Qrm Developer Job at Realign (Toronto)

Intern, Quality Assurance, Global Quality Management System

The BioMarin Summer Internship Program will enable students to gain valuable exp...

Location

United States

Salary:

24.00 - 32.00 USD / Hour

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

Student in their 3rd or 4th year of Undergrad or Master’s Candidates in one of the following fields (or closely related disciplines): Pharmaceutical Sciences
Chemistry / Biochemistry
Chemical Engineering / Biomedical Engineering
Quality Assurance / Regulatory Affairs
Life Sciences (Biology, Microbiology)
Must be available to work full time, 40 hours a week
Must be currently enrolled as a full-time student at an accredited U.S. based university or college and enrolled in the fall term after the completion of the internship OR have graduated within 1 year of the start of the program
Must be able to relocate if necessary and work at the designated site for the duration of the internship for on-site, hybrid roles
Some positions will be open to remote interns, but employee must be within United States borders
Clear written and visual communication: ability to simplify complex ideas for diverse audiences

Job Responsibility

Support initiatives to enhance the user experience and drive continuous improvement during a Quality Risk Management process transformation
Creating practical tools and resources that make QRM concepts accessible and actionable across the pharmaceutical product lifecycle
Developing a visual map illustrating where risk management is applied and how QRM principles integrate across development, manufacturing, and post-market stages
Creating a clear, user-friendly glossary of QRM terms and a communication toolkit to improve cross-functional understanding and application
Designing a beginner-friendly QRM guide and apply it to a small-scale pilot risk assessment for a real or hypothetical process

What we offer

Paid hourly wage
paid company holidays
sick time
Apply skills and knowledge learned in the classroom to on-the-job experiences
Comprehensive, value-added project(s)
Develop skills specific to your major
Opportunities for professional development by building relationships and learning about other parts of the business
Participate in company all hands meetings, monthly community lunches
Corporate office amenities such as: 24/7 on-site gym, coffee truck, snacks
Access to Employee Resource Groups

Fulltime

Qrm developer

Seeking a QRM Developer to support Treasury, ALM, Liquidity, and Risk functions ...

Location

Canada , Toronto

Salary:

230000.00 USD / Year

Realign

Expiration Date

Until further notice

Requirements

Total Experience: 6-8 years
Hands on experience with QRM (ALM, Liquidity, FTP, risk simulations)
Strong PowerShell scripting skills
Ansible automation experience
Solid SQL, data integration, and ETL understanding
Knowledge of Treasury ALM Liquidity IRRBB concepts

Job Responsibility

Build and maintain QRM ALMLRMFTP models
Configure assumptions, behavioral models, forecasting logic, and data mappings
Automate tasks and deployments using PowerShell and Ansible
Support daily weekly QRM runs, troubleshoot issues, and ensure model stability
Manage data ingestion, validation, and ETL flows for QRM
Collaborate with Treasury, Risk, Finance, and IT teams
Maintain documentation, support audits, and ensure model governance

Fulltime

Principal Quant Developer

Principal Quant Developer | Banking. An experienced Principal Quant Developer wh...

Location

Netherlands , Amsterdam

Salary:

Not provided

Levy Professionals

Expiration Date

Until further notice

Requirements

7+ years as a Quant Developer
Minimum 4 years’ experience building market or counterparty risk systems in C++
Background working with cross-functional teams in quantitative and risk-driven environments
Experience reviewing, guiding, and uplifting existing engineering teams is highly preferred
Strong understanding of quantitative concepts such as curve bootstrapping, implied volatilities, and standard pricing models
Solid knowledge of linear products and plain vanilla options, including basic pricing fundamentals
Able to lead design discussions, mentor engineers, and bring industry-standard development practices
Capable of working in a short-term, high-impact engagement where guidance, code review, and architecture leadership are key deliverables
Master of Science degree in a STEM field

Job Responsibility

Review and assess the end-to-end architecture and detailed implementation of existing margin models
Lead requirements analysis and guide the design process for enhancements
Perform ongoing code reviews and mentor IT Risk Engineers throughout the implementation
Collaborate with QRM, quants, IT developers, and business teams to align technical and risk objectives
Drive model accuracy, system performance, and overall reliability

Senior Manager CSSV AI Compliance Lead

This role provides strategic leadership & operational Quality oversight for deve...

Location

United States , Philadelphia

Salary:

124400.00 - 201400.00 USD / Year

Pfizer

Expiration Date

Until further notice

Requirements

Applicant must have a bachelor's degree with at least 6 years of experience
OR a master's degree with at least 5 years of experience
OR a PhD with 1+ years of relevant experience
Experience in Artificial Intelligence qualification and usage in regulated environments
Experience Software Quality Assurance, including risk-based approaches (e.g., CSA, GAMP5, QRM)
Experience of enterprise system validation/compliance/ deployment and good knowledge of Pfizer Digital life cycle methodologies (S/ADLC)
Demonstrated experience with computer system validation lifecycle processes
Intimate knowledge of Computer System Quality and AI regulations/industry guidance
Good understanding of Quality Management System regulations
Experience of interacting with auditors and inspectors.

