Quality assurance technician jobs in Loveland, CO - 228 jobs

LSG Sky Chefs is a leading provider of in-flight food services, delivering high-quality meals to approximately 300 airlines across the globe. With a commitment to innovation and excellence, we operate around 200 service centers in nearly 50 countries, serving over 425 million meals annually. Voted “Airline Caterer of the Year in North America” for three consecutive years 2023, 2024, and 2025 we are committed to excellence and innovation, driven by the dedication and expertise of our talented employees. Our team members are the heart and soul of our success, consistently delivering exceptional culinary experiences and outstanding service to our clients and their passengers across North and Latin America. Our focus on enhancing customer satisfaction and adapting to industry changes positions us as a key player in the airline catering sector. Position Overview As a Quality Assurance Specialist, you'll take the lead in maintaining LSG Sky Chefs' and LHI's Global Quality System, ensuring our Customer Service Center (CSC) consistently meets the highest standards. In this role, you'll champion food safety and regulatory excellence by driving adherence to FDA, USDA, and HACCP guidelines, including seafood-specific protocols. Your expertise will help us deliver world-class service while guaranteeing every product meets stringent customer requirements and regulatory standards, because quality isn't just a goal here, it's our promise. Compensation & Benefits Competitive Base Salary Medical, Dental, Vision - starts Day 1 401(k) with Company Match Paid Time Off, Sick Leave & Holidays Tuition Reimbursement - support for professional development Free Parking & Daily Meals Membership to American Airlines Credit Union Opportunities for Advancement What You'll Do Perform a general walk through of the CSC and take notes of all hygiene, operational and building concerns to be reported promptly to the QA Supervisor/Manager before morning briefing. Conduct internal temperature checks in coolers and on prep racks and record temperature on Daily HACCP Temperature Monitoring Log. Conduct pre-operational inspection of all Food related areas and record findings and Daily Sanitation Report. Follow-up on rejected areas or equipment if necessary. Perform a general walk-through of the CSC before the end of the shift and take notes of all hygiene, operational and building concerns to be reported to the QA supervisor/manager on duty. Conduct an inspection of all Pest & Rodent Control equipment. Building Sanitation Performance and Walk-Through Inspection should be conducted once every week. Assist the QA supervisor on the conduct of GQS internal Hygiene Process audit. Assist the QA Supervisor in the preparation of the GQS Chef table and/or Portion Control of randomly selected prepared food item. Others duties as assigned by QA Manager What We Look for in a Candidate Must demonstrate excellent communication skills, both oral and written. Strong presentation, communication, training and interpersonal skills. Strong knowledge of Food Safety, HACCP, USDA & FDA regulations a plus Must have ability to work under pressure while maintaining composure. Must be a team spirited individual. Must be flexible on days off and start time LSG Sky Chefs is an EEO and Affirmative Action Employer of Women/Minorities/Veterans/Individuals with Disabilities.

Civil Technology Inc. (CTI) is seeking a qualified Field Quality Control Manager to support work to modify and upgrade Baggage Handling Systems (BHS) at Denver International Airport (DEN). This role is instrumental in ensuring the BHS scope is completed as designed and expected, and will work closely with another quality inspector to review design documents and inspect field installation of the BHS system. We are specifically looking for a professional with hands-on experience inspecting electrical systems and process control systems for conveying/transport systems. Prior BHS experience is ideal-however, experience from industrial manufacturing environments manufacturing facilities can translate extremely well to this role. This position will primarily be on the day shift, with flexibility required as construction activities may drive off-hour and night inspections. Key Responsibilities Review project documents including construction drawings, submittals, shop drawings, and approved installation methods related to the BHS installation. Verify BHS components received onsite are supplied and installed in accordance with construction documents, shop drawings, submittals, RFIs, and Certificate of Compliance requirements. Perform shop inspections when needed to confirm compliance and readiness for installation. Verify electrical installation is completed in accordance with approved documents and related RFIs, including: Main power and control power Motors, conveyors, and BHS control systems Inspect and validate process control systems supporting BHS operations, including control devices and logic-driven conveying systems. Perform required site inspections and complete Quality Control Inspection Reports in ACC. Prepare Quality Reports in ACC for night shift inspections, ensuring required inspection scope is understood and executed by night inspectors. Meet with DEN QA representatives, attend quality follow-up inspections, and prepare Quality Reports in ACC. Attend meetings and inspections with DEN Operations (Log Plan) and prepare special reports for distribution with the project team. Perform inspections to document construction progress and re-inspect open structural, electrical, and mechanical issues, tracking status and resolution in ACC. Participate in planned temporary mock-up installations, including conveyor system electrical and control device installation. Provide extensive coordination between contractor personnel/activities and owner representatives to ensure BHS systems are installed correctly and operate as expected. Communicate clearly and professionally (written and verbal) to support issue resolution and maintain alignment across the team. Support other quality-related activities as requested. Preferred Experience Previous work experience with baggage handling systems (BHS) (highly preferred) Strong background inspecting: Electrical systems for conveying and transport systems Process control systems and logic-driven equipment In lieu of direct BHS experience, applicable experience from industrial/manufacturing conveying systems, including: Bottle/can manufacturing facilities (Pepsi, Coca-Cola, Coors, etc.) Automated production lines with process control and sequencing logic Experience supporting manufacturing plants and operations Aviation experience (preferred) Experience working on large, complex, active facilities requiring detailed coordination and communication Work Location & Requirements Work is located 100% onsite at Denver International Airport (DEN) Must be able to pass all required background checks for airport badging and access Why Join CTI? High-Impact Work: Be part of transformational projects shaping Denver's infrastructure. Competitive Compensation: Strong salary and opportunities for growth. Family-Oriented Culture: Supportive, close-knit environment that values collaboration and communication. Tangible Benefits: Full benefits package, competitive 401(k) matching, certification support, and more. Big Impact, Small Team: Your contributions won't get lost in the crowd-they'll be recognized and appreciated. Commitment to Diversity: Certified SBE, M/WBE, DBE, and ESB; we value every voice. Cutting-Edge Projects: Work on complex, high-profile construction management efforts at DEN and beyond. Continuous Learning: Professional development and certification support are core to our culture. Small Business Advantage: Agility and entrepreneurial spirit with the resources and reach of legacy projects. Additional Benefits 401(k) with match Cell phone reimbursement Dental insurance Fuel discounts Health insurance Paid time off Professional development assistance Performance bonuses About Civil Technology Inc. Since 1989, Civil Technology, Inc. (CTI) has been pushing the boundaries of construction and program management in Denver for decades. We don't just manage projects-we elevate them. From pre-design to the final closeout, our team delivers unmatched expertise, ensuring every project not only meets but exceeds expectations.

