Validation Engineer Salary at Motional BETA

Hi Network, One of our clients, a leading Biotech company, is seeking a Quality Validation Engineer with 5–10 years of experience in Medical Devices & Pharmaceutical Drug (Drug-Device Combo, APIs). This is a part-time (20 hours/week) contract-to-FTE opportunity, requiring on-site work (3 days/week) in Cambridge. Key Responsibilities: Oversee late-stage validation for a Class III medical device in a startup environment. Work independently and collaborate with a CDMO manufacturer. Ensure compliance with regulatory standards for drug-device combination products. Utilize science/engineering expertise to support quality assurance efforts. Position starts early May—must be local to Cambridge. Thanks.

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. Role description: Arcadis is seeking a Validation Engineer to join our team and play a critical role in ensuring compliance with industry standards and regulatory requirements for our products and processes. The ideal candidate will have expertise in validation processes and protocols, particularly in the pharmaceutical or biotech industry with a focus on sterilization, environmental monitoring, and utility systems. Role accountabilities: Autoclave Cycle Development and Performance Qualification (PQ): Develop and optimize autoclave sterilization cycles to ensure product steril

Overview: We are excited to share once again TranSystems has been recognized as a top 100 design firm by Engineering News-Record in 2024. TranSystems is committed to building strong relationships with our clients, partners, and communities, because we believe we can go farther together. We act with integrity, use resources wisely, and proactively enhance projects with new thinking for sustainable infrastructure solutions. Our team incorporates these core values every day: All-In Always - Passionate Problem Solvers - Driven to Serve. Interested in joining our team? Great! Were looking for top talent to grow with our firm. Responsibilities: What you'll be challenged to do: TranSystems Boston Massachusetts office has an opening for an Entry Level Bridge Engineer. This position is open to entry level engineers. This position includes structural design, rehabilitation, and inspection of bridges and tunnels along with the preparation of load ratings, construction documents, specifications, a

Required Skills: Validation Engineer Manufacturing Engineer with Packaging, Cleanroom, Equipment machine validation experience Good communication skill Good experience in validations (IQ/OQ/PQ) 5+ years of Working Experience machine shop environment Good communication skill Machining background Has worked in a Packaging, Cleanroom, Equipment machine shop environment (within med device or aerospace preferred) Product / Manufacturing Transfer activities Good experience validations (IQ/OQ/PQ) Understanding of different types of metal/plastic cutting manufacturing processes Basic understanding of Packaging, clean room, milling and or lathe machines Understanding of basic Quality systems

Responsibilities: Authoring and/or reviewing of SOP's (both new and existing). Authoring and/or reviewing Equipment Requirements Specifications. Document calibration and maintenance requirements, generate procedures. Supporting Equipment Management Program. Schedule and work with suppliers to perform service, installation, calibration, maintenance activities for facility, utilities, and equipment. Troubleshoot manufacturing issues to identify root causes and implement corrective actions. Initiate and/or execute Equipment Impact Assessments on failures. Collaborate with cross-functional teams to drive continuous improvement efforts. Communicates technical information within the team. Primarily hands-on workers. Requirements: Authoring and/or supporting efforts on any On the Job Training. Execute Equipment Qualification Protocols. Perform investigations and support CAPAs as needed. Ensure proper documentation is completed to meet quality system requirements. Ensure compliance with all ap

**Working with Us** Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us . **Position:** Manager, Cleaning Validation, Validation Engineer

Project Farma (PF) is the leading advanced therapy technical operations consulting company in the life science industry. We provide biomanufacturing strategy and execution to start up and established gene and cell therapy, pharmaceutical, and biotechnology companies. We are an industry leader in providing project management, validation, engineering, quality/compliance, and consulting services to support our partners in finding ground-breaking treatments and solutions. We are committed to advancing manufacturing to achieve operational excellence and accelerate speed to market for next-generation medicines. Our culture of philanthropy, teamwork, training and development and commitment is the foundation to our teams' and partners' long-term success. Project Farma is a wholly owned subsidiary of Precision Medicine Group, LLC, a leading global life sciences company with over 2,000 employees. Position Summary: The Project Engineer will work collaboratively with partners, vendors, contractors

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. Role description: Arcadis is seeking a CQV Engineer who is responsible for executing and managing QC lab analytical equipment activities to meet cGMP requirements. He/She will initiate equipment validation protocol development, including drafting documents, managing review cycles, and protocol approval. Role accountabilities: Become familiar with the user, functional, installation, operation and performance requirements for assigned projects and tasks. Review requirements and source documentation P&IDs, RDs, URSs, SOPs, Specifications), for use in development of equipment comm