Chemist jobs in Philadelphia, PA

Compensation & Details: 2 Openings Fully onsite role in Malvern, PA - in the laboratory $35-39/hr - exact rate is based on several factors, including skills, experience, and education. Benefit packages for this role will start on the 1st 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 10 PTO Days & 6 Sick Days 12 month extending contract Requirements: Minimum two (2) years of relevant work experience Experience in Medical Device, Biopharmaceutical, or Pharmaceutical industry Working experience in a current Good Manufacturing Practices (cGMP) compliant QC laboratory or equivalent environment and solid understanding of cGMP and current Good Laboratory Practices (GLPs) Must have experience in the following: qPCR, cell culture, Flow Cytometry, and/or ELISA Ability to read/interpret technical documents such as SOPs, work instructions, test methods and protocols Proficient with Microsoft Office applications (Outlook, One Note, Teams, Excel, Word, and PowerPoint) Day to Day: The QC CRS Analyst is responsible for conducting biochemical and testing of drug substance, final product release and characterization samples, and critical reagent qualifications of cell and gene therapy products, including CAR-T. They are responsible for ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations. They typically work with a team of 10 - 15 other Analysts within a functional Clinical Release and Stability (CRS) Laboratory and report to one of two QC CRS Supervisors. Key Responsibilities: Conduct analytical biological testing (ELISAs, qPCR, Flow Cytometry, Cell-based assays, etc.) of clinical and commercial drug product/drug substance samples Perform peer reviews and approvals of laboratory data Use electronic systems (LIMS, MES, Empower, etc.) for execution and documentation of laboratory data Support of New Product Initiatives (NPI) in groups of 3-6 analysts Perform Instrument Calibration and/or Preventative Maintenance, as needed Update CRS-owned documents using the Electronic Document Management System (EDMS) Order/receive supplies and manage inventory Support analytical method qualification, validation, and transfer into and out of the QC lab, owning change control actions, completing testing activities with mentorship from Sr. Analysts on transfer activities Complete change control processes to integrate new methodologies and technologies into and out of the CRS Lab with limited oversight Complete invalid assay and general laboratory investigation records Complete corrective and preventative actions (CAPA) as assigned Assist in the execution of internal audits

At Quaker Houghton, we are experts in the development, production and application of chemical specialties, process fluids, lubricants and coatings for the manufacturing industry. We have been an integral part in the growth of the worlds largest industrial companies and to this day our experience and expertise show in the actions and dedication of our Associates worldwide. Today, we have a global presence, with our corporate headquarters located in Conshohocken, PA. Quaker Houghton is a global publicly traded company with a unique collaborative culture that supports career growth for its associates and offers competitive compensation and benefit programs. Summary: Quaker Houghton is seeking a Development Chemist III to work in our Metalworking Fluid Development Laboratory in Conshohocken, PA. The laboratory supports multiple metalworking fluid product lines including soluble oils, semi-synthetics, and full synthetics. An individual in this role will be responsible for conducting product development, research projects, and product support for Quaker Houghton metalworking fluids. This will require working closely with commercial associates, other RD&E teams, customers, and external partners to design new products and execute tests both in the laboratory and in the field. We are seeking experienced candidates who are highly motivated, have strong collaboration skills, are creative problem solvers, and communicate effectively. What will you do? * Use knowledge of colloid chemistry, tribology, and testing techniques to formulate metalworking fluids that will meet customer needs and provide solutions to application problems. * Work independently with minimal guidance from the laboratory manager. * Act as a mentor to junior development chemists. * Maintain a clear and orderly record all observations and data. * Write detailed reports summarizing product development efforts, laboratory testing, and troubleshooting. * Perform customer requested product analysis and testing to answer questions and address problems at commercial accounts. * Provide legal and archival documentation for patent applications. * Comply with safety regulations and lab procedures. * Provide technical service and knowledge to customers and sales associates based upon the chemists current level of expertise. Visit customers when required. * Provide assistance to Manufacturing to improve the quality and efficiency of the manufacturing process. Assist Manufacturing and the Quality Assurance lab in solving quality and production problems. * Comply with safety regulations and make recommendations towards the improvement of safety and environmental concerns. * Follow all ISO quality and environmental standards as provided in the various procedural manuals. Ensure that all laboratory equipment is calibrated and functioning properly. Education, Experience, Skills & Competencies: * This position requires a Bachelor Degree in Chemistry or equivalent with at least 7 years of experience, a Masters Degree in Chemistry or equivalent with at least 5 years of experience, or a Doctor of Philosophy in Chemistry or equivalent with at least 3 years of experience. * Knowledge of colloid chemistry, surfactants, and tribology is required. * Experience with the formulation of metalworking fluids and field support of machining and grinding operations is highly desired. * Understanding of applied statistics and experimental design is not required, but highly desired. * Must have the ability to operate in a fast-paced environment, to work on different projects at the same time, and to think analytically. * Must have good prioritization and communication skills (oral and writing). * Ability to write detailed reports and presentations which may be used to inform high-ranking members of the Technical Community. What's in it for you: * Competitive pay programs with excellent career growth trajectory * Opportunities to see your efforts contribute toward the success of the business * Work for a global leader in the industrial process fluids industry Quaker Houghton is an equal opportunity employer committed to creating a diverse workforce. Quaker Houghton provides equal employment opportunity for all qualified candidates. Quaker Houghton does not discriminate against any candidate for employment based on race, color, religion, sex, gender, gender identity or expression, affectional or sexual orientation, pregnancy, age, creed, ancestry, national origin, citizenship, marital or domestic partnership or civil union status, veterans status, physical/mental disability, genetic information, or any other category protected by U.S federal, state, and/or local employment law. Furthermore, Quaker Houghton is committed to providing reasonable accommodations to qualified candidates with physical and/or mental disabilities. Applicants with a disability who need assistance applying for a position may email

