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Salary
$104k – $214k per year (Estimated)
Location
In office (Basel)
Seniority
Staff · 8+ years exp
Employment
Full-Time
Overview
Company
Impact
Profile match
Roche is a Swiss healthcare group founded in Basel in 1896 and is unusual in operating two large divisions of comparable importance: prescription medicines and in vitro diagnostics. The pharmaceutical business is built on oncology, neurology, immunology, ophthalmology and haemophilia, with products such as Ocrevus, Hemlibra, Perjeta and Vabysmo, while the diagnostics division supplies laboratory analysers, molecular tests and sequencing systems to hospitals worldwide. The group owns the American biotechnology company Genentech outright and the Japanese firm Chugai in majority, is controlled by a family shareholder pool, and spends among the largest research budgets in the industry.

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

A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche!

Advances in AI, data, and computational sciences are transforming drug discovery and development. Roche’s Research and Early Development organisations at Genentech (gRED) and Pharma (pRED) have demonstrated how these technologies accelerate R&D, leveraging data and novel computational models to drive impact. Seamless data sharing and access to models across gRED and pRED are essential to maximising these opportunities. The new computational sciences Center of Excellence (CoE) is a strategic, unified group whose goal is to harness this transformative power of data and Artificial Intelligence (AI) to assist our scientists in both pRED and gRED to deliver more innovative and transformative medicines for patients worldwide. Within the CoE organisation, the Data and Digital Catalyst (DDC) organisation drives the modernization of our computational and data ecosystems and integration of digital technologies across Research and Early Development to enable our stakeholders, power data-centric science and accelerate discovery.

The Security, Compliance and Validation Technical Project Manager is responsible for defining, implementing, and advancing frameworks that ensure scientific computing platforms and data systems meet regulatory, security, and quality standards. This role operates within the Security, Compliance and Validation (SCV) function and partners closely with Platform Engineering, Platform Enablement, and scientific teams to enable compliant, secure, and high-quality digital solutions. Beyond Scientific Computing, this role will partner closely with Roche Global Information Security, Product Development / pharma Research & Early Development Quality Assurance as well as Legal Officers and the Roche Computer System Validation group to ensure that our work is compliant with Roche Security system standards while meeting regulatory requirements.

This position combines deep expertise with regulatory and quality domain knowledge, ensuring that modern, cloud-native and data-intensive platforms can operate effectively within GxP and other regulated environments. The role emphasizes a risk-based, pragmatic approach to compliance and validation, enabling innovation while maintaining audit readiness and adherence to regulatory expectations.

The Security, Compliance and Validation Technical Project Manager is expected to act as a subject matter expert, influencing strategy, mentoring others, and driving continuous improvement in validation, security, and compliance practices across the organization.

The Opportunity

  • Partner with Quality to co-drive the modernization and optimization of the Computerized System Validation (CSV) framework, including automation, continuous validation, and quality-by-design; drive the efficient application of the CSV processes to products & platforms.

  • Ensure that systems, and workflows adhere to risk-based validation and applicable GCP or GLP regulations & organizational standards.

  • Create & manage lifecycle documentation, including validation plans, test protocols, and traceability artifacts, ensuring complete audit readiness.

  • Perform comprehensive risk assessments for internal systems and vendor solutions, ensuring robust controls are implemented and documented.

  • Provide expert guidance on regulatory expectations, including data integrity, audit trails, and system lifecycle controls.

  • Embed security-by-design into platform and product architectures, including IAM, encryption, and monitoring (i.e. support incident response, vulnerability management, and continuous security improvements).

  • Act as a subject matter expert for the Roche Information Security framework, promoting best practices and compliance awareness across the Computational Sciences organization

Who You Are

  • Bachelor’s degree in Computer Science, Engineering, Life Sciences, or equivalent experience.

  • 8+ years of experience in CSV, GxP compliance, security, and risk assessment within regulated environments.

  • Strong understanding of regulatory requirements, including GxP guidelines, data integrity, and system lifecycle management, and knowledge of security frameworks and standards (e.g., NIST, ISO 27001).

  • Proven experience implementing validation and compliance frameworks for laboratory, cloud-based, or distributed systems, and supporting regulatory inspections or audits.

  • Experience developing SOPs, validation templates, and compliance tooling.

  • Expertise in leading the validation of computerized systems (preferably GCP/GLP) and supporting regulatory inspections.

  • Significant experience with software development lifecycle methodologies (AGILE/SCRUM) and lifecycle management tools (e.g., Jira, ServiceNow).

  • Demonstrated ability to translate complex regulatory requirements into actionable technical guidance for cross-functional scientific and engineering teams.

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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