Quality control analyst jobs in Wilmington, DE

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 ************************.

A career at Resilience is more than just a job - it's an opportunity to change the future. Resilience is a technology-focused biomanufacturing company that's changing the way medicine is made. We're building a sustainable network of high-tech, end-to-end manufacturing solutions to better withstand disruptive events, serve scientific discovery, and reach those in need. For more information, please visit ****************** Position Summary The Senior Analyst II, Quality Control - Flow Cytometry is to support our Quality Control department. The successful candidate will be responsible for performing routine testing for manufacturing release and stability samples of gene (viral vector) and cell therapy products. In this role, the Senior Analyst II will collaborate closely with Manufacturing and Quality Control Operations teams to ensure all required testing is completed accurately, on time, and in full compliance with established standard operating procedures and testing methods. This position reports to the Technical Lead Manager, Quality Control - Analytical, and is based at our East Norriton, PA facility. Job Responsibilities Perform routine sample analysis in support of manufacturing release and stability activities. Sample testing of manufactured products using protein-based assays, molecular methods, and cellular assays. Participate in method qualification/validation activities, as necessary. Analyze, document, and report experimental data in accordance with Resilience requirements. Maintain, calibrate, and operate analytical equipment. Qualify equipment related to testing. Serve as owner of QC equipment and complete necessary owner tasks, as assigned by management. Perform method transfer and qualification activities. Document work in accordance with cGMPs, established business processes and applicable SOPs. Review data, identify discrepancies, and escalate issues to management. Author SOPs, methods, protocols, training materials, and reports in alignment with applicable cGMPs, business standards, and intended use. Own, author, review/approve, and support QC change controls, deviations, and other quality records for the East Norriton site, as applicable. Investigate OOS or OOT events and develop/implement preventive and corrective actions. Mentor, coach and train Quality Control Associates. Completes qualified program requirements necessary to train other employees. Acts as liaison with Clients for site-specific Flow Cytometry, as needed. Other activities as assigned. Minimum Qualifications Experience in mammalian cell culture. Knowledge of general analytical methods. Successful visual acuity test required for this role. Experience in Flow Cytometry. Preferred Qualifications BS in relevant discipline (immunology, cell biology, or related field). 5+ years relevant life science experience. GMP experience preferred. Other Ideal Personal Characteristics: Ability to thrive in ambiguous or complex situations. Highly motivated and self-directed. Thrives in matrix environment. Excellent interpersonal, verbal and written communication skills Resilience is an Equal Employment Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, disability status, physical or mental disability, genetic information, or characteristic, or other non-job-related characteristics or other prohibited grounds specified in applicable federal, state, and local laws. Requests for reasonable accommodation can be made at any stage of the recruitment process. Resilience offers employees a robust total rewards program including an annual cash bonus program, a 401(k) plan with a generous company match and our benefits package which is thoughtfully designed to support our employees with great healthcare (including medical, dental and vision), family building benefits, life and disability insurance, flexible time off, paid holidays, other paid leaves of absence, tuition reimbursement and support for caregiving needs. Our target base pay hiring range for this position is $100,000.00 - $137,500.00 per year. Actual base pay is dependent upon a number of factors, including but not limited to, the candidate's geographical location, relevant experience, qualifications, skills and knowledge. Excited about Resilience and the biomanufacturing revolution? We encourage you to apply and start a conversation with one of our recruiters.

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

We are seeking motivated Production Chemists to join our GMP-compliant pharmaceutical manufacturing team working in both pilot plant and kilolabs. The Production Chemist will be responsible for performing production operations involving chemical processing, batch preparation, and in-process testing to support the manufacture of pharmaceutical products. In addition, the Production Chemist will provide day-to-day supervision and guidance to production operators, ensuring processes are carried out in full compliance with GMP and safety requirements. This position requires strict adherence to cGMP standards, safety regulations, and data integrity practices. The role involves working on a rotating shift schedule, including nights and/or weekends. Key Responsibilities Execute production processes involving weighing, charging, mixing, distillation, and chemical reactions in compliance with SOPs and batch production records. Operate and monitor process equipment (reactors, filtration systems, dryers, etc.) according to validated procedures. Collect, test, and interpret in-process samples to ensure product quality and batch consistency. Maintain accurate, real-time documentation in batch production records, logbooks, and electronic systems to ensure data integrity and regulatory compliance. Supervise and support operators during daily production operations, ensuring tasks are performed according to GMP and safety standards. Provide on-the-floor technical guidance and troubleshoot issues as needed. Adhere to all cGMP, safety, and environmental policies, including proper handling of raw materials, intermediates, and finished products. Support cleaning, equipment setup, and line changeover activities as required. Assist in deviation investigations, corrective and preventive actions (CAPA), and continuous improvement initiatives. Collaborate with Quality Assurance, Engineering, and Maintenance teams to ensure efficient production operations. Participate in training programs and maintain qualifications for GMP manufacturing operations.

