Chemist Jobs in Chester, PA

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

Title: Scientist - II Duration: 12+ Months Pay Range: $30 - $35/hr on W2 • We are currently seeking a temporary scientist for an immediate onsite position within the Analytical Sciences (AS) laboratory within Science and Technology. • The successful candidate will be expected to perform analytical testing of drug products and APIs under the supervision of a senior scientist. • The candidate will have a good understanding of the technical, regulatory, and GMP needs related to drug product development. • The position will report to the Senior Leadership of the Analytical Sciences laboratory. • Strong technical background with a problem-solving skill set as well as the ability to work in teams are considered essential. Position Responsibilities: • Perform analytical testing (e.g., HPLC/UPLC and dissolution) of drug products • Perform data analysis (chromatography/spectroscopy) and present them to the team in a timely manner Quals-- Education and experience: BS with 4-6 years or MS with 1-3 years or Ph.D with 0-2 years of relevant experience in Analytical Chemistry. Required Experience and Skills • Hands-on analytical laboratory experience-e.g., wet chemistry, chromatography. • Expertise in Liquid Chromatography (HPLC/UPLC) and dissolution • Hands-on experience with chromatographic integration and with Empower software (or other chromatographic data acquisition systems) and Electronic Laboratory Notebook (ELN) • Experience collecting and analyzing raw data, preparing graphs and other visualization tools to help interpret results • Demonstrated strong verbal as well as written communication skills and ability to work in an interdisciplinary team environment. Preferred Experience and Skills: • Expertise in UV. • Working knowledge of laboratory GMP, quality, compliance and data integrity requirements and related recent industry trends • Working knowledge of troubleshooting analytical techniques (e.g., chromatography, dissolution, spectroscopy, etc). • Demonstrated ability to work independently in the laboratory • Working knowledge of statistics and tools, e.g., statistical data treatment and/or Excel or Minitab. • Experienced in conducting comparative and or multi-media dissolution studies. Personality: • Collaborative and team player • Independent • Flexible and adaptable Note: 12 months assignment, 100% onsite, lab based role. Key skills: • HPLC and dissolution experience is required. • Analytical chemistry background is required. • Empower expertise is preferred • Pharma industry is preferred Net2Source is an Equal Opportunity Employer. We believe that no one should be discriminated against because of their differences, such as age, disability, ethnicity, gender, gender identity and expression, religion or sexual orientation. Our rich diversity makes us more innovative, more competitive, and more creative, which helps us better serve our clients and our communities. All employment decisions shall be made without regard to age, race, creed, color, religion, sex, national origin, ancestry, disability status, veteran status, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status or any other basis as protected by federal, state, or local law.

Chemical Research Technician- Are you eager to be at the cutting edge of innovation in water treatment solutions? Our laboratory partner, located in Bensalem, PA, is seeking a motivated and dynamic individual to join our team as a Chemical Research Technician. Key Responsibilities: Innovative Solutions: Lead research and development initiatives to create advanced chemical solutions for our valued clients, driving improvements in water treatment performance and ensuring a competitive edge in the industry. Collaborative Development: Partner with the development team to brainstorm, experiment, and analyze results. Your contributions will be essential in shaping the future of water treatment technologies. Project Execution: Utilize your scientific expertise to design, analyze, and evaluate projects while maintaining a focus on business standards and project timelines. You will play a key role in achieving project milestones and ensuring successful execution. Customer-Centric Support: Provide technical assistance and problem-solving expertise to customers in the industrial water sector, addressing their needs effectively and fostering customer satisfaction and loyalty. Qualifications: Educational Background: Bachelor's Degree in Science (Chemistry, Materials Science, Chemical Engineering, Biochemistry, Integrated Science and Technology). Experience: Less than 3 years of industrial chemistry experience. Desired Skills and Attributes: Specialized Knowledge: Experience with wet analytical techniques (e.g., titrations and chemical analyses) is highly advantageous. Mechanical Aptitude: Basic mechanical skills, including the ability to work with tools for piping and fittings, are a plus. Interpersonal Skills: Strong communication skills paired with exceptional interpersonal abilities are essential. You should thrive in a collaborative, fast-paced work environment. Problem-Solving Skills: Demonstrated ability to conceptualize and solve complex problems while implementing creative and innovative solutions. Safety First: A commitment to maintaining strong environmental, health, and safety standards in all aspects of work. Passion for Excellence: Driven by a passion for quality, speed, and continuous improvement, with a relentless pursuit of excellence in all aspects of your work.

