Scientist Jobs in Newark, DE

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

A large retail bank located in Midtown Manhattan looking to bring on board a “ AML Technology Developer/Data Scientist” to join their team. The role is on a hybrid schedule, in office 3 days a week. Responsibilities: -Assist in the development and tuning of transaction monitoring scenarios for AML compliance. -Utilize data science techniques to analyze and improve the efficiency of AML transaction monitoring systems. -Build models to detect suspicious activities and continuously improve transaction monitoring rules. -Collaborate with the AML Technology Manager and compliance teams to integrate and implement new technologies for financial crime prevention. -Stay updated on new tools and techniques in financial crime compliance and make recommendations for system enhancements. -Develop dashboards and reports that provide insights into transaction monitoring performance.

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.

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.

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

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

Outlier is the world's leading expert platform, connecting a network of over 100,000 contributors worldwide to improve AI models by providing expert human feedback. We partner with companies including OpenAI, Meta and Microsoft to enable advanced generative AI models to provide accurate responses and advanced reasoning capabilities. We are looking for advanced Chemistry experts to teach AI how to interpret and solve complex problems by: Evaluate AI-generated content for factual accuracy and relevance in Chemistry. Develop and answer Chemistry-related questions to refine AI understanding. Assess and rank AI responses based on scientific rigor. Required expertise and qualifications: Education: Master's degree or higher (PhD preferred) in Chemistry or a related field (can be currently enrolled) Research Experience: Strong preference for candidates with peer-reviewed publications, patents, conference presentations, research grants, or industry R&D contributions English Proficiency: Ability to read and write with minimal errors Bonus Skills: AI model training experience is not required but helpful Payment: Currently, pay rates for core project work by Chemistry experts range from $30 to $50 per hour USD but varies based on your geographic location (see note below) Opportunities for higher-paying research projects based on performance. Rates vary based on expertise, skills assessment, location, project need, and other factors. For example, higher rates may be offered to PhDs. For non-core work, such as during initial project onboarding or project overtime phases, lower rates may apply. Certain projects offer incentive payments. Please review the payment terms for each project.

