Quality control analyst jobs in Newark, DE - 102 jobs

L3Harris is dedicated to recruiting and developing high-performing talent who are passionate about what they do. Our employees are unified in a shared dedication to our customers' mission and quest for professional growth. L3Harris provides an inclusive, engaging environment designed to empower employees and promote work-life success. Fundamental to our culture is an unwavering focus on values, dedication to our communities, and commitment to excellence in everything we do. L3Harris Technologies is the Trusted Disruptor in the defense industry. With customers' mission-critical needs always in mind, our employees deliver end-to-end technology solutions connecting the space, air, land, sea and cyber domains in the interest of national security. Job Description: The Quality Control Engineer is responsible for ensuring the manufacturing in-process quality and final quality of L3Harris products. This role involves conducting audits, inspections, and quality data reviews to maintain and improve product standards. The Quality Control Engineer will coordinate quality activities related to Engineering, Manufacturing, and other functions, assisting with the implementation of Quality Control requirements, including AS9100 and ISO9001 quality systems. Essential Functions: Conducting audits and inspections and recommend corrective actions or improvement opportunities. Coordinate and provide guidance to assemblers and testers in their performance to our quality procedures and adherence to standards Contribute to RCCA, MRB and non-conformance disposition efforts Interfacing with program, engineering, manufacturing and quality management Ability to coordinate and work with multiple program and operations teams Support Packing and Shipping Identify, write up and report on non-conformances Qualifications: High School Diploma 2-5 years' experience in Manufacturing Operations of electronic assemblies. U.S. Citizenship required. Able to secure a Security Clearance. Proficient in development of manufacturing flow processes and developing inspection plans and inspection procedures, workmanship criteria. Knowledgeable in Part Specification; Identification Marking, Packaging. Knowledgeable in wiring harness specifications & requirements. Knowledgeable of Statistical Process Control techniques and statistics. Experience with auditing. Experience with Test specifications and equipment. Knowledgeable in Surface Mount Technology: printing, placement, and soldering processes. Team oriented, able to work as part of a program team. Preferred Additional Skills: Knowledgeable in MS Office tools: Excel, PowerPoint. Some experience in training or providing guidance to electronic assembly operators. Experience using SAP Experience in Rack assemblies either inspection or assembly Experience working in Aerospace and Defense industries Experience or knowledge of 5-S, Lean Six Sigma work environments In compliance with pay transparency requirements, the salary range for this role is $48,205-127,000. This is not a guarantee of compensation or salary, as final offer amount may vary based on factors including but not limited to experience and geographic location. L3Harris also offers a variety of benefits, including health and disability insurance, 401(k) match, flexible spending accounts, EAP, education assistance, parental leave, paid time off, and company-paid holidays. The specific programs and options available to an employee may vary depending on date of hire, schedule type, and the applicability of collective bargaining agreements. L3Harris Technologies is proud to be an Equal Opportunity Employer. L3Harris is committed to treating all employees and applicants for employment with respect and dignity and maintaining a workplace that is free from unlawful discrimination. All applicants will be considered for employment without regard to race, color, religion, age, national origin, ancestry, ethnicity, gender (including pregnancy, childbirth, breastfeeding or other related medical conditions), gender identity, gender expression, sexual orientation, marital status, veteran status, disability, genetic information, citizenship status, characteristic or membership in any other group protected by federal, state or local laws. L3Harris maintains a drug-free workplace and performs pre-employment substance abuse testing and background checks, where permitted by law. Please be aware many of our positions require the ability to obtain a security clearance. Security clearances may only be granted to U.S. citizens. In addition, applicants who accept a conditional offer of employment may be subject to government security investigation(s) and must meet eligibility requirements for access to classified information. By submitting your resume for this position, you understand and agree that L3Harris Technologies may share your resume, as well as any other related personal information or documentation you provide, with its subsidiaries and affiliated companies for the purpose of considering you for other available positions. L3Harris Technologies is an E-Verify Employer. Please click here for the E-Verify Poster in English or Spanish . For information regarding your Right To Work, please click here for English or Spanish .

