Quality control analyst jobs in Delaware - 46 jobs

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

Intro Marketing Language: Join a team that supports your career growth, advancement and expanding opportunities! At JPMorgan Chase we take pride in valuing our employees' individualities, while supporting an inclusive culture of teamwork. Job Summary: As a Quality Control Analyst within Loan Accounting, you will be part of a team dedicated to navigating the dynamic landscape of client expectations and product complexities. Your role in Wholesale Lending Services is crucial in ensuring the delivery of top-tier products and services to our clients, maintaining the highest quality standards. You will be responsible for conducting quality reviews on the system of record for both new and existing credit facilities. Job Responsibilities: Evaluate, identify, and report any inconsistences between the supporting documentation relative to the proposal data entered in accordance with internal risk policies Ensure organizational requests, queries, and issues sent to the team are actioned accurately and timely Adhere to production queues, exception reporting, and Key Performance Indicators Collaborate with Operations, Credit, and Controls in resolving items and preparing weekly ad hoc reports when requested Required Qualifications, Capabilities, and Skills: Experience reading and interpreting loan documentation and/or working with credit products such as revolving lines of credit, term loans, commercial cards, letters of credit Demonstrated decision-making skills Strong oral and written communication skills Analytical mindset with the ability to probe sensitive issues while maintaining the highest level of integrity and objectivity Ability to prioritize tasks and pivot in response to new developments Preferred Qualifications, Capabilities, and Skills: Bachelor's Degree Intermediate use of Microsoft Word, Excel, Access Experience with loan accounting systems, such as LoanIQ

**Are you looking to power the next leap in the exciting world of advanced electronics?** Do you want to help solve problems that drive success in the rapidly evolving technology and connectivity landscape? Then bring your problem-solving, passion, and creativity to help us power the next leap in electronics. At **Qnity** , we're more than a global leader in materials and solutions for advanced electronics and high-tech industries - we're a tight-knit team that is motivated by new possibilities, and always up for a challenge. All our dedicated teams contribute to making cutting-edge technology possible. We value forward-thinking challengers, boundary-pushers, and diverse perspectives across all our departments, because we know we play a critical role in the world enabling faster progress for all. Learn how you can start or jumpstart your career with us. We are seeking a highly skilled **Technician** to support advanced machining, prototyping, and process development for complex engineering and R&D projects. This role is critical to delivering precision components, improving manufacturing processes, and enabling innovation across multiple product lines. **Key Responsibilities** · Machining & Fabrication: Operate and maintain advanced CNC equipment including routers, mills, lathes, and cutters. Produce high-quality parts and prototypes such as experimental pads, new groove designs, custom windows, carrier plates, fixtures, etc. · Design & Programming: Create accurate part drawings and tool paths using SolidWorks, MasterCAM or similar software. Collaborate with engineers to develop and refine designs for new products and process improvements. · Process Development & Continuous Improvement: Troubleshoot machining and design challenges, refine jigs and templates, and implement creative solutions to enhance efficiency and quality. Support technology transfer and contribute to Lean and Six Sigma initiatives. · Team Collaboration & Leadership: Coordinate equipment scheduling and facilitate communication across teams. Assist in cross-training initiatives to build team capability and flexibility. · Safety & Compliance: Maintain strict adherence to safety protocols and contribute to SOP development and audits. **Qualifications** · Associate degree or equivalent technical training in Mechanical, Electrical, or Manufacturing Technology. · 5+ years of experience in machining, manufacturing, or R&D environments. · Proficiency in SolidWorks and MasterCAM; experience operating CNC equipment. · Strong problem-solving skills, adaptability, and attention to detail. Preferred Skills · Experience with process automation and digital manufacturing tools. · Knowledge of Lean and Six Sigma principles. · Excellent communication and organizational skills. Join our Talent Community (*************************************************************** to stay connected with us! Qnity is an equal opportunity employer. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability or any other protected class. If you need a reasonable accommodation to search or apply for a position, please visit our Accessibility Page for Contact Information (**************************************************** . Qnity offers a comprehensive pay and benefits package. To learn more visit the Compensation and Benefits page (*************************************************************************** . **We use Artificial Intelligence (AI) to enhance our recruitment process.**

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.

