Arcadis
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.
About the Role Arcadis is seeking a talented
Plant Project Engineer
with a strong background in pharmaceutical/biotech facility design, engineering, and project management. The ideal candidate will play a pivotal role in the design, implementation, and optimization of plant processes and equipment in Boston, MA. This role requires a deep understanding of pharmaceutical manufacturing environments, GMP (Good Manufacturing Practices), and the ability to lead cross‑functional teams to deliver engineering solutions that meet operational, compliance, and business needs.
Key Responsibilities Project Management & Execution
Plan, coordinate, and execute engineering projects related to pharmaceutical or biotech plant operations.
Manage timelines, budgets, and resources to ensure successful project delivery.
Interface with stakeholders, vendors, and contractors to align designs with technical and operational requirements.
Lead the design and layout of plant systems, utilities, and manufacturing areas (e.g., cleanrooms, process suites).
Oversee the selection, specification, and installation of plant equipment, ensuring compliance with industry standards.
Collaborate with cross‑functional teams to ensure seamless integration of systems and equipment into operations.
Engineering & Technical Expertise
Provide expertise in plant utilities (e.g., HVAC, WFI, CIP/SIP systems) and process equipment.
Develop and review engineering drawings (P&IDs, equipment layouts, etc.) and documentation.
Identify opportunities for process improvements, energy efficiency, and cost savings.
Compliance & Validation
Ensure compliance with GMP, FDA, OSHA, and other applicable regulatory standards.
Support validation activities, including commissioning, qualification, and documentation of systems and equipment.
Address and resolve technical issues related to plant systems during design, construction, and operation.
Act as a liaison between the engineering team, operations, and quality departments.
Provide mentorship and technical guidance to junior engineers and technicians.
Required Qualifications
Education:
Bachelor’s degree in Mechanical, Chemical, Electrical, or Industrial Engineering (or related field).
Experience:
5+ years of experience in pharmaceutical/biotech plant engineering or project management.
Strong background in facility and process design, including cleanroom environments.
Technical Skills:
Proficient in CAD software (e.g., AutoCAD) and engineering tools.
Familiarity with plant utilities (e.g., HVAC, compressed air, purified water systems).
Knowledge of cGMP, FDA, and EMA regulations.
Soft Skills:
Excellent communication, problem‑solving, and organizational skills.
Preferred Qualifications
Professional Engineer (PE) license or PMP certification.
Experience with advanced technologies like single‑use systems, continuous manufacturing, or automation in pharma/biotech processes.
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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.
About the Role Arcadis is seeking a talented
Plant Project Engineer
with a strong background in pharmaceutical/biotech facility design, engineering, and project management. The ideal candidate will play a pivotal role in the design, implementation, and optimization of plant processes and equipment in Boston, MA. This role requires a deep understanding of pharmaceutical manufacturing environments, GMP (Good Manufacturing Practices), and the ability to lead cross‑functional teams to deliver engineering solutions that meet operational, compliance, and business needs.
Key Responsibilities Project Management & Execution
Plan, coordinate, and execute engineering projects related to pharmaceutical or biotech plant operations.
Manage timelines, budgets, and resources to ensure successful project delivery.
Interface with stakeholders, vendors, and contractors to align designs with technical and operational requirements.
Lead the design and layout of plant systems, utilities, and manufacturing areas (e.g., cleanrooms, process suites).
Oversee the selection, specification, and installation of plant equipment, ensuring compliance with industry standards.
Collaborate with cross‑functional teams to ensure seamless integration of systems and equipment into operations.
Engineering & Technical Expertise
Provide expertise in plant utilities (e.g., HVAC, WFI, CIP/SIP systems) and process equipment.
Develop and review engineering drawings (P&IDs, equipment layouts, etc.) and documentation.
Identify opportunities for process improvements, energy efficiency, and cost savings.
Compliance & Validation
Ensure compliance with GMP, FDA, OSHA, and other applicable regulatory standards.
Support validation activities, including commissioning, qualification, and documentation of systems and equipment.
Address and resolve technical issues related to plant systems during design, construction, and operation.
Act as a liaison between the engineering team, operations, and quality departments.
Provide mentorship and technical guidance to junior engineers and technicians.
Required Qualifications
Education:
Bachelor’s degree in Mechanical, Chemical, Electrical, or Industrial Engineering (or related field).
Experience:
5+ years of experience in pharmaceutical/biotech plant engineering or project management.
Strong background in facility and process design, including cleanroom environments.
Technical Skills:
Proficient in CAD software (e.g., AutoCAD) and engineering tools.
Familiarity with plant utilities (e.g., HVAC, compressed air, purified water systems).
Knowledge of cGMP, FDA, and EMA regulations.
Soft Skills:
Excellent communication, problem‑solving, and organizational skills.
Preferred Qualifications
Professional Engineer (PE) license or PMP certification.
Experience with advanced technologies like single‑use systems, continuous manufacturing, or automation in pharma/biotech processes.
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