Scientist Jobs in Aston, PA

The American Board of Internal Medicine (ABIM) is currently seeking a Measurement Scientist to join our Research & Innovations department. The Measurement Scientist will apply exceptional critical thinking and creative problem-solving skills to help ABIM develop the most advanced assessments in credentialing. Reporting to the Manager, Measurement Research, the Measurement Scientist has the following primary responsibilities: Apply creative problem-solving skills to solve practical problems in assessment. Design and implement innovative approaches to assessment. Develop a coherent research agenda to support valid interpretation and use of test scores. Collaborate with ABIM staff on original research and development projects. Communicate measurement concepts and analytic results to internal and external colleagues. Prepare manuscripts for publication and presentation at professional meetings. Provide psychometric analysis and consultation to improve internal operational testing activities. Perform operational activities to support ABIM exam programs. The ideal candidate has a doctorate in educational/psychological measurement, statistics, or a related field (actively pursuing a doctorate and close to completion will be considered). They should also have strong interpersonal skills and a solid foundation in the principles of psychometrics, including knowledge of test development, item response theory, and equating procedures. They must have demonstrated ability with research design and methodologies, and facility with R, SAS, SPSS, and other programming languages. Experience with the application of Generative AI and/or Natural Language Processing (NLP) in an assessment context is highly desirable. This role requires an on-site office presence at least two days per week. ABIM offices are located in the historic section of Philadelphia, 510 Walnut Street. Our technology and workplace operations teams provide for and support a seamless hybrid work environment for all ABIM employees. * * * At the American Board of Internal Medicine (ABIM), our team of unique and talented professionals, and the inspiring work they do, are essential to meeting the needs and expectations of ABIM's diverse community of physicians. ABIM is like no other workplace, and we are proud of it. We are committed to recognizing the importance of our people by investing in their lives through ongoing learning opportunities and exceptional total compensation & benefit offerings. We look forward to learning more about your interest in joining our team. Cover letter preferred but not required. EOE

We are looking for a talented Scientist to join our team! Key Responsibilities Isolate and expand immune cells, characterizing them using multi-parameter flow cytometry and functional assays Package, titer, and characterize engineered viruses for immune cell transduction, assessing viral infectivity and transduction efficiency using flow cytometry and molecular assays (PCR, VCN analysis). Develop and optimize immunoassays to assess host immune responses to viral vectors and engineered immune cells. Conduct experiments to evaluate CAR-T cell persistence, function, and immunogenicity. Ensure timely execution of experiments and project deliverables with accountability. Maintain compliance Prepare and present research findings Requirements Bachelor's degree in relevant field 0-3 years of industry experience in cell therapy, immunology, or autoimmune disease research. Experience with immune cell-based analytics and assay development, including: Flow cytometry Immunogenicity assays Lentiviral engineering Knowledge of CAR-T or other immune cell therapy approaches is a plus Familiarity with genome editing is a plus. Ability to work both independently and collaboratively in a team environment. Dexian is a leading provider of staffing, IT, and workforce solutions with over 12,000 employees and 70 locations worldwide. As one of the largest IT staffing companies and the 2nd largest minority-owned staffing company in the U.S., Dexian was formed in 2023 through the merger of DISYS and Signature Consultants. Combining the best elements of its core companies, Dexian's platform connects talent, technology, and organizations to produce game-changing results that help everyone achieve their ambitions and goals. Dexian's brands include Dexian DISYS, Dexian Signature Consultants, Dexian Government Solutions, Dexian Talent Development and Dexian IT Solutions. Visit ******************* to learn more. Dexian is an Equal Opportunity Employer that recruits and hires qualified candidates without regard to race, religion, sex, sexual orientation, gender identity, age, national origin, ancestry, citizenship, disability, or veteran status.

Bioanalytical Scientist responsibilities include, but are not limited to, the following: • Execution of assay development experiments for vaccine clinical assays including complex pipetting and plate map schemes • Media and reagent preparation • General laboratory upkeep, maintenance, and ordering of supplies • Work according to established Standard Operating Procedures (SOPs) and regulatory guidance • Maintain accurate records in adherence with documentation standards • Collaborate and communicate within and across the work group • Work in a structured environment under direct to moderate supervision Quals-- • Education: BS degree - no higher or lower • At least 1 year related laboratory experience with demonstrated pipetting skills at various volumes is required • Experience with MSD or Luminex platform preferable • Strong computer, scientific, and organizational skills • Excellent communication (oral and written) and attention to detail • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate and real time records, follow instructions, and comply with company policies • High sense of responsibility, accountability, and professional integrity