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 Microbiology Lead, the QC Analyst will perform routine and non-routine microbiological laboratory activities in support of drug product manufacturing at WuXi STA's Middletown, DE site. This role includes microbiological testing, environmental monitoring, stability sample handling, equipment operation, and documentation in accordance with GMP, corporate quality standards, and regulatory requirements. The QC Analyst will support both startup and steady-state operations, working closely with the QC Microbiology Lead to ensure timely and accurate completion of QC tasks for product release, stability studies, and validation activities. Responsibilities Microbiological Testing and Support Perform microbial QC testing for drug products, raw materials, packaging components, and utilities in accordance with approved methods and SOPs. Conduct tests such as environmental monitoring, bioburden, endotoxin, microbial limits, and microbial identification. Accurately record and report test results in compliance with data integrity principles (ALCOA+). Operate, calibrate, and maintain microbiology laboratory equipment according to GMP requirements. Other QC tasks assigned by microbiology lead. Regulatory Compliance and Documentation Follow all cGMP, safety, and quality policies while executing microbiology laboratory activities. Maintain complete, accurate, and inspection-ready microbiology laboratory records. Assist in the preparation for client and regulatory audits, providing documentation and responding to inquiries. Promptly notify the QC Microbiology Lead of any deviations, out-of-specification (OOS) results, or atypical findings. Qualifications Required Qualifications Associate or bachelor's degree in Microbiology, Biology, or related scientific discipline. 1-3 years of QC microbiology experience in a GMP-regulated pharmaceutical or biotechnology environment; internship or co-op experience considered. Working knowledge of microbiological techniques and instrumentation. Familiarity with GMP regulations, USP , , , , ICH guidelines, and data integrity principles. Preferred Qualifications Experience with LIMS, Empower, or other electronic laboratory systems. Previous work in a CDMO or multi-client environment. Ability to work flexibly across analytical and microbiological testing areas as cross-trained. 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. 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 Click here to get started.

