Quality control analyst jobs in Upper Darby, PA - 142 jobs

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

At DuPont, our purpose is to empower the world with essential innovations to thrive. We work on things that matter. Whether it's providing clean water to more than a billion people on the planet, producing materials that are essential in everyday technology devices from smartphones to electric vehicles, or protecting workers around the world. Discover the many reasons the world's most talented people are choosing to work at DuPont. Why Join Us | DuPont Careers DuPont Water Solutions, a global leader in ion exchange resin and membranes technology, is seeking applicants for an application lab technologist opportunity. In this role, you will work on customer-facing projects, developing the key application know-how to solve real world problems and guide the development of new products. Your work will help us save water and energy, and protect the environment by delivering more effective, efficient products and processes that do more with less impact to our world. We are seeking candidates with 2-5 years of industrial laboratory experience who are motivated to make a difference in our world. Training in our core technologies such as ion exchange resin and membrane technology will be provided. This role will be part of the applications R&D group in the Water Solutions business and will be on-site at the DuPont Experimental Station in Wilmington, DE. Relocation for this role is not supported. The scope of this role includes: Conducting work in the lab developing and testing new products and new applications Working with ion exchange resin technology to overcome processing and purification challenges Working with teams of scientists and engineers to deliver project goals Analyzing data and presenting results, conclusions and recommendations to stakeholders and management Managing a laboratory, including having primary responsibility for several pieces of process and analytical equipment as well as safety and procedural documentation. Required skills and experience: Bachelor of science in chemistry, chemical engineering, or similar discipline Two to five years of experience in an industrial laboratory setting, which may include internship or co-op experience Time management and the ability to work on multiple projects simultaneously Strong interpersonal skills and emotional intelligence for effective work on project teams Proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook) Preferred skills and experience: Experience with ion exchange resins, laboratory-scale packed beds, and/or columns General experience in purification processes using ion exchange resins Experience building and maintaining Swagelok -based or equivalent laboratory equipment Analytical experience such as HPLC, ion analysis, or polymer characterization #LI-TG1 Join our Talent Community to stay connected with us! DuPont 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. DuPont offers a comprehensive pay and benefits package. To learn more visit the Compensation and Benefits page.

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

Piper Companies is seeking a Quality Control Analytical Scientist (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

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

Since 1946, The Jet Pulverizer Company, Inc. has been committed to providing state-of-the-art processing equipment and services. The continuous technological advancement of our line of Micron-Master Jet Pulverizers and ongoing modernization and expansion of our Custom Grinding Division provide our customers with unsurpassed value and quality in both jet pulverizing equipment and custom grinding services. The Quality Technician plays a crucial role in ensuring the safety, quality, and compliance of products manufactured within our FDA-regulated micronization facility. This position involves monitoring production processes, conducting inspections, and collaborating with cross-functional teams to maintain high standards. Requirements Essential Duties of the QC Lac Tech: PRIORITY - Product sample testing as required Complete paperwork on a timely basis Create sample composites and retains as indicated by customer need Generate CoA's as required Stock sample cups and lids Monitor lab consumables and order as needed Maintain clean lab Monitor calibration status of instrumentation and calibrate as required Perform routine inspections of raw materials, intermediate products, and finished goods. Utilize precision measuring instruments and testing equipment to verify product specifications. Identify any deviations from quality standards and report findings promptly. Monitor micronization processes, including particle size reduction, blending, and packaging. Collect samples at various stages of production for analysis. Ensure adherence to standard operating procedures (SOPs) and regulatory guidelines. Maintain accurate records of inspections, test results, and corrective actions. Prepare quality reports and communicate findings to supervisors and management. Collaborate with the Quality Assurance team to address non-conformities. Assist during internal and external audits, including FDA inspections. Ensure compliance with cGMP (current Good Manufacturing Practices) and other relevant regulations. Support the implementation of quality management systems. Provide guidance on quality-related matters to colleagues. Foster a culture of quality awareness and accountability. Must be willing to work overtime as needed, including some mandatory weekend shifts. Experience/Skills HS Diploma required. Associate degree preferred. Computer proficiency - Microsoft Windows/Outlook, Microsoft Office 1 - 2 years lab experience Experience working in an FDA-regulated environment (pharmaceuticals, medical devices, or related industries). Proficiency in using measurement tools (calipers, micrometers, etc.) and analytical instruments. Knowledge of cGMP, ISO standards, and quality control principles. Strong attention to detail, problem-solving skills, and ability to work independently. Excellent communication and teamwork abilities. Salary Description $20 - $21 / hour