Since 1869 we've connected people through food they love. We're proud to be stewards of amazing brands that people trust. Our portfolio includes the iconic Campbell's brand, as well as Michael Angelo's, Pace, Pacific Foods, Prego, Rao's Homemade, Swanson, and V8. In our Snacks division, we have brands like Cape Cod, Goldfish, Kettle Brand, Lance, Late July, Pepperidge Farm, Snack Factory, and Snyder's of Hanover. Here, you will make a difference every day. You will be supported to build a rewarding career with opportunities to grow, innovate and inspire. Make history with us. Why Campbell's… Benefits begin on day one and include medical, dental, short and long-term disability, AD&D, and life insurance (for individual, families, and domestic partners). Employees are eligible for our matching 401(k) plan and can enroll on the first day of employment with immediate vesting. Campbell's offers unlimited sick time along with paid time off and holiday pay. If in WHQ - free access to the fitness center. Access to on-site day care (operated by Bright Horizons) and company store. Giving back to the communities where our employees work and live is very important to Campbell's. Our "Campbell's Cares" program matches employee donations and/or volunteer activity up to $1,500 annually. Campbell's has a variety of Employee Resource Groups (ERGs) to support employees. How you will make history here... The Associate Scientist R&D will be responsible for supporting the Research & Development activities on the Fresh & Frozen Bakery and Cookies Product Development Teams. In this role you will be supporting projects across the Bakery and Cookie Categories, primarily the Pepperidge Farm brand. The scope of the job encompasses supporting the entire Product Development process from idea conception through plant commercialization. What will you do... The Associate Scientist will be responsible for supporting benchtop, pilot plant, and ad-hoc project support. The individual may also work in a lab-based setting using applicable analytical testing equipment. They will be responsible for assisting with research, gathering and analyzing data and reporting findings on assignments/projects that are moderately complex. The Associate Scientist will perform a variety of duties requiring the application of technical knowledge using established processes/protocols. They will independently plan, prioritize, and execute work making basic technical decisions independently. Their day-to-day job responsibilities will require them to work in a team environment ensuring alignment with cross-functional partners, both internal (Marketing, Quality Assurance, Process Development, Packaging Development, Finance, Operations, and Procurement) and external (vendors/suppliers, Campbell's, co-manufacturers). They must be knowledgeable about experimental design (DOE), laboratory documentation, and general food science. Primary Responsibilities Support Product Development Scientists with sandboxing/product ideation, product feasibility testing, plant trials, start-ups, productivity and quality programs. Assist with the assessment and validation of formulations from benchtop through commercialization with support and coaching from R&D manager. Project types include: New product development Cost savings opportunities Quality improvement projects Business continuity initiatives Ensure all proper documentation is done accurately and on schedule, inclusive but not limited to: Pre and post-trial documentation and communication to cross functional team Electronic lab notebook maintenance of formula testing and results Ability to interact and communicate effectively (written and verbal) Conduct and maintain Quality Analytical Testing Data for Product Development team as needed. Apply problem solving skills to identify, interpret and analyze the correct data and provide detailed directions to development projects. Leveraging external suppliers to build knowledge to deliver results Maintain benchtop workspace cleanliness and order Easily adapts to changing priorities. Who you will work with... R&D management, scientists, product development and cross-functional team members. What you will bring to the table... (Required Skills) Bachelor's degree required from an accredited institution in science related field (Food Science, Engineering; or related field) 6 months to 2 years of related experience with a consumer-packaged goods background. Experience in a combination of any of the following: Snacks (such as crackers, chips, pretzels, and cookies) and Bakery (such as breads, buns/rolls, and cakes/frozen desserts). Handle allergens including dairy, peanuts, tree nuts, soy, wheat, eggs and other food ingredient chemicals and allergens while wearing appropriate PPE. Excellent analytical skills, strong attention to details, self-driven, ability to deal with ambiguity, good communication and interpersonal skills. Ability to handle multiple assignments at any given time in a team environment. Experience with Microsoft Office - including formula, data, graph application a plus Must be able to lift up to 40 lbs Anticipated travel up to 25% Compensation and Benefits: The target base salary range for this full-time, salaried position is between $57,800-$83,100 Individual base pay depends on work location and additional factors such as experience, job-related skills, and relevant education or training. Total pay may include other forms of compensation. In addition, we offer competitive health, dental, 401k and wellness benefits beginning on the first day of employment. Please ask your Talent Acquisition Partner for more information about our total rewards package. The Company is committed to providing equal opportunity for employees and qualified applicants in all aspects of the employment relationship, including consideration for employment, without regard to race, color, sex, sexual orientation, gender identity, national origin, citizenship, marital status, protected veteran status, disability, age, religion, or any other classification protected by law.

Veolia is a global leader in environmental services, operating across all five continents with nearly 218,000 employees. Specializing in water, energy, and waste management, Veolia designs and implements innovative solutions for decarbonization, depollution, and resource regeneration, supporting communities and industries in their ecological transformation. Within this framework, Water Tech brings together a dedicated team of experienced professionals committed to tackling the world's most complex challenges related to water scarcity, quality, productivity, and energy. Together, we pursue a shared mission to create a more sustainable future. Job Description As a Junior Process Chemist, you will work closely together with the Manufacturing plants, Technology, Global Engineering and Regional Quality and EHS functions to support variable process chemistry activities related to high risk operations and chemical manufacturing operations. You will coordinate the NAM tolling activities for products for which Veolia does not have the in-house capabilities. In this critical role, you'll provide technical guidance, direction and training to plant staff and operators on process chemistry and process safety, ensuring awareness and adhesion to operational parameters and safety limits. You'll lead and provide onsite support for new and/or improved processes, provide on-time coverage for troubleshooting, participate in root cause analysis and implement corrective and preventive actions. Additionally, you will be responsible for supporting different new business opportunities, manufacturing process optimization, and cost-out initiatives in the business. If you like the idea of doing meaningful work with a company that's doing big things to create a cleaner, more sustainable world for us all, here's more! Key Characteristics: Serves as regional process chemistry expert, representing global standards in meetings and projects while ensuring safety requirements and operational consistency across manufacturing sites. Leads tolling strategy and execution, including supplier qualification, SOP development, audits, and scale-up support to optimize cost and quality outcomes. Champions process safety initiatives and continuous improvement through implementation of hazardous material standards, safety programs, and lean/digital optimization methods. Duties & Responsibilities Represent Global Process Chemistry in team meetings and projects to ensure process chemistry and process safety requirements are covered from a regional point of view while ensuring consistency with global standards. Support Cost-out initiatives by investigating the best operational strategy, in-house production vs tolling. Coordinate the regional tolling activities by assembling and providing toll manufacture SOPs, conducting onsite EHS and Quality audits, and following up on completion of corrective actions. Being a critical part of the qualification team through the entire qualification process, providing guidance and support during scale-up trials, ensuring safe operation, and delivering products meeting quality expectations. Implement the company's internal standards for hazardous processes (e.g. flammable materials, combustible dust handling and neutralization reactions) in cooperation with the Process Safety Chemist and support the manufacturing sites during plant upgrades. Implement, maintain, and improve all aspects of the company's process safety program. Drive and support continuous system and process improvements based on Digitization and Lean Six Sigma methodology. Qualifications Knowledge, Skills & Abilities: Knowledge: Expert understanding of process chemistry principles and global safety standards Comprehensive knowledge of chemical manufacturing processes and hazardous material handling In-depth understanding of quality management systems and audit procedures Advanced knowledge of Lean Six Sigma methodology and digital optimization tools Thorough understanding of tolling operations and supplier qualification processes Skills: Ability to develop and implement process safety programs and protocols Proficiency in conducting EHS and quality audits Strong analytical skills for cost-benefit analysis and operational strategy development Excellence in SOP development and documentation Advanced project management capabilities Skilled in digital tools and process improvement methodologies Abilities: Capacity to lead cross-functional teams and influence stakeholders Ability to balance multiple projects while maintaining attention to detail Capability to translate technical requirements into practical applications Strong problem-solving abilities in complex manufacturing environments Excellent communication skills for presenting technical information to various audiences Education & Experience Required: Master's Degree in Science, Chemistry, or Chemical Engineering (or equivalent experience) Proven experience with chemical plant processes and process safety protocols Demonstrated ability to develop and conduct Process Safety training programs Track record of promoting and maintaining safety compliance culture in chemical industry settings Experience in conducting quality and compliance audits Strong verbal and written communication skills Willingness and ability to travel up to 10% of time Preferred: Two (2) years of professional experience with chemical manufacturing operations Knowledge of industry safety standards and regulations Familiar with NFPA 30 standard, OSHA regulations, Process Safety Management Familiar with Brilliant fulfilment / Lean Manufacturing / Six Sigma Expertise with chemical process instrumentation Knowledge of SAP is helpful Additional Information At Veolia, we realize diverse teams make smarter decisions, deliver better results, and build stronger communities. We're an organization that champions diversity and inclusion at every rung of the ladder and are proud to be an equal opportunity workplace. ● Medical, Dental, & Vision Insurance Starting Day 1! ● Life Insurance ● Paid Time Off ● Paid Holidays ● Parental Leave ● 401(k) Plan - 3% default contribution plus matching! ● Flexible Spending & Health Saving Accounts ● AD&D Insurance ● Disability Insurance ● Tuition Reimbursement Disclaimer: The salary, other compensation, and benefits information is accurate as of the date of this posting. The Company reserves the right to modify this information at any time, subject to applicable law. ****Applicants are required to be eligible to lawfully work in the U.S. immediately; employer will not sponsor applicants for U.S. work authorization (e.g. H-1B visa) for this opportunity**** VWTS does not accept unsolicited resumes from external recruiting firms. All vendors must have a current and fully executed MSA on file before submitting candidates. Any unsolicited resumes and candidate profiles will be deemed the property of VWTS, and no fee will be due. As an inclusive company, Veolia is committed to diversity and gives equal consideration to all applications, without discrimination.

