Quality control analyst jobs in Gloucester, NJ

At Quaker Houghton, we are experts in the development, production and application of chemical specialties, process fluids, lubricants and coatings for the manufacturing industry. We have been an integral part in the growth of the worlds largest industrial companies and to this day our experience and expertise show in the actions and dedication of our Associates worldwide. Today, we have a global presence, with our corporate headquarters located in Conshohocken, PA. Quaker Houghton is a global publicly traded company with a unique collaborative culture that supports career growth for its associates and offers competitive compensation and benefit programs. Summary: Quaker Houghton is seeking a Development Chemist III to work in our Metalworking Fluid Development Laboratory in Conshohocken, PA. The laboratory supports multiple metalworking fluid product lines including soluble oils, semi-synthetics, and full synthetics. An individual in this role will be responsible for conducting product development, research projects, and product support for Quaker Houghton metalworking fluids. This will require working closely with commercial associates, other RD&E teams, customers, and external partners to design new products and execute tests both in the laboratory and in the field. We are seeking experienced candidates who are highly motivated, have strong collaboration skills, are creative problem solvers, and communicate effectively. What will you do? * Use knowledge of colloid chemistry, tribology, and testing techniques to formulate metalworking fluids that will meet customer needs and provide solutions to application problems. * Work independently with minimal guidance from the laboratory manager. * Act as a mentor to junior development chemists. * Maintain a clear and orderly record all observations and data. * Write detailed reports summarizing product development efforts, laboratory testing, and troubleshooting. * Perform customer requested product analysis and testing to answer questions and address problems at commercial accounts. * Provide legal and archival documentation for patent applications. * Comply with safety regulations and lab procedures. * Provide technical service and knowledge to customers and sales associates based upon the chemists current level of expertise. Visit customers when required. * Provide assistance to Manufacturing to improve the quality and efficiency of the manufacturing process. Assist Manufacturing and the Quality Assurance lab in solving quality and production problems. * Comply with safety regulations and make recommendations towards the improvement of safety and environmental concerns. * Follow all ISO quality and environmental standards as provided in the various procedural manuals. Ensure that all laboratory equipment is calibrated and functioning properly. Education, Experience, Skills & Competencies: * This position requires a Bachelor Degree in Chemistry or equivalent with at least 7 years of experience, a Masters Degree in Chemistry or equivalent with at least 5 years of experience, or a Doctor of Philosophy in Chemistry or equivalent with at least 3 years of experience. * Knowledge of colloid chemistry, surfactants, and tribology is required. * Experience with the formulation of metalworking fluids and field support of machining and grinding operations is highly desired. * Understanding of applied statistics and experimental design is not required, but highly desired. * Must have the ability to operate in a fast-paced environment, to work on different projects at the same time, and to think analytically. * Must have good prioritization and communication skills (oral and writing). * Ability to write detailed reports and presentations which may be used to inform high-ranking members of the Technical Community. What's in it for you: * Competitive pay programs with excellent career growth trajectory * Opportunities to see your efforts contribute toward the success of the business * Work for a global leader in the industrial process fluids industry Quaker Houghton is an equal opportunity employer committed to creating a diverse workforce. Quaker Houghton provides equal employment opportunity for all qualified candidates. Quaker Houghton does not discriminate against any candidate for employment based on race, color, religion, sex, gender, gender identity or expression, affectional or sexual orientation, pregnancy, age, creed, ancestry, national origin, citizenship, marital or domestic partnership or civil union status, veterans status, physical/mental disability, genetic information, or any other category protected by U.S federal, state, and/or local employment law. Furthermore, Quaker Houghton is committed to providing reasonable accommodations to qualified candidates with physical and/or mental disabilities. Applicants with a disability who need assistance applying for a position may email

