Quality control technician jobs in Nashua, NH

“WHEN YOU WORK FOR US, WE WORK FOR YOU.”Travel Cath Lab Tech Weekly Gross Pay: $2578.00 - $2778.00 Assignment length: 13 Weeks Minimum years of relevant experience in healthcare: 2 years Job type: Traveler Shift: Day (5x8) Certifications: BCLS/BLS - American Heart Association/RCIS/ARRT(R) Position Highlights 13-week travel contract Competitive weekly pay package Work with an experienced clinical and recruiting team Quick start options available (inquire for details) 🫀 Cath Lab Tech - Nashua, NH 📅 Start: 12/29/2025 | ⏳ Duration: 13 Weeks 💰 Pay: $2,778 Gross Weekly 🌤 Shift: Days 5x8 (7:30 AM-5:00 PM) 📍 Location: 8 Prospect St, Nashua, NH 03060 📞 Contact: Broc Bettell 📲 Call: ************ ext.1052 | 💬 Text: ************** 🏥 Position Highlights • 💡 Experience: 2+ years Cath Lab required | First-time travelers accepted depending on experience • 🪪 Certs: ACLS, ARRT(R), RCIS or ARRT, NH State License • ⚙️ Core Skills: Scrub & maintain sterile field PCI, stents, angioplasty Left & right heart cath Impella insertion Temporary pacemakers Thrombectomy & vascular interventions Rhythm interpretation, vitals, hemodynamic monitoring • 🖥️ Systems: EPIC | Mac-Lab • 🏥 Setting: Elective & emergent PCI, pacemaker & ICD implants, IABP, STEMI • 🔄 Float: None • ☎️ Call: Required | Weekday & weekend call • 📊 Daily Volume: Avg 4 cases/day | 1 procedure room • 🧭 Locals: Accepted • 🎁 Holidays: Per facility need • 🧼 Scrubs: Any • 🌡️ Other: Unit prefers experience with monitoring, ablations, cardiac mapping, and EP procedures 🌆 Fun Things To Do in Nashua, NH 🍽️ Downtown Nashua - boutique shops, breweries & charming restaurants 🌳 Mine Falls Park - forest trails, river views & walking paths 🎳 Boston Billiard Club & Casino - gaming, sports bar & weekend fun 🛍️ Pheasant Lane Mall - shopping, food court & entertainment 🚣 Nashua Riverfront - kayaking, fishing & scenic overlooks Benefits Day-one medical, dental & vision insurance Loyalty bonus after 2,080 hours Life and short-term disability 401(k) with employer match Referral bonus up to $1,500 24/7 recruiter support Licensure and CEU reimbursement Experienced clinical team available to support you throughout your assignment Titan Medical App available on the Apple Store & Google Play Why Travel with Titan Medical Titan Medical provides access to thousands of travel nursing and allied health jobs nationwide. Your dedicated recruiter will help you: Build a strong traveler profile by improving your résumé and showcasing your skills Increase your chances of landing the assignment you want Travel with a top healthcare staffing company in the industry Ready to apply or want more information? Call ************** to connect with Titan Medical today!

Primary Skills: Electrical testing (Expert), Oscilloscopes (Expert), Python (Intermediate), Soldering (Advanced), Test-Execution (Proficient) Contract Type: W2 Duration: 6 Months with possible extension Pay Range: $37.00 - $41.00 Per Hour #LP Job Summary: Join our dynamic Hardware Test Engineering team as a Quality Assurance Engineer, focused on groundbreaking robotic system design. This position involves collaborating with hardware developers and program management to enhance testing capabilities utilizing your critical thinking and problem-solving skills. Ideal candidates will bring in-depth electrical experience to the forefront of new technological advancements in robotics. Key Responsibilities: Collaborate with Test Engineers and developers on tooling and techniques for testing. Maintain and maximize fixture uptime for existing systems. Troubleshoot electrical and control issues efficiently. Develop comprehensive test subsystems and documentation. Execute detailed tests and accurately acquire test data. Must-Have Skills: Proficient in reading and understanding electrical schematics. Experienced with board-level soldering and capable of performing board reworks. Skilled in using standard electrical test equipment (oscilloscopes, multi-meters). Industry Experience: Robotics, Electrical Engineering or related fields with a strong emphasis on testing and troubleshooting hardware. ABOUT AKRAYA Akraya is an award-winning IT staffing firm consistently recognized for our commitment to excellence and a thriving work environment. Most recently, we were recognized Inc's Best Workplaces 2024 and Silicon Valley's Best Places to Work by the San Francisco Business Journal (2024) and Glassdoor's Best Places to Work (2023 & 2022)! Industry Leaders in IT Staffing As staffing solutions providers for Fortune 100 companies, Akraya's industry recognitions solidify our leadership position in the IT staffing space. We don't just connect you with great jobs, we connect you with a workplace that inspires! Join Akraya Today! Let us lead you to your dream career and experience the Akraya difference. Browse our open positions and join our team!

Title: QC Investigations Specialist Employment Type: Contract Status: Accepting Candidates About the role This role supports real-time manufacturing operations by leading investigations, resolving on-floor issues, and ensuring high-quality documentation. You'll partner closely with manufacturing, QC, materials, and facilities teams to maintain operational continuity and compliance. Key Responsibilities • Triage manufacturing issues and lead analytical investigations and root cause analysis. • Write clear, compliant quality documentation including deviations and CAPAs. • Coordinate with SMEs to determine immediate actions, containment, and impact assessments. • Interpret data to support structured problem-solving and continuous improvement. • Provide technical operations support across manufacturing and QC functions. Qualifications • 6+ years pharmaceutical or biotech manufacturing experience. • 4+ years analytical investigation and QC-focused experience. • Strong background in RCA, deviation management, and GxP documentation. • Ability to interpret analytical data and think scientifically under time-sensitive conditions. • Experience partnering cross-functionally with manufacturing, QC, materials, and facilities teams. Compensation (MA Pay Transparency): • Estimated hourly range: $50-$55/hr (W-2). • Final rate within this range will be based on skills, experience, and interview results.