Collectors is the leading creator of innovative technology that provides value-added services for collectors worldwide. We grade, authenticate, vault, and sell millions of record-setting collectibles, all while modernizing and digitalizing the process to further our mission of helping collectors pursue their passions. We're always on the lookout for talented people to join our growing team. Our services span collectible coins, trading cards, Funko Pops!, video games, event tickets, autographs, and memorabilia. Our subsidiaries include PSA, PCGS, SGC, WATA, and Card Ladder. Since our founding in 1986, we have graded and authenticated millions of items. We employ more than 1,900 people across our headquarters in Santa Ana and offices in Jersey City, Tokyo, Shanghai, Hong Kong, Toronto, Guadalajara, Dallas, and Paris. Collectors is the leading creator of innovative technology that provides value-added services for collectors worldwide. We grade, authenticate, vault and sell millions of record-setting collectibles, all while modernizing and digitalizing the process to further our mission of helping collectors pursue their passions. We're always on the lookout for talented people to join our growing team. Our services span collectible coins, trading cards, Funko Pops!, video games, event tickets, autographs, and memorabilia. Our subsidiaries include PSA, PCGS, WATA, Card Ladder, and the Long Beach Expo collectibles trade show. Since our founding in 1986, we have graded and authenticated millions of items. We employ more than 1,700 people across our headquarters in Santa Ana and offices in Jersey City, Seattle, Hong Kong, Paris, Shanghai, and Tokyo. We're looking for a Quality Control Specialist who will work out of The Collectors Vault. They will help conduct audits throughout the building and check on overall accuracy for each department. This role will partner with the operations team to assure all products are received and shipped at a zero % defect rate. This role reports to our General Manager at The Collectors Vault and will work out of our New Castle, DE office. The position schedule will be Wednesday To Saturday from 7:00am - 5:30pm. What You'll Do: Train new hires on procedures, standards, and protocols to ensure consistency and adherence to quality requirements. Work with the operations manager on unique day-to-day projects that arise. Assist the operation manager in tracking and locating exception orders to maintain accurate records while simultaneously updating spreadsheets and identifying problem orders. Responsible for auditing inbound packages to ensure compliance with quality standards and specifications, identifying any discrepancies and initiating corrective actions as necessary. Create and maintain spreadsheets and perform data manipulation. Act as the operations liaison between the operation and customer care teams. Investigate customer complaints and non-conformance issues. Conduct routine audits and inspections across the inbound and outbound processes. Demonstrate meticulous attention to detail in performing day-to-day tasks, including data entry, documentation, and quality control activities, to maintain accuracy and consistency in all aspects of quality assurance operations. Who You Are: Working knowledge of the collections hobby with specialized or detailed understanding of professional sports teams, players, entertainment, pop culture, and historical figures is a plus Ability to work under strict deadlines (Overtime needed depending on the auction cycle) Organizational skill and attention to detail are essential Strong time management skills required Enthusiasm, a willingness to learn and adaptability Common computer software: Microsoft Office, Google Documents, Internet High School or equivalent education background Physical Requirements: Computer Use: Typing, mouse work, and sitting and looking at a computer potentially for long periods of time. Exposure to Machinery: Exposure to machinery noise, which may include noise from forklifts, injection presses, or other machinery. Lifting and Carrying: Ability to lift, carry, and move materials up to 25 pounds. Hand Use: Regular hand use for various tasks. Hearing Requirements: Ability to hear alarms, signals, and verbal instructions. Hourly Rate: The reasonable estimated hourly rate for this position is $19. Actual compensation varies based on a variety of non-discriminatory factors, including location, job level, prior experience and skill set. Reasons To Join Us: Health Insurance: All full-time employees are eligible to enroll in Medical, Dental, and Vision Additional Benefits: Full-time employees are eligible for fertility, commuter, and educational assistance benefits. 401(K) Matching Plan: We are proud to offer a competitive 401k matching plan to our employees to support their future financial goals Vacation: All full-time employees are eligible for paid vacation Holiday Pay: All regular, full-time employees are eligible for ten company paid holidays Employee Discounts: Employees receive discounts on select grading services for approved submissions Flexible Hours: Many of our teams offer flexible schedules with varying shifts and will work with you to accommodate your needs Fun Working Environment: Our team members are invited to participate in celebrations, holiday events, and team building activities Collectors uses e-Verify to validate your ability to work legally in the United States. We are aware that there are instances where individuals are receiving job offers that fraudulently allege to be from Collectors or one of our business units. This type of fraud can be carried out through false websites, through fake e-mails claiming to be from the company or through social media. We never ask for personal information such as your bank account, Social Security numbers or National IDs, nor do we send or request payments for the purchase of business-related equipment. If you suspect fraud, please reach out to *******************. We are committed to equal employment opportunity regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, veteran status, or other class protected by applicable law. We believe that a team that represents a variety of backgrounds, perspectives, and skills will better service the diverse community of collectors we support. If you require an accommodation to apply or interview with us due to a disability or special need, please email ********************* . U.S. residents: for disclosures relating to personal information we collect during the employment application and recruitment process, please see our Privacy Notice for U.S. Applicants . If you are based in California, you can read information for California residents here .