Empower, Innovate, Impact! At Team A-TEK, we EMPOWER people to drive INNOVATION that IMPACTS mission! A-TEK operates at the intersection of mission and innovation by applying our deep domain expertise across the federal markets. Embracing our digital-first strategy, A-TEK provides enhanced capabilities in application development, digital transformation, enterprise IT, and scientific services. Our solutions are designed to modernize, automate, secure, protect, and enhance the operations of our federal clients, ensuring they stay ahead in a rapidly evolving digital landscape. Our work is fueled by a passion to serve our clients' needs and to protect the safety and welfare of Americans. That passion shapes how we nurture our most valuable asset - Our Employees. A-TEK actively cultivates the talent that drives our success and fosters a creative, challenging, and mission-driven work environment for current and future employees. This position will be responsible for performing non-research molecular testing of samples for potentially containing biological threat agents. Ensures incoming operational, QA, and other sample types are processed while maintaining chain of custody. Prepares reports, answers questions, troubleshoots, and makes recommendations to the supervisor for inclusion in comprehensive reports. Maintains and operates equipment properly and in a safe manner, including performing routine calibrations and adjustments. Performs all procedures in accordance with proper handling and storage of various materials. Additionally, will be responsible for maintaining knowledge and skills related to position and program. Laboratory operations are 7 days a week. Team members take turns with weekends and holidays to ensure results are reported each day. In the event of a public health emergency, extended work hours and alternative shift work may be required to maintain temporary emergency 24/7 operations. Kindly be aware that a pre-employment drug screening is a requirement. REQUIRED QUALIFICATIONS: Bachelor's degree from an accredited university in microbiology, molecular biology, or related course work in biological sciences. REQUIRES at least one year of laboratory bench experience, utilizing PCR, aseptic techniques and experience with biological assays. Laboratory training that is assigned or accompanies an associated course is not considered applicable training. Biological Safety Level (BSL)-3 experience is highly desirable. This position supports a federal contract which requires that all employees and job applicants hold a valid Green Card or US Citizenship at the time of application. #LI-OnSite A-TEK, Inc. is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or status as a qualified individual with a disability, or Vietnam era or other protected Veteran status. Verification of education may be requested before or during the hiring process.

Job DescriptionSummary: QC Chemist:This position's purpose is to support the Quality Control lab for analysis of purified water, raw materials, finished and stability samples. Essential Duties and Responsibilities: QC Chemist Sample of Raw materials and Purified water for Analysis Arrange retain samples for raw materials and finished products Performing daily analytical balance verification- as required Performing calibration of pH meters and Fluoride Ion meters as required Preparation and standardization of Volumetric solutions and test solutions as required Arranging chemicals in the lab and checking for their expiration dates as required Arranging quality control documents as needed as required Performing wet analysis for raw materials and finished products, which includes Loss on drying, Viscosity, pH and water content etc. Performing chart replacement for all chart records which monitor temperature and humidity as required. Perform analysis using HPLC/UV-Visible spectrophotometer for raw materials, finished products and stability samples. Qualifications: QC Chemist: Ability to apply comprehensive knowledge of pharmaceutical cGMP's and quality system controls, procedures and records to ensure ongoing quality compliance. Ability to perform all requirements independently with limited managerial oversight. Excellent organizational abilities to meet accelerated timelines, manage multiple shifting priorities and maximize efficiencies in a dynamic customer-focused environment. Superior attention to detail to ensure accuracy of work product. Superior critical-thinking and problem-solving skills; ability to recognize and resolve discrepancies and issues. Education/Experience: QC Chemist: Minimum 2 years industrial experience in Quality Control laboratory functions. Degree (BS or BA) in Biology, Chemistry, Biochemistry, or relevant related field. Or sufficient technical depth or professional experience will be considered in lieu of technical degree. Experience in quality systems, including validation, documentation, compliance department preferred. HPLC analytical experience is a plus. Onsite Personnel is an equal opportunity employer committed to hiring a diverse workforce in an inclusive culture environment. Onsite Personnel does not discriminate based on disability, veteran status or any other basis protected under federal, state, or local laws.