Join a leading life sciences company as a Lab Technician, where you will play a crucial role in ensuring the safety and quality of products across various industries. You will be part of a dynamic team focused on making life and our environment safer, healthier, and more sustainable. Responsibilities Split and homogenize incoming samples in compliance with standard operating procedures and quality systems. Maintain and care for equipment associated with sample processing. Prepare test samples by splitting, grinding, and homogenizing aseptically for further testing. Clean the workplace and equipment following standard operating procedures and general housekeeping requirements. Provide feedback to department management for procedural improvements. Monitor and meet turnaround time (TAT) requirements for sample workflow, informing management of any anticipated delays. Perform operational qualifications prior to analysis as per standard procedures. Log and deliver sample splits to testing departments, obtaining necessary signatures. Log, store, and properly discard sample retains according to procedures. Perform environmental monitoring as needed. Assist in client sample processing with appropriate media and support other technicians in weekly sample preparation and aseptic operations. Essential Skills High School Diploma Proficiency in computers and Excel Ability to work cooperatively and independently Effective verbal and written communication skills Interest or focus in science, biology, or microbiology Authorization to work in the United States indefinitely without restriction or sponsorship Additional Skills & Qualifications Associates Degree or Bachelors Degree preferred Experience in food service is beneficial Ability to lift 50 lbs Punctual, team player, with a growth mindset Experience from a stable work history is advantageous Work Environment Work in a production-based analytical lab with a team of 11 technicians. The lab handles a variety of samples, including protein bars, skincare products, produce, and raw meat, under ambient and cold conditions. Tests conducted include meat study validation and detection of pathogens such as Salmonella, Listeria, and E. Coli. Available Schedules Tuesday - Saturday 9:00 AM - 5:00 PM Tuesday - Saturday 12:00 PM - 8:00 PM Tuesday - Saturday 2:00 PM - 10:00 PM Training is Monday - Friday (3 weeks) Job Type & Location This is a Contract to Hire position based out of Lafayette, CO. Pay and Benefits The pay range for this position is $18.50 - $20.00/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 Lafayette,CO. Application Deadline This position is anticipated to close on Jan 30, 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.

**Our promise to you:** Joining AdventHealth is about being part of something bigger. It's about belonging to a community that believes in the wholeness of each person, and serves to uplift others in body, mind and spirit. AdventHealth is a place where you can thrive professionally, and grow spiritually, by Extending the Healing Ministry of Christ. Where you will be valued for who you are and the unique experiences you bring to our purpose-minded team. All while understanding that **together** we are even better. **All the benefits and perks you need for you and your family:** + Benefits from Day One: Medical, Dental, Vision Insurance, Life Insurance, Disability Insurance + Paid Time Off from Day One + 403-B Retirement Plan + 4 Weeks 100% Paid Parental Leave + Career Development + Whole Person Well-being Resources + Mental Health Resources and Support + Pet Benefits **Schedule:** Part time **Shift:** Day (United States of America) **Address:** 2525 S DOWNING ST **City:** DENVER **State:** Colorado **Postal Code:** 80210 **Job Description:** Adjusts approach based on patient and family understanding of test procedures and troubleshoots equipment malfunctions or patient issues. Prioritizes clinical and administrative work independently and identify process improvements. Other duties as assigned. Assists physicians in performing specialized cardiovascular procedures, including diagnostic and interventional catheterization, pacemaker/defibrillator implantation, intra-aortic balloon pump operation, and electrophysiology studies. Evaluates and documents patient status, responding appropriately to ensure optimal outcomes. Demonstrates clinical expertise, competence, and proficiency in all job responsibilities. Commits to continuous learning and shares knowledge with patients and co-workers. Participates in performance improvement activities to evaluate and enhance care outcomes. Uses evidence-based practices to monitor and improve care according to regulatory and practice standards. Operates equipment, manages time, and utilizes personnel and supplies effectively to deliver high-quality, cost-effective patient care. Adapts to changing workloads, patient needs, technologies, policies, regulations, census, and staffing through priority setting and flexibility. Maintains high skill levels through participation in continuous quality improvement, in-services, ongoing education, and attendance at staff meetings. Recognizes and acts upon unusual patient results or responses by informing the primary healthcare team to ensure patient safety. **The expertise and experiences you'll need to succeed:** **QUALIFICATION REQUIREMENTS:** Bachelor's, Technical/Vocational School (Required) Advanced Cardiac Life Support Cert (ACLS) - RQI Resuscitation Quality Improvement, Basic Life Support - CPR Cert (BLS) - RQI Resuscitation Quality Improvement, Certified Surgical Assistant (CSA) - EV Accredited Issuing Body, Registered Cardiac Electrophysiology Specialist (RCES) - EV Accredited Issuing Body, Registered Cardiovascular Invasive Specialist (RCIS) - EV Accredited Issuing Body, Registered Technologist - Cardiac-Interventional Radiography (R.T(CI)(ARRT)) - EV Accredited Issuing Body, State Certified Surgical Technologist (CST) - EV Accredited Issuing Body **Pay Range:** $32.53 - $60.50 _This facility is an equal opportunity employer and complies with federal, state and local anti-discrimination laws, regulations and ordinances._ **Category:** Medical Assistant & Technician Services **Organization:** AdventHealth Porter **Schedule:** Part time **Shift:** Day **Req ID:** 150659159

