Quality inspector jobs in Toms River, NJ - 172 jobs

The QA Technical Service Rep is responsible for the timely delivery of services as they relate to the quality assurance of Tremco's installed roofing systems within their respective region. $20-33/hour (not including prevailing wage) Benefits, upon satisfaction of applicable eligibility requirements, include but are not limited to: 401K with company match Company Pension Plan Health Insurance Paid time-off Mileage reimbursement Continuing education Duties/Responsibilities, Core knowledge: Lead Technician performing roof patch and repair as necessary and determined by the Quality Assurance Group on Tremco Incorporated roof systems (BUR, Modified Bitumen, Single Ply, Fluid Applied, etc.). Estimate material and labor quantities for roof patch and repair. Work with local WTI Field Representatives and/or Supervisors as required or necessary. Provide accurate and timely documentation to ensure that all work was completed properly and that the customer is fully satisfied. Conduct and foster professional and timely communication (via email, voicemail, in person) with the customers, sales reps, field staff, and internal company personnel on all work-related matters. Demonstrate working knowledge of all services provided. Perform any other duty and/or project as required or assigned by the QA Assurance Group. Skills, Qualifications, Experience, Special Physical Requirements: High school diploma or GED Prior roofing experience including patch and repair skills Knowledge and ability to use basic tools associated with commercial roofing Knowledge and experience monitoring and maintaining Quality Control Functional computer skills Safety training and OSHA knowledge with a commitment to safety at all times Understanding and ability to manage expenses Planning and organizational skills. Able to juggle multiple priorities and demonstrate good task management Work independently, as well as in a team environment, to solve problems and delegate assignments Excellent customer service skills and ability to build relationships Ability to climb up and down interior/exterior ladders to access roofs (minimum of 20 ft) and carry basic hand tools, equipment and/or material up to approx. 100 lbs. over long distances Capable of walking along roof top edges (no fear of heights, good balance, etc.) Ability to handle prolonged exposure to outside weather conditions (heat, cold, etc.) Ability to travel out of town including overnight travel Must have transportation and a valid driver's license Ability to work weekends and/or holidays if needed Ability to pass pre-employment drug test Ability to read, write and speak English The hourly rate for applicants in this position generally ranges between $20 and $33. This range is an estimate, based on potential employee qualifications, operations, needs, and other considerations permitted by law. Qualified applicants will receive consideration for employment without regard to their race, color, religion, national origin, sex, sexual orientation, gender identity, protected veteran status or disability.

Somerset County, NJ Hourly Rate: $20.00 - $23.00 1st Shift 7AM - 3PM 2nd Shift 3PM -11PM (Plus 10% differential for 2nd shift) Responsibilities: Inspect and verify incoming materials and components against specifications Detect and prevent defects or inconsistencies in the assembly line and collaborate with production teams for corrective actions Maintain accurate records of inspection results and communicate findings to supervisors and production staff Ensure all measuring equipment is properly calibrated and maintained Accurately document all inspection activities, non -conformances, and corrective actions in quality management systems Collaborate with the Quality Control Manager to refine inspection processes and implement continuous improvement initiatives Requirements High School Diploma or equivalent; technical or vocational training in quality control or a related field is preferred 2+ years of experience in quality within a manufacturing or assembly environment, preferably with electric products Strong attention to detail and a keen eye for identifying defects Ability to read and interpret engineering drawings, specifications, and technical documents Good communication skills and the ability to work collaboratively with projection and quality teams Knowledge in calibration and equipment maintenance Must be able to lift 50 lbs Benefits We offer a competitive & attractive compensation package including a base salary plus incentives Company subsidized medical & dental insurance Paid Time Off 401K savings plan including company match

Full-time Description Conduct Receiving, In-process and Final Inspections of Parts, Containers, Shelters, and Welded Structural Steel Fabricated Assemblies by performing Dimensional Inspection, VT, and NDE IAW AWS and Military Specifications. Perform wind, light, water leak, and paint performance tests. Witness electrical testing on all components. Sign each traveler line item as each task is performed and checked before movement to next process step to maintain traceability. Calibrate and Maintain TME and Manufacturing equipment. Complete Inspection Reports, and Sign Product Conformance Release Finished Product. Maintain Records of Acceptance to ISO9001 Standard. Report findings to supervisor. Job Summary: This position reports to the Quality Manager. The ideal candidate possesses a basic understanding of manufacturing, fabrication, assembly, and welding processes of Structural Steel Products. Ability to read different types of schematic drawings. Ability to use basic inspection equipment, prepare and write inspection reports. Responsibilities: · Accident prevention - actively identify, correct and/or report safety hazards to prevent accidents. · Actively identify and pursue cost reduction and efficiency/profit improvement opportunities. · Support the ISO 9001 Quality Management System and the Sea Box Quality Policy calling for self-inspection of your work product. · Determines quality and reliability standards by studying drawings and formulas; verifying specifications with engineering staff. · Perform NDE of Welds and Welding Processes IAW AWS, Military, and Customer Specifications. · Identifies raw material condition by inspecting materials samples; conducting inspections and physical tests of materials. · Identifies in-process product condition by inspecting samples during productions process; conducting in-process inspections and physical tests. · Determines disposition of finished products by collecting, classifying, analyzing, and interpreting production and quality data; determine product acceptability in comparison to specifications. · Determines acceptability or rework by conducting inspections and physical tests of reworked product. · Documents finished product status by recording and summarizing raw materials, in-process, and finished-product inspection and physical test data; updating quality assurance data based. · Maintains quality assurance operations by following quality assurance policies and procedures; reporting needed changes. · Contributes to team effort by accomplishing related results as needed. · Perform precision inspection with equipment such as calipers, micrometers, depth gauges, plug gauges and comparator · Performs other duties as assigned · Must be able to fulfill essential job function in a consistent state of alertness and safe manner. Why work for Sea Box? We offer benefits to our full-time employees that include: Health Insurance Dental Insurance Vision Insurance Basic and Voluntary Life Long-Term Disability Flexible Spending Accounts Employee Assistance Program Paid Time Off Paid Holidays, Bereavement, Jury Duty 401(k) with company match Employee Referral Program Employees are eligible for most benefits on the 1st of the month following date of hire. Salary Range: $40,000 - $55,000 Location: This position is onsite (non-remote) at the Company's corporate headquarters in Cinnaminson, NJ. This position may occasionally require working overtime and/or working outside of the Company's normal 8:30am - 5:30pm hours of operation. Requirements Experience: 3-5 years' work related experience. Education: High school diploma or equivalent. ASQ or AWS Certifications helpful. Salary Description $40,000 - $55,000

