Quality control technician jobs in Abington, PA - 319 jobs

Discover Veranova: At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented workforce in our industry. Our commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking innovative individuals who have a mindset open to learning and growth, and a desire to make a difference. Veranova is a global leader in the development and manufacturing of complex active pharmaceutical ingredients (APIs) for pharma and biotech customers. With deep technical expertise and impressive flexibility, we develop solutions and processes that support and accelerate innovation. Join us on our mission to enable current and next-generation therapeutics to improve and save the lives of patients. Role Overview: The Production Technician will manufacture of bulk API pharmaceuticals in accordance with customer and internal specifications. Core Responsibilities: Complete batch records in accordance with FDA and Current Good Manufacturing Practices (cGMP) guidelines Provide process support and troubleshooting necessary to meet all customer requirements Maintain the facility in excellent FDA/cGMP posture ▪ Responsible for safety equipment and active participation in safety program and hazard analysis. Wears appropriate PPE for task. Ensure that waste is appropriately characterized, labelled, stored and disposed in compliance with all Company, state and federal regulations. Works collaboratively with Environmental, Health & Safety, as appropriate. Assure all production/support equipment is in proper operating condition and that all production equipment is appropriately labelled with a current status tag. Works collaboratively with Maintenance, as appropriate. Ensure the security and safe handling of all controlled substances at all times. Strictly adheres to all Company and DEA regulations. Ensure a level of housekeeping appropriate for a pharmaceutical manufacturer and maintain 5S areas. Active member of Emergency Response Team. Participate in Emergency Response Training and related activities. Promote a positive work environment by maintaining a safe work area and ensuring that their team members have the knowledge, skills and appropriate tools to perform their assigned duties and a thorough understanding of their performance expectations. Provide prompt, appropriate feedback to team members, both positive and constructive, in a continuing effort to develop employees to their full potential. Demonstrate a professional and positive attitude, integrity and a strong work ethic and encourages team members to do the same. Cooperate with all root cause investigations and follow corrective actions and compliance with Company policies and procedures, and all state and federal regulations occurs within department. Operate machines and equipment that involves set up and making adjustments to regulate temperature, pressure, flow and reactions or materials safely and in accordance with batch record and work instructions. Basic batch processing and unit operations, able to run all milling operations. Thinking is within well-defined procedures with assistance readily available. Proficient in all tasks/unit operations associated with a processing area ▪ Able to complete basic mechanical work required to keep operation moving Complex batch processing and unit operations, such as hydrogenations, PFD operations etc. Resolve regular technical problems and takes action to ensure the production plan continues to move Qualifications: Required High School Diploma with 5-7 years of experience in an API Manufacturing facility or AA in Chemistry, Engineering, or other related technical field with 3-5 years of experience or BS in Chemistry, Engineering or other related technical field Solid understanding of GMP and FDA Safety Awareness Authenticity and motivation to contribute to team success Ability to independently apply scientific and/or technical knowledge in the performance of job duties Commitment to continuous learning and improvement Effective written and verbal communication Special Factors Walking, standing for long periods of time while in plant, reaching, handling, twisting, and bending spine at waist when operating equipment. Obtain and maintain certification as forklift operator Able to lift 50lbs Must be willing to work a rotating shift Hourly Rate: $26-30 per hour Our Commitment: Health & Wellness: Comprehensive health & wellness benefits. Access to mental health resources and wellness programs. Generous PTO and holiday pay policies. Financial Wellness: Veranova is committed to fair and transparent compensation practices. This includes a competitive base salary, eligibility for performance-based bonuses, and an attractive 401(k) Plan with company match. Salary ranges reflect the scope and expectations of the role, and are based on market data, internal equity, and role-specific factors. Final compensation may vary depending on experience, skills, education, and business needs. Professional Development: Opportunities for continuous learning through LinkedIn Learning, workshops, conferences, and mentorship. Tuition Assistance for Undergraduate and Graduate degree programs. Inclusive Culture: At Veranova, an inclusive culture is integral to our values. We welcome people with diverse experiences and perspectives who share our mission to improve and save lives. Even if you don't meet every qualification, we encourage you to apply. Veterans, first responders, and those transitioning from military to civilian life bring valuable skills that strengthen our team. Additional Information: Applicants for this role must be authorized to work in the United States without further employer sponsorship. Agency and Search Firm Representatives : Veranova does not accept unsolicited resumes from agencies and/or search firms for this job posting. . All your information will be kept confidential according to EEO guidelines. Veranova is an Equal Opportunity Employer. It is the policy of Veranova to provide equal employment access and opportunity to all persons regardless of age, race, color, national origin, religion, sex, sexual orientation, gender identity and/or expression, physical or mental disability, genetic information, citizenship, marital status, veteran status, or any other characteristic protected by federal, state, or local law. All applications are carefully considered, and your details will be stored on our secure Application Management System. This is used throughout Veranova for the selection of suitable candidates for our vacancies as they arise. Veranova respects your privacy and is committed to protecting your personal information. For more information about how your personal data is used please view our privacy notice .

