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We are on the lookout for a dedicated and enthusiastic Validation Engineer to contribute to our validation efforts in regulated sectors such as Pharmaceuticals, Biotechnology, Medical Devices, Chemicals, and Food Manufacturing. The Validation Engineer's primary role will be to ensure that our equipment, systems, and processes comply with regulatory standards, thereby safeguarding product quality and patient safety.Key Responsibilities:Design, develop, and implement validation protocols (IQ, OQ, PQ) for machinery, utilities, facilities, and production systems.Facilitate the validation of laboratory instruments, manufacturing equipment, cleaning procedures, and computerized systems.Ensure adherence to cGMP, FDA, EMA, and other relevant regulatory guidelines.Prepare and evaluate validation documentation, including protocols, reports, SOPs, and risk assessments.Conduct troubleshooting and root cause analysis for any validation or equipment-related discrepancies.Collaborate with multidisciplinary teams (Engineering, Quality, Manufacturing, Laboratory) to achieve project goals.Engage in change control, CAPA, and continuous improvement projects.Maintain precise records and ensure that documentation remains audit-ready at all times.

Validation EngineerLocation: Raleigh, NCFounded in 2014 in Denmark, Eupry Aps is revolutionizing the validation, monitoring, and documentation processes within the life sciences sector by offering innovative solutions for temperature and humidity control. Over the years, we have forged strong partnerships with global leaders such as FedEx, DHL, DSV, AstraZeneca, Novo Nordisk, and AbbVie.As a frontrunner in cold chain mapping and monitoring, Eupry provides some of the most advanced and reliable solutions available today. We go beyond traditional validation by offering state-of-the-art temperature mapping services for various environments, including warehouses, transport, and production. We are also proud to be the first company globally to deliver continuous temperature mapping for aircraft.With a rapidly expanding presence in the United States, our dedicated office in Raleigh, North Carolina, accommodates approximately 20 employees. Internationally, we are approaching a workforce of 100 as we continue to grow to meet increasing demand.Our unique Compliance as a Service model replaces outdated systems with a fully digital, IoT-driven approach, simplifying audits, eliminating manual tasks, and ensuring ongoing compliance across storage and transportation processes. To learn more, visit Eupry.com.About the RoleAs a Validation Engineer, you will play a crucial role in our Validation team in the U.S., leading various validation and qualification projects. Your primary responsibilities will include organizing and executing daily project activities, addressing customer inquiries, and developing comprehensive qualification protocols and documentation. You will also perform temperature mappings, both on-site and remotely as necessary. Success in this position will rely on your ability to collaborate effectively with specialists and maintain robust communication with our clients. You should thrive in a fast-paced startup environment, with travel requirements of up to 100 days annually, primarily domestic, and occasional international trips to Europe. This role is based in our modern Raleigh, NC facility, reporting directly to the Global Validation Manager. Your responsibilities will include:Coordinating and supervising daily project activities related to the validation and qualification of temperature-controlled units, including freezers, refrigerators, and warehouses.Responding to customer inquiries and concerns with clarity and thoroughness to ensure satisfaction.Executing validation projects for a diverse clientele, from smaller firms to large pharmaceutical corporations, ensuring compliance with regulatory standards and quality assurance.Creating and drafting qualification protocols and documentation that align with regulatory requirements, particularly in the pharmaceutical industry.Installing data loggers on-site and remotely as needed.

Are You Ready to Elevate Your Career?CAI, founded in 1996, is a leading professional services firm with a workforce of nearly 800 professionals globally. We specialize in providing critical solutions for mission-driven and regulated industries, ensuring operational readiness and exceptional performance in high-stakes environments. Our profound expertise, honed over 30 years, positions us uniquely to deliver results that redefine industry standards.At CAI, we are driven by a clear purpose: to be your trusted partner in creating a better working world and enhancing the human experience.Our Core Values:- Integrity in all actions- Commitment to serving one another- Dedication to societal improvement- Focused on future advancementsWe are relentless in our pursuit of excellence, consistently challenging the status quo. We are bold, innovative, and thrive at the intersection of technology and human experience. For us, operational readiness is not merely a target; it is our lifestyle. We are committed to progress, precision, and efficiency, always looking to the future.Key Responsibilities:CQV Execution & Safety:- Conduct Commissioning, Qualification, and Validation (CQV) activities prioritizing safety- Ensure C&Q activities are delivered in accordance with project timelines- Monitor and report on CQV progressDocumentation & Compliance:- Assist in creating and reviewing C&Q procedures for client projects- Revise qualification-related documents like SOPs, master plans, and execution plans- Support CQV review and validation of equipment designProject Planning & Coordination:- Aid in planning commissioning spares and consumables- Allocate resources effectively for project execution- Coordinate logistics and support during CQV activitiesTesting & Vendor Management:- Facilitate design reviews, equipment shakedown, commissioning, FATs, IQ, OQ, and PQ activities- Collaborate with contractors and vendors for necessary testing