Piper Companies is seeking a Quality Control Analytical Scientist (Flow Cytometry) to support GMP analytical testing for a late-stage biopharmaceutical organization advancing gene therapies for rare genetic disorders. This onsite role in Exton, PA offers hands-on experience with flow cytometry and related cell-based assays supporting clinical manufacturing. Responsibilities of the Quality Control Analytical Scientist (Flow Cytometry): * Perform GMP-compliant flow cytometry assays to support in-process, drug substance, and drug product testing. * Execute methods such as percent transduction efficiency and CD90 analysis. * Support additional testing platforms including cell culture, ELISA, and qPCR. * Review results for accuracy, data integrity, and compliance with GMP documentation standards. * Conduct investigations, CAPAs, and method troubleshooting as needed. * Maintain laboratory organization, equipment calibration, and readiness for audits. Qualifications of the Quality Control Analytical Scientist (Flow Cytometry): * 3-5 years of QC experience in a GMP-regulated biopharma or biologics environment. * Strong experience with flow cytometry, gating strategies, and data analysis. * 2-3 years of mammalian cell culture experience preferred. * Familiar with analytical assays such as ELISA and qPCR. * BS in Biochemistry, Biology, or related Life Science required. Compensation for the Quality Control Analytical Scientist (Flow Cytometry): * Pay Rate: $40/hour * Type: Contract-to-Hire (benefits included) * Location: Onsite - Exton, PA * Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays Application Period: This position opens for applications on 12/9/2025 and will remain open for a minimum of 30 days from the posting date. Keywords: Quality Control, QC Scientist, Flow Cytometry, FACS, GMP, Analytical Testing, Biologics, Gene Therapy, Cell Culture, ELISA, qPCR, Transduction Efficiency, CD90, Gating Strategy, Data Integrity, CAPA, SOP, Aseptic Technique, QC Assays, Biopharma, Exton PA #LI-JM1 #LI-ONSITE

Job title: AML/KYC Quality Control Analyst Duration: 12+ months contract (with possibility of extension) Job Type: Onsite Job Current Status: Actively Interviewing Please confirm candidate location on resume while submittal. JOB DESCRIPTION: KYC Quality Control ("QC") Analyst work to ensure high quality standards are maintained for KYC and Enhanced Due Diligence (EDD) casework conducted by KYC analysts. The QC Specialist will review cases for adherence to EDD procedures and ensure analyst conclusions are clear, complete and supported by the information in the file. The QC specialist will also identify and escalate critical issues to their Quality Control Supervisor.The QC specialist will assist in identifying problem areas and risks associated with processes and make recommendations to improve quality of KYC analyst file work. KYC QC Specialists will serve as a key support resource for delivering training and guidance to KYC analysts. The KYC QC Specialist will decrease regulatory and reputational risk by exercising sound judgment in approving/rejecting submitted cases. The QC Specialist operates in a team environment and has regular interaction with Business, Operations and AML Compliance management, as well as KYC and QC teams. The QC Specialist should be able to work under minimal supervision. Participate in a risk-based AML-specific testing program, adhering to the Global Compliance Testing standards, in order to provide senior management with comprehensive end-to-end assessments of the regulatory control environment. - Perform Compliance testing processes and activities in accordance with the Global Compliance Testing standards. Ensure the testing is completed timely and within quality expectations including writing clear and concise summaries and reports with the appropriate supporting workpaper documentation. - Become fully familiar with using and incorporating the Global Compliance Testing standards related to research, planning, test execution and reporting/conclusion. Ensuring the workpaper documentation is within the guidelines and standards. - Complete key projects as assigned by the Compliance Testing Management - Recognize, document and assess key risks, control environments, and applicable regulations - Effectively use data analysis to assist in the completion of testing activities - Maintain proactive communication with Senior Management including periodic updates on engagement progress and identified or potential issues. Additional Information This is an urgent opening with one of our banking client at New Castle, DE OR Irving, Texas . Hiring manager is actively interviewing candidate will close this position ASAP. If you are interested and a good match please respond to this posting with your recent updated copy of resume or you can reach me on my direct number ************. Regards, Aditya

