Quality control technician jobs in Easton, PA - 232 jobs

Job Title: QA Technician Reports to: Quality Assurance Manager FLSA Status: Non-Exempt Shift: Nights Department: Quality Assurance Prepared by: Human Resources Approved By: Plant Manager Qualifications: High School diploma or equivalent, undergraduate degree preferred Food, beverage, or liquid consumer product manufacturing a plus. Ability to work a flexible schedule as needed Basic reading, writing, and math skills Functional Knowledge of Excel, Word, Power Point Excellent verbal and written communication skills Responsibilities: QA Tech is responsible for conducting micro testing, wet chemical analysis of water, testing and maintaining the RO, overseeing with the help of the rest of QA that the production QAF's are being filled out and adhered to, policing GMP policies, quarterly CFR testing for bottles and closures, and various other tasks as they arise. GMP & PPE Required While on the production floor in the plant you will be required to follow and help to enforce all GMP regulations in the plant. Anyone entering the production floor must follow the GMP rules in their employee handbook, which includes the required hairnets, beard nets, and earplugs. It is also required that all personnel wear safety glasses. Follows standard operating procedures including quality checks and procedures for all operations. Also follows HACCP and SQF requirements for food quality and safety. Essential Job Duties: Performs daily and quarterly micros Performs wet chemical analysis of product. Performs Quality checks and calibrations. Maintains quality forms and may do cleaning and minor maintenance. Performs daily Plant checks/walkthrough checking QAF and cleanliness. Writes Process deviations and Defective Material Reports. Over sees corrective actions are being implemented Makes sure that Plant personnel are adhering to corporate GMP policies Maintains chemical inventory Must be able to communicate at all levels Non-Essential Job Duties: Performs any and all related work as assigned by the manager and needs of the business. In the absence of this employee, the direct manager or appointee will cover responsibilities. Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Sitting - Approximately 30% Standing - Approximately 60% Walking - Approximately 10% Bending/Stooping - Occasionally Push/Pull - Occasionally Carrying/Lifting up to 40 lbs. - Occasionally Verbal communication - Frequently Written communication - Frequently Hearing normal conversation - Frequently Sight, including near acuity and depth perception - Frequently Work Environment: While performing the duties of this job, the employee is regularly exposed to moving mechanical parts and vibration. The employee is exposed to wet and/or humid conditions, toxic or caustic chemicals, extreme cold, and extreme heat. The employee is frequently exposed to high, precarious places; fumes or airborne particles; risk of electrical shock. The employee is occasionally exposed to outside weather conditions; and a noise level requiring use of hearing protection.

Quality Assurance Technician - Night Shift is $29.19/hr. + $3.00/hr. shift differential = $32.19/hr. Who We Are At Freshpet, our goal is to change the way people nourish their pets forever. We strive to strengthen the bond between people and our pets so that we both live longer, healthier, and happier lives while being kind to the planet. We believe that if we can create fresh, real foods that pets love and help them live healthier lives, that their pet parents will also enjoy the many benefits of a rich life shared with a pet. We started off with a mission to change the way pet parents feed dogs and cats, but we also wanted to be a company that had a thoughtful approach to how we operate. We wanted to do things differently, make great products but be gentle to the planet, good to the people who touch our business, and leave a positive impact with everything we do. We work hard every day to ensure that the original vision is met, starting with making the highest quality foods in our kitchens to running our business with integrity, transparency, and social and environmental responsibility. IT'S AMAZING WHAT CAN HAPPEN WHEN YOU START COMPLETELY FRESH! What You Will Do Looking for a self-motivated and quality driven individual for a Quality Assurance Technician position. The ideal candidate will bring in the knowledge and expertise in GMPs and HAACP programs and ensure compliance with product standards, food safety standards and all regulatory requirements. The QA Technician will be responsible for verifying the execution of Quality systems and processes, perform various product tests, evaluate occurrences, implement corrective actions, and document all data. How You Will Make an Impact Conduct hourly production line audits to evaluate compliance to product standards, food safety standards and regulatory requirements. Document audit data Perform routine product tests during audits, including temperature, pH, oxygen, CEM moisture, net weight, particle size, vacuum, and packaging integrity to determine conformance to standards Be familiar with Freshpet HACCP programs for all products. Conduct and/or verify required HACCP food safety tests Perform product organoleptic evaluations on all pet food batches produced for conformance to standards and document test results Work with operations to evaluate nonconformance occurrences and implement corrective action. Document data on Corrective Action Log Isolate and place nonconforming products or ingredients on hold and document hold by entering data on Hold Log and circulating information to Operations and Quality Management Inspect incoming ingredients for conformance to ingredient specifications, collect representative samples for testing and document audit data Collect routine product, ingredient, or water samples for microbiological or chemical testing, shelf-life evaluations or to use as retention samples Conduct Vacuum Tank Packaging tests on Roasted Meals, Vital Complete Meals, and Single Serve products to evaluate packaging and seal integrity Test diluted sanitizers and foot bath solutions to verify concentration and record data Audit sanitation and perform ATP hygiene tests on food contact surfaces and equipment to determine sanitation effectiveness. Document swab data Take swab and sponge samples from established locations to evaluate plant Micro conditions. Record data Test cooling water for sanitary conditions and add biocides as needed to control water quality. Record test data and chemical addition levels Monitor plant TPR tests and collect required samples for testing Provide technical support to Shift Supervisors and Line Leaders Additional related responsibilities as necessary Any trained or qualified individual will serve as backup to this position What You Will Bring High School Diploma or equivalent required Associate Degree in Science Area preferred Minimum 2 years' experience working in Food Safety/Quality Systems, preferably in food or pet food Capable of performing and understanding mathematical calculations. Understanding of ratios, percentages, and fractions Basic understanding of Biology and/or Chemistry and associated technical terms Basic computer skills to read and write emails and enter data on spreadsheets Basic understanding of food Good Manufacturing Practices Capable of following instructions and conducting routine Quality Assurance tests Good interpersonal and communication skills Sound ethics What We Offer At Freshpet, we offer a competitive salary and an excellent benefits package, including medical, dental and vision insurance, basic and optional life insurance, short- and long-term disability protection, flexible spending accounts, and a 401(k) plan with company match, paid parental leave, pet insurance, tuition assistance, a generous PTO plan and so much more! Our Commitment to a Diverse Workforce: At Freshpet, we embrace and encourage our employees' differences in age, sex, color, disability, ethnicity, family or marital status, gender identity or expression, language, national origin, physical and mental ability, political affiliation, race, religion, sexual orientation, socio-economic status, veteran status, and other characteristics that make our employees unique. Freshpet aims to foster, cultivate and preserve a culture of diversity, equity and inclusion. Our employees are our most valuable assets. The collective sum of the individual differences, life experiences, knowledge, inventiveness, innovation, self-expression, unique capabilities and talent that our employees invest in their work represents a significant part of not only our culture, but our reputation and company's achievement as well. Freshpet is an Equal Opportunity Employer. Disclaimers We are interested in every qualified candidate who is eligible to work in the United States. However, we are not able to sponsor visas. Freshpet is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Freshpet via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Freshpet. No fee will be paid in the event the candidate is hired by Freshpet as a result of the referral or through other means.