Job Title: Quality Compliance Associate Type: Contract Compensation: $26 - $36 per hour Contractor Work Model: Onsite Hours: 8/9 AM - 5/6 PM, Monday to Friday Industry: Pharmaceuticals, Sterile Injectable Products Responsibilities: + Under the oversight of the Associate Manager of Quality Assurance (QA) Compliance, this position will be responsible for establishing the internal QA review system to supervise the Pharmacovigilance Group (PVG) function, which is handled by a third-party vendor. + Additionally, the position is responsible for creating a QA system to notify the U.S. Food and Drug Administration (FDA) of illegitimate products, as and when needed. + This position will also review all finished product batches for compliance with applicable regulatory requirements and current Good Manufacturing Practice (cGMP) standards prior to release for commercial distribution, as needed. + Maintenance and/or improvement of the company's quality systems necessary to support GMP-related activities will also be required. + Prepare, review, and finalize Standard Operating Procedures (SOPs), Master Approval Process Procedures (MAPPs), internal guidelines, and review checklists to supervise the Pharmacovigilance Group (PVG) function of company products. + Coordinate with third-party PVG team to establish the standard review process of PVG reports generated for company products. + Prepare, review, and finalize SOPs, MAPPs, and internal guidelines for creating a QA system to notify the FDA of illegitimate products, as and when needed. + Coordinate and communicate with cross-functional teams (CFTs) to gather the required data and information to notify the FDA of illegitimate products. + Assist the Associate Manager of QA Compliance in notifying the FDA of illegitimate products within the FDA's pre-defined timeline. + As needed, conduct social media monitoring for any product quality or safety-related complaints and inform the third-party PVG team for further processing. + Compile and archive batch-related documents. Keep all GMP records in compliance with Good Documentation Practices (GDP). + Provide periodic updates to the immediate manager on quality-related concerns. Requirements: + Bachelor's degree in a scientific or related field. + Previous experience in a quality assurance or quality compliance role, preferably in a regulated industry such as pharmaceuticals, medical devices, or biotechnology. + Basic knowledge of Pharmacovigilance Group (PVG) processes, FDA Form 3911, SOPs, change control processes, Code of Federal Regulations (CFR), and Good Manufacturing Practice (GMP) regulations. + 1-2 years of experience in the pharmaceutical or biotechnology industry, with knowledge of cGMP regulations as they pertain to active pharmaceutical ingredients (API) and sterile finished drug products. Previous experience in Quality Assurance/Compliance is preferred. + Strong computer skills, including proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook). System One, and its subsidiaries including Joulé, ALTA IT Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law. #M3- #LI- #DI- Ref: #558-Scientific System One, and its subsidiaries including Joulé, ALTA IT Services, CM Access, TPGS, and MOUNTAIN, LTD., are leaders in delivering workforce solutions and integrated services across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible full-time employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan. System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

Night Owl Needed! Be the Quality Guardian of Our Growing Team - Competitive Benefits Package! Do you have a keen eye for detail and thrive in a fast-paced environment? Are you a night owl looking for a challenging and rewarding career with a comprehensive benefits package? Then we want YOU on our team! As a Quality Inspector (Night Shift) , you'll be the guardian of our quality standards in a great custom plastic manufacturing environment , ensuring every product meets our high expectations. You'll perform inspections, maintain records, and collaborate with the team to keep our production line running smoothly. This is your chance to: Be a key player in a rapidly growing company Work alongside a supportive and collaborative team in a great custom plastic manufacturing environment Develop your skills and knowledge in quality control Make a real difference in the quality of our products Here's a glimpse into your world: Additional $3 per hour shift differential Inspect parts and ensure they meet specifications Maintain detailed records and document processes Help develop and implement quality standards And more! To be successful, you'll need: 3+ years of experience as a Quality Inspector A high school diploma (or equivalent) Strong attention to detail and a commitment to quality Excellent analytical and problem-solving skills Ability to work independently and as part of a team Willingness to learn and continuously improve Familiarity with ISO 9001:2015, cGMP standards a plus Bonus points if you have: Experience working in a cleanroom environment Knowledge of SQF standards Experience with gauge calibration or training others Benefits: Medical, Dental & Vision Insurance: We offer comprehensive health coverage options to keep you and your loved ones well. Company-Paid Life Insurance: We've got your back, with life insurance coverage included. Optional Voluntary Benefits: Tailor your benefits package to your needs with a variety of additional options. Paid Time Off & Paid Holidays: Recharge and relax with paid time off and holidays. 401(k) with Company Match: Save for your future with our retirement plan and a company match on your contributions. Profit Sharing: Share in the company's success with our profit-sharing program. Ready to join our growing team? Apply today and let's make quality happen - together!