Adecco Staffing is partnering with a reputable manufacturing facility in Peterborough, NH to hire Quality Control Inspectors for all shifts! This is a temp-to-hire or direct-hire opportunity, depending on your level of Inspection experience. The position offers competitive pay rates and the opportunity to join a growing company. Pay Rate: $17-$26 per hour, depending on experience and shift Schedules Available: 1st Shift Monday through Friday 7:00am-3:30pm, OT available 2nd Shift Monday through Friday 3:15pm-11:45pm, OT available 3rd Shift Sunday through Thursday 11:30pm-7:00am (paid for 8), OT available Job Summary: Responsible for ensuring the quality of processes and product within an assigned functional area. Essential Duties and Responsibilities: The following represent general inspection functions which may or may not be required depending upon the functional area in which you are assigned. Inspectors may be reassigned to a different sub function at any time based on the business need, and training will be provided. Perform dimensional inspection using mechanical and visual inspection equipment, such as an optical comparator, contour reader, dial indicators, inspection hand tools, surface plates, height gauges, air gauges, specialized bearing measurement equipment, and gauge blocks. Measure bearing assemblies and/or component features such as roundness, concentricity, perpendicularity, flatness, sphericity, surface finish, surface noise and vibration levels using specialized equipment. Complete basic control charts, run charts, prepare charts, and histograms. Read and understand drawings, specifications, procedures, standards and instructions. Write inspection rejection reports in accordance with company procedures, and maintain detailed inspection records using appropriate forms. Make recommendations regarding quality and manufacturing improvements as needed. Perform visual inspection of bearing assemblies, and/or bearing components, using microscope and the unaided eye. Communicate with Manufacturing & Quality personnel and other disciplines as required in a timely and professional manner. Why Apply? Competitive pay rates with the potential for overtime. Temp-to-hire or direct-hire opportunity based on your level of experience. Work in a high-level manufacturing facility with advanced equipment and processes. Training and growth opportunities available. If you are interested in this exciting opportunity and feel you have the skills to succeed, please apply today with an updated resume or call 603-###-####! We look forward to hearing from you. Pay Details: $17.00 to $26.00 per hour Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable. Equal Opportunity Employer/Veterans/Disabled Military connected talent encouraged to apply To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: The California Fair Chance Act Los Angeles City Fair Chance Ordinance Los Angeles County Fair Chance Ordinance for Employers San Francisco Fair Chance Ordinance Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

We are seeking a highly motivated Entry-Level Quality Control (QC) Analyst to join our Gene Therapy QC Bioassay group. This is an excellent opportunity for recent graduates or individuals early in their careers to gain hands-on experience in a dynamic and cutting-edge environment supporting AAV-based gene therapy programs. The QC Analyst will be trained to perform cell-based bioassays, ELISAs, and other biological methods in a GMP-regulated setting, while also supporting external laboratory testing. Responsibilities: Learn and perform immunoassays (e.g., ELISA) and cell-based assays under supervision in a GMP environment to support product release and stability testing. Assist in drafting and reviewing standard operating procedures (SOPs) and technical documents. Support method transfer, qualification of critical reagents, and other assay-related activities. Participate in the review and basic trending of QC data. Assist with routine laboratory upkeep, including cell culture maintenance, instrument calibration, and inventory tracking. Collaborate with internal teams and external partners as part of cross-functional project support. Contribute to investigations and deviation reports under guidance. Qualifications: Bachelor's degree in Cell Biology, Molecular Biology, Biochemistry, or a related scientific field. Academic or internship experience with mammalian cell culture and/or ELISAs strongly preferred. Familiarity with basic lab techniques and data analysis methods. Enthusiasm for learning and the ability to work both independently and within a team. Strong organizational, communication, and interpersonal skills. Detail-oriented and eager to develop problem-solving skills in a regulated lab environment.

Job Title: Manufacturing Associate I - Cell Therapy Job Duration: 6 Months with potential to extend Shift Schedule: (There will be 6-8 weeks of training 7 AM - 4 PM, Monday to Friday) Rotational shift schedule PURPOSE AND SCOPE OF POSITION The client seeks Associates within manufacturing who bring enthusiasm, intellectual curiosity, scientific rigor, and a desire to help drive novel programs. The candidate must be goal-oriented, flexible, and able to work efficiently with safety and quality in mind. We are searching for enthusiastic and innovative individuals with a good understanding of good manufacturing practices to support routine manufacturing operations for Cell Therapy. DUTIES AND RESPONSIBILITIES Performing patient process unit operations and support operations described in standard operating procedures and batch records. Work in a cleanroom environment and perform aseptic processing; maintain manufacturing environmental conditions (Non-Viable Particulate(s) and Viable microbial levels per controlled area classification specifications) by performing area disinfection regimen as required to meet global Health Authority requirements. Completing documentation required by process transfer protocols, validation protocols, standard operating procedures, and batch records. Performing tasks in a manner consistent with the safety policies, quality systems, and GMP requirements. Completing training assignments to ensure the necessary technical skills and knowledge. Assisting in setting up manufacturing areas and equipment/fixtures. Perform facility and equipment commissioning activities. Training others on SOPs, Work Instructions to successfully complete manufacturing operations. Executing daily unit operations schedule that includes people, product, and material flow across multiple shifts. REQUIRED COMPETENCIES Education: Bachelor's in a relevant science or engineering discipline is preferred. High school diploma and 2 years of experience in cGMP bioprocessing manufacturing, cell therapy manufacturing, or relevant experience. Preferred Qualifications: Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy manufacturing is preferred.