Job Details Corporate Headquarters - Bristol, PA Full Time Graduate Degree Up to 25%Description ***ALL UCT FACILITIES ARE SMOKE & TOBACCO FREE** (pre-employment includes successfully passing drug/nicotine screening, physical and background check) Searching for a full-time Environmental R&D Chemist. Please read the full job description prior to applying for this position United Chemical Technology (UCT) was founded in 1986 by one of the pioneers of Solid Phase Extraction (SPE), Michael Telepchak, who is still active in the Company and continues to works with our team of talented chemist in our research and development department. UCT is a major competitor in the field of silica based phase extraction technology and silane manufacturing. UCT's mission is to establish and maintain a leadership position in the specialty chemical market for organosilicon products. Our products serve the environmental, forensics, food and beverage, clinical, pharma and cannabis industries. As a company, we consistently strive to distinguish ourselves from competitors in terms of service, pricing and quality. To accomplish this goal, we continue to invest in the best people, providing them with the finest tools available. Through excellence, UCT is committed to meeting not only the customer's needs of today but also those of tomorrow. An opportunity has arisen at our corporate headquarters in Bucks County, PA for a full-time, Environmental R&D Chemist with a focus on sample preparation, method development, use of solid phase extraction and QuEChERs for food safety, cannabis and environmental testing, some research, and who has a solid background with GCMS & LCMS instrumentation. SUMMARY: Primarily responsible for performing routine tests and analysis related to research and development projects. Other responsibilities include archiving test data, troubleshooting analysis problems, method development, sample prep and maintenance of the R&D lab. DUTIES & RESPONSIBILITIES: Perform routine solid phase extractions on a variety of matrices. The successful candidate will play a key role in analyzing and quantifying PFAS compounds across various environmental matrices. This includes conducting laboratory testing, implementing established methods, and maintaining instrumentation to ensure accurate and reliable data on PFAS levels in different samples. Plan and execute method development, method validation and method transfer studies, independently and as part of a team. Assist in the development of new methods to address customers and/ or client's needs or specific requests using existing sample preparation and chromatography products. Operate and maintain analytical instruments including GC-MS, GC-MS/MS and LC-MS/MS Stay up to date with US FDA and EPA guidelines and other industry regulations to ensure UCT products can be used in future methods for food safety, cannabis and environmental testing that involve the use of solid-phase extraction, QuEChERS, and GC-MS or LC-MS analysis. Provide technical laboratory support for research projects involving food safety, environmental testing (e.g., water testing) and cannabis. Execute presentations, training, and educational seminars geared towards food safety, cannabis and environmental markets when called upon. Assist the Quality Control and Production teams as needed to assess the effectiveness and cleanliness of select UCT consumables and sorbents that are commonly utilized in food safety, cannabis, and environmental testing. Must be familiar with basic chemical principals. Design and troubleshoot research projects with assistance from the R&D Manager. Ensure thorough documentation of laboratory activities and experimental data; analyze results using appropriate statistical or analytical methods to support project objectives. Detail-oriented candidate with strong organizational skills and the ability to manage multiple tasks and project simultaneously. Support fellow chemists in maintaining laboratory operations in accordance with established safety guidelines. Excellent verbal and written communication skills; scientific writing experience preferred. Positive attitude and the ability to work both independently and within a multidisciplinary team. Self-motivated individual capable of working efficiently with limited supervision. Qualifications Skills and Abilities: Excellent verbal and written communication skills; scientific writing experience preferred. Positive attitude and the ability to work both independently and within a multidisciplinary group. Must be a highly motivated individual, a self-starter, and be able to work under minimal supervision. Comfortable with public speaking, to include executing or facilitating presentations as it relates to educational or training seminars. Detail-oriented personality with the ability to manage multiple tasks/projects simultaneously. Required Education and Experience: Bachelor's degree in Chemistry, Environmental Science or Food Safety. or a related field; master's degree preferred Minimum of two years method development and/or environmental laboratory experience . Minimum of two years of GC-MS and/or LC-MS experience is required. Prior experience working with sample prep wuch as solid-phase extraction and QuEChERS. Familiarity with US EPA Analytical Methods and US EPA validation guidelines for the analysis of drinking water, wastewater and solid waste extraction, specifically the ************** and 8000 series, and the Unregulated Contaminant Monitoring Rule (UCMR) program, preferred not required. Competitive salary and a comprehensive benefit package. ***Qualified candidates must be eligible to work in the U.S.*** UCT is committed to the principles of equality in employment. It is contrary to our policy to discriminate against individuals because of race, color, creed, ethnicity, religion, ancestry, age, national origin, sex (including childbirth, or related medical conditions), sexual orientation, gender identity or expression, genetic information, physical or mental disability, union affiliation, citizenship status, marital status, pregnancy, military or veteran status or any other status prohibited by applicable federal, state or local law (“protected category”). Equal employment opportunity applies to all terms and conditions of employment, including hiring, placement, promotion, termination, layoff, recall, transfer, leave of absence, compensation, and training. UCT explicitly prohibits any form of unlawful employee harassment or discrimination based on any of the characteristics mentioned above. Improper interference with the ability of other employees to perform their expected job duties will not be tolerated.

Education, Experience, and Skill Requirements * Minimum 5 years relevant lab experience, Associate's degree with 2 yrs relevant Lab experience, or a Bachelor of Science degree in Chemistry * Prior CFR experience preferred - operating and/or maintaining * General mechanical aptitude - ability to perform basic troubleshooting/repair of equipment * Proficient with Microsoft Word, Outlook, and Excel, IT Skills - understanding data bases, Laboratory Information Management Systems (LIMS) and instrumentation networking. * Demonstrated proficiency in all of Role Specific Competencies. * This is a shift-work job that requires flexibility to work days, nights, weekends, and holidays. Key Role Description Assists with Lab technical activities related to all of the refinery processes and products including test methodology, equipment purchases, and equipment calibration and repair. Assists in managing daily operations to insure quality of results, efficient management of inventory to maintain continuity of operations, and the storage and handling of samples for regulatory compliance and inspection purposes. Role Specific Competencies At Monroe, we have identified nine specific competencies we expect all employees of our organization to possess. These competencies are incorporated as a part of our Selection, Performance Management/Review and Developmental processes. The competencies and activities for this role are detailed below: Technical Knowledge - demonstrates the specific skills necessary for the assignments, understands the background and points of leverage to be effective in the role. * Performs technical work in analytical or physical chemistry involving a variety of standardized chemical and physical tests. * Monitors a specialized unit of a laboratory section or the operations of several units or performs complex and specialized chemical laboratory tests. * Conducts analytical and physical tests on finished products. * Requisition and maintainenance of chemistry supplies and equipment. * Conducts analytical or physical testing of a variety of materials. Knowledge of Work Areas and Responsibilities - demonstrates a clear understanding of role and responsibilities within specific area, flexible and agile in adapting to changes or exploring opportunities and challenges. * Maintains schedule flexibility to meet the needs of the business: extended hours, evenings and/or weekends. * Performs special projects as assigned by the Lab Leader. * Attends operational meetings as needed. Communications - Verbal and Written - includes written and verbal communications, delivers presentations and has good listening skills. Problem Solving and Conflict Leadership - strives to understand contributing factors, works to resolve complex situations, and helps individuals to resolve conflicts. Delivering Results - Sense of Urgency - defines appropriate goals, works toward achieving goals, articulates vision and steps for achievement, meets deadlines and provides timely status updates and follow-through. Teamwork/Cooperation - accountable to team, works to meet established deliverables, appreciates view of team members and is respectful of others. Initiative - takes action, seeks new opportunities, and strives to see projects to completion. Work Reliability/Quality - strives to eliminate errors, accurate work is a priority, and seeks opportunities to improve product/services. Integrity and Trust - honest, accountable, upholds ethics standards and maintains confidentiality.

