Chemist Jobs in Delaware

Akkodis is looking for a Manufacturing Scientist onsite in Claymont, DE. This position requires someone who has experience with immunoassays, ELISA, lateral flow assays and/or Document Revision, NCR, or other issues with manufacturing. The pay range is $42-50 an hour on a W2 contract to hire.[~$87k-$104k a year]. Cannot do C2C. Job Summary This is an experienced position. The individual is responsible for supporting the daily production and testing needs of a Reagent Manufacturing team. This includes investigation and resolution of assay failures during in-process or final testing. Including material specification changes due to new material qualification or supplier changes and updating/correcting SOPs in compliance with current quality system standards. This position will support the routine production and testing of reagents for IVD assays. All work will be in compliance with governing regulatory requirements such as FDA, ISO 13485, and QSR. Activities can include Experience with immunoassays is required, ELISA and lateral flow technology is preferred. Principal Duties and Responsibilities: Provide technical expertise and direction in multiple Immunoassay manufacturing areas Lead multi-department teams to support/resolve non-conforming issues for existing products Communicate investigation status reports, proposals for further investigation, etc. via oral and written reports; develop and implement changes to existing documentation in a timely manner Solve immunoassay testing and manufacturing issues as they arise Training of laboratory personnel Assess manufacturing processes and systems, and implement improvements aimed at performance, quality, and cost Assure compliance with FDA Quality System Regulations (QSR), Good Manufacturing Practices (GMP), and ISO regulatory requirements Create protocols, execute, draw conclusions and author reports Interpolate and analyze data using statistical analysis (including control charts) Create and revise standard operating procedures including periodic review. Manage the documentation associated with the Change Control process. Author review and manage quality events including NCRs, Issue Evaluations, and CAPAs. Understands, promotes, and enforces all applicable safety protocols including chemical, biological hazards, labeling, containment, and waste handling. Understand product application and customer expectations Work as a member of interdepartmental project teams This is not an exhaustive list of duties or functions and might not necessarily comprise all of the essential functions for purposes of the Americans with Disabilities Act. Expected Areas of Competence (i.e., knowledge, skills and abilities) Candidates with practical experience in the development, validation and/or manufacture of diagnostic assays is required Work experience with ELISA assays is preferred ISO 13485 or cGMP experience preferred Proficiency in Microsoft Office software is required. The ability to read, interpret and analyze scientific data is required. The ability to effectively communicate through written and oral form is required, along with strong organizational and time management skills Education/Experience Requirements Bachelor's Degree in a scientific or engineering related field is required. Advanced degree (MS/PhD) preferred and can substitute for experience. Minimum 4 years of experience in a relevant production/manufacturing environment. If you are interested in this role, then please click APPLY NOW. Equal Opportunity Employer/Veterans/Disabled Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, an EAP program, commuter benefits, and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Disclaimer: These benefit offerings do not apply to client-recruited jobs and jobs that are direct hires to a client. To read our Candidate Privacy Information Statement, which explains how we will use your information, please visit ****************************************** The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: · The California Fair Chance Act · Los Angeles City Fair Chance Ordinance · Los Angeles County Fair Chance Ordinance for Employers · San Francisco Fair Chance Ordinance

At DuPont, our purpose is to empower the world with essential innovations to thrive. We work on things that matter. Whether it's providing clean water to more than a billion people on the planet, producing materials that are essential in everyday technology devices from smartphones to electric vehicles, or protecting workers around the world. Discover the many reasons the world's most talented people are choosing to work at DuPont. Why Join Us | DuPont Careers We are hiring an Applications R&D Technologist to join our team at the DuPont Experimental Station located in Wilmington, DE We are global leaders in ion exchange resins sand membranes technologies. In this role, you will work on customer-facing projects, developing the key application expertise to solve real world problems and guide the development of new products. Your work will help us save water and energy, and protect the environment by delivering more effective, efficient products and processes that do more with less impact to our world. Your Key Responsibilities: * Conducting work in the lab developing and testing new products and new applications. * Working with ion exchange resin technology to overcome processing and purification challenges. * Collaborating with teams of scientists and engineers to deliver project goals * Analyzing data and presenting results, conclusions and recommendations to stakeholders and management. * Managing a laboratory, including having primary responsibility for several pieces of process and analytical equipment as well as safety and procedural documentation. Qualifications: * Bachelor of science in chemistry, chemical engineering, or similar discipline. * Two to five years of experience in an industrial laboratory setting, which may include internship or co-op experience. * Time management and the ability to work on multiple projects simultaneously. * Strong interpersonal skills and emotional intelligence for effective work on project teams. * Proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook). Preferred skills and experience: * Experience with ion exchange resins, laboratory-scale packed beds, and/or columns. * Broad experience in purification processes using ion exchange resins. * Experience building and maintaining Swagelok-based or equivalent laboratory equipment. * Analytical experience such as HPLC, ion analysis, polymer characterization. Join our Talent Community to stay connected with us! On May 22, 2024, we announced a plan to separate our Electronics and Water businesses in a tax-free manner to its shareholders. On January 15, 2025, we announced that we are targeting November 1, 2025, for the completion of the intended separation of the Electronics business (the "Intended Electronics Separation")*. We also announced that we would retain the Water business. We are committed to ensuring a smooth and successful separation process for the Future Electronics business. We look forward to welcoming new talent interested in contributing to the continued success and growth of our evolving organization. (1) The separation transactions are subject to satisfaction of customary conditions, including final approval by DuPont's Board of Directors, receipt of tax opinion from counsel, the filing and effectiveness of Form 10 registration statements with the U.S. Securities and Exchange Commission, applicable regulatory approvals, and satisfactory completion of financing. For further discussion of risks, uncertainties and assumptions that could impact the achievement, expected timing and intended benefits of the separation transactions, see DuPont's announcement. DuPont is an equal opportunity employer. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability or any other protected class. If you need a reasonable accommodation to search or apply for a position, please visit our Accessibility Page for Contact Information. DuPont offers a comprehensive pay and benefits package. To learn more visit the Compensation and Benefits page.