Join the High-Flying Team at ALOFT AeroArchitects! Ready to elevate your career? At ALOFT AeroArchitects, we seek talented professionals in airplane maintenance, modification, and completion. We craft exceptional client experiences by pushing the boundaries of luxury, performance, and safety. Join our crew! If you're looking for a career where you can make a real impact and work on cutting-edge and luxury aircraft, look no further. Join us at ALOFT AeroArchitects and let's take aviation to new heights! SUMMARY The Quality Control Inspector performs required inspections and conformity inspections of aircraft, articles, and other product in accordance with the Certificated Repair Station (CRS) operating manuals, procedures and standards, in compliance with all applicable regulatory guidance, based on individual ability and advancement in training, under minimal direct supervision. ESSENTIAL DUTIES AND RESPONSIBILITIES Ensure all work is accomplished in accordance with applicable Federal Aviation Regulations, the Repair Station Manual (RSM), Quality System Manual (QSM), Original Equipment Manufacturer specifications, owner/operator requirements, and industry standards acceptable to the Administrator. Perform required inspections and conformity inspections on aircraft and products that have been assigned. Release aircraft, articles, and products for return to service. Maintain proficiency in the use of inspection aides, test equipment and techniques used to determine the quality of airworthiness of a product or aircraft undergoing maintenance, repair, or alteration. Read, understand, apply, and maintain currency with applicable FAA Regulations, FAA Airworthiness Directives, Manufacturer Bulletins, Maintenance Manuals, Engineering Letters, Service letters, and Maintenance Program Manuals. Assist Receiving Department with inspection of incoming material, parts and supplies, and ensure that the proper certification papers are routed to the Inspection Department for aircraft records. Determine airworthiness of subcontracted work performed outside the Repair Station. Ensure the Preliminary and Hidden Damage Inspections are properly executed and record the results as outlined in the RSM and QSM. Ensure unserviceable parts are properly tagged and identified to prevent reuse as serviceable parts. Properly execute FAA Form 337 and / or maintenance release. Verify inspections of completed work are properly performed in accordance with engineering drawings, specified standards, regulations, or manuals. Perform aircraft document audits to assure that the paperwork package is complete prior to aircraft or product being returned to service. Maintain a safe and clean working environment in accordance with company standards. Document actions by completing all required time keeping records. Complete initial / recurrent training requirements in a timely manner. Other duties may be assigned. SUPERVISORY RESPONSIBILITIES None ADDITIONAL RESPONSIBILITIES The individual employed in this position is expected to dress appropriately (determined by area in which their work is performed), report to work on time, have excellent work habits, and have a cooperative and positive attitude in the work setting; exhibits respect and professionalism when interacting with customers, and all employees; must adhere to company policies, procedures and safety standards. QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the minimum knowledge, skill, and/or ability required. Requires High School diploma or equivalent reading, writing, and math abilities. 5+ years' experience in a Repair Station or Military/Commercial equivalent. Must have experience returning aircraft to service. Proficiency in the use of inspection aides, test equipment and techniques to determine quality of airworthiness. Ability to assist, and to provide training and guidance to Inspection staff. Effective computer skills; Microsoft Office software and other company and discipline specific software applications. Effective written and verbal communication skills. Effective analytical and problem-solving skills. Must be detail oriented with the ability to multi-task. Ability and willingness to work extended hours, when needed. Mastered all Quality Control inspectors' essential duties and responsibilities. LANGUAGE SKILLS Read, write, and understand the English language. Read, analyze, and interpret complex regulatory documents, technical documents, engineering drawings, regulations, procedures and manuals CERTIFICATES, LICENSES, REGISTRATIONS FAA Airframe and Powerplant license is required. PHYSICAL DEMANDS The physical 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. Standard safety precautions are required in all areas where hazardous conditions exist. TRAVEL Occasional travel may be required; the employee filling this position must be willing to travel on short notice and possibly for extended periods. WORK ENVIRONMENT The following work environment and characteristics described are representative of those an employee encounters while performing the essential functions of this job. Standard office environment. Infrequent exposure to noise, smells, dust and fumes typically associated in an industrial manufacturing / aviation environment. Occasional, general proximity to several industrial hazards including electrical, mechanical and chemical. SAFETY STATEMENT All employees have a responsibility to cooperate in promoting and maintaining a safe and healthy work environment, to take reasonable care of their own health and safety and to encourage the health and safety of all other team members. The above statements are intended to describe the general nature and level of work being performed by people assigned to this job. They are not intended to be an exhaustive description of all work requirements and responsibilities. The job description does not constitute an employment contract and is subject to change as needed.