Job Title: QC ChemistJob Description We are seeking a skilled QC Chemist who practices the principles of quality on a daily basis. The ideal candidate is hard-working and extremely ambitious, with the ability to learn and manage responsibilities in a dynamic business environment. The analytical group is responsible for analyzing raw materials, in-process materials, stability, and finished products in accordance with cGMP regulations. The group also handles scheduling, calibration, maintenance of equipment, and performs method development and validation for various analytical methods. As a team member, you will be expected to follow and help plan daily operations within the lab, communicating with all areas in the company to meet client and company deadlines. Responsibilities + Demonstrate expertise with analytical instrumentation, including HPLC, UHPLC, Dissolution, Spectrophotometer, GC, KF (potentiometric and coulometric), and ICP-MS. + Understand and apply USP, ICH, and CFR regulatory requirements. + Perform analytical techniques such as Method Development/Validation, chromatography, pipetting, and solution preparation. + Utilize electronic systems like LIMS, electronic laboratory notebooks, TrackWise, OpenLAB, Excel, and Word. + Conduct various analytical tests, including Assay, dissolution, degradants, moisture, hardness, viscosity, and pH. + Execute against monographs, protocols, and SOPs in a cGMP laboratory environment. + Prevent deviations and investigations. + Conduct stability scheduling and studies. Essential Skills + Bachelor's Degree in Chemistry from an accredited US college or university. + At least 1 year of hands-on QC Chemistry experience in a small molecule GMP lab. + Previous related lab experience is required. + Experience with HPLC (Agilent 1100 or 1290). + Experience with Dissolution and FTIR/IR. + Proficiency with LIMS and GMP. Additional Skills & Qualifications + Experience with electronic systems such as TrackWise and OpenLAB. + Capability in Method Development and Method Improvement. + Understanding of wet chemistry and pharmaceutical processes. Work Environment This position requires you to spend the majority of your time in the lab. Please note that salaried employees are compensated for a 50-hour work week. Job Type & Location This is a Permanent position based out of Horsham, PA. Pay and Benefits The pay range for this position is $80000.00 - $80000.00/yr. Health, dental, vision and 401k available2 weeks of vacation Holiday and sick time available Workplace Type This is a fully onsite position in Horsham,PA. Application Deadline This position is anticipated to close on Dec 15, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.

KOMAN Government Solutions, LLC (KGS), a wholly-owned 8(a) subsidiary of the Natives of Kodiak, is an Alaska Native Corporation, providing environmental investigation, remediation, munitions and explosives of concern support, operations and maintenance, long-term monitoring, and construction services to our clients. We have an immediate need for a **Senior Environmental Project Chemist** to support our diverse portfolio of DoD, USEPA, other federal agencies, and private sector projects. This position can be full or part-time depending on the candidate's availability. This is a hybrid position reporting to either our Marlborough, MA or Exton, PA office locations. However, remote candidates will also be considered. In this leadership role, you'll serve as principal contact to internal and external customers for all chemistry-related activities and will manage and direct all internal requests for chemistry support. You will be responsible for mentoring and oversight to our part-time data validator and to additional chemistry and data validation staff as we grow the business. You will assign work and review chemistry and data validation work products for completion and accuracy prior to client submittal. You will be responsible for managing laboratory products and determining which validation assignments may need to be subcontracted, as well as monitoring laboratory and validation subcontracts to ensure they are compliant with the project requirements. **Why Work Here?** + Competitive salary with Paid Time Off and Holidays + Benefits selected start first of month after hire. + Robust benefit options: medical, vision, dental, additional life insurance, critical illness, additional hospitalization coverage, pet insurance, and identity theft offerings. + Company paid 1X salary life insurance, short term disability and long-term disability insurance. + Company match up to 4% on 401K **Typical work assignments include:** + Proposal support: identify preferred environmental analytical laboratories, create requests for price proposals, and obtain competitive pricing. + UFP-QAPP and work plan support: prepare chemistry portion of UFP-QAPPs. Ensure that all work plans prepared by junior staff correctly identify analytical methods, preservation requirements, bottleware, and number and frequency of required QA/QC samples. + Resolve chemistry-related client or regulatory comments on plans and reports. + Laboratory procurement and coordination: Support preparation of analytical laboratory scopes of work; procurement of those laboratories; and coordination with laboratories prior to, and following, sampling events. + Auditing laboratory operations when needed. + Laboratory data report review: ensure reports meet criteria for completeness, correctness, sensitivity, and conformance with requirements. Ensure data received meets the requirements of the UFP-QAPP. + Data validation: follow established DoD and USEPA guidelines to determine the analytical quality of laboratory data. Ensure data validation meets the requirements of the UFP-QAPP. Review all data validation reports prepared by junior staff. + Database management: Follow established procedures for management of analytical data in NIRIS, various USACE chemistry databases (including FUDSChem, ERPIMS, and EDMS), and state-specific databases. + Implementation and monitoring of corrective action, as needed. **Required qualifications:** + Bachelor of Science degree (Master's preferred) in Chemistry or Environmental Chemistry. + Minimum 10 years of experience supporting federal projects. + Expertise in chemical data quality management of environmental analytical data, including working knowledge of industry-standard procedures for environmental data verification and data validation. + Working knowledge of Microsoft Office Suite and Adobe. + Excellent communication skills, both verbal and written. **The ideal candidate will have:** + Commercial environmental analytical laboratory experience. + Experience with validation of data using current DoD QSM requirements for various methods including explosives, perchlorate, PFAS, PCBs, in addition to more common environmental analytical methods. + Experience working on DoD, USEPA, and other federal agency projects and/or state environmental/department of health agencies. + Experience directing and mentoring junior staff/chemists. _As a Federal Contract Employer, KOMAN Families of Companies follows Federal Laws as it pertains to drug testing. All candidates who receive a written offer of employment will be required to undergo drug testing for commonly abused controlled substances in accordance with Federal Law. It is important to note although a State may have legalized a controlled substance, if the controlled substance is illegal per Federal Law, it is then considered to be illegal. KOMAN Families of Companies is a Drug-Free Workplace. Successful completion of a background and DMV record check also must be completed prior to hire._ _Preference will be given to Natives of Kodiak, Inc. Shareholders and Descendants of Shareholders in accordance with Title 43 U.S. Code 1626(g) and Title 42 U.S. Code 2000e - 2(i)_ _KGS is an Equal opportunity employer as to all protected groups, including protected veterans and individuals with disabilities_