Reporting to the QC Analytical Lead, the QC Analytical Scientist will serve as a technical expert in analytical chemistry testing and laboratory operations in support of drug product manufacturing at WuXi STA's Middletown, DE site. This role includes advanced execution and troubleshooting of analytical methods, stability studies, method transfers, and equipment qualification, as well as maintaining compliance with GMP, corporate quality standards, and global regulatory requirements. The QC Analytical Scientist will play a critical role in both startup and steady-state operations, ensuring timely and accurate testing for product release, validation, and regulatory inspections. **Responsibilities** QC Analytical Testing and Support - Perform and review QC analytical testing for drug products, raw materials, packaging components, and stability samples in accordance with approved methods and SOPs. - Execute advanced analytical techniques including HPLC, UPLC, GC, dissolution, UV-Vis, TOC, Karl Fischer, and other relevant compendial and non-compendial methods. - Troubleshoot analytical instrumentation and methods, supporting investigations and continuous improvement. - Author, review, and revise test methods, SOPs, and technical documents. - Mentor and train QC Analysts and Associates in analytical techniques and best practices. - Other QC tasks assigned by analytical lead. Regulatory Compliance and Documentation - Ensure all activities are conducted in strict compliance with cGMP, safety, and quality standards. - Maintain accurate, complete, and inspection-ready laboratory documentation. - Participate in method transfer, qualification, and validation of analytical methods and equipment. - Support client and regulatory audits by presenting data, explaining technical approaches, and preparing responses. - Escalate deviations, out-of-specification (OOS) results, or atypical findings promptly to the QC Analytical Manager. **Qualifications** - Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related scientific discipline with 5+ years of QC analytical laboratory experience in a GMP-regulated pharmaceutical or biotechnology environment; OR - Master's degree with 3+ years or PhD with 1+ years of relevant QC analytical laboratory experience. - Deep expertise in chromatographic and spectroscopic methods (HPLC/UPLC, GC, UV-Vis, TOC, KF, etc.) and data interpretation. - Demonstrated ability to lead laboratory investigations, troubleshoot instrumentation, and author technical reports. - Strong knowledge of GMP regulations, ICH guidelines, and data integrity principles (ALCOA+). Preferred Qualifications - Experience in method transfer, qualification, and validation of analytical methods. - Familiarity with LIMS, Empower, or other electronic laboratory management systems. - Prior experience in a CDMO or multi-client environment. - Strong communication and collaboration skills to support cross-functional teams, audits, and regulatory inspections. An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against based on disability This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. Employees holding this position will be required to perform any other job-related duties as requested by Management. **Need help finding the right job?** We can recommend jobs specifically for you! An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability (************************************************************************************************** **Job Locations** _US-DE-Middletown_ **Job ID** _2025-13807_

