Job Title: Python Developer/DevOps Developer – SDLC ToolsLocation: Calgary, Alberta, Canada (Day 1 Onsite)Local candidates preferred
Client is seeking a hands-on developer to join the Firmwide Developer Tools and Systems Group (MSDE). MSDE is responsible for shaping the Software Development Lifecycle (SDLC) within Morgan Stanley by implementing the tools, systems, and processes used by 12,000+ developers across the firm for software development and deployment.
The candidate will be part of a global team of experts modernizing the Firm’s SDLC platform to enable deployment automation to private/public cloud environments and SaaS-based tooling. This role offers an opportunity to contribute to next-generation development and deployment tooling across diverse technology stacks.Prior financial industry experience is not required—candidates from software companies are welcome
Skills Required:5+ years of hands-on development experience in Python.(Additional experience with Java, C#, or TypeScript is an asset.)Strong technical background and passion for SDLC tooling and processes.Experience with multiple SCM systems, code review systems, issue tracking tools, build tools, test frameworks, code quality tools, CI systems, and IDEs.Experience working as a developer on large-scale projects in an Agile, globally distributed environment.Curious and investigative mindset — “gets to the bottom of things.”
Skills Desired:Experience developing tools for:Build automationVersion control (Bitbucket, GitHub)Issue tracking (Jira)CI/CD (Jenkins, Azure DevOps, GitHub Actions)Deployment orchestration using Terraform, Ansible, or related technologies.Integration experience with Azure or AWS for development and deployment tools.Containerization experience using Docker and Kubernetes.System administration experience on Linux or Windows environments.
Minimum Skills Required (5+ years):Hands-on Python development experience.Familiarity with multiple SDLC and DevOps tools.Proven ability to work in Agile, distributed teams.Strong collaboration and analytical skills.
Job Title: Python Developer/DevOps Developer – SDLC ToolsLocation: Calgary, Alberta, Canada (Day 1 Onsite)Local candidates preferred
Client is seeking a hands-on developer to join the Firmwide Developer Tools and Systems Group (MSDE). MSDE is responsible for shaping the Software Development Lifecycle (SDLC) within Morgan Stanley by implementing the tools, systems, and processes used by 12,000+ developers across the firm for software development and deployment.
The candidate will be part of a global team of experts modernizing the Firm’s SDLC platform to enable deployment automation to private/public cloud environments and SaaS-based tooling. This role offers an opportunity to contribute to next-generation development and deployment tooling across diverse technology stacks.Prior financial industry experience is not required—candidates from software companies are welcome
Skills Required:5+ years of hands-on development experience in Python.(Additional experience with Java, C#, or TypeScript is an asset.)Strong technical background and passion for SDLC tooling and processes.Experience with multiple SCM systems, code review systems, issue tracking tools, build tools, test frameworks, code quality tools, CI systems, and IDEs.Experience working as a developer on large-scale projects in an Agile, globally distributed environment.Curious and investigative mindset — “gets to the bottom of things.”
Skills Desired:Experience developing tools for:Build automationVersion control (Bitbucket, GitHub)Issue tracking (Jira)CI/CD (Jenkins, Azure DevOps, GitHub Actions)Deployment orchestration using Terraform, Ansible, or related technologies.Integration experience with Azure or AWS for development and deployment tools.Containerization experience using Docker and Kubernetes.System administration experience on Linux or Windows environments.
Minimum Skills Required (5+ years):Hands-on Python development experience.Familiarity with multiple SDLC and DevOps tools.Proven ability to work in Agile, distributed teams.Strong collaboration and analytical skills.
Job Title: Technical Writer – Pharma IT ComplianceLocation: Remote, Canada (Must Support EST Time Zone)
Position SummaryWe are seeking a Technical Writer – Pharma IT Compliance to join our client’s global pharmaceutical IT team. The ideal candidate will develop, maintain, and enhance IT process documentation in compliance with GxP and regulatory requirements. This position plays a critical role in ensuring infrastructure qualification, documentation quality, and alignment with global IT compliance standards.The role requires close collaboration with IT Compliance, Quality Assurance, and Global Shared Services teams to ensure all deliverables meet company and industry expectations.