A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. Job Description Performs qualitative and quantitative chemical analysis of raw materials. Coordinates testing responsibilities to ensure QA test support according to the needs of Manufacturing to maintain continuous process flow. Functions as a team member in the QA Chemical Laboratories to provide timely test analysis information on the status of conformance to requirements. Investigates testing abnormalities and implements corrective action. Cross-trains in all testing responsibilities to ensure a fully cross-functional laboratory team environment. Assists with determination of root causes of non- conformance and recommends corrective actions. Maintains laboratory chemical supplies to ensure an adequate supply and prevent testing delays. Audits documentation, device history records, and test methods for compliance . Assists with special projects by supporting the development of new test methods of performing investigative test analyses as required. Assists in projects including the validation of test methods and transfer of new products/processes/test methods. Qualifications Minimum BS degree is required. Additional Information

The Impact You'll Make in this Role As a Senior Research Chemist, you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by: * Leveraging and developing new technologies to drive 3M adhesion science. * Collaborating with a cross-functional team to develop innovative adhesive solutions. * Applying knowledge of chemistry, chemical engineering, mechanical engineering, or material science to solve complex problems. * Strengthening 3M's proprietary position through development of intellectual property. * Collaborating with global, multi-disciplinary teams to identify and implement new solutions toward customer applications. Your Skills and Expertise To set you up for success in this role from day one, 3M is looking for candidates who meet following minimum requirements: * PhD degree (completed and verified prior to start) in a in a chemistry, chemical engineering, or related field from an accredited institution science or engineering discipline from an accredited university. * Substantial experience in laboratory research in a private, public, government or military environment * Fluent in English and German Additional knowledge / nice-to-have skills / preferred qualifications that could help you succeed even further in this role include: * Experience in UV curable polymeric materials. * Experience either direct or through collaborations utilizing modeling and simulation tools to understand and / or predict polymeric material properties. * Self-motivation to identify and execute on new technology development * Results driven and self-motivated, with a growth mindset. * Experience developing intellectual property portfolios in collaboration with legal and other technical experts. * Effective communication skills, proven ability to develop and maintain productive networks within the technical community. Job specifics: * Location: Neuss * On-site job with flexibility (job responsibilities require presence on site at least 3-4 times a week) * Travel expectations: May include up to 20% international travel * -- Please provide your resume in English --- Does this opportunity and our innovative 3M culture align with your career aspirations? If so, we encourage you to apply and embark on a journey of creativity and growth with us. We look forward to hearing from you! Resources for You For more details on what happens before, during and after the interview process, check out the Insights for Candidates page at 3M.com/careers. If you have further questions please reach out to Max (our AI Virtual Assistant) via our Career Page. At 3M, we believe diversity & inclusion are essential to innovation. We seek and value differences in people! This Job ad is addressed to all potential candidates. As an equal opportunity employer 3M will not discriminate against any applicant for employment on the basis of race/ethnicity, nationality, religion, sex, gender identity, sexual orientation, pregnancy/maternity-related matters, age or disability, or any other relevant characteristic protected under applicable local law. Please note: your application may not be considered if you do not provide your education and work history, either by: 1) uploading a resume, or 2) entering the information into the application fields directly. 3M Global Terms of Use and Privacy Statement Carefully read these Terms of Use before using this website. Your access to and use of this website and application for a job at 3M are conditioned on your acceptance and compliance with these terms. Please access the linked document by clicking here, select the country where you are applying for employment, and review. Before submitting your application, you will be asked to confirm your agreement with the terms.

Reference ID: 41717 Are you interested in high-quality, natural, and tasty nutrition? We are! It's our ambition to shape the future of nutrition. Döhler is a leading global producer of natural ingredients and solutions for the food, beverage, lifestyle and nutrition industries. We use innovative technology to process plant-based raw materials and enrich products such as lifestyle drinks, cereals, dairy, and confectionery goods for almost every well-known brand. Close to 10.000 dedicated employees in more than 70 countries share one common goal - to ensure that millions of people around the world enjoy the products created by us. We strive to inspire and empower our employees in everything we do, and we invite you to join our team - together WE BRING IDEAS TO LIFE. Your Role * You bring your technical expertise to the Analytical Science department, especially in the areas of ion chromatography, elemental analysis, and classic wet chemical processes and expand this further * You are characterized by a responsible way of working and a high level of quality awareness * You interpret the results in the context of specified food fraud and authenticity guidelines and develop recommendations for action * You carry out routine preventive maintenance work and ensure the quality of the analyzes * You coordinate the analytical examinations of raw materials, semi-finished products and end products, carry them out independently and then interpret the results independently and competently * You are the internal contact for analytical questions from different areas of the company * You are an integral part of the team and, if necessary, represent the team's interests externally * You support the continuous standardization and optimization of processes Your Profile * You have successfully completed your studies in food chemistry or a comparable field with a focus on analytics (state examination, master's degree, diploma or PhD). * Ideally, you have already gained 1-3 years of professional experience in analytics, authenticity analysis and food fraud topics in the food industry * Your colleagues (m/f/d) appreciate your reliable, communicative and implementation-oriented way of working * You manage to adequately communicate topics and convince your interlocutors, even in difficult situations * Thanks to your open and communicative nature, you will quickly be able to build a professional and cross-departmental network * You keep a cool head in stressful situations and show a high level of initiative * You have high organizational skills as well as very good analytical and conceptual skills * In addition to very good English skills, you are confident in common IT applications Your Benefits * Culture: Friendly and informal atmosphere, family-owned company, flat hierarchies, short communication channels, and helpful colleagues * Impact: You are an integral part of our business success and make an important contribution to the future of nutrition * Empowerment: You can fully unleash your potential and have the opportunity to take on responsibilities * Digitalization: We maintain excellent partnerships with market-leading innovators, allowing you to access and work with state-of-the-art technologies * Anniversary and special payments * Employee referral bonuses * Additional benefits: Christmas parties, events, financial benefits, and online shop discounts (e.g., IT leasing, mobile phone contracts, shopping, and travel discounts, etc.) Equal opportunities for all We welcome applicants, who are just as diverse as we are - regardless of age, ancestry, disability, ethnic origin, gender, nationality, religion, sexual orientation, social background or any other characteristic protected by applicable laws, regulations and ordinances. Become a part of our team and apply online trough our career portal to the attention of Luisa Rhein. Please note that we are unable to consider or return application documents sent by mail.

Agilent Technologies is seeking a Production Chemist for its manufacturing facility in Newport, Delaware. The Newport site is part of Agilent's growing Consumables and Supplies Division (CSD), with a focus on liquid chromatography products. Agilent's product quality and technological innovation lead the market. As a leader, we are entering new phases of product transformation with increased emphasis on new product and process innovation, process standardization and production efficiency. This is a high-visibility and growing product line where you will have the opportunity to make a real difference to one of Agilent's key consumables businesses. Plus, we embrace 6-Sigma and Lean Manufacturing methodologies making for an engaging and rewarding mix of scientific discovery, process improvement, and employee growth and development. Key responsibilities include working individually or as part of multi-discipline, cross-functional teams to: Evolve existing chemistries and design new chemistries Provide support for and/or represent the site on new product introduction projects Scale existing chemistries in support for a rapidly growing line of liquid chromatography consumables Lead project teams to develop and deploy product and process improvements, which include capital projects and continuous improvement projects Support and actively pursue Lean, 6-Sigma, and Safety Improvement projects Provide daily support for the production of silica-based packing for high-performance liquid chromatography columns Resolve yield and scrap issues Execute and support the Management of Change control process, determine the disposition of nonconforming product, and create and execute corrective and preventive action plans to improve safety and quality Maintain SAP data accuracy (bills of materials, recipes) Qualifications Bachelors or Masters Degree in Chemistry, Material Science or equivalent 1+ years of experience in a chemistry based working environment Demonstrated technical and problem solving skills Demonstrated communication skills; written, oral and listening Demonstrated leadership skills Computer and digital skills Additional Details This job has a full time weekly schedule. Applications for this job will be accepted until at least February 26, 2025 or until the job is no longer posted.The full-time equivalent pay range for this position is $79,200.00 - $123,750.00/yr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: ************************************* Agilent Technologies, Inc. is an Equal Employment Opportunity and Affirmative Action employer. We value diversity at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to diversity in the workplace and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_******************* or contact ***************. For more information about equal employment opportunity protections, please visit *************************************** Required: OccasionalShift: DayDuration: No End DateJob Function: Manufacturing

IFF is a world-class science company working to bring creative solutions to health, consumer, and industrial markets. IFF's Health and Biosciences division is currently looking for talented scientists to help in the development of sustainable solutions across technology platforms in Probiotics, HMO, Fibers; Cultures, Enzyme and Biopolymers for markets such as Household & Personal Care, Animal Nutrition, Human Nutrition, and Biofuels. IFF has an exciting opportunity for an adaptive, curious, self-motivated, and passionate scientist for our Lead Polymer Chemist role in the Biological and Interfacial Sciences team at IFF. In this team you will work closely with the business, regulatory scientists, biochemists, and chemical engineers to discover and develop enzymatically derived biopolymers. In this role, the scientist will have responsibility for synthesizing new materials, developing processes, as well as exploring their application in home and personal care applications. The position will be located at the Experimental Station in Wilmington, Delaware, and will be lab-based. Responsibilities: Design, initiate and execute polymer synthesis and functionalization for new product development projects. Partner with biochemists, molecular biologists, engineers, and application experts to discover novel biopolymer biocatalysts. Work closely with process and production engineers to scale-up new products at global manufacturing sites. Translate business needs into research strategies, engage with internal and external stakeholders to identify and evaluate new ideas, and develop the necessary fundamentals to bring new chemistry from concept to commercial success. Execute application studies to develop and enhance key structure-property relationships understanding in home care, personal care, and food applications. Lead and independently drive R&D projects in multi-functional research teams; maintain a state-of-the-art knowledge in biomaterials; Leads by example and acts as a mentor for scientists and other team members. Prepare data summaries, technical reports, presentations, protocols, and other technical and regulatory documents as needed. Lead in ideation, patent application drafting, and intellectual roperty strategy development in collaboration with peers and the legal team. Use and demonstrate solid project management skills working with stakeholders to define scope, impact, and deliverables. On occasion, engage directly with customers on their needs, problems, and prototyping. Maintain a safe and clean work area and follow IFF safety policies and standards. We are a global leader in taste, scent, and nutrition, offering our customers a broader range of natural solutions and accelerating our growth strategy. At IFF, we believe that your uniqueness unleashes our potential. We value the diverse mosaic of the ethnicity, national origin, race, age, sex, or veteran status. We strive for an inclusive workplace that allows each of our colleagues to bring their authentic self to work regardless of their religion, gender identity & expression, sexual orientation, or disability. Visit IFF.com/careers/workplace-diversity-and-inclusion to learn more

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description Performs qualitative and quantitative chemical analysis of raw materials . Coordinates testing responsibilities to ensure QA test support according to the needs of Manufacturing to maintain continuous process flow. Functions as a team member in the QA Chemical Laboratories to provide timely test analysis information on the status of conformance to requirements. Investigates testing abnormalities and implements corrective action. Cross-trains in all testing responsibilities to ensure a fully cross-functional laboratory team environment. Assists with determination of root causes of non-conformances and recommends corrective actions. Maintains laboratory chemical supplies to ensure an adequate supply and prevent testing delays. Audits documentation, device history records, and test methods for compliance. Assists with special projects by supporting the development of new test methods of performing investigative test analyses as required. Assists in projects including the validation of test methods and transfer of new products/processes/test methods. The candidate should be able to work 2nd or 3rd shifts. Need to be flexible on working 2nd or 3rd. Qualifications The candidate should be able to work 2nd or 3rd shifts. Need to be flexible on working 2nd or 3rd. Additional Information Sneha Shrivastava Technical Recruiter (Clinical/Scientific) Artech Information Systems LLC 360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: ************ | Fax: ************ Connect with us on - LinkedIn | Facebook | Twitter

Follows/executes written procedures/protocols with minimal supervision and completes notebook and verification with accuracy. Conducts sample analysis, method development and method qualification/verification/validation under minimum guidance of research scientists/managers. Stability/release testing. Maintains scientific integrity and timeliness of results, clearly documents results and clearly summarizes work in written and verbal form. Ensures maintenance and calibration of lab equipment with minimal supervision. Communicates test results, task status and testing issues to scientists/managers in a timely manner. Participates in department/group meeting activities and cross-functional group activities as needed. Understands and maintains cGMP training records and follows all cGMP company policies, standard operating procedures and best practices. Adheres to safety standards.

Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! The Translational Medicine (TLM) department of QPS is comprised of three laboratory operations units: Biomarker Analysis (BMA), Gene & Sequence Analysis (GSA), and Immunobioanalysis (IBA). An Associate Scientist in any of these units will be a fully-supervised trainee, responsible for gaining mastery of GCP and GDP, conducting assigned studies according to study protocols, and recording study results and observations. Our TLM department is continuing to expand, and has positions available in most of the above units. If you have a Bachelor's degree in Biology, Biochemistry, Immunology or other related disciplines, we would like to hear from you. QPS' Story: Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II - IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life. Team members enjoy challenging and rewarding work, and are encouraged achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, team work and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals. If this sounds like your ideal work environment, then we would love to speak with you, so apply today! Please visit our website (************ for more information and to see all current openings. The Job Perform routine lab operations, such as preparing reagents, pipetting, weighing, monitoring, recording, and replenishing supplies Assist supervisor in performing analysis of drug or other targets in complex biologic matrices Set-up, use and maintain complex instrumentation Document experiment details, calculations, results and observations in accordance with GLPs and SOPs Perform routine mathematical & chemical calculations Work Location This job will be 100% QPS-office/facility based Requirements The successful candidate will hold an undergraduate degree in Biology, Molecular Biology, Biochemistry, Immunology, Pharmacology, Medical Technology, or a related field as follows: Bachelor's Degree Associate's Degree plus 2 or more years relevant experience Desire to learn and grow professionally Why You Should Apply Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals. Structured Career Ladders that provide excellent growth based on your personal aspirations. Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance. Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&D and Short and Long-term Disability Insurance Park-like setting in Newark, Delaware Internal committees designed with the needs and enjoyment of QPS employees in mind. QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.

At DuPont, our purpose is to empower the world with essential innovations to thrive. We work on things that matter. Whether it's providing clean water to more than a billion people on the planet, producing materials that are essential in everyday technology devices from smartphones to electric vehicles, or protecting workers around the world. Discover the many reasons the world's most talented people are choosing to work at DuPont. Why Join Us | DuPont Careers We are hiring an Applications R&D Technologist to join our team at the DuPont Experimental Station located in Wilmington, DE We are global leaders in ion exchange resins sand membranes technologies. In this role, you will work on customer-facing projects, developing the key application expertise to solve real world problems and guide the development of new products. Your work will help us save water and energy, and protect the environment by delivering more effective, efficient products and processes that do more with less impact to our world. Your Key Responsibilities: Conducting work in the lab developing and testing new products and new applications. Working with ion exchange resin technology to overcome processing and purification challenges. Collaborating with teams of scientists and engineers to deliver project goals Analyzing data and presenting results, conclusions and recommendations to stakeholders and management. Managing a laboratory, including having primary responsibility for several pieces of process and analytical equipment as well as safety and procedural documentation. Qualifications: Bachelor of science in chemistry, chemical engineering, or similar discipline. Two to five years of experience in an industrial laboratory setting, which may include internship or co-op experience. Time management and the ability to work on multiple projects simultaneously. Strong interpersonal skills and emotional intelligence for effective work on project teams. Proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook). Preferred skills and experience: Experience with ion exchange resins, laboratory-scale packed beds, and/or columns. Broad experience in purification processes using ion exchange resins. Experience building and maintaining Swagelok -based or equivalent laboratory equipment. Analytical experience such as HPLC, ion analysis, polymer characterization. Join our Talent Community to stay connected with us! On May 22, 2024, we announced a plan to separate our Electronics and Water businesses in a tax-free manner to its shareholders. On January 15, 2025, we announced that we are targeting November 1, 2025, for the completion of the intended separation of the Electronics business (the “Intended Electronics Separation”)*. We also announced that we would retain the Water business. We are committed to ensuring a smooth and successful separation process for the Future Electronics business. We look forward to welcoming new talent interested in contributing to the continued success and growth of our evolving organization. (1) The separation transactions are subject to satisfaction of customary conditions, including final approval by DuPont's Board of Directors, receipt of tax opinion from counsel, the filing and effectiveness of Form 10 registration statements with the U.S. Securities and Exchange Commission, applicable regulatory approvals, and satisfactory completion of financing. For further discussion of risks, uncertainties and assumptions that could impact the achievement, expected timing and intended benefits of the separation transactions, see DuPont's announcement. DuPont is an equal opportunity employer. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability or any other protected class. If you need a reasonable accommodation to search or apply for a position, please visit our Accessibility Page for Contact Information. DuPont offers a comprehensive pay and benefits package. To learn more visit the Compensation and Benefits page.

Job Summary: We are seeking a dedicated and detail-oriented QC Chemist to join our team. The QC Chemist will be responsible for conducting routine and non-routine analyses of raw materials, in-process, and finished products to ensure they meet quality standards and safety regulations. The ideal candidate will have a strong analytical mindset, meticulous attention to detail, and extensive knowledge of laboratory procedures and equipment. Responsibilities * Conduct various chemical and instrumental analyses on raw materials, in-process samples, finished products, packaging, and composites. * Prepare and analyze samples using various procedures, including internal SOPs, specifications, analytical methods, compendial monographs, client procedures, research procedures, and protocols. * Utilize Wet Chemistry techniques (pH, Viscosity, and Titration) and Analytical Testing methods (GC, UV/Vis, and IR). * Maintain sophisticated analytical instruments, schedule preventative maintenance, and ensure trouble-free operation. * Ensure products meet quality standards and specifications, making critical pass/fail decisions. * Troubleshoot quality issues and identify root causes, preventive, and corrective actions. * Prepare and report results from timely preparation of monthly reports. * Maintain compliance with relevant regulations, standards, and guidelines. * Maintain accurate and complete records of all analytical activities. * Provide technical assistance to internal and external customers. * Make risk analysis and usage decisions of non-conformances. Essential Skills * Quality control * GMP * QC testing * Chemistry * Laboratory * Gas chromatography (GC) * Wet Chemistry techniques (pH, Viscosity, Titration) * UV/Vis * IR Additional Skills & Qualifications * Bachelor's degree in Chemistry, Biochemistry, Biology, or a related field. * 1+ years of experience in a QC role within a cGMP facility. * Proficiency with Wet Chemistry techniques such as pH, Viscosity, and Titrations. * Familiarity with analytical techniques such as GC, UV/Vis, and IR. * Strong understanding of cGMP environment and regulatory standards. * Excellent attention to detail and problem-solving skills. * Ability to work independently and as part of a team. * Strong communication and documentation skills. Work Environment The QC Chemist will work in a cGMP-compliant laboratory setting, utilizing a range of sophisticated analytical instruments and equipment. The role requires adherence to safety protocols and regulatory guidelines. The work environment is collaborative, and you will have the opportunity to provide technical support to both internal and external customers. Flexibility and the ability to work independently and within a team are essential. Additional Information: This plant is a 24/7 operation and the QC department works a rotating shift (no set shifts, each employee must do the rotating shift). Ex: 4 12hr night shift followed by 7 days off then 5 8hr day shift followed by 3 days off then back to night. Pay and Benefits The pay range for this position is $30.00 - $30.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Newark,DE. Application Deadline This position is anticipated to close on Apr 16, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: * Hiring diverse talent * Maintaining an inclusive environment through persistent self-reflection * Building a culture of care, engagement, and recognition with clear outcomes * Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

At DuPont, our purpose is to empower the world with essential innovations to thrive. We work on things that matter. Whether it's providing clean water to more than a billion people on the planet, producing materials that are essential in everyday technology devices from smartphones to electric vehicles, or protecting workers around the world. Discover the many reasons the world's most talented people are choosing to work at DuPont. Why Join Us | DuPont Careers We are hiring an Applications R&D Technologist to join our team at the DuPont Experimental Station located in Wilmington, DE We are global leaders in ion exchange resins sand membranes technologies. In this role, you will work on customer-facing projects, developing the key application expertise to solve real world problems and guide the development of new products. Your work will help us save water and energy, and protect the environment by delivering more effective, efficient products and processes that do more with less impact to our world. Your Key Responsibilities: Conducting work in the lab developing and testing new products and new applications. Working with ion exchange resin technology to overcome processing and purification challenges. Collaborating with teams of scientists and engineers to deliver project goals Analyzing data and presenting results, conclusions and recommendations to stakeholders and management. Managing a laboratory, including having primary responsibility for several pieces of process and analytical equipment as well as safety and procedural documentation. Qualifications: Bachelor of science in chemistry, chemical engineering, or similar discipline. Two to five years of experience in an industrial laboratory setting, which may include internship or co-op experience. Time management and the ability to work on multiple projects simultaneously. Strong interpersonal skills and emotional intelligence for effective work on project teams. Proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook). Preferred skills and experience: Experience with ion exchange resins, laboratory-scale packed beds, and/or columns. Broad experience in purification processes using ion exchange resins. Experience building and maintaining Swagelok -based or equivalent laboratory equipment. Analytical experience such as HPLC, ion analysis, polymer characterization. Join our Talent Community to stay connected with us! On May 22, 2024, we announced a plan to separate our Electronics and Water businesses in a tax-free manner to its shareholders. On January 15, 2025, we announced that we are targeting November 1, 2025, for the completion of the intended separation of the Electronics business (the “Intended Electronics Separation”)*. We also announced that we would retain the Water business. We are committed to ensuring a smooth and successful separation process for the Future Electronics business. We look forward to welcoming new talent interested in contributing to the continued success and growth of our evolving organization. (1) The separation transactions are subject to satisfaction of customary conditions, including final approval by DuPont's Board of Directors, receipt of tax opinion from counsel, the filing and effectiveness of Form 10 registration statements with the U.S. Securities and Exchange Commission, applicable regulatory approvals, and satisfactory completion of financing. For further discussion of risks, uncertainties and assumptions that could impact the achievement, expected timing and intended benefits of the separation transactions, see DuPont's announcement. DuPont is an equal opportunity employer. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability or any other protected class. If you need a reasonable accommodation to search or apply for a position, please visit our Accessibility Page for Contact Information. DuPont offers a comprehensive pay and benefits package. To learn more visit the Compensation and Benefits page.

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description Performs qualitative and quantitative chemical analysis of raw materials . Coordinates testing responsibilities to ensure QA test support according to the needs of Manufacturing to maintain continuous process flow. Functions as a team member in the QA Chemical Laboratories to provide timely test analysis information on the status of conformance to requirements. Investigates testing abnormalities and implements corrective action. Cross-trains in all testing responsibilities to ensure a fully cross-functional laboratory team environment. Assists with determination of root causes of non-conformances and recommends corrective actions. Maintains laboratory chemical supplies to ensure an adequate supply and prevent testing delays. Audits documentation, device history records, and test methods for compliance. Assists with special projects by supporting the development of new test methods of performing investigative test analyses as required. Assists in projects including the validation of test methods and transfer of new products/processes/test methods. The candidate should be able to work 2nd or 3rd shifts. Need to be flexible on working 2nd or 3rd. Qualifications The candidate should be able to work 2nd or 3rd shifts. Need to be flexible on working 2nd or 3rd. Additional Information Sneha Shrivastava Technical Recruiter (Clinical/Scientific) Artech Information Systems LLC 360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: ************ | Fax: ************ Connect with us on - LinkedIn | Facebook | Twitter

Wilmington PharmaTech (WPT) is seeking self-motivated Research Scientists to join our dynamic chemistry process department for active pharmaceutical ingredient (API) synthesis in clinical phase drug development. Key Responsibilities: Participates in the production of APIs in a kilolab or pilot plant setting by following batch records under cGMP environment. Records precisely all critical observations and documents all results during the production accurately. Diligently follows company SOPs to clean equipment for production and maintains appropriate cleaning records. Disassembles reactors for cleaning as necessary and reassembles them after the cleaning complete. Ensures and maintains kilolabs and related storage areas are in good condition. Performs routine qualifications for production equipment and maintains related records. Understands cGMP requirements of WPT and strictly follows all company policies, SOPs and best practices. Adheres to safety standards. Potential to conduct hands-on organic research with supervision for process optimization, and collect data to support the production of intermediates/APIs. Participates in the hazard operations (HAZOP) discussion and provide suggestions and solutions as necessary. Assists in trouble shootings and investigations of processes. Maintain good, clear laboratory records. Desired Qualifications: Academic or industrial research experience in organic chemistry. This position offers benefits, competitive salary and an opportunity to advance in a growing company.