JobID: 210692742 JobSchedule: Full time JobShift: : In this highly impactful role, you will drive innovative automation processes and strategies to enhance our global digital learning solutions operations. Your expertise in automation tools and analytics will be essential for streamlining workflows and delivering impactful solutions across the organization. If you are passionate about leveraging technology to elevate learning experiences, we want to hear from you! As a Learn Automation & Quality Associate in Digital Solutions, you will oversee the daily robotic scripting management, processing of HCM Learning management new course and existing course maintenance automation tasks through robotics supporting Business As Usual intake as well as specialty high-impact requests, collaborate with teams to streamline workflows and manage digital learning tools. You will support initiatives that drive efficiency and quality ensuring learning solutions remain effective and scalable. Your work empowers partners across the organization, helping them access reliable and innovative learning experiences. By leveraging emerging technologies you help create a transformative learning environment that fosters ongoing improvement and future-readiness for all learners. Job Responsibilities: * Support learning operations automation technologies, global scalability, process control documentation, field readiness for technology upgrades, and process agility. * Implement a continuous improvement mindset by regularly assessing and refining Digital Solutions tools, and robotic scripts, while aligning to quality standards, and developing scalable automation strategies based on reporting trends, user feedback, industry developments, and organizational needs. * Support change initiatives that advance automation and quality operating enhancements, ensuring seamless transitions and high adoption rates across the organization. * Consult with HCM partners to ensure alignment of HCM functionality with robotic processing. * Stay current with industry trends in automation and quality, particularly in digital operations development, quality validation, effective use of accessibility tools, and measurement and evaluation practices. * Engage with learning partners to understand and document emerging operational refinement needs. * Create strategies and lead initiatives to expand the use of automation technology and quality tools. Required qualifications, capabilities and skills: * Minimum of 3 years of work experience in complex Digital automation tools, Oracle HCM Learning Management tools, troubleshooting, agile workflows, technical infrastructure, multimedia tools, quality controls, accessibility tools and Learning Technologies. * Excellent written and verbal communication skills as well as strong escalation skills * Working knowledge of Oracle HCM Learn Management admin and learner functionality, coding and running scripts supported through Git/Bitbucket, IntelliJ, Cucumber/Gherkins, Jira, Tableau, JDK, Maven, cloud services, and AI tools such as LLMs (ChatGPT). * Experience running & troubleshooting production environment BOT automation in a production operational team. * Strong project management & prioritization skills demonstrated by balancing multiple projects through agility processes, quality, controls & risk management, process scalability, MVP task completion and business impact of deliverables. * Ability to build effective teamwork, collaborate with technical and business partners, openness to leverage multiple perspectives, and ability to work both independently and collaboratively to achieve deliverables. * Ability to identify, learn, grow and troubleshoot new tools, platforms, and production processes. Preferred qualifications, capabilities and skills * Experience researching, evaluating, and prototyping emerging technologies/approaches and consult on potential application in learning. * Strong knowledge of HCM data & digital learning tableau reporting tools, reporting design techniques, data feeds to assure accurate reporting. * Experience designing, developing, and troubleshooting robotic templates. * Working knowledge of Figma, HTML5, xAPI, Microsoft Office Tool, User Experience/User Interface, Computer Science, Learning Technologies, Learning Design and Development, or similar field.

At Eurofins, your work supports global health and safety. We invest in your professional growth with opportunities to advance in the biopharmaceutical industry, backed by collaborative teams, work-life balance, and competitive benefits. Eurofins Scientific is a global leader in life sciences, providing analytical testing across industries-from food and water to pharmaceuticals and advanced materials. We help the world's top companies ensure their products are safe, authentic, and accurately labeled. Relocate to Indianapolis - Join Our Team! Are you ready for a fresh start in a vibrant city? We're seeking a Team Leader - QC Medical Packaging Testing to join our growing Indianapolis facility. This is your chance to advance your career while enjoying all the benefits of living in one of the Midwest's most dynamic cities. Why Indianapolis? We provide relocation assistance to support your move! Affordable cost of living Thriving job market and biotech community Great neighborhoods, schools, and cultural attractions Job Description Testing & Analysis: Perform lab testing on primary and secondary packaging systems, including container closure integrity, mechanical (break loose/glide force, residual seal force), and vibration testing. Sample & Data Management: Receive samples in LIMS, execute test methods, collect and document data, and release results in LIMS. Method Development: Support development and qualification of new test methods. Client Interaction: Communicate with clients to meet business needs promptly. Compliance & Safety: Ensure adherence to safety standards, GMP, and regulatory requirements. Team Leadership: Supervise, coach, and develop team members; foster motivation and morale. Operational Oversight: Coordinate workflow, monitor daily tasks to meet turnaround times (TAT), and manage job plans. Performance & Growth: Conduct performance reviews, manage training records, interview candidates, and support succession planning. Qualifications Bachelor's degree in science, engineering, or technology (or equivalent experience) Professional leadership experience preferred GMP experience Experience with lab testing - container integrity Authorization to work in the U.S. indefinitely without restriction or sponsorship Additional Information Position is full-time, 8:00 am- 5:00 pm Overtime as needed. 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 #LI-EB1 Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