Why Stokes? Stokes Healthcare is a privately-owned business comprised of three divisions: Stokes Pharmacy (503A pharmacy), Epicur Pharma (503B facility) and STEP labs. The these divisions operate out of separate facilities in Mount Laurel, NJ, following different regulations and are guided by different principles. Stokes Pharmacy was founded in 1975. The pharmacy formulates custom prescription medicines for both humans and animals. The business has grown from a small, hometown operation in Medford, New Jersey, to a respected pharmacy serving the entire U.S., enabled by sophisticated online ordering and overnight shipping capabilities. In 2016, Stokes Healthcare built a world-class facility (which became Epicur Pharma), as a testament to the commitment to providing the highest level of quality. Adding a unique offering to the veterinary industry, Epicur Pharma is an FDA Registered 503B Outsourcing Facility, producing drugs such as Tacrolimus Eyedrops, Buprenorphine Injection and Gabapentin tablets. Epicur follows Current Good Manufacturing Practices (cGMP) which are the same rules and regulations followed by commercial manufacturers. Epicur Pharma is proud to be a pioneer in animal drug standards, offering the largest selection of manufactured drugs that are traditionally compounded. Epicur products are distributed directly to veterinary hospitals from our manufacturing facility and offered through Stokes Pharmacy for individual patient prescriptions. STEP Labs is a GMP-compliant laboratory that delivers accurate, reliable analytical testing for manufactured pharmaceutical products. Equipped with advanced instrumentation and operated under strict regulatory standards, STEP Labs provides comprehensive services in microbiological and chemistry analysis with a focus on quality, data integrity, and timely results. Stokes Healthcare has built a reputation for unwavering quality and superb service by holding fast to the founders' commitment to traditional craftsmanship, combined with today's most advanced knowledge and technologies. In a field where many corporate-owned pharmacies try to compete on price, Stokes has always put safety and quality first because patients' lives depend on it. At Stokes, we offer competitive salaries and a comprehensive benefits package that includes medical, dental and vision coverage, life insurance, Health Reimbursement Account, Flexible Spending Account, 401(K) retirement savings plan with a generous employer match, a bonus program, paid holidays, vacation and personal time, and an excellent working environment. We are conveniently located in Mount Laurel, New Jersey, just minutes from Philadelphia and the NJ shore. Job Title Microbiology Analyst I FLSA Status Non-exempt Job Summary The Microbiology Analyst I is responsible for supporting microbiology procedures, assisting in investigations, and performing routine analysis of raw material and finished product according to established specifications and procedures. Starting at $20/hour based on experience plus twice a year cash bonuses. Essential Duties and Responsibilities include the following. Other duties may be assigned. Assist in method validation for sterility, bioburden, and endotoxin of drug products including, but not limited to, injections, ophthalmic preparations, oral tablets, and oral liquids Perform and/or assist in investigations related to sterility assurance and environmental monitoring Perform routine analysis of finished product and raw material according to established specifications and procedures relating to: Sterility Bioburden Endotoxin AET Growth Promotion Perform atypical particulate inspection on finished product Support sampling and microbiological testing on facility water (WFI, CS, etc.) Review and approve data related to sterility, bioburden, AET, and endotoxin testing of finished product and/or raw materials Perform technical review of test results for completeness and compliance to cGMP to ensure that documentation, controls and traceability are in place to maintain integrity Prepare and review preparation of media, reagents, test samples and equipment as required Prepare microorganisms for identification Understand and demonstrate aseptic technique Maintain laboratory cleanliness and inventory of microbiology supplies Familiar with GxP (Good Manufacturing Practice, Good Laboratory Practice and Good Documentation Practice) Assist with environmental monitoring and microbiological trend reports Required Education and Experience B.S. degree in Microbiology, Biology or related scientific field Minimum 1 year of experience in a microbiology laboratory or pharmaceutical industry Knowledge of good analytical and laboratory techniques, GxP, USP and FDA requirements Knowledge in statistical data analysis and its application to pharmaceutical or compounding processes and quality controls Must exhibit good analytical, writing (GDP), interpersonal and organizational skills Must be able to meet deadlines Must be detail oriented and have multi-tasking capabilities with ability to prioritize Must exhibit strong computer skills including but not limited to software packages supporting statistical data analysis, word processing, and project management programs Must have the ability to work in a fast-paced environment Must exhibit excellent problem resolution skills Must be able to work independently and as part of a team Must exhibit punctuality and low absenteeism Must be able to sit, stand, reach and walk for prolonged periods of time Eligibility Qualifications Must develop knowledge of 21 CFR Part 210 and 211 for cGMP operations Must be capable of wearing all protective gear (gown, hair bonnet, mask, beard cover, gloves, goggles) and maintain good personal hygiene (makeup, jewelry and other cosmetics are prohibited from the production areas) May be necessary to work extended hours as needed May require weekend work Competencies Communication Proficiency Time Management Organizational Skills Problem Solving/Analysis Quality Results Driven Technical Capacity Thoroughness Supervisory Responsibility This position has no supervisory responsibilities. Work Environment This job operates primarily in a controlled laboratory environment. This position requires the use of standard office equipment, and frequent standing and walking. 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. Able to sit and/or stand 8-10 hours or more per day as needed May sit, stand, stoop, bend and walk intermittently during the day; may be necessary to work extended hours as needed Finger dexterity to operate office equipment required Ability to lift up to twenty (20) pounds on occasion Position Type and Expected Hours of Work This is a full-time Mon-Fri 7AM-3:30PM position. Because of the nature of the business, work schedules may vary at times. Travel No travel is expected for this position. Disclaimer The above job description is intended to describe the general nature and level of work being performed by employees assigned to this job. It is not designed to capture or illustrate a comprehensive list of all responsibilities, duties, and skills required of employees assigned to this job. AAP/EEO Statement Stokes Healthcare is an Equal Employment Opportunity and Affirmative Action Employer. Monday - Friday 7AM to 3:30PM

