Quality control inspector jobs in Easton, PA

Quality Control Technician - Ingredients Bethlehem, PA The quality control technician is responsible for ensuring Newly Weds Foods standards of quality and safety on all ingredients and finished products. Essential Functions: * Sampling and approving of all incoming ingredients. * Articulate and well-maintained records are necessary. * Flexibility and cooperativeness are essential. * Evaluates finished products for quality and acceptability. Performs all necessary analysis as required, and according to the product specification. * Communicates product quality issues to Production, Supervisors, Production Manager, QC Manager and Supervisor and shipping and customer service staff. * Logs all analysis test results and batch information in the I-Series (AS400) and maintains analysis records and documents necessary for documentation compliance. * Monitors line equipment for functionality, safety, and cleanliness. * Check metal detectors (CCP), magnets, scales and performs critical control point & GMP audits. * Assist in all foreign material and product non-conformance investigations. * Performs batch set-up checks, assists in correction the set ups, and logs discrepancies. * Places product on hold as necessary and release when appropriate. * Rejects product as necessary and completes rejection forms including root cause and correction action analysis. * Checks allergens clean out effectiveness as needed. * Perform Pre-Op audit when necessary (example: equipment down for maintenance). * Perform production scale checks and lab equipment calibration based on calibration schedule. * Collect micro samples as needed and places micro hold products on hold. * Performs special task as assigned by QC manager. * Maintains retain sample area and control sample file. * Follows all GMP's and Safety Procedures. Qualifications: * High school or GED with 1-2 years related work experience. * Ability to use quality control analysis equipment. * Fluency in spoken and written English. * Mathematical Skills * Computer skills and data processing skills required. * Ability to climb ladders to work platforms. * Able to lift 50 pounds.

Inspects in process and finished products for conformance to specifications using fixed or preset measuring instruments. Checks for irregularities and ensures products conform with established tolerance levels for quality and performance. Documents all instances of non-conformance and rejected products in production reports. Prepares required inspection certifications. REPORTING TO Quality Manager ESSENTIAL JOB FUNCTIONS Inspect in process and finished product as required by established procedures. Accurately document the results of inspection and testing results. Perform careful inspections and enforcements of Quality Standards. Maintain all controlled document files of the inspections and testing results. Document and report product or service quality levels. Collaborate with Quality Team Members to solve problems. Maintain records of measuring devices to ensure compliance to standards of QAP, AS9100 and ISO9001. Evaluate problems and make recommendations for possible corrective actions. Monitor critical equipment and instrumentation to ensure proper operation. SKILLS and ABILITIES Good written and verbal communication skills. Knowledge of ISO9001 and AS9100 management systems. Ability to read blueprints and understand GD&T. Working knowledge of measurement instruments. Knowledge of Microsoft Office applications. Strong attention to detail and the ability to follow verbal and written communications. EDUCATION and EXPERIENCE High school diploma or GED equivalent required. Minimum 1 year experience working with quality hand tools, such as calipers, micrometers, gages, etc. Ability to lift to 20 pounds. Vision and depth perception suitable for use of inspection equipment. EEOC Statement: MW Industries, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

PennPak Solutions, in Bethlehem, PA. is seeking a dynamic and self-motived Quality Technician to join our team. This individual will provide Quality oversight during production and have the ability to fill in, as needed, when manufacturing is down. The ideal candidate shall have prior experience in food manufacturing and have flexibility to accommodate the needs associated with an entrepreneurial business start-up. Responsibilities and Expectations Key Responsibilities: Manage, approve, or reject all raw materials, packaging materials, labeling and finished products. Monitor the facility, personnel, and visitors for adherence to GMPs. Perform Pre-Operational Inspections per the stated frequencies. Perform monitoring and verification activities related to food safety and food quality. Activities may include but are not limited to analytical product testing, packaging attribute and weight assessments, label review, food safety verification, sanitation and environmental swabbing, etc. Ensure adherence to Food Safety and HACCP critical control points and preventive controls. Lead and manage investigations and corrective actions as appropriate. Review all production records for legibility, accuracy, and completeness. Oversee document control within production/quality records to ensure the latest revision of procedures are being used at all times. Assist with cleaning duties as assigned. The team member will be responsible for their immediate area during standard production and will be assisting with equipment and facility cleaning as needed and directed during down periods. Engage in learning and working in other areas of production as needed. Other duties as assigned by the QA Manager. All other duties assigned as needed. Qualifications: Proficiency with data entry and basic computer skills required. Must be able to lift at least 35lbs. Ability to reach, pull, push, stop and bend frequently. Ability to stand for approximately 80% of 12-hour shift. Must be able to problem solve, show a high attention to detail and be very self-motivated. Excellent verbal, written, and interpersonal skills. High school diploma or equivalent GED certificate Experience in food manufacturing facility preferred. Experience in record keeping, data entry and stock management is a plus. Work Environment: This position may require working overtime or weekends to meet business needs. This position is on the manufacturing floor almost constantly. Exposure to allergens such as milk, eggs, fish, crustacean shellfish, tree nuts, peanuts, wheat, sesame, and soybeans is likely.