Job Responsibility

Fulfil the Quality Authority responsibilities for Digital-delivered AI in partnership with other Quality SMEs and GPOs (as defined in AILC/SDLC processes).
Support and consult with the GPO/BSO in: AI validation and enablement activities
Confirming the system meets the specified business requirements
Ensuring appropriate business dataset selection for model training
Reporting value delivery/ongoing performance of the solution in support of the L2 process
Collaborate with the CSQ/BUQA function to ensure adequate system validation and ongoing compliance for the target/interfaced GMP/GDP applications
Partner and consult with Digital (for both on-prem and SaaS solutions) in: Oversight and approval of validation deliverables, risk assessments and integrations
Acceptance & endorsement of the model/system for GxP use
Supporting sites to enable timely deployment and adoption
Monitoring of AI models

What we offer

Eligibility for participation in Pfizer’s Global Performance Plan with a bonus target of 17.5% of the base salary
Eligibility to participate in our share based long term incentive program
401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution
Paid vacation, holiday and personal days
Paid caregiver/parental and medical leave
Health benefits to include medical, prescription drug, dental and vision coverage
Relocation assistance may be available based on business needs and/or eligibility.

Fulltime

New

Qualified Person

Joining Moderna offers the unique opportunity to be part of a pioneering team th...

Location

United Kingdom , Oxford

Salary:

Not provided

Moderna

Expiration Date

Until further notice

Requirements

A Life Science degree and/or relevant postgraduate qualification, with a minimum of 10 years’ experience in quality roles within the biotechnology and/or pharmaceutical industry
Eligibility to act as a Qualified Person (QP), with demonstrable knowledge of biologics and sterile manufacturing sufficient to be named on the site’s licences issued by the MHRA
Commitment to maintaining QP status through ongoing Continuing Professional Development
Experience working in GMP-regulated pharmaceutical / biological manufacturing environments
Expert knowledge of Pharmaceutical Quality Management Systems, including their application across the product lifecycle
Extensive understanding of GxP requirements for both early-phase clinical trial materials and commercial products, including interpretation and application of EU GMP and associated MHRA guidance
Demonstrated, in-depth understanding of broader GMP principles, industry standards, and current trends shaping the regulatory landscape
Experience as a qualified pharmaceutical auditor (internal and/or external)
Proven experience hosting and participating in regulatory inspections (e.g., MHRA, FDA, EMA)
Demonstrated ability to influence cross-functional teams, provide leadership and drive organisational change.

Job Responsibility

Acting as the named Qualified Person (QP) on Moderna’s site licence(s)
Certifying and authorising batch releases in full compliance with The Human Medicines Regulations 2012, EU GMP (Annex 16, and where applicable, Annex 13), and MHRA guidance
Ensuring sterile drug product batches meet cGMP, approved specifications, and the conditions of the Marketing or Clinical Trial Authorisation
Maintaining oversight of the PQS as it pertains to QP responsibilities, ensuring it is fit for purpose
Escalating GMP or product quality concerns related to safety and efficacy to senior leadership
Participating as a member of the site and country Quality teams, promoting strong quality culture and QRM principles
Attending and reporting at the Quality Management Review Forum
Overseeing delegated activities and ensuring proper training of personnel or third parties
Leading or participating in self-inspections, external audits, and Quality Risk Assessments
Serving as the QP point of contact for Technical/Quality Agreement reviews and approvals

What we offer

Best-in-class healthcare, plus voluntary benefit programs to support your unique needs
A holistic approach to well-being with access to fitness, mindfulness, and mental health support
Family building benefits, including fertility, adoption, and surrogacy support
Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
Savings and investments to help you plan for the future

Fulltime

New

Software Development Lead Engineer

Join us as Software Development Lead Engineer based in Pune to Develop and deliv...

Location

India , Pune

Salary:

Not provided

Alfa Laval

Expiration Date

Until further notice

Requirements

8+ years of experience in automation engineering, system design, and/or industrial software architecture
Strong hands-on and architectural experience with PLC and HMI systems, with the ability to review and guide implementation rather than execute all development personally
Proven experience defining and applying automation and software standards (ISA S88, PackML, modular architectures, OOP)
Solid understanding of industrial cybersecurity standards and secure system design
Experience with Agile development methodologies (Scrum, DevOps) in multi-team environments
Strong background in industrial communication protocols, networking, and system integration
Experience designing or governing web-based HMIs and IoT-enabled automation solutions
Fluent in English (spoken and written) with strong cross-cultural collaboration skills
Bachelor's or master's degree in electrical, Electronics, or Instrumentation Engineering

