Automation Validation Engineer

Arcadis; Bedford (MA); On-site; USD 80,000 - 200,000; Full time

Job summary

Join a forward-thinking company dedicated to sustainable design and engineering solutions. As an Automation CQV Engineer, you will play a crucial role in pharmaceutical manufacturing, focusing on DeltaV-based control systems and automated processes. This position offers a unique opportunity to collaborate with cross-functional teams, ensuring compliance with GMP standards while delivering impactful solutions. With a commitment to diversity and inclusion, this role not only empowers you to excel in your career but also contributes to a legacy of sustainable practices. Embrace the chance to make a difference in a dynamic environment where your skills will shine.

Benefits

Medical Insurance

Dental Insurance

Vision Insurance

401K

Paid Parental Leave

Tuition Reimbursement

15 days PTO

EAP

Reward & Recognition Program

Wellbeing Benefits

Qualifications

• 5-7 years of experience in automation engineering with DeltaV systems.
• Strong hands-on experience with filling and packaging systems in biopharma.

Responsibilities

• Design and troubleshoot DeltaV DCS and automated systems.
• Execute CQV protocols for automated filling and packaging systems.

Skills

Automation Engineering

Problem-Solving

Communication Skills

Attention to Detail

Knowledge of GMP Compliance

Education

Bachelor’s degree in Science, Engineering, or a related technical field

Tools

DeltaV Distributed Control Systems (DCS)

Job description

This range is provided by Arcadis. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$80,000.00/yr - $200,000.00/yr

Talent Acquisition Specialist at Arcadis DPS Group Global

About The Job

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.

Arcadis is seeking an experienced Automation CQV Engineer to join our team in the Boston area. The ideal candidate will be responsible for the Commissioning, Qualification, and Validation (CQV) of automated systems in pharmaceutical manufacturing, with a primary focus on DeltaV-based control systems and automated filling and packaging equipment. This position requires a hands-on, onsite presence to ensure successful project execution and compliance with Good Manufacturing Practices (GMP) standards.

Responsibilities

1. Design, configuration, testing, and troubleshooting of DeltaV Distributed Control Systems (DCS) and associated automated systems.
2. Execute CQV protocols (IQ, OQ, PQ) for automated filling and packaging systems in alignment with regulatory requirements.
3. Collaborate effectively with cross-functional teams (Engineering, QA, Manufacturing) to support system integration, upgrades, and continuous improvements.
4. Develop and maintain detailed technical documentation, including Standard Operating Procedures (SOPs), User Requirements Specifications (URS), Functional Specifications (FS), and Validation Protocols.
5. Provide ongoing system support, troubleshooting, and optimization to ensure the reliability and performance of automated systems in a production environment.
6. Other duties as assigned.

Qualifications & Experience:

• 5-7 years of experience in automation engineering, specifically with DeltaV systems and CQV activities for automated equipment in a regulated environment.
• Knowledge for EMPQ/smoke visualization is a plus but not required.
• Strong hands-on experience with filling and packaging systems used in biopharma or pharmaceutical manufacturing.
• Bachelor’s degree in Science, Engineering, or a related technical field.
• In-depth knowledge of pharmaceutical manufacturing practices, particularly GMP compliance.
• Excellent communication skills, with the ability to collaborate across teams and document technical information clearly.
• Strong problem-solving abilities and attention to detail.
• Ability to provide legal US work authorization documents required. Will consider US domestic travelers and relocation.

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.

Seniority level

Mid-Senior level

Employment type

Full-time

Job function

Pharmaceutical Manufacturing