Company: Fusion Medical Staffing Job Details Fusion Medical Staffing is seeking a skilled Cath Lab Tech for a 13-week travel assignment in Inglewood, California. As a member of our team, you'll have the opportunity to make a positive impact on the lives of patients while enjoying competitive pay, comprehensive benefits, and the support of a dedicated clinical team. Required Qualifications: One year's recent experience as a Cardiac Cath Lab Tech Current BLS (AHA/ARC) certification ARRT, RCES, or RCIS certification Current ACLS (AHA/ARC) certification Preferred Qualifications: Valid Radiologic Technologist license in compliance within state regulations PALS (AHA/ARC) or ENPC Certifications Other certifications and licenses may be required for this position Summary: The Cath Lab Technologist is responsible for assisting in diagnostic and interventional cardiovascular procedures in the cardiac catheterization lab. This role involves preparing patients and equipment, monitoring hemodynamic data, assisting physicians during procedures, and ensuring patient safety throughout the process. The technologist operates specialized imaging equipment, maintains sterile technique, and collaborates with the healthcare team to provide high-quality patient care. This position requires technical expertise in cardiovascular procedures, critical thinking skills, and the ability to work efficiently in high-pressure situations. Essential Work Functions: Prepare and position patients for cardiac catheterization, angioplasty, stent placement, electrophysiology studies, and other interventional procedures Assist physicians during procedures by passing catheters, wires, balloons, and stents, and operating fluoroscopy and hemodynamic monitoring equipment Operate and maintain imaging equipment, contrast injectors, and hemodynamic monitoring systems, ensuring proper functionality Scrub in and assist with sterile field setup, ensuring adherence to infection control and procedural protocols Perform sheath removal and hemostasis using manual compression or closure devices as directed Maintain accurate documentation, including patient records, imaging data, and equipment logs Assist with inventory management, stocking supplies, and ensuring proper storage of sterile instruments and medications Adhere to radiation safety protocols, ensuring proper use of lead aprons, shields, and dosimeters Ensure compliance with hospital policies, safety guidelines, and regulatory requirements Adhere to hospital safety protocols, infection control guidelines, and regulatory standards Perform other duties as assigned within the scope of practice Required Essential Skills: Critical thinking, service excellence, and good interpersonal communication skills The ability to read, write, and communicate in the English language Ability to read/comprehend written instructions, follow verbal instructions, and proficiency in PC skills Physical Abilities - Must be able to remain in a stationary position, move about, move equipment (50-100lbs), push, pull, and bend Interpersonal Skills - Must be able to work effectively with a variety of personnel (professional and ancillary) to present a positive attitude and professionalism Technical/Motor Skills - Must have the ability to grasp, perform fine manipulation, push/pull, and move about when assisting with procedures and/or using department equipment Mental Requirements - Must be able to cope with frequent contact with the general public and customers while meeting deadlines under pressure. Must be able to work under close supervision occasionally, as well as working without assistance from other personnel. Must be able to contend with irregular activity schedules occasionally and continuous concentration to detail Sensory - Must possess visual acuity and ability to effectively communicate Benefits Include: Highly competitive pay for travel professionals Comprehensive medical, dental, and vision insurance with first day coverage Paid Time Off (PTO) after 1560 hours Life and Short-term disability offered 401(k) matching Aggressive Refer-a-friend Bonus Program 24/7 recruiter support Reimbursement for licensure and CEUs Why Choose Fusion? At Fusion Medical Staffing, our goal is to improve the lives of everyone we touch, and we're always looking for people like you to join our mission. Your passion for helping others deserves a partner just as committed to supporting you - that's why we offer day one insurance, $0 copay for mental health services, scholarships and awards, exclusive discounts, and more. From your personal recruiter to our clinical and traveler experience teams, we're here to guide and celebrate you along your journey. You take care of others; we take care of you. Other Duties Disclaimer: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Other duties may be assigned. This job description is not a comprehensive list of all activities, duties, or responsibilities that are required of the employee for this job and is subject to change at any time with or without notice. Start your rewarding career as a Travel Cath Lab Tech with Fusion Medical Staffing and join our mission to improve lives. Apply now! *Fusion is an EOE/E-Verify Employer #pb12

The Quality Technician - FAI Specialist is responsible for coordinating and supporting the creation of AS9102 First Article Inspection Reports (FAIR) in alignment with industry and customer specific requirements. This position works alongside various other departments and is vital to ensuring success of the AS9102 program. Duties/Responsibilities: Navigates internal company software and database systems to gather information. Accurately completes AS9102 Reports (FAIR) and other dimensional inspection reports as required. Interpret drawings, specifications and customer requirements. Works effectively and communicates with various departments, including: Planning, Marketing, Quality, QC Inspection and Source Inspection. Assures accuracy of FAI programs and records. Assists with identifying opportunities for improvement within the FAIR process to aid in the success of the Quality Department. Maintain a positive work environment by acting and communicating in a manner so that you get along with customers, clients, vendors, co-workers and management. This position may require overtime for coverage on alternate shifts and weekends. Will be required to perform other duties as requested, directed or assigned. Requirements: High School diploma or General Education Degree (GED). Previous experience as a First Article Inspection Specialist is preferred but not required. Must be able to use a computer to maintain records, develop reports, and analyze data and document discrepancies as well as using a computer to perform all other related aspects of the position. Must have excellent communication skills and ability/flexibility to work in a fast-paced environment. Must be able to read and interpret technical drawings, prints and industry/customer specifications. Must be able to read and interpret GD&T requirements. Must be able to display a thorough attention to detail and organization. Amphenol offers a competitive salary and benefits. The candidate must be able to legally work in the United States; we are unable to provide sponsorship. Position requires candidate to be a U. S. person as defined in ITAR, 22 CFR 120. 15 (U. S. Citizenship or Resident Alien Status) and defined by 8 U. S. C. 1101(a) (20). Amphenol is a proud Equal Opportunity Employer as to all protected groups, including Individuals with Disabilities and Protected Veterans. For consideration for this position, please apply online to: ********************* acquiretm. com APC878

