Trabajos chemist en Delaware

Job Description Adesis Inc. - a subsidiary of Universal Display Corporation (Nasdaq: OLED), a global leader in organic light emitting diodes - is a premier contract development and manufacturing organization (CDMO) accelerating our clients’ success in the biotech, pharmaceutical and specialty chemistry industries through our innovative chemistry and solutions. Adesis Inc. encompasses almost 100,000 square feet of state-of-the-art laboratory and manufacturing space in two U.S. locations - New Castle and Wilmington, DE, centrally located in the Mid-Atlantic biotech/ pharmaceutical hub. Our business model provides clients with organic chemistry services in three areas: early-stage research, scale-up and development, and specialty manufacturing. We specialize in organic and organometallic synthesis, from milligrams to multi-kilogram quantities, and our exceptional technical team prides ourselves in our ability to solve challenging chemistry problems for our growing client base. Adesis is an extraordinary company looking for extraordinary talent! Our mission is to accelerate our clients’ success through innovative chemistry and solutions, and we offer promising careers in an inclusive work environment aligned with our values of innovation, ownership and integrity. Job Summary: The manufacturing Process Chemist works both independently and as part of a team to assist in the development, optimization, and technology transfer of commercial manufacturing compounds. The position involves set-up, use, and cleaning of various laboratory equipment as well as running established protocols with the guidance of chemists and senior technical staff. Key Responsibilities: * Develop robust processes for the target compounds to ensure safe and reproducible processes. * Develop alternate synthetic routes to target molecules and modify reactants and/or equipment as required. * Solve complex chemical problems which may arise during process development, optimization or scale up of processes. * Understand the concepts of reaction kinetics, design of experiments, solubility and crystallization, mass transfer, heat transfer and process safety to ensure critical process parameters are identified. * Accountable for documentation to ensure the consistent manufacture of products; including batch records, production instructions, and development / qualification reports. * Performs other related duties as assigned by Management. Technical and Specialized Equipment: * NMR * (UP)LC/MS * EasyMax, PolyBLOCK * Jacketed reactors * GC/MS * Automated Chromatography Systems * Hydrogenation equipment Required Qualifications: * BS or MS in Chemistry or related field required. * At least 2 - 5 years’ experience in technical production, R&D, and/or new product development experience required. * Ability to define problems, collect data, establish facts, and draw valid conclusions. Interpretation of technical instructions from disparate information sources, and deal with several abstract and concrete variables. * Ability to work within a fast-paced, dynamic and team environment. * Working knowledge of ISO-9001, cGMP, and/or ICH Q7 in pharma or chemical regulated environments preferred. * Knowledge of Process Improvement methodology (ie., Lean Manufacturing, Six Sigma, and/or TOC) a plus. * Experience with or ability to master the use of modern research tools such as EasyMax, PolyBlock, Continuous Flow Reactors, and in-situ process monitoring a plus. * Strong computer skills in standard & scientific systems, such as Microsoft Word, Excel, PowerPoint, ChemDraw, Reaxys and Scifinder. Current Benefits at Adesis: * Competitive base salary and annual bonus program * Medical/Prescription Drug coverage, Dental, and Vision for employees and family * Option between Flexible Spending account (FSAs) or Health Savings Account (HSA) * Group Term Life insurance, short term disability, and long-term disability benefits for employees * Employee Stock Purchase Plan (ESPP) * 401(k) company contribution * Annual charitable matching gift * Generous Paid Time Off Annual compensation range: $65k-75k