At Morgan & Morgan, we believe that the work we do has a significant impact. For countless Americans, we serve as their final line of defense against insurance firms, large corporations, and defective products. Our team, comprising attorneys across all 50 states, client support staff, creative marketers, and operational experts, plays a vital role in the fight for consumer rights. With over 6,000 dedicated professionals, we are unified in our mission: For the People.Job SummaryThis position involves collaborating closely with a lead attorney and litigation assistant. We offer competitive compensation alongside a generous bonus structure. Successful candidates will engage in various responsibilities, including but not limited to the following tasks.Key ResponsibilitiesDraft and prepare legal documents such as pleadings, motions, affidavits, complaints, and legal memoranda.Electronically file court documents in both state and federal courts.Maintain effective communication with clients, courts, counsel, and other relevant parties.Conduct legal research and factual investigations.Prepare discovery documents, interrogatories, and responses.Draft and serve summons.Coordinate and summarize depositions.Prepare trial binders and exhibits in conjunction with legal assistants.Organize and maintain pleadings and discovery indexes.Assist attorneys with interrogatories and other discovery requests.Compile relevant information from diverse sources.Act as a liaison between trial teams and both internal and external parties.Facilitate witness preparation.Assist with case settlements.Perform other related duties as assigned to meet the needs of the business.

Are you an experienced Fire Protection Engineer looking to advance your career? Coffman Engineers, Inc. is seeking a skilled Senior Fire Protection Engineer with 10-15 years of experience to join our dynamic team in Raleigh, NC. You will play a crucial role in designing fire protection systems for various projects, ensuring safety and compliance with standards.Your responsibilities will include:Conducting fire protection system design and analysis.Collaborating with project teams to develop innovative solutions.Reviewing and mentoring junior engineers.Interfacing with clients and stakeholders to ensure project requirements are met.Staying current on industry trends and regulations.

Join Us as a Senior Validation EngineerAre you a motivated and experienced Senior Validation Engineer with a passion for driving complex Commissioning, Qualification, and Validation (CQV) projects? At Eupry, we are looking for someone like you! In this pivotal role, you will leverage your technical expertise in temperature mapping along with robust project management skills to deliver exceptional compliance solutions for leading global pharmaceutical manufacturers and distributors.Located in our Raleigh office, this position offers a unique opportunity to take technical ownership of high-impact projects within a rapidly growing, innovation-driven organization.About EupryFounded in Denmark in 2014, Eupry is on a mission to transform how top life science companies validate, monitor, and document temperature and humidity across the value chain. Over the years, we have earned the trust of global organizations such as FedEx, DHL, DSV, AstraZeneca, Novo Nordisk, and AbbVie.As a leader in temperature mapping and monitoring, Eupry provides some of the most advanced and reliable solutions in the industry. We go beyond traditional validation by offering cutting-edge temperature mapping services for warehouses, transport, and manufacturing environments. Notably, we are the first in the world to provide continuous temperature mapping for airplanes.With a strong and rapidly expanding presence in both Europe and the United States, our headquarters in Copenhagen is home to around 80 dedicated employees, while our global team exceeds 100 members and continues to grow to meet increasing demand.Through our innovative Compliance as a Service model, Eupry replaces outdated legacy systems with a fully digital, IoT-driven approach, simplifying audits, eliminating manual processes, and ensuring continuous compliance across storage and transportation.Why Work at Eupry?Collaborating with industry leaders across the United States, Eupry is recognized for providing the easiest solutions to monitor and map storage temperature and humidity. Our “Compliance as a Service” approach redefines the industry, moving away from outdated legacy products into the IoT realm.We value the professional development of our team members and strive to create an engaging environment where everyone can thrive. At Eupry, we are committed to helping you face new challenges, empowering you to work independently, and celebrating your achievements!Your Role and ResponsibilitiesAs a Senior Validation Engineer, you will be the technical and operational backbone of our CQV service delivery. You will own client-facing validation projects from inception to final reporting, guaranteeing that complex temperature mapping strategies are executed flawlessly. Acting as a technical subject matter expert, you will collaborate directly with international colleagues to ensure alignment across global markets.