Changing lives. Building Careers. Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what's possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care. The Lead Quality Inspector serves as a Lead Associate, Quality Inspector for the Plainsboro Manufacturing Site, Collagen Manufacturing Center (CMC). The lead associate is responsible for performing and/or scheduling quality assurance inspections on purchased components, manufactured sub-assemblies and final product. Expectations are to be familiar with and be able to measure critical dimensions as well as to train new quality inspectors and provide guidance to current quality inspectors. Lead Associate, Quality Inspector will perform all duties in accordance with the requirements of overall corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory agencies. This is for a Weekend Lead, the Shift is 12 hours on Friday, Saturday and Sunday from 6am to 6:30pm (will be compensated for 40 hours per week) Job Responsibilities Oversee daily activities in the QC department. Prepare the QC Inspection schedule to ensure that all manufacturing areas are covered in order to meet production schedule. Reports any non-conformances in timely manner. Support NCs and CAPA investigations as required. Assist with product flow between departments. Interface with Manufacturing department in order to coordinate inspections of completed product to ensure the inspections are done in a timely manner. Initiate and /or propose revisions to standard operating procedures involving new processes or process improvements. Train QC Inspectors as required. Perform inspections (incoming, in-process, first article, etc.) by using a variety of inspection measuring equipment to determine acceptance or rejection of material or parts. Interpret and work within the guideline of drawings, specifications, charts, procedures, and other date to determine product or material acceptance. Read and interpret sampling plan as per the American National Standard Institute (ANSI). Oversees physical and electronic quarantine locations. May also perform other related duties, responsibilities, and special projects as assigned. DESIRED MINIMUM QUALIFICATIONS Minimum of 5+ years' experience in document and promotional materials management using electronic document management systems or with manual systems using electronic document storage. Minimum of 5+ years' experience in a Quality Systems / Regulatory Compliance environment with a working knowledge preferably in the medical device, diagnostics or pharmaceutical industries. Familiarity with FDA regulations and ISO series of quality standards preferred. Capable of both written and verbal effective communication skills. Proficient in the Microsoft Office suite of products. Proficient in Oracle R12/Agile preferred. Salary Pay Range: $26.21 - $35.38 USD Hourly Our salary ranges are determined by role, level, and location. Individual pay is determined by several factors including job-related skills, experience, and relevant education or training. In addition to base pay, employees may be eligible for bonus, commission, equity or other variable compensation. Your recruiter can share more about the specific salary range for your preferred location during the hiring process. Additional Description for Pay Transparency: Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance, and savings plan (401(k)). Subject to the terms of their respective policies and date of hire, Employees are eligible for the following ******************************************* Integra LifeSciences is an equal opportunity employer, and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status. This site is governed solely by applicable U.S. laws and governmental regulations. If you'd like more information on your rights under the law, please see the following notices: EEO Is the Law | EOE including Disability/Protected Veterans Integra LifeSciences is committed to provide qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the ADA. If you have difficulty using our online system due to a disability and need an accommodation, please email us at ***********************. Unsolicited Agency Submission Integra LifeSciences does not accept unsolicited assistance from search firms for employment opportunities. All CVs/resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. A formal written agreement is required before engaging any agency, and it must be executed and authorized by the Vice President, Talent Acquisition. Where agency agreements are in place, introductions (the initial sharing of a candidate's name, resume, or background) are position-specific and may only occur within the scope of that approved agreement. Please, no phone calls or emails. Integra - Employer Branding from Integra LifeSciences on Vimeo

Geo-Technology Associates, Inc. (GTA) is seeking a STRUCTURAL STEEL SPECIAL INSPECTOR with 2-7 years of relevant test experience for work in the Somerset, NJ area. SPECIAL INSPECTOR RESPONSIBILITIES: Verify construction is being completed in accordance with all plans and specifications. Carry out inspections, sampling, and testing. Coordinate with clients, general contractors and GTA Project Managers. Record and document construction in daily field reports Contribute to the generation of technical reports and special inspection summaries. Oversee, train, and mentor junior/less-experienced staff. SPECIAL INSPECTOR REQUIRMENTS: At least one of the following: NJ DCA/ICC Structural Steel Bolting NJ DCA/ICC Structural Steel Welding CWI Certifications preferred (not required): NJ DCA/ICC (Soils, Structural Masonry, Reinforced Concrete, etc.) ACI Certified Construction Special Inspector (CCS), ACI Concrete Field-Testing Technician Grade 1, ACI/CRSI Certificate for Post-Installed Concrete Anchor Installation Inspector Own reliable transportation, valid driver's license and satisfactory driving record. Authorized to work in the U.S. Ability to work independently and as a part of a team Ability to lift up to 75 lbs. unaided and up to 100 lbs. with assistance: frequent bending, hammering and repetitious movements. Proficient with Microsoft Word, Excel, PowerPoint and Adobe We ensure nondiscrimination and equal employment opportunity in all programs and activities in accordance with Title VI of the Civil Rights Act of 1964, and all revisions and addendums thereof. #LI-Onsite #breezy GTA

Senior Construction Inspector STV's growing Transportation group in our Lawrenceville or Newark, NJ office is seeking Construction Inspector(s) with highway, bridge, and/or rail experience for multiple long term $25M - $1B bridge, highway and rail reconstruction projects. These individuals should possess inspection experience with asphalt, concrete, rail and steel inspection experience, and the appropriate certifications. If you have a High School Diploma/GED, NICET, NJSAT Asphalt, ACI Concrete certification, and/or an AS or BS in Civil Engineering, and enjoy working outdoors, we want to hear from you. Minimum Required Skills & Relevant Experience: Bachelor's Degree in Civil, Structural Engineering or Construction Management; or equivalent experience 4+ years of construction inspection experience with NICET 2 8+ years of construction inspection experience with NICET 3 or 4 or a PE Experience on roadway/highway, bridge, drainage, utility or other municipal projects. Have experience with DRPA, NJ Transit, NJ Turnpike, NJDOT and/or PANYNJ projects Familiar with construction management software (CapEx, Site Manager, eBuilder, BIM 360) Be able to work nights and weekends, as needed Preferred Skills & Relevant Experience: Minimum of 8 years providing construction inspections for highway or bridge projects $10M or greater Have combination of NJSAT, ACI, and Rutgers TCC, certifications Compensation Range: $75,416.00 - $100,554.00 Don't meet every single requirement? Studies have shown that women and people of color are less likely to apply to jobs unless they meet every single qualification. At STV, we are fully committed to expanding our culture of diversity and inclusion, one that will reflect the clients we serve and the communities we work in, so if you're excited about this role but your past experience doesn't align perfectly with every qualification in the job description we encourage you to apply anyways. You may be just the right candidate for this or other roles. STV offers the following benefits • Health insurance, including an option with a Health Savings Account • Dental insurance • Vision insurance • Flexible Spending Accounts (Healthcare, Dependent Care and Transit and Parking where applicable) • Disability insurance • Life Insurance and Accidental Death & Dismemberment • 401(k) Plan • Retirement Counseling • Employee Assistance Program • Paid Time Off (16 days) • Paid Holidays (8 days) • Back-Up Dependent Care (up to 10 days per year) • Parental Leave (up to 80 hours) • Continuing Education Program • Professional Licensure and Society Memberships STV is committed to paying all of its employees in a fair, equitable, and transparent manner. The listed pay range is STV's good-faith salary estimate for this position. Please note that the final salary offered for this position may be outside of this published range based on many factors, including but not limited to geography, education, experience, and/or certifications.