Medical Device QC Inspector Your responsibilities The QC Inspector will be responsible for performing inspection on medical devices to specified requirements to determine product disposition. Will operate in accordance with company procedures, FDA Regulations, ISO 13485 and Canadian Medical Device Regulations, and other applicable requirements. Responsibilities: Essential Duties · Perform mechanical, visual, packaging and document Inspection of orthopedic medical devices · Complete all required documentation of the inspection results, on handwritten forms, and electronic spreadsheets or databases, in accordance with company procedures and work instructions. · Identify and document potentially non-conforming product. · Ensure non-conforming product is properly segregated and quarantined. · Interface with other departments, to address and resolve any product related issues. · Assist with labeling of product and label reconciliation. · Perform line clearance to ensure that product integrity is maintained. · Read, understand, and follow company procedures and policies. Skills and Qualifications: · Educational Requirements: High school diploma/GED (Required) o Associate's Degree (Desired) · Working knowledge of use of various gauges such as calipers, micrometers, thread gauges, etc. · Knowledge of quality practices, FDA Regulations and ISO 13485. · Knowledgeable of inspection techniques. · Basic understand of reading engineering drawings. · Good verbal and written communication skills. · Strong attention to detail and accurate record keeping. · Basic computer skills including a word processing, and spreadsheet, etc. · Must be flexible and able to adapt to changes in priorities. · Must be able to occasionally lift up to 25 lbs.

Quality Control Inspector Opportunity - Macungie, PA HTSS is seeking a highly meticulous Quality Control Inspector to join a respected electronics manufacturer in the Macungie area. This role is essential for ensuring the quality and reliability of electro-mechanical and printed circuit board PCB assemblies, offering a strong Temp-to-Hire path. Compensation and Schedule Location: Macungie, PA Schedule: Monday-Friday, 7:30AM - 4PM Pay Rate: $19/hour Type: Temp-to-Hire Core Responsibilities As the QC Inspector, you will act as the final check on product quality: Inspection: Inspect components and assemblies, verifying dimensions using precision measuring tools (e.g., calipers, micrometers). Testing: Conduct functional tests on final assemblies according to established procedures, utilizing test equipment. Documentation: Accurately document all inspection results, track defects, and maintain quality records. Quality Assurance: Collaborate with production to resolve quality issues, suggest corrective actions, and ensure adherence to all quality system processes. Support: Assist with inventory processes, ERP data scanning, and participate in rework/repair of defective assemblies, which may include light soldering. Candidate Profile and Requirements We are seeking a detail-focused professional prepared for a fast-paced environment: Required Experience: Previous experience in a Quality Control or similar inspection role is mandatory. Visual Acuity: Strong attention to detail and excellent visual acuity, including accurate color identification. Technical Skills: Able to read and interpret blueprints, schematics, and technical drawings. Proficient with measuring instruments and Microsoft Office (Word, Excel). Physical: Comfortable sitting or standing throughout the shift and lifting up to 30lbs. Preferred: Prior experience in electronics manufacturing, familiarity with IPC-A-610 standards, and soldering experience are a definite plus. Apply Today If you are ready to apply your inspection expertise to a rewarding role, we want to hear from you. Text "QC Inspector" to ************ to apply!

