Supervisor, Manufacturing

Are you ready to work for a more active world?

At 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.

• Lead day-to-day production activity for the Surgical manufacturing line, ensuring safe, efficient, and compliant operations.
• Assign labor, balance workloads, and manage resource allocation to meet production schedules and takt time requirements.
• Execute shift huddles, communication updates, and performance reviews (hour-by-hour boards, tier meetings, etc.).
• Monitor production metrics (throughput, FPY, scrap, downtime, labor efficiency) and take immediate action to address issues.
• Ensure adherence to manufacturing instructions, device history records, SOPs, and regulatory requirements (FDA QSR, ISO 13485).
• Support and document deviations, nonconformances, and quality holds; partner with Quality Engineering to resolve issues.
• Maintain traceability, proper documentation, and batch/lot control throughout production.
• Provide direction, coaching, performance feedback, and development to production team members.
• Manage staffing, timekeeping, training, and cross‑training to ensure adequate skill coverage.
• Lead onboarding for new associates and ensure proficiency in standard work and quality expectations.
• Support performance management, attendance guidance, and corrective action when necessary.
• Partner with Supply Chain to ensure material availability, component accuracy, and inventory integrity.
• Escalate equipment issues promptly and work with Maintenance/Engineering to restore operation.
• Enforce safety standards, ergonomic practices, and proper use of PPE.
• Participate in Production Readiness for NPI/Sustaining Engineering changes.
• Holds oneself and others accountable to conduct business in a manner compliant with Bioventus’ Code of Compliance and Ethics, policies, procedures, and internal controls applicable to their role.
• Other duties as assigned.

• Bachelors degree (preferred) or a high school diploma with relevant experience.
• 3–5 years experience in a regulated manufacturing environment (medical device, pharmaceutical, biotech, or equivalent) required.
• Prior experience in a leadership or supervisory role required.
• Strong understanding of Good Manufacturing Practices (GMP), FDA QSR, and ISO 13485 requirements.
• Demonstrated ability to lead a team, manage production flow, and communicate effectively.
• Proven ability to manage priorities, problem‑solve, and drive performance in a fast‑paced environment.
• Experience with in medical device assembly or surgical product manufacturing, preferred.
• Knowledge of Lean, Six Sigma, standard work, and continuous improvement tools, preferred.
• Experience with ERP systems (SAP preferred).

Reports to:

Director, Manufacturing

Direct Reports:
Yes

Apply now! Hit the “Apply” button to send us your resume and cover letter.

Bioventus 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.

All individuals, regardless of personal characteristics, are encouraged to apply.