Job Title: Scientist I Duration: 12 months Pay Range:$30 - $36 /hr on W2 Qualifications: Education Minimum Requirement: • Master's degree in a relevant field (e.g. Biochemistry, Biology, Biotechnology, Molecular and Cell Biology, Pharmacology; Pharmaceutical Sciences) with 0-3+ years relevant experience • Bachelor's degree in a relevant field (see above) with 5+ years relevant experience Required Experience and Skills: • Cell culture, including routine maintenance using aseptic cell culture technique and ability to perform experiments per established protocols • Track record of working collaboratively in a team environment delivering results for complex in-vitro biological systems • Data analysis and interpretation using tools such as Excel, Graphpad PRISM, ability to document results • Autonomy, attention to detail, critical thinking, growth mindset Preferred Experience and Skills: • Experience conducting in-vitro drug transporter or metabolism studies such as substrate phenotyping and inhibition assays in recombinant cell lines, vesicles and primary hepatocytes or comparable cell-based systems. • Experience with automation and/or developing complex liquid handling methodologies for in vitro experiments • Basic understanding of quantitation using radiometric or LC/MS methods Responsibilities: This position will contribute to Client's drug discovery and clinical development efforts in the Transporter Science Group within the Department of Pharmacokinetics, Pharmacodynamics Drug Metabolism, and Bioanalytics (PDMB) at Client Research Laboratories in West Point, PA. • The main goal of this group is to develop and execute assays that will predict the disposition of drug candidates and provide insights into the potential for drug-drug interactions by being a substrate or inhibitor of drug metabolizing transporters. • Successful candidates should have a passion for generating high quality in vitro data for use by project teams across a range of therapeutic areas and must have independent bench level skills for working with a range of in vitro assay systems as well as the capacity to contribute to complex research projects. • Candidates must have demonstrated leadership as well as excellent written and verbal communication skills. Net2Source is an Equal Opportunity Employer. We believe that no one should be discriminated against because of their differences, such as age, disability, ethnicity, gender, gender identity and expression, religion or sexual orientation. Our rich diversity makes us more innovative, more competitive, and more creative, which helps us better serve our clients and our communities. All employment decisions shall be made without regard to age, race, creed, color, religion, sex, national origin, ancestry, disability status, veteran status, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status or any other basis as protected by federal, state, or local law.

The Associate Investigator is a member of the General Toxicology group in our AAALAC-accredited and GLP-compliant facility. The Associate investigator will be responsible for conducting studies which includes protocol reviews, in-life data collection (both electronically and written), collecting biological samples, and performing procedures according to Standard Operating Procedures (SOPs). *2-5 yrs experience: Laboratory w/ rodent animal handling, basic science skills; BS Degree required Job Responsibilities The duties include, but are not limited to the following: • Ensure the welfare of laboratory rodents in the testing facility. • Uphold study integrity. • Careful handling/restraint of laboratory rodents. • Test material administration by various routes of exposure, e.g. dietary, oral gavage, intraperitoneal injection, subcutaneous injection. • Determining and recording animal body weights, clinical observations, holding for eye exams, and other in-life study functions. • Collecting biological samples which can include, urine, feces, and blood (tail venipuncture). • Data collection using manual and electronic methods (including Provantis and Microsoft software systems). • Collecting, recording, documenting, and reporting results with a high degree of accuracy and precision in a timely manner. • Understanding and following all relevant SOPs, GLPs, and safety guidelines. • Learning and refining new laboratory skills as applicable. • Maintaining study records and data in in a well-organized manner. • Communicating effectively with Study Directors, Supervisors, attending Veterinarians, and other relevant staff members within the company. • Assisting other Associates and completing other tasks as assigned. • Working weekends, holidays, and or external hours on a rotating schedule. Job Requirements • B.S. degree in animal science, biology, or related field or an equivalent of a combination of applicable work experience and higher education. • 2-5 Years of relevant experience. • Ability to work both independently and in a team setting with minimal supervision. • Proficient with Microsoft Office software programs. Work Environment • Most of the tasks required for this position will be conducted in a secured and locked animal vivarium. When entering the vivarium individuals must wear safety glasses with side shields, laboratory coats or scrubs, and shoe coverings. The use of a respirator (usually a particulate filtering mask) is required in areas/rooms where research animals are being housed or handled. Please note: If the employee had visited another animal facility on the same day as work, has had contact with companion-/pet-/wild-rodents, or had contact with snakes/reptiles/birds of prey that are fed rodents, the employee must shower and have a complete change of clothing prior to entering company's animal vivarium. • Employees will be working individually and/or in groups in small animal housing rooms, examination rooms, or special purpose procedures rooms. • Work in a research environment, which requires the use of sharp objects (e.g. needles) and working around mechanical parts such as rodent caging systems, watering systems, cage washing systems. • Working with or near known or unknown toxic chemicals and/or biological hazards. • The employee will work regularly with live animals requiring the use of appropriate PPE to prevent exposure to allergens, biohazards, and/or test material hazards.