Join the High-Flying Team at ALOFT AeroArchitects! Ready to elevate your career? At ALOFT AeroArchitects, we seek talented professionals in airplane maintenance, modification, and completion. We craft exceptional client experiences by pushing the boundaries of luxury, performance, and safety. Join our crew! If you're looking for a career where you can make a real impact and work on cutting-edge and luxury aircraft, look no further. Join us at ALOFT AeroArchitects and let's take aviation to new heights! SUMMARY The Manufacturing Quality Control Inspector performs required inspections of articles and other product(s) in accordance with operating manuals, procedures, and standards, in compliance with all applicable regulatory guidance, based on individual ability and advancement in training, under minimal direct for supervision. ESSENTIAL DUTIES AND RESPONSIBILITIES Read and interpret schematics, drawings, specifications, or other technical data to determine engineering design data requirements Perform visual and dimensional inspections of raw material, complex manufactured components, and assemblies using microscopes, micrometers, dial calipers, snap gages, optical comparator, and other measurement equipment at various stages of inspection (preliminary, in-process, and final). Maintain proficiency in the use of inspection aides, test equipment and techniques used to determine product compliance with design data. Independently determine appropriate inspection setups using the equipment available. Verify part marking of manufactured parts and articles. Make acceptance or rejection decisions based on established procedures. Review and/or analyze documentation of articles, parts, and materials. Maintain all Quality Management System (QMS) records in accordance with applicable policies. Follow company safety policies and procedures while ensuring quality work. Facilitate the control of nonconforming product in accordance with QMS procedures. Be familiar with and compliant to applicable QMS procedural requirements, FAA Regulations, and industry ISO 9001/AS9100 standards. Maintain a safe and clean working environment in accordance with company standards. Document actions by completing all required time keeping records. Complete initial / recurrent training requirements in a timely manner. Other duties may be assigned. SUPERVISORY RESPONSIBILITIES Assist in carrying out administrative duties such as incident reports, accident reports, etc. in a timely manner. Provide training and guidance for the inspection staff. ADDITIONAL RESPONSIBILITIES The individual employed in this position is expected to dress appropriately (determined by area in which their work is performed), report to work on time, have excellent work habits, and have a cooperative and positive attitude in the work setting; exhibits respect and professionalism when interacting with customers, and all employees; must adhere to company policies, procedures and safety standards. QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the minimum knowledge, skill, and/or ability required. Requires High School diploma or equivalent reading, writing, and math abilities. 5+ years inspection / manufacturing experience. Working knowledge of Geometrical Dimensioning and Tolerancing (GD&T) Proficient in the use of inspection aides, test equipment and techniques to determine the quality of the materials, work in progress and the final product. Experience with AS9102 First Article Inspection report desired. Effective computer skills; Microsoft Office software (Outlook, Excel, Word, PowerPoint, SharePoint, Teams), ERP/MRP systems, QMS software, etc. Effective written and verbal communication skills. Effective analytical and problem-solving skills. Must be detail oriented with the ability to multi-task. Ability and willingness to work extended hours, when needed. LANGUAGE SKILLS Read, write, and understand the English language. Ability to read, write, analyze, and interpret complex technical documents, engineering drawings, regulations, procedures and manuals. CERTIFICATES, LICENSES, REGISTRATIONS None. PHYSICAL DEMANDS The physical 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. Standard safety precautions are required in all areas where hazardous conditions exist. TRAVEL Occasional travel may be required; the employee filling this position must be willing to travel on short notice and possibly for extended periods. WORK ENVIRONMENT The following work environment and characteristics described are representative of those an employee encounters while performing the essential functions of this job. Standard office environments. Exposure to noise, smells, dust and fumes typically associated in an aviation environment. Close proximity to several industrial hazards including electrical, mechanical and chemical. SAFETY STATEMENT All employees have a responsibility to cooperate in promoting and maintaining a safe and healthy work environment, to take reasonable care of their own health and safety and to encourage the health and safety of all other team members. The above statements are intended to describe the general nature and level of work being performed by people assigned to this job. They are not intended to be an exhaustive description of all work requirements and responsibilities. The job description does not constitute an employment contract and is subject to change as needed.