Compensation & Details: 2 Openings Fully onsite role in Malvern, PA - in the laboratory $35-39/hr - exact rate is based on several factors, including skills, experience, and education. Benefit packages for this role will start on the 1st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law 10 PTO Days & 6 Sick Days 12 month extending contract Requirements: Minimum two (2) years of relevant work experience Experience in Medical Device, Biopharmaceutical, or Pharmaceutical industry Working experience in a current Good Manufacturing Practices (cGMP) compliant QC laboratory or equivalent environment and solid understanding of cGMP and current Good Laboratory Practices (GLPs) Must have experience in the following: qPCR, cell culture, Flow Cytometry, and/or ELISA Ability to read/interpret technical documents such as SOPs, work instructions, test methods and protocols Proficient with Microsoft Office applications (Outlook, One Note, Teams, Excel, Word, and PowerPoint) Day to Day: The QC CRS Analyst is responsible for conducting biochemical and testing of drug substance, final product release and characterization samples, and critical reagent qualifications of cell and gene therapy products, including CAR-T. They are responsible for ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations. They typically work with a team of 10 - 15 other Analysts within a functional Clinical Release and Stability (CRS) Laboratory and report to one of two QC CRS Supervisors. Key Responsibilities: Conduct analytical biological testing (ELISAs, qPCR, Flow Cytometry, Cell-based assays, etc.) of clinical and commercial drug product/drug substance samples Perform peer reviews and approvals of laboratory data Use electronic systems (LIMS, MES, Empower, etc.) for execution and documentation of laboratory data Support of New Product Initiatives (NPI) in groups of 3-6 analysts Perform Instrument Calibration and/or Preventative Maintenance, as needed Update CRS-owned documents using the Electronic Document Management System (EDMS) Order/receive supplies and manage inventory Support analytical method qualification, validation, and transfer into and out of the QC lab, owning change control actions, completing testing activities with mentorship from Sr. Analysts on transfer activities Complete change control processes to integrate new methodologies and technologies into and out of the CRS Lab with limited oversight Complete invalid assay and general laboratory investigation records Complete corrective and preventative actions (CAPA) as assigned Assist in the execution of internal audits