Our QC Laboratory Technician plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, your responsibilities will include performing basic laboratory support functions related to the management of laboratory samples, materials, and testing supplies. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US. This is a full-time role working Monday through Friday from 8:00 AM to 4:30 PM. This is a set, consistent schedule with minimum overtime requirements and based on site in our Bloomsbury, NJ location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws. What the QC Laboratory Technician Does Each Day: * Verifies information on incoming lab samples and enters sample information into the laboratory database * Place orders and stock laboratory supplies * Light housekeeping, including operation of glassware washer * Ensures all work is performed and documented in a timely manner and according to approved standard operating procedures and in general compliance with cGMPs Our Most Successful QC Laboratory Technicians: * Are accurate and well organized, with strong attention to detail * Express energy, show accountability, can multi-task and work in a fast-paced, quality-rich environment * Fulfill expectations, establish sustainable relationships with team members, maintain effective and meaningful communication channels * Have good interpersonal skills and work effectively and efficiently in a team environment to accomplish goals * Have strong verbal and written communications skills Minimum Requirements for this Role: * A High School diploma or equivalent * Able to successfully complete a drug and background check * Proficient in Microsoft Office, Word and Excel * Able and willing to walk, stoop, stand, bend, and lift up to 50 lbs. throughout each shift, with or without reasonable accommodation * Must be currently authorized to work in the United States on a full-time basis; Quva will not sponsor applicants for work visas Any of the Following Will Give You an Edge: * Bachelor's Degree in life science or related field * 1 to 2 years' experience in data entry/clerical, or related responsibilities Benefits of Working at Quva: * Set, full-time, consistent work schedule * Comprehensive health and wellness benefits including medical, dental and vision * 401k retirement program with company match * 17 paid days off plus 8 paid holidays per year * Occasional weekend and overtime opportunities with advance notice * National, industry-leading high growth company with future career advancement opportunities * Salary Range: $18.85-27.34/hour About Quva: Quva is a national, industry-leading provider of compounded injectable medicines and software solutions that help power the business of hospital and health-system pharmacy. Quva Pharma produces and distributes injectable medicines required by health care providers and critical to patient care. Quva BrightStream partners with health-systems to analyze large amounts of data and through AI and machine learning, develops software solutions that turns the data into insights that are used to better run their pharmacy operation. Quva's overall product and technology offerings help health-systems achieve greater value and deliver the highest-quality patient care. Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is "at will." California Consumer Privacy Act (CCPA) Notice for Applicants and Employees

