Octapharma Plasma, Inc. · 12 hours ago
Center Quality Manager 1
Octapharma Plasma, Inc. is seeking a Center Quality Manager 1 to join their plasma center management team. This role is responsible for ensuring compliance with regulatory requirements and industry standards related to plasma collection and donor safety, while also overseeing quality control processes and leading quality assurance initiatives.
BiotechnologyHealth CarePharmaceutical
Responsibilities
Operate independently of plasma center operations to ensure compliance with all federal, state, local, and industry regulations (e.g., FDA, EMA)
Report critical incidents and negative trends to the Operations team and Regional leadership and collaborate with Operations to ensure product quality and donor safety
Maintain current knowledge of regulations and standards affecting plasma collection and donor safety; execute QA policies and procedures to comply with requirements
Oversee quality control processes, including donor screening, plasma collection, storage, and shipping; ensure QC checks, validations, equipment calibration, and CLIA assessments are performed according to SOPs
Monitor and review quality performance indicators, including deviations, Corrective and Preventive Actions (CAPAs), and complaints; lead monthly Quality Assurance meetings to discuss SOP changes and regulatory requirements
Conduct final QA review and release of all product shipments and associated documents to ensure compliance with customer specifications
Serve as Designated QA Trainer, developing and delivering training on GMP, SOPs, and compliance; provide direction and oversight to Quality backup staff and participate in QA staff selection
Prepare for and lead internal and external audits; maintain audit records and ensure timely completion of audit responses and corrective actions
Perform root cause analyses, implement CAPAs, and conduct effectiveness checks for systemic issues
Continuously assess, promote, and improve quality systems by investigating trends, supporting continuous improvement initiatives, and monitoring outcomes
Provide leadership in the implementation of changes, adjusting strategies as necessary to strengthen quality and compliance
Perform other duties as assigned
Qualification
Required
One (1) year experience in a Quality Assurance role
Preferred
Bachelor's degree preferred
Experience with quality management systems (QMS) and quality control processes preferred
Ability to sit or stand for extended periods
Ability to tug, lift, and pull up to thirty-five (35) pounds
Ability to bend, stoop or kneel
Ability to enter an environment with a temperature of -40°C for short periods of time
Occupational exposure to blood borne pathogens
Ability to view video display terminal less than 18” away from face for extended periods of time
Ability to perform precise tasks that require repetitive small motor skills, such as drawing blood for diagnostic tests
Ability to use a computer and other office equipment
Ability to use assistive devices if needed for mobility or communication
Ability to communicate effectively, both verbally and in writing
Ability to focus and concentrate on tasks for extended periods
Ability to navigate the office environment safely, including stairs and elevators (if applicable)
Ability to travel up to 20% via airplane and vehicle for CQM I and up to 75% for all others
Benefits
Formal training
Outstanding plans for medical, dental, and vision insurance
Health savings account (HSA)
Flexible spending account (FSA)
Tuition Reimbursement
Employee assistance program (EAP)
Wellness program
401k retirement plan
Paid time off
Company paid holidays
Personal time
Company
Octapharma Plasma, Inc.
About Us: Octapharma Plasma, Inc. helps change lives through the incredible power of plasma donation.
Funding
Current Stage
Late StageRecent News
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2025-09-26
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