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

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

Penn Life Sciences is seeking a detail-oriented QC Chemist I to join our team in Langhorne, PA. The QC Chemist I performs routine analytical testing in support of sterile drug product manufacturing, batch release, and stability programs within a cGMP-regulated environment. This role is responsible for generating accurate, compliant laboratory data while executing approved analytical methods and maintaining strict adherence to data integrity and documentation standards. The ideal candidate will have a strong foundation in analytical chemistry, a commitment to quality, and the ability to work effectively within a regulated Quality Control laboratory. This position's responsibilities will include, but not be limited to the following: * Perform routine analytical testing of raw materials, in-process samples, finished drug products, and stability samples using approved QC methods. * Execute wet chemistry and instrumental analyses in compliance with validated methods, specifications, and cGMP requirements. * Accurately document laboratory activities, results, and calculations in laboratory notebooks and electronic systems in accordance with ALCOA+ data integrity principles. * Operate assigned analytical instruments and perform routine checks, calibrations, and basic troubleshooting in accordance with SOPs. * Support stability programs, laboratory investigations (including deviations and OOS events), and analytical data review activities under supervision. * Maintain laboratory organization, sample traceability, and inspection readiness while adhering to all applicable safety and regulatory requirements. We are looking for applicants with: * Bachelor's degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or a closely related scientific discipline required. * 0-3 years of analytical laboratory experience in a pharmaceutical, biotechnology, or regulated laboratory environment; academic laboratory experience will be considered. * Working knowledge of analytical techniques such as HPLC/UPLC, UV-Vis spectroscopy, pH, Karl Fischer, TOC, dissolution, or particle size analysis. * Understanding of good documentation practices and data integrity expectations within a QC laboratory. * Strong organizational, analytical, and communication skills with a high attention to detail. What we offer: * 401(k) with company match * Health, vision, and dental Insurance * Childcare expense reimbursement * Tuition reimbursement * Annual bonus eligibility * Annual merit increases * Paid Time Off and Flexible Holidays Penn Life Sciences is an affirmative action/equal opportunity employer and does not discriminate in hiring or employment on the basis of age, sex, race, color, religion, national origin, gender identity, veteran status, sexual orientation or any other protected status. We encourage you to apply if you feel that you are a match! We look forward to hearing from you.