EPTAM Precision Molding is looking for a Quality Inspector - 2nd Shift to join our team in Phillipsburg, NJ . Join us as we create medical devices that support our OEM partners in creating life-saving parts and positive outcomes for their patients. EPTAM Precision Molding, in Phillipsburg New Jersey , hosts a tightly controlled facility with ISO Class 7 and 8 cleanrooms. Our commitment to exceptional service is reflected in our continuous investment in operational upgrades and the utilization of advanced Toyo and Arburg molding machines. We take great pride in our ISO 13485:2016 and ISO 9001:2015 certifications. EPTAM Solutions , our parent company with locations nationwide, is at the Heart of Manufacturing. We recognize that our parts touch lives, and our teams assume this responsibility with vigor. Our minds never sleep. Join our incredible team at any one of our locations and reap the benefits of an employee-focused company. We excel at what we do for our customers, our employees, and the world. Benefits Include: Professional Development/On the Job Training Health and Wellness Benefits Clean, Friendly, Safe work Environment Recognition and Rewards Program Tuition Re-imbursement Competitive Pay/Merit Increases 401k w/ Company Match Employee Assistance Program (EAP) SCHEDULE: 2nd Shift Monday through Friday 4:00pm to 12:30am In addition to the noted Pay range, there is also an additional 10% Shift differential for those on the 2nd Shift POSITION SUMMARY: Monitor, measure, test, and record data to determine if product meets customer's specifications. Responsible for all incoming, start-up, in-process, and final inspections to ensure product meets specifications including required documentation. Work with production personnel to resolve quality discrepancies and ensure acceptable product. ESSENTIAL FUNCTIONS: Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Utilizes engineering drawings, gauges, comparator, vision system, microscopes, templates, and other inspection equipment/aids to ensure all product meets the customer specifications. Ensures that all required process operations have been performed on the product. Records all quality data and notes into the appropriate electronic or manual systems. Good documentation, record keeping, and communication is required for all personnel. Notifies the appropriate personnel if product defects and/or process problems are identified or if product rejects exceed acceptable levels. Provides timely feedback to manufacturing if non-conforming product is identified. Works closely with and monitors machine/lead operators to ensure product meets quality criteria. Determines and answers questions as to product acceptability. Must be able to relate to other employees beyond giving and receiving instructions. Can get along with co-workers or peers and respond appropriately to feedback in a professional manner. Sorts and Reworks: Sorting and/or reworking product that does not conform to the customer requirements. Properly documents and labels to identify the status of non-conforming product. Sampling and gaging of reject product may also be required. Responsible for keeping areas neat and clean, follow restriction/rules of fire protection, safety, and environmental issues. Follow specifications and procedures for manufacturing, i.e., process sheets, work orders and any other special instructions. Proper handling of all material, parts, and equipment to prevent damage and loss of finished product. MINIMUM JOB QUALIFICATIONS REQUIRED: Education: High School diploma, equivalent or trade school graduate and/or minimum experience. Experience: 2 years of experience within a Quality related environment. LICENSES, CERTIFICATIONS AND/OR REGISTRATIONS: None OTHER MINIMUM QUALIFICATIONS: Must possess good written and verbal communication skills with our internal and external customers. Basic knowledge of equipment. Basic ability to read prints and use measuring equipment along with basic math skills. ADP1414 2X9-251023-446 SCHEDULE: 2nd Shift Monday through Friday 4:00pm to 12:30am In addition to the noted Pay range, there is also an additional 10% Shift differential for those on the 2nd Shift

