Quality control analyst jobs in Upper Chichester, PA - 165 jobs

Please note: For confidentiality purposes, this position is not located in Blue Bell. The role is based in the tri-state area. This role will focus on the validation of analytical methods for products in development or for commercial products when needed. This position involves executing validation studies and optimizing or developing analytical methods when needed to support drug product applications. In addition to analytical method validation, this position will involve R&D T0 and Stability testing for 2-3 drug products in development Key responsibilities. Develops analytical methods that are accurate, precise, and specific for use in both the Quality Control department and the Research department. Methods primarily include HPLC and GC but also include ICP-MS, Karl Fisher, solid-state characterization, and others. Documents the development of the method in the appropriate notebooks for future reference. Performs pre-validation work ahead of transfer to the Validation Department to demonstrate suitability for use. Prepares test method procedures and supporting documentation for use in the Quality Control laboratory. May be required to develop validation protocols and validate analytical methods used in the testing of raw materials, intermediate products, final products, and cleaning samples. Assists in the maintenance and calibration of laboratory analytical instrumentation including, but not limited to HPLC and GC. Maintains accurate records regarding the maintenance and calibration activities. May support manufacturing operations with testing of raw materials, intermediate products, final products, and cleaning samples. The incumbent is expected to operate in a neat and orderly manner and to provide accurate and timely test results. Assists in the maintenance of the QC Laboratory. In addition to routine housekeeping and glassware cleaning, maintains and appropriate inventory of supplies and chemicals. Documents sample preparation, equipment set-up and test results in Laboratory Notebooks or on the appropriate test record form. Documentation must be complete and verified by a second member of the quality group. In addition, laboratory log sheets, those related to equipment usage, calibration, and maintenance, reference standard inventory, QC chemical inventory, or those related to retention samples will be properly maintained. EDUCATION/EXPERIENCE. A Bachelor's Degree in Chemistry (Master's or PhD Degree is preferred) A minimum of 7 years of experience in small molecule pharmaceutical laboratories, with a strong background/proficiency in LC, GC, Dissolution and chromatographic method validation and development. Proficient with Empower software. Strong organizational skills. Good communication skills Good writing skills.

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

Job DescriptionAre you the person who always spots the small stuff? If details jump out at you and you enjoy collaborating to solve problems, you'll fit right in at our Linwood, PA operation. We're looking for someone who keeps products safe, consistent, and compliant-every time. Role at a glance Perform inspections across the flow: receiving, in-process, and final release. Apply gauges, calipers, micrometers, and other test equipment to verify specifications. Document results thoroughly and maintain accurate inspection records. Escalate defects or nonconformities and recommend corrective actions. Partner with production to troubleshoot and improve processes. Participate in quality audits and contribute to the creation of quality control procedures. Keep up with industry standards and best practices to ensure compliance. Must-haves High school diploma or equivalent; extra technical training in quality is a plus. Experience as a quality inspector or similar quality-focused role. Knowledge of quality standards and common inspection/testing methods. Proficiency with measurement tools and equipment. Meticulous attention to detail and strong analytical ability. Team player who can also work independently when needed. Effective verbal and written communication. Proficiency checklist Quality Inspection Experience Tape Measure Reading Blueprint Reading Primary instruments Measurement Gauges Calipers and Micrometers Join a collaborative team where your eye for detail directly elevates product quality and customer confidence.