Job DescriptionBenefits: • Company car, • Health insurance, • Opportunity for advancement, • Paid time off, • Training & development, • Bonus based on performance, • Competitive salary, • 401(k), • Dental insurance, • Vision insurance Environmental Manager BWI - Mid Atlantic WTS, a leading By-Product and Waste Management firm, is seeking an experienced Environmental Manager in the Baltimore Md/Mid Atlantic region. The Environmental Manger is responsible for supervision and on-site coordination of services related to the proper disposition and shipment of hazardous wastes, non-hazardous wastes, packaged laboratory chemicals, materials for recycling. Primary tasks include overall site RCRA compliance, waste characterization, profiling, materials collection, and preparation of shipments, while ensuring regulatory compliance. Full Time Position Basic Required Qualifications Astute Chemistry Knowledge * • Degreed Chemist Preferred, • 3-5 Years Experience in Field Chemistry, • Focused ability to recognize and characterize risks associated with a wide variety of chemicals commonly used in various industrial settings., • Chemical Lab Packing Experience Preferred., • Working Knowledge of Hazardous Waste RCRA Regulations, • Experience in Waste Characterization, • Experience in Waste Profiling, • Experience in HW Manifest Preparation, • Working Knowledge of USDOT (PHSMA) Hazardous Materials Regulations, • Experience in HM Characterization, • Practical Knowledge of Pertinent HM Labeling, Marking, Placarding, Segregation, Packaging Regulations, • Experience in HM Shipping Paper Regulations, • Safety Oriented, • Ability to work independently as well as in a team setting, • Ability to travel as needed, • No restrictions on physical activities supplies, on-site container movement, load supervision, • OSHA Haz Wopper Trained, RCRA training, USDOT HM training preferred, • Located in Baltimore/Philly Region

Job Description Adesis Inc. - a subsidiary of Universal Display Corporation (Nasdaq: OLED), a global leader in organic light emitting diodes - is a premier contract development and manufacturing organization (CDMO) accelerating our clients’ success in the biotech, pharmaceutical and specialty chemistry industries through our innovative chemistry and solutions. Adesis Inc. encompasses almost 100,000 square feet of state-of-the-art laboratory and manufacturing space in two U.S. locations - New Castle and Wilmington, DE, centrally located in the Mid-Atlantic biotech/ pharmaceutical hub. Our business model provides clients with organic chemistry services in three areas: early-stage research, scale-up and development, and specialty manufacturing. We specialize in organic and organometallic synthesis, from milligrams to multi-kilogram quantities, and our exceptional technical team prides ourselves in our ability to solve challenging chemistry problems for our growing client base. Adesis is an extraordinary company looking for extraordinary talent! Our mission is to accelerate our clients’ success through innovative chemistry and solutions, and we offer promising careers in an inclusive work environment aligned with our values of innovation, ownership and integrity. Job Summary The Analytical Chemist I will support the Quality Control laboratory by performing analytical testing of raw materials, in-process samples, intermediates, and finished products. The technician will ensure compliance with ISO-9001 Standards, internal procedures, and client-specific requirements while maintaining accurate documentation and supporting laboratory operations. Essential Duties and Responsibilities Include the following. Other duties may be assigned. * Perform routine analytical testing using techniques such as HPLC, GC, LC-MS, UV-Vis, FTIR, and wet chemistry methods. * Execute raw material, in-process, release, and stability testing in accordance with SOPs and regulatory guidelines. * Prepare, standardize, and document test solutions and reagent. * Calibrate and maintain analytical instruments; promptly report malfunctions. * Maintain accurate laboratory records in compliance with Good Documentation Practices (GDP). * Identify and correct problems with instruments in QC lab. Identify and communicate problems and solutions related to process, procedure, and materials to Analytical team lead and QC Chemists. * Maintain cleanliness and organization of lab by following safety, regulatory, and chemical hygiene plan * Perform daily record keeping in electronic lab notebook, * Responsible for properly managing the generation and accumulation of hazardous and non-hazardous waste * Assist in OOS/OOT investigations and support root cause analysis. * Attend and participate in QC Team meetings. Develop team skills. * Participate in continuous improvement initiatives to optimize laboratory efficiency and data integrity. Required Qualifications * Bachelor’s degree in chemistry, Pharmaceutical Sciences, or related field. * QC analytical