QA/RA Specialist

synergy
  • Dallas, Texas
    30+ days ago

    Job Description

    Description

    Synergy Bioscience is a pharmaceutical and biotech CRDMO providing development, manufacturing, testing, and regulatory compliance consulting services. Our work supports organizations navigating complex quality and regulatory demands across the product lifecycle, with a focus on maintaining rigorous standards in highly regulated environments.

    As a QA/RA Specialist, you will play an important role in helping maintain the quality and regulatory foundation behind laboratory and manufacturing operations. This role is well suited to someone who brings strong judgment, a detail-oriented approach, and the ability to work across teams to support compliant, consistent, and effective quality systems.

    Responsibilities

    • Maintain quality assurance and regulatory affairs documentation in compliance with GLP and GMP standards.
    • Ensure adherence to regulatory requirements from FDA, EMA, and other global regulatory agencies.
    • Conduct internal audits and inspections to assess compliance with quality systems and regulatory standards.
    • Support preparation and management of regulatory submissions and responses to regulatory agencies.
    • Collaborate with cross-functional teams to ensure compliance throughout the product lifecycle.
    • Provide GLP/GMP regulatory compliance training to laboratory and manufacturing staff.
    • Investigate and support resolution of deviations, non-conformances, OOS, and CAPA activities.
    • Maintain readiness of the facility for upcoming audits.


    Requirements
    • Bachelor’s degree in life sciences, pharmacy, chemistry, or a related field.
    • 10+ years of QA/RA experience in pharmaceutical environments working under both GLP or GMP standards.
    • Strong knowledge of FDA, EMA, and ICH regulatory requirements.
    • Hands-on experience conducting internal audits and inspections, investigating deviations, out-of-specification, and CAPA investigations.
    • Experience managing regulatory submissions and responses to regulatory agencies.
    • Experience training laboratory staff on quality system requirements and regulatory standards.


    Benefits

    • Health Care Plan (Medical, Dental & Vision)
    • Paid Time Off (Vacation, Sick & Public Holidays)
    • Training & Development

    Numbers & Facts

    LocationDallas, Texas

    Skills

    • Auditingunmatched
    • Biologyunmatched
    • Biotech and Pharmaceuticalunmatched
    • Chemistryunmatched
    • Consultingunmatched
    • Corrective and Preventative Action (CAPA) Systemsunmatched
    • Cross-Functionalunmatched
    • Detail Orientedunmatched
    • Documentationunmatched
    • FDA (Food and Drug Administration)unmatched
    • FDA Requirementsunmatched
    • GLP (Good Laboratory Practices)unmatched
    • GMP (Good Manufacturing Practices)unmatched
    • Health Planunmatched
    • ICH Regulationsunmatched
    • Insurance Regulationsunmatched
    • Internal Auditunmatched
    • Laboratoryunmatched
    • Laboratory Operationsunmatched
    • Maintain Complianceunmatched
    • Manufacturingunmatched
    • Manufacturing Operationsunmatched
    • Pharmacyunmatched
    • Product Lifecycleunmatched
    • Quality Assuranceunmatched
    • Quality Managementunmatched
    • Quality System Requirements (QSR)unmatched
    • Regulationsunmatched
    • Regulatory Complianceunmatched
    • Regulatory Requirementsunmatched
    • Regulatory Submissionsunmatched
    • Staff Trainingunmatched
    • Testingunmatched

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