Quality control technician jobs in Clinton, NJ - 359 jobs

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

**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._

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

Job Description Are you ready to join our team at C&L Auto Body, an esteemed family-owned MSO in Plainfield, NJ? We are in search of a talented and devoted Quality Control Technician to uphold our dedication to business expansion and client contentment. Your precision and proficiency will be pivotal in reducing customer inconvenience following accidents. This position is a great jumping-off point for higher-paying jobs such as estimating & production management. Compensation: $18 - $30 hourly Responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required: Assure that C&L QC procedures are being followed by all departments Solely responsible for final quality inspections Assure that all repairs to the vehicle match the final invoice Perform other related duties as assigned to ensure an efficient and effective repair Meet & greet customers Review repairs of all vehicles & sign off on ready-for-delivery Deliver vehicles to customers, reviewing repairs & answering any questions Perform ADAS on all vehicles that need scanning or calibrations fill out appropriate paperwork & check in requirements for each vehicle Qualifications: The ideal candidate should have the following experience: Experience working in a Team Environment Prior working knowledge of body repairs and parts Prior experience in multi-tasking, prioritizing, and organizing Ability to effectively communicate Technical knowledge for automotives Ability to learn & adapt quickly customer service experience Quality control experience About Company C&L Autobody is a regional Multiple-Shop Organization (MSO) with 11 body shops throughout Morris, Essex, Sussex, Warren, Union, and Middlesex counties in Northern NJ. We also manage one of the largest towing fleets in the state. As one of NJ's largest family-owned MSOs, we pride ourselves on delivering an unmatched level of customer service and craftsmanship for all your collision repair needs. We offer full benefits (medical, dental, and vision), paid time off, paid holidays, and a 401(k) with a company match. Work hours are Monday through Friday, 8 am to 5 pm, with occasional Saturdays.

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

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

Quality 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.

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 Control Technician Industry Leading Benefits: Medical, Prescription, Dental, Vision, 401K, Pension, Short and Long Term Disability, Life Insurance, Tuition Reimbursement, Overtime as needed. As a Silvi Materials Quality Control Technician, one is responsible for ensuring that concrete chemistry and construction projects comply with plans and specifications. This position includes industry testing of concrete consistency, air, water, color, and chemical content. The qualified candidate will be able to communicate with and interact with construction personnel, inspectors, plant managers, and drivers concerning the concrete materials used on a particular job. Silvi Materials has been expanding our “A” Team of employees since 1947! Our team has grown to 15+ companies, employing over 850 people across 30+ locations in Southeastern Pennsylvania, New Jersey, and North Carolina. Silvi is large enough to provide the stability you need, but small enough that you can feel your individual contribution to our success. We value the fresh ideas and perspectives of each new member of our team. What does Silvi Materials offer you, you may ask? Phenomenal Benefits: Medical, Vision, Dental, Prescription, Vacation, Paid Holidays, and so much more! Your future in mind: With 401(k) (at select locations) and/or pension options. We want all employees to build a great retirement! Growth at Silvi Materials: We offer each employee the opportunity to move into any facet of our complex business. And our tuition reimbursement program is the perfect springboard to help you get there! So, what does a Silvi Materials Quality Control Technician do? You'll be an integral part of our Quality Control/Technical Services Team! Arrives at the plant or job site prior to the first concrete delivery. Performs the initial and ongoing testing of aggregate and concrete for gradation, moisture, slump, air content, and temperature After evaluation of the above factors, maintains contact with plant operations and/or QC, to ensure that necessary adjustments (if required) to the mixture are made. When the concrete comes to the job site places some of the batch in cylinders. In the lab, performs tests that measure the compressive strength of concrete cylinders. Compares that value to the design value to ensure compliance with specifications. Communicates information to the appropriate individuals/agencies. Directly handles concrete during various testing. Qualifications Required: Industry experience is preferred but not required. Some college or further education is preferred but not required. Travel with their own vehicle to and from various plants and client locations. Mileage and tolls will be reimbursed. Valid Driver's license. Work a wide variety of hours and be able to work a flexible schedule as per company and client needs. Is able to work overtime hours. Works Saturdays and night pours as required. Understand the various components that make up the product and how they interact with one another. Understand how to troubleshoot the various problems that occur with the product and how to correct them. Understand the proper techniques for testing concrete. Preferably is ACI Level 1 certified, or willing to undergo paid training and testing to obtain the certification. Has a valid driver's license and is willing to undergo an MVR check. Willing to work outdoors, in all weather, to handle the concrete testing on site. Lift up to 100 lbs of liquid concrete using a wheelbarrow. Physical Requirements In a typical work setting, people in this job: Lift 50 pounds regularly and up to 100 pounds on occasion. Use one or two hands to grasp, move, or assemble objects Stand for long periods of time. Kneel, stoop, crouch, bend, stretch, twist or crawl. Hear sounds and recognize the difference between them. See details of objects that are less than a few feet away. See differences between colors, shades, and brightness. Silvi Materials does not discriminate in employment on the basis of race, color, religion, sex (including pregnancy and gender identity), national origin, political affiliation, sexual orientation, marital status, disability, genetic information, age, membership in an employee organization, retaliation, parental status, military service, or other non-merit factors.