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

Performs inspection of aircraft, components, assemblies, tools or parts during modifications, installation, service, or overhaul to determine airworthiness, safety, or conformance to manufacturer's specifications, FAA accepted/approved data, and AS9100 Quality standards and requirements. This position will be based in Philadelphia, PA Essential Duties and Responsibilities: Duties and Responsibilities: % of Time 1. Performs inspection of aircraft, or parts during modifications, installation, or overhaul and is accountable for the determination of airworthiness, safety, and conformance to FAA accepted/ approved data, Company standards, and AS9100 requirements. 30 2. Interprets and checks engineering drawings for applicability to work scope, both hard copy and electronic, engineering change orders, FAA regulatory procedures, processes, and specifications. 10 3. Reviews engineering technical data for major alterations and major repairs. Documents in detail a description of the work accomplished on a FAA form 337. Determines whether a major repair or major alteration will require a field approval and submit FAA Form 337 to the FAA for a field approval. Responsible for writing Instructions for Continued Airworthiness (ICA's) maintenance work instructions on FAA Form 337. 5 4. Performs review of work orders for completeness, required repair station dedicated forms, and any other mandatory documents. 5 5. Performs research of FAA, EASA, and other foreign civil aviation authorities Airworthiness Directives (AD's). Creates and documents a dedicated compliance list for customer aircraft records. 5 6. Returns aircraft and aircraft parts to service in accordance with 14 CFR Part 43.9 or 14 CFR Part 43.11 by creating and signing an aircraft logbook entry, or completing a FAA Form 8130-3 for aircraft parts. Creates and updates customer aircraft records. 15 7. Interfaces with FAA Safety Inspectors during FAA audits of the Repair Station. 5 8. Supervises the work performed on site, and is responsible for ensuring that the appropriate work instructions are followed, and is responsible for the overall quality of the work performed for travel events (work away from the repair station). 5 9. Liaise with company Technical Representatives and Customer Support Managers for all matters relating to Quality concerning customer aircraft or parts. 5 10. Performs data collection and performs conformity inspections during the development of a STC project. Performs conformity inspections to fabricated parts by a vendor or in-house to ensure part meets engineering design requirements. 5 11. Prepares data package and presents to FAA for any aircraft certification changes. 5 12. Performs other duties and fulfill other responsibilities as assigned. This includes working as an aircraft maintenance technician if required. 5 TOTAL: 100% Qualifications for Position: Education High school diploma (or equivalent) College degree or Technical writing a plus Experience Minimum 5 years hands-on quality control inspector on turbine helicopters in a Part 145 Repair Station environment 5 years hands-on turbine helicopter maintenance experience AgustaWestland A109/A119/AW139/AW169/AW189 maintenance experience is a plus Competencies & Attributes Technical knowledge in the fields of mechanics, hydraulics, electricity, avionics, sheet metal, rigging, instruments, test flights, etc. to determine safety, airworthiness, conformance, and sign off work in aircraft records to meet the requirements of the FAA Federal Aviation Regulations Must be pro-active and team and detail oriented. Must have good working knowledge of FAR Part 145 and related areas. Must possess experience in Microsoft Office suite. Must be able to work independently Ability to travel occasionally. Ability to work weekends and/or be on-call. Licensure/Certification FAA A&P license a must, and Inspection Authorization (IA) rating is a plus Equal Opportunity Employer/Vet/Disability

