Senior Quality Control Inspector

Integra LifeSciences Corporation; Braintree (MA); On-site; USD 31,684 - 42,705; Full time

Job summary

Integra LifeSciences Corporation is seeking a Senior Quality Control Inspector in Braintree, MA to support incoming inspection and release activities. The role collaborates with Manufacturing, Engineering, QA, and Supply Chain to maintain product quality and regulatory compliance.

Responsibilities include inspecting reports, investigations of non-conformances, data analysis, and training teammates in QC standards and procedures. A background in medical devices or regulated industry is preferred.

Qualifications

• Knowledge of QC terms, tools, and methodologies.
• Ability to follow instructions precisely, recognize deviations, and recommend corrective action.
• Detail-oriented with strong time management and organizational skills.

Responsibilities

• Supports QC collaboration with Quality Management to ensure standards are met.
• Inspects products, processes, and systems for compliance with quality standards.
• Investigates non-conformances, identifies root causes, and implements corrective actions.
• Supports documentation and reporting of QC findings and data analyses.
• Assists Review & Release activities reviewing manufacturing, inspection and quality records.

Skills

QC terminology

Data analysis

Attention to detail

Team collaboration

Education

High school diploma or equivalent

Bachelor’s or Associate degree preferred

Tools

Calipers

Rulers

Dataloggers

Job description

## Senior Quality Control InspectorApplylocations: US-MA-Braintree-220-Facilitytime type: Full timeposted on: Posted Todayjob requisition id: JR-6350Changing 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.**SUMMARY**The Sr. Quality Inspector is responsible for supporting Quality Control Incoming Inspection and Review & Release activities to ensure compliance with internal procedures, regulatory requirements, and quality standards. This position serves as a key technical resource within the Quality Control organization, providing support for incoming material inspection, batch record review, product release activities, non-conformance investigations, and continuous improvement initiatives. The role works collaboratively with Manufacturing, Engineering, Quality Assurance, Supply Chain, and other cross-functional groups to support daily operations and maintain operational efficiency. This position is expected to operate flexibly between QC Incoming Inspection and Review & Release functions based on business needs, workload demands, and organizational priorities while ensuring compliance and product quality. Perform the essential duties and responsibilities listed in section below.**ESSENTIAL DUTIES AND RESPONSIBILITIES**To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.Primary responsibilities are to:- Supports QC collaboration with Quality Management to ensure all quality standards are met, including but not limited to inspecting reports are properly updated and completed in a timely manner.-Inspects products, processes, and systems to ensure compliance with quality standards.-Assists in investigating non-conformances, identifying root causes, and implementing corrective actions.-Supports documentation and reporting quality control findings and the analysis of data to recommend process improvements.- Supports Review & Release activities including review of manufacturing, inspection, and quality records to ensure completeness, accuracy, and compliance with established procedures.-Supports Inspection and testing raw materials, intermediates and record test results. Assist as needed in test method validation, implementation, and execution.- Assists in training employees in quality standards, KPIs and procedures.-Assists with the implementation of new or improved quality control systems as needed.-Supports maintaining a working inventory of all department components, materials and solutions.-Ability to assist in root cause analysis and implement corrective actions.-Serves as an informal resource for colleagues with less experience.- Collaborate with Quality Management to ensure compliance with industry regulations, company policies, and safety standards during the transition process.-Provides database support with generating reports and analyzing process data.- Support Quality Management in preparing for and participating in FDA audits, customer audits, etc.-Maintains work areas and equipment in a clean and orderly condition.-Must be able to work in a Team environment, multi-task and communicate effectively.-Demonstrate excellent organizational and time management skills.-Knowledge of industry standards and regulations related to quality control.-Perform other duties as required.**DESIRED MINIMUM QUALIFICATIONS*** High school diploma or equivalent with 5 years of experience; A bachelor’s degree or associate degree in a related field is preferred.* Related work experience is preferred in a medical device, pharmaceuticals, Quality/Regulatory Compliance, or other regulated industry.* Familiarity with application of FDA and/or ISO quality standards in a government regulated industry.* Moderate computer competence, including experience with database and Microsoft Office software to create reports, spreadsheets, analyze data and prepare presentations.* Knowledge of QC terms, tools, and methodologies.* Working knowledge of standard laboratory practices and safety.* Ability to follow instructions precisely, recognize deviations, and recommend corrective action.* Detail-oriented.**TOOLS AND EQUIPMENT USED**Calipers, rulers, dataloggers, standard office equipment (i.e. computers, phones, photocopiers, filing cabinets, other general office equipment).Salary Pay Range:$23.28 - $31.46 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.