Requisition ID 2026-20612 # of Openings 1 Category (Portal Searching) Other Type (Portal Searching) Regular Full-Time This position is responsible for the cleaning and processing of reusable pumps and durable medical equipment. The cleaning and processing of equipment includes all medical infusion and feeding pumps, bili-blankets, dialysis machines, commodes, shower chairs, and other equipment as directed by the Materials Distribution Management Leadership. Responsibilities Assessing the physical condition of the equipment for damage Ensuring the devices will turn on and off to verify basic function Clean each device as per the manufacturer's Instructions for Use (IFU) and established procedures Bag clean devices and transport to clean storage area Stage equipment for pickup ensuring proper storage and charging of devices Maintaining all required electronic documentation for processing equipment and exceeding minimal levels of processing productivity as established by leadership Coordinate transport and pickup for damaged electronic medical equipment with the Biomed Department Responsible for the retrieval of reusable pumps and durable medical equipment throughout the main campus Equipment Inventory Management and Cleaning related projects as assigned by CHOP leadership Complete basic replacement of damaged or missing parts on DME such as shower chairs and commodes Training to maintain cross functional understanding of other areas as well as departmental standards and safety policies Support of other areas should demand for processing equipment reduce the priority of this particular role Implementations of new medical equipment as it is introduced into the Hospital Maintain a clean and orderly Decontamination Room Clean 20-25 pieces of reusable pumps and/or durable medical equipment per hour as per the training material provided. Collection of soiled pumps and durable medical equipment twice per shift or as needed through the employees scheduled shift Other duties as assigned Qualifications High School Diploma or equivalent required Basic working knowledge of computers and programs Must be a "critical thinker" with an ability to quickly adapt to a changing environment Strong product knowledge a must Excellent interpersonal skills, verbal and written communications skills are required for success in this function Demonstrated good ability to prioritize work, strong organizational skills and initiative to improve processes Consistently display a friendly, positive, and professional demeanor Work with limited supervision with no instruction needed on routine work and general instructions given on new lines of work Excellent customer service, professional attitude and appearance are a must Ability to work overtime and meet deadlines. PHYSICAL DEMANDS Ability to lift 40 lbs Repetitive motion Reaching, pushing, pulling carts weighing up to 250lbs Walking, standing for extended periods of time What We Offer: Competitive pay & benefits! Comprehensive training and development programs that prepare employees to advance from within. A company focused on creating a positive work and client environment. Employee discounts on entertainment, products, and services nationwide! Come Join Our Team! Connect With Us! Not ready to apply? We look forward to connecting with you in the future! By joining our Talent Network, you can receive job alerts for new positions that match your skills and experience sent straight to your inbox.

Student employees will support the Theater & Dance department's productions, specifically in the areas of technical production, as required by a specific production's needs. This position will be specialized toward the technology components of the theatrical process (lighting, sound, video, etc.), but will also have crossover with the scenic and carpentry responsibilities as needed. This position will also support the technology needs for campus events taking place in the Kaleidoscope (lectures, dinners, ceremonies, etc.) Work is done in the Kaleidoscope's scene shop, Lenfest Theater, and Blackbox Studio Theater, under the direct supervision of the Theater & Dance department's Technical Director & Production Manager and Performing Arts Technician. Schedule may vary weekly. Some evening and weekend hours will likely be required during a production's load in period and tech weekend, and during campus events taking place in the building. Typical work week may average between 12 and 20 hours. Responsibilities: Learn and practice a variety of skills (depending on the needs of the production) primarily including hanging and focusing lights, setting up microphones and speakers, and (as needed for the production), scenic carpentry, metalworking, scenic painting, and theatrical rigging. Support the technology needs for campus events taking place in the Kaleidoscope (lectures, dinners, ceremonies, etc.) Train on the theaters fly-system and operation along with other specified theatrical equipment. Help with the set-up of both theater spaces for rehearsal and technical rehearsals. Assist in scheduled maintenance and organization of shop and theater gear and equipment. Requirements: Current full-time student at Ursinus College Must learn shop and theater safety requirements and adhere to those protocols during work calls. Must be able to lift 25-50lbs. Must be comfortable with, and/or, willing to, work at heights. Prior experience in technical theater is preferred, but not required. Other Duties: The above statements are intended to describe the general nature and level of work being performed by the individual(s) assigned to this position. They are not intended to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel so classified. Job responsibilities and activities may be modified or changed at any time with or without notice. Job descriptions will be audited periodically by the Ursinus Human Resources department to ensure they are up-to-date and reflect the essential responsibilities and duties of the job. Ursinus EEO Statement Ursinus is an EEO employer. Ursinus College does not discriminate on grounds of race, color, national origin, gender, sexual orientation, gender identity or expression, religion, age, creed, ancestry, veteran status, marital status, disability, or other classification protected by applicable law in the administration of any of its educational programs or activities or with respect to employment.