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

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

We are seeking a motivated and detail-oriented Analytical Scientist to join our team. The ideal candidate will have a Bachelor's degree in Chemistry, Pharmaceutical Sciences, or a related field, with at least 1 year of hands-on experience in analytical testing using techniques such as High-Performance Liquid Chromatography (HPLC) and other modern instrumentation. This role supports the analysis of raw materials, intermediates, and finished products to ensure compliance with regulatory and quality standards. Key Responsibilities: Perform analytical testing using HPLC, UV-Vis, FTIR, dissolution, and other relevant techniques. Support method development, validation, and routine sample analysis in compliance with cGMP regulations. Document all laboratory activities and results accurately in laboratory notebooks and electronic systems. Assist in investigations, OOS (Out of Specification) results, and laboratory deviations as required. Maintain and calibrate laboratory instruments according to SOPs and regulatory standards. Qualifications: Bachelor's degree in Chemistry, Pharmaceutical Sciences, or a related field. Minimum 1 year of experience in a pharmaceutical laboratory environment. Hands-on experience with HPLC is required; familiarity with other techniques like GC, UV, FTIR, and dissolution is a plus. Working knowledge of cGMP, ICH, and FDA regulations. Strong attention to detail, organizational, and documentation skills.

Our client, a world-leading Pharmaceutical Company in Malvern, PA is currently looking for an Analytical Scientist to join their expanding team. Job Title: Analytical Scientist (Liquid Chromatography, Capillary Electrophoresis) Duration: 12 months contract, extendable up to 24 months Location: Malvern, PA Note: The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract. You may participate in the company group medical insurance plan Job Description: Title: Scientist Summary: We are hiring a scientist to support the Separations & Characterization Workcell in Malvern, PA. This Workcell is part of a fully automated laboratory that supports non-GXP process and formulation development. Responsibilities: Support the execution of analytical assays such as Peptide Mapping, CE-SDS, cIEF, and SE-HPLC Instrument maintenance, mobile phase and reagent preparation Data analysis Qualifications: Bachelor's degree in Chemistry, Biology, Biochemistry or related discipline is required. 1+ year of experience is preferred. Must be proficiency in Microsoft Office tools (Excel, Word, PowerPoint) Must have excellent interpersonal skills (written and oral) and the ability to work in a cross-functional customer-focused environment is required. Knowledge and working experience on proteins or therapeutic cell and gene therapy projects is preferred. Experience with BIOVIA, CISPro, and data review is preferred Experience in equipment troubleshooting and routine instrument maintenance is preferred. Experience with automated equipment and software is preferred (Tecan Fluent Control, Biosero Green Button Go ). Experience with liquid chromatography or capillary electrophoresis is preferred.

