North America CQSS QMS Analyst at Johnson & Johnson in Mooresville, NC

North America CQSS QMS Analyst Location: Mooresville, Indiana, United States of America At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world.  We provide an inclusive work environment where each person is considered as an individual.  At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit. Job Function: Quality Job Sub Function: Customer/Commercial Quality Job Category: Professional All Job Posting Locations: Mooresville, Indiana, United States of America Job Description: DePuy Synthes isrecruiting fora(n)North America CQSS/QMS Analyst,locatedin Mooresville, Indiana. The North America CQSS/QMS Analyst supports the effectiveness and continuous improvement of the Quality Management System (QMS) within DePuy Synthes. This role plays a critical part in ensuring compliance with applicable quality system regulations and internal standards while partnering closely with Quality, Regulatory Affairs, andcross‑functionalteams. The position offers the opportunity to directlyimpactproduct quality, patient safety, and regulatory readiness across the North America region by supporting audits, metrics, and quality system processes. Key Responsibilities Support the maintenance, execution, and continuous improvement of the Quality Management System (QMS) in alignment with internal procedures and external regulatory requirements. Assistwith quality system processes including document control, change management, CAPA, internal audits, and management review activities. Compile, analyze, and trend quality data and metrics to support compliance monitoring and leadership reporting. Participate in internal, supplier, and regulatory audits by preparing documentation, responding to requests, and trackingfollow‑upactions. Supportinspectionreadiness activities and ensuretimelyclosure of audit observations and commitments. Collaborate withcross‑functionalpartners to ensure consistent application of QMS requirements across the organization. Contribute toquality system training materials and support training compliance activities. Qualifications Education Bachelor’s degreerequired, preferably in Engineering, Life Sciences, Quality, or a related technical discipline. Advanced degree preferred. Experience and Skills Required: Approximately 2–4 years of experience in Quality, Compliance, or Quality Systems within a regulated environment (medical device, pharmaceutical, or similar). Working knowledge of Quality Management Systems and applicable regulations and standards (e.g., FDA QSR, ISO 13485). Experience supporting audits, inspections, or quality system assessments. Ability to manage multiple priorities and work effectively in across‑functionalenvironment. Preferred: Experience in the medical device industry or orthopedics sector. Familiarity with electronic QMS (eQMS) tools and document management systems. Experience with CAPA, change control, and management review processes. Prior involvement in regulatory authority inspections or notified body audits. Continuous improvement or risk management experience. Strong analytical skills with the ability to interpret quality data and metrics. Effective written and verbal communication skills. Other: Language: Englishproficiencyrequired. Travel: Limited; up to ~10% domestic travel may berequired. Certifications: ASQ or otherquality‑relatedcertifications preferred but notrequired. For more information on how we support the whole health of our employees throughout their wellness,careerand life journey, please visitwww.careers.jnj.com. Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company, operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months, subject to legal requirements, including consultation with works councils and other employee representative bodies, as may be required, regulatory approvals and other customary conditions and approvals. Should you accept this position, it is anticipated that, following conclusion of the transaction, you would be an employee of DePuy Synthes and your employment would be governed by DePuy Synthes employment processes, programs, policies, and benefit plans. In that case, details of any planned changes would be provided to you by DePuy Synthes at an appropriate time and subject to any necessary consultation processes. Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource. #LI-Hybrid #DePuySynthesCareers Required Skills: Preferred Skills: Audit Management, Business Behavior, Coaching, Compliance Management, Continuous Improvement, Data Analysis, Detail-Oriented, Goal Attainment, Internal Controls, Issue Escalation, Problem Solving, Process Oriented, Quality Control (QC), Quality Management Systems (QMS), Quality Standards, Regulatory Environment The anticipated base pay range for this position is : 79,000.00 - 1,42,000.00 USD Annual Additional Description for Pay Transparency: Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)). Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits: Vacation –120 hours per calendar year Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year Holiday pay, including Floating Holidays –13 days per calendar year Work, Personal and Family Time - up to 40 hours per calendar year Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year Caregiver Leave – 80 hours in a 52-week rolling period10 days Volunteer Leave – 32 hours per calendar year Military Spouse Time-Off – 80 hours per calendar year For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits