Lead and oversee engineering, FFS, and NDT services, providing technical leadership, ensuring compliance, and driving continuous improvement.
Responsibilities
Provide technical leadership and oversight for engineering, FFS, and NDT services
Develop, review, and maintain engineering procedures, technical documentation, inspection methodologies, and quality processes
Lead and oversee engineering assessments, including Fitness-for-Service evaluations, remaining-life assessments, damage mechanism reviews, and repair recommendations
Serve as the primary technical authority for professional engineering activities under WQS’s APEGA Permit to Practice
Provide technical guidance on complex inspection findings, engineering calculations, technical risks, and integrity assessment challenges
Requirements
Bachelor’s degree in Engineering
Professional Engineer (P.Eng.) designation in Alberta
Responsible for performing field inspections to ensure compliance with safety policies, project specifications, and quality standards for electrical and mechanical assemblies.
Responsibilities
Conduct inspections to ensure compliance and conformance with project or contract specifications
Conduct inspections in accordance with Quality Control Plan
Read blueprints and specifications
Monitor operations to ensure that they meet specifications
Recommend adjustments to the assembly or installation process
Manages vital clinical projects from initiation through completion, joining a dynamic remote team. This role offers the unique opportunity to align cross-functional activities, mitigate risks, and drive solutions that maintain our high quality standards and deliver a healthier future.
Compensation
The expected salary range for this position based on the primary location of Arizona is 56,400.00 - 104,700.00 USD Annual. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance.
Responsibilities
Manages multiple clinical projects from initiation through completion, ensuring alignment with timelines, scope, and quality standards.
Serves as the primary point of contact for Pharma and Roche clients, ensuring clear communication and stakeholder alignment.
Coordinates project timelines and develops and executes project plans across CDx Pharma Services, aligning cross-functional activities and tracking progress against defined milestones.
Identifies and mitigates risks, gaps, and bottlenecks, driving solutions to maintain project timelines.
Oversees sample testing workflows and data reporting, ensuring accuracy, compliance, and adherence to quality standards.
Requirements
Bachelor’s Degree in Life Sciences, Clinical Research, Healthcare, or a related field
Master’s Degree or completed specialized training in Project Management or Clinical Research
Nice to have: specialized training in Project Management
Manage clinical projects from initiation through completion, coordinating cross‑functional activities, mitigating risks, and ensuring quality standards in a remote team environment.
Compensation
The expected salary range for this position based on the primary location of Arizona is 56,400.00 - 104,700.00 USD Annual. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance.
Responsibilities
Manage multiple clinical projects from initiation through completion, ensuring alignment with timelines, scope, and quality standards.
Serve as the primary point of contact for Pharma and Roche clients, ensuring clear communication and stakeholder alignment.
Coordinate project timelines and develop and execute project plans across CDx Pharma Services, aligning cross‑functional activities and tracking progress against defined milestones.
Identify and mitigate risks, gaps, and bottlenecks, driving solutions to maintain project timelines.
Oversee sample testing workflows and data reporting, ensuring accuracy, compliance, and adherence to quality standards.
Requirements
Bachelor’s Degree in Life Sciences, Clinical Research, Healthcare, or a related field
Master’s Degree or specialized training in Project Management or Clinical Research
Develop, design, and debug embedded software solutions for MSP microcontrollers, leading software development for new and innovative projects within the MSP business unit.
Responsibilities
Write clean and scalable code for MSP microcontrollers
Design software solutions with a test‑driven development approach
Support and own all phases of the software development lifecycle
Collaborate with cross‑functional teams to align on software strategy and customer needs
Debug and address software issues during development and in production systems
Supports initiatives related to User Acceptance Testing (UAT) process and product rollout into production
Conducts a variety of moderately complex process monitoring, product evaluation and audit assignments; reports issues and makes recommendations for solutions
Ensures project standards and procedures exist, are fully clearly documented and followed throughout the software development life cycle; makes recommendations for enhanced documentation
Monitors products for conformance to standards; monitors processes for conformance to procedures
Documents findings and performs preliminary root causes analyses to provide recommended improvements
Requirements
Bachelor’s/University degree or equivalent experience
Nice to have: 5+ years Quality Assurance (QA) experience in the Financial Service industry
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