What we are looking for: The Quality Inspector / Medical Component Finishing (MCF) Operator performs a variety of different functions in support of preparing medical components for final inspection and packaging. The MCF Operator can be assigned duties such as scouring, heating setting, laser cutting, measuring, cutting and/or inspecting. This position may focus on one area of the MCF department or be crossed trained in more than one functional area. Inspection and testing may be performed on braids, yarns, fabrics for commercial and or R & D products. Shift: Monday-Friday 3:00pm-11:00pm with training on 1st shift Monday - Friday 7:00am - 3:00pm for approximately 1 months. What you'll do: Inspects and measures product, either visually or through microscopes, to measure and record fabric characterization such as Ends per Inch (EPI), Pics per Inch (PPI), Courses per Inch (CPI), width, diameter, thickness, etc. Inspects product for defects and contamination, according to Work Instructions (WI), Visual Inspection Criteria, SOP's, and internal specifications. Records and communicates test results manually and/or electronically. Conducts extensive data collection to support the identification of trends to increase yields through process improvement. Utilizes a variety of testing equipment including, but not limited to optical comparator, hot knife equipment, microscopes, and Scanning Electron Microscopy (SEM) technology. Packs product for transfer to final inspection and final packaging Who you are: High school graduate or equivalent. Minimum of 0-1 year related experience. Basic understanding of good manufacturing practices and working within regulated industries. Excellent interpersonal skills with proven ability to get along well with others and work in a team environment. Who we are: The Secant Group is an advanced technology biomaterials company headquartered in Telford, Pennsylvania, with manufacturing facilities in Quakertown and Perkasie, Pennsylvania. Secant provides innovative solutions through next-generation materials, structures, textile designs, and process technologies for the medical device, pharmaceutical, aerospace and energy markets.

What we are looking for: The Quality Inspector / Medical Component Finishing (MCF) Operator performs a variety of different functions in support of preparing medical components for final inspection and packaging. The MCF Operator can be assigned duties such as scouring, heating setting, laser cutting, measuring, cutting and/or inspecting. This position may focus on one area of the MCF department or be crossed trained in more than one functional area. Inspection and testing may be performed on braids, yarns, fabrics for commercial and or R & D products. Shift: Monday-Friday 3:00pm-11:00pm with training on 1st shift Monday - Friday 7:00am - 3:00pm for approximately 1 months. What you'll do: Inspects and measures product, either visually or through microscopes, to measure and record fabric characterization such as Ends per Inch (EPI), Pics per Inch (PPI), Courses per Inch (CPI), width, diameter, thickness, etc. Inspects product for defects and contamination, according to Work Instructions (WI), Visual Inspection Criteria, SOP's, and internal specifications. Records and communicates test results manually and/or electronically. Conducts extensive data collection to support the identification of trends to increase yields through process improvement. Utilizes a variety of testing equipment including, but not limited to optical comparator, hot knife equipment, microscopes, and Scanning Electron Microscopy (SEM) technology. Packs product for transfer to final inspection and final packaging Who you are: High school graduate or equivalent. Minimum of 0-1 year related experience. Basic understanding of good manufacturing practices and working within regulated industries. Excellent interpersonal skills with proven ability to get along well with others and work in a team environment. Who we are: The Secant Group is an advanced technology biomaterials company headquartered in Telford, Pennsylvania, with manufacturing facilities in Quakertown and Perkasie, Pennsylvania. Secant provides innovative solutions through next-generation materials, structures, textile designs, and process technologies for the medical device, pharmaceutical, aerospace and energy markets.