Are you looking to power the next leap in the exciting world of advanced electronics? Do you want to help solve problems that drive success in the rapidly evolving technology and connectivity landscape? Then bring your problem-solving, passion, and creativity to help us power the next leap in electronics. At Qnity, we're more than a global leader in materials and solutions for advanced electronics and high-tech industries - we're a tight-knit team that is motivated by new possibilities, and always up for a challenge. All our dedicated teams contribute to making cutting-edge technology possible. We value forward-thinking challengers, boundary-pushers, and diverse perspectives across all our departments, because we know we play a critical role in the world enabling faster progress for all. Learn how you can start or jumpstart your career with us. We are seeking a highly skilled Technician to support advanced machining, prototyping, and process development for complex engineering and R&D projects. This role is critical to delivering precision components, improving manufacturing processes, and enabling innovation across multiple product lines. Key Responsibilities · Machining & Fabrication: Operate and maintain advanced CNC equipment including routers, mills, lathes, and cutters. Produce high-quality parts and prototypes such as experimental pads, new groove designs, custom windows, carrier plates, fixtures, etc. · Design & Programming: Create accurate part drawings and tool paths using SolidWorks, MasterCAM or similar software. Collaborate with engineers to develop and refine designs for new products and process improvements. · Process Development & Continuous Improvement: Troubleshoot machining and design challenges, refine jigs and templates, and implement creative solutions to enhance efficiency and quality. Support technology transfer and contribute to Lean and Six Sigma initiatives. · Team Collaboration & Leadership: Coordinate equipment scheduling and facilitate communication across teams. Assist in cross-training initiatives to build team capability and flexibility. · Safety & Compliance: Maintain strict adherence to safety protocols and contribute to SOP development and audits. Qualifications · Associate degree or equivalent technical training in Mechanical, Electrical, or Manufacturing Technology. · 5+ years of experience in machining, manufacturing, or R&D environments. · Proficiency in SolidWorks and MasterCAM; experience operating CNC equipment. · Strong problem-solving skills, adaptability, and attention to detail. Preferred Skills · Experience with process automation and digital manufacturing tools. · Knowledge of Lean and Six Sigma principles. · Excellent communication and organizational skills. Join our Talent Community to stay connected with us! Qnity is an equal opportunity employer. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability or any other protected class. If you need a reasonable accommodation to search or apply for a position, please visit our Accessibility Page for Contact Information. Qnity offers a comprehensive pay and benefits package. To learn more visit the Compensation and Benefits page. We use Artificial Intelligence (AI) to enhance our recruitment process.

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

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. 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.

Join our team as an External Reporting Controller! The external reporting function handles the oversight of the financial statements and management reporting, ensuring a sound control environment; understands and applies the accounting treatments and ensures compliance with appropriate corporate and regulatory requirements; coordinates the preparation of quarterly regulatory requirements; validates balance sheet items and understands balance sheet usage and reporting. As an External Reporting Controller within the Corporate sector, you'll engage in producing, reviewing, and filing monthly, quarterly, semi-annual, and annual reports for regulatory agencies. These reports are crucial for regulators to compile widely used statistics on domestic and international portfolio positions and their changes. Job responsibilities: Consolidate, review, and analyze quarterly financial data for accuracy and completeness. Perform quarter-over-quarter variance analytics Coordinate data collection and quarterly business results with various lines of business, Regulatory Controllers and SEC reporting teams Assist in the thorough assessment of the issues and outcomes Communicate financial information to the lines of businesses and able to flag potential issues Adhere to proof & control procedures to ensure accurate reconciliation between regulatory filings, SEC filings and other published financial reports (e.g., Form 10-Q, Annual Report/Form 10-K, Call Report & FR Y-9C, Pillar III, etc) Adhere to various control procedures and edit checks to ensure the integrity of reported financial results Ensure accurate and complete data submission to the Regulators Interpret and define regulatory and/or SEC requirements and coordinate internal and external policies Establish and manage relationships with the line of business as well as with external regulatory agency constituents through ongoing partnership and dialogue Participate in continuous improvement efforts around data quality review and external reporting improvement projects Required qualifications, capabilities, and skills: 3+ years in a Finance organization with exposure to accounting, financial statements, and/or regulatory reporting Strong skills in time management, problem solving, written and oral communication Team player, with ability to work effectively across diverse functions, locations and businesses Excellent Excel and computer skills Strong analytical skills Extremely strong organizational and time management skills Preferred qualifications, capabilities, and skills: Bachelor's degree in Accounting or Finance preferred Experience in Product Control, Financial Control or knowledge of SEC reporting/Reg Reporting a plus Project management experience/skills helpful