The Quality Technician is responsible for performing daily verification activities to ensure that all raw ingredients, raw materials, packaging, and finished products comply with all applicable regulations and meet or exceed the customer's expectations and to act when predefined standards are not met. This position will also help manage product quality tracking systems, state regulatory standards, internal and external audits, etc. The goal for this role is to ensure compliance with all Green Thumb policies and procedures, as well as applicable federal, state, county, and municipal laws, ordinances, and regulations. DUTIES AND RESPONSIBILITIES: Supports the Quality Department and ensures all employees understand and follow all standard operating procedures (SOPs). Perform incoming inspections of materials received and ensure compliance with all specifications and requirements. Execute in-process and finished product sampling as required. Conducts positive release of all finished goods, which includes review of in-process batch documentation, packaging, labeling, logbooks, test results against internal specifications, and other production paperwork as required. Ensures good documentation practices are followed and all records are filed and maintained accordingly. Assist with segregation, control, and disposition of non-conforming product. Identify, recommend, and perform quality training as needed. Ensure maintenance and control of production quality records. Assist Quality Manager and production personnel in the investigation of root causes of quality incidents and non-conformances and assist with documenting and performing corrective and preventative actions. Continually study the existing quality system and make recommendations for improvements. Perform improvement projects as identified. Monitors compliance to established current Good Manufacturing Practice (GMP) guidance. Expected to adhere to safe work practices, follow general GMP and food safety guidelines, maintain sanitary conditions and ensure that product quality is maintained. Report to management any conditions or practices that may adversely affect product safety, product quality or personnel safety. Maintain and foster a positive work atmosphere. Perform pre-operation inspection and sanitation verification of production areas as required. Perform allergen and environmental swabbing activities as needed. Performs other duties as assigned. Working Conditions Work involves daily exposure to allergens (such as cannabis, tree nuts, and coconut oil). PREFERRED EDUCATION, EXPERIENCE AND SKILLS: Associate degree in a related field preferred, or equivalent combination of education, training and/or experience. Prior experience in regulated industry in healthcare, medical devices, pharmaceutical, consumer packaged goods (food), or cannabis is highly desired. Food and Drug Administration (FDA), Good Manufacturing Practices (GMP), Safe Quality Food (SQF) and Hazard Analysis Critical Control Point (HACCP) experience is highly desired. Strong experience with product sampling and inspection. Must have the knowledge and skills required to work in a fast paced and challenging environment Must be able to work variable day shifts dependent on business need Ability to follow written procedures and monitor others for adherence to written procedures. Ability to work independently, handle multiple tasks and problem solve effectively. Exceptional computer skills in Microsoft Office Suite (Access, Excel, Outlook, PowerPoint, Publisher, Word). Should have a solid understanding of the Cannabis laws, rules and regulations or a passion to further their understanding and knowledge of the industry and the laws. Prior cannabis experience not required Additional Requirements Must pass all required background checks Must be and remain compliant with all legal or company regulations for working in the industry Must possess valid driver's license Must be a minimum of 21 years of age Must be approved by state badging agency to work in cannabis industry Our Mission: To promote well-being through the power of cannabis. We're humble-We prefer quiet confidence and don't shout about our success. We're hardworking-We put our heads down and get the job done. We're grateful-Working in our industry is a privilege and an act of service. We're transparent-Honest and open communication keeps us healthy as an organization. We're collaborative-And believe good ideas can come from anywhere. We have a growth mindset-One that's grounded in well-being. At Green Thumb we believe that our corporate community should be a reflection of the communities we serve. We are dedicated to fostering an inclusive culture that celebrates diversity across race, sex, age, gender identity, sexual orientation, disability, nationality, religion, experience, and thought-not only because it is right, but because it makes us better. Our mission-the right to wellness-informs our commitment to champion economic opportunities in communities disproportionately affected by the war on drugs through employment and community involvement. Green Thumb is proud to be an equal opportunity workplace. We can't wait to meet you. As a Green Thumb team member, you will have access to excellent benefits and incentives including: Health, dental, and vision insurance Paid Time Off Employee Discount Mental Health Programs 401(k) Daily Pay Supplemental Insurance Perks Marketplace Flexible Spending Account / Health Spending Account And much more The pay range is competitive and based on experience, qualifications, and/or location of the role. Positions may be eligible for a discretionary annual incentive program driven by organization and individual performance. Green Thumb Pay Range$20-$20 USD

Job Title: Incoming Inspector Employment Type: Full-Time, Onsite Schedule: Monday-Friday, 7:30 AM - 4:00 PM Pay Rate: $20/hour We are seeking a detail-oriented and self-motivated Incoming Inspector to join our Quality Assurance team. In this role, you will be responsible for verifying that purchased parts and materials meet established specifications. In-process inspections of assemblies may also be assigned as needed. Key Responsibilities: Inspect printed circuit boards, components, assemblies, and electro-mechanical assemblies for conformance to IPC standards and product requirements. Perform incoming material inspections using engineering documentation, specifications, procedures, and work instructions. Prepare and maintain accurate inspection reports and records. Retrieve manufacturing or distributor data sheets as needed. Respond to incoming small package deliveries in the absence of Stockroom coworkers. Adhere to all Quality System processes and procedures. Follow safety protocols and wear required PPE (e.g., safety glasses and cleanroom coats). Perform other duties as assigned. Qualifications: Strong attention to detail and high quality standards. Problem-solving skills. Visual acuity for reading small print and identifying colors. Strong communication and organizational skills. Ability to work independently with minimal supervision. Requirements: High school diploma or equivalent. Previous experience in Quality Control, preferably in an electronics manufacturing environment. Ability to read and interpret engineering documentation, material specifications, and relevant industry standards. Experience with inspection tools such as calipers, gauges, multimeters, and stereo microscopes. Basic soldering skills a plus. Familiarity with IPC standards preferred. Basic computer skills (MS Office and ERP systems). Ability to lift up to 30 lbs. Able to work in a seated or standing position for extended periods. If interested, apply today at **************** or text "QC" to ************.

Job Description1st Shift Production Associate Needed in Whitehall, PA! A leading medical device manufacturing company in Whitehall, PA is seeking a reliable and detail-oriented Warehouse Associate to join their team. This role involves hands-on work with ceramics, shipping responsibilities, and opportunities to cross-train in other areas of the warehouse. Warehouse Associate Job Details: Schedule: Monday - Friday 8:30am-4:30pm Pay Rate: $17.00/hour Job Type: Full-Time, Temp-to-Hire Location: Whitehall, PA Warehouse Associate Key Responsibilities: Pour and cut ceramics as part of the production process Handle shipping and receiving tasks Maintain organized work areas and accurate documentation Cross-train in additional warehouse and production duties as needed Contribute to a positive and collaborative team environment Warehouse Associate Requirements: Previous warehouse or manufacturing experience preferred Strong attention to detail and organizational skills Personable, dependable, and adaptable to changing tasks PeopleShare is the leading Staffing Agency in the region and has temporary to hire and permanent jobs across 8 states. Our openings include receptionist, data entry, customer service, collections, office managers, call center, administrative assistant, production technicians, accounts payable clerk, accounts receivable clerk, file clerk, warehouse, assembly, production, pickers, packers, forklift, machine operators, and maintenance mechanics. PeopleShare provides equal opportunities to all employees and applicants for employment without regard to race, religion, color, age, sex, national origin, sexual orientation, gender identity, genetic disposition, neurodiversity, disability, veteran status, or any other protected category or class under federal, state, and/or local laws. This policy applies to all locations and all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. #IND14