The Associate Analytical Technician supports manufacturing operations by performing laboratory analyses, maintaining analytical systems, and ensuring data integrity. This role is ideal for individuals who are detail-oriented, safety-conscious, and eager to grow in a technical laboratory environment. Key Responsibilities: Train under senior team members to perform routine analyses until proficiency is demonstrated. Collect samples in accordance with the Sample Plan and standard operating procedures. Conduct laboratory analyses to support plant operations and product quality. Evaluate the validity of routine analytical data and take appropriate corrective actions. Monitor analytical systems and escalate issues as needed. Perform basic preventive maintenance and calibration of laboratory instruments. Implement and qualify new analytical equipment and methods. Document, communicate, and archive analytical results and data accurately. Follow Environmental Health & Safety (EH&S) and Operating Discipline Management System (ODMS) procedures. Suggest improvements to laboratory processes, tools, and workflows. Maintain lab cleanliness and inventory through regular housekeeping tasks. Escalate non-routine requests or issues to appropriate team members. Preferred Skills & Qualifications: Understanding of analytical/scientific methods and laboratory best practices. Ability to troubleshoot and adapt to non-routine lab analyses. Familiarity with data systems and statistical evaluation tools. Strong attention to detail and commitment to safety and quality. Effective communication and collaboration skills. Schedule: This Lab Tech position is on a Rotating shift schedule but you will have different hours during training. This position will follow a rotating shift schedule with AM and PM shifts switching every two weeks.

Since 1869, we've connected people through food they love. We're proud to be stewards of amazing brands that people trust. Our portfolio includes the iconic Campbell's brand, as well as Cape Cod, Chunky, Goldfish, Kettle Brand, Lance, Late July, Pacific Foods, Pepperidge Farm, Prego, Pace, Rao's Homemade, Snack Factory, Snyder's of Hanover. Swanson, and V8. Here, you will make a difference every day. You will be supported to build a rewarding career with opportunities to grow, innovate and inspire. Make history with us. Why Campbell's… Benefits begin on day one and include medical, dental, short and long-term disability, AD&D, and life insurance (for individual, families, and domestic partners). Employees are eligible for our matching 401(k) plan and can enroll on the first day of employment with immediate vesting. Campbell's offers unlimited sick time along with paid time off and holiday pay. If in WHQ - free access to the fitness center. Access to on-site day care (operated by Bright Horizons) and company store. Giving back to the communities where our employees work and live is very important to Campbell's. Our “Campbell's Cares” program matches employee donations and/or volunteer activity up to $1,500 annually. Campbell's has a variety of Employee Resource Groups (ERGs) to support employees. How You Will Make History Here… As a Senior Technician - QA, you will play a critical role in ensuring the highest standards of food safety and quality in our plant operations. You will manage regulatory compliance, oversee quality assurance programs, and support continuous improvement initiatives that uphold our commitment to excellence. What You Will Do… Execute daily distribution, collection, and review of control documentation for product manufacturing and release, ensuring compliance with quality standards and product specifications. Collaborate with production teams to monitor processes and drive efficiency and continuous improvement. Support preparation and execution of third-party and regulatory audits by maintaining food safety and quality policies, standards, and procedures. Plan and execute work through eMaint Application as Site Administrator. Manage Environmental Monitoring Program (EMP) and Alchemy training program for quality and safety. Oversee in-process quality for plant operations and Kitchen 1869, including routine sample analyses and adherence to Good Laboratory Practices. Conduct GAP assessments, root cause analysis, and manage corrective and preventive actions (CAPA). Support plant safety processes through audits, corrective actions, and document management. Other duties as assigned. Who You Will Work With… You will collaborate closely with: Plant Operations and R&D teams, including Kitchen 1869. Quality Manager and North American Supply Chain Quality group. USDA onsite officials and third-party auditors. What You Bring to the Table… (Must Have) High School Diploma required Minimum 3 years of experience with a BS degree OR 8 years in a fast-paced food manufacturing environment. Strong verbal and written communication skills. Proven planning, organizing, leadership, and teamwork abilities. Knowledge of canning and thermal processing. Background in food processing and quality assurance. Ability to drive quality initiatives in a dynamic environment. Problem-solving and analytical thinking skills. Proficiency with computer systems, SharePoint, and Microsoft Office Suite. It Would Be Great If You Have… (Nice to Have) BS in Food Science preferred. Experience with HACCP/FSP plans and GFSI audit standards. Familiarity with Alchemy training systems and eMaint planning tools. Understanding of regulatory compliance and food safety programs. Compensation and Benefits: The target base salary range for this full-time, salaried position is between $54,600-$78,400 Individual base pay depends on work location and additional factors such as experience, job-related skills, and relevant education or training. Total pay may include other forms of compensation. In addition, we offer competitive health, dental, 401k and wellness benefits beginning on the first day of employment. Please ask your Talent Acquisition Partner for more information about our total rewards package. The Company is committed to providing equal opportunity for employees and qualified applicants in all aspects of the employment relationship, including consideration for employment, without regard to race, color, sex, sexual orientation, gender identity, national origin, citizenship, marital status, protected veteran status, disability, age, religion, or any other classification protected by law.