Join the High-Flying Team at ALOFT AeroArchitects! Ready to elevate your career? At ALOFT AeroArchitects, we seek talented professionals in airplane maintenance, modification, and completion. We craft exceptional client experiences by pushing the boundaries of luxury, performance, and safety. Join our crew! If you're looking for a career where you can make a real impact and work on cutting-edge and luxury aircraft, look no further. Join us at ALOFT AeroArchitects and let's take aviation to new heights! SUMMARY The Manufacturing Quality Control Inspector performs required inspections of articles and other product(s) in accordance with operating manuals, procedures, and standards, in compliance with all applicable regulatory guidance, based on individual ability and advancement in training, under minimal direct for supervision. ESSENTIAL DUTIES AND RESPONSIBILITIES Read and interpret schematics, drawings, specifications, or other technical data to determine engineering design data requirements Perform visual and dimensional inspections of raw material, complex manufactured components, and assemblies using microscopes, micrometers, dial calipers, snap gages, optical comparator, and other measurement equipment at various stages of inspection (preliminary, in-process, and final). Maintain proficiency in the use of inspection aides, test equipment and techniques used to determine product compliance with design data. Independently determine appropriate inspection setups using the equipment available. Verify part marking of manufactured parts and articles. Make acceptance or rejection decisions based on established procedures. Review and/or analyze documentation of articles, parts, and materials. Maintain all Quality Management System (QMS) records in accordance with applicable policies. Follow company safety policies and procedures while ensuring quality work. Facilitate the control of nonconforming product in accordance with QMS procedures. Be familiar with and compliant to applicable QMS procedural requirements, FAA Regulations, and industry ISO 9001/AS9100 standards. Maintain a safe and clean working environment in accordance with company standards. Document actions by completing all required time keeping records. Complete initial / recurrent training requirements in a timely manner. Other duties may be assigned. SUPERVISORY RESPONSIBILITIES Assist in carrying out administrative duties such as incident reports, accident reports, etc. in a timely manner. Provide training and guidance for the inspection staff. ADDITIONAL RESPONSIBILITIES The individual employed in this position is expected to dress appropriately (determined by area in which their work is performed), report to work on time, have excellent work habits, and have a cooperative and positive attitude in the work setting; exhibits respect and professionalism when interacting with customers, and all employees; must adhere to company policies, procedures and safety standards. QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the minimum knowledge, skill, and/or ability required. Requires High School diploma or equivalent reading, writing, and math abilities. 5+ years inspection / manufacturing experience. Working knowledge of Geometrical Dimensioning and Tolerancing (GD&T) Proficient in the use of inspection aides, test equipment and techniques to determine the quality of the materials, work in progress and the final product. Experience with AS9102 First Article Inspection report desired. Effective computer skills; Microsoft Office software (Outlook, Excel, Word, PowerPoint, SharePoint, Teams), ERP/MRP systems, QMS software, etc. Effective written and verbal communication skills. Effective analytical and problem-solving skills. Must be detail oriented with the ability to multi-task. Ability and willingness to work extended hours, when needed. LANGUAGE SKILLS Read, write, and understand the English language. Ability to read, write, analyze, and interpret complex technical documents, engineering drawings, regulations, procedures and manuals. CERTIFICATES, LICENSES, REGISTRATIONS None. PHYSICAL DEMANDS The physical 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. Standard safety precautions are required in all areas where hazardous conditions exist. TRAVEL Occasional travel may be required; the employee filling this position must be willing to travel on short notice and possibly for extended periods. WORK ENVIRONMENT The following work environment and characteristics described are representative of those an employee encounters while performing the essential functions of this job. Standard office environments. Exposure to noise, smells, dust and fumes typically associated in an aviation environment. Close proximity to several industrial hazards including electrical, mechanical and chemical. SAFETY STATEMENT All employees have a responsibility to cooperate in promoting and maintaining a safe and healthy work environment, to take reasonable care of their own health and safety and to encourage the health and safety of all other team members. The above statements are intended to describe the general nature and level of work being performed by people assigned to this job. They are not intended to be an exhaustive description of all work requirements and responsibilities. The job description does not constitute an employment contract and is subject to change as needed.