Key ResponsibilitiesDevelop, author, and maintain IT policies, SOPs, plans, specifications, protocols, and reports.Lead and facilitate IT process improvement initiatives related to documentation and compliance.Act as the Infrastructure Qualification Lead for PSG sites to ensure global/local alignment on qualification deliverables.Guide project teams on GxP processes, qualification strategies, and compliance documentation.Manage and advise on change control processes in accordance with IT compliance standards.Collaborate with Global IT Shared Services to review and prepare GxP documentation for QA approval.Support the creation and review of IT-related agreements and compliance documentation.Participate in audit and inspection preparation, providing IT compliance support as needed.Support qualification/validation of mobile devices, scanners, and computers used in GxP environments.
Required Skills & Qualifications5+ years of experience as a Technical Writer or in IT compliance documentation within the pharmaceutical or life sciences domain.Strong knowledge of GxP regulations, IT validation, and documentation management.Proven ability to author and manage controlled documentation (SOPs, protocols, and reports).Experience with infrastructure qualification and change control processes.Excellent written and verbal communication skills with exceptional attention to detail.Familiarity with audit support, regulatory inspections, and quality systems.Proficient with tools such as SharePoint, ServiceNow, and Power BI.Experience in manufacturing or regulated environments preferred.
EducationBachelor’s degree in Information Technology, Computer Science, Engineering, Life Sciences, or a related field.Master’s degree preferred but not required.
Preferred ExperiencePrior experience in pharmaceutical IT compliance and infrastructure qualification.Understanding of IT lifecycle documentation within regulated manufacturing systems.Ability to collaborate effectively with global and cross-functional teams.
Job Title: Technical Writer – Pharma IT ComplianceLocation: Remote, Canada (Must Support EST Time Zone)
Position SummaryWe are seeking a Technical Writer – Pharma IT Compliance to join our client’s global pharmaceutical IT team. The ideal candidate will develop, maintain, and enhance IT process documentation in compliance with GxP and regulatory requirements. This position plays a critical role in ensuring infrastructure qualification, documentation quality, and alignment with global IT compliance standards.The role requires close collaboration with IT Compliance, Quality Assurance, and Global Shared Services teams to ensure all deliverables meet company and industry expectations.
Key ResponsibilitiesDevelop, author, and maintain IT policies, SOPs, plans, specifications, protocols, and reports.Lead and facilitate IT process improvement initiatives related to documentation and compliance.Act as the Infrastructure Qualification Lead for PSG sites to ensure global/local alignment on qualification deliverables.Guide project teams on GxP processes, qualification strategies, and compliance documentation.Manage and advise on change control processes in accordance with IT compliance standards.Collaborate with Global IT Shared Services to review and prepare GxP documentation for QA approval.Support the creation and review of IT-related agreements and compliance documentation.Participate in audit and inspection preparation, providing IT compliance support as needed.Support qualification/validation of mobile devices, scanners, and computers used in GxP environments.
Required Skills & Qualifications5+ years of experience as a Technical Writer or in IT compliance documentation within the pharmaceutical or life sciences domain.Strong knowledge of GxP regulations, IT validation, and documentation management.Proven ability to author and manage controlled documentation (SOPs, protocols, and reports).Experience with infrastructure qualification and change control processes.Excellent written and verbal communication skills with exceptional attention to detail.Familiarity with audit support, regulatory inspections, and quality systems.Proficient with tools such as SharePoint, ServiceNow, and Power BI.Experience in manufacturing or regulated environments preferred.
EducationBachelor’s degree in Information Technology, Computer Science, Engineering, Life Sciences, or a related field.Master’s degree preferred but not required.
Preferred ExperiencePrior experience in pharmaceutical IT compliance and infrastructure qualification.Understanding of IT lifecycle documentation within regulated manufacturing systems.Ability to collaborate effectively with global and cross-functional teams.
Job Title: Technical Writer – Pharma IT ComplianceLocation: Remote, Canada (Must Support EST Time Zone)
Position SummaryWe are seeking a Technical Writer – Pharma IT Compliance to join our client’s global pharmaceutical IT team. The ideal candidate will develop, maintain, and enhance IT process documentation in compliance with GxP and regulatory requirements. This position plays a critical role in ensuring infrastructure qualification, documentation quality, and alignment with global IT compliance standards.The role requires close collaboration with IT Compliance, Quality Assurance, and Global Shared Services teams to ensure all deliverables meet company and industry expectations.