laboratory experience in a pharmaceutical, biotech, or CDMO environment, preferred. Technical Skills: * Hands-on experience with HPLC, GC, and spectroscopic techniques. * Familiarity with cGMP, ICH, and USP/EP guidelines preferred. * Strong analytical and problem-solving skills with attention to detail. Other Skills: * Proficiency in Microsoft Office and laboratory data systems (e.g., Empower, Open Lab CDS, Mass hunter and LIMS) is a plus. * Excellent written and verbal communication skills. * Strong organizational skills and ability to work both independently and in a team setting. Current Benefits at UDC: * Competitive base salary and annual bonus program * Medical/Prescription Drug coverage, Dental, and Vision for employees and family * Option between Flexible Spending account (FSAs) or Health Savings Account (HSA) * Group Term Life insurance, short term disability, and long-term disability benefits for employees * Employee Stock Purchase Plan (ESPP) * 401(k) company contribution * Annual charitable matching gift * Generous Paid Time Off Annual compensation range: $65k-$75k

Job Description We are seeking a detail-oriented and innovative Associate Chemist to support the development, evaluation, and application of advanced stationary phases for High Performance Liquid Chromatography (HPLC) and analytical methods for biopharmaceutical analysis. This position involves both hands-on laboratory work and technical analysis to support R&D, product method development, and customer application testing. This position is full-time exempt onsite at our Newark, DE location. Requirements: · Master’s degree in Chemistry, Chemical Engineering, Biochemistry, or a related field; or BS with 1–3 years of hands-on in analytical testing. · Strong hands-on experience with HPLC/UPLC systems and familiarity with method development and system troubleshooting. · Working knowledge of techniques such as ELISA, FLD, UV-VIS, RID detection, and basic polymer or protein characterization. · Proficiency in analyzing and interpreting experimental results with attention to detail and data integrity. · Strong organizational and communication skills; able to work both independently and collaboratively in a team environment. Responsibilities: · Develop, optimize, and apply analytical methods for the testing of biologic drug products, including monoclonal antibodies (mAbs), bispecific antibodies, ADCs, fusion proteins, AAVs, and RNA therapeutics. · Perform HPLC/UPLC-based separations using various detection techniques to evaluate the performance of chromatography columns and stationary phases. · Prepare samples, mobile phases, and reagents in support of application testing and method development workflows. · Analyze test data and compile technical summaries, contributing to method performance reports and customer-facing application notes. · Maintain and troubleshoot analytical instrumentation; evaluate and implement emerging technologies. · Prepare technical documents including method SOPs, method transfer records, and method transfer protocols. · Assist with customer support by executing methods for product evaluation, providing data, and answering application-related questions. · Participate in maintaining lab compliance with safety and quality standards. Company DescriptionSepax is a fast-growing technology company and has emerged as a leader in the biological separation industry. Sepax has been developing a wide range of intellectual properties in the areas of particle synthesis, surface modification, LC column packing, bulk media production and purification process development. Sepax Technologies, Inc. focuses on three business areas: 1) bioanalytical solutions, 2) solution-based process purification and 3) medical diagnostics. Sepax Quality Management System is ISO 9001:2015 certified. Sepax Technologies Inc. is an Equal Opportunity Employer. Sepax is an Equal Opportunity Employer.Sepax is a fast-growing technology company and has emerged as a leader in the biological separation industry. Sepax has been developing a wide range of intellectual properties in the areas of particle synthesis, surface modification, LC column packing, bulk media production and purification process development. Sepax Technologies, Inc. focuses on three business areas: 1) bioanalytical solutions, 2) solution-based process purification and 3) medical diagnostics. Sepax Quality Management System is ISO 9001:2015 certified. Sepax Technologies Inc. is an Equal Opportunity Employer.\r\n\r\nSepax is an Equal Opportunity Employer.