Leprino Foods' history dates back over 65 years, when Jim Leprino first started making small batches of mozzarella for local markets and eateries in the Little Italy neighborhood of Denver. We've grown a bit since then. Today, Leprino is the largest manufacturer of mozzarella and lactose in the world, and a leading producer of whey protein. Still owned by Jim and the Leprino family, our sights are set to be the "World's Best Dairy Food and Ingredient Company." To help us achieve that daring vision, we're looking for our secret ingredient: You. A motivated individual who is the best at what you do. Three people in a small corner grocery store in the early 1950s have now grown to over 4,300 employees throughout 16 global locations. Will you join us on our journey? The Greeley Team is seeking a Quality Technician / Team Member II to help us achieve our goals. We Ask of You To: * Be responsible for the safe operation of its associated equipment and/or processes, the quality of incoming raw materials, the quality of the outgoing products in accordance with Standard Operating Procedures (SOP's), Good Manufacturing Practices (GMP) and safe work practices. * Be responsible for maintaining 5S standards and participating in and implementing continuous improvement. * Communicate effectively in relaying information to team members, team leads, supervisors, and managers as applicable. * Have strong time management and organizational skills. * Meet food safety and quality requirements by following the Food Safety Plan, Quality Plan and company policies. We Offer You In Return: At Leprino Foods, starting compensation for this role is $25.00 per hour. * A chance to be part of a global team of individuals passionate about producing and delivering high-quality products that help feed and nourish families around the world. Leprino Foods could not be where it is today without our incredible employees. That is why we share our success together by rewarding you for your hard work. Hiring great people who are in it for the long run is our goal. Through competitive salaries, tuition assistance, vacation, holiday, dedicated sick time, matching 401(k), annual merit increases and bonuses, as well as our annual Profit-Sharing plan. Your impact will be noticed and rewarded, as you seek to further our company, our customers, and one another. You Must Have (Minimum Qualifications): * Must be 18 years of age * Must be able to read, write and speak the English language in order to understand/adhere to Standard Operating Procedures (SOP's) and Good Manufacturing Practices (GMP's), to communicate effectively with others, to complete required documentation both in written and electronic form, and to troubleshoot systems utilizing the English language. * Must have the ability to perform essential job functions * Must wear required personal protective equipment * Must comply with all applicable safety practices * Maintain a clean work area * Complete written reports * Perform basic and intermediate mathematical calculations * Enter data into and pull data from computer systems * Must possess considerable problem-solving ability in dealing with equipment or troubleshooting when supervision is not readily available for consultation * Must have an understanding of basic chemistry or biology, and basic lab equipment and testing through on the job experience, or through high school or college coursework * Experience in instrumentation operation and troubleshooting in a manufacturing environment, experience with computers and programs We Hope You Also Have (Preferred Qualifications): * Advanced level science knowledge (e.g. chemistry, biology); and lab work experience (e.g. computer-assisted analytical equipment, balances, fat extraction, pH meter, incubators, infrared analyzer (FT2) are preferred. Experience in a manufacturing environment is preferred "The culture of Leprino Foods is built by a family of passionate employees who believe in what they do, who understand the value of teamwork and understand that no one person is greater than the other." - Andy, Greeley, Colorado Plant Manager Leprino Foods Company utilizes the services of Psychemedics to perform our Hair Follicle Drug Testing. Additional information about this process can be obtained at ******************** Leprino Foods Company utilizes the services of Psychemedics to perform our Hair Follicle Drug Testing. Additional information about this process can be obtained at ******************** Leprino Foods requires all individuals to wear the appropriate Personal Protection Equipment (PPE) as required by the role and location. Leprino Foods Company supports a drug-free workplace and is an EEO/Affirmative Action Employer - M/F/Disability/Veteran Leprino uses Psychemedics for a 90-day hair follicle drug test as part of the employee pre-employment process and also participates in E-Verify. All employees in our manufacturing facilities are required to wear Personal Protective Equipment (PPE) as mandated by their role and location.

Starting compensation: $25.00 per hour (plus a $1.50 shift differential) Shift Days: Sunday to Thursday Shift Hours: 2:30 PM to Close Shamrock anticipates closing the application window for this job opportunity on or before December 31, 2026 Lead Quality Control Technicians in maintaining all aspects of Quality Assurance to ensure proper, safe and exceptional operation of the department. Essential Duties: * Audit products for quality and safety prior to sending them out to customers. * Audit incoming raw materials for supplier specifications, quality, and food security. * Review incoming ingredients for allergen checks and quality standards. * Responsible for compliance with all regulations and food safety including allergen and pest control. * Fill out necessary paperwork for product audits and HACCP documents. * Review HACCP documents prior to handing paperwork to QA Supervisor/Manager. * Work with operational teams on paperwork, quality checks, and HACCP procedures. * Ensure adherence to all standard work processes, including the Production Sanitation processes. * Aid in plant training requirements and conduct plant training sessions as needed. * Work with QA leaders to ensure plant training requirements and frequencies are met. * Recognize and escalate risks and/or improvement opportunities to improve plant performance. * Other duties as assigned. Qualifications: * High School Diploma or GED. * 3+ year's meat and/or protein experience. * HACCP certified, preferred. * Must be flexible and willing to work the demands of the department which may be subject to evenings, weekends, and holidays. Corporate Summary: At Shamrock Foods Company, people come first - our associates, our customers, and the families we serve across the nation. A privately-held, family-owned and -operated Forbes 500 company, Shamrock is an innovator in the food industry and has been since being founded in Arizona in 1922. Our Mission: At Shamrock Foods Company, we live by our founding family's motto to "treat associates like family and customers like friends." Why work for us? Benefits are a major part of your overall compensation, and we believe offering them at an affordable cost is not only the right thing to do, but it helps keep you and your family healthy. That's why Shamrock Foods pays for the majority of your health insurance, allowing you to take home more of your paycheck. And it doesn't stop there - our associates also enjoy additional benefits such as 401(k) Savings Plan, Profit Sharing, Paid Time Off, as well as our incredible growth opportunities, continued education, wellness programs. Equal Opportunity Employer Shamrock Foods Company is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, veteran status, sexual orientation, gender identity or any other basis protected by applicable law.

Join our dynamic Quality Assurance team at our Organic Dairy Processing facility in Platteville, CO. Be a part of a 2025 Top Workplace USA! Purpose: The Quality Assurance Lab Technician is responsible for in-process and finished product quality testing, maintaining accurate and complete records, and alerting management to any potential quality issues. S hift Days 6am - 6pm Essential Responsibilities: All plant personnel have the responsibility to monitor and report any deviations from our Food Safety and Food Quality (HACCP & SQF) programs to your immediate supervisor. Assist in all in-bound and finished product milk processing including but not limited to: Customer Service, working with our Laboratory and Product Information Management System, Tanker/Silo Inventory Control, administrative assistant duties. Competency in Microsoft Windows and Office products. Responsible for performing process control testing in a manufacturing environment. Maintain accurate and complete laboratory testing result records. Maintain Good Manufacturing Practices, Good Laboratory Practices and Safety Procedures. Communicate any potential quality issues to QA Management. Professional communication and customer service skills in working with multiple departments and external partners. Other Required Responsibilities: Laboratory testing result data entry. Member of HACCP team. Other quality department responsibilities as deemed necessary. Knowledge & Experience: High School Diploma or equivalent. Bachelor's degree in Dairy Manufacturing, Food Science, Microbiology, or related field preferred. Experience in dairy laboratory testing procedures preferred. Knowledge of laboratory testing methods. Detail oriented and team member. Strong, honest work ethic with ability to handle multiple tasks daily. Good communication skills. Physical Requirements: Must be able to sit for extended periods of time; Must be able to stand or walk for more than 50% of the shift. Must be able to bend, stoop, kneel or crawl; reach grasp and lift, push, pull up to 50 lbs. regularly and up to 80 lbs. occasionally.