10 Days of PTO / 6 Sick Days / Paid Holidays Compensation: $35.76/hr to $45.87/hr. Exact compensation may vary based on several factors, including skills, experience, and education. Healthcare benefit packages for this role will start on the 1st day of employment and include medical, dental, and vision insurance, financial protection benefits, as well as HSA, FSA, and DCFSA account options. 401k retirement account access is offered starting on the 90th day with employer matching after one year of service. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law. Required Skills & Experience -Minimum 2 years of relevant GMP work experience in a lab setting -Minimum 1 year of experience working with mammalian cell culture -Experience with one or more of the analytical technologies used in the Cell and Gene Therapy Laboratories such as qPCR, cell culture, Flow Cytometry, and/or ELISA -Bachelor degree in Biology or Chemistry -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) -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) Nice to Have Skills & Experience -CAR-T, Cell and Gene Therapy, or Biochemistry laboratory experience -Basic knowledge of Compendial (USP, EP, JP, etc.) requirements pertaining to their functional area of QC -Ability to complete equipment and software qualification protocols -Experience developing and setting long-term objectives -Experience working in Biosafety Level lab (BSL 2, BSL2+) or aseptic facility -Knowledge of EU/FDA guidance Job Description The QC CRS Analyst is responsible for conducting biochemical and testing of raw material, in-process, final product release and characterization samples, 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 other Analysts within a functional Clinical Release and Stability Laboratory and report to the Senior QC Supervisor. Key Responsibilities: -Conduct analytical biological testing of clinical and commercial drug product/drug substance samples -Perform peer reviews and approvals of laboratory data -Use electronic systems (LIMS, MES, LES, Empower, etc.) for execution and documentation of testing including application of statistical concepts to laboratory data -Support of New Product Initiatives (NPI) including owning a project and perform project management functions with limited to no coaching from supervision/management -Perform Instrument Calibration and Preventative Maintenance -Update CRS-owned documents using the Document Management System (DMS) -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 -Act as a peer subject matter expert in assessing talent by participating in panel interviews for job -Complete invalid assay and general laboratory investigation records -Complete corrective and preventative actions (CAPA) as assigned -Assist in the execution of internal audits

Job Details: Job Title: Lab Instrument Coordinator / Analyst 3 - Laboratory Quality Control Duration: 12 Month Contract The role involves managing and coordinating the onboarding, validation, and maintenance of laboratory instruments, including scheduling vendor services and overseeing routine repairs. The individual will work closely with internal and external teams to ensure lab operations are compliant and efficient. Responsibilities: Coordination and management of instrument onboarding and validation Scheduling vendor routine and repair service Escorting vendors in the lab space Facilitating instrument preventive maintenance, calibration, and repairs; may include some hands-on maintenance and calibration duties Qualifications: Minimum of an Associate's degree is required At least 1+ years of GxP experience is required Must have GMP record keeping experience Experience with chamber management, lab safety and housekeeping Software validation experience Must be proficient in MS Excel and PowerPoint Be able to coordinate activities with internal and external operations and service teams, service providers, IT, site quality, and analysts to ensure lab operation activities are completed and compliant.

IDR is excited to announce an opportunity for a talented Research & Development Technician to join our esteemed client's team in Philadelphia, PA. This role is perfect for individuals who thrive in a dynamic, hands-on work environment and are eager to contribute to innovative research projects. If you are passionate about scientific exploration and eager to make a significant impact within a leading organization, we encourage you to apply today! Position Overview/Responsibilities for the Research & Development Technician: - Assist in the design and execution of experiments, independently conducting these experiments and summarizing the resulting data. - Prepare and evaluate coating formulations using various equipment. - Accurately record test results for all coating formulations. - Troubleshoot laboratory problems, collaborating with research investigators when unexpected results occur. - Maintain a safe working environment, handling and disposing of chemicals safely and routinely. - Manage multiple tasks under strict time constraints. This is a one-year contract position requiring a 2-year or 4-year degree from a college or technical school in a chemical or life-science related field, or equivalent job experience in an industrial laboratory environment. Required Skills for Research & Development Technician: - Strong interpersonal and communication skills, with the ability to work well in both self-managed and team environments. - Ability to manage multiple projects simultaneously, meeting established deadlines. - Comfortable with safely working with hazardous materials. - Strong problem-solving and decision-making skills. - Excellent verbal and written communication skills. - Proficiency in Microsoft Office programs such as Excel, Word, & Teams. What's in it for you? - Competitive compensation package - Full Benefits; Medical, Vision, Dental, and more! - Opportunity to get in with an industry leading organization - Close-knit and team-oriented culture Why IDR? - 25+ Years of Proven Industry Experience in 4 major markets - Employee Stock Ownership Program - Medical, Dental, Vision, and Life Insurance - ClearlyRated's Best of Staffing Client and Talent Award winner 11 years in a row ;