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description • The QC Scientist I will provide testing and technical support in the QC laboratories. • These functions include: Collection, processing and testing of chemical components, bulk products, raw materials, packaging components, finished products, in-process materials, scale up, and cleaning validation samples to conform to specifications and standard operating procedures ( SOPs) . • Maintain inventory of testing supplies, t emperature monitoring, water sample collection and testing, environmental monitoring and other duties as assigned. This position will have a general knowledge of SOPs, USP and other applicable pharmacopeia. Performs tasks with some guidance, but demonstrate the ability to comprehend and perform with experience. • They will support the review, data generation and/or writing of technical documents such as SOPs, laboratory investigations, test protocols and annual product reviews. • This position complies with cGMP, safety training and regulations. Maintain an environment of respect and teamwork with all coworkers. All employees are required to cultivate an environment of quality & compliance in their actions. • This includes attending all required training, adhering to the processes & procedures of their role and the company and displaying the highest level of integrity. • Those who manage others are required to ensure their employees are trained appropriately, create & maintain an environment that promotes employee involvement and doing things right the first time. Qualifications • A minimum of Bachelor's Degree in Microbiology, Chemistry, Biology, Natural Science, Medical Technology, or related science is required. • Minimum 1 year of GMP/GLP microbiology lab experience in a pharmaceutical and/or OTC and/or regulated environment is required. • Experience performing routine laboratory activities is required. • Basic knowledge/exposure of a LIMS system is preferred. Strict compliance with good documentation practices and aseptic techniques is required. • Ability to work independently, manage timeline and decision making is preferred. • This candidate will be based in Fort Washington, PA and will be required to travel less than 10% domestically. Additional Information Sneha Shrivastava Technical Recruiter (Clinical/Scientific) Artech Information Systems LLC 360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: ************ | Fax: ************ Connect with us on - LinkedIn | Facebook | Twitter

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 Run routine assays on instruments including UPLC, LC/MS and NMR Develop or adapt pre-existing methods based on changing needs and new raw materials Data analysis outside of lab Qualifications Bachelors degree in a scientific concentration Authorization to work in the United States indefinitely without restriction or sponsorship. Experience with UPLC, LC/MS Experience with Waters LC systems is a plus, especially UPLC with QDA/PDA Analytical knowledge, especially working with calibration curves Knowledge of ICH guidance for validation of analytical procedures Knowledge of chemistry, especially molecules such as amino acids, sugars, and metals Experience with Empower software is a plus Additional Information This position is Full-Time, Monday through Friday, 9a.m. to 5 p.m with overtime as needed. 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 Run routine assays on instruments including UPLC, LC/MS and NMR Develop or adapt pre-existing methods based on changing needs and new raw materials Data analysis outside of lab Qualifications Bachelors degree in a scientific concentration Authorization to work in the United States indefinitely without restriction or sponsorship. Experience with UPLC, LC/MS Experience with Waters LC systems is a plus, especially UPLC with QDA/PDA Analytical knowledge, especially working with calibration curves Knowledge of ICH guidance for validation of analytical procedures Knowledge of chemistry, especially molecules such as amino acids, sugars, and metals Experience with Empower software is a plus Additional Information This position is Full-Time, Monday through Friday, 9a.m. to 5 p.m with overtime as needed. 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.

Job DescriptionDescription: FLSA Status: Non-exempt/Hourly Schedule: 8:00AM - 4:30PM, Monday - Friday. Occasional 2nd shift work required Are you interested in growing your laboratory career at a fact-paced and expanding environmental testing laboratory? If so, we may have a great role for you; Criterion's Laboratory Analyst (PLM) role primarily performs precise and timely analysis of asbestos bulk samples using polarized light microscopy techniques. This role is responsible for adhering to quality assurance and quality control standards, following Criterion Laboratories' Laboratory Safety Procedures, ensuring a clean work environment, and fostering effective collaboration within a team environment. Essential Duties and Responsibilities: Uses polarized light microscopy to conduct detailed analysis of bulk samples for the identification and quantification of asbestos fibers. Adheres to established analytical protocols and procedures to ensure reliable and reproducible results. Maintains rigorous quality assurance practices to uphold data integrity and compliance with regulatory requirements. Adheres to safety protocols to ensure a secure work environment for all personnel. Maintains cleanliness and organization of the workspace to prevent contamination and ensure optimal working conditions. Collaborates effectively with team members to achieve departmental objectives and contribute to a positive team culture. Participates in training programs and stays abreast of advancements in polarized light microscopy techniques and asbestos analysis methodologies. Requirements: Required Knowledge and Experience: At least six (6) months experience performing analyses via polarized light microscopy Familiarity with regulatory requirements and standards pertaining to asbestos analysis is preferred. Strong attention to detail and the ability to maintain accuracy under tight deadlines. Excellent organizational and communication skills, both verbal and written. Demonstrated ability to work both independently and collaboratively within a team environment. Commitment to maintaining high safety standards and promoting a culture of safety in the workplace. Required Education, Certifications, and Licenses: Bachelor's degree in a relevant scientific field (e.g., Geology, Biology, Chemistry, Environmental Science) and/or an equivalent amount of education and experience. Physical and Mental Requirements: Ability to perform microscopy work for extended periods, including sitting or standing. Capability to lift and handle sample containers and equipment (up to 25 pounds).

