Senior Research Scientist

Siemens Healthineers AG; Ottawa; On-site; CAD 90,000 - 140,000; Full time

Job summary

Siemens Healthineers AG is seeking a Senior Research Scientist (Stability, Verification and Validation) to lead verification and validation activities for handheld products, supporting regulatory submissions and post‑market documentation.

You will independently design experiments, analyze complex data, and prepare technical reports while collaborating with Regulatory Affairs, Clinical Affairs, R&D, Quality, and Marketing. Travel may be required up to 25% in a global role.

Qualifications

• Master's or PhD in a relevant technical discipline or equivalent experience
• Minimum of 8 years of clinical research experience in medical devices, healthcare, or pharmaceutical industry
• Demonstrated expertise in point-of-care blood gas and chemistry analysis within medical diagnostics/clinical labs
• Proven ability to interface with external sites and form collaboration agreements
• Demonstrated success managing complex, high-level technical assignments with minimal oversight
• Excellent written and verbal communication skills

Responsibilities

• Manage planning and execution for internal validation, evaluations, and post-market evaluations; include protocol development and study design
• Perform data acquisition for verification and validation studies (Alpha, method comparison, precision, LOQ, interference)
• Compile, analyze, and interpret study data; prepare technical reports and regulatory summaries
• Coordinate investigational product supply logistics with Export Control, Customs, Shipping
• Contribute to customer-facing collateral with R&D, Quality, Regulatory, Marketing
• Support regulatory submissions (FDA, IVDR, CLIA) as required

Skills

Data interpretation

Cross-functional collaboration

Independent work

Time management

Technical reporting

Presentation skills

Education

Master's or PhD in a relevant technical discipline

Tools

Excel

JMP

Job description

Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably.

Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions.

Position Overview

Under the supervision of the Manager, Stability, Verification and Validation (Handheld), the Research Professional oversees verification and validation activities for both new and on‑market products in support of regulatory submissions and post‑market documentation.

The role operates at a scientist level and requires a high degree of independence and technical expertise. Responsibilities include technical development and experimental screening, as well as the design, execution, and interpretation of complex studies with minimal supervision. The Senior Research Scientist engages and collaborates with cross‑functional stakeholders, including Regulatory Affairs, Clinical Affairs, Marketing, Product Health, Research and Development, and Stability, Verification and Validation.

Responsibilities

• Manages planning and execution activities for internal validation, preliminary evaluations, continuous improvement initiatives, product portfolio life‑cycle management, and post‑market evaluations. This includes protocol development and study design, document management.
• Performs data acquisition for a broad range of in‑house and field verification and validation studies, including but not limited to Alpha studies, method comparison, precision, limit of quantification, and interference testing.
• Compiles, analyzes, and clinically interprets study data, and prepares technical reports and support regulatory summaries.
• Manages investigational product supply logistics, working closely with Export Control and Customs specialists as well as Shipping and Receiving to ensure timely delivery to collaboration sites and to resolve logistical issues as needed.
• Contributes to the development of customer‑facing collateral, including case studies, proof points, white papers, and customer bulletins, in close collaboration with R&D, Quality, Regulatory, and Marketing.
• Supports preparation of regulatory submissions, including but not limited to FDA Pre‑Submissions, FDA 510(k) submissions, IVDR submissions, and CLIA Waiver applications, as required.

Required Knowledge, Skills, Education, and Experience

• Master's or PhD's degree in a relevant technical discipline, or an equivalent combination of education and applicable technical experience.
• Minimum of 8 years of clinical research experience in the medical device, healthcare, or pharmaceutical industry.
• Demonstrated expertise in point-of-care blood gas and chemistry analysis within the medical diagnostics or clinical laboratory environment.
• Proven ability to interface professionally with external sites and to establish and maintain effective working relationships and collaboration agreements.
• Demonstrated success in managing complex, high‑level technical assignments with minimal oversight.
• Highly organized and detail‑oriented, with strong time‑management and prioritization skills.
• Strong ability to work collaboratively in a team environment, with a demonstrated commitment to mentoring and developing others.
• Proficient in the use of data collection and analysis tools, such as Excel and JMP.
• Willingness to proactively identify issues, raise concerns, and propose practical solutions.
• Excellent written and verbal communication skills.
• Comfortable developing and delivering presentations to internal and external stakeholders in both one‑on‑one and group settings.

Preferred Knowledge, Skills, Education, and Experience

• In‑depth understanding of the epoc® blood analysis system, with the ability to apply this knowledge to troubleshoot issues related to sample preparation, testing protocols, workflows, and product performance.
• Experience in launching a commercial product.
• Ability and willingness to travel upon request (less than 25%)

Who we are

We are a team of more than 72,000 highly dedicated Healthineers in more than 70 countries. As a leader in medical technology, we constantly push the boundaries to create better outcomes and experiences for patients, no matter where they live or what health issues they are facing. Our portfolio is crucial for clinical decision‑making and treatment pathways.

How we work

When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skilled specialists, who believe in each individual’s potential to contribute with diverse ideas. We are from different backgrounds, cultures, religions, political and/or sexual orientations, and work together, to fight the world’s most threatening diseases and enable access to care, united by one purpose: to pioneer breakthroughs in healthcare. For everyone. Everywhere. Sustainably.

The expected compensation for this position is

Factors which may affect starting compensation within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate.

Siemens Healthineers offers a variety of health and wellness benefits including a flexible benefits plan, Defined Contribution Pension Plan, Registered Retirement Savings Plan matching contributions, plus a competitive paid time off program including vacation, company holidays, sick leave, and parental leave (all subject to eligibility requirements).

Equal Employment Opportunity Statement

Siemens Healthineers is committed to creating a diverse environment and is proud to be an equal opportunity employer. While we appreciate all applications we receive, we advise that only candidates under consideration will be contacted.

Accessibility

Siemens Healthineers is committed to excellence in serving all employees and customers, including people with disabilities. Siemens Healthineers will strive to ensure that policies and procedures established with respect to the provisions of its goods and services to persons with disabilities are consistent with the principles of dignity, independence, integration and equal opportunity as provided in the Accessibilities for Ontarians with Disabilities Act, 2005. Siemens Healthineers will continue to attempt to meet the needs of all its customers, including but not limited to persons with disabilities, in an effective and timely manner.

Accommodation Request

If you require a reasonable accommodation in completing a job application, interviewing, completing any pre‑employment testing, or otherwise participating in the employee selection process, please fill out the accommodations form here . If you’re unable to complete the form, you can reach out to our HR People Connect People Contact Center for support at [e-mail] . Please note HR People Connect People Contact Center will not have visibility of your application or interview status.

Data Privacy

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Recruitment Agency Policy

To all recruitment agencies: Siemens Healthineers does not accept agency resumes. Please do not forward resumes to our jobs alias, employees, or any other company location. Siemens Healthineers is not responsible for any fees related to unsolicited resumes.

Beware of Job Scams

Please beware of potentially fraudulent job postings or suspicious recruiting activity by persons that are currently posing as Siemens Healthineers recruiters/employees. These scammers may attempt to collect your confidential personal or financial information. If you are concerned that an offer of employment with Siemens Healthineers might be a scam or that the recruiter is not legitimate, please verify by searching for the posting on the Siemens Healthineers career site.