C & L Inspection was built on a mission to be the most trusted US Services Company delivering top-notch performance with uncompromising integrity. This way of thinking has set us above the competition. We are looking for knowledgeable, safety minded people to join our team as we grow. Job Title: Sr. Craft InspectorLocation: Middletown, PA (Surrounding Areas) Duration: 03/010/2024-12/31/2024Job Description:· The Sr. Craft Inspector performs the quality control (QC) function over the contractor's work as a part of the Company's quality assurance program and is responsible for the completion of all activities in his area of assignment in accordance with the appropriate Company specifications and the approved for construction drawings. Duties may include, but are not limited to:· Right-of-Way Clearing and Grading' Ditching, Stringing, and Bending' Lowering, Padding, and Backfilling' Road Boring' Tie-ins' Clean-up' inspection.· The inspector works under the direction of the Chief Inspector may be assigned additional responsibilities as required· The inspector provides quality assurance through inspection of work and materials for conformance to requirements.· The inspector is to complete required documentation (i.e. reports and log books) in a timely, concise, and accurate manner.· Familiarization with the approved construction drawings and the appropriate Company specifications in order to assure the work is performed in accordance with those requirements.· Familiarization with Contract documents (Agreement) as it relates to his or her duties on the project· Familiarization with applicable industry and regulatory codes' Familiarization with the Pre-Job Notes · Familiarization with the sequence of the work and plan inspection of upcoming activities· Report safety issues to the Chief Inspector and Safety Inspector· Drawing markups for as-built records· Hydrostatic tests and any test failures· Quantity, size, wall thickness, grade, heat number, other pipe nomenclature and pipe coating, and its location· Understanding the basics of pipe alignment, welding, and its inspection (specialized inspectors are required for the actual inspection)· Condition of ditch bottom Rocks, roots, clay, and other debris· Lifting and lowering in equipment· Understanding, monitoring, assessing, and reporting on painting and coating activities and items including but not limited to:· Vendor Product data sheet utilization· Proper application of paint and/or coating· Proper setup and use of holiday detector / jeep Requirements:· API 1169· OSHA 10 or OSHA 30· 10 years hands on experience· 5 years supervisor experience C & L Inspection offers a full slate of Inspection, Construction Management and Engineering personnel to the Petroleum, Natural Gas and Telecom Industries. We surpass others in the industry by providing the newest technology, training and support that is unequaled. Working together with our inspectors and clients, our team strives to set a new bar for the Pipeline & Utilities Inspection industry. We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

Quality Assurance Technician- 3rd (11:30pm-8:00am) Pay Range: $25-$28/hr. Your Role at Prestone Our Freehold, NJ Plant is looking for a self-motivated, reliable, and detail-oriented Quality Assurance Technician to be part of our growing team. People that take the initiative and action to pursue production line goals and complete tasks. People that are thorough and accurate in accomplishing tasks. People that hold a high standard for safety, quality, production, and teamwork. If you are this person, we encourage you to apply! What You'll Be Doing Review of production line parameters and performance for adherence to Company Standard Operating Procedures, Quality Guidelines and Facility Procedures Testing samples for physical and chemical properties for adherence to Quality Specifications Include raw materials and Finished Products Generating and shipping samples for outside analytical testing Maintenance of the Quality Retain Program Responsible for laboratory cleanliness and organization Responsible for documentation of testing, holding product, internal investigations and root cause analysis Ordering lab supplies Maintenance of Instrument Calibration Program Other duties as assigned What You'll Bring High school diploma or equivalent 2-3 years of hands on Quality Systems experience, manufacturing preferred Must be able to work 3rd shift Ability to work in a fast paced, time sensitive environment Able to lift to 50 pounds periodically throughout the manufacturing shift and meet physical requirements of position including lifting, bending, standing for extended periods, reaching with both hands/arms, ability to visually inspect product Excellent math and problem solving skills Excellent communication skill set (verbal, written, etc.) Bilingual English/Spanish preferred What You Will Get PRESTONE offers a competitive salary and comprehensive benefits including health, wellness, dental, vision, life, and disability insurance. You can plan for your future with PRESTONE's retirement savings options including employer match. PRESTONE also recognizes the importance of continuing education and offers Education Assistance to our employees to encourage continued personal development and growth.

Job Description 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 PositionExperienceEducationEssential Duties and Major ResponsibilitiesQuality Technician I1-2 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 II3-6 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 III7+ 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. Powered by JazzHR lX14NZcm8H

Changing lives. Building Careers. Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what's possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care. The **Quality Inspector II** will be responsible for performing quality assurance inspections on purchased components, manufactured sub-assemblies and final product. The Quality Inspector will perform all duties in accordance to the requirements of overall corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory agencies. Expectations are to be familiar with and able to measure critical dimensions. **ESSENTIAL DUTIES AND RESPONSIBILITIES** + Perform inspection by using a variety of inspection measuring and test equipment to determine acceptance or rejection of material or parts. + Perform first article, incoming/receiving, and in-process inspections of materials or parts; determine acceptance or rejection after inspection and/or testing of materials, parts, and/or equipment. + Interpret and work within the guideline of drawings, specifications, charts, procedures, and other data to determine acceptance or rejection of materials. + Read and interpret sampling pan as per the American national standard institute (ANSI), + Assist in the review and disposition of non-conforming material and customer returned material, including rework, scrap, and return to vendor. + Maintain accurate and current inspection and/or testing records such as nit not limited to Material Certifications, Inspection/Test Results and reports, Certificates of Conformance, Rejection reports/tags, as required by applicable procedure and/or specification. + Coordinate and inform other departments of inspection and/or testing status in support of production and project goals and initiatives. + Promote and participate in continuous improvement initiatives. + Responsible for the maintenance of appropriate conditions of all quarantine locations. + Maintain the QC inspection areas in an orderly fashion conducive to carrying out safe and efficient inspections and procedures. + Inspection requirements include training and working in classified clean rooms as necessary to perform in process inspections. + Maintain records of inspection and all testing performed on the appropriate test records. + Perform line clearances and quality reviews in manufacturing, labeling, or other assigned areas during manufacturing activities. + Identify and implement opportunities for continuous improvement, including document revisions in order to maintain accurate SOPs. + Provide quality support to various departments as needed, e.g. engineering, product development, etc.) + Assist in training new associates according to the Quality System Regulations and company SOPs as applicable. + May also perform other related duties, responsibilities, and special projects as assigned. **DESIRED MINIMUM QUALIFICATIONS** + Associate degree in science is preferred. + 3-7 years of relevant GMP/GLP experience specific to incoming, line clearance, in-process, and finished goods inspections in pharmaceutical or medical device industry. + QA experience in the medical device industry preferred. + Must have strong written and verbal communication skills. + Strong organizational skills, self-directed, strong problem solving and interpersonal skills. + Knowledge of CAPA, Validations, Change Control, preferred. + Working knowledge of ISO 13485, 21CFR820 FDA QSR, and cGMP. + Knowledgeable in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) preferred. Salary Pay Range: $21.12 - $27.98 USD Hourly Our salary ranges are determined by role, level, and location. Individual pay is determined by several factors including job-related skills, experience, and relevant education or training **.** In addition to base pay, employees may be eligible for bonus, commission, equity or other variable compensation **.** Your recruiter can share more about the specific salary range for your preferred location during the hiring process. Additional Description for Pay Transparency: Subject to the terms of their respective plans, employees and/or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs: medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance, and savings plan (401(k)). Subject to the terms of their respective policies and date of hire, Employees are eligible for the following ******************************************* Integra LifeSciences is an equal opportunity employer, and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status. This site is governed solely by applicable U.S. laws and governmental regulations. If you'd like more information on your rights under the law, please see the following notices: EEO Is the Law (********************* | EOE including Disability/Protected Veterans (******************************************************************** Integra LifeSciences is committed to provide qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the ADA (************************************************** . If you have difficulty using our online system due to a disability and need an accommodation, please email us at ***********************. Unsolicited Agency Submission Integra LifeSciences does not accept unsolicited assistance from search firms for employment opportunities. All CVs/resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. A formal written agreement is required before engaging any agency, and it must be executed and authorized by the Vice President, Talent Acquisition. Where agency agreements are in place, introductions (the initial sharing of a candidate's name, resume, or background) are position-specific and may only occur within the scope of that approved agreement. Please, no phone calls or emails. Integra - Employer Branding from Integra LifeSciences on Vimeo (*****************************************

