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The PositionAs the Process Engineer, you will ensure robust automation, clean utility, and manufacturing processes by providing technical support to multiple Reagent Manufacturing laboratories and Site Operations. You will carry out CAPA, root cause investigations, process improvements, and change control practices in support of cGMP processes. In this role, you will participate in the installation and commissioning of new systems, and processes.
The Opportunity
- You will provide engineering support and technical troubleshooting for automation systems, cGMP Process Utility systems, and general equipment upgrades.
- You will troubleshoot hardware and software for the Process Control System (PCS), which controls Bulk Reagent Formulation, Solvent Delivery, Site, and Process Utility operations.
- Author and maintain system support and specification documentation, including Change Requests, SOPs, Equipment Non-Conformances, User Requirements Specifications, and User Acceptance Testing.
- Contribute to the planning and design review of automation processes, including EHS reviews (e.g., HAZOP), equipment evaluations, tests, and approvals.
- Maintain high equipment reliability utilizing maintenance, engineering, and appropriate resources to resolve availability issues.
- Participate in engineering projects involving instrumentation selection, wiring diagram generation, issue diagnosis, and solution implementation while addressing quality-related issues like CAPAs and audits.
Who You Are
- You have a Bachelor’s degree in Engineering, Computer Science, or a related field (or an equivalent combination of education and work-related experience).
- You have 2+ years of experience with increasing responsibilities in process engineering and automation within a manufacturing environment, including at least 1 years in a bioprocess, pharma, or diagnostic site.
- You will carry out root cause investigations and execute change control practices to maintain cGMP compliance.
- You will collaborate across maintenance, engineering, and quality teams to resolve equipment availability and compliance issues.
Preferred Qualifications
You have experience with the design and operation of cGMP clean utility systems and manufacturing equipment (e.g., Purified Water Generation/Distribution, Clean Steam, CIP, Autoclaves, Glass Washers, and Manufacturing Process Vessels).
Knowledge, Skills and Abilities
- Solid understanding of mechanical systems, including valves, pumps, motors, seals, and bearings.
- Experience with PLCs, industrial maintenance, and computer control systems.
- Strong diagnostic, problem-solving, and troubleshooting skills for hardware and software systems.
- Ability to read and interpret schematics, including P&IDs, mechanical, electrical, and control diagrams.
- Willingness and ability to fulfill operational work environment requirements, including wearing required PPE, performing Lock Out Tag Out, climbing ladders, and maintaining a valid driver's license.
- Flexibility to carry a company-issued cell phone for off-hours response, work weekends during facility shutdowns (4 times per year), and perform overtime as needed.
Willingness to travel up to 10%.
Relocation benefits are not available for this position.
The expected salary range for this position based on the primary location of Branchburg, NJ is 77,100.00 - 143,100.00 USD Annual. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.
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. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.
Skills Required
- Bachelor's degree in Engineering, Computer Science, or a related field, or equivalent education and work experience
- At least 2 years of progressively responsible process engineering and automation experience in a manufacturing environment
- At least 1 year of experience in a bioprocess, pharmaceutical, or diagnostic site
- Experience conducting root-cause investigations and executing change control practices in a cGMP environment
- Experience with PLCs, industrial maintenance, and computer control systems
- Ability to troubleshoot hardware and software systems and interpret P&IDs, mechanical, electrical, and control schematics
- Valid driver's license
- Ability to wear required PPE, perform Lockout/Tagout, climb ladders, work overtime, and respond during off-hours
- Experience designing and operating cGMP clean utility systems and manufacturing equipment, including purified water, clean steam, CIP, autoclaves, glass washers, and process vessels
Roche Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Roche and has not been reviewed or approved by Roche.
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Retirement Support — U.S. materials describe a 401(k) with both matching and an additional company contribution, supported by formal plan documents and true‑up features. This structure is positioned as a standout element of the total package, particularly at Genentech.
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Leave & Time Off Breadth — Time‑off provisions include substantial vacation, a year‑end shutdown, and a paid six‑week sabbatical after six years. These elements indicate a recharge‑oriented approach within the U.S. offering.
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Healthcare Strength — Company materials emphasize comprehensive medical, dental, vision, and mental‑health resources alongside well‑being programs. Benefits pages consistently highlight breadth across core health coverage elements.
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What We Do
Roche is a global pioneer in pharmaceuticals and diagnostics focused on advancing science to improve people’s lives. The combined strengths of pharmaceuticals and diagnostics under one roof have made Roche the leader in personalised healthcare – a strategy that aims to fit the right treatment to each patient in the best way possible. Roche is the world’s largest biotech company, with truly differentiated medicines in oncology, immunology, infectious diseases, ophthalmology and diseases of the central nervous system. Roche is also the world leader in in vitro diagnostics and tissue-based cancer diagnostics, and a frontrunner in diabetes management. Founded in 1896, Roche continues to search for better ways to prevent, diagnose and treat diseases and make a sustainable contribution to society. The company also aims to improve patient access to medical innovations by working with all relevant stakeholders. Thirty medicines developed by Roche are included in the World Health Organization Model Lists of Essential Medicines, among them life-saving antibiotics, antimalarials and cancer medicines. Roche has been recognised as the Group Leader in sustainability within the Pharmaceuticals, Biotechnology & Life Sciences Industry ten years in a row by the Dow Jones Sustainability Indices (DJSI).








