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Resumes 1 - 10 of 192 |
Toronto, ON, Canada
... Regulatory Familiarity: Knowledgeable about clinical laboratory guidelines (FDA, CAP, CLIA, CLSI, IQMH). Administrative Competence: Demonstrated administrative practices across diverse settings. Analytical Skills: Effective problem-solving, critical ...
- Apr 13
Toronto, ON, Canada
... • Hands-on experience in the execution of production protocols, GMPs-FDA part 11, HACCP, Quality ISO- 9001, environment 14001 procedures, ISO/IEC 17025 standard and ISO 13485 (medical device license) • Summary of experience: QA/QC Manager in ...
- Mar 21
Brampton, ON, Canada
... • Engaged with external governing bodies personnel (such as CFIA,FDA,NSF ) for external audits • Conduct CFIA, 3rd party audits, customer audits and internal audits and follow up on corrective actions. • Ensure Hold and Release process is functional ...
- Mar 08
Richmond Hill, ON, Canada
... - Reviewed the efficacy, safety and cost-effectiveness of diagnostic, treatment, and management options, by synthesizing results from landmark trials and late-breaking abstracts, FDA and EMA approvals, international guidelines, health technology ...
- Feb 23
Toronto, ON, Canada
... APOTEX INC., THE APOTEX GROUP – Toronto Jul 2003 – Sep 2004 Project Manager & Senior Consultant, Consulting Services Managed the complete lifecycle of a multi-year internal program to re-engineer all applications that had to comply with FDA 21CFR ...
- Feb 21
Toronto, ON, Canada
... Verification and Validation plans and reports and maintaining DHF • Expertise in adhering to regulatory guidelines including FDA, EU-MDR, PMDA, and 62304 • ISTQB certified with advanced certification in progress, skilled in Agile and SCRUM ...
- Feb 14
Toronto, ON, Canada
... with WHODD ● Strong knowledge of Pharmacovigilance (PV) process and aware of regulatory guidelines (ICH GCP, MHRA, US FDA and Health Canada) ● Experienced in triage, processing and review of reports received from Health Canada ● Subject Matter ...
- Feb 13
Toronto, ON, Canada
... Post assessment - facilitated guidance for solutions implementation and establishing IT controls to comply with HIPPA, FDA and FOIP requirements and standards. Responsibilities AHS IT Control Framework o An AHS Baseline Self-Assessment Formalized ...
- Jan 24
Toronto, ON, Canada
... FDA & EPA, Health Canada, ECHA/REACH, OECD & ICH for Drugs and medical devices Long term oriented on high impact treatment interventions, testing new drugs and contribute to Precision medicine practice Work Experience Medical Assistant Pediatric ...
- Jan 12
Brampton, ON, Canada
... • Advanced knowledge of ICH-GCP, FDA, and Health Canada regulations and guidelines. • Eager to learn and adapt, I often seek opportunities to acquire new skills that contribute to efficiency, cost-effectiveness, and quality improvements. • Highly ...
- 2023 Dec 05