Key ResponsibilitiesDevelop, author, and maintain IT policies, SOPs, plans, specifications, protocols, and reports.Lead and facilitate IT process improvement initiatives related to documentation and compliance.Act as the Infrastructure Qualification Lead for PSG sites to ensure global/local alignment on qualification deliverables.Guide project teams on GxP processes, qualification strategies, and compliance documentation.Manage and advise on change control processes in accordance with IT compliance standards.Collaborate with Global IT Shared Services to review and prepare GxP documentation for QA approval.Support the creation and review of IT-related agreements and compliance documentation.Participate in audit and inspection preparation, providing IT compliance support as needed.Support qualification/validation of mobile devices, scanners, and computers used in GxP environments.
Required Skills & Qualifications5+ years of experience as a Technical Writer or in IT compliance documentation within the pharmaceutical or life sciences domain.Strong knowledge of GxP regulations, IT validation, and documentation management.Proven ability to author and manage controlled documentation (SOPs, protocols, and reports).Experience with infrastructure qualification and change control processes.Excellent written and verbal communication skills with exceptional attention to detail.Familiarity with audit support, regulatory inspections, and quality systems.Proficient with tools such as SharePoint, ServiceNow, and Power BI.Experience in manufacturing or regulated environments preferred.
EducationBachelor’s degree in Information Technology, Computer Science, Engineering, Life Sciences, or a related field.Master’s degree preferred but not required.
Preferred ExperiencePrior experience in pharmaceutical IT compliance and infrastructure qualification.Understanding of IT lifecycle documentation within regulated manufacturing systems.Ability to collaborate effectively with global and cross-functional teams.
Job Title: Technical Writer – Pharma IT ComplianceLocation: Remote, Canada (Must Support EST Time Zone)
Position SummaryWe are seeking a Technical Writer – Pharma IT Compliance to join our client’s global pharmaceutical IT team. The ideal candidate will develop, maintain, and enhance IT process documentation in compliance with GxP and regulatory requirements. This position plays a critical role in ensuring infrastructure qualification, documentation quality, and alignment with global IT compliance standards.The role requires close collaboration with IT Compliance, Quality Assurance, and Global Shared Services teams to ensure all deliverables meet company and industry expectations.
Key ResponsibilitiesDevelop, author, and maintain IT policies, SOPs, plans, specifications, protocols, and reports.Lead and facilitate IT process improvement initiatives related to documentation and compliance.Act as the Infrastructure Qualification Lead for PSG sites to ensure global/local alignment on qualification deliverables.Guide project teams on GxP processes, qualification strategies, and compliance documentation.Manage and advise on change control processes in accordance with IT compliance standards.Collaborate with Global IT Shared Services to review and prepare GxP documentation for QA approval.Support the creation and review of IT-related agreements and compliance documentation.Participate in audit and inspection preparation, providing IT compliance support as needed.Support qualification/validation of mobile devices, scanners, and computers used in GxP environments.
Required Skills & Qualifications5+ years of experience as a Technical Writer or in IT compliance documentation within the pharmaceutical or life sciences domain.Strong knowledge of GxP regulations, IT validation, and documentation management.Proven ability to author and manage controlled documentation (SOPs, protocols, and reports).Experience with infrastructure qualification and change control processes.Excellent written and verbal communication skills with exceptional attention to detail.Familiarity with audit support, regulatory inspections, and quality systems.Proficient with tools such as SharePoint, ServiceNow, and Power BI.Experience in manufacturing or regulated environments preferred.
EducationBachelor’s degree in Information Technology, Computer Science, Engineering, Life Sciences, or a related field.Master’s degree preferred but not required.
Preferred ExperiencePrior experience in pharmaceutical IT compliance and infrastructure qualification.Understanding of IT lifecycle documentation within regulated manufacturing systems.Ability to collaborate effectively with global and cross-functional teams.
Job Title: Technical Writer – Pharma IT ComplianceLocation: Remote, Canada (Must Support EST Time Zone)
Position SummaryWe are seeking a Technical Writer – Pharma IT Compliance to join our client’s global pharmaceutical IT team. The ideal candidate will develop, maintain, and enhance IT process documentation in compliance with GxP and regulatory requirements. This position plays a critical role in ensuring infrastructure qualification, documentation quality, and alignment with global IT compliance standards.The role requires close collaboration with IT Compliance, Quality Assurance, and Global Shared Services teams to ensure all deliverables meet company and industry expectations.