Job Description Job Summary We are seeking motivated Production Chemists to join our GMP-compliant pharmaceutical manufacturing team working in both pilot plant and kilolabs. The Production Chemist will be responsible for performing production operations involving chemical processing, batch preparation, and in-process testing to support the manufacture of pharmaceutical products. In addition, the Production Chemist will provide day-to-day supervision and guidance to production operators, ensuring processes are carried out in full compliance with GMP and safety requirements. This position requires strict adherence to cGMP standards, safety regulations, and data integrity practices. The role involves working on a rotating shift schedule, including nights and/or weekends. Key Responsibilities · Execute production processes involving weighing, charging, mixing, distillation, and chemical reactions in compliance with SOPs and batch production records. · Operate and monitor process equipment (reactors, filtration systems, dryers, etc.) according to validated procedures. · Collect, test, and interpret in-process samples to ensure product quality and batch consistency. · Maintain accurate, real-time documentation in batch production records, logbooks, and electronic systems to ensure data integrity and regulatory compliance. · Supervise and support operators during daily production operations, ensuring tasks are performed according to GMP and safety standards. · Provide on-the-floor technical guidance and troubleshoot issues as needed. · Adhere to all cGMP, safety, and environmental policies, including proper handling of raw materials, intermediates, and finished products. · Support cleaning, equipment setup, and line changeover activities as required. · Assist in deviation investigations, corrective and preventive actions (CAPA), and continuous improvement initiatives. · Collaborate with Quality Assurance, Engineering, and Maintenance teams to ensure efficient production operations. · Participate in training programs and maintain qualifications for GMP manufacturing operations. Qualifications · Bachelor’s degree in Chemistry, Chemical Engineering, Pharmaceutical Sciences, or a related field is required. · Experience in pharmaceutical manufacturing, chemical production, or other regulated industries is preferred. · Knowledge of GMP, GLP, and FDA/EMA regulatory requirements is an advantage. · Recent graduates with strong academic backgrounds in chemistry or related fields are encouraged to apply. · Strong understanding of chemical principles and laboratory techniques. · Ability to follow detailed instructions and complete precise documentation. · Excellent problem-solving and analytical skills. · Effective communication and teamwork abilities. · Commitment to safety and compliance in a regulated environment. · Willingness to work rotating shifts (day/night/weekend). Company DescriptionWilmington PharmaTech is a rapidly growing CRO/CMO serving the pharmaceutical industry.Wilmington PharmaTech is a rapidly growing CRO/CMO serving the pharmaceutical industry.

Job DescriptionIGK is looking for a chemist/customer service rep to join our research team and participate in high-level, complex research projects. We seek a qualified candidate who has an expert understanding of lab procedures. They will test chemical substances through various methods to ensure the safety, functionality, and quality of a chemical product. The chemist will also be responsible for generating comprehensive technical reports that provide insight into a project, allowing the team to devleop solutions as needed and conduct any additional tests. Objectives of this role: • Prepare, weigh and use solutions for various laboratory procedures;, • Analyze chemical substances to identify their composition;, • Customize formulas and run tests to improve the quality of a chemical product;, • Draft detailed reports conveying experimental results and presenting findings to other scientists;, • Monitor laboratory equipment to minimize malfunctions and adhere to safety regulation;, • Customer visits for problem shooting and product research development;Responsibilities, • Develop and conduct tests for chemical ingredients, substances, and materials;, • Participate in high-level chemical research projects and create improved testing methods;, • Sterilize all used equipment and organize tools in safe areas;, • Use chemical substances or sources like heat and energy to produce reactions;Skills and Qualifications, • Bachelor's degree (or equivalent) in chemistry, or other relevant field;, • Strong knowledge of laboratory technology, tools and tests;, • Clear written communication skills to produce accurate lab reports;, • Solid understanding of lab health and safety regulations;, • Exceptional analytical research skills;, • Adequate computer skills;Preferred Qualifications, • Experience working in a laboratory setting;, • Additional certifications relevant to region;, • Excellent time-management skills when meeting important deadlines;, • Ability to think strategically and develop effective solutions;, • Expereince in sealant manufacturing is an asset;, • Motivated and a positive attitude a must;, • Assist in customer trials;, • Ready to be available for customer site visits;, • Assist production in new product development;