Our large pharmaceutical clients is seeking an Associate Scientist to join their growing Biophysics & Molecular Attributes Group in Spring House, PA. The Biophysics & Molecular Attributes Group within Biologics Discovery uses innovative biophysical, biochemical, and mass spectrometry based analytical tools to help select best therapeutic candidates for clinical development. You will be a critical member of the Higher Order Structure (HOS) team that characterizes developability attributes like thermal stability, chemical stability, solubility, and aggregation on a broad range of biologics platforms including monoclonal antibodies, multi-specific antibodies, antibody drug conjugates, antibody radio conjugates, and other therapeutic proteins. You will design and perform experiments using a variety of technologies like HPLC, DSF, DSC, cIEF, GXII, DLS, and more. Key Responsibilities: Execute automated methods for biophysical and structural characterization of antibody therapeutics. Integrate robotic liquid handling systems (e.g., Hamilton, Tecan) with analytical platforms to improve efficiency, consistency, and sample throughput. Execute analytical analysis of biologics candidates using a wide variety of technologies such as size-exclusion HPLC, plate-based HIC/Heparin binding, DSF. Evaluate results to deliver scientifically supported conclusions and recommendations that are documented in appropriate technical reports. Maintain lab and equipment. Collaborate with colleagues in the global organization to support discovery projects. Assist in developing recommendations for improving standard procedures. Qualifications: Master's or Bachelor's Degree in a related field of study Minimum of 1 year of protein/antibody analytical methods experience Experience using HPLC, DSF or DLS Salary: $70,000-$75,000 (flexible based on experience) Hours: Monday-Friday, 8:00am-5:00pm Hiring Method: Multiyear contract - After 1 year on contract, the individual will have the opportunity to apply for a permanent role or have their contract renewed for another year PTO: 10 PTO days, 6 paid sick days annually & paid Holidays Benefits: Medical, Dental, Vision and 401K plans available Exact compensation may vary 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.

At Quaker Houghton, we are experts in the development, production and application of chemical specialties, process fluids, lubricants and coatings for the manufacturing industry. We have been an integral part in the growth of the world's largest industrial companies and to this day our experience and expertise show in the actions and dedication of our Associates worldwide. Today, we have a global presence, with our corporate headquarters located in Conshohocken, PA. Quaker Houghton is a global publicly traded company with a unique collaborative culture that supports career growth for its associates and offers competitive compensation and benefit programs. Summary: Quaker Houghton is seeking a Development Chemist III to work in our Metalworking Fluid Development Laboratory in Conshohocken, PA. The laboratory supports multiple metalworking fluid product lines including soluble oils, semi-synthetics, and full synthetics. An individual in this role will be responsible for conducting product development, research projects, and product support for Quaker Houghton metalworking fluids. This will require working closely with commercial associates, other RD&E teams, customers, and external partners to design new products and execute tests both in the laboratory and in the field. We are seeking experienced candidates who are highly motivated, have strong collaboration skills, are creative problem solvers, and communicate effectively. What will you do? * Use knowledge of colloid chemistry, tribology, and testing techniques to formulate metalworking fluids that will meet customer needs and provide solutions to application problems. * Work independently with minimal guidance from the laboratory manager. * Act as a mentor to junior development chemists. * Maintain a clear and orderly record all observations and data. * Write detailed reports summarizing product development efforts, laboratory testing, and troubleshooting. * Perform customer requested product analysis and testing to answer questions and address problems at commercial accounts. * Provide legal and archival documentation for patent applications. * Comply with safety regulations and lab procedures. * Provide technical service and knowledge to customers and sales associates based upon the chemist's current level of expertise. Visit customers when required. * Provide assistance to Manufacturing to improve the quality and efficiency of the manufacturing process. Assist Manufacturing and the Quality Assurance lab in solving quality and production problems. * Comply with safety regulations and make recommendations towards the improvement of safety and environmental concerns. * Follow all ISO quality and environmental standards as provided in the various procedural manuals. Ensure that all laboratory equipment is calibrated and functioning properly. Education, Experience, Skills & Competencies: * This position requires a Bachelor Degree in Chemistry or equivalent with at least 7 years of experience, a Master's Degree in Chemistry or equivalent with at least 5 years of experience, or a Doctor of Philosophy in Chemistry or equivalent with at least 3 years of experience. * Knowledge of colloid chemistry, surfactants, and tribology is required. * Experience with the formulation of metalworking fluids and field support of machining and grinding operations is highly desired. * Understanding of applied statistics and experimental design is not required, but highly desired. * Must have the ability to operate in a fast-paced environment, to work on different projects at the same time, and to think analytically. * Must have good prioritization and communication skills (oral and writing). * Ability to write detailed reports and presentations which may be used to inform high-ranking members of the Technical Community. What's in it for you: * Competitive pay programs with excellent career growth trajectory * Opportunities to see your efforts contribute toward the success of the business * Work for a global leader in the industrial process fluids industry Quaker Houghton is an equal opportunity employer committed to creating a diverse workforce. Quaker Houghton provides equal employment opportunity for all qualified candidates. Quaker Houghton does not discriminate against any candidate for employment based on race, color, religion, sex, gender, gender identity or expression, affectional or sexual orientation, pregnancy, age, creed, ancestry, national origin, citizenship, marital or domestic partnership or civil union status, veteran's status, physical/mental disability, genetic information, or any other category protected by U.S federal, state, and/or local employment law. Furthermore, Quaker Houghton is committed to providing reasonable accommodations to qualified candidates with physical and/or mental disabilities. Applicants with a disability who need assistance applying for a position may email ************************.