Provide expert technical and analytical support to the Quality Control (QC) function including instrumentation and methodology troubleshooting, non-routine analysis, and the evaluation of new technology. Individual should be qualified to Bachelor of Science level/or higher in a scientific field with a minimum of 3 years' experience in a GMP laboratory environment. Strong knowledge of analytical chemistry and laboratory instrumentation and GMP/GLP. Required skills: Individual should be qualified with a Bachelor of Science or graduate level degree in a scientific discipline with a minimum of 3 years' experience in GMP laboratory environment. Strong knowledge of analytical chemistry, laboratory instrumentation, and GMP/GLP. Mandatory Science Degrees/Experience/ Certifications: Bachelor of Science degree in a scientific discipline (i.e. chemistry, analytical chemistry, biochemistry, etc.) HPLC or HPIC experience 3 years minimum post-grad experience Semi-automatic dissolution bath experience Experience in a GMP environment and an understanding of those requirements Desirable skills: Validation Experience, Technical Transfer Methods, Experience with Lab Data Management Systems (LIMS or 1Lab) Preferred schedule 6am - 3pm or 10am - 7pm

Compensation & Additional Details: Fully onsite in Malvern, PA 10 PTO Days + 6 Sick Days 12 month extending contract Compensation: $29-$32/hr exact rate is based on several factors, including skills, experience, and education. Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law. Minimum Qualifications: -Bachelor's degree in scientific field, preferably Biotech -Minimum 1 year of experience working in a lab environment, preferably GMP -Minimum 1-2 years of experience working within cell culture (not just academia) -Minimum 1 year of experience working with Aseptic techniques -cGPMP, GMP, GDP (Good documentation practice) -Strong attention to detail -Extremely motivated individual -Cell Banking experience (preferred) Day-to-Day: One of our large pharmaceutical clients is looking to hire an Associate Scientist of Cell Banking to perform Cell Banking for the Cell Culture processes and/or bio-analytical testing within the API Large Molecule Process Development group in Malvern PA. The candidate's primary responsibilities will include but are not limited to the production, testing, inventory, and supply of Master, Working, and development Cell Banks for clinical, and commercial production as well as analytical testing for J&J biopharmaceutical and cell therapy products. Responsibilities will include: -Support Cell banking organization by performing Cell banking for Cell Culture processes and analytical testing. -Execute production, testing, and release of Master, Working, development, and analytical cell Banks and ensures the timely supply to customers. -Work in a team environment as well as contributing individually to meet project timeline and objectives. -Participate in Cell culture and cryopreservation of cells using aseptic techniques under GMP Compliant conditions. -Execute all activities per established procedures and protocols -Interface with internal and external customers to ship cell banks and supply critical information as per their requirements. -Collaborate cross-functionally to represent Cell Banking department. -Author, review, and approve technical documents, SOPs, and batch records.

We are seeking a highly skilled Fermentation Process Scientist / Senior Scientist with expertise in fermentation process development and optimization to join our team. The successful candidate will focus on the development, optimization, and scaling of fermentation-based processes for various applications. This role requires a strong background in biochemical engineering, microbiology, or a related field, with hands-on experience in fermentation technologies and process development. Key Responsibilities: Develop and optimize fermentation processes for Saccharomyces cerevisieae . Design, execute, and analyze fermentation experiments in shake flasks and fermenters to improve yield, productivity, and scalability. Collaborate with cross-functional teams to integrate fermentation processes into larger production workflows. Monitor and troubleshoot bioreactors, ensuring optimal process conditions and identifying areas for improvement. Work with a contract manufacturing network to scale up fermentation processes from lab to pilot and production scales while maintaining product quality. Analyze process data and apply statistical tools to optimize performance. Prepare technical reports, SOPs, and documentation for regulatory compliance and knowledge sharing. Function as the process owner for all scales of the process Stay updated on advancements in fermentation technology and bioprocess engineering. Qualifications & Experience: Master's or Ph.D. in Biochemical Engineering, Microbiology, Biotechnology, or a related field with 3+ year of experience. Salary and job title will be commensurate with experience. Hands-on experience with fermentation process development, bioreactors, and microbial cultivation. Strong knowledge of metabolic pathways, microbial physiology, and bioprocess optimization. Experience with Design of Experiments and technoeconomic analysis Experience with process scale-up and technology transfer. Proficiency in data analysis software and statistical modeling. Excellent problem-solving and critical-thinking skills. Strong written and verbal communication skills for technical documentation and research dissemination. Relentless drive to deliver the best product to customers. Ability to wear many hats and thrive in a startup environment. Preferred Qualifications: Prior experience optimizing Saccharomyces cerevisiae cell lines for efficient commercial production. Prior experience producing polysaccharides, polymers, or natural products in Saccharomyces cerevisiae . Familiarity with automation, sensors, and control strategies for fermentation. Benefits & Opportunities: Competitive salary and benefits package including equity. Access to state-of-the-art fermentation and bioprocessing facilities. Opportunities for career growth, collaboration, and publishing in peer-reviewed journals. Engagement in innovative research projects with real-world applications. Collaborate with a driven team of domain experts to develop a biomaterial with unrivaled biomedical potential in a well-funded company. If you are passionate about fermentation technology and bioprocessing and are eager to contribute to cutting-edge process development, we encourage you to apply!