Job Description At Amuneal, each product we create is influenced by exploration, research, investment, and a never-ending focus on the highest quality materials, cutting-edge technologies, and skilled craftsmanship. With nearly 60 years of experience, Amuneal operates two divisions in Philadelphia, each with a focus on the highest quality products, fed by a strategy focused on diversification. Amuneal's Technical Products Division is the country's largest and most respected supplier of magnetic shielding, while our award-winning Custom Fabrication Division creates original designs for high-end residential and commercial interiors. Amuneal Manufacturing is seeking a dedicated Quality Control Inspector to join our fast-paced, dedicated, and extremely talented team. Candidates should bring in a high level of excitement and punctuality. They will be responsible for performing set-up and production operations on projects of a wide variety, while maintaining standards for safety & quality. This role will operate on a 4 day, 10 hour work week of 6:00AM-4:30PM Monday-Thursday Responsibilities: Inspect - Conduct routine and non-routine inspection of materials at incoming, in-process, and final. First Article Inspection when required by the customer or quality management. Inspect - Perform tests, interpret test results, compare them to established specifications and control limits, and make recommendations on appropriateness of data/material for release. Calibration - Maintain inspection equipment in accordance with Amuneal's internal procedures and any relevant customer specifications. Document - Ensure drawings, work instructions, and procedures are maintained to current revision and accessible. Audit - Perform routine internal audits of processes and persons, as directed by relevant management. Train - Provide training and guidance to junior members of the Quality team. This includes the provision of oversight, and implementation of disciplines when it is necessary, as well as reporting on progress, or lack thereof, to relevant management. Straighten: Arrange items that are needed so that they are ready & easy to use. Clearly identify locations for all items so that anyone can find them & return them once the task is completed. Shine: Clean the workplace & equipment on a regular basis to maintain standards & identify defects. Standardize: Revisit the first three of the 5S on a frequent basis to maintain standards & identify defects. Sustain: Keep the rules to maintain the standard and continue to improve every day. Qualifications: High School Diploma/ GED required. Associates Degree, Bachelors Degree, or Technical school preferred. Knowledge of ISO 9001 Ability to read and understand blueprints Technically apt, with experience using Microsoft Suites. Use of CMM/ FARO Arm Preferred. Our work is custom in nature and highly evolving. As part of a team, you will work on a diverse set of challenging projects. Applicants should have experience and be able to thrive both in a collaborative setting and on solo tasks. This role offers a competitive salary in addition to inclusion in the company's profit sharing, 401K, medical, and dental programs. Benefits: 401(k) 401(k) matching Dental insurance Flexible schedule Health insurance Life insurance Paid time off Referral program Vision insurance Schedule: 4 Day Work Week Weekends as needed Ability to commute/relocate: Philadelphia, PA 19124: Reliably commute or planning to relocate before starting work (Required)

