Quality Specialist

CSLHazel Crest, IL
3d$18 - $21

About The Position

Responsibilities: • Under general direction, monitors plasma center processes to ensure compliance with Standard Operating Procedures (SOPs) and applicable local, state and federal requirements • Partners with management to have the center “inspection ready” at all times by managing compliance to SOPs and the quality system • Ensures compliance to quality processes, regulatory requirements, SOPs and necessary training for plasma center and business operations • Coordinates training and facilitates processes to support timely reporting of biologic product deviations to Food & Drug Administration (FDA) • Performs/ensures center records quality review to ensure thoroughness, accuracy and timeliness of required information • Initiates investigation to ensure documentation of deficiencies and development of corrective action plans, in partnership with management • Ensures training materials/documents are maintained and modified regularly; maintains the Learning Management System to ensure data integrity, report generation and data analysis • Leads internal audits to monitor facility compliance with SOPs, cGMP, OHSA, FDA, and other regulations, as applicable Qualifications: • Bachelor’s/Associate degree in business administration or biological sciences preferred, or equivalent combination of education, training and experience • 3-5 years’ experience in quality within Plasma or related industry • Minimum 1-year supervisory/leadership experience or equivalent of 1-year experience in a regulated environment • Knowledge of cGMP, OHSA, FDA, and other applicable regulations • Strong customer service skills • Equivalent combination of education and professional work experience required The expected base pay for this position at hiring is $18.10/hour - $20.75/hour. Please note this wage range reflects what CSL expects to pay for this position at the listed location as of the time of this posting. Individual base pay for a successful candidate within this range is determined by qualifications, skill level, experience, competencies and other relevant factors. Different qualifications or responsibilities may apply based on local legal and/or educational requirements. Refer to local job documentation where applicable.

Requirements

  • Bachelor’s/Associate degree in business administration or biological sciences preferred, or equivalent combination of education, training and experience
  • 3-5 years’ experience in quality within Plasma or related industry
  • Minimum 1-year supervisory/leadership experience or equivalent of 1-year experience in a regulated environment
  • Knowledge of cGMP, OHSA, FDA, and other applicable regulations
  • Strong customer service skills
  • Equivalent combination of education and professional work experience required

Responsibilities

  • Under general direction, monitors plasma center processes to ensure compliance with Standard Operating Procedures (SOPs) and applicable local, state and federal requirements
  • Partners with management to have the center “inspection ready” at all times by managing compliance to SOPs and the quality system
  • Ensures compliance to quality processes, regulatory requirements, SOPs and necessary training for plasma center and business operations
  • Coordinates training and facilitates processes to support timely reporting of biologic product deviations to Food & Drug Administration (FDA)
  • Performs/ensures center records quality review to ensure thoroughness, accuracy and timeliness of required information
  • Initiates investigation to ensure documentation of deficiencies and development of corrective action plans, in partnership with management
  • Ensures training materials/documents are maintained and modified regularly; maintains the Learning Management System to ensure data integrity, report generation and data analysis
  • Leads internal audits to monitor facility compliance with SOPs, cGMP, OHSA, FDA, and other regulations, as applicable
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