Job Details Leominster - Leominster, MA Manufacturing DESCRIPTION QC Inspector FLSA: Non-Exempt REPORTS TO: Vanessa Torres FUNCTION: Relative visual inspection of company product verifying conformance to order specific paperwork using established sampling plans, color/fabric samples and aesthetic requirements. Verify size and quantity of product presented for inspection for conformance to order. Minimal computer skills required. Shop Math. Individually inspect each small part of negligible weight in each lot, following simple verbal instructions. Use direct reading gauges to separate good and defective parts. RESPONSIBILITES: Visual & dimensional inspection of company product to drawing, production paperwork & quality standards. Knowledge of the use of handheld measuring instruments a plus. Knowledge of reading blueprints a plus. Knowledge of welding operations a plus. Will record data and enter reports. High level of accuracy and attention to detail required. Qualifications REQUIREMENTS: Must be willing to work overtime hours needed to complete job. Bi-lingual a plus. Must be neat and detail oriented. Ability to work OT is also required. Previous Inspection experience is a plus. PHYSICAL REQUIREMENTS: PHYSICAL DEMANDS NEVER OCCASSIONALLY .25 - 2.5 Daily HRS FREQUENTLY 2.5 - 5.5 DAILY HRS CONTINUOUSLY 5.5 - 8 DAILY HRS PHYSICAL DEMANDS NEVER OCCASSIONALLY .25 - 2.5 Daily HRS FREQUENTLY 2.5 - 5.5 DAILY HRS CONTINUOUSLY 5.5 - 8 DAILY HRS SITTING x WALKING x STANDING x DRIVING x BENDING x REACHING x GRIPPING x STOOPING x PUSHING/PULLING x TWISTING x 0- 10 LBS 10-20 LBS 20-50 LBS 50-100 LBS LOW MODERATE HIGH VERY HIGH LIFTING/ CARRING x STRESS LEVEL x At AIS, we have a strong set of values that guide our business and help us align with our customers. We listen to our Customers. We rely on our Employees. We honor Integrity. We embrace Continuous Learning. We lead with Design. We create Value. We work to make the World better. EEO/AA Statement As an EEO/AA employer, AIS will not discriminate in its employment practices due to an applicant's race, color, sex, pregnancy, national origin, ancestry, citizenship, sexual orientation, gender identity or expression, protected genetic information, age, disability, marital status, veteran status, religion, height, weight, other protected group status, or any other basis protected by the laws where we employ people. This organization participates in E-Verify Employment Eligibility Verification. AIS is a Federal Contractor and required to comply with Executive Order 14042. This means that all employees of AIS must (a) be vaccinated, (b) have a medical exemption, or (c) have a religious, moral or ethical exemption that meets EEOC requirements. As a condition of employment, you must meet one of these three requirements at the time of hire or within 60 days of your initial employment date. DISCLAIMER The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required of personnel so classified.

75 Plumb Pak Drive, Winchester, New Hampshire 03470 United States of America Why Oatey? Since 1916, Oatey has provided reliable, high-quality products for the residential and commercial plumbing industries, with a commitment to delivering quality, building trust and improving lives. Today, Oatey operates a comprehensive manufacturing and distribution network comprised of industry leading family of companies: Oatey, Cherne, Keeney, Quick Drain, Hercules, Dearborn, GF Thompson, William H. Harvey, Masters, Contact, Belanger, Lansas, and Durgo. At Oatey, we're doing big things - and by joining us, you'll have the chance to do big things too. You can build a strong career in an innovative, inclusive, high-performance environment, with the confidence that your company cares - about you, our customers and our world. Ready to make an impact in a place where you matter? - Position Summary: Ensures the quality of all processes, procedures, materials, processes rework and finished products. Also performs scheduled tasks as support for environmental and safety functions with additional responsibilities as assigned. This position is a second shift 3:00PM-11:30PM Monday-Friday work schedule and reports directly to Quality Manager. Position Responsibilities: Conduct daily quality inspections in all departments to audit the following: Procedure compliance/documentation with ISO9001 quality systems. In-process quality inspections, using established procedures. Incoming inspection, including first piece inspection, verification of Supplier's Certificates of Analysis, etc. Validation of product quality conformance to specifications. Complete ongoing Reliability Testing to ensure current products continue to meet product performance and/or formulation specs. Provide disposition and segregation of rejected materials and/or products. Summarize data and provide appropriate reports. Maintains rework inventory. Provides samples and sample data. Maintain calibration/verification records for all lab testing instrumentation and hand-held devices. Prepare test pipes (go-no go Gauges) for fit testing. Supply manufacturing with calibrated measuring and test equipment. Provide organizational quality support by assisting with problem resolution on the shop floor which includes gathering information on any quality-related issues, conducting root cause analysis and providing resolution for non-conformities. Participate in manufacturing CIP meetings as the QA representative and in ongoing quality training of manufacturing and QA staff. Maintain good housekeeping in lab, office and storage areas. Maintain and keep organized all QA files and documentation for easy reference and ISO9001 documentation compliance. Other duties as assigned. Knowledge and Experience Good communication and organizational skills. Computer literacy with Microsoft Office software applications. Excellent problem-solving and analytical skills. Basic understanding of quality concepts including variation, process control and root cause analysis. Cooperative attitude toward co-workers and supervisors. Knowledge of various equipment used in a laboratory (Fill machines, pallet jack, box knife, batch gun, mix tanks, drum mover, microscope, viscometer, Gas Chromatograph, and computer). Education and Certification High School Diploma required. Associate's Degree in a business, engineering or scientific course of study or equivalent experience in a manufacturing or laboratory environment preferred.

Job Description About Us Stellar Industries is a rapidly growing industry leader in manufacturing metalized ceramics. We are a major supplier of innovative, high-quality parts to the Aerospace, Photonics, Telecommunications, and Commercial industries. The company was acquired by TRUMPF Photonics in 2019 and has significant growth goals. About the Role The Quality Control Inspector Level II maintains quality standards by inspecting incoming materials from outside suppliers, in-process production, and finished products in accordance with the quality standards and operating procedures set forth by the Head of Quality Control/Quality Assurance. What You Get to Do Works independently with minimal supervision. Maintain an organized and clean work area. Uses Hand tools, including but not limited to tweezers, calipers, and micrometers. Confirms specifications by conducting visual and measurement tests. Works with a variety of blueprints and technical drawings; must be able to interpret changing requirements as products and builds vary. Completes a General Inspection Report by documenting inspection findings regarding product dimensions, quantity of parts accepted/rejected, and basis of rejection. Uses Vision Systems and documents results into the computer. Follow all safety protocols. Cross-train as requested in other areas of the company. About You Minimum of 3 years of quality control experience. Must be able to work in a sitting position for up to 10 hours. Must be able to wear a lab coat, spittle mask, and gloves while working. The position requires working with measuring devices and microscopes. Individuals must have previous experience working in a similar environment. Must be able to work independently and demonstrate extremely high levels of precision and accuracy. line, High-Temperature BTU Furnaces, as well as various facility-related items, including air handlers, air compressors, air filtration units, etc. What We Offer Competitive pay A generous benefits package that includes medical, dental, 401K plan, and PTO Employer-paid vision plan, Employer paid Basic Life and AD&D Insurance, and Employer Paid Disability Insurance Tuition Reimbursement 4-Day workweek, Monday-Thursday 12 pm-10:30 pm Monday-Thursday 12:00 pm - 10:30 pm