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

The Quality Associate tests product batches, as necessary, to ensure compliance with customer specifications and quality standards. Tests incoming raw materials and maintains/ files Certificates of Analysis (COA) from suppliers. ESSENTIAL DUTIES & RESPONSIBILITIES: Follows and complies with all safety and work rules and regulations. Maintains departmental housekeeping standards Performs standard tests on all product line finish materials and on some incoming raw materials as needed, ensuring they meet both GEON and the customer's specifications. Acts as a technical resource to production addressing issues related to the final quality of all products. Recommends to production and may develop process adjustments to meet final product specifications. Records test results in lab software or other customer specific data files. Maintains reference files. Completes and maintain all required paperwork, records, documents, etc. Ensures all gages and test equipment are verified and all lab standards are conducted and recorded daily. Participates in the investigation of complaints and corrective actions as needed. Completes and sends documentation to customers (i.e. COA) if needed. Willing to work some amount of overtime as needed. Other duties as assigned. MINIMUM QUALIFICATIONS: To perform this position successfully, an individual must be able to perform each job duty satisfactorily. The requirements listed below are representative of the knowledge, skills, and/or abilities required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential duties. Required Education: Requires high school diploma or GED equivalency. Knowledge, Skills & Abilities: Must be able to read/comprehend both written and oral instructions in English; read and comprehend safety rules, operating and maintenance instructions, technical lab procedure manuals and product recipes/material identifications. Must be able to write legibly to keep records and to correspond. Must have strong mathematical skill to add, subtract, multiply and divide and the ability to perform these operations using units of weight measurement, volume, and distance. Must be able to effectively communicate one-on-one and in small group situations. Requires matching proficiency, including the ability to color match. Must have ability to reason and address problems involving a few concrete variables in standardized situations. Must have manual dexterity sufficient to use a wide variety of standard lab equipment including a scale, ovens, viscometers and the ability to operate standard office equipment such as a computer, a calculator, telephone, fax, and photocopier. Individual must be able and willing to work with fellow associates in a professional manner at all times. The individual should demonstrate a positive attitude at all times with other work associates in a manner conducive to improving the quality and productivity of the company. Required Length & Type of Experience: 1 year of related manufacturing lab/quality experience. Required Certification, Licenses, Registration: May require obtainment of a Forklift Operator's License. PHYSICAL DEMANDS: The characteristics listed below are representative of the physical demands required by an individual to successfully perform the essential duties of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential duties. While performing the duties of this job, the employee is regularly required to stand; walk; stoop, kneel, crouch or crawl; use hands to finger, handle, or feel objects, tools, or controls; talk and/or hear. Occasionally required to sit. The employee must frequently lift and/or move up to 10 pounds and occasionally handle up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus. WORK ENVIRONMENT: The characteristics listed below are representative of the work environment typically encountered by an individual while performing the essential duties of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential duties. Requires the use of safety equipment as dictated by the work area such as safety glasses and shoes, dust mask, hard hat, respirator, face shield, hearing protection, chemical suit, gloves, aprons, etc. This position may be an 8 hour or 12-hour work shift. Work is inside and the typical noise level fluctuates from moderate to loud. Occasionally exposed to moving mechanical parts and fumes or airborne particles. The employee may be occasionally exposed to vibration. The employee may be occasionally exposed to toxic or caustic chemicals and risk of electrical shock.

We don't like to brag, but we've crafted solutions for real-world bath and home needs for almost 100 years. Since our modest start in 1929, Mayzon has compiled a long list of firsts in manufacturing, production, design and marketing innovations for our homes. But we're about much more than the past. Looking toward a brighter tomorrow, we've committed to innovate using sustainable methods and environmentally friendly practices whenever possible. So, yeah, maybe we do like to brag a little. A lot of companies say it, but we mean it: At Mayzon, our people are our best asset. We are growing! We empower our team members to be creative problem solvers. We provide tools, training and an environment to help them thrive. We're not perfect. But we're happiest when our people have an impact on our customers' lives. We offer great benefits! BC/BS for medical, dental, & vision. 11 paid holidays. Bonuses (Referral, sign-on, quarterly)..... Please ask. Department: Quality Control Shift: 2nd Shift FLSA Status: Non-Exempt Reports To: Quality Manager / QA Supervisor Position Summary The Quality Control Inspector is responsible for performing in-process and final inspections of manufactured and purchased components to ensure compliance with engineering specifications, customer requirements, and internal quality standards. This role supports defect reduction, process compliance, and continuous improvement within a high-volume manufacturing environment. Qualifications Essential Duties and Responsibilities Perform in-process and final inspections of assemblies, materials, packaging, and finished goods in accordance with written inspection procedures, work instructions, and sampling plans Review and interpret engineering drawings, specifications, bills of material (BOMs), work orders, and quality documentation Conduct first article, first-run, random, and hourly inspections per quality standards Use measuring and inspection equipment including tape measures, digital calipers, gauges, meters, and scales Identify, document, and report nonconforming material using Defective Material Reports (DMRs) Verify material availability and accuracy during production set-up and changeovers Assess aesthetic and functional quality, determine defect classification, and quantify defect levels Stop or escalate production activity when major non-compliance or quality risks are identified Communicate quality issues to Quality, Engineering, and Production leadership in a timely manner Support rework, sorting, containment, and corrective action activities Participate in quality improvement initiatives, audits, and investigations Maintain accurate inspection records and quality documentation Perform additional duties as assigned to support operational and quality objectives Required Qualifications High School Diploma or GED required Minimum 3-5 years of experience in a manufacturing quality, inspection, or production environment Ability to read and interpret engineering drawings and inspection instructions Proficient in the use of mechanical measuring devices Basic computer proficiency (data entry, inspection records, reports) Strong attention to detail with solid analytical and problem-solving skills Basic math skills and accurate color vision Ability to stand, walk, bend, and inspect products for extended periods Preferred Qualifications Prior experience with in-process inspection, final inspection, or quality auditing Experience in assembly, plastics, metal, or consumer product manufacturing Familiarity with sampling plans, quality standards, and corrective action processes Competencies Quality-focused and detail-oriented Clear written and verbal communication Ability to work independently and collaboratively Organized with strong documentation discipline Comfortable working in a fast-paced production environment Work Environment & Physical Requirements Manufacturing environment with exposure to noise, moving equipment, and production lines Standing and walking for extended periods Manual handling of parts and inspection tools Occasional off-site work may be required Equal Employment Opportunity Statement The Company is an Equal Opportunity Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other protected status under applicable law.