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

Responsibilities · Prepare reagents, standards, and control samples · Analyze samples using various techniques specific to department · Operate analytical equipment · Maintain analytical equipment · Ensure lab area is clean and inspection ready at all times · Remove lab waste · Record tasks in accordance with Good Documentation Practices (GDP) · Learn and apply regulatory requirements; GLP, GCP, 21CFR Part 11 · Follow applicable SOPs and procedural documents · Learn how to review and evaluate data results · Other tasks as assigned Education, Experience & Qualifications · BA/BS or higher; all experiences will be evaluated · Able to perform basic lab work · Able to work in a regulated environment · Able to work effectively and contribute within a team · Able to work with computer systems · Able to document clearly

IFF Health and Biosciences is looking for a Senior Scientist in our Microbiome & Microbiology R&D group. Our IFF laboratories are located within the Experimental Station research site in Wilmington, Delaware. The successful candidate will work with a highly interactive multidisciplinary research team applying rigorous, state of the art science toward the development and discovery of new health products. We are searching for a candidate to join our immune health team who has broad experience working in BSL-2 laboratories and demonstrates conceptual and technical expertise that can be applied to investigations at the intersection of the Mucosal Microbiota and host immune systems. Responsibilities The primary responsibilities of the position will involve technical operations within our tissue culture facility establishing cellular assays using cell lines and primary cells isolated from humans and animals to study host microbiota interaction. In addition to cell culture responsibilities, familiarity with immunological techniques and technologies involved in downstream analysis and the ability to design and develop assays will be required. Most importantly the candidate will need to be team oriented, adaptable, self-motivated, and able to operate within a dynamic professional environment. Desired Skills General lab organization, project planning, and task coordination among team members. Experience with pre-clinical models of host-microbe interaction. Sterile technique and safe handling of samples of human origin. Isolation of Peripheral Blood Mononuclear Cells (PBMCs) from human blood of healthy donors (Buffy coats/leukapheresis paks) Immunoaffinity separations of cells from PBMC preps. (ex: MACS / FACS). Primary immune cell isolation from host tissue and culture techniques. Cell line development by using CRISPR/Cas9. Tissue models; 3D (e.g.Mattek), organoids, co-cultures. Microscopy / immunohistology. Flow cytometry, cytometric bead arrays, Western Blot, ELISA, EliSpot, RNA-Seq. Qualifications PhD in Immunology/Cell biology/mucosal Microbiology or related field. 6+ years of post-PhD laboratory research experience in immunology, cell biology, host-microbe interaction, microbiome-host relationships. 3+ years industrial experience is strongly preferred. Demonstrated knowledge of basic Immunology, cell biology, molecular biology, biochemistry techniques and microbiology, Sterile techniques and experience in the isolation and cultivation of microorganisms, preferably with experience in an anaerobic environment The successful candidate must be motivated, creative, have strong problem solving and critical thinking skills to meet technical objectives and milestones. Excellent written and verbal communication skills and the desire to work as a bench-scientist within a multidisciplinary team are required.

Principal Scientist, Analytical Chemistry - Philadelphia, PA . The selected candidate will take a lead role in execution of analytical programs. He/she will design and develop studies to advance and progress the expertise and capabilities in the nanoparticle innovation space. Results of research/progress will be communicated regularly to executive leadership. Job Responsibilities Willingly and enthusiastically work at the bench to solve analytical challenges encountered within drug development. Can be relied upon to work independently and develop a variety of analytical methods in-house or in collaboration with contract organizations for starting materials, intermediates, and final drug products, including but not limited to GPC, HIC, Ion Exchange Chromatography, Size Exclusion Chromatography (SEC), UPLC/HPLC, RP-HPLC, LC-MS, MS, High Resolution Mass Spectroscopy (HRMS), MALDI-TOF, GC-FID, KF, Field Flow Fractionation, FFF-MALS-DLS, Asymmetric Flow Field AF-MALS, NMR, SERS, XPS, TGA, DSC, DLS, Zeta Potential, UV-vis, ELISA, TEM, AFM, Fluorimetry, Endotoxin Testing, BET, LAL, Flow Cytometry, Infrared (IR) and Raman Spectroscopy, FTIR, SDS-PAGE and Gel Electrophoresis. Assess existing analytical methods and identify areas for further improvements and optimization. Perform new analytical method development, qualification and validation and support the technology transfer of analytical methods. Ability to bring analytical methods developed at CROs/CDMOs in-house. When required, perform routine chemical/physical testing of raw materials, in-process, finished product and stability samples according to in-house methods and compendial methods as applicable, generating reliable and interpreting data in support of clinical studies. Prepare and review analytical method protocols, reports and SOPs, as required. Other duties as assigned. Required Skills and Competencies and Education Demonstrated/proven abilities to develop, optimize, and validate analytical methods and testing procedures. Gold Nanoparticle, Nanoparticle, LNP, Biologics, Proteins, Small Molecules, Large Molecules experience. Demonstrated expertise in creating chromatographic methods for purity, impurities, surface chemistry and charge, surface homogeneity, size and ligand distributions, chemical bonding, and integrity for synthetic large molecule PEGylated nanoparticles is highly preferred. Excellent communications skills with demonstrated ability to communicate clearly in English in both written and spoken form. Excellent data analysis, plotting, summary and presentation skills. Demonstrated ability to work on multiple projects in parallel in collaboration with outside vendors and internal research teams. Experience in collaborating analytical CROs/CDMOs and the ability to work one-on-one with the counterparts in these contract organizations. An advanced degree in analytical chemistry or relevant field is highly preferred. Bachelor's degree with significant industry experience will be considered. 5-10 years of previous industry experience is required.

