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Contract Testing Jobs in Quebec (NOW HIRING)

Intact Financial

Senior Developer

Montreal, QC · Hybrid

Hands-on experience with mocking/stubbing, contract testing, data management, and mitigation of flaky tests. * CI/CD integration (reports, gates, artifacts) and a strong sense of performance ...

L3HHCM20

Contracts Administrator

Mirabel, QC · On-site

CA$120K/yr

The Contract Administrator reports to the Manager of Contracts. He/She is mainly responsible for ... L3Harris maintains a drug-free workplace and conducts pre-employment drug and alcohol testing and ...

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Contract Testing information

What is the difference between Contract Testing vs Software Tester?

AspectContract TestingSoftware Tester
Primary FocusVerifies interactions between services or components based on predefined contractsEnsures overall software quality through manual or automated testing of functionalities
Skills & CertificationsKnowledge of API testing, contract frameworks, possibly some automation toolsTesting methodologies, scripting, automation, certifications like ISTQB
Work EnvironmentOften in Agile teams, working closely with developers and QACan vary from manual testing to automation, in various development environments

Contract Testing specializes in validating interactions between services based on contracts, while Software Testers focus on overall software quality through various testing methods. Both roles require testing skills but differ in scope and focus.

What are some common challenges faced by professionals working in contract testing, and how can they be addressed?

Professionals in contract testing often encounter challenges such as ensuring clear communication between frontend and backend teams, maintaining up-to-date test suites when APIs evolve, and managing test flakiness due to changes in dependencies. Addressing these challenges typically involves regular collaboration with development teams, implementing automation for contract verification, and using robust mocking tools. Being proactive in reviewing contract changes and participating in cross-functional meetings can greatly enhance the reliability and efficiency of contract testing processes.

What is contract testing?

Contract testing is a software testing approach used to ensure that different services or components in a system interact correctly according to a set of agreed-upon rules, known as contracts. It is especially useful in microservices architectures, where independent services must communicate reliably. By verifying that the provider and consumer of an API adhere to the same contract, contract testing helps prevent integration issues and reduces the risk of breaking changes during development.

What are the key skills and qualifications needed to thrive as a Contract Tester, and why are they important?

To thrive as a Contract Tester, you need a solid understanding of software testing principles, API interactions, and experience with contract testing frameworks like Pact or Postman, often supported by a background in computer science or QA. Familiarity with version control systems such as Git, CI/CD pipelines, and relevant certifications like ISTQB can be highly beneficial. Strong analytical thinking, attention to detail, and effective communication are crucial soft skills for collaborating with development teams and stakeholders. These skills are essential to ensure seamless integration between services, reduce bugs, and deliver reliable software systems.
What are the most commonly searched types of Testing jobs in Quebec? The most popular types of Testing jobs in Quebec are:
Contract Testing jobs near you
Infographic showing various Contract Testing job openings in Quebec as of May 2026, with employment types broken down into 19% Full Time, and 81% Contract. Highlights an 100% In-person job distribution.

Chemistry Manufacturing & Controls (CMC) Manager

Milestone Pharmaceuticals

Montreal, QC • On-site

Full-time

Posted 21 days ago

Job description

WHY JOIN MILESTONE
At Milestone, we aspire to advance and implement paradigm shifts for cardiac therapy. We are currently focused on developing anti‐arrhythmia treatments for self‐administration outside of the emergency department or hospital setting for patients with acute episodes of paroxysmal supraventricular tachycardia (PSVT) and atrial fibrillation (AFib), as well as other episodic cardiovascular conditions.
In addition to our science and innovation, we are a team guided and driven by our core values. Patient needs and empowerments are continually upheld as central to our mission. Our teamwork is strengthened in an environment in which we support and challenge each other while enjoying and celebrating our achievements. We maintain an entrepreneurial, proactive, and action‐oriented mindset that places high value on grit, courage, and resolve. Decision‐making is based on evaluating information and an idea’s merits; data‐driven proposals are both supported and sought. We act individually and as a team with humility, candor, empathy, and unwavering integrity.
We have been successful in attracting and empowering best‐in‐class talent, and we seek those with passion to join on our journey to develop treatments and to motivate change. We are excited about the possibilities of this team and what we can accomplish together.
YOU WILL BE RESPONSIBLE FOR
  • Manage external manufacturing and analytical activities at contract development and manufacturing organizations (CDMOs) to support commercial supply and clinical programs, ensuring collaboration, communication and scientific expertise.
  • Manage GMP production of drug substance/drug product at CDMOs intended for nasal administration.
  • Manage and support outsourced analytical development, validation and testing activities.
  • Manage stability programs and trending.
  • Provide technical expertise to support the development of new processes and formulations, scale-up, technology transfer and validation.
  • Review batch production records, certificate of analysis, stability reports, validation protocols and reports to ensure technical and cGMP compliance.
  • Review and approve deviations, investigations, CAPAs and change controls as technical subject matter expert and make recommendations to Quality Assurance.
  • Review technical drug substance and drug product documents in a timely matter for regulatory submissions.
EDUCATION AND RESPONSIBILITIES
  • BSc or MSc in Pharmaceutical Sciences, Chemistry, Chemical Engineering, Biochemistry or related field.
  • 5+ years of experience in the biotech or pharmaceutical industry with at least 3+ years in cGMP environment.
  • Hands-on experience with one or more of the following: drug substance/drug product GMP manufacturing, tech transfer, process scale-up and validation, analytical development and validation, formulation development, experience working with CDMOs or contract testing laboratories.
  • Knowledge of GMP, FDA and EU regulations, ICH guidelines, as well as CMC content of regulatory submissions.
  • Proficiency with Word, Excel, PowerPoint, SharePoint, Teams and Acrobat.
KEY ATTRIBUTES
  • Superior interpersonal abilities - including working in a multi-cultural, multi-lingual environment.
  • Exceptional communication skills, with both written and oral presentation abilities.
  • Demonstrated ability to successfully work with and influence contract manufacturing partners while maintaining positive working relationships.
  • Attention to details, strong organization and troubleshooting skills.
  • Able to travel approximately 15% of the time, including international travel when appropriate.

EEOC STATEMENT: Milestone believes in a diverse environment and is committed to equal employment opportunities for all its employees and qualified applicants. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status. Milestone will make reasonable accommodations for qualified individuals with known disabilities in accordance with applicable law.

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