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

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

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

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

Hours: 40 Pay Details: $72,280 - $108,160 USD TD is committed to providing fair and equitable compensation opportunities to all colleagues. Growth opportunities and skill development are defining features of the colleague experience at TD. Our compensation policies and practices have been designed to allow colleagues to progress through the salary range over time as they progress in their role. The base pay actually offered may vary based upon the candidate's skills and experience, job-related knowledge, geographic location, and other specific business and organizational needs. As a candidate, you are encouraged to ask compensation related questions and have an open dialogue with your recruiter who can provide you more specific details for this role. Line of Business: Governance & Control Job Description: The Senior Governance & Control Analyst - Treasury Data Controls and Quality Assurance provides specialized data governance, control & assurance guidance and support for a business or functional area and implement policies / processes and/or initiatives to meet business governance and control objectives for US Treasury. **This position is in office in either our Mount Laurel NJ, Portland ME, or Charlotte NC locations** Depth & Scope: SME level professional role requiring in-depth business knowledge/expertise in own domain/field of specialty and working knowledge of broader related areas Integrates the broader organizational context into advice and solutions within own area Understands a certain aspect of the industry, competition and the factors that differentiate the organization Applies best practices to implement process, product or service improvements Leads projects of moderately to complex risk and resource requirements; may lead end-to-end processes or functional programs Contributes to setting standards within area of expertise Solves complex problems requiring analysis of multiple variables, including consultation with multiple stakeholders Uses advanced methods to contribute to new solutions and recommend standards against which others will operate Interprets guidelines, standards, policies and results of analysis to inform decision making at senior levels Works independently as a SME or lead and guides others within area of expertise Education & Experience: Undergraduate degree preferred Broad and deep knowledge of business and risk and control environment 5+ years of relevant experience Proficient knowledge of governance, risk and control procedures, strategies & tactics Proficient Knowledge of current and emerging trends Skill in mentoring/ coaching others Skill in using analytical software tools, data analysis methods and reporting techniques Skill in using computer applications including MS Office Ability to communicate effectively in both oral and written form Ability to work collaboratively and build relationships Ability to work successfully as a member of a team and independently Ability to exercise sound judgment in making decisions Ability to analyze, research, organize and prioritize work while meeting multiple deadlines Ability to process and handle confidential information with discretion Preferred Qualifications: Data control testing Executing control tests Comfortable working in an ambiguous, quickly evolving, and maturing environment Customer Accountabilities: Provides specialized business governance and control related advice/support to management/leadership and respective teams for area(s) of specialization Leads on the implementation of governance and control initiatives in support of the overall business/function strategy Manages a set of business governance and control work activities requiring coordination across multiple areas Reviews processes and controls and connects the dots across issues and control deficiencies in order to increase standardization of solutions, processes and controls Supports/manages the integrated implementation of policies/processes/procedures/changes across multiple functional areas Provides subject matter expertise to projects/initiatives, and participates in identifying, designing and testing solutions and supporting implementation activities Shareholder Accountabilities: Ensures programs/policies/practices are well-managed, meet business needs/priorities, and comply with internal/external requirements Exercises discretion in managing communication/correspondence, information and all matters of confidentiality Conducts research projects; supports the development/delivery of materials and presentations to management or broader audience Adheres to enterprise frameworks or methodologies that relate to activities for own business area May lead work streams by acting as a project lead/SME for medium-scale projects/initiatives in accordance with project management methodologies Protects the interests of the organization - identifies and manages risks, and escalates non-standard, high-risk transactions/activities as necessary Maintains a culture of risk management and control, supported by effective processes in alignment with risk appetite Is knowledgeable of and complies with Bank Code of Conduct Employee/Team Accountabilities: Participates as a member of the team, supports a positive work environment and ensures timely communication Supports team by regularly enhancing knowledge/expertise in own area and participates in knowledge transfer Keeps current on emerging trends/developments and grows knowledge of the business, related tools and techniques Keeps others informed about the status/progress of projects Contributes to team development of skills and capabilities through mentorship of others, by sharing knowledge and experiences and leveraging best practices Contributes to a fair, positive and equitable environment Acts as a brand ambassador for your business area/function and the Bank Physical Requirements: Never: 0%; Occasional: 1-33%; Frequent: 34-66%; Continuous: 67-100% Domestic Travel - Occasional International Travel - Never Performing sedentary work - Continuous Performing multiple tasks - Continuous Operating standard office equipment - Continuous Responding quickly to sounds - Occasional Sitting - Continuous Standing - Occasional Walking - Occasional Moving safely in confined spaces - Occasional Lifting/Carrying (under 25 lbs.) - Occasional Lifting/Carrying (over 25 lbs.) - Never Squatting - Occasional Bending - Occasional Kneeling - Never Crawling - Never Climbing - Never Reaching overhead - Never Reaching forward - Occasional Pushing - Never Pulling - Never Twisting - Never Concentrating for long periods of time - Continuous Applying common sense to deal with problems involving standardized situations - Continuous Reading, writing and comprehending instructions - Continuous Adding, subtracting, multiplying and dividing - Continuous The above statements are intended to describe the general nature and level of work being performed by people assigned to this job. They are not intended to be an exhaustive list of all responsibilities, duties and skills required. The listed or specified responsibilities & duties are considered essential functions for ADA purposes. Who We Are: TD is one of the world's leading global financial institutions and is the fifth largest bank in North America by branches/stores. Every day, we deliver legendary customer experiences to over 27 million households and businesses in Canada, the United States and around the world. More than 95,000 TD colleagues bring their skills, talent, and creativity to the Bank, those we serve, and the economies we support. We are guided by our vision to Be the Better Bank and our purpose to enrich the lives of our customers, communities and colleagues. TD is deeply committed to being a leader in customer experience, that is why we believe that all colleagues, no matter where they work, are customer facing. As we build our business and deliver on our strategy, we are innovating to enhance the customer experience and build capabilities to shape the future of banking. Whether you've got years of banking experience or are just starting your career in financial services, we can help you realize your potential. Through regular leadership and development conversations to mentorship and training programs, we're here to support you towards your goals. As an organization, we keep growing - and so will you. Our Total Rewards Package Our Total Rewards package reflects the investments we make in our colleagues to help them and their families achieve their financial, physical and mental well-being goals. Total Rewards at TD includes base salary and variable compensation/incentive awards (e.g., eligibility for cash and/or equity incentive awards, generally through participation in an incentive plan) and several other key plans such as health and well-being benefits, savings and retirement programs, paid time off (including Vacation PTO, Flex PTO, and Holiday PTO), banking benefits and discounts, career development, and reward and recognition. Learn more Additional Information: We're delighted that you're considering building a career with TD. Through regular development conversations, training programs, and a competitive benefits plan, we're committed to providing the support our colleagues need to thrive both at work and at home. Colleague Development If you're interested in a specific career path or are looking to build certain skills, we want to help you succeed. You'll have regular career, development, and performance conversations with your manager, as well as access to an online learning platform and a variety of mentoring programs to help you unlock future opportunities. Whether you have a passion for helping customers and want to expand your experience, or you want to coach and inspire your colleagues, there are many different career paths within our organization at TD - and we're committed to helping you identify opportunities that support your goals. Training & Onboarding We will provide training and onboarding sessions to ensure that you've got everything you need to succeed in your new role. Interview Process We'll reach out to candidates of interest to schedule an interview. We do our best to communicate outcomes to all applicants by email or phone call. Accommodation TD Bank is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, status as a protected veteran or any other characteristic protected under applicable federal, state, or local law. If you are an applicant with a disability and need accommodations to complete the application process, please email TD Bank US Workplace Accommodations Program at ***************. Include your full name, best way to reach you and the accommodation needed to assist you with the applicant process.