Job Description Quality Assurance Inspector Inspects high reliability printed circuit board assemblies, cables, and wires under a microscope. 2 years inspection experience working with Military / Avionics / Medical IPC Class 3 assemblies required. Knowledge and certification to any of the following industry Standards a plus: IPC-A-610, IPC J-STD-001 Quality Assurance Internal Auditor Knowledgeable in ISO-9001, ISO-13485 and AS9100 standards Internal auditing experience, assessments and reporting Completion of AS9102 First Article Inspection Reports Data management, data entry

Job Description Date 05/2025 Title Technician, QC Analytical Department Quality Control Reports to Manager, Chemistry Laboratory FLSA (Exempt or Non-Exempt Non-Exempt Role Overview We are seeking a detail-oriented and skilled Laboratory Technician to join our Chemistry Lab division. The successful candidate will support physical and chemical testing of raw materials, R&D, Method development / Stability and finished products using various analytical instruments / Equipment's and techniques to ensure compliance with internal specifications. Areas of Responsibility Prepare samples, Mobile Phase, Buffer solution, Dissolution Media, Sample digestion etc. for analysis according to standard operating procedures (SOPs) or as per suitable method provided by senior management. Perform chemical analyses using techniques such as UV-Vis, Dissolution, FTIR, titration, Microwave Digestion system, TOC water sample and physical testing using apparatus and equipment's' such as Disintegration, Bulk Density, Tap Density, Loss on Drying, Karl Fisher, etc. Accurately record, and report test results in compliance with GLP/GMP standards. Calibrate, maintain, and troubleshoot laboratory instruments and equipment. Example-pH meter, Weighing Balance, etc. Maintain a clean, organized, and safe work environment. Assist in the development and validation of analytical methods under supervision. Document laboratory activities and results in lab notebooks, Raw Datasheets, and on computer system with validated excel. Dispose of chemical waste properly and follow all environmental, health, and safety (EHS) protocols. Participate in quality audits and continuous improvement initiatives. Must be able to work extended hours as needed and occasional weekends. Other duties and responsibilities as assigned. Other Responsibilities Including Safety: Works in a safe and responsible manner to create an injury-free and incident-free workplace. Complies with all job-related safety and other training requirements. Keeps management informed of area activities and of any significant problems. Requirements Education & Qualification: Associate's or Bachelor's degree in Chemistry, Biochemistry, or related scientific field. 0-3 years of hands-on experience in an analytical chemistry lab (academic or industrial). Strong understanding of laboratory safety and quality standards (e.g., GMP, GLP, ISO). Good problem-solving and organizational skills with attention to detail. Ability to work independently and collaboratively within a team. Certifications, Licenses, Credentials: N/A Skills & Ability Ability to maintain integrity and honesty at all times and to communicate with transparency. Ability to work independently or as part of a team. Solid understanding of cGMP's and GLP and is familiar with 21 CFR Part 11 Strong working knowledge of Microsoft Word, Excel. Good documentation practices and able to write simple, clear reports Meets commitments on time and practices time-management skills Seeks to identify continuous improvement needs Experience with Shimadzu LC2010, Nexera, GC2010, Thermo ICP-MS, Labsolution and Waters Empower Lab Software a plus. Physical Requirements (lifting, etc.): May execute 90%-100% of their work at the bench level either standing or sitting on a stool. Uses hands to finger, handle, feel, or operate objects or controls, lifting to waist height and/or above shoulder height, frequent bending from the waist, or squatting, walking short distances and leaning over equipment as well as kneeling on the floor to clean under the equipment. Must be able to wear all PPE including a lab coat, face mask, booties, gloves, safety glasses/goggles, and respirators. On occasion may need to lift up to 35 lbs. Ability to navigate office, lab, and/or plant floor working environments. Work Environment (Office, Warehouse, temperature extremes, etc.): Approximately 80% of work performed in a laboratory environment which may have unpleasant odors or hazardous conditions. Temperatures can be moderate, exposure to dust, odors, noise, and fumes. The noise level is usually moderate. Employees can be exposed daily to chemicals and cleaning agents. The above statements are intended to describe the general nature and level of work being performed by people assigned to this job. They are not intended to be an exhaustive list of all the job responsibilities, duties, skill, or working conditions. In addition, this document does not create an employment contract, implied or otherwise, other than an "at will" relationship. USPL is proud to be an Equal Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy), sexual orientation, gender identity or expression, national origin, age, genetic information, disability, protected veteran status, or any other characteristic protected by applicable local, state, or federal law. Benefits And Compensation: Our benefits are designed to help you move forward in your career, and in areas of your life outside of USPL. From health and wellness benefit options including: medical, dental, vision, short and long term disability, basic life insurance, supplemental life insurance, AD&D insurance. We also offer a matched 401(k) savings plan. Employees have the opportunity to receive compensation in the form of premium pay such as overtime, shift differential, holiday pay, sick time, etc. Newly hired employees receive up to 10 days of vacation the first year, which grows to 12 days starting the second year of employment. Office Hours: 8:30 AM - 5:00 PM 9:00 AM - 5:30PM