At Spindrift, we're making every beverage a positive force of nature. Founded in 2010, we believe the best flavors come directly from nature. That's why every Spindrift beverage is made the hard way-with real squeezed fruit, never from concentrate. From sourcing the best-tasting fruit globally to maintaining a carefully honed manufacturing process, we believe in doing things the hard way, the intentional way, the better albeit more challenging way, the right way - because, in the end, it's worth it. Spindrift sparkling water is available nationwide, and Spindrift Spiked and Spindrift SODA is available in select markets. We are also a proud member of 1% for the planet, donating to environmental causes. Spindrift is headquartered in Newton, MA. The Quality Technician Role The Quality Technician will be responsible for supporting the Spindrift quality program across Spindrift's beverage portfolio, assist with maintenance of the retain library, assistance with recruiting and training internal sensory panelists, assist with collecting, synthesizing and archiving data as it relates to quality initiatives. Responsibilities include: Assisting the Sensory Analyst with managing the Spindrift sensory program by supporting new panelist onboarding and training, product retain tastings onsite, raw material evaluations, and standard production retains Assisting with managing the Product Retain Library to ensure it is neatly organized at all times, including maintaining an orderly process of receiving/processing product retains into the library upon arrival and the disposal/removal of out-of-date code samples Supporting the creation and organization of quality documentation (i.e. SOPs, protocols, training documents and more as needed) Collaborating with various teams within operations on the following activities: Finished product releases as needed, including review of finished micro reports and sensory evaluations Production holds as needed, including performing sensory evaluations on finished product and communicating results to relevant parties Assist with qualification of new suppliers, including performing required sensory evaluation of raw materials to determine acceptability for use Data entry and approval for specified raw materials into quality management system Assist with consumer complaint process, to include but not limited to: data entry, sample collection, investigation support Requirements Previous food safety experience, with experience in HACCP, GMP, USDA, or FDA preferred. Previous experience with SQF, ISO, GFCO, and/or FDA audits desirable Excellent verbal and written communication skills Thrives in an entrepreneurial environment and considers no task too small nor too large Consistently demonstrates accuracy, thoroughness and dependability Establishes and maintains effective channels of communications with internal and external contacts Adjusts tasks and focus in accordance with changing deadlines and priorities Available to travel up to 10% Able to work in the Newton, MA office Benefits Hourly rate for this part-time position is $22 - $25 / hour, 24-32 hours per week.

We're hiring a Metrology Quality Technician to join our quality team. This role is hands-on with CMM programming, precision inspections, and GD&T, ensuring our products meet the highest standards. You'll support engineering, new product development, and quality investigations while working with cutting-edge inspection tools. Key Responsibilities Program and troubleshoot CMMs;perform precision inspections including FAIs. Apply GD&T and ASME standards to ensure product compliance. Use a variety of inspection tools (calipers, micrometers, vision systems, 3D scanning, etc.). Partner with engineers and quality teams to improve inspection methods and support new product development. Document inspection results and contribute to quality investigations. Qualifications Associate degree or higher in engineering, design, or manufacturing. 3+ years of experience in measurement, CMM programming, and GD&T. 6+ years in a manufacturing environment. Strong knowledge of inspection tools and ASME Y14.5 (certification preferred). Proficiency with Microsoft Office;strong communication and teamwork skills. Why Join Us Work with advanced inspection technology in a clean, collaborative environment. Be part of a team dedicated to precision, quality, and continuous improvement. Opportunities to grow your skills and contribute to impactful projects.

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. This position will have the primary responsibility for daily formulation activities to ensure schedule activities are completed, formulation materials and equipment are maintained, as well as the responsibility for performing corrective and preventative actions. As a secondary function, provide troubleshooting expertise for manufacturing of products both internally and externally of the company. Essential Duties and Responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The basic duties and responsibilities include the following, but other duties may be assigned. Has ownership for the daily formulation activities to ensure scheduled all scheduled tasks/events are completed Is responsible for critical steps in the formulation process including but not limited to, lab setup and process flows, in-process testing, API dissolution and final QS while ensuring safety, batch integrity and prevention or errors that could lead to product and or finical loss Initiate the production of batch documentation used for engineering and cGMP production. Prepare and update Master Production Batch records and SOPs accurately for communicating and initiate the documentation change process for needed documentation changes Complete executed Batch Records accurately and completely prior to submission to supervision for review Comply with all area SOPs and ensure logbooks are completed, and adhere to cGMP requirements Author process deviations when these occur within the department, participate in investigations, and contribute to identifying corrective and preventative actions Cross train to increase technical skills across the department Accountable for timely communication to management and clients of issues, challenges as well as opportunities for process improvements. As a member of the manufacturing team, you will perform other manufacturing tasks for example filling, capping etc., as needed. Work with enabling groups to improve/implement processes. Other duties as assigned. Strong interpersonal skills Strong working knowledge of MS Office suite is preferable Attention to detail and positive attitude are key attributes Able to follow rules and regulations perfectly Works directly with aseptic and non-aseptic personnel. Works closely with Quality Assurance, MTS, Validation etc. Qualifications: The requirements listed below are representative of the knowledge, skill, and/or ability required for the stated position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Required: High School education or AS degree or BS degree in Chemical Engineering/ Bio Chemistry or other industry related discipline is preferred Experience and knowledge of formulation/compounding tools and equipment Minimum 1-2 year's work experience in a GMP environment preferably in fill finish pharmaceutical operations Demonstrated ability to prioritize multiple projects and activities Full Professional Proficiency: Ability to speak, read, and write fluently and accurately on all levels pertinent to professional needs. #LI-KC1 Join us and be part of building the bridge between life changing therapies and patients. Let's talk future Equal Employment Opportunity (EEO) Statement: PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