At Eurofins, your work supports global health and safety. We invest in your professional growth with opportunities to advance in the biopharmaceutical industry, backed by collaborative teams, work-life balance, and competitive benefits. Eurofins Scientific is a global leader in life sciences, providing analytical testing across industries-from food and water to pharmaceuticals and advanced materials. We help the world's top companies ensure their products are safe, authentic, and accurately labeled. Relocate to Indianapolis - Join Our Team! Are you ready for a fresh start in a vibrant city? We're seeking a Team Leader - QC Medical Packaging Testing to join our growing Indianapolis facility. This is your chance to advance your career while enjoying all the benefits of living in one of the Midwest's most dynamic cities. Why Indianapolis? We provide relocation assistance to support your move! Affordable cost of living Thriving job market and biotech community Great neighborhoods, schools, and cultural attractions Job Description Testing & Analysis: Perform lab testing on primary and secondary packaging systems, including container closure integrity, mechanical (break loose/glide force, residual seal force), and vibration testing. Sample & Data Management: Receive samples in LIMS, execute test methods, collect and document data, and release results in LIMS. Method Development: Support development and qualification of new test methods. Client Interaction: Communicate with clients to meet business needs promptly. Compliance & Safety: Ensure adherence to safety standards, GMP, and regulatory requirements. Team Leadership: Supervise, coach, and develop team members; foster motivation and morale. Operational Oversight: Coordinate workflow, monitor daily tasks to meet turnaround times (TAT), and manage job plans. Performance & Growth: Conduct performance reviews, manage training records, interview candidates, and support succession planning. Qualifications Bachelor's degree in science, engineering, or technology (or equivalent experience) Professional leadership experience preferred GMP experience Experience with lab testing - container integrity Authorization to work in the U.S. indefinitely without restriction or sponsorship Additional Information Position is full-time, 8:00 am- 5:00 pm Overtime as needed. 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 #LI-EB1 Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Responsibilities: LAB RELEASES Maintain accuracy and transcribe large volumes of analytical data to support products on SAP system through data entry. Review, obtain QC Supervisor approval and release non-GMP products in SAP. Performs MMBE and MB1B SAP functions to also release or block non-regulated products in warehouse database. Also, update inventory out-of-balance screens and found inventory. In support of maintaining the accuracy of analytical data and releasing products on-time, occasionally require Technical and/or IT support from Sr. QA Analysts to ensure proper alignment with Avantors methods and procedures; CofA error corrections and repush to the CofA website. Creates 05 IL as needed Work with Contract labs to coordinate test results and escalate priorities/rush jobs SAMPLE SHIPMENTS Assist with gathering documents to ship samples to outside labs Sample shipment shipping documentation (i.e. MSO, Chain of Custody and MSDS) are generated and submitted. Samples are packaged and delivered to Distribution for pick up and shipment. Communicate with outside lab to ensure sample arrival, are on schedule for testing and for the lab to receive the CofA on time. Capture, manage and make available to management sample shipments via Google Drive spreadsheet. FINANCIAL Inventories and orders office and lab supplies to ensure a smooth work process flow. Communicate with Receiving to ensure supply arrivals are delivered to the lab. Upon receipt of office and lab supplies; packing slips, invoices are reviewed to ensure the QC Lab received all materials and all order transactions are invoiced correctly. Responsible for generating purchase requisitions for purchase orders and maintaining office equipment preventative maintenance and notifying service techs for service. Monthly P-Card reconciliation. Capture, manage and make available to management PO requests, office and lab supply orders each via Google Drive spreadsheets. OOS Investigations (20%) of the time: The successful candidate with assist in OOS investigations and performing root cause analysis. The candidate will be responsible for events/CAPA's that are opened in response to the OOS investigations. Follow thru until completion. Handle general administrative tasks, manages the meeting rooms booking as per needs Works closely with Finance representatives to have all inventory records updated Keep track of all docs needed by/for the accountancy company (invoices, contracts and other) Archiving of company documents according local law Maintains a record of entry and exit of documents and registers them *Other duties as assigned