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

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

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

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

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)

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

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at ******************* Job Function: R&D Operations Job Sub Function: Laboratory Operations Job Category: Professional All Job Posting Locations: Spring House, Pennsylvania, United States of America Job Description: About Innovative Medicine Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at *******************/innovative-medicine We are searching for the best talent for an Analyst II, Laboratory Operations to be located in Spring House, PA. Purpose: This position is part of the global Discovery, Product Development & Supply (DPDS) Operations Team responsible for operations within the Therapeutic Discovery (TD) and Preclinical Safety and Translational Sciences (PSTS) organizations. The Lab Operations team in DPDS Operations looks after the lab workspace to enable the scientists to focus on their science using a knowledge of project management, drug discovery instrumentation and automation, and process excellence to evaluate, develop and deliver drug discovery laboratory processes and infrastructure. The Analyst II functions by planning and performing operational activities and acquisitions linked to the lab workspace. They work effectively in multi-disciplinary teams and collaborates with internal and external partners - such as Safety, Business Operations, Facility Management, Finance - thus ensuring flawless execution of all projects and processes connected to the lab workspace. The function requires a hands-on mentality and the ability to work autonomously for longer term activities independently adapting to project developments and proposing next steps. You will be responsible for: Overseeing and managing the day-to-day activities involving provisioning, instrumentation, facility maintenance and upkeep to optimize laboratory operations. Managing laboratory projects end to end, from idea through onboarding and installation of new instruments. Coordinating laboratory moves for facility projects. Ensuring routine and unscheduled equipment maintenance is performed within acceptable timeframes, effectively collaborating with external partners/organizations. Collaborating with IT to manage and maintain computer and automation systems, including systems upgrades and issue resolution. Working closely with scientific staff and leaders to ensure a steady and ongoing relationship with intent for efficient operation, improved automation, and workflow process improvements. Collaborating effectively with fellow team/project members following procedures, priorities and timelines. Maintaining general laboratory safety standards. Qualifications / Requirements: Education: A minimum of a Bachelor's degree in a Scientific field, Engineering, Information Systems or Business is required. An advanced degree is preferred. Experience and Skills: Required: A minimum of 2 years of relevant experience is required. Strong interpersonal communication skills, effective organization, communication, and customer service skills are required. Excellent attention to details is required. Strategic and critical thinking, prioritization, and ability to execute on those strategies are required. Preferred: Proven project management success and change management experience is highly preferred. Solid working knowledge of laboratory or highly controlled facilities operations, information systems, instrumentation, automation, safety, and compliance are highly preferred. Prior laboratory experience on the bench or laboratory/operational management experience for science background candidates is preferred. Prior facility or laboratory renovation project management is a plus. Prior experience and understanding of laboratory automation is a plus. Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via *******************/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource. #LI-Onsite Required Skills: Preferred Skills: Analytical Reasoning, Business Behavior, Coaching, Communication, Data Management and Informatics, Data Savvy, Ethical and Participant Safety Considerations, Inventory Management, Laboratory Operations, Laboratory Safety, Mental Agility, Molecular Diagnostics, Preclinical Research, Problem Solving, Research and Development, Toxicology, Use of Laboratory Equipment