H&K does not discriminate in employment opportunities or practices on the basis of race, color, religion, gender, national origin, age, disability, veterans' status, or any other characteristic protected by law. We are always looking for the best, most qualified people to join our team. Pre-employment drug testing (EOE) Great Benefits offered! Environmental Scientist US-PA-Skippack Job ID: 2025-2657 Type: Regular Full-Time Category: Other Engineering & Environmental Services Overview H&K Group, Inc. is seeking an Environmental Scientist to join our team! The Scientist will work within Engineering and Environmental Services in support of company facilities/projects and consultation services pertaining to environmental regulation, permitting and compliance. This position provides the opportunity to gain valuable experience in a broad range of technical areas within the environmental sciences. Why work for H&K Group, Inc.? Competitive salary commensurate with experience 100% Company-paid Health Benefits (high deductible plan) 401(k) Savings and Investment Plan Tuition reimbursement programs available to qualifying employees for approved programs Additional training programs including on the job, online through H&K Academy, manufacturer offered training, and more Responsibilities Essential Duties and Responsibilities Conducts field sampling of soil, water, and waste materials for laboratory analysis. Assists with the preparation of documents, forms, and reports related to field observations and laboratory results and compares them to relevant regulatory standards. Conducts National Pollutant Discharge Elimination System (NPDES) discharge water sampling and assists with regulatory reporting and permit applications. Assists in the development, monitoring and implementation of comprehensive Spill Prevention, Control and Countermeasure (SPCC) and Preparedness, Prevention and Contingency (PPC) Plans. Conducts site inspections for compliance with Federal, State and Local regulations including but not limited to Solid Waste Management, SPCC/PPC, EPCRA/SARA, NPDES, Erosion and Sediment Control, Stormwater Pollution Prevention, Surface Mining Permits, and Management of Fill. Completes annual reporting related to Emergency Planning and Community Right-to-Know Act (EPCRA) and Residual Waste (26R) for H&K Group, Inc. facilities. Provides technical assistance in the event of a spill or release of a regulated substance; identifies potential pollutant sources, determines potential impacts and liabilities, and recommends and assists in the implementation of corrective actions. Maintains working knowledge of new technologies, practices, standards, and regulations developed by industry and regulatory sources. Maintains a positive and constructive attitude and strives to build upon relationships with internal personnel and external clients. Other duties as assigned. Qualifications Qualifications To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Education and/or Experience Bachelors degree (B.S.) and one to three years related experience and/or training; or equivalent combination of education and experience in the environmental health and safety, physical sciences, or other relevant programs with a focus on environment, health, and safety. OSHA 40 Hour HAZWOPER Training a plus. Language Skills Ability to read and interpret documents such as regulations, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively to customer contacts and coworkers. Mathematical Skills Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. Ability to compute rate, ratio, and percent and to draw and interpret graphs. Reasoning Ability Ability to apply common sense understanding to carry out instructions furnished in written, oral, or diagram form. Ability to deal with problems involving several concrete variables in standardized situations. Equipment/Computer Skills To perform this job successfully, an individual should have knowledge of Database software; Internet software; Spreadsheet software and Word Processing software. Experience with ArcGIS, AutoCAD a plus. Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is frequently required to stand; walk; sit; use hands to finger, handle, or feel; reach with hands and arms and talk or hear. The employee is occasionally required to climb or balance and stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. Work Environment The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is frequently exposed to wet and/or humid conditions; moving mechanical parts; fumes or airborne particles and outside weather conditions. The employee is occasionally exposed to high, precarious places; toxic or caustic chemicals; risk of electrical shock and vibration. The noise level in the work environment is usually moderate. Other Qualifications Valid drivers license, good driving record. H&K Group, Inc. provides complete heavy civil contracting and construction materials solutions with safety, speed, quality, efficiency, and value. Beginning as a small family business a half century ago, we are now a dynamic group of vertically integrated companies that has been growing and prospering for 50 years. Thank you for your interest in employment with H&K Group, Inc. At H&K, we invest in our people, providing the essential training, instruction, and supervisory support that they need to develop and grow within our company. We acknowledge that H&Ks strength and success is directly related to our employees and the talents, dedication, and job performance they exemplify. We seek dynamic, motivated people who are driven to make a difference. H&K does not discriminate in employment opportunities or practices on the basis of race, color, religion, gender, national origin, age, disability, veterans status, or any other characteristic protected by law. We are always looking for the best, most qualified people to join our team. Pre-employment drug testing (EOE) Pre-employment Physical 100% Company-Paid Health Benefits! PI10334ded84c5-29***********5 RequiredPreferredJob Industries Agriculture & Environment

