II position at Integra LifeSciences?
Changing lives. Building Careers.
Joining us is a chance 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, our colleagues are challenging what’s possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care.
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
Primary responsibilities are to:
- Perform all required quality inspections according to inspection instructions and/or product drawings.
- Utilize department databases to track and manage inspection workload and rejected products.
- Adhere to SOPs, policies, and ISO/QSR requirements.
- Complete archival activities for device history records for inspected lots.
- Write and process Material Reject Reports as necessary.
- Manage inventory on hold for quality inspection.
- Review and update inspection plans as needed.
- Handle transactional duties for incoming, work-in-process, and finished goods processing in the designated product line.
- Cross-train in two or more product lines.
Note: Other duties may be assigned as necessary.
DESIRED MINIMUM QUALIFICATIONS
Education & Experience:
- High School or Trade School Graduate (or GED) minimum is required.
- Certified Quality Technician (ASQ CQT) would be a plus.
- Minimum three (3) years of experience in Quality Inspection (or minimum six (6) years in a manufacturing environment where responsible for measurement of products) and preferably in an FDA regulated environment is required
- Ability to interpret instructions, blueprints, and drawings to effectively inspect product is required.
- Ability to utilize multiple gauges and measurement tools for inspection of manufactured components and assemblies is required.
- Use of math skills relative to physical measurement of product (calculations involving basic functions and metric units) is required.
- Knowledge of ISO, FDA and QSR concepts and guidelines preferred.
- Excellent communication and organizational skills.
- Outstanding attention to detail.
- Strong interpersonal skills and ability to work with others in a positive and collaborative manner.
- Demonstrated ability to work accurately, follow instructions/schedules/timelines and handle multiple priorities.
- Knowledge of various MS Office applications such as: Word, and Excel
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:
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
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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