Key ResponsibilitiesDevelop, author, and maintain IT policies, SOPs, plans, specifications, protocols, and reports.Lead and facilitate IT process improvement initiatives related to documentation and compliance.Act as the Infrastructure Qualification Lead for PSG sites to ensure global/local alignment on qualification deliverables.Guide project teams on GxP processes, qualification strategies, and compliance documentation.Manage and advise on change control processes in accordance with IT compliance standards.Collaborate with Global IT Shared Services to review and prepare GxP documentation for QA approval.Support the creation and review of IT-related agreements and compliance documentation.Participate in audit and inspection preparation, providing IT compliance support as needed.Support qualification/validation of mobile devices, scanners, and computers used in GxP environments.
Required Skills & Qualifications5+ years of experience as a Technical Writer or in IT compliance documentation within the pharmaceutical or life sciences domain.Strong knowledge of GxP regulations, IT validation, and documentation management.Proven ability to author and manage controlled documentation (SOPs, protocols, and reports).Experience with infrastructure qualification and change control processes.Excellent written and verbal communication skills with exceptional attention to detail.Familiarity with audit support, regulatory inspections, and quality systems.Proficient with tools such as SharePoint, ServiceNow, and Power BI.Experience in manufacturing or regulated environments preferred.
EducationBachelor’s degree in Information Technology, Computer Science, Engineering, Life Sciences, or a related field.Master’s degree preferred but not required.
Preferred ExperiencePrior experience in pharmaceutical IT compliance and infrastructure qualification.Understanding of IT lifecycle documentation within regulated manufacturing systems.Ability to collaborate effectively with global and cross-functional teams.
Job Title: Technical Writer – Pharma IT ComplianceLocation: Remote, Canada (Must Support EST Time Zone)
Position SummaryWe are seeking a Technical Writer – Pharma IT Compliance to join our client’s global pharmaceutical IT team. The ideal candidate will develop, maintain, and enhance IT process documentation in compliance with GxP and regulatory requirements. This position plays a critical role in ensuring infrastructure qualification, documentation quality, and alignment with global IT compliance standards.The role requires close collaboration with IT Compliance, Quality Assurance, and Global Shared Services teams to ensure all deliverables meet company and industry expectations.
Key ResponsibilitiesDevelop, author, and maintain IT policies, SOPs, plans, specifications, protocols, and reports.Lead and facilitate IT process improvement initiatives related to documentation and compliance.Act as the Infrastructure Qualification Lead for PSG sites to ensure global/local alignment on qualification deliverables.Guide project teams on GxP processes, qualification strategies, and compliance documentation.Manage and advise on change control processes in accordance with IT compliance standards.Collaborate with Global IT Shared Services to review and prepare GxP documentation for QA approval.Support the creation and review of IT-related agreements and compliance documentation.Participate in audit and inspection preparation, providing IT compliance support as needed.Support qualification/validation of mobile devices, scanners, and computers used in GxP environments.
Required Skills & Qualifications5+ years of experience as a Technical Writer or in IT compliance documentation within the pharmaceutical or life sciences domain.Strong knowledge of GxP regulations, IT validation, and documentation management.Proven ability to author and manage controlled documentation (SOPs, protocols, and reports).Experience with infrastructure qualification and change control processes.Excellent written and verbal communication skills with exceptional attention to detail.Familiarity with audit support, regulatory inspections, and quality systems.Proficient with tools such as SharePoint, ServiceNow, and Power BI.Experience in manufacturing or regulated environments preferred.
EducationBachelor’s degree in Information Technology, Computer Science, Engineering, Life Sciences, or a related field.Master’s degree preferred but not required.
Preferred ExperiencePrior experience in pharmaceutical IT compliance and infrastructure qualification.Understanding of IT lifecycle documentation within regulated manufacturing systems.Ability to collaborate effectively with global and cross-functional teams.