Quality Assurance Technician Objective: Inspects and tests materials and products for form, fit, and functions at various stages of production, including incoming, in-process, and final. Compiles and evaluates data to determine and maintain quality and reliability of products. Essential Duties Performs receiving inspection of incoming material using various measuring devices such as comparators, Calipers, micrometers, meters, etc. Verifies documentation such as picking lists, vendor supplied test data, purchase orders, etc. Interprets and utilizes inspection procedures, blueprints, schematics, assembly drawings, work orders, specifications, and process documentation to perform quality tasks Confers with management, engineering, and production to determine quality and reliability standards. Selects appropriate inspection sample and performs appropriate inspections based on established inspection procedures or creates new procedures if necessary. Prepares charts, graphs, reports, and other documentation using various software applications. Work closely with production departments to assure manufactured products maintain conformance. Practices good housekeeping and safety procedures and adheres to all company policies. Knowledge, Skills and Abilities: To perform the job successfully, an individual should demonstrate the following knowledge, skills and abilities: Ability to verify parts meet specifications, visual inspection, confirm color codes. Ability to interpret drawings, ECN's, sketches, schematics, etc. Tools: micrometers, calipers, CMM's, depth mic's, etc. PC software knowledge ( Microsoft Office Suite) Able to analysis problems and provide solutions. Ability to work close with production personnel provide guidance and possibly training to enhance quality. Qualifications Education/ Experience: 5+ years QA experience. Or 3 years + Associates degree in related field Or 1 year + Bachelors degree in related field Additional Information All your information will be kept confidential according to EEO guidelines.

Country: United States of America Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: U.S. citizenship is required, as only U.S. citizens are authorized to access information under this program/contract. Security Clearance: None/Not Required Pratt & Whitney is working to once again transform the future of flight-designing, building and servicing engines unlike any the world has ever seen. And because transformation begins from within, we're seeking the people to drive it. So, calling all curious. Come ready to explore and you'll find a place where your talent takes flight-beyond the borders of title, a country or your comfort zone. Bring your passion and commitment and we'll welcome you into a tight-knit team that takes our mission personally. Channel your drive to make a difference into shaping an organization and an industry that's evolving fast to the future. At Pratt & Whitney, the difference you make is on display every day. Just look up. Are you ready to go beyond? We have an immediate need for Quality Assurance Inspector 1st Shift (onsite) FUNCTION: Perform dimensional and visual inspections following standardized methods and established techniques, which may involve surface plate work, or standard measuring techniques to verify accuracy of parts, tools, gages or other equipment. What You Will Do: Accept or reject material based on findings. Work from applicable written inspection procedures drawings and other pertinent instructions to plan and perform dimensional and visual inspection on parts tools, gages and other equipment, accepting material or referring for rework or quality review based on findings. Use a variety of fixed and variable measuring instruments including automated measuring machines where program instructions are well defined to check dimensions and record results. Perform necessary mathematical computations to determine extent of nonconformance and complete appropriate paperwork. Follow proper procedures to perform in-line checks and verification of dimensions and make sure that operation sheets are followed. Recognize need and arrange for repair or replacement of equipment used in performing the work as necessary. May be assigned to carry out tasks, not specifically listed within the scope and skill level of this job description in support of department objectives. Qualifications You Must Have: High School Diploma or GED equivalent. U.S. citizenship is required, as only U.S. citizens are authorized to access information under this program/contract. Must be able to make arithmetical calculations involving the use of decimals and fractions, angles, and apply substitution of numbers in simple formulas. One-year relevant experience working from drawings and use precision measuring equipment such as Vernier calipers and height gages, indicators, size blocks and sine bars. Qualifications We Prefer: Familiarity with inspection tooling and techniques. Strong communication skills and the ability to work within a group setting and interface directly with shop floor operators and inspection personnel. Knowledge / experience with quality systems and standards such as AS9100. Proficient in the use of continuous improvement tools, such as robust root cause analysis (RRCA) and principles of lean manufacturing. ASQ - CQE a plus. Qualifications We Value: In compliance with the collective bargaining agreement, priority consideration is given to candidates who are INTERNAL (and recall) to the Pratt & Whitney IAM Bargaining Unit members of District Lodge 26 and Affiliated Locals 700 and 1746 (Connecticut Operations). Learn More & Apply Now! Must be a U.S. Citizen. This position may require access to systems/tools that are restricted to individuals who possess US citizenship. Pratt & Whitney in East Hartford, CT is a FAA regulated facility and as such under the U.S. Departments of Transportation's Federal Aviation Administration (FAA). This position is considered safety sensitive in accordance with FAA Guidelines. Candidate will be subject to drug and alcohol testing per FAA's regulation 14 CFR part 120, as well as 49 CFR part 40. This role is: • Onsite: Employees who are working in Onsite roles will work primarily onsite. This includes all production and maintenance workers, as they are essential to the development of our engines. Candidates will learn more about role type and current site status throughout the recruiting process. For onsite and hybrid roles, commuting to and from the assigned site is the employee's personal responsibility. As part of our commitment to maintaining a secure hiring process, candidates may be asked to attend select steps of the interview process in-person at one of our office locations, regardless of whether the role is designated as on-site, hybrid or remote. Hired applicants may be eligible for benefits, including but not limited to, medical, dental, vision, life insurance, short-term disability, long-term disability, 401(k) match, flexible spending accounts, flexible work schedules, employee assistance program, Employee Scholar Program, parental leave, paid time off, and holidays. Specific benefits are dependent upon the specific business unit as well as whether or not the position is covered by a collective-bargaining agreement.Hired applicants may be eligible for annual short-term and/or long-term incentive compensation programs depending on the level of the position and whether or not it is covered by a collective-bargaining agreement. Payments under these annual programs are not guaranteed and are dependent upon a variety of factors including, but not limited to, individual performance, business unit performance, and/or the company's performance.This role is a U.S.-based role. If the successful candidate resides in a U.S. territory, the appropriate pay structure and benefits will apply.RTX anticipates the application window closing approximately 40 days from the date the notice was posted. However, factors such as candidate flow and business necessity may require RTX to shorten or extend the application window. RTX is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or veteran status, or any other applicable state or federal protected class. RTX provides affirmative action in employment for qualified Individuals with a Disability and Protected Veterans in compliance with Section 503 of the Rehabilitation Act and the Vietnam Era Veterans' Readjustment Assistance Act. Privacy Policy and Terms: Click on this link to read the Policy and Terms