This is a laboratory-based position that will aid in improving our various water analysis products as well as help design and implement new products. This position will report to the Director of R&D and has no direct reports. Job Responsibilities: Works safely Develops new and improved reagents and products. Develops formulations for tableted or powdered reagents Develops formulations for liquid and dried reagents Develops formulations for test strip reagents Ability to perform reagent calibrations on colorimeter/photometers Ability to use spread sheets and other data analysis applications Provides technical assistance to Customer Service and Marketing personnel. Resolves technical problems. Provides technical support to QC, QA, to resolve problems. Performs related laboratory duties as assigned. Conducts performance evaluations of our products versus competitor's products of similar specifications. Prepares calibration standards for checking performance of instruments. Provides technical input for quotations and product costs. Provides technical input for the preparation of SDS, instructions and labels. Maintains laboratory notebook and/or electronic notes and records. Prepares pre-production batches of reagents to establish specifications. Writes SOPs, TIs, operation instructions and manuals as needed. Participates in staff meetings as needed. Miscellaneous: Participates in lean activities, including but not limited to Lean training and lean events such as kaizen or a 5-day event. 5-S program in the various departments assigned. DMAICs. Continuously looks for ways to improve both departments' and own individual efficiencies and time management, as well ways to improve any aspect of the Company's operations and develops and implements DMAICs accordingly. Notifies Manager of any production, equipment, safety or personnel problems, etc. and cooperates in resolving such issues as well. For example, requests assistance when systems prevent the efficient performance of duties or when a system fails. Provides Manager with feedback to determine where additional training would benefit and obtains additional training as necessary. Complies with all Company policies (i.e. personnel, safety, etc.). Performs other duties as assigned. (Such duties may or may not be essential functions of the job. Travel will be required to our Chestertown facility of 10%-20%. Qualifications/Requirements: Requires a minimum of B.S. or B.A. degree in chemistry from an accredited institution, with 2 or more years of lab experience in chemistry or a related field (i.e. biochemistry), and/or an advanced degree in chemistry or pharmaceutical chemistry. Must have good laboratory skills to safely handle chemicals and instruments used in R&D laboratory, be familiar with computer-assisted instrumentation, possess good color perception and adequate manual dexterity, maintain accurate records, work according to established laboratory procedures, work independently without requiring day-to-day supervision and have proficient computer skills using Microsoft Office at a minimum, additional computer skills with data analysis applications an advantage. Environmental Factors/Physical/Mental Capabilities: Works indoors in temperature controlled environment.Handles various chemicals. Requires good problem solving, judgment, communication skills, math skills and color perception. Requires walking, standing, sitting, good manual dexterity and some transporting up to 30 lbs. LaMotte Company, a 100+ year-old global industry leader in developing and manufacturing premier water analysis solutions, operating in Newark, DE, Chestertown, MD and Warwick, UK. Our products are used around the world to accurately, quickly, and conveniently test water in a multitude of applications. LaMotte offers paid time off including vacation, sick leave, and paid holidays. Full-time employees, who regularly work at least 30 hours per week, are eligible for employer-provided insurance including health, dental, vision, disability, life insurance, and supplemental insurance. Full-time employees are eligible to contribute to our 401(k) plan with an employer match available. LaMotte is committed to a policy of Equal Employment Opportunity and will not discriminate against an applicant or employee on the basis of race, color, religion, creed, national origin or ancestry, sex, age, disability, military status, genetic information, sexual orientation, or any other legally recognized protected basis under federal, state, or local laws.