Introduction Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong. Our success comes from a specific focus in these rapidly evolving diagnostic areas, our commitment to customers, and our dedication to innovation and quality. We're passionate about providing healthcare professionals the most valuable and complete solutions to improve hospital efficiency and enhance patient care. Overview If you're a QC expert when it comes to manufacturing, Immucor has an exciting opportunity for you! We are looking to hire a Quality Control Technologist III medical device, and/or the pharmaceutical industry. This critical role will Lead QC stability projects, perform Incoming, In-process, final release and stability testing in the Quality Control Laboratory. Act as Team Lead in the QC lab to assist supervisor and Director in daily operations of the Quality Control Laboratory and provide guidance to the QC staff. This position is not eligible for sponsorship for work authorization by Immucor, Inc. Therefore, if you will require sponsorship from us for work authorization now or in the future, we cannot consider your application at this time . Responsibilities Job Summary This role will be the team SME (subject matter expert) on product stability. This will include writing stability protocols and reports, performing product testing, and trending stability data. They may lead QC projects, perform Incoming, In-process, final release, and stability testing in the Quality Control Laboratory. They will be a Team Lead in the QC lab to assist the supervisor/ manger and Director in daily operations of the Quality Control Laboratory and provide guidance to the QC staff. Key Accountabilities Monitors stability testing time points, ensures samples are pulled and tested at the correct intervals, and performs data analysis to support QA/QC management. Drafts stability protocols and reports. Performs trend analysis onstability data throughout the stabiity protocol timeline. Develops timeline for annual stability and determines which products are required. Provides direction and guidance to Quality Control staff in the performance of daily tasks. Creates daily and weekly scheduling of all QC related activities Performs and schedules testing for incoming raw material, in-process, final release and inspection of BioArray products according to approved Standard Operating Procedures (SOP's) and other applicable documents within defined timeframes. Performs and schedules stability, method validations, equipment validations, threshold analysis process and other special testing. Act as OJT trainer to train new employees and current employees on new test methods. Guides QC technicians training activities and ensures that the appropriate training records are completed as per the role functions Reports and escalates out-of-specification results and deviations to the department supervisor/manager. Assists and leads the investigations, root cause analyses, and reports for out-of-specification results and deviations. Writes/Revises SOPs, WI, QC Specification/testing documents. Maintains accurate, legible, and complete records according to Current Good Manufacturing Procedures (cGMP's). Performs all assigned tasks following applicable laboratory SOPs, OSHA regulations and cGMP regulations (i.e. Blood borne pathogens and chemical hazards). Maintains work area, equipment, department, and all storage areas in a clean, neat, and orderly manner. Performs, schedules and delegates equipment calibration and manintenance. Qualifications Bachelor's degree in biology or chemistry or related field. Four (4) or more years experience in a medical device or pharmaceutical GMP quality laboratory. Experience working under 21 CFR Part 210/211 and/or 820 regulations required. Knowledge of ISO 13485 desired. Two (2) or more years of experience performing stability testing required. Experience writing stability protocols, performing data trending, and writing stability reports preferred. Eperience performing OOS Phase I investigations, in alignment with FDA guidelines, required. Expereince training QC technicians desired. Expereience performing PCR (Polymerase chain reaction) desired. Management has the discretion of substituting relevant work experience for a degree and/or making exceptions to the years of experience requirement. Quality Control Technologist III-Stability Closing If you are interested in constantly learning and being challenged on a daily basis we encourage you to submit your resume or CV. Werfen is an Equal Opportunity employer and is committed to a diverse workplace. Werfen strictly prohibits unlawful discrimination, harassment or retaliation based upon an individual's race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other protected characteristic as defined by applicable state or federal law. If you have a disability and need an accommodation in relation to the online application process, please contact ****************************** for assistance. We operate directly in over 30 countries, and in more than 100 territories through distributors. Annual revenue is approximately $2 billion and more than 7,000 employees around the world comprise our Werfen team. **************

