Inspector, QC

Job Title: (Inspector, QC) About Kyyba: Founded in 1998 and headquartered in Farmington Hills, MI, Kyyba has a global presence delivering high-quality resources and top-notch recruiting services, enabling businesses to effectively respond to organizational changes and technological advances. At Kyyba, the overall well-being of our employees and their families is important to us. We are proud of our work culture which embodies our core values; incorporating value, passion, excellence, empowerment, and happiness, creates a vibrant and productive atmosphere. We empower our employees with the resources, incentives, and flexibility that they need to support a healthy, balanced, and fulfilling career by providing many valuable benefits and a balanced compensation structure combined with career development. Job Description Position Summary Responsible for ensuring compliance with all applicable Corporate and Divisional procedures, Quality System requirements, and regulatory expectations. Performs detailed quality assurance review and line support activities for Relabeling, Addendum, and related production documentation. Ensures complete and accurate review of LHR/eLHR, SAP transactions, and controlled documents while supporting Engineering, maintaining audit readiness, and promoting continuous improvement within the department. Essential Duties & Responsibilities: • Performs comprehensive QA reviews of LHR/eLHR, SAP transactions, and related documentation to verify accuracy, completeness, correct document revision use, and procedure adherence. • Audits materials, documentation, components, and line activities through visual checks, sampling, system verification, and comparison to specifications. • Supports reduction of documentation and process errors through thorough review, timely issue escalation, and consistent adherence to established quality practices. • Provides daily line support to Relabeling and Addendum operations, ensuring correct labeling, traceability, and documentation practices. Supports approval of required training holds. • Assists Engineering with assigned subtasks including demonstrations, scrapping, AQL sampling, testing of SAP/LHRBM or document changes, and support of other technical evaluations as required. • Contributes to documentation accuracy and continuous improvement by identifying process or documentation enhancements and supporting Change Order updates. Assists with assigned document updates and collaborates on development of controlled documents. • Executes SAP transactions and inventory movements accurately. Handles and documents discrepant materials in accordance with approved dispositions and all applicable procedures. • Supports internal and external audits by ensuring documentation is complete, organized, and available. Maintains full audit readiness through consistent compliance with procedural and documentation requirements. • Supports Quality, Operations, and Engineering with activities related to COA requests, ICS signature requests, retains management. • Maintains personal accountability for schedule adherence, accurate timecard entry, completion of required training, safe work practices, and participation in team activities such as daily stretches. • Provides safety recommendations or near miss submissions and actively participates in sustaining a culture of safety and compliance. • Achieves and maintains required certifications including QCRI, Relabeling, Addendum (if assigned), and QA Review recertification. Supports JI Assessor duties and other assigned quality responsibilities. • Performs additional duties as required in support of Divisional initiatives, Quality Management System objectives, Environmental Management System requirements, and other cross functional business needs. Knowledge, Skills & Competencies: • Strong attention to detail with the ability to perform accurate, complete, and compliant documentation review in a regulated environment. • Working knowledge of SAP, LHR/eLHR systems, AQL sampling methods, and document control practices. • Ability to understand and apply procedures, material specifications, drawings, and regulatory standards. • Effective communication skills with the ability to convey findings, collaborate with cross functional teams, and support training activities. • Familiarity with medical device regulatory frameworks such as ISO 13485 and 21 CFR 820 preferred. Location: (Temecula, CA) Disclaimer: Kyyba is an Equal Opportunity Employer. Kyyba does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other basis covered by appropriate law. Minorities / Females / Protected Veterans / Individuals with Disabilities are encouraged to apply. All employment is decided on the basis of qualifications, merit, and business need." It is the policy of Kyyba to provide reasonable accommodation when requested by a qualified applicant or employee with a disability, unless such accommodation would cause an undue hardship. The policy regarding requests for reasonable accommodation applies to all aspects of employment, including the application process. If reasonable accommodation is needed, please contact Kyyba at 248-813-9665 Rewards: Medical, dental, vision 401k Term life Voluntary life and disability insurance Optional Pre-paid legal plan Optional Identity theft plan Optional Medical and dependent FSA Work-visa sponsorship Opportunity for advancement Long-term assignment with opportunity for hire by client SELECT AWARDSAn INC 5000 company for 10 yearsCorp! 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