Quality Compliance Associate

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.The Quality Compliance Associate supports the site Quality Management System (QMS) by performing routine quality system and compliance activities in accordance with internal procedures and regulatory requirements. Primary responsibilities include supporting complaint handling and investigations, Nonconformance (NC) and CAPA processes, maintaining quality documentation, and providing quality assurance support to manufacturing and product development teams. This role works under the guidance of senior quality personnel and contributes to continuous improvement initiatives.ResponsibilitiesSupports the maintenance of the site Quality Management System (QMS) to ensure compliance with applicable regulations, standards, and internal procedures.Assists with complaint intake, documentation, investigation support, and timely closure in accordance with complaint handling procedures.Supports the initiation, review, processing, and completion of Nonconformance (NC) records in the electronic quality system.Gathers information and supporting data for complaint investigations, NCs, and CAPAs, and assists with root cause analysis activities.Maintains quality system documentation, including procedures, forms, and records, ensuring accuracy and document control compliance.Assists with quality data collection, trending, and reporting of quality metrics in accordance with established procedures.Provides quality assurance support to manufacturing, product development, and other functional areas by addressing quality questions and ensuring procedural adherence.Supports internal and external audits by preparing documentation, responding to requests, and participating as needed.Participates in quality-focused meetings, communicates status updates, and tracks actions to completion.Escalates potential quality issues, compliance risks, or delays to senior quality personnel in a timely manner.Participates in continuous improvement activities and special projects as assigned.Completes required training and maintains awareness of applicable quality system requirements and regulatory expectations.Minimum QualificationsAssociate’s degree in a scientific, technical, or related discipline or a minimum of 2 years of experience working within a regulated industry (e.g., medical device, pharmaceutical, biotechnology, or similar).Previous experience supporting quality systems, complaint handling, nonconformance management, or documentation control preferred.Basic understanding of regulated quality environments (e.g., FDA, ISO, or similar standards).Strong attention to detail and organizational skills with the ability to manage multiple tasks and meet deadlines.Effective written and verbal communication skills.Ability to clearly document findings and follow established procedures.Must be able to read and write in English.Salary Pay Range:$62,100.00 - $85,100.00 USD SalaryOur 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 VeteransIntegra 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 View email address on click.appcast.io 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 #J-18808-Ljbffr