Job Description The job of the Quality Control Technician is to ensure compliance with cGMP requirements and company procedures while providing support to the QC team and throughout the QA and Operations departments. Additionally, this role is responsible for coordinating QC sample preparation and external laboratory shipments in relation to Environmental Monitoring activities and other required sampling. This role will work closely with the Production team and report quality data to department management, as needed. Duties/Responsibilities: Maintain retention materials and disposal when required. Assist with review and release of raw materials, API, excipients, and sterile supplies. Coordination of Biohazard waste destruction. Perform sampling and inspection of in-process and finished products. Assists with Environmental Monitoring and microbiological sample evaluation activities. Coordination of submitting samples for testing with third party vendors on their respective web portals or paper submissions. Logbook and controlled document generation. Assist with investigations and develop and implement corrective and preventive actions geared toward continuous process improvements. Review GMP documents including production environmental monitoring forms, room and equipment logs, etc. Support quality management system activities including document control and training program management. Other duties and tasks, as assigned. Required Skills/Abilities: Excellent independent judgement, written communication, verbal communication, and interpersonal skills. Strong attention to detail. Familiarity with Good Manufacturing Practices and FDA Regulations. Proficient in using Microsoft Word, Excel, PowerPoint, Outlook. Education and Experience: 1-3 Years as a Quality Control Technician Pharmaceutical, Medical Device, or biotechnology industry experience, preferably in support of manufacturing. Associate degree in the sciences or equivalent experience preferred. Physical Requirements: Ability to work in a clean room setting Prolonged periods of sitting at a desk and working on a computer. Must be able to lift up to 15 pounds at times. 7:00 am to 3:30 pm, Monday through Friday

Pay Type: Salary Estimated Wage Range $57,600 - $67,700/Annually Amrize is building North America. From bridges and railways to data centers, schools, offices and homes, our solutions are inside the buildings and infrastructure that connect people and advance how we live. And we invite you to come and build with us. As the partner of choice for professional builders, we offer advanced branded solutions from foundation to rooftop. Wherever our customers are, whatever their job, we're ready to deliver. Our 19,000 colleagues work across 1,000 sites supported by an unparalleled distribution network. Infrastructure, commercial and residential, new build, repair and refurbishment: We're in every construction market. Amrize listed on the New York Stock Exchange and the SIX Swiss Exchange on June 23, 2025, following our spinoff as an independent company. Join us and build _your_ ambition. Learn more at ********************** (****************************************** Description: Join Amrize as a Quality Control Technician II and help construct whats next. If you're ready to put your skills to work on projects that matter - and build a career with a company that's building North America - we want to hear from you! **ABOUT THE ROLE** Collects samples and performs accurate quality control testing to ensure product quality. Provides verbal and/or written test results to management and production staff in a timely manner. Assists manager with customer service issues as directed. Certifies results of laboratory findings. Provides QC support on various residential and commercial projects. **WHAT YOU'LL ACCOMPLISH** + Demonstrates a commitment to communicating, improving and adhering to safety policies in all work environments and areas. + Ensures that all testing is conducted efficiently and consistently to ensure accurate results. + Prepare required documents with test results to be presented to production personnel and quality control management. + Maintains mix designs as required by DOT or local city/county specifications or to ensure accuracy of products used in mix. + Ensure that safety, compliance and environmental requirements are followed. + Examines laboratory samples to determine their physical properties. Uses a variety of instruments and calculations to determine conformity. Performs various tests to make certain that samples meet required standards. + Records, analyzes, certifies and prepares summaries of findings. Maintains records of test results using various databases. + Provide technical support for production. + Assist in the investigation and testing, and sampling of raw materials and finished products to help solve quality problems. + Demonstrate a commitment to communicating, improving and adhering to health, safety andenvironmental policies in all work environments and areas. Promote a culture of safety and exhibit these behaviors. **WHAT WE'RE LOOKING FOR** **Education:** High school diploma or equivalent **Required Work Experience:** 3-5 year **Required Training/Certifications** : State regulated or industry certifications, as required **Travel Requirements:** 5% **Additional Requirements:** + Successful candidates must adhere to all safety protocols and proper use of Amrize approved Personal Protection Equipment (PPE), including but not limited to respirators. Employees that are required to wear respirators must be clean shaven where the respirator seal meets the face in order to pass the qualitative and quantitative fit test **WHAT WE OFFER** + Competitive salary + Retirement Savings: Choose from 401(k) pre-tax and/or Roth after-tax savings + Medical, Dental, Disability and Life Insurance + Holistic Health & Well-being programs + Health Savings Accounts (HSAs), Flexible Spending Accounts (FSAs) for health and dependent care + Vision and other Voluntary benefits and discounts + Paid time off & paid holidays + Paid Parental Leave (maternity & paternity) + Educational Assistance Program + Dress for your day Accepting applications through 12/23/25 **Amrize is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.** _We thank all applicants for their interest; however, only those selected for an interview will be contacted._ **BUILDING INCLUSIVE WORKSPACES** At Amrize, there is endless opportunity for you to play your part. Whether you're in a technical, managerial, or frontline role, you can shape a career that works for you. We're seeking builders, creative thinkers and innovators. Come put your expertise to work while developing the knowledge and skills to drive your career forward. With us you'll have the chance to build your ambition! Amrize North America Inc. takes pride in our hiring processes and our commitment that all qualified applicants will receive consideration for employment without regard to age, race, color, ethnicity, religion, creed, national origin, ancestry, gender, gender identity, gender expression, sex, sexual orientation, marital status, pregnancy, parental status, genetic information, citizenship, physical or mental disability, past, current, or prospective service in the uniformed services, or any other characteristic protected by applicable federal, state or local law. Amrize North America Inc, and its respective subsidiaries are Equal Opportunity Employers, deciding all employment on the basis of qualification, merit and business need. Amrize Canada Inc. is committed to the principles of employment equity and encourages the applications from women, visible minorities, and persons with disabilities. In compliance with the ADA Amendments Act (ADAAA), if you have a disability and would like to request accommodation in order to apply for a position with us, please email recruiting-accommodations@amrize.com . This email address should only be used for accommodations and not general inquiries or resume submittals. In Ontario, our organization/business is committed to fulfilling our requirements under the Accessibility for Ontarians with Disabilities Act. Under the Act, accommodations are available on request for candidates taking part in all aspects of the selection process. While we sincerely appreciate all applications, only candidates selected for an interview will be contacted. **Nearest Major Market:** Denver