Supports Quality Assurance and Control activities to ensure products and procedures meet all applicable internal and external requirements. Supports the administration and maintenance of quality systems. Provides support for quality projects dictated by the Quality Leadership. ESSENTIAL FUNCTIONS AND RESPONSIBILITIES * Supports the administration and maintenance of in-process inspection reports, final inspection reports, and First Article inspection Reports compliant with AS9102 using Discus inspection report software. * Maintain calibrated test equipment, ensures equipment is calibrated, validated and maintained properly, maintains the calibration system, prepare test data, and identify areas for improvement. * Reads and interprets work instructions and to determine dimensions and tolerances. * Reads blueprints or specifications to determine dimensions and tolerances. * Collates test data and drafts quality reports. * May interpret test results and compare them to the specifications and control limits in place while providing recommendations on the appropriateness of data. * Supports QMS activities including but not limited to CAPA, Internal Audits, Document Control, Records Management, etc. * Maintain QMS documentation; revise and update documentation, assign training based on documentation changes. * May interpret Geometric Dimensioning & Tolerance * Strong attention to detail, organization, and documentation skills. * May verify specified dimensions of product or raw material using verniers, micrometers, CMM, height gages, comparator, scales or other tools. * Assists in other areas in support of product conformity. * Demonstrates responsibility and accountability for creating a professional, safe, and clean environment evidenced by: being at work on time to perform assigned duties, following the policies of Granite State Manufacturing, always wearing safety glasses in designated areas, maintaining a neat and orderly work area, and following safety practices to prevent errors. * Demonstrates commitment to teamwork by establishing effective relationships and networks with both managers/directors and workers and collaborating with them to accomplish shared purposes and goals. * Complies with federal and state laws, regulations, specifications and company standards. * Abides by GSM Code of Ethics and Business Conduct standards and strictly observes all U.S. and foreign laws and regulations.

Job Title: Quality Technician Pay: $22-$25 per hour, depending on experience Hours: Monday - Thursday, 6:00 AM - 2:30 PM, and a half day on Friday! 36 hours a week! As a Quality Technician, you'll help ensure that all customer and company quality standards are met-from raw materials to finished goods. You'll work closely with the Quality Manager and other team members to support inspections, documentation, and compliance activities that keep operations running smoothly. What You'll Do As a Quality Technician, you will be responsible for: Reviewing and approving testing reports from third-party laboratories Maintaining up-to-date knowledge of ASME regulations and applicable industry codes Receiving and inspecting returned products to determine quality and return category Evaluating inbound goods, preparing documentation, and managing return transactions Using metrology hand tools and small test fixtures to perform mechanical inspections Collaborating with the MRB team to determine the disposition of nonconforming materials Supporting company quality standards and 6S organization practices Working independently with minimal supervision Performing additional duties as assigned by the Quality Manager What You'll Bring The ideal candidate for this role will have: High school diploma or equivalent (technical education preferred) At least 5 years of experience in a similar quality technician or inspection role Strong math and mechanical aptitude Ability to read and interpret blueprints Familiarity with ASME Section II and IV (preferred) Proficiency with Microsoft Office and general computer use Experience with ERP systems such as M2K (inventory moves, RGA processing, etc.) Excellent communication, organization, and time management skills Ability to lift up to 35 pounds and work in a fast-paced environment Why Join Us in Rochester, NH? Stable schedule: Enjoy a four-and-a-half-day workweek with Fridays ending early Great pay: Competitive hourly rate based on experience Career opportunity: Temp-to-hire position with long-term potential Affordable health and prescription coverage with no waiting period Employer benefits available upon permanent hire Ask about our Referral Bonus Program to earn extra cash! Location & Schedule This position is on-site in Rochester, NH and follows a Monday-Thursday 6:00 AM-2:30 PM, Friday half-day schedule. 36/HRS a week! Ready to Take the Next Step? If you're ready to start a rewarding career as a Quality Technician in Rochester, NH, apply today or contact our recruiting team to learn more. Don't wait - we're hiring now!

Job Description The Quality Technician - FAI Specialist is responsible for coordinating and supporting the creation of AS9102 First Article Inspection Reports (FAIR) in alignment with industry and customer specific requirements. This position works alongside various other departments and is vital to ensuring success of the AS9102 program. Duties/Responsibilities: Navigates internal company software and database systems to gather information. Accurately completes AS9102 Reports (FAIR) and other dimensional inspection reports as required. Interpret drawings, specifications and customer requirements. Works effectively and communicates with various departments, including: Planning, Marketing, Quality, QC Inspection and Source Inspection. Assures accuracy of FAI programs and records. Assists with identifying opportunities for improvement within the FAIR process to aid in the success of the Quality Department. Maintain a positive work environment by acting and communicating in a manner so that you get along with customers, clients, vendors, co-workers and management. This position may require overtime for coverage on alternate shifts and weekends. Will be required to perform other duties as requested, directed or assigned. Requirements: High School diploma or General Education Degree (GED). Previous experience as a First Article Inspection Specialist is preferred but not required. Must be able to use a computer to maintain records, develop reports, and analyze data and document discrepancies as well as using a computer to perform all other related aspects of the position. Must have excellent communication skills and ability/flexibility to work in a fast-paced environment. Must be able to read and interpret technical drawings, prints and industry/customer specifications. Must be able to read and interpret GD&T requirements. Must be able to display a thorough attention to detail and organization. Amphenol offers a competitive salary and benefits. The candidate must be able to legally work in the United States; we are unable to provide sponsorship. Position requires candidate to be a U.S. person as defined in ITAR, 22 CFR 120.15 (U.S. Citizenship or Resident Alien Status) and defined by 8 U.S.C. 1101(a) (20). Amphenol is a proud Equal Opportunity Employer as to all protected groups, including Individuals with Disabilities and Protected Veterans. For consideration for this position, please apply online to: ********************************** APC878

