Company Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. Job Description Eurofins Scientific, Inc. is seeking a highly skilled and detail-oriented Food Product Testing Specialist to join our team in Des Moines, IA. In this role, you will provide advanced technical leadership in the oversight, development, and optimization of food product testing operations. You will leverage your expertise in analytical chemistry to ensure scientific rigor, data integrity, and regulatory compliance across testing programs, while working collaboratively with cross-functional teams in a primarily remote environment. Key Responsibilities: • Provide technical leadership in the development, validation, verification, and transfer of analytical methods for food testing, including chemical contaminants, residues, and nutritional analyses. • Critically evaluate complex analytical datasets (e.g., chromatographic and mass spectrometric data), ensuring scientific validity, accuracy, and compliance with regulatory standards. •Collaborate with intercompany facilities to manage client product testing and timely delivery of results [major US site locations: California, Iowa, New Orleans, Wisconsin] • Review and interpret data generated from advanced instrumentation (HPLC, GC, LC-MS/MS, ICP-MS), identifying trends, anomalies, and potential sources of error.. • Lead and support complex investigations (OOS/OOT), applying root cause analysis methodologies and implementing scientifically justified corrective and preventive actions (CAPAs). • Provide expert-level troubleshooting support by diagnosing method, instrumentation, or matrix-related issues in collaboration with on-site laboratory teams. • Oversee method transfer and comparability studies, ensuring reproducibility and alignment across laboratories and client requirements. • Develop and review technical documentation including validation protocols, study reports, risk assessments, and scientific justifications. • Ensure data integrity through rigorous review of electronic records, audit trails, and compliance with regulatory expectations (e.g., ISO, HACCP, GMP where applicable). • Collaborate with Quality Assurance and regulatory teams to support audits, inspections, and responses to regulatory inquiries. • Act as a technical subject matter expert (SME) for analytical chemistry within food testing operations, supporting internal teams and client engagements. • Provide advanced training and mentorship to laboratory and junior staff on analytical techniques, data interpretation, and scientific best practices. • Liaise with clients to provide high-level technical consultation, interpret results, and support method selection or problem-solving efforts. • Stay current with emerging analytical technologies, instrumentation, and regulatory developments relevant to food safety and testing. • Support operational strategy by identifying opportunities for process optimization, efficiency gains, and scientific innovation. •Track and manage change requests from internal and external sources •Assisting with logistics for timely sending and receiving samples, ensuring proper tracking and handling customs matters (FDA compliance) Qualifications Required Qualifications: • Bachelor’s degree (+ 5 years’ experience) or Master’s degree (+1 year experience) in Analytical Chemistry, Chemistry, Food Science, or a closely related scientific discipline • 5-10 years of experience in analytical laboratory environments • Advanced expertise in chromatographic and spectrometric techniques (HPLC, GC, LC-MS/MS, ICP-MS, or similar) • Strong understanding of method development, validation, and lifecycle management • In-depth knowledge of regulatory and quality standards (ISO, HACCP, GMP/GLP as applicable) • Demonstrated ability to interpret complex analytical data and solve technical challenges • Proficiency in statistical analysis and data evaluation tools • Excellent technical writing and documentation skills • Ability to work independently and collaboratively in a remote team-oriented environment • Strong organizational and project management skills Preferred Qualifications: • Familiarity with laboratory information management systems (LIMS) and electronic data integrity principles • Experience supporting audits and regulatory inspections • Knowledge of food chemistry, contaminants, and regulatory limits • Experience with continuous improvement methodologies (e.g., Lean, Six Sigma) WORKING CONDITIONS: • This position is primarily remote, involving advanced data analysis, technical review, and virtual collaboration. • Occasional on-site presence may be required for critical investigations, audits, or method transfer activities. • Extended periods of computer-based work, including data evaluation and report writing. • Flexibility to accommodate project timelines, cross-functional collaboration, and occasional extended hours. • Work is conducted in a secure digital environment to ensure data integrity and regulatory compliance. Additional Information What we offer: - Excellent full time benefits including comprehensive medical coverage, dental, and vision options - Life and disability insurance - 401(k) with company match - Paid vacation and holidays Eurofins USA Food Testing is a Disabled and Veteran Equal Employment Opportunity employer.