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

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

Quality Technician The role of the Quality Technician is to ensure GMP compliance throughout the execution of labeling, assembly, and packaging activities. The Quality Technician is responsible for supporting Operational activities that directly impact manufacturing. The primary activities include performing line clearance verifications, adjustment of AQL sampling quantities, completing real-time and end of batch review of documentation such as batch records and logbooks, and taking Finished Good and Special Request samples as required throughout the labeling, assembly, and packaging processes. ESSENTIAL DUTIES AND RESPONSIBILITIES: The following is a list of minimum responsibilities required of the Quality Technician position. Other duties may also be assigned. • Ensure all batch record documentation is accurate (lot numbers, expiration dates, items number and related data are consistent throughout the record; AQL Report is accurate), and complete. • Read and understand process steps within the batch record to ensure compliance during the packaging process. • Review batch records for any additional requests, memos, deviations, change controls, material request transfer forms, etc. and ensure appropriate actions are taken. • Ensure room/equipment cleaning logs have been completed as applicable. • Pull all Finished Good (Reference, Retain and Reserve) and special request samples as required in batch record and material request transfer forms • Support operations by completing line clearance verifications after room clean activities. • Responsible for notifying supervision if any abnormal occurrences are observed while performing job responsibilities. QUALIFICATIONS: To perform this job successfully, the candidate must be detailed oriented. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. • One (1) year of related pharmaceutical experience or training. • General knowledge of FDA regulations related to cGMPs is required. • General knowledge of quality control/assurance is required. • Strong written and verbal communication skills are required. • Strong foundation in basic mathematical skills (addition, subtraction, multiplication, and division) • Strong problem solving and critical thinking skills. • Strong organizational and planning skills are required. SUPERVISORY RESPONSIBILITIES: This position will have no supervisory responsibilities. PREFERRED / REQUIRED EDUCATION and/or EXPERIENCE: An associate or bachelor's degree is preferred 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 accommodation may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to sit, stand, walk and use hands to finger, handle, or feel. The employee is occasionally required to reach with hands and arms. The employee must occasionally lift and/or move up to 35 pounds. Specific vision abilities required by this job include close vision, and color vision. WORK ENVIRONMENT: The work environmental characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is normally exposed to moving mechanical parts. The noise level in the work environment is usually moderate. DISCLAIMER: This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities, and activities may change, or new ones may be assigned at any time with or without notice.

Line of Business: Asphalt About Us Heidelberg Materials is one of the world's largest suppliers of building materials. Heidelberg Materials North America operates over 450 locations across the U.S. and Canada with approximately 9,000 employees. What You'll Be Doing Conduct sampling and testing of hot mix asphalt to ensure compliance with specifications Maintain accurate records of test results and report deviations promptly Calibrate and operate testing equipment in accordance with quality standards Collaborate with production teams to identify and resolve quality issues Support continuous improvement initiatives related to asphalt quality and performance What Are We Looking For Demonstrated ability to follow testing procedures and interpret results accurately Strong attention to detail and commitment to quality assurance Effective communication skills and ability to work collaboratively across teams Familiarity with hot mix asphalt production and testing protocols Capability to work independently in a fast-paced, outdoor environment Conditions of Employment Successful candidate must submit to post-offer pre-employment physical examination, drug/alcohol screen, and background check Must meet company safety standards and comply with all regulatory requirements Work Environment Role operates primarily in environments where the conditions include moving mechanical equipment, inclement weather, heat, cold, humidity, and elevated noise level What We Offer $23-30 per hour 401(k) retirement savings plan with an automatic company contribution as well as matching contributions Highly competitive benefits programs, including: Medical, Dental, and Vision along with Prescription Drug Benefits Health Saving Savings Account (HSA), Health Reimbursement Account (HRA) and Flexible Spending Account (FSA) AD&D, Short- and Long-Term Disability Coverage as well as Basic Life Insurance Paid Bonding Leave, 10 days of Paid Vacation, 40 hours of Paid Sick Leave and 10 Paid Holidays Equal Opportunity Employer - Minority / Female / Veteran / Disabled

Job DescriptionNeeds 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.

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.