Milliken & Company is a global manufacturing leader whose focus on materials science delivers tomorrow's breakthroughs today. From industry-leading molecules to sustainable innovations, Milliken creates products that enhance people's lives and deliver solutions for its customers and communities. Drawing on thousands of patents and a portfolio with applications across the textile, flooring, chemical and healthcare businesses, the company harnesses a shared sense of integrity and excellence to positively impact the world for generations. Discover more about Milliken's curious minds and inspired solutions at Milliken.com and on Facebook, Instagram, LinkedIn and Twitter. POSITION TITLE / LOCATION: Quality Control Technician I: 3rd Shift / Salisbury, MA TÍTULO DEL PUESTO / UBICACIÓN: Técnico de Control de Calidad I: 3er turno / Salisbury, MA JOB CLASSIFICATION: Non-Exempt CLASIFICACIÓN DE TRABAJO: No exento POSITION REPORTS TO: Quality Control Supervisor REPORTE DE POSICIÓN A: Supervisor de Control de Calidad POSITION OVERVIEW - RESUME DE LA POSICION Entry level QC technician responsible for conducting standard quality control test methods and process auditing. Técnico de control de calidad de nivel de entrada responsable de realizar métodos de prueba de control de calidad estándar y auditoría de procesos ESSENTIAL JOB DUTIES AND RESPONSIBILITIES DEBERES Y RESPONSABILIDADES LABORALES ESENCIALES * Adhere to all safety policies Cumplir con todas las políticas de seguridad * Understand and follow current good manufacturing practices as defined within Ovik procedures Comprender y seguir las buenas prácticas de fabricación actuales, tal y como se definen en los procedimientos de Ovik * Understand and follow good documentation practices Comprender y seguir las buenas prácticas de documentación * Maintain awareness of ISO 13485 Mantener el conocimiento de la norma ISO 13485 * Understand the manufacturing process from beginning to end Comprender el proceso de fabricación de principio a fin * Understand all QC procedures and be able to perform all QC checks and audits Comprender todos los procedimientos de control de calidad y ser capaz de realizar todas las comprobaciones y auditorías de control de calidad * Update QC test results in SAP Actualizar los resultados de las pruebas de control de calidad en SAP * Prepare and send the QC shift report Preparar y enviar el informe de turno de control de calidad * Prepare test samples and use all QC lab equipment Prepare muestras de prueba y utilice todo el equipo de laboratorio de control de calidad * Correct handling and disposition of nonconforming product Manejo y disposición correctos del producto no conforme * Conduct standard analytical test methods after method and equipment training Llevar a cabo métodos de prueba analíticos estándar después de la capacitación sobre métodos y equipos * Record test data and escalate findings appropriately to supervisor or manager Registre los datos de las pruebas y escale los hallazgos de manera adecuada al supervisor o gerente MINIMUM QUALIFICATIONS - CUALIFICACIONES MÍNIMAS * High school diploma or equivalent PREFERRED QUALIFICATIONS - CALIFICACIONES PREFERIDAS * Laboratory experience Experiencia en laboratorio * Medical device manufacturing experience Experiencia en la fabricación de dispositivos medicos * Bilingual (English/Spanish) Bilingüe (Inglés/Español) SKILL REQUIREMENTS - REQUISITOS DE HABILIDAD * Ability to read, write, and perform basic math at an 8th grade level Capacidad para leer, escribir y realizar matemáticas básicas a un nivel de 8º grado * Competency in Microsoft Outlook, Excel, and Word Competencia en Microsoft Outlook, Excel y Word AUTHORIZED TRAINING TIME - TIEMPO DE FORMACIÓN AUTORIZADO 90 days/90 dias MACHINES, TOOLS AND EQUIPMENT USED: MÁQUINAS, HERRAMIENTAS Y EQUIPOS UTILIZADOS: * Laboratory measuring equipment (scale, viscometer, pH meter, tensile tester, unwind tester, calipers, rulers, beakers, pipettes, etc.) Equipos de medición de laboratorio (báscula, viscosímetro, medidor de pH, probador de tracción, probador de desenrollado, calibradores, reglas, vasos de precipitados, pipetas, etc.) * Sample preparation equipment (knives, die cutters, roll down machine, etc.) Equipo de preparación de muestras (cuchillas, troqueladoras, máquina de enrollar, etc.) PERSONAL PROTECTIVE EQUIPMENT USED: EQUIPOS DE PROTECCIÓN PERSONAL UTILIZADOS: * Safety Eyewear (additional when executing certain tasks) Gafas de seguridad (adicionales al ejecutar ciertas tareas) * Steel Toe Safety Shoes/Zapatos de seguridad con punta de acero * Hairnet/Redecilla * Cut resistant gloves, chemical gloves, etc. as needed/Guantes resistentes a cortes, guantes químicos, etc. según sea necesario * Bump cap/hard hat as needed/Gorra de golpe/casco según sea necesario PHYSICAL REQUIREMENTS FREQUENCY, AMOUNT, OR DESCRIPTION REQUISITOS FÍSICOS FRECUENCIA, CANTIDAD O DESCRIPCIÓN * Standing: Ability to stand while working 80% of day Estar de pie: Capacidad de estar de pie mientras se trabaja * Sitting: Ability to sit down 20% of day Sentado: Capacidad para sentarse * Moving: Ability to move throughout plant: 100% of day Movimiento: Capacidad de moverse a través de la planta: * Lifting: Ability to lift to 25 lbs. 100% of day Elevación: Capacidad de levantar hasta 25 libras * Ascending/Descending: Ability to walk upstairs, climb to top of range (approx. 16 ft) 75% of day Ascendente/Descendente: Capacidad de subir las escaleras, subir a la cima del rango (aprox. 16 pies) * Push/Pull/Reach: Ability to push/pull fabric rolls, A-frames (approx.1500lbs) 10% of day Empujar/Tirar/Alcanzar: Capacidad de empujar/tirar de rollos de tela, marcos en A (aprox. 1500 libras) * Bending: Ability to pick up objects from the floor 25% of day Agacharse: Capacidad de recoger objetos del suelo * Visual Acuity: Visual acuity adequate to perform job duties, including reading information from printed sources and computer screens. 90% of day Agudeza Visual: Agudeza visual adecuada para realizar las tareas laborales, incluyendo la lectura de información de fuentes impresas y pantallas de ordenador. * Cognitive: Alert. Able to make decisions, reason, and understand information. 