Join CRB as a Senior Manager of Commissioning, Qualification, and Validation (CQV) and be a key player in delivering exceptional CQV services to our esteemed Life Sciences clients. This dynamic role requires a proactive and self-driven individual to oversee the daily operations of the CQV team, ensuring effective collaboration with both internal and external resources across various regional projects from the proposal phase through to facility turnover. Your responsibilities will encompass guiding teams through regulatory compliance, formulating and implementing strategies, and managing timelines while mitigating risks.In this leadership position, you will utilize your exceptional organizational, communication, and interpersonal skills to forge strong relationships with clients and stakeholders. You will represent CRB with professionalism and contribute directly to our success by assisting in securing new projects.Lead the CQV team’s daily operations, including resource management across regional projects.Oversee the creation and execution of validation protocols, studies, and comprehensive final reports.Review and approve User Requirements Specifications (URS), Functional Specifications (FS), Design Specifications (DS), and process Failure Mode and Effects Analysis (FMEA).Act as a subject matter expert in discussions with clients and regulatory bodies.Collaborate on the development of tailored CQV plans that integrate with design and construction initiatives.Implement and manage periodic system reviews and requalification activities.Develop execution schedules for all ONEsolution projects.Engage with regulatory authorities during audits.Mentor and train both internal and external employees on CQV methodologies pertinent to each project.Support the formulation of internal qualification documentation.Evaluate the impact of new systems and changes on validated statuses using a quality risk-based approach.

Join Veeva Systems, a mission-driven leader in industry cloud solutions, dedicated to accelerating the delivery of therapies to patients. As one of the fastest-growing SaaS companies, we achieved over $2 billion in revenue in our last fiscal year and continue to expand rapidly.Our core values—Do the Right Thing, Customer Success, Employee Success, and Speed—guide us in everything we do. In 2021, we made history by becoming a public benefit corporation, emphasizing our commitment to balancing the needs of customers, employees, society, and investors.As a Work Anywhere organization, we prioritize flexibility, allowing you to work from home or the office in an environment that suits you best.Be part of our mission to transform the life sciences industry and make a positive impact on our customers, employees, and communities.Role OverviewAs the Director of Validation Management Strategy, you will spearhead the growth of Veeva’s Validation Management solutions across North America. Your mission will be to assist life sciences companies in digitizing and managing their Commissioning, Qualification, and Validation (CQV) processes via a centralized cloud platform.We are looking for a visionary leader who can align sales, marketing, products, and services into a unified strategy, driving measurable growth. You should possess a profound understanding of the technical and regulatory standards needed for the qualification of manufacturing environments, utilities, equipment, and the validation of intricate analytical and production processes.In this capacity, you will act as a trusted advisor and thought leader within the industry, fostering executive relationships and guiding clients through their transition from traditional paper methods to a data-driven digital solution. Your efforts will position Veeva Validation Management as the leading solution for next-generation validation management.This full-time position allows you to work from anywhere, with processes designed to maximize your productivity in the environment that suits you best.

Are you a passionate Full Stack Developer looking to make a real impact in a dynamic R&D team? At Bandwidth, we strive to innovate and create solutions that redefine communication technology. Join us in our mission to empower businesses through cutting-edge software development!As a Full Stack Developer, you will work on both front-end and back-end technologies, collaborating with cross-functional teams to design and implement robust applications. Your contributions will be pivotal in enhancing our platforms and ensuring seamless user experiences.

Join Aretetechnologies Inc. as an Expert Specialist where your skills will make a significant impact. We are seeking a dynamic individual who is passionate about technology and innovation. This role will involve working closely with clients to provide expert solutions and insights that drive success in their projects.

Join Verkada as a Healthcare Subject Matter Expert, where you will leverage your deep expertise in healthcare systems to drive innovative solutions and improve patient outcomes. In this dynamic role, you will work closely with our product and engineering teams to enhance our offerings tailored for the healthcare sector. Your insights will help shape our strategy and ensure we meet the unique needs of healthcare organizations.

