Role Description Responsible for leading teams to deliver project(s) that span across one or more business units. Proficient in coordination, scheduling and delivery of internally initiated improvements and product-driven initiatives, and to proactively identify areas of risk related to scope, resource constraints, and process breakdowns. Identify complex data source and independently extract to build own analysis methodologies. SME to ensure project entrance and exit criteria are being met, to drive the prioritization of projects, and to ensure that resources are being utilized efficiently. Ability to make advanced/complex level decisions and actions. Ability to develop systemic solutions that can be implemented and developed into framework guidelines for other team members. Main Responsibilities - Successfully execute project scope and ensures program milestones and objectives are met. - Able to articulate a persuasive argument for a business decision through financial acumen within departmental boundaries. - Able to escalate work at a team activity level on behalf of your own projects as well as the collective projects of your team. - Manage the development and implementation process of a company's products and services. - Interpret market requirements and converts to engineering and program deliverables. - Organizes cross-functional activities, ensuring completion of the project i.e. product on schedule and within budget constraints. - Plan and manage company resources to execute development project or project components from design phase through implementation. - Reporting and metrics from multiple order entry, workflow and inventory systems as well as support data marts/databases. - Use specific knowledge about one or more technical areas to research, plan, communicate and achieve objectives through program/project team. Qualifications - Project Management Professional (PMP) certification preferred. - 5 plus years technical project management experience. - Proficient with Microsoft Office Suite (Excel, Word, Power Point). - Experienced in analyzing complex issues, distilling and communicating their relevant aspects. - Able to mentor peers on priorities within the team and across functional areas. - Able to draw conclusions from research and analysis and determine next steps and course of action. - Understands interdependencies between technology, operations and business needs. Requirements - Bachelor's Degree. - PMP Certification in process. Preferred Education, Skills and Experience - Experience: 5+ yrs. - Education Level: Bachelor's Degree and PMP certification preferred. - Field Of Study: Engineering, Production or other relative field. - Attention to detail with good analytical and organizational capabilities. - Ability to prioritize with good scope, time and cost management skills. Compensation This information reflects the anticipated base salary range for this position based on current national data. Minimums and maximums may vary based on location. Individual pay is based on skills, experience and other relevant factors. - $84,629 - $112,838 in these states: AL, AR, AZ, FL, GA, IA, ID, IN, KS, KY, LA, ME, MO, MS, MT, ND, NE, NM, OH, OK, PA, SC, SD, TN, UT, VT, WI, WV, WY. - $88,860 - $118,480 in these states: CO, HI, MI, MN, NC, NH, NV, OR, RI. - $93,092 - $124,122 in these states: AK, CA, CT, DC, DE, IL, MA, MD, NJ, NY, TX, VA, WA. Benefits Lumen offers a comprehensive package featuring a broad range of Health, Life, Voluntary Lifestyle benefits and other perks that enhance your physical, mental, emotional and financial wellbeing. Life at Lumen Life at Lumen is human and connected, even in a fast moving, AI‑focused organization. We set clear expectations and trust people to meet them. With real support and shared accountability, teams collaborate better, move faster, and deliver meaningful outcomes. Equal Employment Opportunities We are committed to providing equal employment opportunities to all persons regardless of race, color, ancestry, citizenship, national origin, religion, veteran status, disability, genetic characteristic or information, age, gender, sexual orientation, gender identity, gender expression, marital status, family status, pregnancy, or other legally protected status (collectively, “protected statuses”). We do not tolerate unlawful discrimination in any employment decisions, including recruiting, hiring, compensation, promotion, benefits, discipline, termination, job assignments or training.

• Lead multidisciplinary teams through all phases of environmental projects • Serve as the primary client liaison and oversee contract compliance • Manage project planning, execution, schedules, budgets, and financial performance • Provide technical leadership and mentorship • Prepare and review technical quality assurance for federal environmental deliverables • Contribute to proposal development • Collaborate with safety and quality personnel for compliance