Join Our Team as an International QA/RA Associate. We're seeking a detail-oriented and globally minded International Regulatory Affairs & Quality Assurance (RA/QA) Associate to support our growing international business. This role plays a critical part in ensuring regulatory compliance across global markets while partnering closely with internal teams and international distributors. If you thrive in a fast-paced, regulated environment and enjoy navigating complex global regulations, this is an exciting opportunity to make an impact at a mission-driven company. What You'll Do as an International RA/QA Associate: Regulatory Affairs - International Coordinate and prepare regulatory documents, submissions, and registration dossiers for international markets, including establishment registrations, product registrations, renewals, and Certificates of Free Sale. Review international product labels, claims, and marketing materials to ensure compliance with region-specific regulations (EU, UK, GCC, Canada, Australia, LATAM, Asia-Pacific, and more). Maintain current knowledge of global regulatory frameworks and emerging regulatory changes affecting dietary supplements, foods, cosmetics, and related product categories. Interpret international regulatory guidance, standards, and directives, providing clear regulatory direction to internal stakeholders. Prepare, update, and maintain technical files for global registrations and regulatory audits. Conduct regulatory pathway assessments for new product launches in foreign markets. Track submission timelines, approvals, renewals, and regulatory commitments. Evaluate ingredient acceptability, formulation compliance, and permissible claims based on international regulatory requirements. Support regulatory assessments related to product changes, formula updates, and labeling revisions. Documentation & Certificates Management Prepare comprehensive international documentation packages, including Manufacturer's Declarations, Certificates of Free Sale, GMP/ISO certificates, specifications, ingredient documentation, and test reports. Provide regulatory and technical documentation to international distributors and partners. Import / Export Compliance Support compliance with international import/export requirements, including HS codes, EORI numbers, customs documentation, and country-specific clearance requirements. Assist in resolving regulatory-related customs holds or international shipment delays. Quality Assurance Support Support quality system processes such as document control, change control, and deviations as they relate to international products. Participate in cross-functional projects and provide regulatory guidance as needed. Who You Are Bachelor's degree in a related field. 3+ years of QA/RA experience within the nutraceutical or dietary supplement industry. Experience working in a cGMP-regulated environment. Working knowledge of FDA food and dietary supplement regulations (21 CFR 111, 21 CFR 117, DSHEA). Strong attention to detail with excellent documentation and organizational skills. Ability to interpret and apply international regulatory requirements accurately. Comfortable managing multiple projects and shifting priorities in a fast-paced environment. Strong written and verbal communication skills, including collaboration with international partners. Proficiency with Microsoft Office and regulatory documentation systems. Preferred Qualifications 3+ years of international regulatory affairs experience. Familiarity with foreign regulatory frameworks (EU, UK, Canada NNHPD, Australia TGA, GCC, LATAM, Asia-Pacific). Experience with botanical, CBD, peptide, or hormone regulatory environments. Experience supporting or preparing international product registrations. Regulatory Affairs Certification (RAC) or similar credential. Multilingual abilities are a plus. Work Environment & Schedule Full-time, salary/exempt position. Monday-Friday, 8:30am-5:00pm with flexibility as business needs require. Hybrid schedule available. Why You'll Love Working Here At Quicksilver Scientific, we're committed to supporting the health, well-being, and professional growth of our team. We offer a comprehensive benefits package that includes: Medical, Dental, and Vision Insurance Health Savings Account (HSA) & Flexible Spending Account (FSA) options Company Paid Life, Short-Term & Long-Term Disability Insurance 401(k) with up to 4% Company Match Four (4) weeks Paid Time Off Gym Membership Reimbursement Compensation: $63,000 to $67,000 About Quicksilver Scientific At Quicksilver Scientific, we believe in transforming health through science and innovation. Our mission is to help people live healthier, more vibrant lives with natural medicine that works. We are proud to foster a diverse, inclusive, and collaborative workplace. Ready to make a global impact? Apply today and join a team where your expertise truly matters. Quicksilver Scientific is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.

At Food Lion, Associates are the most important assets to our organization. We want associates to have meaningful careers full of variety and challenges. Each associate contributes to the overall success of Food Lion, and in return, we strive to provide all associates with a fulfilling work experience and reward performance and commitment. We are committed to the professional development of our associates through on-the-job learning opportunities and training. Provide our customers with a clean, safe, inviting place to shop by maintaining standards in accordance with the standard practice manual. Minimize shrink through proper utilization of standard practice. Duties and Responsibilities: Maintain an atmosphere of enthusiastic customer awareness with primary emphasis on fast, friendly, and accurate customer service to create a positive shopping experience Courteous and helpful to other associates Sweep and clean floors on nights with no scheduled vendor services Weekly cleaning of Produce, Market and Deli Departments Clean and organize the store mop room Find more efficient ways to do the job and seek to reduce costs and improve labor productivity Follow QA daily check list and sanitation standards set by Food Lion Follow current Standard Practices regarding cleanup of Hazardous Waste product Maintain a complete understanding of and adherence to company guidelines, policies and standard practice Understand and follow Food Safety and Workplace Safety guidelines and procedures Observe and correct all unsafe conditions that could cause associate or customer accidents Report all associate and customer accidents in accordance with established Food Lion procedures to the Manager on Duty Ensure compliance with local, state and federal regulations Wear the Food Lion uniform complete with name badge, when on duty, has a neat and clean appearance while adhering to the Food Lion dress code Successfully complete Computer Based Training (CBT), Training Packet and Training Aid courses Perform all other duties as assigned Qualifications: High school graduate or equivalent preferred Excellent interpersonal, organizational, communication and customer service skills Ability and willingness to learn multiple tasks and technical requirements of the job Ability to use technical information to solve problems Must meet minimum age requirements to perform specific job functions Must be able to meet the physical requirements of the position, with or without reasonable accommodations Physical Requirements: Ability to use computers and other communication systems required to perform job functions Perform repetitive hand and arm motions Bend and lift products weighing up to 15 lbs. continuously, 25 lbs. frequently, and 50 lbs. on occasion Pull or push up to 75 lbs. on occasion Stand 100% of the time, frequently walking short distances Be able to handle a variety of substances associated with cleaning and packaging materials, fresh fruits, vegetables, house plants/flowers and household cleaners Use hands to frequently/continuously handle currency (paper and coin) as well as operate a variety of equipment such as cash register, lottery machine (where applicable), scanner, computer, and calculator Frequent reaching and grasping at waist level: occasionally above shoulder or below waist level Meet established volume activity standards for the position Tolerate working in extreme hot/cold temperatures for up to 20 minutes at a time Have sufficient visual ability to check ID cards, checks, invoices and other written documents Food Lion provides equal employment opportunities to all associates and applicants for employment without regard to race, color, religion, sex (including pregnancy, childbirth and related conditions) national origin, age, disability, sexual orientation, veteran status, gender identity or gender expression or any other characteristic protected by law. If you have a disability and require assistance in the application process, please contact our Recruiting Department at ***********************

