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Quality Systems Manager

Job in Stamford, Fairfield County, Connecticut, 06925, USA
Listing for: Jobtailor
Full Time position
Listed on 2026-07-22
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist
  • Management
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 60000 - 85000 USD Yearly USD 60000.00 85000.00 YEAR
Job Description & How to Apply Below

Responsibilities

  • Evaluates processes, develops action plans, and coordinates the strategic implementation of quality system processes and corrective actions at the plasma donor center.
  • Maintains oversight of the center’s quality management system and ensures continuous quality improvement, by addressing deficiencies in a timely manner and communicating concerns to the appropriate parties.
  • Directs and monitors processes and ensures center compliance with all applicable state, federal, and company-designated regulations. Implements Standard Operating Procedures (SOPs) for quality control and overall regulatory compliance.
  • Maintains oversight of center training program by ensuring compliance to program requirements promoting staff competency in their assigned job duties. Maintains and audits training records and files.
  • Collaborates with Center Manager to ensure the donor center operates in a manner which assures product quality, donor suitability and donor safety are maintained.
  • Responsible for the personnel functions of the Quality Systems Associate; including direction, assignment of work, hiring, development and training, disciplinary actions, termination, maintenance of personnel records, work schedule and delegation/follow-up of tasks.
  • Responsible for oversight of all aspects of internal and external audits including audit preparation, execution, response, implementation of corrective/preventative actions, assessment of corrective actions, and follow-up as required.
Requirements
  • Bachelor of Science degree or equivalent.
  • Typically requires 2 years of related experience in a medical and/or cGMP regulated environment.
  • Experience with plasma or whole blood preferred.
  • Command of interpersonal communication, organizational and problem-solving abilities.
  • Ability to understand and assess FDA regulations.
  • Strong integrity and commitment to quality and compliance.
  • Full command of mathematics.
  • Legible handwriting.
  • High level of proficiency with computers.
  • Proficient in root cause analysis and corrective/preventative actions.
  • Ability to balance multiple competing priorities.
  • Strong time management abilities.
  • Proven ability to maintain a high level of quality and compliance and to become a valuable member of the center leadership team.
  • Ability to work with minimal supervision.

    Ability to travel when needed for meetings, events, and occasional support of other centers.
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