Polytek Development Corp. is a leading manufacturer of mold making and casting materials. Polytek is currently looking for a highly motivated, experienced, and extremely organized individual to join our rapidly expanding company. Essential Job Functions: Major tasks and other key responsibilities include: Perform QC tests on incoming raw materials as described in QC SOP. Perform QC tests on production samples as described in QC SOP. Mixing and curing test samples. Run Titrations, Viscosity measurements, Hardness measurements. Work with analytical equipment (including FTIR, TGA, rheometer, DSC). Hazardous chemical handling, storage, and disposal. Physical property testing (including viscosity, specific gravity, tensile/tear strength). Perform any testing and inspection required for customer returns. Perform any testing and inspection required for customer complaints and product non-conformance. Perform additional testing as required for off-specification raw materials and batches. Perform additional testing, ie. Soak tests, physical properties, product application, etc as directed. Interact with production personnel on pilot batches and production problems. Generate weekly QC Reports. Keep laboratory work area neat and uncluttered. Organize and maintain QC retain product samples and cured samples. Understand hazards of Polytek products through company provided training and reading SDSs and labels. Wear proper personal protective equipment (e.g., gloves and safety glasses) and follow all safety rules. Report safety concerns immediately to your supervisor. Perform other duties as assigned. Physical Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Must be able to work in a laboratory environment. Must be able to climb a ladder, frequently lift up to 8 lb, and occasionally lift up to 40 lb. Must be able to bend, squat, walk, stand, use hands to finger, handle or feel, reach with hands and arms, and repeatedly ascend/descend short flights of stairs/ladders for a full shift. Must be able to talk, hear and see with vision abilities including close/near, distance, color and peripheral vision, depth perception and ability to adjust focus. Must wear required Personal Protective Equipment (PPE) when entering laboratory or manufacturing areas. Education and Experience: Must be able to understand, speak, write, and read English. Bachelor's Degree in Chemistry or related field required. 1 - 3 years experience in quality control function in a chemical manufacturing environment is a plus. Skilled in quality processes and statistical techniques. Must have ability to work a flexible schedule, including occasional overtime. Must be proficient in Microsoft Office Suite. Must have the ability to work independently in a fast-paced environment. Strong verbal and written communication, organizational, and time management skills. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Job DescriptionWe are seeking an innovative, creative, and detail-oriented Quality Control Sample Coordinator to join our team in Bridgewater, New Jersey. This individual will play a critical role in ensuring the seamless handling, tracking, and shipping of analytical samples in support of assay execution for the Quality Control (QC) teams. This position acts as the central point of contact between Manufacturing, Analytical teams (multi-site), and other cross-functional stakeholders in managing sample logistics and documentation. All activities are performed in accordance with cGMP guidelines and are supported by departmental and inter-departmental policies and standard operating procedures. Candidates should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows.Responsibilities Create and maintain sample schedule, from sample creation through QC testing Track sample shipments between internal and external sites Receive samples from clients or other Cellares sites and ensure proper logging, handling, & reconciliation Maintain visibility into sample storage locations, including LN2 and -80°ree;C freezers Manage documentation related to the shipping and receiving of samples Document sharing & coordinate ordering cryoports/cryopods with the Warehouse team and coordinate shipment/reshipment logistics for analytical samples Be comfortable working with LN2 systems Work with QC teams in developing and managing sample batching approaches Deliver required samples to the QC team in real time Monitor for and address discrepancies (labels not accurate, vial missing, wrong concentration, etc) proactively Be available to support unplanned analytical re-executions Review the assay execution schedule and monitor turnaround times for data release to ensure alignment with project timelines Ensure sample retains are shipped to appropriate long-term storage locations after assay execution Assist in general upkeep of the laboratory and maintain a clean work environment Perform other duties as assigned Requirements Bachelor's degree in a science discipline required, or comparable experience 2+ years of experience in cGMP or cGxP at an operational level supporting manufacturing in a pharmaceutical or biotech environment is preferred Prior experience related to LN2 sample handling is preferred Prior experience with scheduling/planning tools (e.g Binocs) is preferred Knowledge of pharmaceutical cGMP (US and EU) is preferred Must have excellent verbal, written, interpersonal, and organizational and communication skills Must be able to commute to Bridgewater, New Jersey Self-awareness, integrity, authenticity, and a growth mindset Cellares total compensation package contains competitive base salaries, highly subsidized Medical, Dental, and Vision Plans, 401(k) Matching, Onsite lunches, and Stock options. All displayed pay ranges are approximate, negotiable, and location dependent.This is Cellares Cellares is the first Integrated Development and Manufacturing Organization (IDMO) and takes an Industry 4.0 approach to mass manufacturing the living drugs of the 21st century. The company is both developing and operating integrated technologies for cell therapy manufacturing to accelerate access to life-saving cell therapies. The company's Cell Shuttle integrates all the technologies required for the entire manufacturing process in a flexible and high-throughput platform that delivers true walk-away, end-to-end automation. Cell Shuttles will be deployed in Cellares' Smart Factories around the world to meet total patient demand for cell therapies at global scale. Partnering with Cellares enables academics, biotechs, and pharma companies to accelerate drug development and scale out manufacturing, lower process failure rates, lower manufacturing costs, and meet global patient demand.The company is headquartered in South San Francisco, California with its commercial-scale IDMO Smart Factory in Bridgewater, New Jersey. The company is backed by world-class investors and has raised over $355 million in financing. Leveling will be based on overall experience, education, and demonstration of knowledge throughout the interview process. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Job DescriptionSalary: $17.00 - $25.00/hour or commensurate with experience LifeLens Technologies, Inc. is a medical device developer located in beautiful Bucks County, PA. We are pioneering innovative, next-generation treatment devices for personal health monitoring. We are hiring a Quality Control (QC) Technician. In this role, you are responsible for the testing and evaluation of finished devices, printed circuit board assemblies (PCBAs), mechanical and electronic sub-assemblies. Duties will also include reviewing electronic and paper records associated with the processing, inspection, and testing of finished devices and executing Quality Assurance release of product that conforms to specified requirements including Good Documentation Practices (GDP). You play an essential role in product testing, acceptance, and defect tracking. This is a full-time, on-site position. Responsibilities: Conduct quality inspections and testing throughout the production process, including incoming, in process and final inspections. Inspect PCBAs for defects, including solder quality and visual damage. Confirm all documentation including production and quality records supporting product release fully adheres to acceptance criteria and good Documentation Practices (GDP) including data integrity. Escalate any discrepancies immediately. Maintain, monitor, and manage the batch record management system, including closure and disposition, data collection, and archiving of the records. Log data from batch records into the quality metrics database. Generate reports on manufacturing yields and defects for management and engineering staff. Education and Training: Associates degree in a science or technical field, or HS diploma with applicable work experience. Direct experience and knowledge of Good Documentation Practices (GDP) Knowledge of quality management systems and regulatory compliance requirements FDA Quality System Regulation ISO 13485 is preferred. Strong organizational and attention to detail skills. Experience: Minimum of 2 years of experience in a QA or QC role in medical device manufacturing or related industry. Manufacturing Quality Record review experience is strongly preferred. Experience using a variety of measurement tools, including multimeters, calipers and micrometers. Experience with PCB assembly and/ or electronics manufacturing Proficient in Microsoft Office Suite (Word, Excel, PowerPoint). Excellent communication and interpersonal skills. Ability to work independently and manage multiple priorities Physical Demands: Able to use standard office equipment (computer, mouse, keyboard, printer, etc.) Specific vision abilities required by this job include close vision, color vision, peripheral vision, depth perception, and the ability to adjust and focus. Must be able to lift 30 lbs. Benefits: Health Insurance Dental & Vision Insurance Stock Options Paid Time Off Flextime

