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Roche

Control Strategy Scientist

Mississauga, ON, Canada
Canada Pharma Campus, Canada

Full-time

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Job details

Job type: Full-time
Apply by: Nov 20, 2026
Experience: Experience: 7-10+ years in the pharmaceutical or biopharmaceutical industry, in QC, analytical development or CMC.
Posting language: English
Posted: Nov 6, 2026

Original job description

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.

The Position

Roche is a global pioneer in pharmaceuticals and diagnostics focused on advancing science to improve people’s lives. As one of the world’s largest biotech companies and a global leader in in-vitro diagnostics, Roche is dedicated to driving innovative healthcare solutions that provide significant benefits to patients and healthcare providers alike. Our commitment to excellence is reflected in our culture of collaboration, where we empower our people to challenge the status quo and deliver life-changing medical breakthroughs. At Roche Canada, we foster a diverse and inclusive environment that encourages creative thinking and rewards the pursuit of excellence in our mission to shape the future of healthcare.

Network Quality Control, part of Roche Parma Technical Quality and Compliance (PTQ), supports Roche's internal QC sites and contract partners worldwide, including emerging markets, with advanced scientific and technical expertise. We are looking for a Control Strategy Scientist (CSS) in Mississauga to join our global team of scientists.

As Control Strategy Scientist (CSS) you are the single accountable owner of the commercial analytical control strategy for one or more products of an expanding portfolio of biologics. That covers specifications, analytical methods, from in-process controls to release and shelf life, across all manufacturing and testing sites. You lead in a matrix without line authority: you work with QC sites, Analytical Development, MSAT, Regulatory and Quality, and you are a standing member of the cross-functional commercial product technical teams. Your work enables robust and efficient QC testing, faster approvals, and reliable supply of medicines to patients.

The Opportunity

Own the control strategy for biologics. Keep specifications, methods and stability programs lean, state-of-the-art and harmonized across the network. Lead the global analytical subteam for one or more products and evaluate release and stability data end-to-end across sites.
Shape new products before launch. From late-stage development onward, influence method design, validation, specifications, reference standards and stability studies so they work in commercial QC. Drive the analytical knowledge transfer from Phase III to commercial QC.
Manage the lifecycle. Plan and deliver lifecycle management of control strategies. Own the overall stability budget and shelf-life extensions. Be accountable for analytical comparability protocols and reports, including statistical acceptance criteria.
Lead the regulatory content. Own responses to health authority information requests, author the analytical, comparability and stability sections of submissions, and support inspections and annual quality reviews.
Solve problems across sites. Support product-specific multi-site investigations. Own global changes and corrective and preventive actions for control system gaps. Assess temperature excursions, method monitoring results and reference standard changes.
Drive innovation. Bring in platform methods, new QC technologies, automation and digital solutions, and contribute to industry best-practice discussions.

Who you are

Education: PhD or MSc in analytical chemistry, biochemistry or another relevant life-science discipline.
Experience: 7-10+ years in the pharmaceutical or biopharmaceutical industry, in QC, analytical development or CMC.
Technical expertise: Experience in analytical methods for biologics such as chromatography, electrophoresis or bioassays; method validation and transfer; experience with stability and shelf-life setting; statistical data evaluation. Experience with synthetic peptide or oligonucleotide parenterals or combination products is considered a plus.
Regulatory knowledge: cGMP, ICH guidelines and global CMC requirements. Experience authoring CTD Module 3 sections is an asset.
Leadership: You influence without authority, communicate clearly in writing and in person, and build trust with sites, partners and health authorities. You follow the science, act as one team and simplify radically.

**Relocation not eligible for this role**

The expected salary range for this position based on the primary location of Mississauga is 136,936.00 and 179,728.50 of hiring range. Actual pay will be determined based on experience, qualifications, and other job-related factors as determined by the company.

We use artificial intelligence to screen, assess or select applicants for this role.

This posting is for an existing vacancy at Hoffmann-La Roche Ltd.

Who we are

A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.

Let’s build a healthier future, together.

Roche is an Equal Opportunity Employer.

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More about this job

Responsibilities

The Control Strategy Scientist serves as the accountable owner for the commercial analytical control strategy for a portfolio of biologics. They lead global analytical subteams to ensure robust QC testing, regulatory compliance, and effective lifecycle management of analytical methods.

Requirements

Candidates must hold a PhD or MSc in analytical chemistry, biochemistry, or a related life-science discipline. A minimum of 7-10 years of experience in the pharmaceutical or biopharmaceutical industry, specifically in QC, analytical development, or CMC, is required.

Skills

Analytical chemistry
Biochemistry
Control strategy
Method validation
Method transfer
Stability testing
Statistical data evaluation
Chromatography
Electrophoresis
Bioassays
Regulatory compliance
cGMP
ICH guidelines
CMC
Lifecycle management
Technical leadership

Visa sponsorship

Not detected in the job text

Keywords

Biologics
Pharmaceuticals
Diagnostics
QC
Analytical Development
CMC
CTD Module 3
Stability programs
Reference standards
Comparability protocols
Health authority
Regulatory submissions
Automation
Digital solutions
Synthetic peptide
Oligonucleotide
Combination products
Matrix leadership
Quality control
Technical quality

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