Principal Project Engineer Packaging & Device Assembly (US)
Roche
Summary
This role is an integral part of our Equipment Engineering team, dedicated to delivering cutting-edge solutions for Device Assembly and Finished Goods Packaging systems that ensure safe, efficient, and compliant pharmaceutical manufacturing. As a member of this team, you will collaborate with global stakeholders, equipment manufacturers, and multidisciplinary project teams to drive the successful delivery of capital projects.
Job description
The Opportunity
As a Principal Project Engineer Packaging & Device Assembly (US), you will lead and manage the technical execution of equipment sub-projects, driving collaboration across global teams and ensuring compliance with industry standards. You will be accountable for delivering innovative, high-quality solutions that support the manufacturing of Roche's life-saving medicines.
- Independently plan, design, and implement mechanical and process engineering projects, ensuring full compliance with Roche Guidelines, Global Standards, and Health Authority Requirements.
- Manage the approved sub-project budget and schedule, define priorities, and provide regular updates on progress, risks, mitigation strategies, and escalations.
- Serve as the primary interface with equipment manufacturers, managing technical specifications, design reviews, performance validation, and compliance requirements.
- Drive mechanical and automation engineering for state-of-the-art assembly systems for pre-filled syringes, autoinjectors, and pen injectors in compliance with relevant standards and regulations.
- Lead and coordinate Factory Acceptance Tests (FATs), Site Acceptance Tests (SATs), commissioning, and qualification activities to ensure operational readiness of equipment.
- Direct and manage external engineering firms, service providers, and contractors to ensure timely and quality-compliant project execution.
- Guide overall project scope, including options analysis, project planning, detailed scheduling, and resource allocation.
- Mentor and coach less experienced engineers, fostering technical growth and professional development across the team.
- Act as a technical Subject Matter Expert (SME) for manufacturing equipment and machine safety during regulatory inspections and audits.
Who You Are
- You possess a Bachelor's Degree in Mechanical Engineering, Chemical Engineering, or a related discipline with 8+ of experience, or a Master's Degree with 6+ years of experience in device assembly or finished goods packaging equipment; an MS in Engineering and/or an MBA is preferred.
- You possess extensive years of experience in international management of capital projects related to device assembly and finished goods packaging, with typical project budgets ranging from 18 to 60 M USD.
- You have proven experience collaborating with equipment manufacturers, leading FAT/SAT efforts, and managing equipment commissioning and qualification activities.
- You possess significant knowledge of regulatory (FDA, EMA) and GMP requirements, as well as machine directives and relevant standards for combination products with demonstrated success in delivering complex projects in pharmaceutical manufacturing environments.
- Significant travel (50% +) assignment requiring weekly commuting and/or temporary remote assignment as required to meet the business need (including on-site presence). International project assignment of 1 to 3 years as required to meet the business need.
Requirements
- Bachelor's Degree in Mechanical Engineering, Chemical Engineering, or a related discipline with 8+ years of experience, or a Master's Degree with 6+ years of experience in device assembly or finished goods packaging equipment
- MS in Engineering and/or an MBA is preferred
- Extensive years of experience in international management of capital projects related to device assembly and finished goods packaging, with typical project budgets ranging from 18 to 60 M USD
- Proven experience collaborating with equipment manufacturers, leading FAT/SAT efforts, and managing equipment commissioning and qualification activities
- Significant knowledge of regulatory (FDA, EMA) and GMP requirements, as well as machine directives and relevant standards for combination products
- Demonstrated success in delivering complex projects in pharmaceutical manufacturing environments
- Significant travel (50% +) assignment requiring weekly commuting and/or temporary remote assignment
- International project assignment of 1 to 3 years as required
Benefits
- Discretionary annual bonus
- Medical, Dental & Vision
- 401(k) Matching
- Paid Time Off
Company overview
Roche is a Swiss multinational healthcare company and a global pioneer in pharmaceuticals and diagnostics, founded in 1896 and headquartered in Basel, Switzerland. As the world's largest biotech company and the fifth-largest pharmaceutical company by revenue, Roche operates through two primary divisions: Pharmaceuticals and Diagnostics. The company is renowned for its leadership in personalized healthcare, combining strengths in both drug development and diagnostic testing to deliver tailored treatments for patients. Roche maintains a strong focus on oncology, immunology, infectious diseases, ophthalmology, and central nervous system disorders, with a portfolio that includes over 30 medicines on the World Health Organization's Model Lists of Essential Medicines. The company owns significant subsidiaries including Genentech, Chugai Pharmaceuticals, Ventana Medical Systems, and Foundation Medicine. With approximately 103,000 employees worldwide and operations in over 100 countries, Roche has established itself as a leader in cancer treatments globally while maintaining a robust pipeline of innovative therapies and diagnostic solutions. The company's commitment to sustainability has been recognized through ten consecutive years as Group Leader in the Dow Jones Sustainability Indices within the Pharmaceuticals, Biotechnology & Life Sciences Industry.