Department: Quality Assurance Reports To: Quality Assurance Manager Hours: Monday to Friday Dependent upon Shift Performs laboratory sampling, testing, and activities consistent with a viable quality assurance program. Activities to include but not limited to bacteriological, analytical, and organoleptic testing. Maintenance of recorded documentation for finished product, raw material, and packaging testing to follow finished product specifications, raw material specifications, and standard lab & quality procedures. Primary Responsibilities ● Monitor and maintain hold and release program ● Proper sampling and analytical techniques ● Complete, orderly, accurate and legible documentation ● Teamwork within quality department and other departments ● Identify & communicate potential problems related to quality & food safety ● Verifying Netweight ● Testing of all seasoning ● Returns SQF (Safe Quality Food) Compliance It is the responsibility of every employee to ensure that Ancient Crunch's food safety and quality management systems complies with food safety regulations and SQF compliance. In turn, our customers are assured that the product has been produced, processed, prepared, and handled according to the highest possible standards. All employees are required to comply and promote compliance with Ancient Crunch's food safety program and polices, including but not limited to: Hazard Prevention: Help to keep all work areas clean and free of unsafe obstacles. Educate: Educate yourself and others on the correct standard operating procedures for the task you are responsible for. Accountable: It's your responsibility to understand and comply with the Company's SQF policies and procedures. Report Food Safety Issues: It is your responsibility to communicate any food safety and quality problems to your supervisor to initiate action. Training: Attend all required training and pass all necessary knowledge or skill-based evaluations. Key Activities ● Sample Preparation & Testing Records Maintenance. ● Positive Release Program. ● Responsible for complying with all Safe Quality Food (SQF) polices/procedures and requirements for position. ● Monitor GMP's, sanitation procedures,and quality procedures as set forth by QA and/or supervisors in all areas of the plant. ● Maintain sanitary conditions, organize, monitor inventory of supplies and report equipment faults in the laboratory. ● Performs other duties as assigned by the QA Manager. Performance Metrics ● Attendance ● Prompt communication of hold information ● Primary responsibilities ● Company Values ● Project work Key External Interface Outside Vendors Key Internal Interface ● Quality Assurance Manager/Supervisor ● Warehouse Management ● Production Management ● Production/Maintenance personnel Skills Required ● Computer Skills (Databases, Excel, Word, etc) in order to prepare reports to communicate outcomes of quality activities ● Mathematical Skills ● Attention to Detail ● Strong Communication skills - Verbal and Written ● Data Collection and Analysis ● Problem Analysis and Problem Solving ● Quality Minded and Good Judgement ● Customer Service Oriented ● Team Oriented ● Ability to work independently ● Responsible for complying to all Safe Quality Food (SQF) polices/procedures and requirements for position. ● Responsible for following Safety (OSHA) regulations and procedures. ● Performs other duties as assigned by management. Necessary Experience ● 2 - 4 Years in the food Industry. ● High School education. ● Some Post High School education preferred but not required Absence of Supervisor In the absence of your direct supervisor it is your responsibility to refer to key personnel of equal status for any food safety issues. Please refer to the organization chart of responsibility or ask your Manager for further clarification. Job Type: Full-time Physical Demands AND WORK Environment The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the functions. While performing the duties of this position, the employee is regularly required to talk or hear. The employee frequently is required to use hands or fingers, handle or feel objects, tools, or controls. The employee is regularly required to stand; walk; sit; and reach with hands and arms. The employee must frequently lift and/or move up to 50 pounds. Specific vision abilities required by this position include close vision, distance vision, and the ability to adjust focus. The noise level in the work environment is usually low to moderate. NOTE This job description in no way states or implies that these are the only duties to be performed by the employee(s) incumbent in this position. Employees will be required to follow any other job-related instructions and to perform any other job-related duties requested by any person authorized to give instructions or assignments. All duties and responsibilities are essential functions and requirements and are subject to possible modification to reasonably accommodate individuals with disabilities. To perform this job successfully, the incumbents will possess the skills, aptitudes, and abilities to perform each duty proficiently. Some requirements may exclude individuals who pose a direct threat or significant risk to the health or safety of themselves or others. The requirements listed in this document are the minimum levels of knowledge, skills, or abilities. This document does not create an employment contract, implied or otherwise, other than an at will relationship. The company is an Equal Opportunity Employer, drug free workplace, and complies with ADA regulations as applicable.