• Proactively identify and solve customer business needs • Manage relationships with senior level technical personnel • Lead value-based sales conversations • Demonstrate product value to advance customer business objectives

• Lead the delivery and evolution of live Varicent product enablement sessions. • Ensure learners understand and can confidently apply their knowledge. • Deliver virtual instructor-led training sessions (vILT) for the Admin Enablement Program and What’s New webinar series. • Collaborate with instructional designers and product SMEs to develop and iterate on vILT curriculum. • Identify gaps and opportunities within the learning ecosystem and propose new modules or formats. • Maintain alignment between training objectives and customer success goals. • Deliver polished virtual training sessions and facilitate interactive learning experiences. • Support post-session follow-up and contribute to refinement of future sessions. • Mentor and support facilitators offering guidance on instructional techniques and facilitation strategies. • Represent Education in cross-functional working groups.

Title: Regulatory Specialist / Engineer III, RA Location: Remote Mexico Full time Remote   As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.   Position Summary: Regulatory Specialist is overall responsible for supporting RA with the tasks described as below. Furthermore, the employee shall provide continuous regulatory support to the organization with review and update of EU MDR/IVDR Technical Files and support to the RA mailbox regarding Change Orders, product related questions, complaints and non-conformities, etc. for sites in Tijuana, Monterrey and Roskilde.   Key Responsibilities: - Work for regulatory activities in cooperation with the existing RA team and Sr RA Manager - Support product development by facilitating globally focused regulatory strategies to drive market access. - Draft regulatory plans and verification reports to ensure products meet regulatory requirements in all target market regions. - Responsible for updating the CE technical files for medical products. - Participate in and ensure follow up on customer requests in the RA mailbox. - Review and approve product development reports, non-conformance reports, product changes, label content and new product data. - Provide general quality support to the organization e.g. TrackWise, complaint, observations, CAPA, NC, CO’s, product registration and technical file questions etc. - Additionally, be part of the risk evaluation in related quality tasks. - Optimize, document and implement RA processes in QMS regarding regulatory procedures. - Support external and internal audits. E.g. participate in the Notified Body audit back office to provide documentation and explanation for the technical file documentation. Minimum Requirements/Qualifications: - Minimum BA/BS degree in a scientific or engineering field (preferred: biology, chemistry, material science, polymer science). - At least 2 years of experience in a regulated industry (pharmaceutical or medical device). - Strong working knowledge of US and EU Medical Device and In vitro Diagnostic requirements - Analytical mind-set and a great ability to learn new professional fields and business processes - Great ability to structured and goal-oriented manner - Excellent communication and team-building skills   Successful Candidate Will Possess   - A positive approach and motivated by challenges - Team-player mentality - Dedicated with the ability to handle tasks independently - Flexibility to handle shifting priorities - Confidence in collaborating with colleagues at all levels - Strong written communication skills, with technical writing experience being a plus - Excellent critical thinking and decision-making skills - A continuous improvement approach - Innovative problem-solving ability - Strong organizational skills with attention to detail   How will you make an impact? The Regulatory Specialist will support the Laboratory Plastics Essentials business by working closely with global manufacturing sites including locations in Tijuana (MX), Monterrey (MX) and Roskilde (DE) to ensure overall product safety and regulatory compliance. This position will be responsible for maintaining and updating Technical Documentation on regulated products and ensuring continuous improvement as it relates to changes in global standards and regulations. In addition, the RA specialist will assist with risk analysis or health hazard assessments for product recalls or field actions relating to a non-conforming product. The RA Specialist will also act as a regulatory consultant to ensure all products comply global and regional regulations and market needs (REACH/SVHC, California Proposition 65, RoHS).   What will you do?       - Ensure availability of up-to-date technical documentation and Standard Operating Procedures - Work together with LPE global teams for supporting customer requests with related RA mailboxes - Work with the global environmental compliance team to oversee the management of compliance information for all sourced materials, components and finished goods - Support international registrations with related technical documentation - Function as an RA subject matter expert on new product introductions, capacity expansion projects and custom product development and manufacturing  - Complete timely regulatory safety evaluations on customer complaints and manufacturing non-conformance activities for regulated products - Provide regulatory input to QA in Deviations, CAPAs, Management Review and complaints - Provide guidance regarding regulatory and performance test requirements for product claims and the design verification and validation of products (including sterilization, biocompatibility, labelling, clinical, and packaging validation)