Product chemistry Development Tech needs 3 years or more related experience in the Rubber, Plastics Compounding or Coatings Industry Product chemistry Development Tech requires: Bachelors degree (B.A.) in a Chemistry related or Material Science field from a four-year college or university with 3 years or more related experience in the Rubber, Plastics Compounding or Coatings Industry; or Associates Degree (A.A.) in Chemistry related or Material Science field with five or more years related experience and / or extensive training in the Rubber, Plastics Compounding or Coatings Industry; or equivalent combination of education and experience. Product chemistry Development Tech duties: Work with multiple chemistry adhesive type products Develop tests and reports on formulations Independently works to perform tests needed per product. Performs gauge R&R on batches produced in lab Executes lab testing and generates test data and documentation necessary Ensures SHE and compliance is met with lab safety and hygiene Communicate with various internal functions Comfortable lifting items and utilizing equipment for lab procedures.

Summary of Quality Control Technician - Precision Machining Inspector DAY SHIFT - MONDAY-THURSDAY 7:00am-4:30pm; Friday 7:00am-11am (estimated) We are seeking a detail / results oriented, Quality Control Technician for our plant in South Eastern Pennsylvania. We have been in business for more than 75 years and are considered a leader in our industry, making precision machined parts for a variety of OEM's. Family oriented culture with focus on Integrity, Accountability and Responsibility. What we do matters! The Quality Control Technician will monitor the quality of incoming and outgoing products or materials. Also, the position requires inspecting parts, analyzing measurements, and overseeing the capability of the production processes which must meet the dimensional specifications of the mechanical engineering drawing. Final and lot inspections are also critical aspects of this role which will be performed as required. Duties Include: Approve incoming materials by confirming specifications, conducting a visual and measurement test, and rejecting and returning unacceptable materials Approve in-process production by confirming required specifications, conducting visual and measurement tests, and communicating the required adjustments. Approve all finished products by confirming specifications and conducting required tests Return products for re-work if needed and complete documentation to confirm re-work Document and update inspection results by completing reports and logs Keep measurement equipment operating by following operating instructions, calling for repairs, and keeping gages calibrated. Roving manufacturing audits for part and systems compliance Approve first piece inspections using any combination of manual or advanced equipment and methods. Requirements include: Prefer a working knowledge of measuring equipment including CMM, Optical Comparator, Vision Systems, Non-Contact Measuring systems, Micrometers, Calipers, and all other handheld measuring tools. Effective communication skills. Detail oriented team player Strong blueprint reading skills. Familiarity with Geometric Dimensioning & Tolerancing. First Article inspections; Capability Studies. Developing and maintaining inspection reports. High School diploma or equivalent. 3+ year's experience in a fast paced precision machining environment Skills, Knowledge and Abilities Gage R & R studies. Inspection & Quality Planning. Ability to complete product layouts from blueprints. Material & Process Certifications and Test Report Verifications. Proficient in Microsoft Word & Excel and Quality software. Knowledgeable performing first piece, final inspection, in process and receiving inspection. Calibration of measuring instruments a plus. Operation of CMM and OGP vison system (or equivalent) a plus. SPC and Control / Run / Trend Analysis & Charting. Process / Equipment capability studies. Previous Aerospace Manufacturing Quality experience a plus. Background in ISO9001 and AS9100 a plus a plus. Lean Manufacturing experience & knowledge. Six Sigma Green Belt or equivalent knowledge a plus. FULL COMPREHENSIVE BENEFITS OFFERED SALARY TO COMMENSURATE WITH EXPERIENCE Must be a US citizen and be able to own a firearm due to ITAR and FFL requirements.