Domino's Pizza, Inc. in Raleigh is looking for a Delivery Expert to join the team. This position focuses on delivering fresh pizza and providing friendly service to customers at their homes or workplaces. Delivery Experts play a key role in keeping orders on schedule and making sure every meal arrives with a positive attitude. Key Responsibilities Bring pizza and other menu items to customers quickly and accurately throughout the Raleigh area Use local knowledge to navigate routes efficiently and keep food hot Maintain a friendly and upbeat attitude during each delivery Contribute to a smooth and enjoyable customer experience from start to finish Requirements Reliable and responsible approach to work Interest in providing excellent customer service Ability to follow directions and navigate local streets Friendly personality and a positive outlook for every shift

Role overview Domino's Pizza, Inc. seeks an Assistant Manager for its Raleigh location. This position plays a key part in daily store operations, working to keep service levels high and every order up to Domino's standards. Assistant Managers help guide team members on each shift. Supporting a positive and productive work environment is central to this role. What you will do Assist with daily operations and store routines Help maintain quality and service standards for every order Support and guide team members during shifts Promote a positive workplace atmosphere Location This position is based in Raleigh.

About Sobi Sobi is a biopharmaceutical company focused on developing treatments for rare diseases. Our team works to advance therapies that make a difference for patients worldwide. Role Overview The Analytical Expert in Pharmaceutical Products will join the product development team in Raleigh. This position centers on applying analytical expertise to support and refine our pharmaceutical product portfolio. The goal: maintain and improve quality standards throughout development. What You Will Do Apply analytical methods to support product development projects Contribute to the optimization of pharmaceutical products Help ensure products meet established quality standards

Join our dynamic team at 360 IT Professionals as a SAS Expert in Raleigh, NC! We are seeking a highly skilled professional with expertise in SAS to contribute to our projects and deliver top-notch data analytics solutions. This role requires a strong understanding of statistical analysis and data management.

Join our dynamic team at Prosidian Consulting as a Cloud Subject Matter Expert. In this pivotal role, you will leverage your expertise to provide top-notch procurement assistance and IT research, advisory, and consulting services. Your insights will help shape strategic decisions and enhance operational efficiencies for our clients.

Getlabs is a pioneering platform transforming at-home diagnostics.Our innovative healthcare solutions enable organizations to dispatch skilled mobile phlebotomists directly to patients’ homes, facilitating lab collections, vital signs monitoring, and advanced diagnostic services. By collaborating with Getlabs, partners enhance patient adherence and bridge care gaps with our same-day, nationwide service.With over $50M raised from key investors, including the premier diagnostic labs in the United States, Labcorp and Quest, Getlabs is on a mission to save lives by broadening access to essential diagnostics for all.About the Role:We are actively seeking a PRN Mobile Phlebotomist who is eager to contribute to a high-growth startup. Ideal candidates will have extensive experience in hospital, office, or mobile settings and demonstrate a commitment to excellence with minimal supervision.The PRN shift operates from 5 AM to 1 PM, with a required availability of at least 3 days between Monday and Friday.We are looking for individuals who are not only skilled but also friendly, empathetic, and truly care about patient well-being. While our focus is on mobile phlebotomy, our identity as a patient experience company is paramount. Each patient interaction is an opportunity to provide an extraordinary experience.Please check out this Day in the life of a Getlabs phlebotomist video!

Become Part of Collibra’s Tax Team As a member of Collibra’s Global Tax Team, you will engage with a progressive group committed to enhancing our financial infrastructure as we expand internationally. Reporting directly to the Tax Director, your core responsibility will be overseeing the daily operations and management of our global indirect tax function. You will take charge of our US Sales and Use Tax (SUT) filings while serving as the internal lead for our international compliance process in collaboration with external partners. A significant aspect of this role is driving digital transformation; you will spearhead the implementation of an automated solution for US SUT return preparation and filing, while also identifying and assessing long-term automation strategies for our global operations. You will enhance the overall efficiency of the department by supporting direct tax reporting, filings, and various workflows, particularly during peak periods. At Collibra, we value transparency, technical excellence, and a proactive approach, maintaining high compliance standards in a rapidly growing environment. This position offers a hybrid work model based in our Raleigh office, requiring you to work from the office at least two days a week. This arrangement fosters connectivity, collaboration, and continuous team progress.

Prosidian Consulting is seeking an experienced IT Subject Matter Expert to provide procurement assistance, IT research, advisory, and consulting services. In this role, you will leverage your expertise to guide clients on best practices, improve their IT procurement processes, and ensure optimal utilization of technology resources.