Job Summary We are seeking a detail-oriented and highly responsible Quality Control Site Safety Health Officer (QC/SSHO) to support a government services contract. This individual will be responsible for overseeing quality control and site safety practices in accordance with Federal and State regulations. A key aspect of the role includes documenting and uploading field observations (photos, statements, reports) into the computerized database system such as NCMMS/Maximo or similar. This is a mission-critical role that ensures safety, compliance, and accurate reporting on all aspects of the contract work carried out. Key Responsibilities: Serve as the primary Quality Control and Safety point of contact on-site. Ensure compliance with all federal, state, and local safety and environmental regulations, as well as project-specific guidelines. Conduct daily Safety Inspections and QC audits on completed and ongoing contract work to identify and mitigate potential hazards and quality issues. Document all findings with photographs and written statements to be entered into NCMMS/Maximo or similar system in a timely and accurate manner as part of the role. Coordinate and lead preparatory, initial, and follow-up QC meetings in accordance with the approved Quality Control Plan Responsible for leading safety meetings, toolbox talks, and driving safe work performance at all times Develop and submit activity hazard analyses (AHAs) and ensure their implementation in the field. Enforce all job site safety protocols and OSHA standards. Interface with government representatives, subcontractors, and field staff to maintain compliance with contract specifications.Maintain detailed site logs, inspection reports, and records in alignment with contract and computerized maintenance system requirements. Investigate incidents or near-misses, gather statements, and contribute to root cause analysis and corrective actions. Provide leadership with overviews of all incidents no matter the severity for compliance, follow up, and safety reporting purposes. Qualifications: Prior experience working as a QC Manager or SSHO on federal or DoD projects (NAVFAC, USACE, GSA) preferred experience). Familiarity with mechanical systems and related inspection procedures. Familiarity with custodial procedures and services (if applicable). Familiarity with grounds maintenance procedures and services (if applicable). Working knowledge of NCMMS/Maximo or similar asset management platforms OSHA 30-Hour Construction Safety Certification (required). EM 385-1-1 certification (required by contract). USACE Construction Quality Management (CQM) certification or equivalent certification. Strong verbal and written communication skills. Proficient in photo documentation and digital reporting processes. Ability to work independently, manage time effectively, and adhere to strict government protocols. U.S. Citizenship is required due to access requirements for military installations. Additional Requirements: Must be able to pass background checks and security clearance as required for access to applicable contract. Must adhere to all PPE guidelines. This includes wearing appropriate PPE at all times and following all site-specific safety procedures/plans. Ability to climb ladders, navigate construction sites, and stand for extended periods. Ability to bend, stoop, pick up items up to 50lbs. Must have a valid driver's license, Read ID, and/or Passport Primary Place of Performance Philadelphia PA, Shipyard and Mechanicsburg PA. Compensation and Benefits Pay Range: $80,000 - $85,000 Medical, Dental, Vision, Supplementary insurances, 401k match EQUAL OPPORTUNITY EMPLOYER…..FORTIS is an Equal Opportunity Employer. Prospective employees will receive consideration without discrimination because of race, color, religion, creed, gender, national origin, age, disability, marital or veteran status, sexual orientation, or any other legally protected status. We are committed to Equal Employment Opportunity and providing reasonable accommodations to applicants with physical and/or mental disabilities. FORTIS is an E-Verify employer Applicant must receive favorable background and drug screen results and meet eligibility requirements for access to government computer systems and or facilities if necessary. Drug screens follow Federal guidelines.

Job Description An independent, family-owned business in Philadelphia, I. Rice & Co. has been making quality food products and flavors since 1884. With considerable growth and expansion, we are looking for qualified employees to help in a variety of positions. As a food manufacturing plant, I. Rice & Co. offers a diverse range of employment opportunities, from production coordination to warehouse stocking and inventory organization. With a passionate community, competitive pay, and generous bonus incentives, I. Rice offers ample opportunity for personal and professional growth. QUALITY CONTROL SENIOR LAB TECHNICIAN This permanent, full-time position supports the Quality Assurance department. The Senior Lab Technician plays a critical role in maintaining and enhancing our commitment to food safety and quality. This hands-on position combines technical expertise with leadership, performing daily functions in the lab, while also supporting the Director of Quality Assurance with administering department operations, validating program CCPs, and participating in audits. Knowledge of laboratory principles is required. Product testing includes brix, pH, water activity, titrations, viscosities and organoleptic evaluations. Environment is a clean and modern lab working with terrific people. Essential Job and Duties - Perform analytical tests on raw materials and finished products - Maintain extensive record keeping - Assist with auditing and maintaining SQF, GMP, & HACCP programs at the plant - Calibrate laboratory equipment - Participate in company audits - Work with production to make adjustments to batches in order to adhere to product specifications - Run batch freezer to make finished product for further study and sensory evaluation - Measure and verify raw materials needed for batching - Respond to customer questions or concerns in a professional and appropriate manner - Inspection of inbound receipts - Maintain the finished goods retention library - Sample finished product for microbial analysis - Maintain raw material specification documentation and product specification documentation - Maintain finished product specification documentation This position is supported by a team of technicians performing similar tasks. Our products, equipment, and methods are continually evolving. The duties associated with this position will change and evolve as needed. This individual is required to be willing and able to take on new responsibilities as needed. Education and Experience - Bachelor's Degree in Food Science, R&D, or related course of study preferred - 5 years of related quality assurance or lab experience - Experience with FDA, USDA, GFSI, SQF, FSMA, GMP, GLP, HACCP preferred Skills and Expectations - Ability to prioritize and organize ones work load - Ability to work in a team environment as well as individually in an environment with changing priorities - Comfortable working on an active busy production floor among batching and packaging equipment. - Ability to manage time effectively - Maintain proper lab conditions and equipment maintenance - Maintain proper record keeping and perform data entry - Be capable of working in various work settings of the facility including laboratory, office and plant areas - Perform basic math skills - Proficient computer skills, including above average knowledge of MS Excel - Understand and perform scaling/measuring in standard and metric formats - Food industry experience preferred. - Lifting and carrying up to 50 pounds - Being able to withstand extended periods of time on one's feet - Working and walking in a wet environment Benefits Benefits and Compensation - Weekly pay with direct deposit - Health insurance - Various supplemental insurance policies available after 90-day introductory period - Life insurance available after completion of 90-day introductory period - 401-K retirement plan available after one year of employment - Option to participate in uniform program - Annual bonus incentives I.Rice is an equal opportunity employer and derives our staff skills through a diverse and talented workforce. This person will work closely with all departments and persons in our facility and must conduct themselves professionally at all times.

