“MasterControl” jobs in Canada

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• 2d

  Operations Technical Writer - 12 month contract

  Whitchurch-Stouffville, ON

  Full Time

  

  Teva Pharmaceutical

  1+ YOETeva Pharmaceutical needs candidates with a college diploma in science or a related field and at least one year in a GMP-regulated manufacturing environment. Candidates must have strong technical writing skills, experience writing controlled documents, and knowledge of cGMP.

  Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Visio, TrackWise, Veeva

• 9d

  Document & Training Specialist, Radioconjugate PQS

  Hamilton, ON

  Full Time

  FP

  Fusion Pharmaceutical Inc Company

  2+ YOEFusion Pharmaceuticals needs candidates with a bachelor's degree in a life sciences, engineering or business-related field and 2-5 years of relevant experience. Knowledge of GxP, document control, change control and eDMS or LMS systems such as Veeva Vault or ComplianceWire is an asset.

  Veeva Vault, ComplianceWire, SuccessFactors, Microsoft 365, Power BI, Tableau

• 9d

  Document & Training Specialist, Radioconjugate PQS

  Hamilton, ON

  On-siteFull Time

  

  AstraZeneca

  2+ YOECandidates need a bachelor's degree in a life sciences, engineering, information management, or business field, plus 2-5 years of relevant experience. GxP, quality management, and document control knowledge is an asset, as is familiarity with Veeva Vault or ComplianceWire. Candidates must be able to stand for long periods and lift up to 40 lbs.

  Veeva Vault, ComplianceWire, SuccessFactors, Cornerstone, MasterControl, Microsoft 365

• 9d

  Quality Engineer

  Richmond Hill, ON

  Full Time

  

  Fresenius Medical Care: Fresenius Medical Care is the world’s leading provider of products and services for individuals with renal diseases.

  3+ YOEFresenius Medical Care needs candidates with a bachelor's degree in engineering or life sciences and 3-5 years in quality engineering in a regulated medical device or pharmaceutical setting. They must know the Medical Devices Regulations, ISO 13485 and ISO 14971, and have experience with audits and an electronic QMS.

  QTRAK, Windchill, TrackWise, MasterControl

• 9d

  Quality Engineer

  Richmond Hill, ON

  HybridFull Time

  CF

  CAN Fresenius Medical Care

  3+ YOECandidates need a bachelor's degree in engineering, life sciences or a related field and 3-5 years in quality engineering in a regulated medical device or pharmaceutical setting. They must know the Medical Devices Regulations, ISO 13485 and ISO 14971, and have experience with audits and an electronic QMS.

  QTRAK, Windchill, TrackWise, MasterControl

• 14d

  Director of Sales, U.S. division

  Ontario

  RemoteFull Time

  

  Medisca

  7+ YOE6+ MgmtCandidates need seven to ten years of sales management experience, six years of leadership experience, and at least five years of physician detailing in the pharmaceutical industry. A bachelor's degree in a business field, a valid passport, and the ability to travel to the U.S. up to 12 weeks a year are also required.

  CRM, MasterControl, Microsoft Excel, Microsoft Word, Microsoft Outlook, Microsoft Teams

  29d

  Chef de la conformité l Compliance Manager

  Montréal, QC

  Full Time

  

  Medisca

  5+ YOEBaccalauréat en sciences; 5 à 7 ans d'expérience en qualité, conformité ou affaires réglementaires; Connaissance des réglementations FDA, Santé Canada, TGA et EMA

  Microsoft Word, Microsoft Excel, Microsoft Outlook, MasterControl, Creatio

• 19d

  Product Manager

  Montréal, QC

  HybridFull Time

  

  GenAIz

  5+ YOECandidates need 5+ years of B2B product management, at least 3 years serving pharma, biotech, medical device or CDMO customers, and working knowledge of GxP quality and manufacturing processes. A bachelor's degree in life sciences, engineering or computer science and fluent English are required; French is a strong asset.

  Veeva Vault QMS, MasterControl, TrackWise, SAP QM, EDC, QMS

• 20d

  Specialist II, Validation

  Mississauga, ON

  $70k–$96k/yrFull Time

  RB

  Resilience Biotechnologies Inc.

  2+ YOECandidates need working knowledge of cGMP, FDA and Health Canada requirements, and 21 CFR Part 11 and EU GMP Annex 1, 11 and 15. A bachelor's degree in engineering or science is preferred, along with strong technical writing skills and experience in a biopharmaceutical setting.

  TrackWise, Veeva, MasterControl, Microsoft Word, Microsoft Excel, Microsoft Visio

• 24d

  OmniaBio: Associate I Quality Assurance (MQA)

  Hamilton, ON

  CF

  Centre for Commercialization of Regenerative Medicine

  1+ YOECandidates need a high school diploma plus college courses in science or engineering, and 1-2 years of GMP quality experience in cell therapy, biologics or a similar regulated industry. They must understand Health Canada and FDA GMP regulations and QA principles.

  MasterControl

• 26d

  Spécialiste formation

  Acton Vale, QC

  Full Time

  LS

  Life Science Nutritionals inc.

  Expérience en formation technique en fabrication; Connaissance des BPF et de la sécurité alimentaire; Maîtrise d'outils comme MasterControl et Dozuki

  MasterControl, Dozuki

• 26d

  Quality Assurance Associate

  Brantford, ON

  $30/hrOn-siteTemporary

  ?

  Do you have a passion for quality, an eye for detail, and experience working in a regulated manufacturing environment?; This role is ideal for a quality professional with pharmaceutical, radiopharmaceutical, or…

  Quality assurance, Quality control systems, Quality control, Good manufacturing practices, Documentation, MasterControl

• 28d

  Repair Solutions Engineer II

  Edmonton, AB

  Full Time

  TC

  TDW Canada

  Candidates need a P.Eng., engineering experience, and proficiency in 3D modeling, tolerance analysis, GD&T, FEA and DFMEA. They should know CAD software such as Siemens NX or SolidWorks, ANSYS is preferred, and have strong written and verbal communication skills.

  ANSYS, SolidWorks, Siemens NX, Teamcenter, MasterControl

• 29d

  Senior Quality Management System (QMS) Quality Engineer

  Oakville, ON

  Full Time

  

  VitalBio

  7+ YOECandidates need a bachelor's degree in engineering, life sciences or a related field, at least 7 years of quality systems work in medical devices, and experience running ISO 13485 and FDA-compliant systems and eQMS platforms.

  eQMS platform, MasterControl, Greenlight Guru, Veeva, ETQ Reliance, TrackWise

13 companies