Location: This position will work a hybrid model (remote and in office one day per week). Ideal candidates will live within 50 miles of one of our Pulse Point locations in Wilmington, DE, Newton, MA, Indianapolis, IN, Norfolk, VA, Mason, OH, Atlanta, GA, Portland, ME, St. Louis, MO, Wallingford, CT, Louisville, KY or Washington, D.C. The Research Scientist is responsible for Carelon Research line of business; specific projects ranging from retrospective to large-scale, prospective studies in areas including population health, health economics, clinical effectiveness (drug, procedures, vaccine, and medical device), health outcomes, safety surveillance, risk management, pharmacoepidemiology, pharmacoeconomics, and comparative effectiveness research. How you will make an impact: * Leads high quality research project proposal development from early conceptual stages for external and internal submissions. * Provides scientific rigorous input in the design and development of the research studies to fulfill study objectives. * Executes statistical analyses plans independently with effective problem solving and decision making as principal investigator across a broad program of studies related to a therapeutic area and/or external collaborator. * Collaborates with biostatisticians to implement the study design and statistical analyses plans utilizing advanced statistical techniques such as propensity score modeling, GEE (generalized estimate equation) and graduate-level statistics in performing research study design and analysis. * Conducts review of administrative claims and clinical data and statistical output to ensure accuracy of results. * Summarizes key findings and generates value messages for incorporation into project deliverables, publications, and presentations. * Prepares study reports and manuscripts for submissions to peer-review journals demonstrating subject matter expertise. * Performs key project functions with minimal oversight. * Collaborates with business and Public Affairs partners, researchers, clinicians, medical writers, subcontractors, or other support staff effectively to keep projects on scope, cost and on schedule. Minimum Requirements: Requires a MS in health sciences or related advanced degree, or clinical degree such as PharmD, or MD, combined with Master level degree and a minimum of 5 years of experience in health service research, biostatistics, epidemiology, health policy, economics or related field; or any combination of education and experience which would provide an equivalent background. Preferred Skills, Capabilities and Experiences: * Ph.D. or MD strongly preferred. * Postgraduate or post-doctoral training or relevant experience in conducting observational and/or prospective research studies strongly preferred. * Clinical or therapeutic area knowledge, familiarity with clinical practice guidelines, and/or understanding of the U.S. health care system strongly preferred. For candidates working in person or remotely in the below location, the salary* range for this specific position is $142,876.00 - $214,314.00. Location: Washington, D.C. In addition to your salary, Elevance Health offers benefits such as, a comprehensive benefits package, incentive and recognition programs, equity stock purchase and 401k contribution (all benefits are subject to eligibility requirements). The salary offered for this specific position is based on a number of legitimate, non-discriminatory factors set by the Company. The Company is fully committed to ensuring equal pay opportunities for equal work regardless of gender, race, or any other category protected by federal, state, and local pay equity laws. * The salary range is the range Elevance Health in good faith believes is the range of possible compensation for this role at the time of this posting. This range may be modified in the future and actual compensation may vary from posting based on geographic location, work experience, education and/or skill level. Even within the range, the actual compensation will vary depending on the above factors as well as market/business considerations. No amount is considered to be wages or compensation until such amount is earned, vested, and determinable under the terms and conditions of the applicable policies and plans. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law. Please be advised that Elevance Health only accepts resumes for compensation from agencies that have a signed agreement with Elevance Health. Any unsolicited resumes, including those submitted to hiring managers, are deemed to be the property of Elevance Health. Who We Are Elevance Health is a health company dedicated to improving lives and communities - and making healthcare simpler. We are a Fortune 25 company with a longstanding history in the healthcare industry, looking for leaders at all levels of the organization who are passionate about making an impact on our members and the communities we serve. How We Work At Elevance Health, we are creating a culture that is designed to advance our strategy but will also lead to personal and professional growth for our associates. Our values and behaviors are the root of our culture. They are how we achieve our strategy, power our business outcomes and drive our shared success - for our consumers, our associates, our communities and our business. We offer a range of market-competitive total rewards that include merit increases, paid holidays, Paid Time Off, and incentive bonus programs (unless covered by a collective bargaining agreement), medical, dental, vision, short and long term disability benefits, 401(k) +match, stock purchase plan, life insurance, wellness programs and financial education resources, to name a few. Elevance Health operates in a Hybrid Workforce Strategy. Unless specified as primarily virtual by the hiring manager, associates are required to work at an Elevance Health location at least once per week, and potentially several times per week. Specific requirements and expectations for time onsite will be discussed as part of the hiring process. Candidates must reside within 50 miles or 1-hour commute each way of a relevant Elevance Health location. The health of our associates and communities is a top priority for Elevance Health. We require all new candidates in certain patient/member-facing roles to become vaccinated against COVID-19 and Influenza. If you are not vaccinated, your offer will be rescinded unless you provide an acceptable explanation. Elevance Health will also follow all relevant federal, state and local laws. Elevance Health is an Equal Employment Opportunity employer and all qualified applicants will receive consideration for employment without regard to age, citizenship status, color, creed, disability, ethnicity, genetic information, gender (including gender identity and gender expression), marital status, national origin, race, religion, sex, sexual orientation, veteran status or any other status or condition protected by applicable federal, state, or local laws. Applicants who require accommodation to participate in the job application process may contact ******************************************** for assistance. Qualified applicants with arrest or conviction records will be considered for employment in accordance with all federal, state, and local laws, including, but not limited to, the Los Angeles County Fair Chance Ordinance and the California Fair Chance Act.