Skill Source is a leading placement service specializing in manufacturing operations both on the production floor and front office. We work hard finding the right complimentary fit for both client and qualified candidates. We facilitate this by asking not just the right questions technically but the right questions to fit you personally. We have a substantial client base to work with so there is a very good chance we can find you the next step in a more satisfying career. Submit your hard earned resume today and let us see what we can do for you! Job Description My growing client is looking for a skilled Metal Anodizing/Plating Technician. Full time position with a growing up and coming manufacturing company! Great pay and benefits! First shift position. Growth opportunities available. Qualifications At least 2yrs experience processing metal coatings (anodizing) onto metal parts (medical device or aerospace a plus) MUST have experience disposing hazardous materials in compliance with OSHA and/or HAZMAT guidelines Chemistry Degree - Associates or better strongly preferred. Additional Information These are permanent positions NOT contract! Excellent pay (Pay commensurate with experience) and benefits packages! Some of our clients pay FULL medical! Please feel free to review our other opportunities at ***************************

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

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

Piper Companies is seeking a Quality Control Analytical Scientist (qPCR) to join a growing biopharmaceutical organization pioneering gene therapies for rare genetic disorders. This onsite position in Exton, PA provides the opportunity to perform advanced molecular testing and DNA-based assays that directly support GMP manufacturing and product quality operations. Responsibilities of the Quality Control Analytical Scientist (qPCR): * Perform GMP-compliant qPCR testing to support bulk, drug substance, and final product analysis. * Conduct DNA extraction and assays including Vector Copy Number (VCN) and VSVG testing. * Support complementary methods such as cell culture, ELISA, and flow cytometry. * Review data for accuracy, integrity, and compliance with GMP and documentation standards. * Execute OOS investigations, CAPAs, and method troubleshooting as needed. * Maintain laboratory organization, calibration schedules, and audit readiness. Qualifications of the Quality Control Analytical Scientist (qPCR): * 3-5 years of QC experience in a GMP-regulated biopharma or biologics environment. * Strong proficiency in qPCR methodology, DNA extraction, and molecular analysis. * 2-3 years of mammalian cell culture experience preferred. * Familiarity with analytical platforms such as ELISA and flow cytometry. * Excellent attention to detail, communication, and documentation skills. * BS in Biochemistry, Biology, or related Life Science required. Compensation for the Quality Control Analytical Scientist (qPCR): * Pay Rate: $40/hour * Type: Contract-to-Hire (benefits included * Location: Onsite - Exton, PA * Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave as required by law, and Holidays Application Period: This position opens for applications on 11/17/2025 and will remain open for a minimum of 30 days from the posting date. Keywords: Quality Control, QC Scientist, qPCR, Vector Copy Number, VCN, DNA Extraction, VSVG, GMP, Biologics, Gene Therapy, Molecular Testing, Analytical Methods, Cell Culture, ELISA, Flow Cytometry, CAPA, SOP, Data Integrity, Aseptic Technique, ALCOA, Good Documentation Practices, QC Assays, Biopharma, Exton PA #LI-JM1 #LI-ONSITE

