Quality Assurance Inspector I

Integra LifeSciences Corporation; Utah; On-site; USD 23,419 - 30,307; Full time

Job summary

Integra LifeSciences Corporation in West Valley City, UT is seeking a Quality Assurance Inspector I to perform incoming, in-process, and finished goods inspections, ensuring compliance with specifications and GDP.

You will review drawings, maintain inspection records, support CAPA activities, and work with QA Engineers and Production to resolve issues; 1–5 years in medical device QC preferred; ISO 13485, FDA 21 CFR 820 familiarity encouraged.

Qualifications

• 1–5 years in quality inspection in medical device or regulated manufacturing.
• Familiarity with ISO 13485, FDA 21 CFR 820, GMP preferred.
• Ability to read drawings and specifications.

Responsibilities

• Conduct incoming inspections of raw materials and components to verify specifications.
• Perform in-process inspections to ensure assemblies meet standards.
• Inspect finished goods from sterilization for final release criteria.
• Verify labels and packaging for regulatory compliance.
• Maintain inspection records per GDP and company policies.
• Support continuous improvement and root cause analysis.

Skills

Inspection techniques

Measurement tools

Technical drawings

Documentation

MS Office & eQMS

Cross-department collaboration

Job description

## Quality Assurance Inspector IApplylocations: US-UT-West Valley-106-Facilitytime type: Full timeposted on: Posted Todayjob requisition id: JR-6243Changing 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.**Key Responsibilities**To perform this job successfully, an individual must be able to execute the following responsibilities satisfactorily:* Conduct **incoming inspections** of raw materials and components to verify compliance with specifications.* Perform **in-process inspections** to ensure assemblies meet quality and regulatory standards.* Inspect **finished goods** returning from sterilization to ensure compliance with final release criteria.* Verify **labels and packaging** for accuracy and compliance with regulatory requirements.* Ensure **assembly instructions** are properly followed by reviewing Lot History Records.* Identify and document **nonconformities** through the Nonconforming Material Reports (NCMR) process.* Work collaboratively with **Quality Engineers and Production teams** to resolve quality issues.* Maintain complete and accurate inspection records in compliance with Good Documentation Practices (GDP).* Support **continuous improvement initiatives** and participate in root cause analysis and corrective actions.* Maintain a clean and safe working environment in accordance with company policies.* Perform other related duties as required.**Desired Minimum Qualifications****Education & Experience*** 1 – 5 years of experience in quality inspection or a similar role within the medical device, pharmaceutical, or regulated manufacturing industry.* Equivalent combination of education and experience will be considered.* Familiarity with ISO 13485, FDA 21 CFR 820, and Good Manufacturing Practices (GMP) is preferred.**Skills & Competencies*** Strong knowledge of inspection techniques, measurement tools, and quality control methods.* Ability to interpret technical drawings, specifications, and work instructions.* Excellent attention to detail and documentation skills.* Proficiency in Microsoft Office (Excel, Word, Outlook) and ability to use electronic quality management systems (eQMS).* Effective communication and collaboration skills to work across departments.Salary Pay Range:$16.68 - $22.12 USD HourlyOur salary ranges are determined by role, level, and location. Individual pay is determined by several factors including job-related skills, experience, and relevant education or training**.** In addition to base pay, employees may be eligible for bonus, commission, equity or other variable compensation**.** Your recruiter can share more about the specific salary range for your preferred location during the hiring process.Additional Description for Pay Transparency: Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance, and savings plan (401(k)). Subject to the terms of their respective policies and date of hire, Employees are eligible for the following Total Rewards | Integra LifeSciencesIntegra 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 [e-mail] Agency SubmissionIntegra LifeSciences does not accept unsolicited assistance from search firms for employment opportunities. All CVs/resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. A formal written agreement is required before engaging any agency, and it must be executed and authorized by the Vice President, Talent Acquisition. Where agency agreements are in place, introductions (the initial sharing of a candidate’s name, resume, or background) are position-specific and may only occur within the scope of that approved agreement. Please, no phone calls or emails.Integra - Employer Branding from Integra LifeSciences on Vimeo### About Us**Whatever your specialty, you’ll find an ideal setting for building a rewarding career.**Along the way, you’ll have the satisfaction of knowing your work matters, that it’s making patients’ lives better, making a positive and lasting difference. You’ll find that the pace is exhilarating – because the need is so urgent. You’ll be challenged – and supported – by the most dynamic and inspiring people in your profession. And you’ll grow a career that is more impactful and fulfilling then you thought possible. More than 4,200 Integra employees already know we’re a great place to build a career. Here’s your chance to discover that for yourself.