About us Delva Tool & Machine (DTM) and its 6 locations specialize in precision machining, fabrication, and assembly highly engineered components. With over 175 years of combined experience, 300,000 sq. ft. of floor space, 250 CNC machines and 350 talented employees between 6 locations across the United States and Canada, we leverage our combined expertise and state of the art CNC machining capabilities to deliver quality machined parts to customers all across the globe. Our primary commitment is to provide our customers with a quality product, on-time delivery, and competitive pricing. Core Values Relentlessly Driven to Excel - We take pride in mastering our craft, pushing ourselves to be the best, and constantly improving. “Good enough” is never enough. Tech-Forward Problem-Solvers - We embrace challenges with a solution-oriented mindset, thinking critically and adapting quickly to get the job done. We seek out and leverage the best technology and processes, appropriately automating to be more agile and lean. Accountable & Dependable - We take ownership of our work, meet deadlines, and follow through on our commitment; no excuses and no self-victimizing. Team-First Mentality - We collaborate, communicate, and support each other, knowing that success comes from effective collaboration. Integrity in Everything - We do what's right, even when no one is watching. Honesty, transparency, and respect guide our decisions. Position Summary Delva Tool & Machine (DTM) is seeking a Quality Technician for our Cinnaminson, NJ location. The Quality Technician will work with the Quality Manager and other manufacturing personnel to support our overall quality objectives by developing, implementing, and maintaining reports for customers. If you are looking for an organization and career that will match your strong work ethic and passion for success, Delva Tool & Machine is a great place to start! *This position works a schedule of Monday through Friday from 7:30 a.m. to 4:00 p.m. The salary range for this role is between $41,000 - $83,200 per year, and applies to Quality Technician I, II, and III, with final compensation determined by level, experience, and qualifications* Essential Duties and Responsibilities Position Experience Education Essential Duties and Major Responsibilities Quality Technician I 1-2 years' experience in a manufacturing or production environment, preferably within CNC machining, aerospace, defense, or precision manufacturing. High school diploma or equivalent required; technical training, trade school coursework, or relevant quality/manufacturing certifications are preferred and may substitute for formal education based on experience. Perform basic visual, dimensional, and documentation inspections on incoming, in-process, and final products under close supervision. Follow established inspection procedures, quality standards, and work instructions to verify product meets customer and Delva/CMT requirements. Review material certifications, supplier documents, and outside process paperwork for completeness and accuracy. Assist in assembling technical data packages and inspection documentation. Promptly identify, document, and report any nonconforming conditions or discrepancies. Maintain inspection records, logs, and reports in accordance with AS9100/ISO procedures. Support first article inspection preparation by gathering prints, certifications, and required documentation. Perform basic gauge checks, tool verifications, and equipment calibration support tasks as directed. Communicate clearly with Quality and Production personnel regarding inspection results. Adhere to all safety guidelines and maintain a clean and organized inspection area. Assist with other quality-related tasks as assigned. Quality Technician II 3-6 years' experience in a manufacturing or production environment, preferably within CNC machining, aerospace, defense, or precision manufacturing. High school diploma or equivalent required; technical training, trade school coursework, or relevant quality/manufacturing certifications are preferred and may substitute for formal education based on experience. Perform complex dimensional, mechanical, and documentation inspections with minimal supervision. Develop, update, and maintain inspection documentation including control plans, technical data packages, and customer-required forms. Submit first article reports (AS9102), control plans, and supporting data to customers as required. Review drawings, specifications, and customer requirements to determine proper inspection methods. Ensure products and all associated documentation meet defined requirements per customer specifications and the Delva quality system. Review and verify outside processing documentation, material certifications, and supplier compliance records. Identify quality issues, investigate root causes at the inspection level, and communicate findings promptly. Assist in implementing and monitoring quality standards, parameters, and inspection criteria. Support process troubleshooting and collaborate with cross-functional teams on problem resolution. Record inspection results, maintain traceability, and ensure compliance with AS9100/ISO documentation standards. Train junior technicians and production operators on inspection procedures, documentation, and quality expectations. Participate in continuous improvement initiatives, including scrap reduction, takt-time improvement, and bottleneck support. Assist with special projects, audits, and customer support activities as assigned. Quality Technician III 7+ years' experience in a manufacturing or production environment, preferably within CNC machining, aerospace, defense, or precision manufacturing. High school diploma or equivalent required; technical training, trade school coursework, or relevant quality/manufacturing certifications are preferred and may substitute for formal education based on experience. Lead complex inspections, including advanced dimensional verification, GD&T interpretation, and multi-step documentation reviews. Develop, implement, and improve quality processes to ensure products meet all specifications for quality, function, and reliability. Create, manage, and deliver comprehensive technical data packages, first article reports, and customer-required quality documentation. Establish and refine product-specific quality standards, acceptance criteria, and inspection parameters. Conduct detailed document reviews of drawings, materials, and external process certifications to ensure full compliance. Act as a quality liaison to customers, engineering, outside processors, and production teams for technical quality issues. Drive root cause investigations, corrective action development, and long-term quality improvement strategies. Lead training efforts for operators, supervisors, and lower-level technicians on updated inspection methods or process modifications. Support and lead efforts to reduce scrap, improve process stability, and enhance throughput in quality bottleneck areas. Provide guidance during audits and customer reviews; ensure all required documentation is accurate, complete, and available. Use advanced quality tools, measurement equipment, and software (CAD, FAI/AS9102 tools, databases). Maintain expert-level understanding of AS9100/ISO, quality assurance methods, and industry requirements. Assist Quality Manager with reporting, metrics, and strategic quality initiatives. Perform other advanced or leadership-level duties as needed. Benefits and Perks Our comprehensive benefits package includes, but is not limited to, a competitive pay rate, accrued vacation time, sick time, paid holidays, 401(k) with company match, health, dental, and vision insurance as well as Short-Term Disability, Long-Term Disability, and life/AD&D insurance. We are a drug-free workplace / Equal Opportunity Employer and Prohibit Discrimination and Harassment of Any Kind: We are committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions are based on business needs, job requirements, and individual experience and qualifications, without regard to a person's sexual orientation, gender identity, gender expression, religion, disability, race, creed, color, sex, age, national origin or ancestry, or any other status protected by the laws or regulations in the locations where we operate.