Are you ready to take on a new challenge and ensure top-tier quality within a Senior QC Analyst role? This could be your next opportunity to make an impact! Hobson Prior is seeking a dedicated Senior QC Analyst to focus on ensuring the quality and safety of cell therapy products through various microbiological tests. You will work in a dynamic environment that may require flexibility with shifts, including weekends and holidays. Responsibilities: Conduct daily laboratory tests to ensure product quality. Monitor cleanroom environments for safety and compliance. Analyse test results and report findings promptly. Ensure all activities comply with industry standards. Investigate any discrepancies in test results. Assist in solving technical issues and improving processes. Document procedures and findings accurately. Review data and provide feedback to team members. Train new staff on testing procedures. Maintain high productivity and quality standards. Key Skills and Requirements: Degree in biological sciences or a related field. Experience in quality control within the pharmaceutical industry. Strong attention to detail and technical skills. Ability to manage multiple tasks efficiently. Knowledge of industry regulations and practices. Effective communication and teamwork skills. For more information, please contact Danielle Hull. Apply now If you are interested in learning more or applying to this exciting opportunity then please click 'Apply' and upload a copy of your CV. Alternatively for further details or to talk directly to a life sciences recruitment specialist directly please select 'Contact me' at the top of this page. Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy. By providing your details and submitting this form you confirm you have read and understood our privacy policy. We only share your personal details with our group companies at acaciumgroup.com/affiliates and those categories of third parties in our privacy policy at hobsonprior.com/privacy-policy.

Immediate need for a talented Quality Control Analyst 2. This is a 12+ Months Contract opportunity with long-term potential and is located in Fortwashington, PA (Onsite). Please review the job description below and contact me ASAP if you are interested. Job ID:25-63901 Pay Range: $35 - $40.70/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location). Key Responsibilities: Compiles and analyzes data on reoccurring product defects to determine root cause. Documents analysis results. Analyzes raw material inspection logs for consistent failures. Notifies purchasing and quality departments about suppliers that have provided inferior products. Studies work processes, measurements and performance metrics to identify improvement areas. Recommends new or modified procedures based on findings. Interfaces with customers, suppliers and associates to define and improve quality standards and expectations. Participates on process improvement teams. Monitors and scrutinizes internal and external complaints and compiles data to be used in reports. Performs analyses in order to determine compliance with specifications using a wide variety of chemical, biological and physical standard procedures. Key Requirements and Technology Experience: Skills-Compiles and analyzes data on reoccurring product defects to determine root cause. Documents analysis results. Analyzes raw material inspection logs for consistent failures. BACHELOR'S DEGREE MUST Generally Requires 2-4 Years Work Experience. University/Bachelors Degree or Equivalent Our client is a leading Healthcare Industry and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration. Pyramid Consulting, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. By applying to our jobs you agree to receive calls, AI-generated calls, text messages, or emails from Pyramid Consulting, Inc. and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here.