Reporting to the QC Analytical Lead, the QC Analytical Scientist will serve as a technical expert in analytical chemistry testing and laboratory operations in support of drug product manufacturing at WuXi STA's Middletown, DE site. This role includes advanced execution and troubleshooting of analytical methods, stability studies, method transfers, and equipment qualification, as well as maintaining compliance with GMP, corporate quality standards, and global regulatory requirements. The QC Analytical Scientist will play a critical role in both startup and steady-state operations, ensuring timely and accurate testing for product release, validation, and regulatory inspections. Responsibilities QC Analytical Testing and Support • Perform and review QC analytical testing for drug products, raw materials, packaging components, and stability samples in accordance with approved methods and SOPs. • Execute advanced analytical techniques including HPLC, UPLC, GC, dissolution, UV-Vis, TOC, Karl Fischer, and other relevant compendial and non-compendial methods. • Troubleshoot analytical instrumentation and methods, supporting investigations and continuous improvement. • Author, review, and revise test methods, SOPs, and technical documents. • Mentor and train QC Analysts and Associates in analytical techniques and best practices. • Other QC tasks assigned by analytical lead. Regulatory Compliance and Documentation • Ensure all activities are conducted in strict compliance with cGMP, safety, and quality standards. • Maintain accurate, complete, and inspection-ready laboratory documentation. • Participate in method transfer, qualification, and validation of analytical methods and equipment. • Support client and regulatory audits by presenting data, explaining technical approaches, and preparing responses. • Escalate deviations, out-of-specification (OOS) results, or atypical findings promptly to the QC Analytical Manager. Qualifications • Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related scientific discipline with 5+ years of QC analytical laboratory experience in a GMP-regulated pharmaceutical or biotechnology environment; OR • Master's degree with 3+ years or PhD with 1+ years of relevant QC analytical laboratory experience. • Deep expertise in chromatographic and spectroscopic methods (HPLC/UPLC, GC, UV-Vis, TOC, KF, etc.) and data interpretation. • Demonstrated ability to lead laboratory investigations, troubleshoot instrumentation, and author technical reports. • Strong knowledge of GMP regulations, ICH guidelines, and data integrity principles (ALCOA+). Preferred Qualifications • Experience in method transfer, qualification, and validation of analytical methods. • Familiarity with LIMS, Empower, or other electronic laboratory management systems. • Prior experience in a CDMO or multi-client environment. • Strong communication and collaboration skills to support cross-functional teams, audits, and regulatory inspections. An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against based on disability This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. Employees holding this position will be required to perform any other job-related duties as requested by Management.

At Eurofins, your work supports global health and safety. We invest in your professional growth with opportunities to advance in the biopharmaceutical industry, backed by collaborative teams, work-life balance, and competitive benefits. Eurofins Scientific is a global leader in life sciences, providing analytical testing across industries-from food and water to pharmaceuticals and advanced materials. We help the world's top companies ensure their products are safe, authentic, and accurately labeled. Relocate to Indianapolis - Join Our Team! Are you ready for a fresh start in a vibrant city? We're seeking a Team Leader - QC Medical Packaging Testing to join our growing Indianapolis facility. This is your chance to advance your career while enjoying all the benefits of living in one of the Midwest's most dynamic cities. Why Indianapolis? We provide relocation assistance to support your move! Affordable cost of living Thriving job market and biotech community Great neighborhoods, schools, and cultural attractions Job Description Testing & Analysis: Perform lab testing on primary and secondary packaging systems, including container closure integrity, mechanical (break loose/glide force, residual seal force), and vibration testing. Sample & Data Management: Receive samples in LIMS, execute test methods, collect and document data, and release results in LIMS. Method Development: Support development and qualification of new test methods. Client Interaction: Communicate with clients to meet business needs promptly. Compliance & Safety: Ensure adherence to safety standards, GMP, and regulatory requirements. Team Leadership: Supervise, coach, and develop team members; foster motivation and morale. Operational Oversight: Coordinate workflow, monitor daily tasks to meet turnaround times (TAT), and manage job plans. Performance & Growth: Conduct performance reviews, manage training records, interview candidates, and support succession planning. Qualifications Bachelor's degree in science, engineering, or technology (or equivalent experience) Professional leadership experience preferred GMP experience Experience with lab testing - container integrity Authorization to work in the U.S. indefinitely without restriction or sponsorship Additional Information Position is full-time, 8:00 am- 5:00 pm Overtime as needed. 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 #LI-EB1 Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.