Duties and Responsibilities: Work effectively with the Quality, Operations, and R&D departments to perform all work accurately, with a sense of urgency and a positive attitude. Activities include the following: In-Process and Final Device Inspection and Test : Support Manufacturing as the QC inspector for clean-room & packaging inspection activities. Perform and document in-process and final inspection/test of devices and sub-assemblies. Provide inspection/test assistance to R&D, Operations and Quality Engineering in support of design and process verification/validation activities. Receiving Inspection and Test : Perform and document receiving inspection/test of device components & raw materials in accordance with drawings/specifications. Maintain accurate & timely records of inspection activities and recording such activities in the QC Receiving Log. Non-Conforming Materials : Identify, segregate and quarantine non-conforming materials resulting from inspection activities. Initiate NCRs and notify the workstream owner in a timely manner. Execute and record disposition activities in accordance with approved NCRs. Microbiological Monitoring : Participates in periodic microbiological and particulate testing of the cleanroom and products as required. Returned Goods Authorization : Perform timely inspections and maintain accurate records of all returned TriSalus products through the RGA process. Correctly dispositions returned product as defined in approved procedures. Quality Record maintenance : Receive, verify, scan and physically file Quality Records in an organized manner as needed. Shipping QC : Verify TriSalus products and associated paperwork are accurate and complete prior to shipment. Audit Assistance : Help retrieve, review, organize and re-file documentation during all TriSalus site audit activities (internal, FDA, ISO registrar). GP Dynamics : Transfer released materials in the ERP software for material management as needed. Training Record support : Enter complete training/certification records into the eQMS as needed. General : Perform other quality inspection, test or administration activities as assigned. Qualifications Education & Certifications: High School diploma. Advanced education or certifications a plus. Work Experience: 2+ years of Quality Control / Inspection experience in a medical device or similar technical product manufacturing company. Experience working with sterile disposable products in a cleanroom environment a plus. Knowledge, Skills & Abilities: Able to read and interpret engineering drawings, specifications and detailed technical documents. Able to read and follow quality procedures and detailed work instructions (QLPs/OPs). Able to perform component and product inspection/testing using tools such as microscopes, calipers, micrometers, pin gauges, depth gauges, pull force test systems and vision measuring systems. (Sufficient knowledge to select and use the correct measurement tool for the required inspection accuracy. Able to accurately document results of inspections using good documentation practices. Able to understand and apply inspection sampling plans, such as C=0 or ANSI Z1.4. Able to utilize basic math skills. Able to use MS Word and MS Excel. Must possess strong attention to detail. Possess good communication skills and able to interact with peers in a professional manner. Possess knowledge and application of US and international standards for quality management (FDA 21 CFR 820, ISO 13485). Demonstrates excellent critical thinking skills. Ability to adapt to and rapidly learn new processes. Strong verbal and written communication skills and confidence in making inspection related decisions. Participates as a member of cross functional technical teams to support process improvements, special projects and investigations as needed. Approaches work tasks with a positive attitude and seeks feedback on performance to continually improve. Physical Requirements: Ability to safely and successfully perform the essential job functions consistent with the ADA, FMLA and other federal, state and local standards, including meeting qualitative and/or quantitative productivity standards. Must be able to lift and carry up to 30 lbs. Ability to maintain regular, punctual attendance consistent with the ADA, FMLA and other federal, state and local standards.

Starting compensation: $25.00 per hour (plus a $1.50 shift differential) Shift Days: Sunday to Thursday Shift Hours: 2:30 PM to Close Shamrock anticipates closing the application window for this job opportunity on or before December 31, 2026 Lead Quality Control Technicians in maintaining all aspects of Quality Assurance to ensure proper, safe and exceptional operation of the department. Essential Duties: Audit products for quality and safety prior to sending them out to customers. Audit incoming raw materials for supplier specifications, quality, and food security. Review incoming ingredients for allergen checks and quality standards. Responsible for compliance with all regulations and food safety including allergen and pest control. Fill out necessary paperwork for product audits and HACCP documents. Review HACCP documents prior to handing paperwork to QA Supervisor/Manager. Work with operational teams on paperwork, quality checks, and HACCP procedures. Ensure adherence to all standard work processes, including the Production Sanitation processes. Aid in plant training requirements and conduct plant training sessions as needed. Work with QA leaders to ensure plant training requirements and frequencies are met. Recognize and escalate risks and/or improvement opportunities to improve plant performance. Other duties as assigned. Qualifications: High School Diploma or GED. 3+ year's meat and/or protein experience. HACCP certified, preferred. Must be flexible and willing to work the demands of the department which may be subject to evenings, weekends, and holidays. Corporate Summary: At Shamrock Foods Company, people come first - our associates, our customers, and the families we serve across the nation. A privately-held, family-owned and -operated Forbes 500 company, Shamrock is an innovator in the food industry and has been since being founded in Arizona in 1922. Our Mission: At Shamrock Foods Company, we live by our founding family's motto to “treat associates like family and customers like friends.” Why work for us? Benefits are a major part of your overall compensation, and we believe offering them at an affordable cost is not only the right thing to do, but it helps keep you and your family healthy. That's why Shamrock Foods pays for the majority of your health insurance, allowing you to take home more of your paycheck. And it doesn't stop there - our associates also enjoy additional benefits such as 401(k) Savings Plan, Profit Sharing, Paid Time Off, as well as our incredible growth opportunities, continued education, wellness programs. Equal Opportunity Employer Shamrock Foods Company is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, veteran status, sexual orientation, gender identity or any other basis protected by applicable law.