The Associate investigator will be responsible for conducting studies which includes protocol reviews, in-life data collection (both electronically and written), collecting biological samples, and performing procedures according to Standard Operating Procedures (SOPs). Job Responsibility The duties include, but are not limited to the following: Ensure the welfare of laboratory rodents in the testing facility. Uphold study integrity. Careful handling/restraint of laboratory rodents. Test material administration by various routes of exposure, e.g. dietary, oral gavage, intraperitoneal injection, subcutaneous injection. Determining and recording animal body weights, clinical observations, holding for eye exams, and other in-life study functions. Collecting biological samples which can include, urine, feces, and blood (tail venipuncture). Data collection using manual and electronic methods (including Provantis and Microsoft software systems). Collecting, recording, documenting, and reporting results with a high degree of accuracy and precision in a timely manner. Understanding and following all relevant SOPs, GLPs, and safety guidelines. Learning and refining new laboratory skills as applicable. Maintaining study records and data in in a well-organized manner. Communicating effectively with Study Directors, Supervisors, attending Veterinarians, and other relevant staff members within the company. Assisting other Associates and completing other tasks as assigned. Working weekends, holidays, and or external hours on a rotating schedule. Job Requirements B.S. degree in animal science, biology, or related field or an equivalent of a combination of applicable work experience and higher education. 2-5 Years of relevant experience. Ability to work both independently and in a team setting with minimal supervision. Proficient with Microsoft Office software programs.

AnalytiChem is a global company founded in 2021 that assists analytical testing laboratories in the industrial, environmental, and materials markets to collect actionable data to optimize their business. Our mission is to enable our customers' science by providing a solutions-oriented and integrated range of products that help them collect their best data. We are experiencing rapid growth, both organically and through acquisition, with 8 companies worldwide and counting. Our brands include SCP Science, Chem Service, Bernd Kraft, OREAS, Chem-Lab, Northeast Laboratories and BioTRADING and we support customers in a wide range of industries from Industrial to environmental and animal health. If you are looking for a dynamic work environment in a fast-growing organization where you can make a difference, AnalytiChem might be the challenge you are seeking. What will you do We are looking for a reliable Quality Control Chemist to ensure that all external and internal requirements for production of chemical reference materials are met before our high-quality product reaches our customers, while managing a team of two (2) quality control analysts. You will be responsible for developing and performing various tests on candidate reference materials, including techniques such as Gas Chromatography (GC-FID & GC-MS), HPLC, FT-IR, pH-testing, UV absorption testing and alike. An excellent Quality Control Supervisor is highly experienced in various instrumental and wet chemical testing methods and passionate about top quality products. The goal is to assure the high quality of our operations and services aiming to the long-term success of our business. Your main skills Plan and perform quality control inspections on candidate reference materials Define standard methods and their acceptance criteria for analysis of CRM Perform HPLC, GC, UV, FT-IR and similar instrumental QC tests Perform titrations, pH-tests and other wet-chemistry tests Document results in lab notebooks and ERP systems Perform Proficiency Tests to demonstrate the lab competence Writing standards operating procedures and method documentations. Handle all non-conformities and corrective actions Communicate with external quality assurance officers and assessors during on-site inspections What we are looking for Proven experience as a quality control analyst or similar relevant role Thorough knowledge (min 3 years) of methodologies of quality testing techniques and methods Experience handling Reference Materials according to ISO 17025 and/or ISO 17034. Good knowledge of MS Office Good communication skills Great attention to detail and a results driven approach Reliable and Trustworthy BSc/BA in Chemistry or another relevant field

