Skip to main content
Tallo logoTallo logo

Find Jobs

Find Jobs Near You – Available Work in Your Location

Skip to job details

Back to Results

Apply for this opportunity

To apply for this job, you'll continue to an external website or email application.

Octapharma

Center Quality Manager 1

Career Insights for Quality Assurance Auditor

See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.

Scorecard

Based on Florida data

Review key factors to help you decide if this role fits your goals. How is this calculated?

Were these scores useful?

What they do

A Quality Assurance Auditor regularly evaluates the quality control systems in place and verifies compliance with quality and safety standards.

$55,660 / year median in Florida

-2% projected decline

Explore Career

Job Description

Center Quality Manager 1 Octapharma Pembroke Pines, FL Job Details Full-time 23 hours ago Benefits Wellness program Health savings account Paid holidays Health insurance Dental insurance 401(k) Flexible spending account Tuition reimbursement Paid time off Employee assistance program Vision insurance Qualifications Computer operation Computer literacy Typing Full Job Description Job Summary This role serves as a member of the plasma center management team. The position will ensure all activities and processes related to plasma collection, donor eligibility, and product quality comply with regulatory requirements, industry standards, and company policies. This is What You'll Do Operate independent of plasma center Operations to ensure compliance with all applicable federal, state, and local regulations, as well as industry standards (e.g., FDA, EMA). Maintain current knowledge of regulations and standards affecting plasma collection and donor safety. Reports critical incidents and negative trends to plasma center Operations team and Regional Quality Director. Collaborate with the plasma center Operations team to ensure product quality and donor safety. Monitor and review quality performance indicators, including deviations, CAPAs (Corrective and Preventive Actions), and complaints. Oversee the quality control processes, including donor screening, plasma collection, storage, and shipping. Perform final QA review and release for all product shipments and associated documents to ensure shipment meets customer specifications. Execute QA policies and procedures to comply with regulatory requirements. Quality Control (QC) checks and validation activities are performed in accordance with SOP. Prepare for and lead internal and external audits and inspections. Develop and implement audit responses ensuring timely completion and adherence to quality standards. Maintain audit records and follow up on audit findings and corrective actions. Serve as Designated QA Trainer and responsible for training Quality backup staff and Plasma Center Quality Manager I. Develop and deliver training programs for staff on quality-related topics, including GMP (Good Manufacturing Practice), SOPs (Standard Operating Procedures), and regulatory compliance. Proficiency surveys and CLIA-required competency assessments are performed in accordance with the required timeframes defined in SOP. Equipment maintenance and calibration documentation comply with Standard Operating Procedures (SOPs). Perform root cause analysis, implement corrective/preventive actions, and conduct effectiveness checks for systemic issues. Continuously assess, promote, and improve the effectiveness of the quality systems in the plasma center through the investigation of trends resulting from failures in the execution of procedures. Support the implementation of continuous improvement initiatives. Monitor the effectiveness of implemented changes and adjust strategies as necessary. Prepare agenda and lead monthly Quality Assurance Meeting to discuss SOP changes and regulatory requirements are conducted, documented and minutes are communicated to all donor center staff. Participate in the selection process for the Quality Assurance Back-up role. Provide direction and oversight of Quality Back-up staff, ensuring required quality tasks are completed within required time frames. Perform other duties as assigned. This is What it Takes B.S. degree preferred. Other combinations of education and experience may be considered. One (1) year experience in a Quality Assurance role required. Experience with quality management systems (QMS) and quality control processes preferred. Physical Requirements Ability to work day and evening hours, weekends, holidays, and extended shifts. Ability to sit or stand for extended periods for up to four (4) hours at a time. 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, up to four (4) hours at a time. Ability to perform precise tasks that require repetitive small motor skills, such as drawing blood for diagnostic tests. Ability to type and use basic computer skills. Ability to use assistive devices if needed for mobility or communication.
https:
//careers.octapharmaplasma.com/us/en/center-quality-manager-i Do Satisfying Work. Earn Real Rewards and Benefits We're widely known and respected for our benefits and for leadership that is supportive and hands-on. Managers who truly want you to grow and excel. 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

Benefits

  • Paid Time Off (PTO)
  • Financial Aid/Assistance
  • 401(k) Plans
  • Other Retirement and Savings