Kedrion Biopharma

Traveling Quality Manager

Kedrion Biopharma$71K — $98K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree required; minimum three years in plasma industry or four to five years in a regulated industry.
  • Ability to travel up to 80% to donor centers by plane and car.
  • Strong written and verbal communication skills for presentations.
  • Proven ability to work effectively with diverse teams and stakeholders.
  • Proficient in English, both spoken and written.
  • Strong technical aptitude, including experience with donor management systems and Microsoft Office applications.

Responsibilities

  • Ensure compliance with cGMP, SOPs, and regulatory requirements at donor centers.
  • Promote understanding of regulations and corporate policies across the region.
  • Partner with management to support product and employee safety.
  • Monitor quality performance for continuous inspection readiness.
  • Lead and mentor Quality Assurance teams to enhance performance and compliance.
  • Identify and evaluate quality and compliance issues and contributing factors.
  • Support SOP updates and ensure compliant implementation across centers.

Benefits

  • Full medical, dental, and vision coverage.
  • Life insurance, AD&D, and retirement savings plans.
  • Paid time off, sick leave, and paid holidays.
  • Training programs and development opportunities.
  • Employee discounts, wellness initiatives, and more!
Full Job Description
Posting Start Date: 9/17/26

State/Province: New Jersey

Job Location: Fort Lee

Place of Employment:

Contract Duration: Permanent

Hiring Pay Range Min: 71800

Hiring Pay Range Max: 98000

Traveling Quality Manager

Job Summary

Lead quality across the network-on the ground, on the move, and at the center of compliance.
As a Traveling Quality Assurance Manager, you will play a critical role in safeguarding product quality, donor and employee safety, and regulatory compliance across assigned donor centers. Working closely with regional and center leadership, you will ensure adherence to cGMP, SOPs, and company standards while mentoring quality teams and driving continuous improvement. This is a highly visible, travel-intensive role that offers exposure to audits, corrective actions, training, and special quality initiatives across multiple locations.

What you'll do

  • Ensure assigned donor centers maintain compliance with cGMP, SOPs, company standards, and applicable FDA, EMEA, customer, and other regulatory requirements
  • Promote understanding and consistent application of state and federal regulations, industry expectations, and corporate policies across the assigned region
  • Partner with Regional and Center Management to support product quality, donor safety, and employee safety initiatives
  • Monitor quality performance and facilitate required QA activities to maintain continuous inspection readiness
  • Lead, train, coach, and mentor Quality Assurance Managers and Quality Assurance Specialists to strengthen performance and regulatory knowledge
  • Identify potential, serious, or recurring quality and compliance issues and evaluate contributing factors such as procedures, training, facilities, and equipment
  • Participate in the review, development, and updating of SOPs and validation processes at both the center and corporate level
  • Ensure timely, accurate, and compliant implementation of new or revised SOPs across donor centers
  • Support donor center operations with investigations and documentation related to Non-Conformance Reports, Post Donation Reports, error and accident reports, and complaints
  • Develop, implement, and track corrective and preventive actions, ensuring timely completion and proper closure
  • Assist with the review and qualification of equipment calibration and maintenance activities and verify documentation completeness
  • Track and verify donor center compliance using the Donor Management System
  • Actively encourage and participate in continuous quality improvement initiatives
  • Review epidemiological data submissions and support centers on Viral Marker Alert by identifying root causes and implementing corrective actions
  • Provide support for special traveling quality projects, including warehouse inventory reconciliation and release activities
  • Provide temporary coverage and on-site quality support as directed by Regional Quality Management
  • Support donor centers in preparation for and during regulatory and customer audits


Qualifications and need-to-know

  • Bachelor's degree required with a minimum of three years of experience in the plasma industry, or four to five years of commensurate experience in a related regulated industry
  • Ability to travel up to 80% by plane and/or car to donor centers
  • Strong written and verbal communication skills, including the ability to conduct oral presentations
  • Proven ability to work effectively with diverse teams and stakeholders
  • Ability to speak, read, and write in English
  • Professional appearance and demeanor
  • Strong technical aptitude, including experience with donor management systems and Microsoft Office applications


Employment eligibility verification will be required at the time of hire. This position does not offer visa sponsorship now or in the future.

Salary ranges are determined based on relevant experience, education, and certifications.

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

About Kedrion Biopharma

Kedrion Biopharma is a biopharmaceutical company that specializes in the development, production, and distribution of plasma-derived products for the treatment of rare and serious diseases. The company's product portfolio includes immunoglobulins, coagulation factors, and albumin, which are used to treat a variety of conditions, including immune deficiencies, bleeding disorders, and shock. Kedrion Biopharma operates in more than 100 countries worldwide and has a strong presence in Europe, North America, and Asia. The company is committed to improving the lives of patients with rare and serious diseases by providing high-quality, safe, and effective therapies. Kedrion Biopharma is headquartered in Fort Lee, New Jersey.
Learn more about Kedrion Biopharma
Size
2,500 employees
Industry

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