Join the High-Flying Team at ALOFT AeroArchitects! Ready to elevate your career? At ALOFT AeroArchitects, we seek talented professionals in airplane maintenance, modification, and completion. We craft exceptional client experiences by pushing the boundaries of luxury, performance, and safety. Join our crew! If you're looking for a career where you can make a real impact and work on cutting-edge and luxury aircraft, look no further. Join us at ALOFT AeroArchitects and let's take aviation to new heights! SUMMARY The Quality Control Inspector performs required inspections and conformity inspections of aircraft, articles, and other product in accordance with the Certificated Repair Station (CRS) operating manuals, procedures and standards, in compliance with all applicable regulatory guidance, based on individual ability and advancement in training, under minimal direct supervision. ESSENTIAL DUTIES AND RESPONSIBILITIES Ensure all work is accomplished in accordance with applicable Federal Aviation Regulations, the Repair Station Manual (RSM), Quality System Manual (QSM), Original Equipment Manufacturer specifications, owner/operator requirements, and industry standards acceptable to the Administrator. Perform required inspections and conformity inspections on aircraft and products that have been assigned. Release aircraft, articles, and products for return to service. Maintain proficiency in the use of inspection aides, test equipment and techniques used to determine the quality of airworthiness of a product or aircraft undergoing maintenance, repair, or alteration. Read, understand, apply, and maintain currency with applicable FAA Regulations, FAA Airworthiness Directives, Manufacturer Bulletins, Maintenance Manuals, Engineering Letters, Service letters, and Maintenance Program Manuals. Assist Receiving Department with inspection of incoming material, parts and supplies, and ensure that the proper certification papers are routed to the Inspection Department for aircraft records. Determine airworthiness of subcontracted work performed outside the Repair Station. Ensure the Preliminary and Hidden Damage Inspections are properly executed and record the results as outlined in the RSM and QSM. Ensure unserviceable parts are properly tagged and identified to prevent reuse as serviceable parts. Properly execute FAA Form 337 and / or maintenance release. Verify inspections of completed work are properly performed in accordance with engineering drawings, specified standards, regulations, or manuals. Perform aircraft document audits to assure that the paperwork package is complete prior to aircraft or product being returned to service. Maintain a safe and clean working environment in accordance with company standards. Document actions by completing all required time keeping records. Complete initial / recurrent training requirements in a timely manner. Other duties may be assigned. SUPERVISORY RESPONSIBILITIES None ADDITIONAL RESPONSIBILITIES The individual employed in this position is expected to dress appropriately (determined by area in which their work is performed), report to work on time, have excellent work habits, and have a cooperative and positive attitude in the work setting; exhibits respect and professionalism when interacting with customers, and all employees; must adhere to company policies, procedures and safety standards. QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the minimum knowledge, skill, and/or ability required. Requires High School diploma or equivalent reading, writing, and math abilities. 5+ years' experience in a Repair Station or Military/Commercial equivalent. Must have experience returning aircraft to service. Proficiency in the use of inspection aides, test equipment and techniques to determine quality of airworthiness. Ability to assist, and to provide training and guidance to Inspection staff. Effective computer skills; Microsoft Office software and other company and discipline specific software applications. Effective written and verbal communication skills. Effective analytical and problem-solving skills. Must be detail oriented with the ability to multi-task. Ability and willingness to work extended hours, when needed. Mastered all Quality Control inspectors' essential duties and responsibilities. LANGUAGE SKILLS Read, write, and understand the English language. Read, analyze, and interpret complex regulatory documents, technical documents, engineering drawings, regulations, procedures and manuals CERTIFICATES, LICENSES, REGISTRATIONS FAA Airframe and Powerplant license is required. PHYSICAL DEMANDS The physical 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. Standard safety precautions are required in all areas where hazardous conditions exist. TRAVEL Occasional travel may be required; the employee filling this position must be willing to travel on short notice and possibly for extended periods. WORK ENVIRONMENT The following work environment and characteristics described are representative of those an employee encounters while performing the essential functions of this job. Standard office environment. Infrequent exposure to noise, smells, dust and fumes typically associated in an industrial manufacturing / aviation environment. Occasional, general proximity to several industrial hazards including electrical, mechanical and chemical. SAFETY STATEMENT All employees have a responsibility to cooperate in promoting and maintaining a safe and healthy work environment, to take reasonable care of their own health and safety and to encourage the health and safety of all other team members. The above statements are intended to describe the general nature and level of work being performed by people assigned to this job. They are not intended to be an exhaustive description of all work requirements and responsibilities. The job description does not constitute an employment contract and is subject to change as needed.

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_

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. 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 Click here to get started.

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.