Location: This position will work a hybrid model (remote and in office one day per week). Ideal candidates will live within 50 miles of one of our Pulse Point locations in Wilmington, DE, Newton, MA, Indianapolis, IN, Norfolk, VA, Mason, OH, Atlanta, GA, Portland, ME, St. Louis, MO, Wallingford, CT, Louisville, KY or Washington, D.C. The Research Scientist is responsible for Carelon Research line of business; specific projects ranging from retrospective to large-scale, prospective studies in areas including population health, health economics, clinical effectiveness (drug, procedures, vaccine, and medical device), health outcomes, safety surveillance, risk management, pharmacoepidemiology, pharmacoeconomics, and comparative effectiveness research. How you will make an impact: * Leads high quality research project proposal development from early conceptual stages for external and internal submissions. * Provides scientific rigorous input in the design and development of the research studies to fulfill study objectives. * Executes statistical analyses plans independently with effective problem solving and decision making as principal investigator across a broad program of studies related to a therapeutic area and/or external collaborator. * Collaborates with biostatisticians to implement the study design and statistical analyses plans utilizing advanced statistical techniques such as propensity score modeling, GEE (generalized estimate equation) and graduate-level statistics in performing research study design and analysis. * Conducts review of administrative claims and clinical data and statistical output to ensure accuracy of results. * Summarizes key findings and generates value messages for incorporation into project deliverables, publications, and presentations. * Prepares study reports and manuscripts for submissions to peer-review journals demonstrating subject matter expertise. * Performs key project functions with minimal oversight. * Collaborates with business and Public Affairs partners, researchers, clinicians, medical writers, subcontractors, or other support staff effectively to keep projects on scope, cost and on schedule. Minimum Requirements: Requires a MS in health sciences or related advanced degree, or clinical degree such as PharmD, or MD, combined with Master level degree and a minimum of 5 years of experience in health service research, biostatistics, epidemiology, health policy, economics or related field; or any combination of education and experience which would provide an equivalent background. Preferred Skills, Capabilities and Experiences: * Ph.D. or MD strongly preferred. * Postgraduate or post-doctoral training or relevant experience in conducting observational and/or prospective research studies strongly preferred. * Clinical or therapeutic area knowledge, familiarity with clinical practice guidelines, and/or understanding of the U.S. health care system strongly preferred. For candidates working in person or remotely in the below location, the salary* range for this specific position is $142,876.00 - $214,314.00. Location: Washington, D.C. In addition to your salary, Elevance Health offers benefits such as, a comprehensive benefits package, incentive and recognition programs, equity stock purchase and 401k contribution (all benefits are subject to eligibility requirements). The salary offered for this specific position is based on a number of legitimate, non-discriminatory factors set by the Company. The Company is fully committed to ensuring equal pay opportunities for equal work regardless of gender, race, or any other category protected by federal, state, and local pay equity laws. * The salary range is the range Elevance Health in good faith believes is the range of possible compensation for this role at the time of this posting. This range may be modified in the future and actual compensation may vary from posting based on geographic location, work experience, education and/or skill level. Even within the range, the actual compensation will vary depending on the above factors as well as market/business considerations. No amount is considered to be wages or compensation until such amount is earned, vested, and determinable under the terms and conditions of the applicable policies and plans. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company's sole discretion, consistent with the law. Job Level: Non-Management Exempt Workshift: Job Family: RDA > Research Data Please be advised that Elevance Health only accepts resumes for compensation from agencies that have a signed agreement with Elevance Health. Any unsolicited resumes, including those submitted to hiring managers, are deemed to be the property of Elevance Health. Who We Are Elevance Health is a health company dedicated to improving lives and communities - and making healthcare simpler. We are a Fortune 25 company with a longstanding history in the healthcare industry, looking for leaders at all levels of the organization who are passionate about making an impact on our members and the communities we serve. How We Work At Elevance Health, we are creating a culture that is designed to advance our strategy but will also lead to personal and professional growth for our associates. Our values and behaviors are the root of our culture. They are how we achieve our strategy, power our business outcomes and drive our shared success - for our consumers, our associates, our communities and our business. We offer a range of market-competitive total rewards that include merit increases, paid holidays, Paid Time Off, and incentive bonus programs (unless covered by a collective bargaining agreement), medical, dental, vision, short and long term disability benefits, 401(k) +match, stock purchase plan, life insurance, wellness programs and financial education resources, to name a few. Elevance Health operates in a Hybrid Workforce Strategy. Unless specified as primarily virtual by the hiring manager, associates are required to work at an Elevance Health location at least once per week, and potentially several times per week. Specific requirements and expectations for time onsite will be discussed as part of the hiring process. Candidates must reside within 50 miles or 1-hour commute each way of a relevant Elevance Health location. The health of our associates and communities is a top priority for Elevance Health. We require all new candidates in certain patient/member-facing roles to become vaccinated against COVID-19 and Influenza. If you are not vaccinated, your offer will be rescinded unless you provide an acceptable explanation. Elevance Health will also follow all relevant federal, state and local laws. Elevance Health is an Equal Employment Opportunity employer, and all qualified applicants will receive consideration for employment without regard to age, citizenship status, color, creed, disability, ethnicity, genetic information, gender (including gender identity and gender expression), marital status, national origin, race, religion, sex, sexual orientation, veteran status or any other status or condition protected by applicable federal, state, or local laws. Applicants who require accommodation to participate in the job application process may contact ******************************************** for assistance. Qualified applicants with arrest or conviction records will be considered for employment in accordance with all federal, state, and local laws, including, but not limited to, the Los Angeles County Fair Chance Ordinance and the California Fair Chance Act.

