Quality inspector jobs in Lakewood, NJ - 172 jobs

Job Description Quality Control - Cable Assembly 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

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.

Job SummaryVisual and dimensional inspection of customer materials, system/process audits, non-conformance investigation.Job Description Key Accountabilities: Accurately inspect materials and products with gauges, scales, or other measurement instruments as required and according to work instructions. Management of non-conforming parts or material. Maintain the system for the documentation for work performed. Perform data entry of work results into appropriate databases. May be required to identify causes of non-conformance. Ability to access and work in SAP or other Warehouse Management System. Meets TKMNA Employee Attributes/Competencies. The above is intended to describe the general content of and requirement for the performance of this job. It is not to be construed as an exhaustive statement of duties, responsibilities or requirements. This position has been identified as “safety sensitive” by thyssenkrupp under applicable laws. Accordingly, any application for this position that is considered for employment with thyssenkrupp requires successful completion of pre-employment drug testing, which may include testing for marijuana in accordance with any applicable federal, state, and local laws. Qualifications: Minimum Requirements: This position requires access to export-controlled technical data or technology. Employment is contingent upon obtaining any required export authorization from the appropriate government agency or agencies. When export authorization is necessary, the length of time to obtain the authorization by the government is outside of the Company's control. Prior experience using basic measurement instruments and blueprint interpretation. Prior experience in a quality assurance inspection position. Prior experience with CMM inspection equipment. Ability to read and write English and perform basic math problems. Basic computer knowledge to complete data entry. Attention to detail and accuracy. Ability to accurately inspect material, commodities, and/or processes. Preferred requirements: Some college courses or certificates in Quality Assurance-related field of study Benefits Overview We offer competitive company benefits to eligible positions, such as : Medical, Dental, Vision Insurance Life Insurance and Disability Voluntary Wellness Programs 401(k) and RRSP programs with Company Match Paid Vacation and Holidays Tuition Reimbursement And more! Benefits may vary based on job, country, union role, and/or company segment. Please work with your recruiter or tk representative for applicable benefits information. Disclaimer This is to notify the general public that some individuals/entities are using the thyssenkrupp (“TK”) name, trademark, domain name, and logo without authorization. They are posing as employees, representatives, or agents of TK and its associated/group companies. These individuals/entities are fraudulently offering jobs online through texts, websites, telephone calls, emails, or by issuing fake offer letters. They are also soliciting jobseekers to deposit money in certain bank accounts or providing jobseekers with fraudulent checks to obtain banking information. TK does not ask, solicit, or accept any monies in any form from candidates, job applicants, or potential jobseekers, who have applied to or wish to apply to TK, whether online or otherwise as a pre-employment requirement. TK bears no responsibility for money being deposited/withdrawn therefrom in response to such fake offers. TK does not: 1. Send job offers from free email services like Gmail, Rediffmail, Yahoo mail, etc.; 2. Request payment of any kind from prospective jobseekers or candidates for employment; 3. Authorize anyone to collect money or agree to any monetary arrangement in return for a job at TK; 4. Send checks to job seekers; or 5. Make job offers through third parties. In the event TK uses professional recruitment services through a third party, offers are always made directly by TK and not by any third parties. PLEASE NOTE: 1. TK strongly recommends that potential jobseekers do not respond to such fake solicitations, in any manner; 2. TK will not be responsible to anyone acting on an employment offer that is not directly made by TK; 3. Anyone making an employment offer in return for money is not authorized by TK; and 4. TK reserves the right to take legal action, including criminal action, against such individuals/entities. TK follows a formal recruitment process through its own HR department and applications are evaluated by its HR department through pre-defined processes. Please visit our official careers website at ******************************** to view authentic job openings at TK. If you receive any unauthorized, suspicious, or fraudulent offers or interview calls, please email us at **********************************************. We shall not accept any liability towards the representation made in any fraudulent communication or its consequences, and such fraudulent communication shall not be treated as any kind of offer or representation by TK or its group companies and affiliates.