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

* Inspect finished product samples in the lab for compliance with specifications, including appearance, integrity, and performance criteria. - Perform sampling and testing procedures: collect representative samples, execute lab tests, and record results accurately. - Document all inspection activities in accordance with SOPs and audit requirements. - Support investigations for out-of-spec results and assist in corrective/preventive actions within the lab environment. - Maintain lab compliance: ensure proper labeling, cleanliness, and adherence to cGMP and QA protocols. - Collaborate with QC team members to uphold safety and compliance culture. Skills Inspection, Quality control, Quality assurance, Laboratory, Gmp, Quality inspection Top Skills Details Inspection,Quality control,Quality assurance,Laboratory,Gmp,Quality inspection Additional Skills & Qualifications Ability to work independently and maintain high attention to detail. Experience with finished product inspections and lab-based quality systems. Knowledge of ERP systems for tracking and reporting. Experience Level Entry Level Job Type & Location This is a Contract to Hire position based out of Wharton, NJ. Pay and Benefits The pay range for this position is $22.00 - $23.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Wharton,NJ. Application Deadline This position is anticipated to close on Jan 23, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

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

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

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

A primary focus of this role is creating and modifying LIMS test plans to support QC activities while adhering to regulatory and data integrity guidelines. The LIMS Coordinator is responsible for tracking and managing laboratory inventories within the LIMS system and to perform and verify daily verification of laboratory data for accuracy and completeness, ensuring compliance with GxP standards before submission for review. Essential Functions: Register samples and input relevant test results, instrument data, and laboratory information into the LIMS system as per QC procedures. Manage laboratory inventories, ensuring timely replenishment and accurate record-keeping within the LIMS system as well as generate and run standard reports from the LIMS system for Laboratory Resource tracking. Perform and verify daily verification data for accuracy and completeness before submitting it for review. Create, troubleshoot and modify LIMS Test, worksheets, and test plans as needed to support QC activities. Train new peers in LIMS operations, including sample manager and resource modules. Assist QC personnel with sample registration and label generation using the LIMS software Additional Responsibilities: Performs other functions as required or assigned. Hands on to follow compendial (USP/EP/BP/JP) procedures for wet chemical tests. Must understand and apply cGMP requirements applicable to quality control laboratory. Follow up on sample status and testing progress within the LIMS system. Participate in continuous improvement initiatives to optimize LIMS functionality and workflows. Education: Associate Degree - Required Bachelors Degree (BA/BS) Chemistry or related field - Preferred Experience: 1 year or more in Pharmaceutical/manutfacturing Skills: Proficient in laboratory informatics - Intermediate Strong understanding of regulatory compliance (FDA, GMP). - Intermediate Proficiency in inventory management systems and data analysis tools. - Intermediate Excellent organizational, communication, and problem-solving skills. - Intermediate The hourly rate for this position ranges from $22.00 to $26.00 per hour. In addition, Amneal offers a short-term incentive opportunity, such as a bonus or performance-based award, with this position within the first 12 months. Amneal ranges reflect the Company's good faith estimate of what Amneal reasonably believes that it will pay for said position at the time of the posting. Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, experience, geographic location and other relevant skills. At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement. We also promote employee well-being with programs that help you enjoy your career alongside life's many other commitments and opportunities.

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

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

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