Manufacturing Quality Inspector BH Job ID: 3365 SF Job Req ID: 15972 Ingersoll Rand is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, color, family or medical care leave, gender identity or expression, genetic information, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran status, race, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by applicable laws, regulations and ordinances. Job Title: Manufacturing Quality Inspector Location: Ivyland, PA (Milton Roy - 201 Ivyland Rd. Warminster, PA 18974) Shift: 1st Shift Mon - Fri (7am - 330pm) About Us: Imagine a company with technology leadership of over 160 years, yet it operates with the energy of a startup. Ingersoll Rand has dedicated itself to Making Life Better for its employees, customers, shareholders, and planets. We produce innovative and mission-critical flow creation and life science technologies - from compressors to precision handling of liquids, gasses, and powers - to increase industrial productivity, efficiency, and sustainability. Supported by over 80+ brands, our products are used in various end-markets including life sciences, food and beverage, clean energy, industrial manufacturing, infrastructure, and more. Across the globe, we're driving growth with an entrepreneurial spirit and ownership mindset. Learn more at irco.com and join us to own your future. Job Overview: We are currently seeking a reliable and knowledgeable individual to join our Quality team. This role will be responsible for inspecting materials and products, providing quality support through knowledge of inspection procedures and tools, identify deviations, work with production team members to document non-conforming materials and communicate with engineering team within in a manufacturing facility. A Quality Inspector works with a team to ensure all products meet established quality standards. The ideal candidate is adaptable, a team player, a great communicator, and can meet deadlines and prioritize multiple projects. Responsibilities: * Perform inspection on in-house and vendor-supplied parts and complete in-process inspections as required. Ability to use ESDS materials when working with electronic materials (i.e. wrist straps, grounded rubber mats). Operate Positive Material Identification (PMI) Gun to check materials against blueprints or drawings. Use Keyence measurement programming and CMM operation experience * Interpret engineering drawings/specifications and geometric dimensioning and tolerancing (GD&T). Conduct process audits of assigned value streams focusing on adherence to standard work. Identify and document defects, deviations, or non-conforming items and processing defects. * Perform final product inspection/verification before shipment for customer orders. Identify and report defects or issues in the assembly process and necessary adjustments or repairs to ensure product quality. Partake in the occasional inspection of soldering workmanship and electronic assemblies Perform quality checks by established quality procedures and ISO requirements. * Collect samples of products or materials for testing and coordinate with the quality control laboratory if further analysis is required. Collaborate with team members to optimize workflow and achieve daily and monthly targets. Ensure inspection tools and equipment are properly calibrated and maintained and report issues. * Maintain accurate records of inspection results, quality control data, and non-conforming products. Generate reports and documentation as required * Inspect finished products for quality and adherence to specifications. Perform quality checks by established quality procedures and ISO requirements. Identify and report defects or issues in the assembly process and necessary adjustments or repairs to ensure product quality. Test and troubleshoot assemblies. * Participate in training programs to improve maintenance skills and product knowledge. Attend monthly EHS trainings. Follow all policies and procedures (i.e. report on time and ready to work - Start/Lunch/Breaks). Participate in continuous improvement initiatives by suggesting process enhancements and participating in root cause analysis, writing the NCM, and disposing of waste accordingly (RTV, Scrap, Rework) * Follow all safety guidelines, including wearing appropriate personal protective equipment (PPE). Test PSI limit no greater than 30,000. Report any safety hazards or incidents to supervisors promptly. Follow 5S principles (Sort, Set in order, Shine, Standardize, Sustain). Test PSI limit no greater than 30,000. Lift a maximum of 35 lbs for an individual and 70 lbs for a team lift. Maintain a clean and organized work area. Requirements: * High School Diploma or GED * 2+ years' experience in Manufacturing/Industrial Quality Inspection * 1+ years of experience in Using Precision measuring tools and blueprints Core Competencies: * Lifting: Must be able to lift up to 35 pounds occasionally with hoist to be used on objects over 40 pounds. * Standing: Standing is required in periods of up to three hours at a time. * Stooping: Would be required to lift objects off pallets * Hand Dexterity: Must be able to work with hand tools, screws and gauges, as well as operating buttons on controls. * Verbal Communication: Must be capable of clear communication between co-workers and supervisor. * Carrying: Capable of carrying 40 pounds for a distance of up to 25 feet. Preferences: * Ability to read and understand the bill of materials and work instructions, blueprints, or technical drawings * Ability to operate precision tools such as micrometers, calipers, thread gauges, comparators, and others * Demonstrated time management skills, strategic thinking, and adaptability * Proficient computer knowledge (i.e. log on credentials (SSO), JD Edwards, and Microsoft Outlook, Word and Excel) Travel & Work Arrangements/Requirements: This position will be based at our site in Ivyland, PA no travel. What we Offer: At Ingersoll Rand, we embrace a culture of personal ownership - taking responsibility for our company, our communities, and our environment, as well as our individual health and well-being. Our comprehensive benefits package is designed to empower you with the tools and support necessary to take charge of your health, ensuring that together, we can continue to make life better. Our range of benefits includes health care options like medical and prescription plans, dental and vision coverage, as well as wellness programs. Additionally, we provide life insurance, a robust 401(k) plan, paid time off, and even an employee stock grant, among other offerings. These benefits are our commitment to you, so you can be your best at work and beyond. Ingersoll Rand Inc. (NYSE:IR), driven by an entrepreneurial spirit and ownership mindset, is dedicated to helping make life better for our employees, customers and communities. Customers lean on us for our technology-driven excellence in mission-critical flow creation and industrial solutions across 40+ respected brands where our products and services excel in the most complex and harsh conditions. Our employees develop customers for life through their daily commitment to expertise, productivity and efficiency. For more information, visit *************