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 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

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

Country: United States of America Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: This job requires a U.S. Person. A U.S. Person is a lawful permanent resident as defined in 8 U.S.C. 1101(a)(20) or who is a protected individual as defined by 8 U.S.C. 1324b(a)(3). U.S. citizens, U.S. nationals, U.S. permanent residents, or individuals granted refugee or asylee status in the U.S. are considered U.S. persons. For a complete definition of “U.S. Person” go here. ********************************************************************************************** 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 a Quality Assurance Inspector 2nd shift (Onsite) FUNCTION: Perform Dimensional and visual inspections following standardized methods and established techniques. This may involve surface plate work or standard measuring techniques to verify accuracy of parts, tools, gages or other equipment. Accept or reject material based on findings What You Will Do: Work from applicable written inspection procedures drawings and other pertinent instructions to plan and perform dimensional and visual inspection on parts, tools and gages. 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 ensure that operation sheets are followed. Recognize the need and arrange for repair or preplacement of equipment used to perform necessary work. Perform routine servicing throughout assigned area following specified procedures and written instructions such as inspector's check list for upkeep and assure equipment operates properly. Assist others who are responsible for specialized inspection processes such as those found in statistical process control or other similar quality assurance programs. Investigation of unusual nonchanged inspection sequences and other specialized assignments within the conformance and new or changed inspection sequences. Specialized assignments within the scope and skill level of this . Refer difficulties to leader or supervisor. 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 and to develop individuals' skills. Qualifications You Must Have: High School Diploma or GED. Proficient reading blueprints U.S. citizenship is required, as only U.S. citizens are authorized to access information under this program/contract. Qualifications we prefer: 1-3 years of inspection experience. 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. In addition to transforming the future of flight, we are also transforming how and where we work. We've introduced role types to help you understand how you will operate in our blended work environment. 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

THEM is a rapidly growing, family-owned company with two locations in South Jersey. We collaborate with some of the biggest consumer packaged goods companies offering flexible packaging alternatives that continue to create breakthrough solutions in the packaging industry. Our employees are our #1 asset, and we are committed to investing in our people, maintaining the highest safety standards and creating a culture and dynamic work environment where motivation and teamwork are keys to the continued success of the company. Our benefits package reflects the company's commitment to its employees offering: competitive compensation employee raises based on performance quarterly bonuses based on company performance outstanding 401K with company contributions medical, dental, vision, prescription drug plan, FSA paid vacation paid holidays We care about our employees and the world we all share. With heightened consumer awareness in the importance of “green” packaging and lowering the impact of packaging production and use on the environment, T.H.E.M. encourages sustainability in packaging production through: Ongoing efforts to achieve significant source reduction Recognizing supply chain impact on space utilization, storage, transportation and distribution Assuring consumer ability to recycle most, if not all, packaging components Come join us and be a part of our family tradition of expertise, creativity, and drive to produce great packaging. For more information, please visit our website at ************* ___________________________ POSITION SUMMARY As a QA Technician, this position will have ownership and overall responsibility for the quality of product in Primary/Secondary Packaging; i.e., inspection of product in process as well as inspection of finished product as per Batch Records and Master Run Sheet specifications. The QA Technician will be responsible for addressing quality issues and support and comply with all quality management systems, food safety and employee safety programs and other responsibilities, as assigned. PRINCIPLE DUTIES AND RESPONSIBILITIES Assure consistent quality of production. Follow company Standard Operating Procedures and comply with Good Manufacturing Practices Inspect in process and finished product as specified in our Standard Operating Procedures and on Master Run Sheet Assure the effective completion and documentation of QA inspections on Batch Production Records entry to assure products adhere to quality specifications Perform magnet and screen inspections as specified in our HACCP program and documents results Perform Pre-Operational and Changeover inspections as required Perform scale calibrations, as needed Responsible for addressing quality issues as necessary. Take actions when there is a non-conformance to food safety requirements and/or product quality specifications, including placing products on hold, re-testing of products, and ensuring all actions taken are properly documented Responsible for releasing all incoming materials into production Follow all safety procedures. Maintain safe and efficient use of equipment and tools. Report any injury or accident and/or any unsafe conditions immediately to supervisor. Follow all Company policies and procedures Work shifts, as needed. Overtime required, as needed. Regular and appropriate attendance is expected. Commitment to Food Safety and Quality, GMP and SOP rules and regulations. Perform all other duties as assigned or needed. Qualifications QUALIFICATION/REQUIREMENTS High School Diploma and minimum 3 years experience in Quality Assurance in a food manufacturing, pharmaceutical or medical device environment Must be self motivated, possess high energy and be able to work in a high pace environment Must have excellent verbal and written communication skills. Must be able to read and interpret basic written instructions and perform tasks and projects. Must be able to interact in a dynamic team environment Must have basic computer skills with Microsoft Word Support and comply with all quality management systems, food safety and employee safety programs. PHYSICAL DEMANDS AND ENVIRONMENT The physical demands and work environment characteristics described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Physical Demands: Employee is required to be able to lift up to 25 lbs and work in both a seated and standing position. Must be able to twist/turn, reach over shoulders and stand/walk on a continual basis. Work Environment: This position requires one to work in a production and warehouse environment. There is a moderate level of noise. GENERAL INFORMATION The above statements are intended to describe the general nature and level of work being performed by individuals assigned to this position. They are not intended to be an exhaustive list of all duties, responsibilities, and skills required of personnel so classified.