At Customers Bank, we believe in working hard, working smart, working together to deliver memorable customer experiences and having fun. Our vision, mission, and values guide us along our path to achieve excellence. Passion, attitude, creativity, integrity, alignment, and execution are cornerstones of our behaviors. They define who we are as an organization and as individuals. Everyone is encouraged to have personal development plans. By doing so, our team members are on their way to achieve their highest potential and be successful in their personal and professional lives. Must be legally eligible to work in the United States without sponsorship, now or in the future. Who is Customers Bank? Founded in 2009, Customers Bank is a super-community bank with over $22 billion in assets. We believe in dedicated personal service for the businesses, professionals, individuals, and families we work with. We get you further, faster. Focused on you: We provide every customer with a single point of contact. A dedicated team member who's committed to meeting your needs today and tomorrow. On the leading edge: We're innovating with the latest tools and technology so we can react to market conditions quicker and help you get ahead. Proven reliability: We always ground our innovation in our deep experience and strong financial foundation, so we're a partner you can trust. What you'll do: The Quality Control (QC) Specialist in Fraud Operations is responsible for ensuring that casework, investigations, alerts and transactions handled by the fraud team are accurate, complete and compliant. Core Purpose: Detect and remediate errors, inconsistencies or missed steps in fraud handling. Ensure fraud operations staff follow internal procedures, regulatory requirements, and escalation paths. Act as the final checkpoint within the fraud operations team Case Review & Sampling: Conduct routine and targeted reviews of fraud alerts, disputes and investigations to confirm accuracy, completeness, and compliance with internal policies, established procedures, and applicable regulations. Accuracy & Compliance Verification: Ensure documentation, investigative decisions, and customer communications are correct, complete, and in adherence with regulatory requirements (e.g., Bank Secrecy Act, Reg E, NACHA) as well as bank policy. Error Tracking, Trending & Reporting: Identify errors and deficiencies, record trends, and develop and maintain processes for tracking and reporting quality metrics. Provide timely feedback to analysts and management. Root Cause Analysis & Remediation: Analyze recurring issues to identify systemic gaps or training needs and partner with management to implement corrective actions that strengthen fraud prevention effectiveness. Policy & Procedure Support: Assis in refining, document, and maintaining departmental procedures to ensure clarity, consistency and alignment with compliance and operational requirement. Training and Coaching: Develop and deliver results-based training or coaching to fraud operations staff when deficiencies are identified through quality reviews. Projects, Audits & Initiatives: Participate in departmental projects, audits, and initiatives as needed, ensuring that quality control insights are incorporated into broader fraud prevention strategies. What do you need? 2-5 years of experience in fraud operations, financial crimes investigations or risk/compliance roles. Prior experience in quality assurance/control or audit strongly preferred Analytical Skills: Ability to review fraud cases, identify errors, spot trends, and conduct root cause analysis. Attention to Detail: Precision in reviewing documentation, decisions, and communications to ensure accuracy and compliance. Regulatory Knowledge: Working understanding of key banking regulations (e.g., Bank Secrecy Act, Reg E, NACHA) and internal fraud policies. Problem-Solving: Skills in diagnosing issues and recommending practical, risk-based solutions. Communication Skills: Clear verbal and written communication to provide feedback, draft reports and collaborate across teams. Coaching & Training Ability: Capacity to provide constructive feedback, develop training materials and deliver targeted coaching. Process Orientation: Ability to follow established procedures while recognizing opportunities for process improvements. Technical/System Skills: Familiarity with fraud monitoring systems, case management tools, and reporting software (Excel or Business Intelligence tools often helpful) Time Management & Prioritization: Skill in managing multiple reviews, projects and reporting deadlines efficiently. Customers Bank is an equal opportunity employer. We do not discriminate based upon race, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics. We also provide “reasonable accommodations”, upon request, to qualified individuals with disabilities, in accordance with the Americans with Disabilities Act and applicable state and local laws. Diversity Statement: At Customers Bank, we believe in working smart, working together, and having fun while delivering innovative solutions and memorable experiences for our customers. We are committed to the continual advancement of a culture which reflects the value we place on diversity, equity, and inclusion. We honor the diverse experiences, perspectives, and identities of our team members, and we recognize that it is their passion, creativity, and integrity that drives our success. Step into your future with us! Let's take on tomorrow.