What we are looking for: The Quality Control Technician conducts inspection and testing activities at various manufacturing states including incoming, in process, and final release. 2nd Shift: Monday-Friday 3:00pm-11:00pm What you will do: Performs first article, in process, and final release testing for raw materials, as well as textile-based products. Utilizes a variety of testing equipment, including tensile testing machines, microscopes, and vision systems. Records and communicates test results manually and/or electronically. Inspects product for defects and contamination, according to Work Instructions (WI), Visual Inspection Criteria, SOP's, and internal specifications. Conducts extensive data collection to support the identification of trends to increase yields through process improvement. Enters visual inspections results as well as physical testing results into the applicable tracking databases. Packages and labels components in preparation for release. Generates certification documentation to accompany shipments. Enters information and uses ERP system to report quantities. Other duties as assigned Who you are: High School diploma or equivalent required. 0-1-year related experience preferred. Strong attention to detail. Intermediate computer skills. Proficiency in MS Word and MS Excel. Basic understanding of GMP and working within regulated industries. Demonstrated ability to communicate effectively with peers and management. Ability to multi-task change direction with shifting priorities. What we offer: Paid Breaks Generous Paid Time off and Holiday Pay Annual Bonuses Health Insurance: Medical with Rx plan / Dental / Vision 401k (retirement savings) with excellent company match Company Paid Short-Term and Long-Term Disability

What we are looking for: The Quality Control Technician conducts inspection and testing activities at various manufacturing states including incoming, in process, and final release. 2nd Shift: Monday-Friday 3:00pm-11:00pm What you will do: Performs first article, in process, and final release testing for raw materials, as well as textile-based products. Utilizes a variety of testing equipment, including tensile testing machines, microscopes, and vision systems. Records and communicates test results manually and/or electronically. Inspects product for defects and contamination, according to Work Instructions (WI), Visual Inspection Criteria, SOP's, and internal specifications. Conducts extensive data collection to support the identification of trends to increase yields through process improvement. Enters visual inspections results as well as physical testing results into the applicable tracking databases. Packages and labels components in preparation for release. Generates certification documentation to accompany shipments. Enters information and uses ERP system to report quantities. Other duties as assigned Who you are: High School diploma or equivalent required. 0-1-year related experience preferred. Strong attention to detail. Intermediate computer skills. Proficiency in MS Word and MS Excel. Basic understanding of GMP and working within regulated industries. Demonstrated ability to communicate effectively with peers and management. Ability to multi-task change direction with shifting priorities. What we offer: Paid Breaks Generous Paid Time off and Holiday Pay Annual Bonuses Health Insurance: Medical with Rx plan / Dental / Vision 401k (retirement savings) with excellent company match Company Paid Short-Term and Long-Term Disability

SUMMARY: This position is primarily responsible for maintaining all instruments, standards, and other necessary analytical items and to accurately analyze and report results for incoming raw material, in process and final product as required by EFC's quality system. DUTIES AND RESPONSIBILITIES: • Ensures all analytical instrumentation is maintained in qualified and operational condition at all times, reporting and exceptions to the Lab Supervisor. • Completes all preventive and corrective maintenance and calibration activities in a timely and accurate manner. • Ensures laboratory standards, reagents, consumables and other supplies are maintained in stock or are available to support quality control activities. • Performs analysis for incoming raw material, in process and final product as required by EFC's quality system. • Prepares and maintains analytical documentation on all conducted analyses as required by EFC's quality system. • Completes all analytical or other tasks required by EFC's quality, SHE, or other systems as assigned. • Attends training to develop relevant knowledge and skills. • Performs other related duties as assigned or needed. SUPERVISORY RESPONSIBILITIES: • This job has no supervisory responsibilities. QUALIFICATIONS: • High school diploma or general education degree (GED); or 1-3 years of related experience and/or training, or equivalent combination of education and experience. • Computer skills required: Microsoft Office Suite; ERP system. COMPETENCIES: • Diversity - Demonstrates knowledge of EEO policy; Shows respect and sensitivity for cultural differences; Educates others on the value of diversity; Promotes a harassment-free environment; Builds a diverse workforce. • Ethics - Treats people with respect; Keeps commitments; Inspires the trust of others; Works with integrity and ethically; Upholds organizational values. • Analytical - Synthesizes complex or diverse information; Collects and researches data; Uses intuition and experience to complement data; Designs work flows and procedures. • Change Management - Develops workable implementation plans; Communicates changes effectively; Builds commitment and overcomes resistance; Prepares and supports those affected by change; Monitors transition and evaluates results • Customer Service - Manages difficult or emotional customer situations; Responds promptly to customer needs; Solicits customer feedback to improve service; Responds to requests for service and assistance; Meets commitments. • Innovation - Displays original thinking and creativity; Meets challenges with resourcefulness; Generates suggestions for improving work; Develops innovative approaches and ideas; Presents ideas and information in a manner that gets others' attention. • Problem Solving - Identifies and resolves problems in a timely manner; Gathers and analyzes information skillfully; Develops alternative solutions; Works well in group problem solving situations; Uses reason even when dealing with emotional topics. • Professionalism - Approaches others in a tactful manner; Reacts well under pressure; Treats others with respect and consideration regardless of their status or position; Accepts responsibility for own actions; Follows through on commitments. • Quality - Demonstrates accuracy and thoroughness; Looks for ways to improve and promote quality; Applies feedback to improve performance; Monitors own work to ensure quality. • Attendance/Punctuality - Is consistently at work and on time; Ensures work responsibilities are covered when absent; Arrives at meetings and appointments on time; necessary to reach goals; Completes tasks on time or notifies appropriate person with an alternate plan. • Oral Communication - Speaks clearly and persuasively in positive or negative situations; Listens and gets clarification; Responds well to questions; Demonstrates group presentation skills; Participates in meetings. • Safety and Security - Observes safety and security procedures; Determines appropriate action beyond guidelines; Reports potentially unsafe conditions; Uses equipment and materials properly. • Technical Skills - Assesses own strengths and weaknesses; Pursues training and development opportunities; Strives to continuously build knowledge and skills; Shares expertise with others. • Written Communication - Writes clearly and informatively; Edits work for spelling and grammar; Varies writing style to meet needs; Presents numerical data effectively; Able to read and interpret written information. PHYSICAL DEMANDS AND WORK ENVIRONMENT: • Continually required to stand, walk, utilize hand and finger dexterity. • Occasionally required to climb, balance, bend, stoop, kneel or crawl, sit, talk or hear. • Continually work near moving mechanical parts. • Frequently work around fumes, airborne particles, or toxic chemicals. • Occasionally exposure to outside weather conditions. • While performing the duties of this job, the noise level in the work environment is usually moderate. • The employee must frequently lift and/or move up to 100 pounds. The above is intended to describe the general content of and requirements for the performance of this job. It is not to be construed as an exhaustive statement of duties, responsibilities or physical requirements. Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Job description: QC Inspector Trainee (Manufacturing) Phillipsburg, NJ Pay: $17-$20 per hour Schedule: Monday-Friday, 7:30 AM - 4:30 PM Type: Temp-to-Hire We're seeking a Quality Control Inspector Trainee to join our client's manufacturing team in Phillipsburg, NJ. A quality control (QC) inspector ensures products and processes meet established standards by inspecting materials, conducting tests, and documenting any defects. They use tools like micrometers and other instruments, analyze data, identify trends, and collaborate with production teams to implement corrective actions and improve overall quality. Their role is crucial for maintaining product consistency, ensuring safety, complying with regulations, and customer's specifications. Responsibilities: Conduct visual inspections and measurements on raw materials and finished goods to identify defects or deviations from standards. Documentation & Reporting: Record inspection results, document any non-conformities or defects, and assist in entering results into the computer system. Tool & Equipment Management: Operate and maintain testing equipment and instruments, ensuring their accuracy and reliability for consistent results. Skills and Qualifications Attention to Detail: A keen eye for identifying small flaws and discrepancies in products and processes. Analytical & Problem-Solving Skills: The ability to interpret data and validate test method procedures. Technical Knowledge: Understanding of measurement tools like calipers, gauges, and micrometers, preferred but training will be provided Organizational Skills: Necessary for managing tasks, prioritizing, and maintaining an orderly workspace. Physical Stamina: The job involves standing for long periods, lifting heavy objects (up to 60 lbs.) with team lift and moving materials. Basic Math Skills: Required for tasks such as counting, weighing, and measuring goods. Computer Literacy: Proficiency in using computers is preferred but training will be provided. Communication Skills: Ability to communicate effectively and professionally with other plant employees as well as vendors when needed. Why Join Temp-to-hire opportunity with a stable, growing manufacturing company. Full-time, consistent schedule. Weekly pay through OneSource Staffing. Supportive team environment with room to grow. How to Apply Apply today to join a growing and stable manufacturing team! Submit your resume to onesourcestaffing.com or Call OneSource Staffing - Easton Office at 610-750-9198 for immediate consideration. Benefits: Dental insurance Health insurance Vision insurance

