| Resume alert | Resumes 21 - 30 of 193 |
Project Manager Scrum Master
Ajax, ON, Canada
... Successfully managed over 50+ highly visible projects from 100k to 15M ranging from software application/Analysis, Implementation, Quality assurance/Regulatory (ISO and FDA), IT Infrastructure, Asset management, Operations and process improvement ... - 2023 Jan 17
... Successfully managed over 50+ highly visible projects from 100k to 15M ranging from software application/Analysis, Implementation, Quality assurance/Regulatory (ISO and FDA), IT Infrastructure, Asset management, Operations and process improvement ... - 2023 Jan 17
Data Entry Research Intern
Toronto, ON, Canada
... assigned, ensure compliance and adherence with study protocols, ICH-GCP guidelines, SOPs and applicable regulatory requirements (TPD, FDA, EMEA) ● Regulatory/IRB Submissions: Generate and maintain IRB/REB documentation for internal and international ... - 2022 Sep 28
... assigned, ensure compliance and adherence with study protocols, ICH-GCP guidelines, SOPs and applicable regulatory requirements (TPD, FDA, EMEA) ● Regulatory/IRB Submissions: Generate and maintain IRB/REB documentation for internal and international ... - 2022 Sep 28
Data Entry Laboratory Technician
Markham, ON, Canada
... of study files after study completion ·Procure and/or process biological samples as required to conduct a clinical study ·Properly complete documentation of clinical activities according to GCP, SOP ·guidelines, and/or FDA/TPD regulations. ... - 2022 Aug 10
... of study files after study completion ·Procure and/or process biological samples as required to conduct a clinical study ·Properly complete documentation of clinical activities according to GCP, SOP ·guidelines, and/or FDA/TPD regulations. ... - 2022 Aug 10
Assurance Analyst Qa Tester
Toronto, ON, Canada
... Review, assess and provide recommendations on current test verification activities against compliance to FDA/ISO requirements at Laborie; Provide technical input to verification teams - assist in design reviews as they pertain to system verification ... - 2022 Mar 30
... Review, assess and provide recommendations on current test verification activities against compliance to FDA/ISO requirements at Laborie; Provide technical input to verification teams - assist in design reviews as they pertain to system verification ... - 2022 Mar 30
Mechanical Engineer Quality Controller
Toronto, ON, Canada
... Strong knowledge of ISO 9001:2015, ISO 13485:2016, ISO 9100, FDA, REACH & ROHS and California Proposition 65 regulations. Competent computer skills, including Microsoft Office and working Knowledge of AutoCAD 2012 Extensive experience in researching ... - 2022 Mar 15
... Strong knowledge of ISO 9001:2015, ISO 13485:2016, ISO 9100, FDA, REACH & ROHS and California Proposition 65 regulations. Competent computer skills, including Microsoft Office and working Knowledge of AutoCAD 2012 Extensive experience in researching ... - 2022 Mar 15
Sponsor Clinical Research
Toronto, ON, Canada
... research regulations and guidelines: ICH/ Good Clinical Practice (GCP), Good Pharmacoepidemiological Practices (GPP), FDA and Health Canada TPD Valued as a dynamic, highly motivated, compassionate, and proactive team-player Recognized by peers ... - 2021 Oct 21
... research regulations and guidelines: ICH/ Good Clinical Practice (GCP), Good Pharmacoepidemiological Practices (GPP), FDA and Health Canada TPD Valued as a dynamic, highly motivated, compassionate, and proactive team-player Recognized by peers ... - 2021 Oct 21
Research Manager Medical Writer
Etobicoke, ON, Canada
... Burnaby, BC (Biotech/Life Sciences) 05/2014 – 07/2015 Vancouver, BC office Clinical Research Leader & RA •Interprets CMDR, FDA 21CFR820 and 510(K) guidance and in collaboration with RA manager, establishes appropriate regulatory strategy, SOP, WI ... - 2021 Jul 23
... Burnaby, BC (Biotech/Life Sciences) 05/2014 – 07/2015 Vancouver, BC office Clinical Research Leader & RA •Interprets CMDR, FDA 21CFR820 and 510(K) guidance and in collaboration with RA manager, establishes appropriate regulatory strategy, SOP, WI ... - 2021 Jul 23
QA Manager/QA Supervisor/HACCP coordinator
Brampton, ON, Canada
... during the processing and packaging of food Conducts tests on food additives and preservatives to ensure organizational and FDA compliance on such factors as color, texture, and nutrients Assists food scientist in research and development and ... - 2021 Jul 20
... during the processing and packaging of food Conducts tests on food additives and preservatives to ensure organizational and FDA compliance on such factors as color, texture, and nutrients Assists food scientist in research and development and ... - 2021 Jul 20
Manager Mental Health
Mississauga, ON, Canada
... Contributed to Pre-market Notification (510(k)) submission for FDA’s review and Medical Device Single Audit Program (MDSAP) audits for Merge PACS. Recognized and thanked team members regularly. Utilized manager empowerment funds to celebrate project ... - 2021 Apr 12
... Contributed to Pre-market Notification (510(k)) submission for FDA’s review and Medical Device Single Audit Program (MDSAP) audits for Merge PACS. Recognized and thanked team members regularly. Utilized manager empowerment funds to celebrate project ... - 2021 Apr 12
Safety Engineer
Toronto, ON, Canada
... He has extensive experience in Drug Safety and Pharmacovigilance, Process Compliance & Improvement, Quality Assurance, Life Sciences Regulatory Compliance for ICH, FDA, DSCSA, EMA, PMDA - 21 CFR Part 11 and GAMP Framework. Expertise in Computer ... - 2021 Mar 15
... He has extensive experience in Drug Safety and Pharmacovigilance, Process Compliance & Improvement, Quality Assurance, Life Sciences Regulatory Compliance for ICH, FDA, DSCSA, EMA, PMDA - 21 CFR Part 11 and GAMP Framework. Expertise in Computer ... - 2021 Mar 15