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

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

Site Name: USA - Pennsylvania - King of Prussia As a QC Scientist you would be responsible for testing drug product and drug substance samples for release and stability as well as sample, test, and release raw materials for production use and/or Performing environmental monitoring of the production areas This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: * Perform and train others on physical testing of laboratory samples (raw materials, drug product, drug substance, in-process, water, etc) utilizing various chemical and biochemical techniques including Immunoassay, Separations, Compendial or various microbiological techniques and assays including Environmental Monitoring, Bioburden, and Endotoxin (see Section C for details). * Prepare laboratory samples for analysis and prepares laboratory standards and solutions. * Perform sampling and laboratory testing (instrumental and wet chemistry) of raw materials for quality disposition in support of manufacturing operations, technical transfers, and special studies within the product supply chain. * Manage samples and associated documentation for duration of sample lifecycle, both physically and electronically. * Author and Participate in laboratory investigations. * Author, review, and revise SOP's and support Electronic Notebook template development (testing electronic lab notebook templates, author user requirement specifications, etc) * Reviews and approves laboratory data. * Performs routine departmental GMP activities (lab instrument calibrations, preventive maintenance, audits, work orders, etc) * Support analytical and instrument lifecycle, technical transfer, and/or validation * Laboratory upkeep, maintenance, and continuous improvement (5S, routine equipment/glassware cleaning, etc) Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: * Bachelor's degree in Chemistry, Biochemistry, or science related field * 2+ years of experience in pharmaceutical industry * Or 2+ years of experience in a science related field Preferred Qualifications: * If you have the following characteristics, it would be a plus: * Biopharmaceutical testing experience is preferred, ability to learn various techniques and assays. Assays * include (but not limited to) - pH, SEC * Protein Concentration, HPLC/UPLC, Wet Chemistry. * System experience preferred - SAP/ERP, LES, LES-EM, Geostatistical, Empower, Hamilton (automated liquid handling), analytical instrument software (SoftMax, etc) * Experience with MS Excel, Word, PowerPoint * Working knowledge of cGXP, ICH guidelines, FDA, USP/EP/JP and data integrity guidelines and regulations * Weekend work and off-shift coverage is required at times for HPLC role due to on demand testing. Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees. Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases - to impact health at scale. People and patients around the world count on the medicines and vaccines we make, so we're committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at ************** (US Toll Free) or *************** (outside US). GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at *********************************

As a QC Scientist you would be responsible for testing drug product and drug substance samples for release and stability as well as sample, test, and release raw materials for production use and/or Performing environmental monitoring of the production areas This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: Perform and train others on physical testing of laboratory samples (raw materials, drug product, drug substance, in-process, water, etc) utilizing various chemical and biochemical techniques including Immunoassay, Separations, Compendial or various microbiological techniques and assays including Environmental Monitoring, Bioburden, and Endotoxin (see Section C for details). Prepare laboratory samples for analysis and prepares laboratory standards and solutions. Perform sampling and laboratory testing (instrumental and wet chemistry) of raw materials for quality disposition in support of manufacturing operations, technical transfers, and special studies within the product supply chain. Manage samples and associated documentation for duration of sample lifecycle, both physically and electronically. Author and Participate in laboratory investigations. Author, review, and revise SOP's and support Electronic Notebook template development (testing electronic lab notebook templates, author user requirement specifications, etc) Reviews and approves laboratory data. Performs routine departmental GMP activities (lab instrument calibrations, preventive maintenance, audits, work orders, etc) Support analytical and instrument lifecycle, technical transfer, and/or validation Laboratory upkeep, maintenance, and continuous improvement (5S, routine equipment/glassware cleaning, etc) Basic Qualifications: We are looking for professionals with these required skills to achieve our goals: Bachelor's degree in Chemistry, Biochemistry, or science related field 2+ years of experience in pharmaceutical industry Or 2+ years of experience in a science related field Preferred Qualifications: If you have the following characteristics, it would be a plus: Biopharmaceutical testing experience is preferred, ability to learn various techniques and assays. Assays include (but not limited to) - pH, SEC Protein Concentration, HPLC/UPLC, Wet Chemistry. System experience preferred - SAP/ERP, LES, LES-EM, Geostatistical, Empower, Hamilton (automated liquid handling), analytical instrument software (SoftMax, etc) Experience with MS Excel, Word, PowerPoint Working knowledge of cGXP, ICH guidelines, FDA, USP/EP/JP and data integrity guidelines and regulations Weekend work and off-shift coverage is required at times for HPLC role due to on demand testing. Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees. Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases - to impact health at scale. People and patients around the world count on the medicines and vaccines we make, so we're committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people. If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at ************** (US Toll Free) or *************** (outside US). GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law. Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at *********************************