Take Your Construction Career to the Next Level! Are you ready to be challenged, make a difference, and experience professional growth in your career? Kleinfelder's Construction Services team is looking for you! From construction management and observation/inspection services to laboratory testing and materials and forensic engineering, our Construction Services market helps to develop and maintain America's infrastructure and supply chain and is a recognized industry leader with more than 25 accredited laboratories. Step into Your New Role Kleinfelder's Mt. Laurel, NJ office is seeking a Laboratory Construction Materials Testing Technician to join our team. We provide construction inspection and material testing services to a broad range of local and national clients. We are looking for individuals who are interested in in joining a dynamic team and building their career in the field of construction inspection and materials testing. We're looking for a person with strong initiative, who will perform routine to complex testing of construction materials in the laboratory, to verify conformance to construction plans and specifications and geotechnical engineering purposes. The Laboratory Technician will manage all activities related to performance of laboratory testing in support of the Mount Laurel Geotechnical and Construction Materials Engineering and Testing Laboratory. They will meet agreed upon project deadlines by performing testing; coordinating with superiors to manage workload. They will correctly perform testing, calibrations, and calculations and computations by implementing and maintaining the requirements of the Kleinfelder Quality Management System. Works moderately independently on day-to-day activities, testing, and reporting. The successful candidate will be a valuable asset to the operations of the Mount Laurel CoMet team. Responsibilities: * Supervise operational personnel (laboratory staff), including resource coordination, internal quality control, and management of deliverables.• Communicate with coworkers to successfully and profitably deliver laboratory services on a consistent basis.• Responsible for making sure project deadlines are met by providing proper scheduling, coordination, and organization of items to be tested and available resources.• Responsible to perform routine to complex lab testing including soils, aggregates, and concrete.• Responsible for performing the testing, documentation, computations, and quality review in accordance with Kleinfelder's Quality Management System Manual and applicable testing standards (e.g. ASTM, AASHTO, etc.).• Ensures that laboratory equipment is properly maintained and calibrated in accordance with internal procedures. * Maintenance of Kleinfelder's local lab accreditations. Position Requirements: * Ability to work independently and as a team member, maintaining composure, and working effectively in a high-pressure environment with changing priorities.• Must have excellent interpersonal, verbal, and written communication skills. • Able to use a company provided laptop or tablet computer and a working knowledge of MS Office programs (e.g. Word, Excel, Outlook, etc.).• Organization and multi-tasking ability. • A good work ethic, attention to detail, and high level of personal integrity. • Authorization to work in the United States. Preferred Shills / Experience: American Concrete Institute (ACI) certifications: * Aggregate Testing Technician - Level 1 or 2 * Aggregate/Soils Base Testing Technician * Concrete Strength Testing Technician * Concrete Field-Testing Technician - Grade 1 * Concrete Laboratory Testing Technician - Level 1 or 2 The successful candidate will be encouraged to expand their skills and certifications through company provided training and mentoring. This is a career opportunity to become a member of a highly successful, fast paced team with a steady and growing backlog of large projects. Must be able to use a computer and a general knowledge of MS Office including Word, Excel, and Outlook is required. Must have own vehicle, a valid driver's license and clean driving record required. Majority of work will be at the Irving Office Laboratory but must be willing to travel locally as required to fulfill project assignments. Education: High school diploma or equivalent required. Move Forward with Kleinfelder Kleinfelder has been connecting great people to the best work since 1961. We are engineers, scientists, and construction professionals providing solutions that improve our clients' transportation, water, energy, and other private infrastructure. As a responsive, cross-disciplinary team of bright, curious, and innovative problem-solvers, we are dedicated to doing the right thing, every day, on every project from over 85 offices in the US, Canada, and Australia. Connecting great people to the best work is our purpose - together, we deliver. Progress with an Employer that Values You Kleinfelder is an inclusive organization free from discrimination. We are a stronger organization when we are a diverse workforce and believe that through diversity, equity, and inclusion comes creativity, innovation, and unity. We are proud to offer the following: Benefits: Kleinfelder offers an excellent compensation and benefits package, including: medical, dental, vision, life insurance, 401(k) plan, and paid holidays. Career Development: We are committed to investing in the professional development of our staff, offering each employee every opportunity to grow, develop, and take control of their career paths. We support these efforts through reimbursements for continuing education as well as many of the expenses associated with trainings and certifications, and opportunities for career development through our internal Mentoring Program. Equal Opportunity: Kleinfelder is an Equal Opportunity Employer - Minorities/Women/Disabled/Veterans. (Compliant with the new VEVRAA and Section 503 rules) NOTICE TO THIRD PARTY AGENCIES Please note that Kleinfelder does not accept unsolicited resumes from recruiters or employment agencies. In the absence of a signed Recruitment Fee Agreement, Kleinfelder will not consider or agree to payment for any referral compensation or recruiter fee. In the event a recruiter or agency submits a resume or candidate without a previously signed agreement, Kleinfelder explicitly reserves the right to pursue and hire those candidate(s) without any financial obligation to the recruiter or agency. Any unsolicited resume, including those submitted to hiring managers, are deemed to be the property of Kleinfelder.

