• Lead the EU CMC strategy for multiple clinical programs • Translate technical changes into regulatory robust strategies • Develop solutions for comparability, specifications and process changes • Identify regulatory risks early and define pragmatic mitigation measures • Lead CMC activities for clinical trial applications and amendments • Prepare structured, high-quality submission documentation • Design strategies for communications with regulatory authorities • Prepare for and support interactions with EU authorities • Ensure regulatory compliance of external manufacturing partners • Work closely with Quality and technical functions • Actively monitor regulatory developments in the CMC space • Contribute to the advancement of regulatory standards within the company

Join Us in Elevating Clinical Excellence: Assessment Specialist  At our organization, we believe that meaningful clinical work starts with precision, collaboration, and a deep commitment to quality care. We are building a team of dedicated professionals who value integrity, thoughtful assessment, and doing things the right way. If you bring both clinical rigor and genuine care to your work, this is your opportunity to make a lasting impact. About the Role This is a full-time, salaried position focused on supporting and conducting high-quality clinical assessments while contributing to strong foundational care for clients. You will play a key role in shaping treatment direction through detailed assessment work, collaboration, and clinical insight. Schedule: Monday through Friday during regular business hours Work Expectation: 40-hour work week Roles and Responsibilities As an Assessment Specialist, you will: Maintain a consistent 40-hour work week Assist in developing individualized treatment plans and clinical goals Support timely and accurate submission of clinical documentation Collaborate with clinical staff to ensure high-quality assessment practices Maintain accurate assessment records and ensure compliance with all internal and external standards Take on additional responsibilities as needed based on business needs This role is designed for someone who values structure, accuracy, and collaboration, and who understands that strong assessments are the foundation of effective care.

• Create high-quality content that enables medical device innovators to understand the QMS and audit requirements of EU MDR, UK MDR, MDSAP, 510(k), ISO 13485 and others. • Design education-grade materials, including slides, diagrams, lesson plans, and voiceover scripts. • Lead structured dialogues clarifying core concepts and aligning medical device innovators on what “good” looks like. • Work closely with auditors to ensure published material reflects a consistent, aligned regulatory view.

In a world of possibilities, pursue one with endless opportunities. Imagine Next! At Parsons, you can imagine a career where you thrive, work with exceptional people, and be yourself. Guided by our leadership vision of valuing people, embracing agility, and fostering growth, we cultivate an innovative culture that empowers you to achieve your full potential. Unleash your talent and redefine what’s possible. Job Description: Parsons is looking for an amazingly talented Environmental Specialist to join our team! In this role you will join an environmental team providing support on the TSSC contract for the FAA. What You'll Be Doing: - Determine level of NEPA review and environmental permitting for each governmental action. - Prepare all necessary NEPA documentation for all proposed government actions - Conduct environmental analysis and assess environmental impacts of all projects - Coordinate and consult with relevant federal, state, and local agencies - Advise on matters related to compliance with environmental regulations What Required Skills You'll Bring: - 3+ years of related work experience - Bachelor's Degree in Environmental Engineering, Environmental Sciences, Planning or related field. - Experience in producing NEPA-related documentation What Desired Skills You'll Bring: - Familiarity with environmental standards, procedures, and approval processes. - Excellent writing and oral communication skills - Knowledge and experience with NEPA/environmental support for federal facilities and related infrastructure Security Clearance Requirement: None This position is part of our Federal Solutions team. The Federal Solutions segment delivers resources to our US government customers that ensure the success of missions around the globe. Our intelligent employees drive the state of the art as they provide services and solutions in the areas of defense, security, intelligence, infrastructure, and environmental. We promote a culture of excellence and close-knit teams that take pride in delivering, protecting, and sustaining our nation's most critical assets, from Earth to cyberspace. Throughout the company, our people are anticipating what’s next to deliver the solutions our customers need now. We value our employees and want our employees to take care of their overall wellbeing, which is why we offer best-in-class benefits such as medical, dental, vision, paid time off, 401(k), life insurance, flexible work schedules, and holidays to fit your busy lifestyle! This position will be posted for a minimum of 3 days and will continue to be posted for an average of 30 days until a qualified applicant is selected or the position has been cancelled. Parsons is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, veteran status or any other protected status. We truly invest and care about our employee’s wellbeing and provide endless growth opportunities as the sky is the limit, so aim for the stars! Imagine next and join the Parsons quest—APPLY TODAY! Parsons is aware of fraudulent recruitment practices. To learn more about recruitment fraud and how to report it, please refer to https://www.parsons.com/fraudulent-recruitment/.