Date 05/2025 Title Technician, QC Analytical Department Quality Control Reports to Manager, Chemistry Laboratory FLSA (Exempt or Non-Exempt Non-Exempt 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.

Job Title: Quality Control (QC) Inspector Company: Hansome Energy Systems Employment Type: Full-Time Hansome Energy Systems is a privately held industry leader in rotating electrical machinery, proudly supporting the U.S. Navy and other critical defense and industrial applications. We specialize in high-performance, precision-engineered equipment designed, built, and inspected to perform in the most demanding environments. Our commitment to quality, reliability, and mission readiness is the foundation of our work. Location & Facility Transition This position is currently based at our Linden, NJ facility and will be relocating to our new East Windsor, NJ facility. Candidates must be able to work in Linden during the transition and remain with the company through the move. Position Overview Hansome Energy Systems is seeking a highly detail-oriented Quality Control (QC) Inspector to ensure that mechanical and electrical components meet stringent defense and industrial quality standards. This role is critical to ensuring product reliability, regulatory compliance, and flawless execution of mission-critical equipment. The QC Inspector will perform dimensional inspections, documentation review, in-process checks, and final inspections. Key Responsibilities Perform incoming, in-process, and final inspections on mechanical, electrical, and precision-machined components. Verify parts and assemblies against drawings, specifications, and quality standards. Use precision measurement tools such as calipers, micrometers, height gauges, bore gauges, dial indicators, and other inspection equipment. Inspect for workmanship, proper assembly practices, dimensional accuracy, and material conformity. Document inspection results, discrepancies, and nonconformances clearly and accurately. Assist with root-cause investigations and corrective actions when defects are detected. Review manufacturing documentation such as travelers, work instructions, certificates of compliance, and material certifications. Ensure products meet all requirements before release to the next production stage. Collaborate closely with production, engineering, and quality teams to resolve issues. Support continuous improvement and maintain compliance with internal and external quality requirements. Qualifications Required High school diploma or equivalent. 1-3 years of experience in quality inspection or manufacturing. Strong understanding of mechanical drawings, tolerances, and inspection requirements. Proficiency with measurement tools such as calipers, micrometers, and gauges. Strong attention to detail, accuracy, and documentation skills. Ability to lift up to 50 lbs and stand for extended periods. Ability to work in Linden, NJ during the transition and relocate to East Windsor, NJ upon facility move. Must be a US Citizen Preferred Experience in defense, aerospace, or other high-reliability manufacturing environments. Familiarity with quality systems such as ISO 9001 or MIL-STD requirements. Experience with nonconformance reporting (NCR), MRB processes, or internal audits. Basic electrical knowledge or experience inspecting rotating electrical equipment. Experience with statistical process control (SPC) or advanced measurement tools (CMM, height gage, etc.). Work Environment Full-time, on-site QC inspection role. Work involves manufacturing floor, inspection stations, and documentation work areas. Exposure to shop environments, machinery, and moderate noise (with proper PPE). Quality- and safety-focused culture supporting defense and industrial programs. Benefits Competitive compensation Health, dental, and vision insurance Paid time off and holidays Retirement plan options Ongoing training and skill development Opportunity to ensure quality for products supporting U.S. Navy and critical applications How to Apply Qualified candidates are encouraged to submit their resume and/or application to the Hansome Energy Systems hiring team.

Kleinfelder's Mt. Laurel, NJ office is seeking a Senior Laboratory Construction Materials Testing Technician to join our team. As a Senior CoMET Laboratory Testing Technician, you will perform routine testing of soils, aggregate, concrete, asphalt and other construction materials to verify conformance to specifications and meet the rigorous schedule demand of our clients. With over 25 accredited laboratories across the nation, Kleinfelder is a recognized industry leader, and we'd like you on our team! Kleinfelder's Construction Materials Engineering and Testing (CoMET) operation provides 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. Your responsibilities may include but are not limited to: * Reading and understanding applicable testing methods * Performing applicable testing on construction materials including Soils, Concrete, Masonry, according to appropriate methods. * Performing strength testing procedures * Preparing materials for laboratory testing * Reporting verification of conformance to construction plans and testing methods * Communicating effectively with clients, field technicians, lab supervisor and other design professionals * Maintenance of Kleinfelder's local lab accreditations. Requirements and Qualifications: * Minimum 5+ years of Experience in CoMET or equivalent * Valid driver's license with a clean driving record and ability to pass drug test. * Ability to work independently and as a team member, maintain composure, and work effectively in a high-pressure environment with changing priorities. * Excellent interpersonal, verbal, and written communication skills. * Ability to use a company provided laptop or iPad and a working knowledge of MS Office programs (e.g. Word, Excel, Outlook, etc.). * Authorization to work in the United States * Bend, stoop, and lift up-to 50 pounds (22.68 kg) repetitively and over 50 pounds (22.68 kg) using handling equipment (hand truck, etc.) * Ability to operate heavy equipment as necessary (i.e., concrete cylinder press, etc.). * Authorization to work in the United States. Preferred Certifications (or ability to obtain) include: * ACI Concrete Lab Testing Technician * ACI Aggregate Base Testing Technician * ACI Aggregate Testing Technician 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. 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.