Role and Responsibilities This position is responsible for working cross functionally to support Quality Assurance & Quality Control tasks, with focus on visual inspection of drug products. The Quality Technician will support Belmar Pharma Solutions in carrying out the mission of the company. This position reports to the Quality Manager. Responsibilities include: Primary responsibility to perform visual inspection of parenteral pharmaceutical products in accordance with regulatory guidelines Create & review all labels (in-process and finished goods) and Batch Production Records for accuracy and adherence to Good Documentation Practices (GDPs) Incoming materials receipt: inspect, document, unpack, label, shelve, and organize materials Obtain samples of raw, in-process, and finished goods materials and send to third party labs for testing. Results to be entered into applicable spreadsheets. Review Logs of Use and Maintenance (LUMs) for accuracy and GDP Finished drug product batch release checks Perform Quality checks on in-process product and facility controls as needed Sterilization: Prepare, receive, and organize product for sterilization Environmental Monitoring (EM): Collect routing EM samples. Enter, report and trend sample data. Identify nonconformances and escalate to leadership Attend all required meetings and provide clear, professional verbal and email communications. Special projects as assigned by Management Other duties as assigned

The Quality Technician II is responsible for maintaining the Quality Management System by following the required procedures and ensuring customer requirements are identified and met. Essential Duties & Responsibilities Reads part drawings and assesses dimensions. Supports inspection equipment operation within the production cell as required, including Coordinate Measurement Machine. Initiates Management Review Board and performs actions as assigned. Performs Final Inspection - Ensures required documentation from all inspections are complete and all functions of the manufacturing process have been verified as complete. Ensures correct product identification and traceability of materials is maintained throughout the operations process. Initiates Quality-related turnbacks and communicates with production. Creates basic and intermediate certifications as required by the Work Order, including FAIRs. Performs specialised inspection, including visual and dimensional checks. Assists with Internal Auditing as required. Assists with measurement tool calibration as required. Creates basic CMM programs in the production cell to aid in inspection. Participates in small projects or other tasks as required. Education and Experience This position requires a High School Diploma or GED equivalent. This position should have 2-3 years of experience in a quality role in a manufacturing environment. Experience with QMS compliance software (e.g., Qualtrax) and enterprise resource planning system (e.g., JD Edwards or SAP) is required. Knowledge, Skills, and Abilities Must have the ability to multitask in a fast-paced environment. Excellent interpersonal skills and ability to effectively communicate with all levels of the organization both written and verbal in English. Ability to work in a team environment. Must have a high level of attention to detail and excellent problem-solving skills. Must be proficient with Microsoft Office, specifically Excel and Outlook, and general computer skills. High knowledge of materials and material requirements as they relate to customer orders. High knowledge of purchase order requirements. Ability to read blueprints and product drawings and interpret requirements as needed. Must be able to operate various inspection tools such as dial calipers, micrometers, optical comparator, height gages, pin & plug gages, pi tape and microscopes. Must have excellent math aptitude. Work Environment/Physical Demands/Equipment Used This position is located in a manufacturing facility which requires prolonged sitting, standing, walking, squatting, twisting, and bending. This position will spend about 90% of their time on the production floor where heavy machinery is present and loud sounds exist. Requires manual dexterity for typing and considerable time at a computer. Health and Safety - PPE Requirements Safety Glasses to be worn at all times when on the production floor Safety Shoes to be worn at all times when on the production floor Must wear appropriate PPE for all work activities performed; varies based work

Join RK as a Quality Inspector - Where Excellence Meets Opportunity At RK, quality isn't just a standard-it's our promise. As a Quality Inspector, you'll be the cornerstone of that commitment, ensuring every project meets the highest level of precision and craftsmanship. This is your chance to work alongside skilled professionals in both shop and field environments, contributing to diverse, impactful projects that shape industries. Self. Made. at RK At RK, Self. Made. isn't a tagline, it's how work gets done. People here build more than projects; they build capability, confidence, and careers they can be proud of. With so much work designed and fabricated in-house, ideas move quickly from concept to shop floor to job site. Teams collaborate across disciplines, solve real-world challenges, and grow through hands-on work that truly matters. RK Company Overview RK Industries is a second-generation family-owned company led by brothers Rick and Jon Kinning. With seven specialized business units working together, we deliver construction, fabrication, manufacturing, and building services with a focus on safety, quality, and craftsmanship. People join RK for the craftsmanship, complexity, and the ability to make a real impact. Our in-house capabilities mean employees see their ideas become real solutions, creating meaningful collaboration and clear visibility into how work gets built. Growth happens through challenging projects, mentorship from experienced builders, and opportunities that stretch your skill set. With RK University, accredited apprenticeships, competitive benefits, and deep community investment, RK offers the stability of a family-owned company with the opportunity and momentum of an industry leader. Position Summary The Certified Welding Inspector (CWI) is responsible for ensuring conformance with internal quality standards and external accreditation requirements (ISO 9001, AISC, and ASME). CWIs conduct inspections, support audits, and collaborate with production teams to ensure high-quality fabrication practices. This role plays a key part in maintaining certifications and creating a culture of continuous quality improvement. The role and responsibilities expand with each level of experience and competency. Role Responsibilities * Responsible for assessing corporate conformance to the Quality Management System (QMS), AISC Certification, and ASME Certification * Assist with all inspection and testing services provided by RK * Monitor activities relating to client expectations of the company. * Report QMS progress, activities, and observations to Quality Manager. * Review plans to ensure they meet building codes, local ordinances and zoning regulations * Monitor construction sites/fabrication facilities to ensure overall compliance * Use survey instruments, testing equipment, and other systems to ensure that product meets code and requirements * Verify alignment, level, and elevation of products * Keep daily logs, including photographs taken during inspection * Provide written feedback related to the findings * Other duties as assigned Qualifications * Indirect supervision. * Fully competent in all conventional aspects of subject matter or functional area. * Plans and conducts work requiring judgment in independent evaluation, selection and substantial adaptation/modification of standards. * Devises new solutions to problems encountered. * Independently performs most assignments with instruction * Receives guidance for unusual or complex problems and supervisor approval for changes in standards. * College/university graduate or equivalent combination of skills and experience generally expected for specified technical roles. * CWI Preferred Minimum Physical Requirements and Accountability * Work outside, inside, and in dusty, noisy and hazardous areas. * Work in high places, tight places, confined spaces and/or other adverse locations. * Climb, balance, squat, kneel and crouch. * Work in all types of weather. * Must have working knowledge of all trade materials and tools. * Ability to lift, move, and/or carry 50 lbs. What Sets RK Industries Apart * Safety: Our unmatched culture of safety is our foremost core value, guiding everything we do each day: Health, Safety, & Environmental * Awards: Whether in Construction, Manufacturing, Fabrication, or Service, RK Industries is highly recognized and accredited throughout the industry: Accreditations & Recognition * Benefits: RK Industries offers competitive benefits to support your growth and well-being: Benefits & Rewards * Philanthropy: RK Industries not only builds our community through our projects, but also invests in it by supporting local services for over a decade through the RK Foundation: RK Foundation * Development: Through RK University, we provide hands-on training and development opportunities that empower employees to advance their careers and grow within the company, to include leadership and technical learning opportunities, we well as our accredited apprentice program: RK University & RK Apprenticeship Program Applications are accepted on an ongoing basis