The Quality Technician in microbiology aseptic processes ensures products meet microbiological standards and are manufactured in a sterile environment. This role monitors quality assurance standards and encourages the team to consistently deliver excellent results. The Quality Technician is responsible for executing best practices, goals, and established standards for the team. Primary Responsibilities * Perform tests to identify harmful microorganisms, maintain a sterile environment, and ensure regulatory compliance * Document and analyze test results following good laboratory practices for microbiology and quality control laboratories * Identify and address production issues, contributing to corrective action * Inspect work daily, maintain cleanliness, organize supplies, and assemble sterile products using aseptic technique * Handle biohazard spills, train new hires, and demonstrate the use of cleaning chemicals * Uphold quality standards, follow GFSI, HACCP, and GMP guidelines, and participate in food safety inspections * Support sanitation operations, monitor performance, and provide report * Address customer complaints, conduct audits, and contribute to quality assurance improvements * Promote continual improvement and collaborate on cross-functional projects * Perform routine environmental monitoring within cleanrooms and production areas to detect microbial contamination * Conduct microbiological assays on raw materials, in-process samples, and finished products using various techniques * Accurately record and interpret test results, maintaining detailed documentation of activities, including deviations, investigations, and corrective actions * Participate in investigations for out-of-specification (OOS) results, deviations, and complaints related to microbiology testing * Ensure proper calibration and maintenance of laboratory equipment used for microbiological analysis and QC testing Prior Knowledge/Experience * Bachelor's Degree in Microbiology, Biology, or related field * 1-3 years of experience in quality; food processing experience preferred * Strong understanding of aseptic techniques and microbiology principles * Experience with various microbiological testing methods, including plate counting, membrane filtration, and rapid microbial detection * Proficiency in data analysis, documentation, and recordkeeping * Excellent attention to detail; ability to work independently and in team environments * Familiarity with GMP regulations and quality systems * Ability to utilize provided PPE - safety glasses, ear plugs/muffs, bump caps, dust masks, company uniform, safety shoes * Ability to be respirator certified if required * Physical ability to sit, stand, walk, climb, stoop for up to 8 hours; lift 55 lbs consistently; lift/hold objects overhead for extended periods * Ability to climb and work on a 40-foot extension ladder for extended periods as needed; work at heights up to 50 feet * Ability to maneuver and work in confined areas with variations in temperature, humidity, and air quality The following common allergens are processed in our facilities: wheat, eggs, dairy, and soy. Looking for a Career for Good? We offer a competitive compensation and benefit package, designed to promote a Happier, Healthier You which includes: Compensation: * Compensation for this role is hourly and will be based on your experience, skills, and location, with a typical range between $24.69/HR and $30.87/HR. * This role is eligible for a targeted annual bonus equal to $3500. Final bonus payouts are determined by both individual and company performance. Benefits: * Medical coverage starts the first of the month-no waiting period * Immediate 401(k) eligibility with fully vested matching contributions * Over 5 weeks of paid time off in your first year * Free life coaching, onsite health exams, and 24/7 access to Registered Nurses * Lifestyle Spending Account #LI-DNI Apply now * Apply Now * Start applying with LinkedIn

