{"id":4283811,"url":"https://alion.io/job/bioventus-manufacturing-engineer-ii","title":"Manufacturing Engineer II","company":{"id":2812900,"name":"Bioventus","domain":"bioventus.com","url":"https://alion.io/company/bioventus","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"B","score":75,"open_postings":4,"ghost_share":0,"stale_share":1,"repost_share":0,"time_to_fill_p50_days":null,"computed_at":"2026-11-14T05:58:10Z"}},"role":"Industrial Engineering","role_family":"Industrial Engineering","seniority":"middle","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Memphis, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":null,"experience_years_min":2,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"21 CFR Part 820","optional":false},{"name":"Design Controls","optional":false},{"name":"GMP","optional":false},{"name":"ISO 13485","optional":false},{"name":"Microsoft Office","optional":false},{"name":"Outlook","optional":false}],"status":"live","first_seen_at":"2026-11-13T21:11:47Z","employer_posted_date":"2026-11-13","last_verified_at":"2026-11-14T15:54:18Z","board_verified":true,"closed_at":null,"days_open":1,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":1},"description":"Are you ready to work for a more active world?\nAt Bioventus, our business depends on developing our people. We invest in you and challenge you to be the best. We value our colleagues for their different perspectives and individual contributions, and our leaders listen. Our success rests on working together to achieve shared goals and rewards. Join a diverse team of global colleagues driven to help patients resume and enjoy active lives.\nThe Manufacturing Engineer is responsible for support and sustaining of existing products. The position is also responsible for delivering technical service of products including: installation qualification, upgrades, troubleshooting, repair and preventative maintenance. The responsibilities also include optimizing system performance to minimize equipment downtime and to ensure maximum overall customer satisfaction.Key Responsibilities:\n1. Responsible for managing manufacturing activities and technical operations functions.\n2. Serve as technical subject matter expert (SME) for all medical device products.\n3. Collaborate with new product development teams to ensure successful integration of new products into manufacturing.\n4. Visit external manufacturing sites as needed to provide technical and validation support and training to contract manufacturing organizations. \n5. Create and maintain technical product specifications, standard work, drawings, bill of materials, batch records, procedures, and Global Unique Device Identification Database (GUDID).\n6. Lead development, troubleshooting, and manufacturing process improvements with external vendors including preparation of design controls and design transfer. \n7. Develop product packaging and establishes test requirements per ISO, and ASTM standards. \n8. Using Lean principles, identify and implement processes to reduce waste and improve manufacturing yield and throughput. \n9. Responsible to serve as SME for designing, assembling, modifying, and supporting custom designed and off-the-shelf processing equipment. \n10. Develop, manage, and perform all process validation/verification and equipment qualification activities, including writing protocols, analyzing data, investigating deviations, non-conformances, corrective and preventative actions, and writing reports. \n11. Develop standard operations procedures (SOP’s) to ensure best practices are consistently followed across the organization. \n12. Identify opportunities and resolve process/service issues; gather, analyze and interpret data to determine root cause or errors/nonconformances and implement appropriate corrective actions. \n13. Measure assigned performance goals for manufacturing operations. Understand internal business processes and lead cross-functional teams in development of new and improved processes. \n14. Hold oneself and others accountable to conduct business in a manner compliant with Bioventus’ Code of Compliance and Ethics, policies and procedures and internal controls applicable to their role.\n15. Collaborates with Audit & Risk Management function to identify business risks, and develop and implement preventive strategies for functional area.\n16. Other duties as assigned.\nEducation and Experience (Knowledge, Skills & Abilities)\nBachelor or higher degree in Engineering (preferably Mechanical Engineering) and 2 or more years’ experience required.\nKnowledge of applicable state, federal, and international regulatory requirements (i.e. ISO 13485, FDA 21 CFR 820, etc.) for surgical products (i.e. requirements for current good manufacturing practice (CGMP’s) for medical devices and biologics. \nClean room manufacturing experience is preferred.\nExperience in mechanical design of tools, fixtures, and gauges.\nExperience in implementing design to reduce manufacturing costs.\nExperience in Lean concepts, including Root Cause Analysis and DMAIC thinking. Green Belt certification preferred. \nSound decision making and innovative thinking. \nExcellent communications skills (written and verbal).\nProficient using MS Office products (Word, Excel, PowerPoint, Visio, Adobe, Outlook).\nExperience using statistical software for data analysis. \nExperience using solid modeling (CAD.CAM) software preferred. \nExperience using document control software. \nKnowledge of SAP or other integrated software application is strongly desired but not required.\nAre you the top talent we are looking for?\nApply now! Hit the “Apply” button to send us your resume and cover letter.\nBioventus is committed to fostering an inclusive and diverse community of employees with a strong sense of belonging. We believe we are bettered by all forms of diversity and take pride in working with top talent from every walk of life. In the spirit of inclusivity, qualified applicants will be considered without regard to age, ethnicity, disability, gender, veteran status, gender expression, gender identity, nationality, race, religion or sexual orientation. 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