“CTD” jobs in Canada

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• 15d

  Freelance Full-Time English into Simplified Chinese (China) CTD Module Language Lead

  Montréal, QC +2

  RemoteContract

  T

  TransPerfect

  2+ YOECandidates need a translation or linguistics degree, or equivalent translation experience, plus excellent English and Simplified Chinese skills. Expertise in CTD and pharmaceutical content, and experience leading or reviewing others, are preferred.

  CAT tools, Translation memories, Termbases

• 7h

  Control Strategy Scientist

  Mississauga, ON

  Full Time

  

  Hoffmann-La Roche Limited

  7+ YOECandidates need a PhD or MSc in analytical chemistry, biochemistry or a related life science, plus 7 to 10+ years in pharmaceutical or biopharmaceutical QC, analytical development or CMC. Strong knowledge of biologics analytical methods, validation, stability, statistics, cGMP and ICH guidelines is required.

• 10d

  Sales Execution Coordinator

  Concord, ON

  Full Time

  

  Toromont Cat: Established in 1993, Toromont Cat is a division of Toromont Industries (TSX: TIH), a publically traded, diversified growth company incorporated in…

  2+ YOEToromont Cat needs candidates with post-secondary education and at least 2 years in an administrative or service role. They must know equipment sales and deal administration, be able to configure and price Cat machines, and be proficient in Microsoft Word, Excel and PowerPoint.

  Microsoft Excel, Microsoft Word, Microsoft PowerPoint, DBS, COTI, IQuote

• 12d

  AI Specialist, Regulatory and Medical Writing

  Remote in Canada

  $110k–$135k/yrRemoteFull Time

  

  IntuitionLabs

  5+ YOECandidates need 5 to 10 years in regulatory or medical writing at a biotech, pharma company or CRO, plus knowledge of ICH guidelines and the CTD structure. A life science PhD is preferred, and daily AI tool use with flawless English is required.

  Claude, ChatGPT

• 14d

  Sr. / Principal Medical Writer (Regulatory focus) - Sponsor-dedicated; NA/CAN/UK

  Remote in Canada

  RemoteFull Time

  

  Syneos Health, LLC

  5+ YOECandidates need at least 5 years of lead regulatory writing experience, including Phase 2 and 3 studies and documents such as CSRs, IBs, patient narratives and integrated summaries. Strong project management, client-facing and time management skills are required.

  eCTD

• 15d

  Spécialiste de la conformité réglementaire

  Saint-Laurent, QC

  HC

  Haleon Canada - Saint-Laurent

  5+ YOEDEC ou baccalauréat en sciences ou diplôme connexe; Cinq ans d'expérience en qualité, conformité ou affaires réglementaires; Connaissance pratique des BPF et de la Loi sur les aliments et drogues

  Microsoft Office, SAP, Veeva QualityDocs

• 15d

  Spécialiste de la conformité réglementaire

  Montréal, QC

  Full Time

  H

  Haleon

  5+ YOEDEC ou baccalauréat en sciences ou domaine connexe; Minimum de cinq ans en qualité ou affaires réglementaires; Connaissance pratique des BPF et de la Loi sur les aliments et drogues

  Microsoft Office, SAP, Veeva QualityDocs

• 15d

  Spécialiste de la conformité réglementaire

  Saint-Laurent, QC

  Full Time

  PC

  PF Consumer Healthcare Canada ULC / PF Soins De Sante SRI

  5+ YOEDEC ou baccalauréat en sciences ou domaine connexe; Minimum de cinq ans d'expérience en qualité, conformité ou affaires réglementaires; Connaissance pratique des BPF et de la Loi sur les aliments et drogues

  Microsoft Office, SAP, Veeva QualityDocs

• 15d

  Principal Medical Writer - Nonclinical Focus

  Remote in Canada

  RemoteFull Time

  SI

  Synchrogenix Information Strategies, LLC

  7+ YOEVeristat needs candidates with a bachelor's degree (MS or PhD preferred) and at least 7 years of regulatory writing experience, including nonclinical CTD sections. Candidates should know regulatory guidelines, lead writing teams, and handle submission-level documents.