Job DescriptionOVERVIEW: Quality Control Technician:The Quality Control Technician will play a critical role in ensuring products are packaged correctly and meet quality standards before they are shipped to customers. The primary objective of the Quality Control Technician - Manufacturing is to identify and rectify defects or deviations from established quality criteria to maintain high product quality. This position runs Monday - Friday, with the following shifts: 2nd Shift: 2:00 PM - 10:30 PM 3rd Shift: 10:00 PM - 6:30 AM QUALIFICATIONS: Quality Control Technician: High school diploma or equivalent qualification. Certification in quality control is preferred. Must have food manufacturing experience. A minimum of 2 years' experience in a similar role. Excellent knowledge of MS Office. Good math, technical, and communication skills. Strong understanding of quality control standards and testing techniques. KEY RESPONSIBILITIES: Quality Control Technician: Perform thorough inspections of raw materials, components, and finished products to check for defects, non-conformities, and deviations from quality standards. Work closely with production teams to ensure that manufacturing processes are in compliance with quality standards and are carried out correctly. Inspect finished produced goods to ensure their quality and adherence are up to specifications. Keep detailed records of inspections, testing results, and any deviations from the quality standards up-to-date and maintained. Reject all products and materials that fail to meet quality expectations. Collect and take samples of production batch to ensure products are meeting standards. Identify opportunities for process improvement and suggestions on changes to enhance efficiency and product quality. Ensure that inspection and testing equipment are regularly calibrated to maintain accuracy and reliability. Investigate the root causes of quality issues, collaborate with cross-functional teams, and recommend corrective and preventive actions to prevent future occurrences. Conduct internal audits of manufacturing processes and procedures to ensure ongoing compliance with quality standards and regulations. Maintain open and effective communication with production staff, quality assurance teams, and management to ensure everyone is aligned on quality goals and expectations. Prioritize safety in the manufacturing environment, ensuring that quality control activities are carried out safely and in accordance with safety protocols. Other duties as assigned. Onsite Personnel is an equal opportunity employer committed to hiring a diverse workforce in an inclusive culture environment. Onsite Personnel does not discriminate based on disability, veteran status or any other basis protected under federal, state, or local laws

Job Title: QA Inspector (3rd Shift, Tuesday-Saturday) Job Type: Full-Time About Us: As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates' purpose is to put better health within reach, every day for millions of patients around the world. We are a trusted, reliable partner and dependable source of over 760 high-quality generic, specialty and branded pharmaceutical products that hospitals, physicians and pharmacists need to treat their patients across North America, the Middle East, North Africa and Europe. Through our global footprint of 30+ manufacturing plants, 8+ R&D centers, and 9,000+ empowered employees, we are committed to making high-quality medicines accessible to the people who need them. Description: We are committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds. We are seeking a talented and motivated QA Inspector to join our team for monitoring in-process product quality for Filling and Inspection and Packaging of parenteral products. Key Responsibilities: * Regular and predictable onsite attendance and punctuality. * Performs in-coming tasks which include pallet checking, raw material sampling, review of test results, release of components, raw materials and production supplies. * Contacts QA Coordinator or QA Supervisor for daily line assignments. * Samples/Checks/Verifies Controlled Substances during in-coming monitoring and raw material sampling. * Must pass frocking qualification for controlled areas and pass the respirator requirements for sampling raw materials * Samples using analytical instrumentation such as Analytical balances, glove boxes and compressed gases. * Be able to push pallet(s) of raw material with the use of a pallet jack * Maintains good housekeeping and safe working conditions. * Accurately and clearly documents sampling/ inspection/test results in accordance to department and site SOPs. * Performs other duties to support production or validation as determined by QA Supervisor. * Participates in rotation for weekend coverage to support production. May work flexible hours and overtime on a short notice to support production. Qualifications: We value the skills and experiences candidates bring to the table. While we have listed some qualifications below, we encourage candidates to apply even if they do not meet all of them: * Associate's degree in science OR Bachelor's Degree with 0-2 years applicable laboratory, pharmaceutical manufacturing, or related experience. * 0-2-year applicable laboratory or pharmaceutical production experience (QA preferred). * Possesses proficient mathematical skills (addition, subtraction, multiplication, division, algebra, unit conversions, rounding significant figures, dividing polynomials, solving rational equations). * Familiar with cGMPs, EU, CFR and the USP * Demonstrates good attention to detail and accuracy * Good organizational skills and ability to multi-task and perform work in a timely manner * Demonstrates ability to work in a team environment with good communication skills and ability to communicate effectively with peers, department management and production personnel * Knowledge of computer systems at a level proficient to navigate input and/or reference computerized data * Must have sound judgment and demonstrate good analytical skills to assess risk to issues related to the manufacturing process * Must be able to pass the respirator requirements established for the Inspector position * Ability to stand/walk 85% of the shift to sample raw material and deliver to labs * Good manual dexterity to repetitively manipulate syringes to sample filled units for in-process monitoring * Good close visual acuity (eye exam required) * Noise levels on production lines may be moderate to high * Able to lift 15 lbs. * Able to pull/push raw materials with use of a pallet jack. Compensation: Hourly Rate: $24.00 per hour. The compensation for this position will be determined during the interview process and will vary based on multiple factors, including, but not limited to, work location, prior experience and job-related knowledge, relevant skills and expertise, current business needs, and market factors. The Talent Acquisition team can provide more details about the specific salary range for the job location during the hiring process. What We Offer*: * Annual performance bonus, commission, and share potential * Auto enrollment in a Hikma-sponsored 401(k) program at a pre-tax contribution rate of 3% of eligible pay. Hikma will match 100% of the first 6% of eligible pay that you contribute * A generous paid time off (PTO) bank starting with 20 days (prorated based on hire date). Additional days granted upon reaching work milestone anniversaries * 3 personal days (prorated based on hire date) * 11 company paid holidays * Comprehensive benefits including health, dental, vision, mental health, disability, life insurance, prescription drug coverage, and a variety of voluntary benefits * Employee discount program * Wellbeing rewards program * Safety and Quality is a top organizational priority * Career advancement and growth opportunities * Tuition reimbursement * Paid maternity and parental leave * Eligibility requirements apply to some benefits and depend on the job classification, role, and length of employment. Benefits are subject to change as well as specific plan or program terms. Recruiters: Please note that Hikma has a set roster of approved recruiters for specific roles agreed to in advance and does not accept unsolicited resumes or calls from third-party recruiters or employment agencies regarding open positions. In the absence of a signed agreement and approval from Hikma's Human Resources department to submit resumes for a specific position, Hikma will not approve, nor will be under an obligation to make, any payment to such non-approved third-parties in the event a candidate they refer is hired by Hikma. Equal Opportunity Employer: Hikma Pharmaceuticals USA Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law. Location: Cherry Hill, NJ, US, 08003 Nearest Major Market: Philadelphia