Process Engineer

DPS Group Global; Boston (MA); Presencial; USD 90.000 - 130.000; Jornada completa

Descripción de la vacante

Arcadis is seeking experienced Process Engineers to support pharmaceutical manufacturing operations in a GMP environment. The role covers upstream, downstream, and utility systems with emphasis on troubleshooting and continuous improvement.

Ideal candidates will review P&IDs, SOPs, specs and drawings; collaborate across Manufacturing, Engineering, Quality, Validation, and Automation; and assist with startup, qualification and readiness activities as needed.

Formación

• Bachelor’s degree in Chemical Engineering, Biochemical Engineering, Mechanical Engineering, or related discipline preferred.
• Experience in pharmaceutical/biotech/biologics or GMP‑regulated manufacturing.
• Strong knowledge of process equipment and/or utility systems.
• Experience with P&IDs, SOPs, specifications, protocols, and engineering drawings.
• Strong troubleshooting, communication, and cross‑functional collaboration skills.

Responsabilidades

• Provide process engineering support for upstream, downstream, and/or utility systems.
• Support manufacturing equipment and process troubleshooting, optimization, and continuous improvement.
• Review and support P&IDs, process flow diagrams, equipment specifications, and technical documentation.
• Work cross‑functionally with Manufacturing, Engineering, Quality, Validation/CQV, Automation, and Maintenance teams.
• Support equipment/system startup, commissioning, qualification, and operational readiness activities as needed.
• Assist with investigation and resolution of process or equipment‑related issues.
• Ensure engineering activities are completed in accordance with GMP requirements and site procedures.

Conocimientos

Process engineering

GMP knowledge

Troubleshooting

Cross-functional collaboration

Educación

Bachelor’s degree in Chemical Engineering or related

Herramientas

P&IDs

SOPs / specifications / engineering drawings

Descripción del empleo

Arcadis is the world's leading company delivering sustainable design, engineering, and consultancy solutions for natural and built assets.

We are more than 36,000 people, in over 70 countries, dedicated to improving quality of life. Everyone has an important role to play. With the power of many curious minds, together we can solve the world’s most complex challenges and deliver more impact together.

We are seeking experienced Process Engineers to support pharmaceutical/biopharmaceutical manufacturing operations. The ideal candidates will have hands‑on engineering experience supporting upstream processing, downstream processing, and/or process/clean utilities within a regulated GMP environment.

• Provide process engineering support for upstream, downstream, and/or utility systems.
• Support manufacturing equipment and process troubleshooting, optimization, and continuous improvement.
• Review and support P&IDs, process flow diagrams, equipment specifications, and technical documentation.
• Work cross‑functionally with Manufacturing, Engineering, Quality, Validation/CQV, Automation, and Maintenance teams.
• Support equipment/system startup, commissioning, qualification, and operational readiness activities as needed.
• Assist with investigation and resolution of process or equipment‑related issues.
• Ensure engineering activities are completed in accordance with GMP requirements and site procedures.

Preferred Experience:

Experience with one or more of the following biopharmaceutical manufacturing systems and processes:

• Upstream: Bioreactors/fermenters, cell culture or microbial processes, media preparation, seed expansion/inoculation, and harvest systems
• Downstream: Chromatography, TFF/UFDF, filtration, purification processes, and buffer preparation
• Utilities: WFI/purified water, clean steam, process gases, HVAC, and clean/process utility systems

Qualifications & Experience:

• Bachelor’s degree in Chemical Engineering, Biochemical Engineering, Mechanical Engineering, or related discipline preferred.
• Previous engineering experience within pharmaceutical, biotechnology, biologics, or other GMP‑regulated manufacturing.
• Strong knowledge of process equipment and/or utility systems.
• Experience working with technical documentation such as P&IDs, SOPs, specifications, protocols, and engineering drawings.
• Strong troubleshooting, communication, and cross‑functional collaboration skills.

Why Arcadis?

We can only achieve our goals when everyone is empowered to be their best. We believe everyone's contribution matters. It’s why we are pioneering a skills‑based approach, where you can harness your unique experience and expertise to carve your career path and maximize the impact we can make together.

You’ll do meaningful work, and no matter what role, you’ll be helping to deliver sustainable solutions for a more prosperous planet. Make your mark, on your career, your colleagues, your clients, your life and the world around you.

Together, we can create a lasting legacy.

Join Arcadis. Create a Legacy.

Our Commitment to Equality, Diversity, Inclusion & Belonging

We want you to be able to bring your best self to work every day which is why we take equality and inclusion seriously and hold ourselves to account for our actions. Our ambition is to be an employer of choice and provide a great place to work for all our people. We are an equal opportunity and affirmative action employer. Women, minorities, people with disabilities and veterans are strongly encouraged to apply. We are dedicated to a policy of non‑discrimination in employment on any basis including race, creed, color, religion, national origin, sex, age, disability, marital status, sexual orientation, gender identity, citizenship status, disability, veteran status, or any other basis prohibited by law.

Arcadis offers benefits for full time and part time positions. These benefits include medical, dental, and vision, EAP, 401K, STD, LTD, AD&D, life insurance, paid parental leave, reward & recognition program and optional benefits including wellbeing benefits, adoption assistance and tuition reimbursement. We offer nine paid holidays and 15 days PTO that accrue per year. Salaries will vary and are based on several factors, such as experience, education, budget, internal equity, project and location.