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

Full-time Description 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

We are seeking a skilled QC Chemist who practices the principles of quality on a daily basis. The ideal candidate is hard-working and extremely ambitious, with the ability to learn and manage responsibilities in a dynamic business environment. The analytical group is responsible for analyzing raw materials, in-process materials, stability, and finished products in accordance with cGMP regulations. The group also handles scheduling, calibration, maintenance of equipment, and performs method development and validation for various analytical methods. As a team member, you will be expected to follow and help plan daily operations within the lab, communicating with all areas in the company to meet client and company deadlines. Responsibilities * Demonstrate expertise with analytical instrumentation, including HPLC, UHPLC, Dissolution, Spectrophotometer, GC, KF (potentiometric and coulometric), and ICP-MS. * Understand and apply USP, ICH, and CFR regulatory requirements. * Perform analytical techniques such as Method Development/Validation, chromatography, pipetting, and solution preparation. * Utilize electronic systems like LIMS, electronic laboratory notebooks, TrackWise, OpenLAB, Excel, and Word. * Conduct various analytical tests, including Assay, dissolution, degradants, moisture, hardness, viscosity, and pH. * Execute against monographs, protocols, and SOPs in a cGMP laboratory environment. * Prevent deviations and investigations. * Conduct stability scheduling and studies. Essential Skills * Bachelor's Degree in Chemistry from an accredited US college or university. * At least 1 year of hands-on QC Chemistry experience in a small molecule GMP lab. * Previous related lab experience is required. * Experience with HPLC (Agilent 1100 or 1290). * Experience with Dissolution and FTIR/IR. * Proficiency with LIMS and GMP. Additional Skills & Qualifications * Experience with electronic systems such as TrackWise and OpenLAB. * Capability in Method Development and Method Improvement. * Understanding of wet chemistry and pharmaceutical processes. Work Environment This position requires you to spend the majority of your time in the lab. Please note that salaried employees are compensated for a 50-hour work week. Job Type & Location This is a Permanent position based out of Horsham, PA. Pay and Benefits The pay range for this position is $80000.00 - $80000.00/yr. Health, dental, vision and 401k available 2 weeks of vacation Holiday and sick time available Workplace Type This is a fully onsite position in Horsham,PA. Application Deadline This position is anticipated to close on Dec 15, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

At Eurofins, your work supports global health and safety. We invest in your professional growth with opportunities to advance in the biopharmaceutical industry, backed by collaborative teams, work-life balance, and competitive benefits. Eurofins Scientific is a global leader in life sciences, providing analytical testing across industries-from food and water to pharmaceuticals and advanced materials. We help the world's top companies ensure their products are safe, authentic, and accurately labeled. Relocate to Indianapolis - Join Our Team! Are you ready for a fresh start in a vibrant city? We're seeking a Team Leader - QC Medical Packaging Testing to join our growing Indianapolis facility. This is your chance to advance your career while enjoying all the benefits of living in one of the Midwest's most dynamic cities. Why Indianapolis? We provide relocation assistance to support your move! Affordable cost of living Thriving job market and biotech community Great neighborhoods, schools, and cultural attractions Job Description Testing & Analysis: Perform lab testing on primary and secondary packaging systems, including container closure integrity, mechanical (break loose/glide force, residual seal force), and vibration testing. Sample & Data Management: Receive samples in LIMS, execute test methods, collect and document data, and release results in LIMS. Method Development: Support development and qualification of new test methods. Client Interaction: Communicate with clients to meet business needs promptly. Compliance & Safety: Ensure adherence to safety standards, GMP, and regulatory requirements. Team Leadership: Supervise, coach, and develop team members; foster motivation and morale. Operational Oversight: Coordinate workflow, monitor daily tasks to meet turnaround times (TAT), and manage job plans. Performance & Growth: Conduct performance reviews, manage training records, interview candidates, and support succession planning. Qualifications Bachelor's degree in science, engineering, or technology (or equivalent experience) Professional leadership experience preferred GMP experience Experience with lab testing - container integrity Authorization to work in the U.S. indefinitely without restriction or sponsorship Additional Information Position is full-time, 8:00 am- 5:00 pm Overtime as needed. Excellent full-time benefits including comprehensive medical coverage, dental, and vision options Life and disability insurance 401(k) with company match Paid vacation and holidays #LI-EB1 Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