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

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

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.

Job Description Quality Control Technician Waste Gas Fabricating Company Fairless Hill, PA (Full Time, Permanent Opportunity) Waste Gas Fabricating Co., Inc., is proud to be an Employee Owned and Operated premier Steel Fabrication and Manufacturing company. We've been in business since 1976 and our 100,000 square foot facility is located in Fairless Hills, PA. Waste Gas Fabricating has a rich history in press brake metal forming, metal rolling, and structural steel fabrication, stainless steel fabrication, fiber laser cutting and the assembly of custom equipment. We are Machine Shop * Laser Cutting * Steel Fabrication * Heavy Steel Plate & Large Metal Parts Experts. We are seeking a qualified, full-time, Quality Control Technician to work in our newly constructed Quality Control Center. Candidates for this position should be: Detail oriented Have good written and verbal communication skills Have experience with basic computer usage and skills Have good math skills in order to calibrate and measure to specifications Have the ability to use good judgement regarding workmanship If you would like to join our team, and become a part of the success of our company, please send your resume along with salary requirements to: ******************** Please visit us at: **************** EOE Prior work in a manufacturing setting is a plus Experience in blueprint reading Experienced with the use of basic inspection hand tools such as "calipers and micrometers" Knowledge of CMM operation Familiarity with ISO 9001 standards and procedures is preferred, but not mandatory Benefits: Our Benefits include: *Health Insurance *Dental Insurance *Vision Insurance *Life Insurance *Long Term/Short Term Disability *401k with Company Match *Employee Stock Ownership Plan (100% employer-funded) *Paid Time Off