IFF Health & Biosciences applies expert science to advance market-driven, healthy and sustainable solutions to serve areas including health, food, beverage, dietary supplement and animal nutrition. We use cutting-edge biotechnology across a range of markets to advance bio-based solutions to meet the needs of a growing population, while protecting our environment for future generations. We are innovative solvers who help our customers turn challenges into high-value business opportunities. We are currently seeking an Associate Scientist of Microbiology to strengthen our Animal Nutrition and Health research program, based in Wilmington, DE. The candidate will be working with a group of scientists with expertise in Microbiology, Molecular biology, Animal Science and Biochemistry. In addition to predominantly laboratory-based workflows, the candidate is expected to interact with technical supports and customers from different animal farms. For this role, the candidate must have proven experience and a strong technical understanding of Microbiology, Molecular Biology, and good knowledge of genomics approaches. Experience in animal science is very helpful. Responsibilities Actively interact with IFF Animal Nutrition & Health service laboratories, execute experiments to explore the impact of probiotics and enzymes on animal nutrition and health. Actively participate in the routine operation and maintenance of our service laboratories. In-lab processing of samples collected from poultry, swine, ruminant, and pets. Routine general microbiological experiments involving bacterial extraction, plating, and counting. General molecular biology operations of DNA extraction, RNA extraction, PCR, qPCR etc. Good knowledge of data collecting and processing using Excel. Knowledge of more sophisticated data processing tools will be a plus. Interact with animal farms and IFF field support technical managers to provide data summaries and feedback for animal trial-related research activities. Actively participate in technical advancement and protocol optimization within the animal service laboratories. Explore and implement new methods and technologies when needed. Job Requirements BS degree in Microbiology, Molecular Biology, Animal Science, Food Science, Biotechnology, or other related biological disciplines with 2-4 years of experience; or M.S. degree with 1-2 years of similar experiences. Some research experience in animal sample collection and processing. 1-3 years of experience with general molecular biology operations including DNA isolation and quantification, and PCR. General understanding of microbiological techniques such as aseptic technique, media preparation, serial dilutions, and microbe culturing. Hands-on-mentality in laboratory settings and a strong affinity for lab work. Demonstrated ability to work as part of a multi-functional team and to collaborate with others. Demonstrated good communication and interpersonal skills. Goal oriented and capable of task-oriented delivery. Willing to learn new skills and techniques. Able to adapt to changes, take initiatives, and thrive in a fast-paced R&D environment. Demonstrated organizational skills and excellent attention to detail. Able to deliver consistent high-quality experimental data. We are a global leader in taste, scent, and nutrition, offering our customers a broader range of natural solutions and accelerating our growth strategy. At IFF, we believe that your uniqueness unleashes our potential. We value the diverse mosaic of the ethnicity, national origin, race, age, sex, or veteran status. We strive for an inclusive workplace that allows each of our colleagues to bring their authentic self to work regardless of their religion, gender identity & expression, sexual orientation, or disability. Visit IFF.com/careers/workplace-diversity-and-inclusion to learn more

Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! QPS, LLC has an opening for an Associate Scientist I in our GBA group. In this role, you will play a pivotal part in QPS' continued expansion of our bioanalytical capabilities to support small molecule, antibody drug conjugate, protein, and gene therapy drug development. As an Associate Scientist I in our Bioanalytical department, you will be a fully-supervised trainee, responsible for sample preparation by various extraction methods; analysis of drug and metabolites in biological samples to support preclinical and clinical drug development programs under GLP regulations; and recording study results and observations. QPS' Story: Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II - IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life. Team members enjoy challenging and rewarding work, and are encouraged achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, team work and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals. If this sounds like your ideal work environment, then we would love to speak with you, so apply today! Please visit our website (************ for more information and to see all current openings. The Job Perform routine lab operations, such as sample extraction, preparing reagents, operating automatic liquid handling equipment, pipetting, weighing, monitoring, and recording, in a neat/clean manner Assist Principal Investigator in performing quantitative analysis of drug and metabolites in biological samples utilizing validated liquid chromatography-tandem mass spectrometry (LC-MS/MS) methods under GLP regulations Document experiment details, calculations, results and observations in accordance with GLPs and SOPs Basic math skills to perform routine calculations Work Location This job will be 100% QPS-office/facility based Requirements The successful candidate will hold a degree in Analytical Chemistry, Biochemistry, Pharmacology, or related scientific discipline as follows: Bachelor's degree Will also consider Associate's degree in Chemistry Why You Should Apply Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals. Structured Career Ladders that provide excellent growth based on your personal aspirations. Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance. Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&D and Short and Long-term Disability Insurance Park-like setting in Newark, Delaware Internal committees designed with the needs and enjoyment of QPS employees in mind. QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.