COMPANY CULTURE Our focus is to deliver world-class solutions to our customers, on time and of the highest quality as the preferred supplier of highly engineered, energetic, and pyrotechnic devices while developing our associates and maximizing long-term value for our shareholders through organic growth and targeted acquisitions. GENERAL STATEMENT OF DUTIES: Responsible for the Quality Inspection and Testing of Aircraft, Military, and Industrial Gas and Oil production Equipment. Collect and report data to be presented to the customer for reporting purposes. The Quality Technician is responsible for providing inspection and administrative support in order to ensure that all general matters in Quality are handled timely and efficiently. ESSENTIAL DUTIES AND RESPONSIBILITIES: The Quality Technician is a hands-on representative of the Quality department whose job is to help ensure all basic visual and test inspections are performed to ensure product integrity and compliance to all specifications at the production facilities. Perform visual and dimensional inspection on components and ensure conformance against the technical data (Product Verification Audits). Responsible for receiving inspection, in-process and final inspection of repairable parts/components channeled into the cell(s). Support and participate in EH&S, Quality, Ethics and continuous improvement projects and initiatives. Support generation of FAI and corresponding documentation. Review incoming FAI to ensure compliance to Collins and AS9102 standards. Any other function(s) as assigned by management Maintain calibration records Maintain tools Perform other related duties as assigned. Qualifications You Must Have Typically requires HS Diploma or AA/AS degree (or other 2-year post high school training) with a minimum of 2 years of relevant experience U.S. citizenship is required, as only U.S. citizens are authorized to access information under this program/contract MSOffice skills Knowledge of GD&T PHYSICAL DEMANDS: Must possess sight/hearing senses, or use prosthetics that will enable these senses to function adequately so that the requirements of this position can be fully met. Physical activity includes walking, standing, bending, squatting, reaching above shoulders and lifting up to 40lbs. The candidate for this position may have to spend long hours using a computer, which can cause eye strain. This position will have to manage a number of requests and situations at one time. Stress may be caused by the need to complete tasks within tight deadlines. WORK ENVIRONMENT: Performs office activities in a lighted and ventilated area. May be subject to changes in temperature and exposure to dust. May be exposed to uncontrolled environmental conditions. Will work in a normally acceptable office environment, with no abnormal hazards or risks. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. DISCLAIMER The above information on this description has been designed to indicate the general nature and level of work performance by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to this job. Cartridge Actuated Devices is an Equal Opportunity Employer and encourages the application of female, minority, disabled, and veteran candidates. Due to the potential for exposure to ITAR controlled data, the incumbent in this role must be a US Person (US Citizen or US Permanent Resident). Due to the nature of our products, To the extent applicable to an employee's role, each employee must be able to obtain (and maintain) the ATF Possessor License as a condition of employment. Employment with Cartridge Actuated Devices is contingent upon the successful completion of a background investigation, including any required Bureau of Alcohol, Tobacco, Firearms and Explosives (ATF) screening, and drug screening, as permitted by applicable law. The background investigation may include verification of employment history, education, criminal records, ATF-mandated checks, and other relevant information to determine suitability for employment. The drug screening will be conducted in accordance with state and federal regulations. Failure to successfully pass the background check, ATF screening, or drug screening, or the provision of false or misleading information during the application process, may result in withdrawal of a job offer or termination of employment. By proceeding with the application process, you acknowledge and consent to the background, ATF, and drug screening requirements as described above.

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.