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Qeen Biotechnologies
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  • Company Description Qeen Biotechnologies is a global Center of Excellence for biomanufacturing nontraditional therapeutics. Our biologics biomanufacturing facility in Gatineau, QC is equipped with ISO-6, ISO-7, and ISO-8 GMP compliant cleanrooms to address the phage care continuum for AMR infections. Our patient-centric approach aims to provide precise phage treatments efficiently and cost-effectively, ultimately improving patient outcomes. Role Description This is a full-time on-site role for a Quality Assurance Specialist at Qeen Biotechnologies in Gatineau, QC. The Quality Assurance Specialist will be responsible for quality control, quality assurance, quality management, GMP practices, and quality auditing tasks to ensure the highest standards of biologics production and regulatory compliance. Qualifications Quality Control and Quality Assurance expertiseKnowledge of Quality Management and Good Manufacturing Practices (GMP)Experience in Quality AuditingAttention to detail and strong analytical skillsExcellent communication and documentation skillsAbility to work effectively in a team environmentBachelor's degree in Biology, Chemistry, Pharmaceutical Sciences, or related fieldCertifications in Quality Assurance or GMP are a plus

  • Quality Assurance Specialist  

    - Gatineau

    Company Description Qeen Biotechnologies is a global Center of Excellence for biomanufacturing nontraditional therapeutics. Our biologics biomanufacturing facility in Gatineau, QC is equipped with ISO-6, ISO-7, and ISO-8 GMP compliant cleanrooms to address the phage care continuum for AMR infections. Our patient-centric approach aims to provide precise phage treatments efficiently and cost-effectively, ultimately improving patient outcomes.
    Role Description This is a full-time on-site role for a Quality Assurance Specialist at Qeen Biotechnologies in Gatineau, QC. The Quality Assurance Specialist will be responsible for quality control, quality assurance, quality management, GMP practices, and quality auditing tasks to ensure the highest standards of biologics production and regulatory compliance.
    Qualifications Quality Control and Quality Assurance expertise Knowledge of Quality Management and Good Manufacturing Practices (GMP) Experience in Quality Auditing Attention to detail and strong analytical skills Excellent communication and documentation skills Ability to work effectively in a team environment Bachelor's degree in Biology, Chemistry, Pharmaceutical Sciences, or related field Certifications in Quality Assurance or GMP are a plus

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Astrid-Lindgren-Weg 12 38229 Salzgitter Germany