Primary Duties & Responsibilities Member of prototype fabrication team: * Project planning, execution, tracking and reporting * Develop and improve processing methods for inorganic composite materials (preform fabrication, metal casting, mold production and assembly, programming and operation of advanced furnaces, programming and operation of CNC machining centers, precision finishing/lapping of hard materials, and other associated activities) * Characterization of materials properties * Measurement of dimensions, both manually and via computer controlled CMMs * Interface with outside entities (raw materials suppliers, equipment vendors, toll manufacturers, machine shops, and test labs) * Transfer successful products to manufacturing, including documentation and training Education & Experience * New AAS in Engineering or Science fields (or equivalent training and experience) * Relevant certifications a strong plus, such as CAM, CAD, ISO, Lean, CMM, others Skills * Familiarity with manufacturing and/or lab environment * Experience with advanced equipment (materials processing, furnaces, CNC machining centers, CMMs, etc.) * Knowledge of assembly operations * Strong mechanical aptitude * Strong computer aptitude (data summaries, programmable furnaces and machining centers, etc.) Working Conditions Position requires on-site activities for prototype fabrication. Work schedule is 5 days, 40 hrs per week, first shift. Working in lab, production and office Physical Requirements Hands-on, lab-based job environment: * Required to frequently lift/push/pull a minimum of 35 lbs * Must be able to sit, bend, squat and walk about facility * Depending on project assignment, may be required to walk/stand for entire 8 hour day Safety Requirements All employees are required to attend scheduled training, follow the site EHS procedures and Corporate EHS standards. This includes the use of proper protective equipment (PPE) as required by the job responsibilities. Managers will ensure that all safety and environmental procedures are followed consistently. They will ensure that risk assessments are performed, proper training, work instructions, required PPE is available, and will monitor compliance. Quality and Environmental Responsibilities Depending on location, this position may be responsible for the execution and maintenance of the ISO 9000, 9001, 14001 and/or other applicable standards that may apply to the relevant roles and responsibilities within the Quality Management System and Environmental Management System. Culture Commitment Ensure adherence to company's values (ICARE) in all aspects of your position at Coherent Corp.: Integrity - Create an Environment of Trust Collaboration - Innovate Through the Sharing of Ideas Accountability - Own the Process and the Outcome Respect - Recognize the Value in Everyone Enthusiasm - Find a Sense of Purpose in Work Coherent Corp. is an equal opportunity/affirmative action employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law. If you need assistance or an accommodation due to a disability, you may contact us at ******************************.

Job Description 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 ************************ .

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.

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.

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 1/5/2026 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

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_

Quality Control Chemist Apex Systems has an immediate opening for a Chemist to join a Pharma company in the Southern New Jersey area. The incumbent demonstrates proficiency through a wide exposure to pharmaceutical analyses and has a firm grasp of scientific principles and skill in applying this knowledge. The incumbent has practical experience in pharmaceutical analyses and routinely performs analysis in two of the functional areas (HPLC, GC, or Wet Chemistry). The incumbent performs and trains on routine chromatographic analyses. The incumbent works independently. ESSENTIAL DUTIES AND RESPONSIBILITIES: * Provides analytical support for production. * Performs GC, HPLC and/or Wet chemistry analyses on Raw Material, In-process and Finished Lot samples. * Supports Analytical and Chemical Development by testing samples. * Provides quick turnaround of In-process samples to production. * Thoroughly documents all results in a laboratory notebook as well as compile all data into an ancillary. * Empties HPLC and Organic waste containers. * Discards completed samples. * Makes retains of all production samples and maintains the inventory of retain samples. * Calibrates production pH meters. * Support Laboratory Investigation through testing. * Performs all tasks in accordance with cGMP compliance. * Assists in writing of SOPs, testing standards, protocols and reports. * Assists in training of lab personnel on instrumentation, methods, and cGMP. * Shares in the responsibilities of housekeeping (i.e. Glassware, waste, retains, etc.) * Provides ideas/feedback for areas where efficiency can improve. * Has in-depth understanding of most analytical methods. * Ability to troubleshoot most methods and equipment. * Reviews and releases analytical results. * Performs any other laboratory tasks deemed necessary by the QC Production Support Manager. * Adheres to personal moral, ethical, legal, and behavioral conduct that is in compliance with the Siegfried Code of Conduct. * Adheres to all applicable SHE and cGMP regulations. Requirements: * Bachelor degree in Chemistry or other science related field. Please send all resumes to David Neto [email protected] EEO Employer Apex Systems is an equal opportunity employer. We do not discriminate or allow discrimination on the basis of race, color, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), age, sexual orientation, gender identity, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, disability, status as a crime victim, protected veteran status, political affiliation, union membership, or any other characteristic protected by law. Apex will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. If you have visited our website in search of information on employment opportunities or to apply for a position, and you require an accommodation in using our website for a search or application, please contact our Employee Services Department at [email protected] or ************. Apex Systems is a world-class IT services company that serves thousands of clients across the globe. When you join Apex, you become part of a team that values innovation, collaboration, and continuous learning. We offer quality career resources, training, certifications, development opportunities, and a comprehensive benefits package. Our commitment to excellence is reflected in many awards, including ClearlyRated's Best of Staffing in Talent Satisfaction in the United States and Great Place to Work in the United Kingdom and Mexico. Apex uses a virtual recruiter as part of the application process. Click here for more details. Apex Benefits Overview: Apex offers a range of supplemental benefits, including medical, dental, vision, life, disability, and other insurance plans that offer an optional layer of financial protection. We offer an ESPP (employee stock purchase program) and a 401K program which allows you to contribute typically within 30 days of starting, with a company match after 12 months of tenure. Apex also offers a HSA (Health Savings Account on the HDHP plan), a SupportLinc Employee Assistance Program (EAP) with up to 8 free counseling sessions, a corporate discount savings program and other discounts. In terms of professional development, Apex hosts an on-demand training program, provides access to certification prep and a library of technical and leadership courses/books/seminars once you have 6+ months of tenure, and certification discounts and other perks to associations that include CompTIA and IIBA. Apex has a dedicated customer service team for our Consultants that can address questions around benefits and other resources, as well as a certified Career Coach. You can access a full list of our benefits, programs, support teams and resources within our 'Welcome Packet' as well, which an Apex team member can provide. Employee Type: Contract Location: Pennsville Township, NJ, US Job Type: Date Posted: December 15, 2025 Pay Range: $36 - $39 per hour Similar Jobs * QC Specialist * R&D Chemist 1 * Sr R&D Chemist - Polymer Science * Senior PM (Biotech - Phase III) * Lab Technician

