Who You’ll Work With
You will join one of our 45 offices in the US, be part of a committed team of over 1500 professionals, and work in teams and directly with our clients doing work that is shaping the world around us. You will be welcomed into a rapidly growing business and team and empowered to make an impact. You will be valued, cared for, and challenged on your path to becoming a world-class professional consultant and surrounded by leaders who are committed to creating an environment that enables you to realize your own success and fulfillment.
When you join Design Group as an Entry-Level Validation Engineer, you are joining a team that will challenge you and position you for growth. In this role, you will work with a team of industry experts to help the world’s leading companies solve their most difficult problems. You will join our Regulatory Compliance Practice and partner with seasoned leaders, technical specialists, and subject matter experts to deliver the highest quality solutions to our clients with consistency and accuracy.
What You’ll Do
You’ll work individually and in teams to support capital projects and implement solutions for our clients. Together, you will help our clients make critical changes to improve their performance and realize their most important goals.
- Develop and execute a variety of validation and FDA compliance related documents/protocols for pharmaceutical equipment
- Assist in the design of manufacturing processes, help manage projects, and develop facilities
- Conduct yourself with integrity in pursuit of individual and business goals
- Become a passionate and successful business family member
- Handle FAT, SAT, IQ and OQ documentation development and execute on automated systems projects
- Assist in the development and execution of QMS procedures, ICH Q1 (stability protocols/reports), CFR 21 Part 211, CFR 21 Part 820, ICH Q8, ICH Q9, and ICH Q10
- Conduct investigations and troubleshoot issues related to validation
- Prepare written validation reports
- Make an impact day-to-day with your skills and expertise, strengthening that relationship with our clients and team
What You’ll Bring
- Solid interpersonal skills and the ability to interact with management, clients, and vendors
- Strong technical writing and oral communication skills
- Proficiency in Microsoft Office, Microsoft Project, and AutoCAD
- Co-op or project experience with validation of automation, packaging, utilities, or facilities (preferred)
- Co-op or project experience in the pharmaceutical or medical device environments (preferred)
- A willingness to travel for project requirements including installation and start-up activities, client and company sponsored meetings, trainings, industry related seminars, forums, and conventions
- A bachelor of science in bioengineering, biomedical engineering, chemical engineering, or a related technical degree
Our culture and commitment to our people is what sets us apart. We foster an environment of mutual respect, integrity, and unconditional interest in the individual and collective success of our professionals. Our model and entrepreneurial mindset offer a rewarding, challenging, and highly flexible path. As a Entry Level Controls Engineer, you will build a meaningful and fulfilling career with the support of professional development resources and mentorships including our First Year Experience program, Individual Development Plans, and Career Path resources and tools. You will be surrounded by exceptional talent who will support your development as both a world-class engineer and a highly effective leader.
Feel like you’re on the path to becoming an Entry Level Validation Engineer but you’re not quite there yet? We’d love to connect with you to see if we can take you from where you are today and grow you into a BW Design Group Engineering Consultant.