**Technician, Quality Control** **Princeton NJ, US** **On-Site** The QC Technician is responsible for maintaining conducting analyses, results entry and reporting and processing of quality related deviations, to ensure products meet specified standards defined, to help ensure that the products manufactured are safe, reliable, and meet both internal and external requirements, promoting customer satisfaction and trust in the business. **Your key responsibilities** + Perform Lab Tests: Independently carry out routine quality control analyses following set procedures. + Data Integrity & Documentation: : Confidently handle all steps of testing, including preparation, execution, and accurate documentation. + Check Results: Review test results for accuracy and consistency before submission. + Initial OOS Testing: Conduct first-level tests for out-of-spec results as per procedures. + Escalate Issues: Identify recurring problems and escalate them to the appropriate person or team. + Maintain Equipment: Take care of assigned lab equipment, including calibration and basic maintenance, following GMP and safety standards. **We bring** + Empowerment to make meaningful contributions while upholding ethical standards. + Recognition and celebration of your efforts and accomplishments. + Opportunities for growth and advancement for those who embrace innovation and take initiative. + Collaboration with experts in health, nutrition, and beauty to drive progress. + Customer-first approach, working with world-renowned brands to turn ideas into impactful solutions. + Opportunity to build a career making a significant impact on billions of lives, with the freedom to shape your own path. + Dedication to creating better futures for customers, communities, people, and the planet. + Responsibility and accountability in living company values and driving sustainable solutions. + Supportive environment where individuals are empowered to progress and contribute to meaningful change. **You bring** + Education: Bachelor's degree in Science, or a related field preferred. + Experience: Minimum of 2 years of experience in quality control. + Fluency in local language a requirement, other languages encouraged. The salary provided reflects the pay range dsm-firmenich expects to pay the successful candidate for the position. Individual pay offered will be based on the applicant's job-related skills, experience, relevant education, or training, and primary work location. $47,000 - $68,000 In addition to base salary, we also offer a comprehensive total rewards package, inclusive of annual incentive pay, a retirement savings plan, health care coverage, paid time off, recognition programs and a broad range of other benefits. All benefits and incentives are subject to eligibility requirements. **About dsm-firmenich** At dsm-firmenich, we don't just meet expectations - we go beyond them. Join our global team powered by science, creativity, and a shared purpose: to bring progress to life. From elevating health to making fortified food and sustainable skincare, the impact of your work here will be felt by millions - every single day. Whether it's fragrance that helps you focus, alternative meat that's better for the planet, or reducing sugar without losing flavor, this is where you help shape the future of nutrition, health, and beauty for everyone, everywhere. And while you're making a difference, we'll make sure you're growing too. With learning that never stops, a culture that lifts you up and the freedom to move across businesses, teams, and borders. Your voice matters here. And your ideas? They're essential to our future. Because real progress only happens when we **go beyond, together** . **Inclusion, belonging and equal opportunity statement** At dsm-firmenich, we believe being a force for good starts with the way we treat each other. When people feel supported, included, and free to be themselves, they do their best work - and that's exactly the kind of culture we're building. A place where opportunity is truly equal, authenticity is celebrated, and everyone has the chance to grow, contribute, and feel they belong. We're proud to be an equal opportunity employer, and we're serious about making our hiring process as fair and inclusive as possible. From inclusive language and diverse interview panels to thoughtful sourcing, we're committed to reflecting the world we serve. We welcome candidates from all backgrounds - no matter your gender, ethnicity, sexual orientation, or anything else that makes you, you. And if you have a disability or need any support through the application process, we're here to help - just let us know what you need, and we'll do everything we can to make it work. **Agency statement** _We're managing this search directly at dsm-firmenich. If you're applying as an individual, we'd love to hear from you. We're not accepting agency submissions or proposals involving fees or commissions for this role._