Job Responsibility

Define and own end-to-end system and solution architectures for multiple automation and digital projects, from concept through commissioning and lifecycle support
Provide architectural guidance for SIEMENS-based automation systems, ensuring compliance with standards such as ISA S88, PackML, and modular design principles
Review and govern PLC, HMI, and software designs, ensuring consistency, reusability, scalability, and adherence to architectural standards
Lead architectural decision-making for control systems, IoT integration, data flows, and enterprise connectivity, balancing technical trade-offs and business needs
Design and guide the integration of automation systems with industrial networks, IoT platforms, and enterprise systems
Define architecture principles for web-based HMIs, real-time monitoring, and secure data exchange across systems
Establish and enforce cybersecurity-by-design practices, ensuring solutions comply with applicable cybersecurity and data protection standards
Ensure data integrity, availability, and security across automation and IoT frameworks
Work closely with cross-functional and international teams, providing architectural oversight across multiple concurrent projects
support on-site engagements as needed

What we offer

Participate in the development of exciting and technologically advanced products
Work in a global company with great career opportunities
Interesting and challenging position in an open and friendly environment
Opportunity to build a global network with different nationalities
True impact on Alfa Laval's future success

Fulltime

New

Deputy Project Manager

The Deputy Project Manager (DPM) plays a critical role in supporting the overall...

Location

United States , Washington

Salary:

Not provided

NTT DATA

Expiration Date

Until further notice

Requirements

Bachelor's degree
Minimum 10 years of experience in leading projects or contracts, with the ability to manage projects and provide guidance and direction for specific tasks or sub-tasks.
Minimum 3 years of experience with ServiceNow and end-to-end Content Management System
Minimum 1 year of experience with Rapid Application Development (RAD) applications, including Customer Relationship Management (CRM) tools.
Project Management Professional (PMP) certification
Ability to obtain a Public Trust Clearance

Job Responsibility

Assist the SPM in planning, executing, and finalizing projects according to scheduled milestones and budget constraints.
Plan, initiate, and manage IT programs, guiding technical staff and serving as the liaison between business and technical aspects of the program.
Develop program stages, assess business implications for each stage, and monitor progress to ensure deadlines, standards, and cost targets are met.
Prepare and disseminate reports on all aspects of responsible programs and projects.
Manage program execution to ensure adherence to budget, schedule, and scope.
Submit program deliverables while ensuring compliance with quality standards.
Monitor and control resources, including personnel, budgets, and materials, within program areas.
Develop specific goals and plans to prioritize, organize, and accomplish work effectively.
Communicate with internal and external stakeholders, including Government representatives, supervisors, co-workers, and subordinates, using various methods such as telephone, teleconferencing (e.g., Microsoft Teams), email, or in-person meetings.
Represent the organization to external parties, including customers, the public, and government entities.

New

Business Analyst: Exotic Interest Rate and Credit Derivatives

We are looking for a senior Business Analyst in the Interest Rate Exotic Derivat...

Location

United Kingdom , Belfast

Salary:

Not provided

Citi

Expiration Date

Until further notice

Requirements

Proven experience working on enterprise level project as a BA or QA Analyst
Ability and proven experience of driving functionality/project from analysis to successful production
Proven experience as an owner of delivering successful project outcomes
Ability to communicate productively and efficiently with business (FO Traders, Business Managers etc.)
Ability to translate business requirements into functional requirements
Experience in writing detailed Functional/Technical specifications, use cases for development and QA teams
Experience with writing documentation for mapping different data formats between each other
Experience with XML: xpath, xsd (to be able to build xml schema, xpath etc), JSON
SQL knowledge to be able to query and analyze database data
Ability to create complex sql queries

Job Responsibility

The BA will assist in defining new products and treatments, and generating functional and technical specification and test cases, managing the product through end-to-end delivery
Act as trusted partner to our business clients to represent their requirements for technology solutions in the Exotic derivatives domain
Define, document and generate actionable functional and technical requirements for our in-house development team
Guide and mentor other team members
Own and be accountable for cross-asset initiatives, influencing strategic technical direction and driving re-use of our data infrastructure
Build a strong partnership with our upstream and downstream business and technology partners
Grow and curate our catalogue of common assets, such as code templates, libraries, utilities, services, etc.
Troubleshoot performance and scalability issues, take ownership of issues and their technical remediation

What we offer

Generous holiday allowance starting at 27 days plus bank holidays
increasing with tenure
A discretionary annual performance related bonus
Private medical insurance packages to suit your personal circumstances
Employee Assistance Program
Pension Plan
Paid Parental Leave
Special discounts for employees, family, and friends
Access to an array of learning and development resources

Fulltime

Qrm Developer

Realign

Location:
Canada , Toronto

Category:
IT - Software Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
March 21, 2026

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