Job Summary: We are seeking a dedicated and detail-oriented QC Chemist to join our team. The QC Chemist will be responsible for conducting routine and non-routine analyses of raw materials, in-process, and finished products to ensure they meet quality standards and safety regulations. The ideal candidate will have a strong analytical mindset, meticulous attention to detail, and extensive knowledge of laboratory procedures and equipment. Responsibilities + Conduct various chemical and instrumental analyses on raw materials, in-process samples, finished products, packaging, and composites. + Prepare and analyze samples using various procedures, including internal SOPs, specifications, analytical methods, compendial monographs, client procedures, research procedures, and protocols. + Utilize Wet Chemistry techniques (pH, Viscosity, and Titration) and Analytical Testing methods (GC, UV/Vis, and IR). + Maintain sophisticated analytical instruments, schedule preventative maintenance, and ensure trouble-free operation. + Ensure products meet quality standards and specifications, making critical pass/fail decisions. + Troubleshoot quality issues and identify root causes, preventive, and corrective actions. + Prepare and report results from timely preparation of monthly reports. + Maintain compliance with relevant regulations, standards, and guidelines. + Maintain accurate and complete records of all analytical activities. + Provide technical assistance to internal and external customers. + Make risk analysis and usage decisions of non-conformances. Essential Skills + Quality control + GMP + QC testing + Chemistry + Laboratory + Gas chromatography (GC) + Wet Chemistry techniques (pH, Viscosity, Titration) + UV/Vis + IR Additional Skills & Qualifications + Bachelor's degree in Chemistry, Biochemistry, Biology, or a related field. + 1+ years of experience in a QC role within a cGMP facility. + Proficiency with Wet Chemistry techniques such as pH, Viscosity, and Titrations. + Familiarity with analytical techniques such as GC, UV/Vis, and IR. + Strong understanding of cGMP environment and regulatory standards. + Excellent attention to detail and problem-solving skills. + Ability to work independently and as part of a team. + Strong communication and documentation skills. Work Environment The QC Chemist will work in a cGMP-compliant laboratory setting, utilizing a range of sophisticated analytical instruments and equipment. The role requires adherence to safety protocols and regulatory guidelines. The work environment is collaborative, and you will have the opportunity to provide technical support to both internal and external customers. Flexibility and the ability to work independently and within a team are essential. Additional Information: This plant is a 24/7 operation and the QC department works a rotating shift (no set shifts, each employee must do the rotating shift). Ex: 4 12hr night shift followed by 7 days off then 5 8hr day shift followed by 3 days off then back to night. Pay and Benefits The pay range for this position is $30.00 - $30.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: - Medical, dental & vision- Critical Illness, Accident, and Hospital- 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available- Life Insurance (Voluntary Life & AD&D for the employee and dependents)- Short and long-term disability- Health Spending Account (HSA)- Transportation benefits- Employee Assistance Program- Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Newark,DE. Application Deadline This position is anticipated to close on Apr 16, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: + Hiring diverse talent + Maintaining an inclusive environment through persistent self-reflection + Building a culture of care, engagement, and recognition with clear outcomes + Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

Reference ID: 41809 Are you interested in high-quality, natural, and tasty nutrition? We are! It's our ambition to shape the future of nutrition. Döhler is a leading global producer of natural ingredients and solutions for the food, beverage, lifestyle and nutrition industries. We use innovative technology to process plant-based raw materials and enrich products such as lifestyle drinks, cereals, dairy, and confectionery goods for almost every well-known brand. Close to 10.000 dedicated employees in more than 70 countries share one common goal - to ensure that millions of people around the world enjoy the products created by us. We strive to inspire and empower our employees in everything we do, and we invite you to join our team - together WE BRING IDEAS TO LIFE. Your role: * You define and coordinate measures to set the foundations for safe food production * You ensure that consistent inspections, tests and assessments are carried out in all teams worldwide to ensure product and process conformity * You define, review and update quality assurance methods to ensure that they are consistent with our organizational goals and the highest industry standards * You work closely with suppliers and external partners to ensure that all of the organization's quality requirements are met * You drive digital transformation in your area of responsibility and use innovative technologies to optimize our quality assurance processes * You successfully coordinate and implement digitalization projects in close cooperation with various interfaces * You provide tools for monitoring and analyzing quality assurance data to identify trends, deviations and potential for improvement * You conduct training, offer mentoring and promote the further development of the team in order to continuously expand specialist knowledge * You support the introduction of the SAP QM module and, in collaboration with IT, are responsible for implementing updates in the area of responsibility Your profile: * Leadership skills and the ability to motivate and develop a global team * Completed degree or comparable qualification in quality management, quality assurance or a closely related field * Several years of experience in quality assurance, ideally in a manufacturing environment, preferably FMCG * Sound knowledge in the application of quality assurance methods and standards * Experience in managing and coordinating projects, especially in the area of digitalization * Experience in the introduction and support of SAP QM modules * Very good knowledge of data analysis and the use of appropriate tools * Strong communication skills and interdisciplinary collaboration Your Benefits * Culture: Friendly and informal atmosphere, family-owned company, flat hierarchies, short communication channels, and helpful colleagues * Impact: You are an integral part of our business success and make an important contribution to the future of nutrition * Empowerment: You can fully unleash your potential and have the opportunity to take on responsibilities * Digitalization: We maintain excellent partnerships with market-leading innovators, allowing you to access and work with state-of-the-art technologies * Anniversary and special payments * Employee referral bonuses * Additional benefits: Christmas parties, events, financial benefits, and online shop discounts (e.g., IT leasing, mobile phone contracts, shopping, and travel discounts, etc.) Equal opportunities for all We welcome applicants, who are just as diverse as we are - regardless of age, ancestry, disability, ethnic origin, gender, nationality, religion, sexual orientation, social background or any other characteristic protected by applicable laws, regulations and ordinances. Become a part of our team and apply online trough our career portal to the attention of Valerie Krämer. Please note that we are unable to consider or return application documents sent by mail.