The Quality Technician's role will be seen as pivotal in our efforts to drive at-source quality at ALMAG. The role requires the individual to support new product introduction, provide quality training, support, and to work collaboratively with various teams to develop standard work and ensure compliance. DUTIES AND RESPONSIBILITIES The quality technician's primary responsibility is to positively support the various departments in assuring that the requirements of the customer and quality management system are being met throughout each department. Additionally, the quality technician contributes to the continuous improvement of Almag's quality system. The duties and responsibilities of the Quality Technician are detailed below, but not limited to the following: Supporting the New Product Introduction process by assuring new customer requirements are understood and achieved. Responsible for performing audits of various departments to ensure that the QMS requirements are being met. Communicate new product status, its performance based on data, and provide samples and feedback to the respective departments with continuous improvement approach in mind. Responsible for collecting samples as required for various customer and internal requirements. Responsible for tracking and supporting Quality Containment processes for nonconforming product in all departments. Responsible for supporting production team in achieving customer requirements through training, auditing, and development of standard documents. Provide direction and support to any special sorting if needed, with the focus on accuracy and efficiency of sorting. Perform product testing for mechanical properties. Support team lead and shift supervisors to determine criteria for acceptance or rejection when there is uncertainty. Provide direction to the team if clarification is required for WO notes or requirements. Perform other related duties as assigned. Requirements MINIMUM QUALIFICATIONS Education/Experience At least 3 years' experience in quality, working in manufacturing environment. ASQ Certified Quality Technician (CQT) would be an asset. Certified Internal Auditor would be an asset. Technical Skills/Competence Excellent teamwork and collaboration across departments and within teams Work Efficiently Flexibility/Adaptability to meet customer business requirements. Communicate clearly and effectively, verbally and in writing. Must be able to read and understand engineering drawings. Basic knowledge of GD&T would be an asset. Ability to work and make decisions independently. Good mechanical aptitude and attention detail. Must be competent in the use of measuring instruments i.e. Calipers, micrometers. Basic proficiency with MS-office (Excel, Word, PowerPoint). Fork Lift Certified Benefits Profit Sharing Education Assistance Program Social Events Safety Shoe and Glasses Allowance Internal Growth and Development Health and Dental Life and AD&D Vision Critical Illness Insurance 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

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

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

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: Associate's 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

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

KMM Group offers rewarding opportunities to propel the world forward through mission critical components for air, space, life-saving equipment and more. You don't want to miss out on this opportunity! A few of our Company Values: Paid to Think Make it Fun Choose Positive Support Each Other Strive for Excellence Inspire Passion Job requirements Quality Technician, Wire Grind (QTWG) 📍 Hatboro, PA | Full-Time At KMM Group, Ltd., we craft mission-critical components that fuel life-saving medical devices and cutting-edge aerospace systems. We are seeking a Quality Technician, Wire Grind (QTWG) to join our team. The QTWG requires an acute eye for detail and strong visual acuity. Though there is some aspect of dimensional measurement in the position, a greater percentage of the work is connected to the visual inspection of critical characteristics of guidewires/corewires (GW/CW) 🔧 What You'll Do Tactical Responsibilities a. Visual inspection of GW/CW i. Roll test ii. Length test iii. PTFE damage b. Tensile testing as required c. Perform final dimensional inspection operations as required (if applicable) d. Perform FAI as required (if applicable) e. Document all findings using Good Documentation Practices (GDP) f. Wash wires g. Package wires Strategic Responsibilities Become proficient at all aspects of the visual inspection process for GW/CW in order to maximize the throughput of wires through QC Physical Requirements and Demands: Keen attention to detail is required for success in QC Ability to sit at a desk, or QC work station, for prolonged periods of time ✅ What You Bring: High School diploma or equivalent Prefer experience in a manufacturing-based pre-apprenticeship program which offers; i. Basic understanding of GD&T ii. Basic understanding of use of measuring instruments 🚀 Why Join KMM Group? Meaningful Work - Build and inspect parts that power technologies protecting and improving lives Innovation Culture - We live our values: Paid to Think, Make it Fun, Support Each Other, Strive for Excellence, Inspire Passion Team-Driven Environment - Join a group of professionals who value precision, integrity, and impact Career Growth - Expand your technical skillset and shape your career within a forward-thinking organization 🛡️Benefits & Perks Offered: Healthcare: Medical, Prescriptions, Dental Vision Insurance Life & Disability Insurance Supplemental: Health Insurances (Hospital Indemnity, Critical Illness Care, etc. - Paid by Employee Total Wellbeing Programs & Mobile Mental Health Hub Financial Academy Paid Holidays and PTO 401k Plan w/Employer Match Employee Assistance Program (EAP) Professional Development Programs, Education Dedicated Manager of Training Dedicated HR staff to support your needs Benefits related Employee Advocacy Team ***All benefits listed herein are for information purposes and subject to change. NOTE: KMM is an ITAR Registered Facility and thus anyone applying for this role must be a US Citizen or have a valid Green Card. ***Offered Compensation is commensurate with experience. All done! Your application has been successfully submitted! Other jobs