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description Run routine assays on instruments including HPLC, UPLC, LC/MS and NMR Develop or adapt pre-existing methods based on changing needs and new raw materials Data analysis outside of lab Qualifications Bachelors degree in a scientific concentration Authorization to work in the United States indefinitely without restriction or sponsorship. Experience with HPLC, UPLC, LC/MS Experience with Waters LC systems is a plus, especially UPLC with QDA/PDA Analytical knowledge, especially working with calibration curves Knowledge of ICH guidance for validation of analytical procedures Knowledge of chemistry, especially molecules such as amino acids, sugars, and metals Experience with Empower software is a plus Additional Information This position is Full-Time, Monday through Friday, 9a.m. to 5 p.m with overtime as needed. Candidates currently living within a commutable distance of Malvern, PA are encouraged to apply. Excellent full time benefits including comprehensive medical coverage, dental, and vision options. Life and disability insurance 401(k) with company match Paid vacation and holidays Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

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

At R-V Industries, our work is much more than designing and building world-class industrial process equipment. Not only are we impacting everyday life in the world we serve, but we are providing a quality of life for our employees and their families. Every day, we come together to build stronger relationships with our vendors, our customers, and each other, so we can solve challenging problems, and continue to improve the safety, quality, and efficiency of all that we do. Caring matters at R-V. We care for each other, our safety, our quality, our learning, and our growth. We seek out diversity of thought, experience, and strengths in individuals, so we can continue to innovate as a team. We believe when we bring our true full selves to serve others, it elevates the quality of life for all. As with all s at R-V, this job is considered safety-sensitive. GENERAL JOB DESCRIPTION We are seeking an experienced Quality Inspector to join our team at our Honey Brook and Morgantown, PA locations. This position is responsible for providing day-to-day quality engineering support within our General Fabrication, ASME Section VIII, and NQA-1 markets. This position will play an integral role in the growth and improvement of the RVII organization through elevating first pass quality, increased project throughput, on-time delivery, and project expectations. DUTIES/RESPONSIBILITES Provide technical support to RVII manufacturing facilities Supports gathering and presenting key KPI measurements to the organization Participate in pre-job contract review. Develop and implement inspection and test plans for manufactured and purchased components Interface with vendors to ensure timely resolution of Quality non-conformances Conduct internal quality system process audits Coordinate and host outside inspection agencies and customer inspectors Prepare, revise, and implant Quality System procedures, policies, and work instructions Conceptualize and analyze designs to ensure technical outcomes are consistent with customer and company specifications Perform non-destructive and dimensional inspections in accordance with approved procedures, customer specifications, and governing codes. Maintain control and maintain an inventory of non-conforming products. Review contracts to determine deliverables and ensure compliance with specifications Plan, schedule, and coordinate NDE Inspection activities daily in conjunction with the manufacturing department. Maintain adherence with all M&TE requirements, testing requirements, and procedures SKILLS/QUALIFICATIONS NDE (Non-Destructive Evaluation) qualifications - minimum of Level II in VT/MT/PT/BLT/UT-T Must possess a valid American Welding Society - Certified Welding Inspector credential Must have advanced knowledge of ASME Y14.5 specification Must have fundamental knowledge of ASME Sections VIII and V Prior experience with ASME NQA-1 and 10CFR50 Appendix B preferred Ability to work independently and direct coworkers Bachelor's degree in engineering or quality related field with 2+ years of experience or 10+ years in Quality Control role Strong verbal and