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

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

Mount Laurel, New Jersey, United States of America **Hours:** 40 **Pay Details:** $72,280 - $108,160 USD TD is committed to providing fair and equitable compensation opportunities to all colleagues. Growth opportunities and skill development are defining features of the colleague experience at TD. Our compensation policies and practices have been designed to allow colleagues to progress through the salary range over time as they progress in their role. The base pay actually offered may vary based upon the candidate's skills and experience, job-related knowledge, geographic location, and other specific business and organizational needs. As a candidate, you are encouraged to ask compensation related questions and have an open dialogue with your recruiter who can provide you more specific details for this role. **Line of Business:** Governance & Control **Job Description:** The **_Senior Governance & Control Analyst - Treasury Data Controls and Quality Assurance_** provides specialized data governance, control & assurance guidance and support for a business or functional area and implement policies / processes and/or initiatives to meet business governance and control objectives for US Treasury. ** **This position is in office in either our Mount Laurel NJ, Portland ME, or Charlotte NC locations**** **Depth & Scope:** + SME level professional role requiring in-depth business knowledge/expertise in own domain/field of specialty and working knowledge of broader related areas + Integrates the broader organizational context into advice and solutions within own area + Understands a certain aspect of the industry, competition and the factors that differentiate the organization + Applies best practices to implement process, product or service improvements + Leads projects of moderately to complex risk and resource requirements; may lead end-to-end processes or functional programs + Contributes to setting standards within area of expertise + Solves complex problems requiring analysis of multiple variables, including consultation with multiple stakeholders + Uses advanced methods to contribute to new solutions and recommend standards against which others will operate + Interprets guidelines, standards, policies and results of analysis to inform decision making at senior levels + Works independently as a SME or lead and guides others within area of expertise **Education & Experience:** + Undergraduate degree preferred + Broad and deep knowledge of business and risk and control environment + 5+ years of relevant experience + Proficient knowledge of governance, risk and control procedures, strategies & tactics + Proficient Knowledge of current and emerging trends + Skill in mentoring/ coaching others + Skill in using analytical software tools, data analysis methods and reporting techniques + Skill in using computer applications including MS Office + Ability to communicate effectively in both oral and written form + Ability to work collaboratively and build relationships + Ability to work successfully as a member of a team and independently + Ability to exercise sound judgment in making decisions + Ability to analyze, research, organize and prioritize work while meeting multiple deadlines + Ability to process and handle confidential information with discretion **Preferred Qualifications:** + Data control testing + Executing control tests + Comfortable working in an ambiguous, quickly evolving, and maturing environment **Customer Accountabilities:** + Provides specialized business governance and control related advice/support to management/leadership and respective teams for area(s) of specialization + Leads on the implementation of governance and control initiatives in support of the overall business/function strategy + Manages a set of business governance and control work activities requiring coordination across multiple areas + Reviews processes and controls and connects the dots across issues and control deficiencies in order to increase standardization of solutions, processes and controls + Supports/manages the integrated implementation of policies/processes/procedures/changes across multiple functional areas + Provides subject matter expertise to projects/initiatives, and participates in identifying, designing and testing solutions and supporting implementation activities **Shareholder Accountabilities:** + Ensures programs/policies/practices are well-managed, meet business needs/priorities, and comply with internal/external requirements + Exercises discretion in managing communication/correspondence, information and all matters of confidentiality + Conducts research projects; supports the development/delivery of materials and presentations to management or broader audience + Adheres to enterprise frameworks or methodologies that relate to activities for own business area + May lead work streams by acting as a project lead/SME for medium-scale projects/initiatives in accordance with project management methodologies + Protects the interests of the organization - identifies and manages risks, and escalates non-standard, high-risk transactions/activities as necessary + Maintains a culture of risk management and control, supported by effective processes in alignment with risk appetite + Is knowledgeable of and complies with Bank Code of Conduct **Employee/Team Accountabilities:** + Participates as a member of the team, supports a positive work environment and ensures timely communication + Supports team by regularly enhancing knowledge/expertise in own area and participates in knowledge