H&K does not discriminate in employment opportunities or practices on the basis of race, color, religion, gender, national origin, age, disability, veterans' status, or any other characteristic protected by law. We are always looking for the best, most qualified people to join our team. Pre-employment drug testing (EOE) Great Benefits offered! Environmental Scientist US-PA-Skippack Job ID: 2025-2657 Type: Regular Full-Time Category: Other Engineering & Environmental Services Overview H&K Group, Inc. is seeking an Environmental Scientist to join our team! The Scientist will work within Engineering and Environmental Services in support of company facilities/projects and consultation services pertaining to environmental regulation, permitting and compliance. This position provides the opportunity to gain valuable experience in a broad range of technical areas within the environmental sciences. Why work for H&K Group, Inc.? Competitive salary commensurate with experience 100% Company-paid Health Benefits (high deductible plan) 401(k) Savings and Investment Plan Tuition reimbursement programs available to qualifying employees for approved programs Additional training programs including on the job, online through H&K Academy, manufacturer offered training, and more Responsibilities Essential Duties and Responsibilities Conducts field sampling of soil, water, and waste materials for laboratory analysis. Assists with the preparation of documents, forms, and reports related to field observations and laboratory results and compares them to relevant regulatory standards. Conducts National Pollutant Discharge Elimination System (NPDES) discharge water sampling and assists with regulatory reporting and permit applications. Assists in the development, monitoring and implementation of comprehensive Spill Prevention, Control and Countermeasure (SPCC) and Preparedness, Prevention and Contingency (PPC) Plans. Conducts site inspections for compliance with Federal, State and Local regulations including but not limited to Solid Waste Management, SPCC/PPC, EPCRA/SARA, NPDES, Erosion and Sediment Control, Stormwater Pollution Prevention, Surface Mining Permits, and Management of Fill. Completes annual reporting related to Emergency Planning and Community Right-to-Know Act (EPCRA) and Residual Waste (26R) for H&K Group, Inc. facilities. Provides technical assistance in the event of a spill or release of a regulated substance; identifies potential pollutant sources, determines potential impacts and liabilities, and recommends and assists in the implementation of corrective actions. Maintains working knowledge of new technologies, practices, standards, and regulations developed by industry and regulatory sources. Maintains a positive and constructive attitude and strives to build upon relationships with internal personnel and external clients. Other duties as assigned. Qualifications Qualifications To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Education and/or Experience Bachelor's degree (B.S.) and one to three years related experience and/or training; or equivalent combination of education and experience in the environmental health and safety, physical sciences, or other relevant programs with a focus on environment, health, and safety. OSHA 40 Hour HAZWOPER Training a plus. Language Skills Ability to read and interpret documents such as regulations, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively to customer contacts and coworkers. Mathematical Skills Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. Ability to compute rate, ratio, and percent and to draw and interpret graphs. Reasoning Ability Ability to apply common sense understanding to carry out instructions furnished in written, oral, or diagram form. Ability to deal with problems involving several concrete variables in standardized situations. Equipment/Computer Skills To perform this job successfully, an individual should have knowledge of Database software; Internet software; Spreadsheet software and Word Processing software. Experience with ArcGIS, AutoCAD a plus. Physical Demands The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is frequently required to stand; walk; sit; use hands to finger, handle, or feel; reach with hands and arms and talk or hear. The employee is occasionally required to climb or balance and stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. Work Environment The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is frequently exposed to wet and/or humid conditions; moving mechanical parts; fumes or airborne particles and outside weather conditions. The employee is occasionally exposed to high, precarious places; toxic or caustic chemicals; risk of electrical shock and vibration. The noise level in the work environment is usually moderate. Other Qualifications Valid driver's license, good driving record. H&K Group, Inc. provides complete heavy civil contracting and construction materials solutions with safety, speed, quality, efficiency, and value. Beginning as a small family business a half century ago, we are now a dynamic group of vertically integrated companies that has been growing and prospering for 50 years. Thank you for your interest in employment with H&K Group, Inc. At H&K, we invest in our people, providing the essential training, instruction, and supervisory support that they need to develop and grow within our company. We acknowledge that H&K's strength and success is directly related to our employees and the talents, dedication, and job performance they exemplify. We seek dynamic, motivated people who are driven to make a difference. H&K does not discriminate in employment opportunities or practices on the basis of race, color, religion, gender, national origin, age, disability, veterans' status, or any other characteristic protected by law. We are always looking for the best, most qualified people to join our team. Pre-employment drug testing (EOE) Pre-employment Physical 100% Company-Paid Health Benefits! PI035781eb754d-26***********5

The Research Chemist is responsible for conducting laboratory experiments, applying the principles of chemistry and processing towards new products while supporting current applications. They will assist with production scale-up in a manufacturing environment. The Chemist will interact with customers and within professional groups in support of the business. Responsibilities Support current chemistry applications within the business activities for the Highway group; Develop professional expertise in the company's core technologies and identify new opportunities for business growth and cost reductions Translate advances in materials chemistry, including paint formulations, into new product improvements and offerings Manage experiments for product improvement and new product development; Understands and optimizes water-based paint formulation Interface with customers in a support role to support technical initiatives; Coordinate process scale-up and production trial activities Maintain a high level of product knowledge of both legacy and new product offering; Investigate independently and collaborate with other groups on quality problems and recommend changes as needed Interface with sales and tech support to ensure customer requests are interpreted correctly into product advancements.; Interface with customers in a support role to support initiatives; Participate in professional trade meetings and conferences; Provide chemical and processing support to manufacturing plants to improve manufacturing efficiencies and capabilities Maintain a clean lab environment; Use established prudent practices in the laboratory while working; Follow manufacturing plant safety guidelines while on site Qualifications Bachelors Degree or higher in Chemistry, Chemical Engineering, or Materials Engineering 3 to 6 years of Chemist/Lab experience required 3 to 6 years of Manufacturing R&D Lab experience preferred Paint and Coatings experience preferred Glass chemistry, glass composition and optics experience are a plus Skills & Knowledge Microsoft Office - strong in Excel Laboratory Equipment Experience Ability to communicate clearly with manager and co-workers Good housekeeping and Lab cleanliness skills Strong attention to Detail and Organization Consistency and Accuracy for Lab Results

Title: Chemist Duration: 1 year Perform experiments and data review according to SOPs and protocols. Qualifications: Bachelor's degree or equivalent, in Biology, Chemistry, Biochemistry or related subject area, with a minimum of 2 or more years of related industry laboratory experience is required or Master's degree with 1 or more years of related industry laboratory experience is required. Strong technical writing and verbal communication skills are required. Demonstrates excellent interpersonal skills (written and oral) and the ability to work in a cross-functional customer-focused environment is required. Experience with cell culture and aseptic technique, cell-based potency assays and ELISA is required. Experience working in a cGMP environment is preferred. Experience with electronic laboratory notebook is preferred.