written communication skills Self-motivated with attention to detail and accurate reporting Proficient in MS Office suite products EDUCATIONAL/PHYSICAL REQUIREMENTS Two- or four-year college degree or relevant experience in inspection activities Everyday bending, crouching, stooping, standing, and overhead reaching Everyday exposure to moving machinery, dust, dirt, grease or other disagreeable elements Lifting up to 50-75 lbs. Must be able to pass and complete a physical assessment Must be able to perform the essential functions of the job with or without accommodation R-V Industries, Inc. is an equal opportunity employer. R-V Industries, Inc. is an equal opportunity employer. Monday-Thursday 6:00 am - 4:00 pm

The Quality Control Inspector I is responsible for inspecting, testing, and auditing raw materials and finished products, as well as releasing finished products. Attention to detail is an expectation. Demonstration of commitment to patient safety and product quality by maintaining compliance with the Quality Policy and all other documented quality processes and procedures. Inspect and release raw materials, components, sub-assemblies, and finished devices according to procedure. Drives continuous improvement activities with cross-functional team members. Generate non-conformances and escalate to the Material Review Board in a timely manner. Interacts with production areas, manufacturing and design engineering, marketing, quality, and management. Job Duties: Promotes a work environment of continuous improvement that supports CQ Medical's Quality Policy, Quality System, and the appropriate regulations. Assists with communicating business-related issues or opportunities for improvement to management. Accountable for compliance with applicable US and International regulations and directives including, but not limited to, Food & Drug Administration (FDA), Canadian and European Union regulations. Works in a team environment to achieve metrics. Interprets engineering drawings, schematic diagrams, sampling tables, or formulas and confers with management or engineering staff to determine quality and reliability standards. Selects products for tests at specified stages in production process, and tests products for variety of qualities such as dimensions, performance, mechanical, or chemical characteristics. Records test data, applying statistical quality control procedures using GMP documentation practices. Recommends modifications of existing quality or production standards to achieve optimum quality within limits of equipment capability. Quarantines all incoming material until testing is accepted. Quarantines all non-conforming material during any step of the manufacturing process until the Material Review Board dispositions the material. Purging of records as required. Maintains a neat and organized work area. Remains current on all required training. Conducts calibrations and works with 3 rd party calibration providers to ensure inspection equipment meets specifications. Conducts transactions in the Quality Management System and/or ERP system to detail the disposition of incoming and in-process materials. Working Conditions: 50 lbs. of lifting required for this role Hearing protection, safety glasses, safety shoes, and gloves are required for this role Required exposure to biohazard Job Qualifications: Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively before groups of auditors or employees of our organization. Ability to interact effectively with individuals and teams. Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. Ability to compute rate, ratio, percent, and interpret bar graphs. Decision-making ability. Ability to use testing equipment. Must be able to manage multiple tasks and perform with accuracy and a high attention to detail. Ability to identify priorities and function independently required. Ability to apply common sense understanding to carry out detailed but uninvolved written or oral instructions. Identify various discrepancies (product, process, documentation, etc.) Analytical and problem-solving skills. Computer proficiency, including data entry. MS Office Suite (Word, PowerPoint, and Excel) experience required. Education and/or Experience High school diploma or general education degree (GED). Medical device or manufacturing experience a plus. Preferred demonstration of leadership.