transfer + Keeps current on emerging trends/developments and grows knowledge of the business, related tools and techniques + Keeps others informed about the status/progress of projects + Contributes to team development of skills and capabilities through mentorship of others, by sharing knowledge and experiences and leveraging best practices + Contributes to a fair, positive and equitable environment + Acts as a brand ambassador for your business area/function and the Bank **Physical Requirements:** Never: 0%; Occasional: 1-33%; Frequent: 34-66%; Continuous: 67-100% + Domestic Travel - Occasional + International Travel - Never + Performing sedentary work - Continuous + Performing multiple tasks - Continuous + Operating standard office equipment - Continuous + Responding quickly to sounds - Occasional + Sitting - Continuous + Standing - Occasional + Walking - Occasional + Moving safely in confined spaces - Occasional + Lifting/Carrying (under 25 lbs.) - Occasional + Lifting/Carrying (over 25 lbs.) - Never + Squatting - Occasional + Bending - Occasional + Kneeling - Never + Crawling - Never + Climbing - Never + Reaching overhead - Never + Reaching forward - Occasional + Pushing - Never + Pulling - Never + Twisting - Never + Concentrating for long periods of time - Continuous + Applying common sense to deal with problems involving standardized situations - Continuous + Reading, writing and comprehending instructions - Continuous + Adding, subtracting, multiplying and dividing - Continuous The above statements are intended to describe the general nature and level of work being performed by people assigned to this job. They are not intended to be an exhaustive list of all responsibilities, duties and skills required. The listed or specified responsibilities & duties are considered essential functions for ADA purposes. **Who We Are:** TD is one of the world's leading global financial institutions and is the fifth largest bank in North America by branches/stores. Every day, we deliver legendary customer experiences to over 27 million households and businesses in Canada, the United States and around the world. More than 95,000 TD colleagues bring their skills, talent, and creativity to the Bank, those we serve, and the economies we support. We are guided by our vision to Be the Better Bank and our purpose to enrich the lives of our customers, communities and colleagues. TD is deeply committed to being a leader in customer experience, that is why we believe that all colleagues, no matter where they work, are customer facing. As we build our business and deliver on our strategy, we are innovating to enhance the customer experience and build capabilities to shape the future of banking. Whether you've got years of banking experience or are just starting your career in financial services, we can help you realize your potential. Through regular leadership and development conversations to mentorship and training programs, we're here to support you towards your goals. As an organization, we keep growing - and so will you. **Our Total Rewards Package** Our Total Rewards package reflects the investments we make in our colleagues to help them and their families achieve their financial, physical and mental well-being goals. Total Rewards at TD includes base salary and variable compensation/incentive awards (e.g., eligibility for cash and/or equity incentive awards, generally through participation in an incentive plan) and several other key plans such as health and well-being benefits, savings and retirement programs, paid time off (including Vacation PTO, Flex PTO, and Holiday PTO), banking benefits and discounts, career development, and reward and recognition. Learn more (*************************************** **Additional Information:** We're delighted that you're considering building a career with TD. Through regular development conversations, training programs, and a competitive benefits plan, we're committed to providing the support our colleagues need to thrive both at work and at home. **Colleague Development** If you're interested in a specific career path or are looking to build certain skills, we want to help you succeed. You'll have regular career, development, and performance conversations with your manager, as well as access to an online learning platform and a variety of mentoring programs to help you unlock future opportunities. Whether you have a passion for helping customers and want to expand your experience, or you want to coach and inspire your colleagues, there are many different career paths within our organization at TD - and we're committed to helping you identify opportunities that support your goals. **Training & Onboarding** We will provide training and onboarding sessions to ensure that you've got everything you need to succeed in your new role. **Interview Process** We'll reach out to candidates of interest to schedule an interview. We do our best to communicate outcomes to all applicants by email or phone call. **Accommodation** TD Bank is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, status as a protected veteran or any other characteristic protected under applicable federal, state, or local law. If you are an applicant with a disability and need accommodations to complete the application process, please email TD Bank US Workplace Accommodations Program at *************** . Include your full name, best way to reach you and the accommodation needed to assist you with the applicant process. Federal law prohibits job discrimination based on race, color, sex, sexual orientation, gender identity, national origin, religion, age, equal pay, disability and genetic information.