100% of the day Cognitivo: Alerta. Capaz de tomar decisiones, razonar y comprender información. WORK ENVIRONMENT/SAFETY-SENSITIVE POSITION ENTORNO DE TRABAJO/POSICIÓN SENSIBLE A LA SEGURIDAD This job operates in a manufacturing facility. This position is a safety-sensitive position and regularly works around moving mechanical parts and powered industrial vehicles. Noise level is generally loud. Temperatures can be more than 100 degrees Fahrenheit. Humidity level can be more than 98% for 100% of day. Este trabajo se realiza en una planta de fabricación. Esta posición es sensible a la seguridad y trabaja regularmente alrededor de piezas mecánicas móviles y vehículos industriales motorizados. El nivel de ruido es generalmente alto. Las temperaturas pueden ser de más de 100 grados Fahrenheit. El nivel de humedad puede ser superior al 98% durante el 100% del día. SHIFT/WORK HOURS - TURNOS/HORAS DE TRABAJO Shift schedule will depend on open positions at time of hire and will be communicated with new hire paperwork. Weekends and holidays are scheduled depending on business demands. El horario de turnos dependerá de los puestos vacantes en el momento de la contratación y se comunicará con la documentación de los nuevos contrataciones. Los fines de semana y días festivos se programan en función de las demandas del negocio * To be determined at time of hire A determinar en el momento de la contratación * OT when scheduled OT cuando esté programado Pay Transparency/ Transparencia Salarial: The hourly rate range for this position is $22.00 to $23.00; the exact hourly rate depends on several factors such as experience, skills, education and budget. El rango de salario por hora para este puesto es de $22.00 a $23.00; la tarifa exacta por hora depende de varios factores como la experiencia, las habilidades, la educación y el presupuesto. Milliken is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to actual or perceived race, color, creed, religion, sex or gender (including pregnancy, childbirth or related medical condition, including but not limited to lactation), sexual orientation, gender identity or gender expression (including transgender status), ancestry, national origin, citizenship, age physical or mental disability, genetic information, marital status, veteran or military status or any other characteristic protected by applicable law. It is unlawful in Massachusetts to require or administer a lie dectector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Job Title: Intermediate Quality Technician Company: Munters Schedule: Monday-Thursday, 6:00 AM - 4:30 PM Salary: $26.17/hr. - $33.10/hr. About Us: Munters is a global leader in climate solutions for mission-critical processes. We offer innovative, efficient and sustainable solutions for customers in industries where controlling indoor humidity, temperature and energy efficiency is mission-critical. Climate control systems often account for a large percentage of the energy consumption in many of our customers' operations. With an optimal climate system, we can help them to more efficiently use energy or water resources, and thereby reduce their climate and environmental impact. Sustainability is an important part of Munters' business strategy and value creation. We pride ourselves on fostering a dynamic and inclusive work environment where interns are valued members of the team and are given meaningful projects to work on. Job Description: Work as part of final test team, analyzing and correcting electrical problems. Keeps the Team Leader and Quality Manager informed of all issues affecting the performance of the department or product quality or delivery. Responsibilities: Assumes delegated responsibilities from the Team Leader of the Quality department. When working with lower graded electrical personnel, assumes some responsibility to coordinate the mutual effort and provide guidance and direction to perform the work in a safe and workmanlike manner and the installation be in compliance with specifications, established standards and the National Electric Code Understands electrical theory and practice as applied to the operation of such components as electric motors, motor starters, contractors, control relays, time delay relays, circuit breakers, and other related electrical, pneumatic and mechanical components Applies trade knowledge and experience to recognize errors or potential problems with schematics, assembly drawings, parts lists or instructions. Advise supervisor of problems or questions and, if possible, recommends solutions Prepares, without supervision, electrical components and subassemblies at the bench or on the product following specified methods and techniques. Cuts or extends lead wires, attaches terminals or connections. Interconnects wires according to diagrams or schematics Inspects repair jobs, prepare list of parts to be replaced or repaired. Tests repaired or reconditioned unit for compliance with specifications or established standards Installs, without supervision, a complete electrical and/or pneumatic system utilizing electrical conduits, fittings, boxes and wire, following electrical diagrams and schematics. Insures that the components are secure and free from any interference and functioning properly Performs trouble-shooting as necessary on parts or subassemblies to identify and resolve the problem Tests unit using required test equipment and complete test reports Performs work and/or delegated responsibilities without supervision and with either verbal or written instructions. Ensures work area is clean and orderly Work in other areas when needed. Maintain ISO standards Observe all safety rules Requirements: Understands electrical theory and practice Capability of reading electrical diagrams and schematics Requires at least 1 year of experience in manufacturing or relevant experience High school diploma or equivalent Medium Work: Exerting up to 50 pounds of force occasionally and/or up to 20 pounds of force frequently, and/or up to 20 pounds of force constantly to move objects Climbing, stooping, kneeling, crouching, reaching, standing, walking, pushing, pulling, lifting The worker is required to have close visual acuity to perform an activity such as: preparing and analyzing data, viewing computer terminal, expansive reading, etc. The worker is not substantially exposed to adverse environmental conditions Benefits: Competitive salary Comprehensive health, dental, and vision insurance plans. Flexible work schedule Generous vacation and paid time off. 401(k) retirement savings plan with employer matching. Professional development opportunities, including tuition reimbursement and conference attendance. Company-sponsored social events and team-building activities. State-of-the-art equipment and tools to support your work. Equal Opportunity Employer: We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status. All offers are contingent on a pre-employment drug test and background check, as applicable for the position. #HPMUNTERS