**MasTec Professional Services** provides end-to-end engineering, design, and integrated services to the power, oil & gas pipeline, and gas distribution industries across the country. With a genesis in construction and a skilled team of multidiscipline engineers and project management professionals, the company delivers best-in-class infrastructure solutions, including design, asset integrity management, feasibility studies, surveys, constructability reviews, turnkey delivery services, and more. MasTec Professional Services creates collaborative partnerships with clients by building trust and consistently delivering the highest standards of performance. MasTec Professional Services is a purpose-driven company. Our core values guide our strategy, performance, and culture. We believe in maintaining an environment where team members can make an impact, grow, and thrive. A place where they find meaning and purpose in doing the important work of ensuring communities have the vital energy, light, and communications to prosper. Our culture is inclusive and welcoming. Our teams are empowered with abundant training, tools, and opportunities to follow their curiosity and ambitions. Everyone has an equal chance to advance. Everyone is supported, respected, and challenged to be their best. We're always looking for talented and dedicated people to join us and love where they work. MasTec Professional Services is a proud subsidiary of MasTec (NYSE: MTZ), a Fortune 500 Company ranked by Energy News-Record as one of the leading contractors in the country. MPS is part of the MasTec Power Delivery segment. We are certified as a minority-controlled company by the National Minority Suppliers Development Council (NMSDC). Our rich diversity of people and ideas makes us a stronger, more innovative organization. **Job Summary** We are currently seeking a full Wetland Delineator/Environmental Scientist/Wetland Specialist/Permitting Specialist who will perform fieldwork for jurisdictional wetland surveys and waters, primarily in the Mid-Atlantic area especially for projects located in Pennsylvania and New Jersey. Candidate must also be willing to learn other aspects of the business which may not necessarily be related to wetland delineations work. Responsibilities + Perform fieldwork for jurisdictional wetland surveys and waters of the US. + Knowledgeable with the Philadelphia, Pittsburgh and Baltimore ACOE region regulatory requirements + Provide initial desktop investigations + Perform plant identifications, soil analysis and identify hydrological characteristics. + Prepare wetland reports summarizing field findings for soil types, vegetation and hydrological characteristics. + Provide wetland delineations and flagging. + Perform GPS location survey of wetland delineation flagging. + Perform preliminary field investigation for evidence of wetlands + Perform Joint permit applications. + Prepare Requests for Jurisdictional Determination to USACOE as needed. + Learn other aspects of the business Qualifications + Minimum 3 years of wetland delineation experience + S. or M.S degree in Environmental Science, Environmental Engineering, Biology, Ecology, Botany, Geology or related field + Strong knowledge of wetlands and aquatic resources + CADD experience a plus + Strong technical writing skills + Strong organization and time management skills. + Able to work under pressure and meet deadlines + Certified Professional Wetland Scientist or Delineator preferred but not required. + Rutgers University Wetland Training Certification a plus + Minimum 3 years of wetland delineation experience + S. or M.S degree in Environmental Science, Environmental Engineering, Biology, Ecology, Botany, Geology or related field + Strong knowledge of wetlands and aquatic resources + CADD experience a plus + Strong technical writing skills + Strong organization and time management skills. + Able to work under pressure and meet deadlines + Certified Professional Wetland Scientist or Delineator preferred but not required. + Rutgers University Wetland Training Certification a plus + Perform fieldwork for jurisdictional wetland surveys and waters of the US. + Knowledgeable with the Philadelphia, Pittsburgh and Baltimore ACOE region regulatory requirements + Provide initial desktop investigations + Perform plant identifications, soil analysis and identify hydrological characteristics. + Prepare wetland reports summarizing field findings for soil types, vegetation and hydrological characteristics. + Provide wetland delineations and flagging. + Perform GPS location survey of wetland delineation flagging. + Perform preliminary field investigation for evidence of wetlands + Perform Joint permit applications. + Prepare Requests for Jurisdictional Determination to USACOE as needed. + Learn other aspects of the business

