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Salary
≈ $106k – $249k per year (Estimated)
Location
In office (Basel)
Seniority
Staff · 8+ years exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 31, 2026. First seen by Alion on Oct 29, 2026. Roche scores A on the Alion truth index.

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

As a Section Lead DP Process Engineering in Pharmaceutical Development in Basel, Switzerland, you are a member of the global Drug Product Process Engineering and Manufacturing team as part of the Department Biologics Pharmaceutical Development. The Department Biologics Pharmaceutical Development is responsible for the development of parenteral drug products (synthetic molecules and biologics) from Phase 1 up to Launch, including formulation and aseptic process development. The Pharmaceutical Development Process Engineer ensures robust clinical and commercial process designs for effective process validation and successful commercialization of sterile drug products.

This position is focused on robust process development for parenteral drug products to drive excellence and innovation and ensure seamless network-wide execution across biologics, synthetic molecules, and peptides.

The Opportunity:

In this role, you will lead a team of process engineers focused on developing sterile DP manufacturing processes across clinical and commercial stages. As part of the global team, you will ensure the implementation of harmonized, science- and risk-based strategies that enable efficient technology transfers and process validation in collaboration with internal and external manufacturing network partners. Furthermore, the Section Lead will foster a growth-oriented, high-performing team environment, enabling staff to develop their skills and contribute their best work.

  • Provide technical oversight and strategic guidance for a team responsible for the development of robust manufacturing processes for parenteral liquid and lyophilized formulations including scale-up, process characterization & validation and transfer to global commercial manufacturing sites.
  • Lead, coach and develop a team of approximately 8-12 process engineers focused on drug product process development across various modalities such as Biologics, synthetic molecules, peptides
  • Ensure process designs for clinical and commercial stages are robust for effective validation and successful commercialization
  • Represent the function during interactions with various interfaces and in stakeholder meetings, emphasizing global harmonization through collaboration, Lean principles, and an innovation mindset.
  • Collaborate cross-functionally and with manufacturing sites, including partnerships with CMOs, to ensure alignment and successful project execution.

Who you are

  • You hold a Ph.D. in relevant scientific or engineering disciplines (preferred) or have commensurate experience.
  • You have at least 8 years of relevant experience in the biopharmaceutical industry and proven ability to shape and lead teams.
  • You have experience in leading or managing groups of scientists and engineers, as well as working with departmental senior staff for project and people decisions.
  • You demonstrate capabilities to lead, motivate, and develop people, focusing on optimum utilization of talent and skills.
  • You possess strong technical expertise in parenteral process development and readiness to oversee end-to-end pharmaceutical development, including regulatory submissions
  • You have a proven ability to prioritize resources effectively across the network and sponsor strategic process engineering projects, ensuring alignment and successful execution within complex organizational structures
  • You are able to travel up to 20% domestically and internationally

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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