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Quality Assurance Specialist

2 months ago

Gilroy, California, United States SOFIE Full time
Job Description

Job Title: Quality Assurance Specialist

Job Summary:

The Quality Assurance Specialist will be responsible for overseeing the Quality Assurance program and the Quality Management System at the site level. This role will ensure product quality and regulatory compliance by applying quality assurance processes and procedures at the site level.

Key Responsibilities:

  • Maintain oversight of the QA program and Quality Management System (QMS) at a single SOFIE manufacturing facility producing products under both 21 CFR Part 212 and 211 (as needed) regulations.
  • Apply quality assurance processes and procedures at the site level to ensure product quality and regulatory compliance.
  • Collaborate with the Facility Manager and Operations team to ensure strong communication and problem-solving efforts.
  • Write, review, approve, and implement procedures, specifications, processes, and methods as required.
  • Oversee the examination and evaluation of each lot of incoming material before use to ensure that the material meets its established specifications.
  • Ensure that components, containers, closures, in-process materials, packaging materials, labeling, and finished dosage forms are examined and approved or rejected to ensure that all these meet their current specifications.
  • Ensure that personnel are properly trained and qualified. Ensure that the training is documented.
  • Conduct periodic audits of the site to monitor compliance with established procedures and practices. May infrequently audit another site.
  • Liaise with internal and external inspectors and representatives, particularly on QA-related topics.
  • Oversee the metrology program at the site (i.e., equipment, personnel qualifications, validations, etc.).
  • Ensure manufacturing and analytical equipment is appropriately maintained and calibrated. Ensure applicable facility certifications are maintained. Identify to management problems in personnel, equipment, and the facility that require correction.
  • Review documents associated with the site's QA program for completeness, errors, and omissions. Review executed CGMP records and product batch records to ensure compliance and product quality.
  • Review trends (e.g., environmental monitoring, deviations, facility issues, etc.) to initiate corrective and preventive actions and/or for continuous process improvement.
  • Conduct continuous review of aseptic operations to ensure compliance to internal procedures (e.g., gowning, cleaning, sanitation, sterility, environmental monitoring, etc.) and USP/FDA regulations.
  • Ensure any deviations from normal procedures are documented and justified.
  • Ensure an investigation is performed and documented when required, and corrective and preventative actions are taken (i.e., follow and maintain corporate CAPA, deviation, and OOS protocols).
  • Ensure compliance to all applicable standard operating procedures and regulations, including 21 CFR Part 212 (and 211 as needed) requirements.
  • Ensure product complaints are managed in a manner consistent with Company SOPs and FDA regulations.
  • Responsible for opening change controls and initiating, maintaining, and reviewing SOFIE network and site-specific procedures relative to their job functions.
  • Oversee the site-level change control process. Ensure that changes in the laboratory are accepted or rejected as appropriate, and ensure the changes are appropriately documented.
  • Attend quality and operational meetings. Interface with Corporate QA and Operations on quality-related issues. Provide status updates as required by management.

Requirements:

  • Associate's or Bachelor's Degree, at minimum
  • Relevant certifications and/or experience may be substituted in lieu of this requirement
  • 1-2 years of QA, Pharmacy, and/or CGMP manufacturing experience