Allegient Defense (DBA BCS Allegient) is a leader in advanced technology research and solutions development, and we are growing quickly. We are looking for a Scientist to support the Joint Program Executive Office for Chemical, Biological, Radiological and Nuclear Defense (JPEO-CBRND) Headquarters (HQ) in Edgewood, MD. This position is a fully onsite role. Essential Job Functions Provide technical guidance on threat defense programs, supporting risk planning, strategic execution, process improvements, and communication strategies. Provide expert guidance on protocol development, collaborate on test projects, assess program risks, and review reports and summaries. Provide scientific/technology advice, technical oversight, and acquisition support in the areas of science and technology availability, technology maturity, and applicability of proposed candidate CBRN detection, protection, and decontamination devices and systems through advanced development, production, and fielding. Provide technical knowledge to support the product team in establishing a link between early research and middle TRL, developing a robust research and/or test strategy, and defining project schedules. Conduct research projects to produce effective solutions for maintaining cost, schedule, and performance parameters. Review documentation pertaining to a range of scientific efforts addressing multiple threat types, providing feedback in support of program efforts. Prepare documentation/presentations to summarize technical results, to include displaying results in “layman's” terms, formulating conclusions, and developing technical strategies in response to the data outcomes. Maintain current knowledge on new technologies and methodologies that may benefit the program. Assist Government personnel in leading requirements generation efforts and development of Request for Proposals (RFPs), Request for Information (RFIs), and Statement of Objectives (SOOs). Advise Government personnel in the development and implementation of program planning, budgeting, and execution strategies, tracking and monitoring obligations and expenditures. Requirements A master's degree in chemistry, biology, or a related discipline, as well as twelve (12) years of general experience and eight (8) years of relevant experience At least eight (8) years of experience in acquisition of CBRN systems and portfolio management (i.e., investment decisions based on the risk management process). At least five (5) years of recent experience in protocol development and execution, advanced development specific to nerve agent, toxins, and/or biological or chemical related countermeasures inclusive of a general understanding of testing and manufacturing of chemical and biological threats. At least eight (8) years of experience working with decontamination or detection products, encapsulated products, and/or chemical or biological countermeasures. At least eight (8) years of experience in the discussion, preparation, and review of cycles required for program management, product development, acquisition program strategic planning, contract guidance, oversight, and advisory services. Eight (8) years of working experience with Microsoft Office, to include Outlook, PowerPoint, Excel, and Word.

Stefanini Group is looking for Scientist - West Chester, PA · The Scientist in Clinical Pharmacology and Pharmacometrics will be involved in the clinical pharmacology (CP) strategy, planning, direction, execution and data analysis/interpretation of clinical pharmacology studies. · The incumbent will participate to the CP activities for one or more programs in the early development portfolio and may represent the CP department at internal meetings (study, project, clinical team). · In addition, the incumbent will participate in the CP sections in documentation submitted to the regulatory authorities and in any required communication or interaction such as replies regarding CP questions during submissions. · This candidate will apply model based drug development concepts to impact decision making and is expected to have experience and relevant training in pharmacokinetics/pharmacometrics. · Candidates with less experience will be paired with a supervisor and will bear less responsibilities at the program level. · This is a full time position, less than 40 hours a week can be discussed/negotiated. Permanent hire for the right candidate is a possibility, contract is a minimum of 1 year. Qualifications • Education: • PhD in pharmaceutical sciences/pharmacology or other relevant life sciences. • PharmD (clinical pharmacology background/experience). • Problem solving skills. • Demonstrated ability to work in a team environment. • Ability to work in a complex multi-disciplinary and global environment. • English proficiency with strong presentation and communication skills. • Interest in clinical pharmacology and in clinical research (designing/managing clinical studies and Good Clinical Practices). • Experience in PK and or population PK/PD analysis (Phoenix WinNonlin training preferred, other modeling software a plus). • Minimum 2-3 years prior experience (including any post-doctoral project with Universities, Pharma or regulatory agencies) • Less experience acceptable especially with strong technical or clinical pharmacology skills

