CQV Engineer

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 a motivated Junior CQV Engineer to support Commissioning, Qualification, and Validation (CQV) activities for a fast-paced GMP manufacturing project involving the installation and qualification of new process, laboratory, and utility equipment. The Junior CQV Engineer will work alongside senior CQV professionals to ensure equipment and systems are qualified and ready for GMP operation in compliance with regulatory and company requirements.

This is an excellent opportunity for an early-career engineer looking to gain hands-on experience in pharmaceutical commissioning, qualification, validation, and startup activities.

• Support execution of commissioning, qualification, and validation activities for GMP equipment, utilities, and facility systems.
• Assist in development and execution of Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols.
• Participate in walkdowns, system inspections, and turnover activities.
• Review engineering documentation including P&IDs, equipment specifications, SOPs, and User Requirements Specifications (URS).
• Execute field verification testing and document results in accordance with GDP requirements.
• Support commissioning activities including FAT/SAT review and startup testing.
• Assist with generation and resolution of deviations, discrepancies, and punch list items.
• Maintain validation documentation and support preparation of final reports and turnover packages.
• Collaborate with Engineering, Quality, Operations, Manufacturing, and Vendor teams to support project milestones.
• Ensure all activities are performed in accordance with GMP, FDA, and site safety requirements.

• Bachelor's degree in Chemical Engineering, Mechanical Engineering, Biomedical Engineering, Biotechnology, or related technical discipline.
• 0–3 years of experience in pharmaceutical, biotechnology, medical device, or regulated manufacturing environments.
• Understanding of GMP/cGMP principles and validation concepts.
• Strong technical writing and documentation skills.
• Proficiency in Microsoft Office Suite.
• Strong communication and problem-solving skills.
• Ability to work onsite in a fast-paced project environment.
• Ability to provide legal U.S. work authorization documents required; will consider U.S. domestic travelers and relocation.

• Medical, dental, and vision coverage.
• EAP.
• 401K.
• STD, LTD, AD&D, life insurance.
• Paid parental leave.
• Reward & recognition program.
• Optional wellbeing benefits, adoption assistance, and tuition reimbursement.
• Nine paid holidays and 15 days PTO accruing per year.

Arcadis is 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, veteran status, or any other basis prohibited by law.