Job Details Division: Nucor Rebar Fabrication Northeast Other Available Locations: N/A Welcome to Nucor, where our unique culture sets us apart. Joining Nucor means becoming part of North America's largest steel and steel products manufacturer, offering unmatched career opportunities and stability. We are known for our innovative sustainability practices and are the continent's largest recycler. Our vibrant culture, built on personal connections and teamwork, empowers every team member with the freedom to innovate and contribute to our collective success. Experience a workplace where safety, efficiency, and meaningful personal connections define every day, enriching both our teammates and the communities we serve. Nucor supports its teammates with top-tier benefits like Medical, Dental, Vision, and Disability Insurance, 401K and Roth accounts, Profit sharing, Pay-for-performance bonuses, Paid parental leave, Tuition reimbursement, Stock program, Scholarships and more. Basic Job Functions: * Must adhere to Nucor's safety programs and standards. * Demonstrate conduct consistent with Nucor's vision and values. * Perform and document all tests required (per the Quality Manual) during a production shift. * Participate in non-conformance root cause analysis. * Report and document any non-conformance to the Quality Manual requirements. * Report and document any non-conformance to tests performed. * Perform other tasks and duties as assigned Safety is the most important part of all jobs within Nucor; therefore, candidates must be able to demonstrate the ability to initiate, lead, and uphold safety policies, practices, procedures, and housekeeping standards at all times.Minimum Requirements: * Legally authorized to work in the United States without company sponsorship now or in the future. * High school diploma, GED or state/local equivalent Preferences: * Knowledge of CRSI quality standards * Proficiency in MS Office, including strong Excel and Word.Physical Demands: * Some heavy lifting may be necessary * Working conditions can be noisy, dusty, hot, cold Special Demands: * Must be able to work overtime when required * Some travel may be required * Must be able to work any shift * Must be familiar with and adhere to shop safety policies and procedures * Communication with various DOT customers * Communication with CRSI * Maintain and update CRIS QM as needed * Maintain DOT certifications with all states as needed * Understanding of ASTM coating and fabrication standards Nucor is an Equal Opportunity/Affirmative Action Employer - M/F/Disabled/Vets - and a drug - free workplace