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 ***************************

Salary: Do you want to work for a construction company unlike any other? At JGM, we challenge the industrys status quo. Known as the team that delivers When You Need It Yesterday, weve built a culture around safety, quality, and speed. At JGM, were more than a company-were a family. Working side by side, we support one another, building trust by knowing we can count on each other. Driven by our core values, mission, and purpose, we stay focused on our vision for the future. The result? A team environment that fuels exceptional employee satisfaction, which in turn drives extraordinary client experience and continued company growth. The only question is: Are you ready to join our growing family and be part of something truly special? Be an integral part of the JGM family by living our core values: We Plan. We Adapt. We Succeed. Uncompromising Safety & Quality. Family is Our Foundation. Create Value Through Better Solutions. Whatever it Takes. Commitment to Self-improvement. Our Purpose (FOREVER): Develop Elite Leaders Today, So We Can Build Tomorrows Future Our Vision (ONE DAY): Driven to be the Safest, Fastest, and Most Effective Industrial Construction & Fabrication Partner in North America Our Mission (TODAY): Solve Our Clients Toughest Challenges with Safety and Quality Top of Mind Position Overview JGM is seeking a talented QC Inspector to join our growing team! The perfect candidate is a professional who thrives on tackling challenges in an exciting, fast-paced environment. This position will inspect raw materials, in-process work and finished products for conformance to shop drawings, specifications, and codes by performing the below duties. Responsibilities Conduct complete layout inspections, measuring dimensions (length, height, angles, radii, etc.) using precision instruments (micrometers, calipers, gauges, etc.) to ensure compliance with drawings, specifications, and codes. Verify quality at all stages: incoming materials, in-process work, and final products. Visually inspect parts, welds, bolts, coatings, and assemblies; compare pieces to detect variations; enforce standards and legal requirements. Interpret and apply shop drawings, specifications, ASTM codes, AISC standards, DOT requirements, and welding/bolting/painting codes. Maintain accurate inspection records, defect lists, and calibration of measuring equipment; coordinate with departments to resolve quality issues. Support operator training on measurement, visual acceptability, and processes; assist with internal and external audits. Manage NDE (Non-Destructive Examination) training, testing, certification, and documentation; maintain CWI certification. Review and approve quality-related purchase orders, reports, and testing requirements. Assist in developing procedures, quality summaries, and corrective actions; enforce non-conformance protocols. Serve as liaison with outside inspectors; investigate shop/field errors and support resolutions. Perform other QA-related tasks as required by supervision. Qualifications Strong knowledge of welding symbols and diagrams, and inspection tools. Highly proficient in reading blueprints and other printed instructional material. Basic Math & Geometry/Trigonometry. Familiar with variety of weld processes: Flux Core Arc Welding (FCAW), Sub Arc Welding (SAW), Gas Metal Arc Welding (GMAW), and/or Gas Tungsten Arc Welding (GTAW) Ability to perform and document inspection activities during fabrication and welding of structural piece members. Microsoft Office. CWI preferred. Self-motivated, collaborative team member. Safety focused. Operates equipment and champions safety initiatives. Education High School Degree or GED Equivalent preferred Minimum of seven years related experience and/or training in steel fabrication; or an equivalent combination of higher education and experience in the steel fabrication industry or closely related fields. Physical Requirements The demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Requires prolonged walking, standing, sitting, bending, squatting, stooping, climbing, regular lifting and carrying to move up to 50 lbs., talking, hearing, reaching, feeling, grasping, and push/pulling. Must be able to work in various weather conditions/temperatures. Regular mental and visual attention much or all the time with manual coordination. General office environment conditions. Flexibility required to travel. JGM offers a competitive wage and benefit package: Participate in the companys yearly performance bonus program Medical, Vision & Dental PTO & Holidays 401(k) + Matching Life Insurance Short/Long-Term Disability Employee Assistance Program Generous Referral Program Training and Further Education This job description is subject to change based on the needs of the business and is notall-inclusive. JGM is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

At Quaker Houghton, we are experts in the development, production and application of chemical specialties, process fluids, lubricants and coatings for the manufacturing industry. We have been an integral part in the growth of the 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

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 1/5/2026 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

Mindlance is a national recruiting company which partners with many of the leading employers across the country. Feel free to check us out at ************************* Job title: AML/KYC Quality Control Analyst Location: ONE PENNS WAY, BLDG 1, NEW CASTLE, DE 19720 USA OR Irving, Texas 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. 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. 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.