Kedrion Biopharma Inc. is an international company specializing in the collection and fractionation of blood plasma to produce and distribute plasma-derived therapeutic products. Our therapies help treat and prevent serious diseases, including Hemophilia, Primary Immune System Deficiencies, and Rh-Sensitization.
Kedrion Biopharma Inc. is committed to providing equal employment opportunities to all employees and applicants. We prohibit discrimination and harassment based on race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This policy applies to all employment terms, including recruitment, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.
Salary ranges are determined based on relevant experience, education, and certifications.
If you require assistance with your employment application or need reasonable accommodations to perform job duties, please contact our Talent Acquisition team at kedtalent@kedrion.com.
Employee Benefits
At Kedrion Biopharma Inc., we believe in taking care of our people. Our benefits package is designed to support your health, happiness, and future, including:
- Health & Wellness – Full medical, dental, and vision coverage
- Financial Security – Life insurance, AD&D, and retirement savings plans
- Work-Life Balance – Paid time off, sick leave, and paid holidays
- Career Growth – Training programs and development opportunities
- Extra Perks – Employee discounts, wellness initiatives, and more!
For specific inquiries please reach out to us
Bring your leadership to the heart of life-saving manufacturing.
At Kedrion Biopharma, every step of our work contributes to therapies that improve and save lives. As a Manufacturing Supervisor, you’ll lead a team of associates to ensure safe, efficient, and compliant operations that directly impact patients worldwide.
You’ll oversee daily operations for plasma fractionation and purification, driving “Right First Time” execution while meeting cGMP and regulatory standards. You’ll also guide process improvements, documentation updates, CAPA implementation, and equipment qualification. Your leadership will build a culture of safety, quality, and continuous improvement.
What You’ll Do
- Lead daily manufacturing operations to meet safety, quality, production, and financial goals.
- Assign and monitor tasks to ensure timely, compliant execution.
- Provide on-the-floor leadership (minimum 85% of time) to guide staff and resolve issues.
- Manage accurate batch documentation, logbooks, and SAP orders.
- Develop and update SOPs and Master Batch Records; train staff on changes.
- Implement and track CAPAs and change controls with timely, effective completion.
- Support activities such as buffer prep, equipment assembly, and parts washing.
- Oversee equipment and facility maintenance and cleaning schedules.
- Troubleshoot issues and drive process improvements.
- Track metrics and ensure department KPIs are achieved.
- Collaborate cross-functionally with QA, Facilities, Validation, and QC teams.
- Coach and mentor team members to ensure a motivated, compliant workforce.
- Maintain a safe, clean, and organized production environment.
- Prepare daily shift reports on safety, schedule adherence, and attendance.
Qualifications
- Bachelor’s degree in science or engineering with 5+ years cGMP manufacturing experience; or high school diploma with 8+ years relevant experience.
- 2+ years leadership or supervisory experience.
- Experience in fractionation, purification, or biopharma manufacturing preferred.
- Strong leadership skills with ability to coach and motivate teams.
- Proficiency in Microsoft Office, SAP, and production software.
- Excellent written, verbal, and problem-solving skills.
- Ability to work weekends or supplemental hours to support 24/7 operations.
Kedrion Biopharma Inc. participates in E-Verify and provides the federal government with Form I-9 information to confirm employment authorization. For more information, please contact the Department of Homeland Security.