Method Development: Perform analytical method development utilizing instruments including LC, GC, LCMS, and ICPMS for raw materials and intermediates, in compliance with ICH standards and regulatory guidelines. Method Validation, Verification, and Transfer: Perform analytical method validations, method verifications, and method transfers utilizing LC, GC, LCMS, ICPMS, UV, IR, and KF instruments according to ICH and USP requirements while maintaining compliance with current regulatory trends. Phase-Appropriate Method Development and Validation: Perform phase-appropriate analytical method development and validation for Phase I, Phase II, and Phase III projects. Analytical Techniques and Instrumentation: Use HPLC, GC, LCMS, ICPMS, KF, ROI, UV, and IR instruments, with comprehensive knowledge in troubleshooting. Documentation and Reporting: Document and report preparation in compliance with GMP environments. Ensure adherence to regulatory guidelines and maintain accurate records for audits and inspections (FDA, EMA, and ICH regulations). Project Management and Coordination: Work closely with departments (Chemical Development, QC, Regulatory Affairs, Production, and QA) to ensure smooth cross-functional collaboration, drive projects forward to meet timelines and regulatory standards. Manage priorities, troubleshoot challenges, and facilitate effective communication between teams. Training and Compliance: Maintain proper personal training records and ensure compliance with all required SOPs and regulatory guidelines. Client and Team Interaction: Coordinate between departments to ensure smooth project execution. Manage cross-functional teams, address client needs, and maintain strong communication to meet project timelines. Ensure project objectives align with regulatory and compliance standards. Handle and analyze controlled substances and high-potent compounds in compliance with regulatory and safety guidelines. Adhere to DEA regulations, GMP standards, and other regulatory requirements. Work properly in a controlled substance environment. Use Empower(Waters), and LIMS, Master Control, and Track Wise software. EDUCATION AND EXPERIENCE REQUIREMENT: Requires a Bachelor's degree in Pharmacy and 3 years of experience in job offered or 3 years of experience in the Related Occupation RELATED OCCUPATION: Scientist or any other job title performing the following job duties: Method Development: Perform analytical method development utilizing instruments including LC, GC, LCMS, and ICPMS for raw materials, in-process samples, API's and Drug products, in compliance with ICH standards and regulatory guidelines. Method Validation, Verification, and Transfer: Perform analytical method validations, method verifications, and method transfers utilizing LC, GC, LCMS, ICPMS, UV, IR, and KF instruments according to ICH and USP requirements while maintaining compliance with current regulatory trends. Analytical Techniques and Instrumentation: Use HPLC, GC, LCMS, ICPMS, KF, ROI, UV, and IR instruments, with comprehensive knowledge in troubleshooting. Documentation and Reporting: Document and report preparation in compliance with GMP environments. Ensure adherence to regulatory guidelines and maintain accurate records for audits and inspections (FDA, EMA, and ICH regulations). Project Management and Coordination: Work closely with departments (Chemical Development, QC, Regulatory Affairs, Production, and QA) to ensure smooth cross-functional collaboration, drive projects forward to meet timelines and regulatory standards. Manage priorities, troubleshoot challenges, and facilitate effective communication between teams. Training and Compliance: Maintain proper personal training records and ensure compliance with all required SOPs and regulatory guidelines. Coordinate between departments to ensure smooth project execution. Managed cross-functional teams, address FDA queries, and maintain strong communication to meet project timelines. Ensure project objectives align with regulatory and compliance standards. Handle and analyze controlled substances and high-potent compounds in compliance with regulatory and safety guidelines. Adhere to DEA regulations, GMP standards, and other regulatory requirements. Work properly in a controlled substance environment. Use Empower(Waters), LIMS and PRAGMA software. SALARY RANGE: $81,806.00 to $108,000.00/year JOB TIME: Full Time #LI-DNI