Under the general direction of the Quality Control Manager, the Quality Control Inspector is responsible for the inspection of products with the objective of meeting quality initiatives in a diverse manufacturing environment. This is a full-time, on-site, non-exempt position. Essential Functions - To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Document Receiving, First-Piece, In-Process and Final Inspections on AS9102 and similar reporting formats Roaming In-Process Inspections on the floor Visual inspections for general workmanship Manually balloon customer prints and create inspection reports, as needed Assist in calibration activities, as needed Prepare documentation packages, as needed Qualifications Experience/Education Able to read and understand blueprints with an emphasis of GD&T Able to use micrometers, dial indicators, optical comparators and height gages for inspecting dimensions as fine as .0002” Able to use attribute gages such as pins, thread gages Able to read and understand Military and other specifications. Have strong verbal and written communication skills Have a keen eye for detail CMM experience a plus Physical ability to stand for long periods Willingness to assist in all other duties as assigned

Bring precision, curiosity, and craftsmanship to a team that builds components trusted by the U.S. Navy. At Interstate Connecting Components (ICC), a division of Heilind Mil-Aero, we take pride in engineering excellence. As a Quality Control Inspector, you'll play a key role in ensuring that every part we ship meets the highest standards of performance and safety. If you have experience inspecting, measuring, or testing mechanical, electrical, or assembled products - or even a background in pharmaceutical or chemical manufacturing where precision is everything - this could be the perfect next step in your quality career. What You'll Do Perform inspection and testing of incoming materials and finished products using precision tools (calipers, micrometers, thread gauges, drop gauges, etc.). Interpret engineering drawings and verify that products meet specifications before they reach our customers. Serve as the liaison between Quality and Warehouse teams, ensuring materials flow seamlessly from receipt to shipment. Conduct and coordinate Customer Source Inspections when required. Support investigations of nonconforming materials and contribute to process improvements. Accurately document inspections and results in our ERP system (Inventory, Order Entry, Purchasing, and Production modules). Assist with continuous improvement projects, developing better inspection methods and tools. Why You'll Love Working Here Purpose-driven work: Your inspections directly impact mission-critical equipment used in military and aerospace applications. Skill development: Get hands-on exposure to diverse products and inspection techniques in a growing organization. Comprehensive benefits package including medical, dental, and vision coverage; 401(k) with company match; PTO and holidays; tuition reimbursement; wellness and pet insurance programs; and referral bonuses.

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