Needs to make sure that products being produced meet the expectations of the consumer. They examine jobs to make sure they meet quality expectations then assess the final product after production. Their role is to establish an acceptable variation range for jobs and identify when something fails to meet those requirements. Responsible for monitoring and ensuring that each stage of production is followed by all the necessary procedures and each product coming out of the production process. Document the results of their inspections and make recommendations on how to prevent common errors. Responsible for ensuring the quality control of all printing and sign products as well as packaging and shipment/delivery of all products. Responsible for checking in all vended products and ensuring they are ready for delivery or shipment. Duties and Responsibilities ● Must have attention to detail on quality and packaging for all outgoing shipments. ● Must be very organized while maintaining the ability to multitask. ● Coordinate with shipping companies like FedEx, UPS and others and ensure timely delivery. ● Work effectively with the center manager and sales team for quality delivery and escalations. ● The job requires repetitive lifting of sometimes heavy boxes. ● Must be a team player, dependable and have a good work ethic. ● Good written and verbal communication skills ● Excellent problem-solving and analytical skills ● Keen attention to detail ● Basic computer and math skills to calibrate and measure specifications ● Ability to use measuring devices like scales and tape measures ● In-depth understanding of company standards ● Understanding of target market and consumer needs ● Documentation and reporting skills ● Teamwork and collaboration ● Comfortable standing or walking for long periods of time Some cross training into bindery or other areas of the company will be required at times if another teammate is out. Experience Entry Level Job Full time Print Smith, Shipleap and Microsoft Office knowledge is a huge plus. Compensation: $15.00 per hour At AlphaGraphics, we offer careers for everyone! Whether you are just starting out, looking for that next great growth opportunity, or seeking a change, we have exciting roles to suit you. We pride ourselves on our training programs in management, sales, operations, print, signs, design, and marketing. Join us with or without experience, and we will succeed together as a team! We invite EVERYONE to apply! *AlphaGraphics centers (locations) are independently owned and operated. The posted positions are offered by individual franchisees who interview, hire, manage and pay the employees hired for positions in a specific local location (center) through their specific business.

The employee is responsible for all quality control activity on their assigned line on the production floor. They are responsible for using only the equipment that is assigned to them, along with complying with all departmental safety requirements. Job Functions Check daily schedules to assure that no changes have taken place Read all work order information prior to start up Match all component numbers to work order making sure they match Review all printed material for accuracy and appropriateness for use Match batch approval to work order signing if information is correct Take temperature of product and record on the QC worksheet. Inspect all codes on lines, jars, bottles, labels, folding cartons, packers, and shippers. Any mechanical problems found at this time should be conveyed to the mechanic and line leader. All issues concerning paperwork, components or batching will be reported to the Lead. Make sure all information is correct and sign the paperwork. If the information is not correct call the Lead Attach any reject reports to the work order and wrap with special marking instruction tape to identify the rejected item Rejected items are to be placed on a skid at the end or beginning of the line Requirements To perform this position, the employee must be able to read and write English, do mathematical calculations, and read measuring equipment Must be able to work under pressure and meet deadlines, while maintaining a positive attitude and providing exemplary customer service Ability to work independently and to carry out assignments to completion within parameters of instructions given, prescribed routines, and standard accepted practices Must be able to work overtime as needed Employee is required to pass a drug and/or alcohol test While performing the job the employee must be able to sit, push/pull, climb, stoop/crouch, crawl/kneel, twist, balance and reach occasionally during shift While performing the job the employee must be able to lift and carry 25 to 50 lbs occasionally during shift

Job Title: Quality Technician Department: Quality Department Job Function: Quality Control, Calibration, Auditing FLSA Status: Salaried Non-Exempt Reports To: Director of Quality Schedule: 1 st Shift SUMMARY The Quality Technician is responsible for driving quality system excellence and ISO 9001 compliance at the Pennsylvania facility while supporting corporate-wide quality initiatives. This role leads internal audits across all locations, manages RMA and calibration programs for the PA site, supports NSF certification processes, and performs investigations into incoming and in-process quality issues. This position collaborates cross functionally to improve quality performance, maintain regulatory compliance, and support data-driven decision-making across production, supplier management, and customer feedback. ESSENTIAL DUTIES AND RESPONSIBILITIES Serve as primary ISO 9001 internal audit lead for all facilities and supports the Director of Quality for the yearly registrar audit. Maintain and improve QMS documentation, procedures, and records for the PA facility. Coordinate NSF audit preparation and ongoing certification maintenance. Support customer, regulatory, and 3rd-party audits. XRF inspection of incoming brass to confirm lead-free. Issue certifications to customers for country of origin, Prop 65, AIS, etc. Lead corrective action (CAPA) activity for PA facility and support corporate CAPAs. Oversee supplier corrective actions and validate results as necessary. Manage and process RMA activity; coordinate disposition and root-cause actions. Support production operations regarding any quality issues and identify potential issues for preventative actions. Manages the calibration program for PA facility and coordinates external calibration vendors. Support containment, root cause analysis, and verification of effectiveness for corrective actions. Identify and drive improvements in inspection, audit, and documentation processes. Support continuous improvement initiatives. Assist with the maintenance of training records for the PA facility. Manages the shelf-life program for the facility. Process non-conformance reports. SUPERVISORY RESPONSIBILITIES This position has no direct reports but may direct daily activities for both support and production personnel, or for trainees under the guidance of Management. TRAVEL Occasional travel may be required (less than 10%) for training, supplier visits, or off-site calibration/lab support. QUALIFICATIONS REQUIRED High school diploma or GED required; Associate degree in a technical discipline or formal metrology training preferred (GD&T). 3+ years manufacturing quality or QMS administrator/auditor experience. Knowledge of ISO 9001 standards and internal auditing methodology. Experience with nonconformance investigations and corrective actions. Strong proficiency with MS Office and ERP-based quality workflows. Excellent communication and documentation skills. PREFERRED Calibration program oversight experience. NSF or third-party compliance experience. Familiarity with machining environments print reading. Root cause and problem-solving methodology training (8D, A3, PDCA, etc.). ASQ Certification (CQE, CQT, or CQA) a plus. PHYSICAL DEMANDS Frequent standing, walking, and manual handling of parts and gaging equipment. Occasional lifting of materials up to 30 pounds. While performing the duties of this job, the employee is regularly required to sit and talk or hear. The employee frequently is required to walk. The employee is occasionally required to stand. Specific vision abilities required by this job include close vision, depth perception, and ability to adjust focus. WORK ENVIRONMENT Must adhere to safety protocols and maintain a clean, organized work area. The noise level in the work environment is usually moderate, but at times very loud.