  Microsoft Word

• 21d

  Client Dedicated CMC Regulatory Manager/Senior Manager - FDA

  Alberta

  Full Time

  TF

  Thermo Fisher Scientific

  10+ YOECandidates need a master's or PhD in biotechnology, pharmaceutical sciences or bioengineering, plus at least 10 years of CMC regulatory experience for biologics. Strong knowledge of FDA, Health Canada, EMA and ICH requirements, and experience leading biologics submissions, is required.

  Regulatory compliance, Reporting, Manufacturing processes, Biotechnology, Project management, Communication skills

• 22d

  Analyste d'affaires junior / Junior Business Analyst

  Laval, QC

  Full Time

  D

  digi-centre

  Pensée analytique et résolution de problèmes; Maîtrise des logiciels de veille, bases de données et outils BPM; Communication, présentation et facilitation

  Microsoft Visio, JIRA, Zoho, Odoo, Microsoft Dynamics, Google Business applications

• 22d

  Writer

  Toronto, ON

  On-siteFull Time

  I

  INKspire

  Candidates need experience preparing clinical regulatory documents with minimal supervision, knowledge of regulatory and compliance requirements, and strong written and oral communication skills. Familiarity with Microsoft Office, Adobe Acrobat, SharePoint and project management is also needed.

  Microsoft Office, Adobe Acrobat, SharePoint, Document management systems

• 25d

  Manager, Regulatory Affairs

  Mississauga, ON

  On-siteFull Time

  

  AstraZeneca

  7+ YOECandidates need at least 7 years of regulatory affairs experience with drugs and biologics in pharma, and a detailed knowledge of Canadian Food and Drug Regulations. A life science degree and a regulatory affairs certification are required, with an advanced degree preferred.

  CTD format, AI tools

• 29d

  Medical Director/Senior Medical Director - Endocrinology(Remote U.S)

  Toronto, ON

  RemoteFull Time

  PD

  PPD Development, LP

  2+ YOECandidates need an MD or equivalent and formal endocrinology training with about two years of patient treatment experience. Senior roles also require clinical trial or pharmacovigilance experience and knowledge of FDA, ICH, EMA and GCP guidelines.

  Clinical trials, Communication skills, Corporate social responsibility, Risk management, Research, Decision making

  29d

  Client Dedicated CMC Regulatory Manager/Senior Manager - FDA

  Remote in Canada

  RemoteFull Time

  PD

  PPD Development, LP

  10+ YOECandidates need a Master's or PhD in biotechnology, pharmaceutical sciences or bioengineering and at least 10 years of CMC regulatory experience for biologics. They also need proven leadership of biologics submissions, knowledge of EMA, ICH and biologics requirements, and strong project management and cross-functional communication skills.

  Regulatory compliance, Reporting, Manufacturing processes, Biotechnology, Project management, Communication skills

• 29d

  Manager, Regulatory Affairs

  Mississauga, ON

  Full Time

  AP

  Alexion Pharma Canada Crp Company

  7+ YOECandidates need at least 7 years of regulatory affairs experience for drugs and biologics in pharmaceuticals, plus a detailed understanding of Canadian Food and Drug Regulations. A life science degree and a regulatory affairs certification are required, with an advanced degree preferred.

  Artificial intelligence tools

• 29d

  Investment Associate

  Burlington, ON

  $95k–$120k/yrHybridFull Time

  

  Adi Development Group

  3+ YOECandidates need 3 to 6 years of real estate private equity, development or investment banking experience, including development underwriting, plus an MBA. Advanced Excel and modeling skills and the ability to lead transactions and present to senior leaders and investors are required.

  Excel

  29d

  Analyst, Investments

  Burlington, ON

  $85k–$110k/yrHybridFull Time

  

  Adi Development Group

  2+ YOECandidates need 2 to 4 years of real estate private equity, development or analytical experience, with strong Excel and financial modelling skills. A bachelor's degree in finance, real estate or economics is required, and a demonstrated ability to use AI tools in analytical work is required.

  Excel

16 companies