Founded in 1950, CDI Corporation is an Engineering and Technology Services Firm providing client-focused solutions in select global industries. CDI provides Global Engineering and Technology Solutions and Professional Staffing Services through its global business operations. The Company also provides staffing services through its franchised Management Recruiters International, Inc. (MRI) operating unit. Job Description Our Client: The company is a prominent maker of medical diagnostics equipment and its medical health-care division, which generates about 12 percent of the company's total sales, is its second-most profitable unit, after the industrial automation division. The company is a component of the Euro Stoxx 50 stock market index. Qualifications Job Title: Scientist 1 - JOB ID SIMNJP00038611 Location: Newark, DE 19702 Type: 11 Months Contract Potential to Convert to Full time: Yes Position Overview: • Bachelor's degree in Biochemistry, Chemistry, Biology, Medical Technology. • Provides assistance in research, analysis, and experimentation for product and process development of clinical chemistry methods. Assists with assay validations and routine tests following written protocols. • Familiar with making up chemical solutions, use of typical laboratory equipment, some clinical chemistry analyzer familiarity a plus, but not required. • Obtains, correlates, and analyzes technical information needed to accomplish routine tasks. Provides assistance in preparing reports, charts, graphs, and other documents. • Good working knowledge of MS Word and Excel, basic understanding of statistics. • Weekend and off day shift may be required. Additional Information If you're interested you can contact me ************** / ************ Look for MARTHA

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Perform routine cGMP testing of samples for biopharmaceutical clients in a BSL-2 laboratory which may include HPLC, SEC, peptide/oligosaccharide mapping, turbidity, and/or osmolality Troubleshoot assay or instrumentation problems Conduct analysis and reporting of data in accordance with requirements set forth by the department in electronic notebooks Apply GMP/GLP in all areas of responsibility, as appropriate Demonstrate strong client service skills, teamwork, and collaboration Proactively plan and multitask to maximize productivity Meet all quality and productivity metrics Qualifications Basic Minimum Qualifications: Bachelor's degree in Engineering or Biochemistry, or other related scientific concentration with 3 years industry experience, OR Relevant Masters with 1 year industry experience, OR PhD. Authorization to work in the United States indefinitely without restriction or sponsorship Basic understanding of Chemistry of amino acids and protein structure Knowledge of LC and LC/MS preferred Operate automation equipment using established protocol Method development experience preferred Additional Information This position is Full-Time, Monday - Friday, 9:00 a.m. - 5:00 p.m. with overtime as needed and the potential for some off shift hours as dependent on project. Candidates currently living within a commutable distance of Malvern, PA are encouraged to apply. Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Perform routine cGMP testing of samples for biopharmaceutical clients in a BSL-2 laboratory which may include HPLC, SEC, peptide/oligosaccharide mapping, turbidity, and/or osmolality Troubleshoot assay or instrumentation problems Conduct analysis and reporting of data in accordance with requirements set forth by the department in electronic notebooks Apply GMP/GLP in all areas of responsibility, as appropriate Demonstrate strong client service skills, teamwork, and collaboration Proactively plan and multitask to maximize productivity Meet all quality and productivity metrics Qualifications Basic Minimum Qualifications: Bachelor's degree in Engineering or Biochemistry, or other related scientific concentration with 3 years industry experience, OR Relevant Masters with 1 year industry experience, OR PhD. Authorization to work in the United States indefinitely without restriction or sponsorship Basic understanding of Chemistry of amino acids and protein structure Knowledge of LC and LC/MS preferred Operate automation equipment using established protocol Method development experience preferred Additional Information This position is Full-Time, Monday - Friday, 9:00 a.m. - 5:00 p.m . with overtime as needed and the potential for some off shift hours as dependent on project. Candidates currently living within a commutable distance of Malvern, PA are encouraged to apply. Excellent full time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Who We Are:

Our mission is to inspire children through science, sparking lifelong imagination and curiosity. For over 25 years, we have delivered unique, hands-on science experiences for children through our after-school programs, birthday parties, workshops, special events, and summer camps. Our innovative programs are as entertaining as they are educational! Mad Science is the world's leading provider of fun science programs for elementary-aged children. As a Mad Scientist, you will lead students through an inquiry-based discovery method involving instructor demonstrations, hands-on activities, and amazing take-home projects that will illustrate how science affects the world around us. Build and fly rockets, demonstrate lasers, explore the states of matter using dry ice, and create slime and other polymers. You will inspire the next generation of scientists through our innovative activities that show kids what science is really about. Responsibilities Facilitate a one-hour after-school science enrichment program using a pre-set curriculum. · Attend orientation and training prior to starting your programs.· Ensure the safety of the kids during programs· Engage with the kids during the activities and experiments. The goal is for the the kids to have fun, not sit through a lecture.· Must be able to lift equipment in kits, can vary in size and weight (heavier kits have wheels). Your vehicle must be able to accommodate the equipment. · Must be able to drive to and from the program with your own vehicle. Programs near you include locations in Haddonfield, Moorestown, and more. Schedule and Pay- You will be scheduled at a school close to you where you will report to at the same day and time each week for either 6 or 8 consecutive weeks. Programs typically start at between 3-3:45PM and last 1.5 hours. - $40 for a 1.5 hour program- Mileage is compensated for any program over 25 miles round trip. Qualifications- Must have experience working with children.- Your own reliable car and license.- Must be over 18 years of age. - Must be vaccinated for COVID-19.- A background in science and/or experiencing performing is a plus! Compensation: $40.00 per hour Mad Science is a powerhouse brand with locations around the globe! For over 35 years, we have sparked imaginative learning through our summer camps, birthday parties, in-class workshops, after-school programs, and special events for kids ages 3-12. Become part of our team and help us inspire the next generation of scientists and engineers. Our locations are always looking for part-time instructors and full-time office staff.

Title: Scientist Locati on: Exton, PA Full-time Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials. Position Summary: We are seeking a highly skilled and motivated Scientist with experience in flow cytometry to join our team. The successful candidate will play a crucial role in the execution and analysis of experiments related to cellular analysis with the guidance of the team lead. This position offers an exciting opportunity to contribute to cutting-edge drug development in a fast-paced and collaborative environment. Position Responsibilities: Develop and optimize flow cytometry protocols for the detection and quantification of specific cellular markers and analytes. Perform sample preparation, staining, data acquisition, and analysis using flow cytometry platforms. Ensure adherence to quality control measures, troubleshoot technical issues, and implement corrective actions. Collaborate with cross-functional teams to support project goals, provide scientific expertise, and contribute to the development of new assays and methodologies. Maintain accurate records of experiments, protocols, and results in accordance with company policies and regulatory requirements. Participate in the training and supervision of junior staff members, fostering a collaborative and productive work environment. Position Requirements: BS or MS in Biology, Immunology, Biochemistry, or a related field. Experience in the design, execution, and analysis of flow cytometry experiments, including multi-color panel design, compensation, and gating strategies. Experience with cell-based assays and knowledge of cellular markers, surface antigens, and intracellular targets. Hands-on experience with flow cytometry instrumentation (e.g., BD FACSCanto, FACSLyric, BC Navios, CytoFLEX, Cytek Aurora). Data Analysis and template design for multiparameter flow cytometry panels using dedicated analysis platform, (FlowJo, Kaluza, FCSExpress) Experience in performing ligand binding assays, including assay optimization, data analysis, and troubleshooting. Excellent organizational skills, attention to detail, and the ability to manage multiple tasks simultaneously. Strong teamwork and collaboration skills, with the ability to work effectively in a cross-functional environment. Salary and Benefits : Frontage Laboratories offers a competitive compensation and benefits package including health and dental insurance, a 401(k) plan, disability insurance, and life insurance. Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.