Job Title: Technical Writer – Pharma IT ComplianceLocation: Remote, Canada (Must Support EST Time Zone)
Position SummaryWe are seeking a Technical Writer – Pharma IT Compliance to join our client’s global pharmaceutical IT team. The ideal candidate will develop, maintain, and enhance IT process documentation in compliance with GxP and regulatory requirements. This position plays a critical role in ensuring infrastructure qualification, documentation quality, and alignment with global IT compliance standards.The role requires close collaboration with IT Compliance, Quality Assurance, and Global Shared Services teams to ensure all deliverables meet company and industry expectations.
Key ResponsibilitiesDevelop, author, and maintain IT policies, SOPs, plans, specifications, protocols, and reports.Lead and facilitate IT process improvement initiatives related to documentation and compliance.Act as the Infrastructure Qualification Lead for PSG sites to ensure global/local alignment on qualification deliverables.Guide project teams on GxP processes, qualification strategies, and compliance documentation.Manage and advise on change control processes in accordance with IT compliance standards.Collaborate with Global IT Shared Services to review and prepare GxP documentation for QA approval.Support the creation and review of IT-related agreements and compliance documentation.Participate in audit and inspection preparation, providing IT compliance support as needed.Support qualification/validation of mobile devices, scanners, and computers used in GxP environments.
Required Skills & Qualifications5+ years of experience as a Technical Writer or in IT compliance documentation within the pharmaceutical or life sciences domain.Strong knowledge of GxP regulations, IT validation, and documentation management.Proven ability to author and manage controlled documentation (SOPs, protocols, and reports).Experience with infrastructure qualification and change control processes.Excellent written and verbal communication skills with exceptional attention to detail.Familiarity with audit support, regulatory inspections, and quality systems.Proficient with tools such as SharePoint, ServiceNow, and Power BI.Experience in manufacturing or regulated environments preferred.
EducationBachelor’s degree in Information Technology, Computer Science, Engineering, Life Sciences, or a related field.Master’s degree preferred but not required.
Preferred ExperiencePrior experience in pharmaceutical IT compliance and infrastructure qualification.Understanding of IT lifecycle documentation within regulated manufacturing systems.Ability to collaborate effectively with global and cross-functional teams.
Job Title: Technical Writer – Pharma IT ComplianceLocation: Remote, Canada (Must Support EST Time Zone)
Position SummaryWe are seeking a Technical Writer – Pharma IT Compliance to join our client’s global pharmaceutical IT team. The ideal candidate will develop, maintain, and enhance IT process documentation in compliance with GxP and regulatory requirements. This position plays a critical role in ensuring infrastructure qualification, documentation quality, and alignment with global IT compliance standards.The role requires close collaboration with IT Compliance, Quality Assurance, and Global Shared Services teams to ensure all deliverables meet company and industry expectations.
Key ResponsibilitiesDevelop, author, and maintain IT policies, SOPs, plans, specifications, protocols, and reports.Lead and facilitate IT process improvement initiatives related to documentation and compliance.Act as the Infrastructure Qualification Lead for PSG sites to ensure global/local alignment on qualification deliverables.Guide project teams on GxP processes, qualification strategies, and compliance documentation.Manage and advise on change control processes in accordance with IT compliance standards.Collaborate with Global IT Shared Services to review and prepare GxP documentation for QA approval.Support the creation and review of IT-related agreements and compliance documentation.Participate in audit and inspection preparation, providing IT compliance support as needed.Support qualification/validation of mobile devices, scanners, and computers used in GxP environments.
Required Skills & Qualifications5+ years of experience as a Technical Writer or in IT compliance documentation within the pharmaceutical or life sciences domain.Strong knowledge of GxP regulations, IT validation, and documentation management.Proven ability to author and manage controlled documentation (SOPs, protocols, and reports).Experience with infrastructure qualification and change control processes.Excellent written and verbal communication skills with exceptional attention to detail.Familiarity with audit support, regulatory inspections, and quality systems.Proficient with tools such as SharePoint, ServiceNow, and Power BI.Experience in manufacturing or regulated environments preferred.
EducationBachelor’s degree in Information Technology, Computer Science, Engineering, Life Sciences, or a related field.Master’s degree preferred but not required.
Preferred ExperiencePrior experience in pharmaceutical IT compliance and infrastructure qualification.Understanding of IT lifecycle documentation within regulated manufacturing systems.Ability to collaborate effectively with global and cross-functional teams.