Role Description NOTE TO CANDIDATES - This is a 100% remote opportunity. Our Livonia, MI laboratory is looking for a Senior Project Manager to join their Client Services team specifically focusing on our Federal Programs! A Senior Project Manager is a key member of the Client Services Team, serving as a client advocate and laboratory liaison. This role is responsible for managing a significant portfolio of primarily premier clients and clients with complex needs and technical requirements. The Sr. Project Manager is expected to build strong working relationships with our clients and technical staff. The Sr. Project Manager is deeply involved with project management process refinement and training within the team. This role is responsible for guiding successful, on-time completion of the clients' project beginning with the first contact through the lab to the final deliverables and invoicing. The Sr. Project Manager manages a dedicated portfolio of high profile clients with high annual analytical spend. The Sr. Project Manager will work within a functional group consisting of a Project Manager Assistant and Project Managers. The Sr. Project Manager is expected to become familiar with the complexities of their own projects and the ongoing work within their group. The Sr. Project Manager will also be responsible for training the PM I and/or PM II on high-level, technical aspects of project management and environmental regulatory requirements, as well as training and delegating tasks to the Project Manager Assistants. Job functions: - Acts as the main point of contact/client services representative for a dedicated list of high profile clients with high annual analytical spend. - Aids the client with all aspects of project setup, including the initial quote, supply order, sample receipt, data reporting, and invoicing. - Responsible for training the PM I and/or PM II on high-level, technical aspects of project management and environmental regulatory requirements, and delegating tasks to the Project Manager Assistants. - Fosters collaborative relationships with the client, laboratory operations, and sales team to support long term, successful relationships between all parties. - Staff meetings and client meetings are critical to relay information about past, current, and upcoming projects. - Acts as the client liaison to the laboratory to ensure all aspects of the project are carried out in the best interest of the client and laboratory operations to meet TAT deadline. - Responsible for keeping all accounts project managed and up to date and accurate. - Monitors project status and provides regular updates through proactive communication to the client, lab operations, and sales team related to project status. - Understands all applicable aspects of the client project, including rationale for the project, regulations that affect the project, and the different methods employed by the client and laboratory to produce results. - Documents and executes client requests including bottle orders, tracking samples, LIMS login, change orders, etc. - Reviews project data and invoicing for accuracy and completeness before sending final reports to the client. - Participates in offsite and/or virtual client meetings as coordinated with the Sales team. - Promotes a positive working atmosphere and represents SGS in a positive manner inside and outside of the laboratory. - Performs other duties as assigned to ensure that SGS can fulfill its mission of quality, service, and growth. - Establishes and sets up laboratory protocols for the execution of complex or atypical analytical and reporting requirements. Qualifications - Associates' degree or equivalent industry experience (Required) - Minimum of 5 years experience as a Project Manager (Required) - Experience with High Volume Clients or Complex PM work (Required) - Bachelor’s degree in Environmental Science, Biology, Chemistry, or a related field (Preferred) - 3+ years of experience as a Client Project Manager II (Preferred) - Advanced oral and written communications skills (Required) - Self-initiative and Resource Utilization (Required) - Advanced English language, reasoning, and mathematical skills (Required) - Advanced computer skills (Required) - Excellent attention to detail (Required) - Solid critical thinking skills to anticipate and solve problems in a systematic manner (Required) - Ability to manage and coordinate multiple projects in a fast-paced, highly professional environment (Required) Company Description SGS is the world's leading Testing, Inspection and Certification company. We operate a network of over 2,700 laboratories and business facilities across 119 countries, supported by a team of 99,250 dedicated professionals. With over 145 years of service excellence, we combine the precision and accuracy that define Swiss companies to help organizations achieve the highest standards of quality, safety and compliance. Our brand promise, when you need to be sure, underscores our commitment to reliability, integrity and trust — enabling businesses to thrive with confidence. We proudly deliver our expert services through the SGS name and trusted specialized brands, including Brightsight, Bluesign, Maine Pointe and Nutrasource. SGS is publicly traded on the SIX Swiss Exchange under the ticker symbol SGSN (ISIN CH0002497458, Reuters SGSN.S, Bloomberg SGSN:SW).

Role Description The Clinical Affairs Project Manager has the responsibility of planning, organizing and executing the GLP preclinical and early clinical studies with Robeauté’s robotic brain biopsy and local drug delivery device, including support of regulatory submissions for clinical studies across geographies, IDE submission to the FDA, reporting to Head of Clinical. - Plan and coordinate the preclinical and clinical studies together with the Head of Clinical and surgeon collaborators. - Preclinical and clinical study design (including GLP animal studies and animal model exploration). - Writing preclinical and clinical protocols. - Preparing documentation for submission to local Ethics Committees, competent authorities in various geographies including to the US FDA (IDE). - Clinical study site contracting. - CRO selection and contracting, including management of both GLP preclinical studies and clinical studies. - Communication and collaboration with surgeon KOLs on study design, protocols and their execution. - Data collection and data management after testing. - Writing of detailed reports after preclinical or clinical use based on the data collected. - Planning and participation in conferences, medical scientific communication and publication support. In parallel, the Clinical Affairs Project Manager is expected to gain detailed knowledge of the clinical applications of Robeauté’s device and connect with and curate surgeon relationships with the goal of growing the surgeon community with mutual respect. The Clinical Affairs Project Manager will collaborate with the technical team that designs hardware and software by giving feedback after any device use in a preclinical or clinical context, on the robot’s performance and in order to develop the platform’s performance with an eye for the global development of the platform. Furthermore, the Clinical Affairs Project Manager will collaborate with Head of Clinical on Medical Affairs management, the representation of Robeauté’s platform at conferences, the creation of a publication pipeline and the medical scientific value communication within the surgeon community. This role is open to candidates based in EMEA locations. Qualifications - MD, Master’s or Ph.D. in a Life Sciences field, Biomedical Engineering and/or M.Eng. and equivalent work experience in relevant areas. - At least 5 years experience in preparation and execution of clinical trials with medical devices, including preclinical (GLP) and/or regulatory submissions (IDE preferred) and subsequent study execution. - Device test experience in lab and clinical environments. - Good written, communication and documentation skills in English required and French preferred. Requirements - Good knowledge of anatomy and physiology and ability to relate to surgeons and the surgeon community. - Ability to communicate Robeauté's product and mission to the surgeon community. - Good ability and predisposition for teamwork as well as ability to work independently. - Strong interdisciplinary understanding of robotics, electronics and control.