Qrm developer Job at Realign (Toronto)

Qrm Developer

QRM Developer Toronto, ON - Onsite

Location

Canada , Toronto

Salary:

309000.00 USD / Year

Realign

Expiration Date

Until further notice

Requirements

Seeking a QRM Developer to support Treasury, ALM, Liquidity, and Risk functions by developing QRM models and automating operational workflows using PowerShell and Ansible.
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

Associate Director, Product Quality Assurance

The Associate Director of Product Quality for Cell and Gene Therapy Programs wil...

Location

United States , Cambridge

Salary:

185000.00 - 225000.00 USD / Year

Beam Therapeutics

Expiration Date

Until further notice

Requirements

Bachelors or Advanced degree in scientific discipline
12+ years’ experience in the pharmaceutical/biotech industry in combination with drug substance/drug product manufacture, development and/or quality with at least 4 years of which should have been in a CMC-focused position in Cell and Gene Therapy Quality role
Detailed knowledge and understanding of GMP regulations and Food and Drug Administration (FDA) requirements
Ability to influence without direct authority
Ability to develop into a primary PQL for Beam programs
Excellent verbal and written communication skills, detail-oriented personality and ability to work and drive change across functions
Experience interacting with regulatory health authorities at pre- and post-approval inspection
Strong team player that has a customer service approach and is solution oriented
Attention to detail and the ability to work individually, within a multi-disciplinary team, as well as with external partners and vendors
Excellent listening, communication and interpersonal skills fostering team spirit

Job Responsibility

Provides strategic Quality CMC-focused support based on Program Team timelines, milestones, and regulatory commitments
Drives and takes action on Phase Appropriate Quality strategy for Beam’s products
Performs Quality review/approval of records and documentation related to manufacturing such as process defining documentation
Performs product quality impact assessments for product complaints, manufacturing deviations, OOT/OOS results, MRB, adverse trends, etc
Quality reviewer and approver of select technical documents (e.g. complaints, temperature excursion reports, justification of specification (JoS), specifications, method validations, critical quality attribute (CQA) assessment, comparability, risk assessments, continued process verification (CPV), tech transfer, ad hoc testing / characterization protocols, etc.)
Ad hoc Quality representative on Program Team and CMC Team in support of primary PQL
Ensures alignment with regulatory requirements, industry standards / best practices, and Beam initiatives
Support clinical to commercial analytical control strategy
Strategic and technical support across product lifecycle (manufacturing process and analytical method changes, tech transfer, characterization, comparability, validations, technology improvements, etc.)
Reviews manufacturing process performance, analytical method performance, stability data, etc. for signals / trends / patterns to proactively monitor and if necessary, support mitigations

Fulltime

Senior Associate, Capital Markets & Risk

Senior Associate, Capital Markets & Risk LMCRO provides oversight of Capital On...

Location

United States , McLean

Salary:

111200.00 - 126900.00 USD / Year

Capital One

Expiration Date

Until further notice

Requirements

Bachelor's degree or Military experience
At least 2 years of experience in Market Risk Management or Capital Markets
Master's degree in Economics, Finance, Data Science, or an MBA
Professional certifications such as CFA as or FRM
Experience with regulatory reporting and compliance related to interest rate risk
Strong analytical skills and attention to detail

Job Responsibility

Develop and implement strategies to mitigate interest rate risk, including balance sheet positioning and hedging strategies
Daily and month-end risk monitoring and reporting for a collection of programs. This will include producing risk analytics and income forecasts on banking programs including card, commercial lending, derivatives, and structured products
Conduct scenario analyses and stress testing to evaluate the impact of various interest rate movements to the bank’s financial position
Utilize QRM or similar ALM modeling software to assess and manage the bank’s interest rate risk exposure
Prepare and present comprehensive risk reports to senior leadership
Collaborate with cross-functional teams, including Finance, Risk Management, and Business Units, to ensure alignment on risk management strategies
Stay informed about market trends and regulatory changes affecting interest rate risk management

What we offer

Performance based incentive compensation, which may include cash bonus(es) and/or long term incentives (LTI)
comprehensive, competitive, and inclusive set of health, financial and other benefits

Fulltime

Transformative career opportunity within Balance Sheet Model Development

Location

United Kingdom

Salary:

75000.00 GBP / Year

Star Actuarial Futures

Expiration Date

Until further notice

Requirements

Experienced financial modeller fluent in major platforms
Previous QRM skills not a prerequisite
Must be willing to apply modelling experience to quickly learn QRM
Thrives in technically complex environments
Advanced Excel skills

Job Responsibility

Help drive multiple tactical QRM-based solutions across 2026, 2027 and beyond
Improve granularity of treasury, liquidity and business-forecasting models
Lead the design and build of enhanced forecasting and modelling capabilities within QRM
Improve existing modelling of core products (mortgages, savings, treasury instruments)
Develop new forecasting approaches (inc. credit cards, commercial and current accounts)
Liaise across financial planning, treasury, capital, ALM and transformation teams

What we offer

10% pension
discretionary annual bonus
28 days holiday (30 days with service)
income protection
6xDIS

Fulltime

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

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

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

New

IT Training Lead

The IT Training Lead will drive technology learning and user adoption across the...

Location

United States , Delray Beach

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

Experience in IT training, instructional design, technical enablement, or learning and development
Strong knowledge of Microsoft 365
Excellent communication, facilitation, and content development skills
Ability to translate technical concepts into practical, user-friendly training.

Job Responsibility

Design, develop, and deliver IT training programs in instructor-led, virtual, and self-paced formats
Take lead in the Microsoft Copilot and AI training strategy, including onboarding, advanced use cases, responsible AI usage, and ongoing enablement
Partner with IT leadership to support new technology rollouts, system upgrades, and digital transformation initiatives
Create and maintain training content, including videos, guides, tutorials, and job aids
Identify skill gaps and develop targeted learning solutions to improve adoption and productivity
Gather feedback and measure training effectiveness to continuously improve programs.

Select Country

Qrm developer

Job Description

Job Responsibility

Requirements

Nice to have

Looking for more opportunities?

Qrm developer

Qrm Developer

Associate Director, Product Quality Assurance

Senior Associate, Capital Markets & Risk

Transformative career opportunity within Balance Sheet Model Development

Qualified Person

Senior Manager CSSV AI Compliance Lead

Principal Quant Developer

IT Training Lead

Our AI answers in your language