At ALS, we encourage you to dream big. When you join us, you'll be part of a global team harnessing the power of scientific testing and data-driven insights to build a healthier future. Microbiology Analyst Imagine your future with us! At ALS, we encourage you to dream big. When you join ALS, you join a purpose and values-driven team that empowers you to innovate, create, and thrive. Our global team turns up each day with passion and commitment to do amazing things, always challenging our thinking to find ways to solve some of the world's most complex problems for a safer, healthier world. General Accountability: The primary purpose of this position is to perform microbiology analyses on drinking water, waste water and biosolids according to method specification and client requirements. Specific Responsibilities: Analyze drinking water, wastewater and sludge/solid samples for microbiological parameters such as coliform, E. coli, fecal coliforms, and standard plate count. Perform all quality control requirements associated with the microbiology methods and maintain appropriate records. Prioritize work by creating schedules to complete daily assignments and data review and reporting promptly. Interpret and author SOPs, perform reagent formulation, record bench level observations, and keep records in bound and electronic notebooks. Be responsive and responsible for meeting method holding times and incubation cycle times by pulling and interpreting media within method prescribed parameters. Meets production levels on a daily and weekly basis in order to meet client deadlines. Able to work independently with little supervision. Make timely notifications for public water compliance on regulated drinking water samples. Able to work in a team with co-workers and participate in schedule rotations as needed to meet microbiology department needs. Assist in maintaining a clean audit ready laboratory at all times Ensure compliance with assigned SOP's, QA manual and HSE policies. Recognize and maintain safe working conditions. Follow PPE policies. Handle hazardous material appropriately and safely. Maintain a clean, orderly work environment. Perform other duties as assigned and directed. About you Required Knowledge, Skills & Abilities: Experience in document control, the use of SOP's, reagent formulation, and bench level observation and recordkeeping in bound and electronic notebooks. An understanding of basic quality assurance parameters specifically measure of precision and accuracy is preferred. Experience in the analysis of environmental samples for microbiological and wet chemistry parameters using EPA methodologies. Able to work independently with little supervision as well as the ability to work as a team, be a team player and support fellow co-workers. Produces quality, error free work. Attitude and cooperation - has an upbeat and positive attitude, offers ideas and solutions to correct problem areas Seeks assistance when needed before a situation gets “out of hand” Professional appearance and conduct to both ALS staff and clients. Diligent work ethic. Adaptable and able to change an approach or method quickly to fit different situations Communicates information well to co-workers / team members to include all those involved in the decision-making process. Motivated and fast paced personality. Multi-tasked, organized, detail oriented, and possess excellent problem solving capabilities; will have good time management capabilities. Must be dependable and reliable. Able to learn new software/computer systems for inventory management. Ability to work overtime when needed. Required Qualifications: A Bachelor of Science in Biology or a related field Previous laboratory experience is preferred. Computer skills, Microsoft programs. Physical Demands: The ability to stand, bend and sit for 100% of shift. Able to speak and hear clearly while communicating with staff, management and clients. Able to lift 50+ lbs. on a consistent basis (may use a dolly for situations requiring heaving loads). Dexterity in hands and fingers to operate computers and instrumentation. Average vision and able to see to read reports and operate instrumentation. Hearing and speech to communicate in person and over the telephone. Able to perform repetitive motion actions. Ability to work overtime when needed. We would like to thank everyone for their interest in ALS Environmental but only candidates selected for an interview will be contacted. “ALS Group is proud to be an equal opportunity employer committed to achieving and maintaining a workforce which reflects and affirms the diversity of our society” EOE AA M/F/Vet/Disability Click Here to view the EEO is the Law poster Working at ALS The ALS team is a diverse and dedicated community united by our passion to make a difference in the world. Our values are important to us, and shape how we work, how we treat each other and how we recognise excellence. At ALS, you'll be supported to develop new skills and reach your full potential. We invest in our people with programs and opportunities that help you build a diverse career with us. We want everyone to have a safe, flexible and rewarding career that makes a positive impact on our people, the planet and our communities. Everyone Matters ALS is proud to be an equal opportunity employer and is committed to fostering an inclusive work environment where the strengths and perspectives of each employee are both recognised and valued. Qualified candidates will be considered without regard to race, colour, religion, national origin, military or veteran status, gender, age, disabilities, sexual orientation, gender identity, pregnancy and pregnancy-related conditions, genetic information and any other characteristics protected by the law. We invite resumes from all interested parties, including women, members of minority groups, and persons living with disabilities. ALS also welcomes applications from people with all levels of ability. Accommodation is available on request for candidates taking part in all aspects of the selection process. Eligibility To be eligible to work at ALS you must be a Citizen or Permanent Resident of the country you are applying for, or either hold or be able to obtain, a valid working visa. How to apply Please apply on-line and provide a cover letter and CV that best demonstrate your motivation and ability to meet the requirements of this role.