Sr. QC Analyst, Microbiology needed! The Senior Quality Control Analyst- Microbiology will support quality control testing operations. The quality control testing programs include in-process and final drug product microbial testing such as bioburden, endotoxins, mycoplasma, gram stain, environmental monitoring, and sterility techniques. This position works across different shifts. Depending on your assigned shift, you may be required to work overtime, weekends, and holidays to complete assigned work. Essential Functions and Responsibilities: Perform daily cGMP quality control laboratory microbiological testing activities. Perform environmental monitoring of the cleanroom areas as scheduled. Perform data analysis and result reporting of microbiology assays to support product lot release with adherence to turnaround times. Perform all activities for cGMP compliance. Support thorough cGMP investigations for out-of-specification test results. Support technical problem-solving. Support product stability programs, including execution of stability testing, stability data analysis, and final reporting of stability data. Support generation and revisions of documentation, such as SOP, protocols and reports, deviations, laboratory investigations, CAPAs, and change controls Perform peer review of laboratory data and logbooks. Provide input to functional laboratory and cross functional team meetings. Act as subject matter expert (SME) on one or more assays and train new laboratory personnel. Solid understanding and functional knowledge with hands on experience with the following: environmental monitoring, endotoxins, sterility, growth promotion, and mycoplasma. Proficient in performing technical writing (e.g., test methods, SOPs, protocols, deviations, CAPAs, change controls, etc.) Extremely detail oriented Ability to effectively manage multiple priorities involving aggressive timelines at a high level of productivity. Support inspections as needed. Operate at a consistent and exemplary efficiency level, producing high-quality and accurate results. Work in a cleanroom with biohazards, human blood components, and chemicals Comply with Safety SOPs, SDS sheets, and laboratory procedures per company policy and OSHA regulations. Perform miscellaneous duties as assigned. Required Education, Skills, and Knowledge: Bachelor's degree in a relevant discipline (biological sciences or equivalent) Minimum five (5) years of experience in the pharmaceutical industry within a Quality Control role Successfully interface with multi-disciplined teams Extremely detail-oriented with strong technical skills Ability to effectively manage multiple priorities involving aggressive timelines at a high level of productivity. High level of ownership and accountability Demonstrate a sense of urgency; ability to recognize time sensitivity. Previous experience with GDP, GLP, GMP Preferred Education, Skills, and Knowledge Advanced degree (MSc. preferred.) Experience with cell therapy products is a plus. The physical demands described here represent those that an employee must meet to perform the essential functions of this job successfully. Reasonable accommodations may be made upon request to enable individuals to perform essential functions. Please contact Human Resources to request an accommodation. Physical Demands and Activities Required: The physical demands described here represent those that an employee must meet to perform the essential functions of this job successfully. Reasonable accommodations may be made upon request to enable individuals to perform essential functions. Please contact Human Resources to request an accommodation. Must be able to wear appropriate cleanroom attire and all Personal Protective Equipment (PPE), i.e., scrubs, gowning coveralls, masks, gloves, etc. Must be able to work in a cleanroom lab setting with biohazards / various chemicals. Must meet requirements for and be able to wear a half-face respirator. Able to stand and/or walk 90% (and sit 10%) within your scheduled workday, which may include climbing ladders or steps. Ability to crouch, bend, twist, reach, and perform activities with repetitive motions. Must be able to lift and carry objects weighing up to 45 pounds. Mental: Clear and conceptual thinking ability; excellent judgment, troubleshooting, problem-solving, analysis, and discretion; ability to handle work-related stress; ability to manage multiple priorities simultaneously; and ability to meet deadlines. Work Environment: This position will work in both an office and a manufacturing setting. When in the lab, you may be exposed to various chemicals/biochemical, including latex and bleach. Additionally, there is potential for variable noise levels, equipment hazards, strong odors, and other detergents/sanitizers. Able to work in cleanroom with biohazards, human blood components, and chemicals. Potential exposure to noise and equipment hazards and strong odors.

The Development Chemist III in the surface treatment lab shall Autonomously manage and execute development assignments, determinations and tests under general direction of the manager/supervisor or in assistance to a more senior level Chemist or Scientist. Provides guidance to junior level Chemists. Company Overview: 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. Position Summary: * Independently develop and improve chemical products used in a variety of manufacturing and mechanical systems in order to enhance processes, safety and quality in order to meet customer needs and provide solutions to complex application problems. Take pricing, timing and priority setting into consideration. * Investigate applicability of new and alternative raw materials in order to enhance performance and minimize cost. Evaluate and implement alternative raw materials in existing products. * Design, develop, and implement specified tests and determinations, in order to answer questions and address problems of customers. Develop and perform customer requested product analysis and testing. * Independently select and execute analytical tests in order to determine quantitative and qualitative composition of raw materials, formulations, competitive products and other chemical (field) samples. * Determine performance characteristics of competitive products using physical, instrumental and wet analysis techniques. * Clearly and orderly record all observations and data. Report results in a clear and concise manner to enhance technical exchange. Provide legal and archival documentation for patent applications. * Develop, improve and execute test methods to enhance R&D, efficiency and field performance predictability. * Provide technical service and knowledge to customers and sales associates based upon the chemists current level of expertise. Visit customers when required to assist the Commercial team, develop and deliver presentations, and engage in discussions on complex matters with customers. * Provide assistance to manufacturing in order to improve the quality and efficiency of the manufacturing process. Assist manufacturing and the quality assurance lab in solving quality and production problems. * Maintain equipment glassware and workspace in order to keep them clean and well-functioning. Properly dispose of all laboratory waste. Participate in ensuring good management of laboratory equipment and storage spaces for chemicals and raw materials. Comply with housekeeping rules. Job Accountabilities: * Train and guide more junior level chemists, lab technicians and trainees in executing routine analysis at the Development Laboratory. Deliver internal trainings for new hires or employees when needed. * 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: * 5+ years related chemistry experience required. Equivalent combination of education (minimum bachelors degree) and experience will be considered. * Must have the ability to work in a fast pace environment, to work at different projects at the same time, and to think analytically. In addition, must have good prioritization and communication skills (oral and writing). * Must be involved, careful, precise, team player, flexible, result/customer oriented and takes initiative. Ability to write presentations. In the addition to the above, an individual must have demonstrated the ability to perform the functions of this position. * Must be involved, careful, precise, team player, flexible, result/customer oriented and takes initiative. While performing the duties of this job the employee is regularly required to carefully, and precisely manipulate samples, apparatus, and sensitive instruments. The employee is frequently required to stand and reach with hands and arms. The employee is occasionally required to walk sit and talk or hear. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision and ability to adjust focus. EEO STATEMENT: It is Quaker Houghton's policy to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. Houghton International will also provide reasonable accommodations for qualified individuals with disabilities. This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here:*************************************** DISCLAIMER: The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position.

