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
Job Description for Manufacturing Supervisor
Manufacturing Supervisor
Job Description for Manufacturing Supervisor
Manufacturing Supervisor
Job Description
Bring your leadership to the heart of life-saving manufacturing.
At Kedrion Biopharma, every step of our manufacturing process contributes to therapies that improve and save lives for people with rare and serious conditions. As a Manufacturing Supervisor, you’ll lead a dedicated team of manufacturing associates, ensuring that each operation is performed safely, efficiently, and to the highest quality standards. This is more than just production — it’s about precision, compliance, and the knowledge that your work impacts patients worldwide.
You’ll oversee the daily operations for the fractionation and purification of plasma intermediates, ensuring a “Right First Time” execution of tasks while adhering to cGMP and all regulatory requirements. You will also guide critical projects to improve processes, develop documentation, implement Corrective and Preventive Actions (CAPAs), and qualify equipment. Your leadership will inspire operational excellence and build a culture of safety, quality, and continuous improvement.
What You’ll Do:
- Lead and supervise daily manufacturing operations to meet safety, quality, production, and financial goals.
- Plan, assign, and monitor daily tasks to ensure timely completion in compliance with cGMP and regulatory standards.
- Provide on-the-floor leadership presence (minimum 85% of time) to guide operations, solve problems, and support staff.
- Manage the timely and accurate execution and review of batch documentation, logbooks, and SAP orders.
- Develop and update SOPs and Master Batch Records; train staff on new or revised procedures.
- Implement and track CAPAs and change controls, ensuring timely completion and effective corrective measures.
- Support manufacturing activities such as buffer preparation, equipment assembly, and parts washing operations.
- Supervise equipment and facility maintenance, including cleaning schedules and repair work orders.
- Troubleshoot operational issues and drive process improvement initiatives to increase efficiency and quality.
- Track performance metrics and ensure department goals and KPIs are consistently achieved.
- Foster cross-functional collaboration with Quality Assurance, Facilities, Validation, and QC teams.
- Coach, mentor, and develop team members to ensure a motivated, knowledgeable, and compliant workforce.
- Maintain a safe, clean, and well-organized production environment that complies with all EHS standards.
- Prepare and deliver daily shift reports on safety, schedule adherence, and attendance.
Qualifications:
- Bachelor’s degree in a scientific or engineering discipline and at least 5 years’ cGMP manufacturing experience; or high school diploma with 8+ years’ relevant experience.
- Minimum of 2 years of leadership or supervisory experience.
- Experience in fractionation, purification, or manufacturing operations for biopharmaceuticals preferred.
- Strong leadership skills with the ability to coach, mentor, and motivate teams.
- Proficiency in Microsoft Office, SAP, and production equipment software.
- Excellent written and verbal communication skills.
- Strong problem-solving skills and the ability to work under pressure in a fast-paced, multi-tasking environment.
- Ability to work weekends or supplemental hours to support a 24/7 schedule.
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.