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

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

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

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.

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.

Job Details East Coast Distribution Center - WESTAMPTON, NJ Full Time $20.00 - $22.00 Hourly Mid ShiftDescription Join our innovative team at TLCH Foods where we are committed to help more food brands redefine the dining experience for their customers by blending creativity, practicality, and smart solutions. Our team of culinary experts includes award-winning chefs, presidents of iconic food brands, and over 70 years of combined business, operations, and technology experience-not to mention, an unwavering passion for food. We are currently seeking highly motivated individuals to fill Quality Control Inspector role at our food manufacturing facility in Westampton, NJ. The primary responsibilities of this role is to monitors and inspect established food safety and quality assurance functions in support of our commitment to our customers and our Mission Statement. What will you be doing: Responsible for inspections, process audits, product testing, analyzing measurements and overseeing production processes to ensure high quality products. Responsible for maintaining quality control standards by properly investigating, correcting and communicating any in process or finished product quality issues immediately. Responsible for completing and reviewing in process and finished product documentation to ensure accuracy. Ability to perform basic food safety practices in the production center with a high degree of attention to detail and internal customer service. Ability to consistently execute tasks according to SOP (Standard Operating Procedures) SSOP (Sanitation Standard Operating Procedure) and GMP (Good Manufacturing Practices) for the production center as trained. Ability to provide support in all areas related to the lab and testing of products. Ability to demonstrate accurate and safe use of basic warehouse equipment including but not limited to pH meter and luminometer. Qualifications Who you are and why you're right for us: At least 6 months experience in warehouse setting is preferred. Ability to read and follow written and/or verbal instructions in English. Attention to detail, accuracy, thoroughness, and flexibility required Basic computer skills required (Microsoft Word, Internet search, Data Entry, Email) Ability to work in a fast-paced environment, a variety of shifts, weekends, and overtime as needed. Ability to work independently and or in a group setting, with minimal supervision. Ability to work in a refrigerated environment (-9º-42º Fahrenheit) for 8 or more hours and in some instances, in a dark environment Why Join Us: Medical, Dental, Vision and Life Insurance HSA and FSA account options Employee assistance program Employee discount 401(K) with a match Paid Holiday and additional 2 Floating Holidays Paid time off (PTO) Access to our weekly internal Farmer's Market, where you can take home free quality produce and pantry items.

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

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