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

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. 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 Minimum Requirements: Bachelor 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 is 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

Compensation & Details: 2 Openings Fully onsite role in Malvern, PA - in the laboratory $34-$38/hr - exact rate is based on several factors, including skills, experience, and education. Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law 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

Detail-oriented and passionate about quality? Hobson Prior is looking for a QC Analyst to elevate our standards! The successful candidate will be part of a team ensuring the quality and safety of cell therapy products through various testing methods. This position requires flexibility with shifts and may include overtime, weekends, and holidays. Responsibilities: Conduct daily quality control tests in the lab with accuracy and compliance. Monitor cleanroom environments regularly. Analyse data and report results to support product release. Assist in solving technical issues related to quality control. Participate in stability testing and data analysis. Update and create necessary documentation like protocols and reports. Train new team members on specific tests. Review lab data and records for accuracy. Contribute to team meetings and discussions. Follow safety guidelines and company policies. Key Skills and Requirements: Degree in biological sciences or a similar field. Experience in quality control within the pharmaceutical industry. Strong attention to detail and technical skills. Ability to manage multiple tasks efficiently. Familiarity with industry standards like GDP, GLP, GMP. Experience with cell therapy is beneficial. Physical ability to perform lab tasks and wear protective gear. For more information, please contact Danielle Hull. Apply now If you are interested in learning more or applying to this exciting opportunity then please click 'Apply' and upload a copy of your CV. Alternatively for further details or to talk directly to a life sciences recruitment specialist directly please select 'Contact me' at the top of this page. Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy. By providing your details and submitting this form you confirm you have read and understood our privacy policy. We only share your personal details with our group companies at acaciumgroup.com/affiliates and those categories of third parties in our privacy policy at hobsonprior.com/privacy-policy.

Shift: Wed. - Sat. 7:00am - 6:00pm Essential Functions and Responsibilities Performs deviation investigations for all areas within Quality Control Perform out of specification investigations with an emphasis on QC analytical assays (flow cytometry, ELISA, and other cell-based assays) and microbiology assays Work cross-functionally to create relevant corrective/preventative actions (CAPA). Support maintenance of a database in support of QC metrics and KPl's. Revise quality documents in support of deviation mitigation and/or CAPAs Support programs to improve on-time closure rates for all quality records. Other responsibilities as determined. Required Education, Skills, and Knowledge Bachelor's degree in a relevant discipline (biological sciences or equivalent) 1-3 years of experience in the biopharmaceutical industry within a cGMP Quality Control role Basic knowledge of biological drug development with respect to Quality Control Extremely detail-oriented with strong analytical, written, and verbal communication skills Demonstrate sense of urgency; ability to recognize time sensitivity Flexible and adaptable style with an eagerness to take on challenges Preferred Education, Skills, and Knowledge Experience with cell and/or gene therapy products GMP regulated laboratory experience Knowledge of investigation writing Pay Range: $35-38/hr