Job Details Corporate Headquarters - Bristol, PA 4 Year Degree Up to 25% ResearchDescription United Chemical Technology (UCT) was founded in 1986 by one of the pioneers of Solid Phase Extraction (SPE), Michael Telepchak, who is still active in the Company and continues to works with our team of talented chemist in our research and development department. UCT is a major competitor in the field of silica based phase extraction technology and silane manufacturing. UCT's mission is to establish and maintain a leadership position in the specialty chemical market for organosilicon products. Our products serve the environmental, forensics, food and beverage, clinical, pharma and cannabis industries. As a company, we consistently strive to distinguish ourselves from competitors in terms of service, pricing and quality. To accomplish this goal, we continue to invest in the best people, providing them with the finest tools available. Through excellence, UCT is committed to meeting not only the customer's needs of today but also those of tomorrow. We are looking for a Forensics R&D Chemist who will be ready to hit the ground running and assist our R&D team who will assist in developing contacts and opportunities by writing journal articles, white papers, posters and technical presentations through interactions with other core members of the Technical Support Team in assisting with customer inquiries, technical phone calls and "on site" support, and traveling with our sales team. Some duties and responsibilities are as follows: Duties and Responsibilities: Assist in designing and troubleshooting research projects using solid-phase extraction (SPE) and other suitable sample preparation techniques, strictly adhering to appropriate regulatory guidelines where applicable. Assist in developing new UCT product applications to generate new uses for our products and potential new applications and products. Follow the project plans of the laboratory concerning the order that projects are to be performed. Operate and maintain analytical instruments including GC, GC-MS and LC-MS/MS. Provide support to all customer inquiries and technical specialists requests in a timely and precise manner addressing the customer's needs. Educate customers and UCT employees as to areas of forensic and toxicology science that are needed for sales calls, applications, and the appropriate use of UCT applications. Take an active role in the American Academy of Forensic Sciences (AAFS), Society of Forensic Toxicologists (SOFT), and other professional groups that will lead to better understanding of the applications of SPE in the Forensic and Toxicological Fields. Publish at least twice yearly a scientific paper or poster on a newly developed application for the use of our products. Keep up on the current trends and new techniques, and if possible, apply our products to those applications for comparison. Travel with sales representative or alone to customer sites to perform demonstrations or solve technical issues. Support sales team as needed to close sales. Assist Quality Control team when needed to assess the effectiveness and cleanliness of select UCT consumables and sorbents that are commonly utilized in forensic toxicology and clinical testing. Execute presentations, training, and educational conference seminars geared towards the forensic toxicology and clinical markets when called upon. Technically support and train both domestic and international sales force and customer base on UCT published application notes and products with a forensic toxicology and clinical concentration. Qualifications A bachelor's or masters in the Forensic Toxicology field with an emphasis on chemical analysis with more than 1 to 3 years' experience in a forensic laboratory performing forensic drug analysis and method development. Candidates must show an interest in performing Toxicological analysis using SPE products and have a familiarity with competitors' products. Knowledge to create new methods, validation criteria, and have a keen eye towards trends in the industry regarding new analytical approaches. Experience using SPE, GC, GC-MS, LC and LC-MS/MS. GC-MS/LC-MS extensive operation experience required. Have published or presented at least three papers on their scope of their activities in their field of interest in Forensic Toxicology. Strong method development/R&D skills for the use of SPE coupled with GC-MS and LC-MS/MS analysis The ability to work in the laboratory extensively utilizing both GC-MS and LC-MS/MS equipment and think independently to solve analytical problems. Ability to work with current products and make recommendations on how to improve UCT's products and their applications. Be adaptable to handle multiple projects and tight timeframes. Strong organizational and interpersonal skills. Ability to think critically. Positive attitude and the ability to work both independently and within multidisciplinary groups. Excellent verbal and written communication skills; scientific writing experience preferred. Ability to effectively present information and respond to questions from managers, sales staff and customers.

We are seeking a skilled QC Chemist who practices the principles of quality on a daily basis. The ideal candidate is hard-working and extremely ambitious, with the ability to learn and manage responsibilities in a dynamic business environment. The analytical group is responsible for analyzing raw materials, in-process materials, stability, and finished products in accordance with cGMP regulations. The group also handles scheduling, calibration, maintenance of equipment, and performs method development and validation for various analytical methods. As a team member, you will be expected to follow and help plan daily operations within the lab, communicating with all areas in the company to meet client and company deadlines. Responsibilities * Demonstrate expertise with analytical instrumentation, including HPLC, UHPLC, Dissolution, Spectrophotometer, GC, KF (potentiometric and coulometric), and ICP-MS. * Understand and apply USP, ICH, and CFR regulatory requirements. * Perform analytical techniques such as Method Development/Validation, chromatography, pipetting, and solution preparation. * Utilize electronic systems like LIMS, electronic laboratory notebooks, TrackWise, OpenLAB, Excel, and Word. * Conduct various analytical tests, including Assay, dissolution, degradants, moisture, hardness, viscosity, and pH. * Execute against monographs, protocols, and SOPs in a cGMP laboratory environment. * Prevent deviations and investigations. * Conduct stability scheduling and studies. Essential Skills * Bachelor's Degree in Chemistry from an accredited US college or university. * At least 1 year of hands-on QC Chemistry experience in a small molecule GMP lab. * Previous related lab experience is required. * Experience with HPLC (Agilent 1100 or 1290). * Experience with Dissolution and FTIR/IR. * Proficiency with LIMS and GMP. Additional Skills & Qualifications * Experience with electronic systems such as TrackWise and OpenLAB. * Capability in Method Development and Method Improvement. * Understanding of wet chemistry and pharmaceutical processes. Work Environment This position requires you to spend the majority of your time in the lab. Please note that salaried employees are compensated for a 50-hour work week. Job Type & Location This is a Permanent position based out of Horsham, PA. Pay and Benefits The pay range for this position is $80000.00 - $80000.00/yr. Health, dental, vision and 401k available 2 weeks of vacation Holiday and sick time available Workplace Type This is a fully onsite position in Horsham,PA. Application Deadline This position is anticipated to close on Dec 15, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost. Job Description • The QC Scientist I will provide testing and technical support in the QC laboratories. • These functions include: Collection, processing and testing of chemical components, bulk products, raw materials, packaging components, finished products, in-process materials, scale up, and cleaning validation samples to conform to specifications and standard operating procedures ( SOPs) . • Maintain inventory of testing supplies, t emperature monitoring, water sample collection and testing, environmental monitoring and other duties as assigned. This position will have a general knowledge of SOPs, USP and other applicable pharmacopeia. Performs tasks with some guidance, but demonstrate the ability to comprehend and perform with experience. • They will support the review, data generation and/or writing of technical documents such as SOPs, laboratory investigations, test protocols and annual product reviews. • This position complies with cGMP, safety training and regulations. Maintain an environment of respect and teamwork with all coworkers. All employees are required to cultivate an environment of quality & compliance in their actions. • This includes attending all required training, adhering to the processes & procedures of their role and the company and displaying the highest level of integrity. • Those who manage others are required to ensure their employees are trained appropriately, create & maintain an environment that promotes employee involvement and doing things right the first time. Qualifications • A minimum of Bachelor's Degree in Microbiology, Chemistry, Biology, Natural Science, Medical Technology, or related science is required. • Minimum 1 year of GMP/GLP microbiology lab experience in a pharmaceutical and/or OTC and/or regulated environment is required. • Experience performing routine laboratory activities is required. • Basic knowledge/exposure of a LIMS system is preferred. Strict compliance with good documentation practices and aseptic techniques is required. • Ability to work independently, manage timeline and decision making is preferred. • This candidate will be based in Fort Washington, PA and will be required to travel less than 10% domestically. Additional Information Sneha Shrivastava Technical Recruiter (Clinical/Scientific) Artech Information Systems LLC 360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960 Office: ************ | Fax: ************ Connect with us on - LinkedIn | Facebook | Twitter