Starting compensation: $21.00 per hour (plus a $1.50 shift differential) Shift Days: Sunday to Thursday Shift Hours: 2:30 PM to Close Shamrock anticipates closing the application window for this job opportunity on or before December 31, 2026 Maintains all aspects of Quality Assurance to ensure proper, safe and exceptional operation of the department. Essential Duties: * Audits products for quality and safety prior to sending out to customers. * Audits incoming raw materials for supplier specifications, quality, and food security. * Reviews incoming ingredients for allergen checks and quality standards. * Responsible for compliance with all regulations. Food Safety - plant in proper sanitary condition at all times, including allergen control, pest control, guidelines followed. * Fills out necessary paperwork for product audits and HACCP documents. * Reviews HACCP documents prior to handing paperwork to QA Supervisor/Manager. * Work with operational teams daily with paperwork, quality checks, and HACCP procedures. * Ensure adherence to all standard work processes, including the Production Sanitation processes. * Aides in plant training requirements and training frequencies. Work with QA Supervisor/ Manager to ensure plant training requirements and frequencies are met. Conduct plant training sessions as needed. * Maintain understanding of processes and functional interdependencies. Recognize and escalate, as needed, those issues identified as risks to, or opportunities to improve, plant performance. * Must be able to work within timelines and in pressure situations. * Other duties may be assigned. Qualifications: * High School Diploma or GED preferred * Meat Protein Experience * HACCP certified, preferred Corporate Summary: At Shamrock Foods Company, people come first - our associates, our customers, and the families we serve across the nation. A privately-held, family-owned and -operated Forbes 500 company, Shamrock is an innovator in the food industry and has been since being founded in Arizona in 1922. Our Mission: At Shamrock Foods Company, we live by our founding family's motto to "treat associates like family and customers like friends." Why work for us? Benefits are a major part of your overall compensation, and we believe offering them at an affordable cost is not only the right thing to do, but it helps keep you and your family healthy. That's why Shamrock Foods pays for the majority of your health insurance, allowing you to take home more of your paycheck. And it doesn't stop there - our associates also enjoy additional benefits such as 401(k) Savings Plan, Profit Sharing, Paid Time Off, as well as our incredible growth opportunities, continued education, wellness programs. Equal Opportunity Employer Shamrock Foods Company is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, veteran status, sexual orientation, gender identity or any other basis protected by applicable law.

Job Description Join Our Team as an International QA/RA Associate. We're seeking a detail-oriented and globally minded International Regulatory Affairs & Quality Assurance (RA/QA) Associate to support our growing international business. This role plays a critical part in ensuring regulatory compliance across global markets while partnering closely with internal teams and international distributors. If you thrive in a fast-paced, regulated environment and enjoy navigating complex global regulations, this is an exciting opportunity to make an impact at a mission-driven company. What You'll Do as an International RA/QA Associate: Regulatory Affairs - International Coordinate and prepare regulatory documents, submissions, and registration dossiers for international markets, including establishment registrations, product registrations, renewals, and Certificates of Free Sale. Review international product labels, claims, and marketing materials to ensure compliance with region-specific regulations (EU, UK, GCC, Canada, Australia, LATAM, Asia-Pacific, and more). Maintain current knowledge of global regulatory frameworks and emerging regulatory changes affecting dietary supplements, foods, cosmetics, and related product categories. Interpret international regulatory guidance, standards, and directives, providing clear regulatory direction to internal stakeholders. Prepare, update, and maintain technical files for global registrations and regulatory audits. Conduct regulatory pathway assessments for new product launches in foreign markets. Track submission timelines, approvals, renewals, and regulatory commitments. Evaluate ingredient acceptability, formulation compliance, and permissible claims based on international regulatory requirements. Support regulatory assessments related to product changes, formula updates, and labeling revisions. Documentation & Certificates Management Prepare comprehensive international documentation packages, including Manufacturer's Declarations, Certificates of Free Sale, GMP/ISO certificates, specifications, ingredient documentation, and test reports. Provide regulatory and technical documentation to international distributors and partners. Import / Export Compliance Support compliance with international import/export requirements, including HS codes, EORI numbers, customs documentation, and country-specific clearance requirements. Assist in resolving regulatory-related customs holds or international shipment delays. Quality Assurance Support Support quality system processes such as document control, change control, and deviations as they relate to international products. Participate in cross-functional projects and provide regulatory guidance as needed. Who You Are Bachelor's degree in a related field. 3+ years of QA/RA experience within the nutraceutical or dietary supplement industry. Experience working in a cGMP-regulated environment. Working knowledge of FDA food and dietary supplement regulations (21 CFR 111, 21 CFR 117, DSHEA). Strong attention to detail with excellent documentation and organizational skills. Ability to interpret and apply international regulatory requirements accurately. Comfortable managing multiple projects and shifting priorities in a fast-paced environment. Strong written and verbal communication skills, including collaboration with international partners. Proficiency with Microsoft Office and regulatory documentation systems. Preferred Qualifications 3+ years of international regulatory affairs experience. Familiarity with foreign regulatory frameworks (EU, UK, Canada NNHPD, Australia TGA, GCC, LATAM, Asia-Pacific). Experience with botanical, CBD, peptide, or hormone regulatory environments. Experience supporting or preparing international product registrations. Regulatory Affairs Certification (RAC) or similar credential. Multilingual abilities are a plus. Work Environment & Schedule Full-time, salary/exempt position. Monday-Friday, 8:30am-5:00pm with flexibility as business needs require. Hybrid schedule available. Why You'll Love Working Here At Quicksilver Scientific, we're committed to supporting the health, well-being, and professional growth of our team. We offer a comprehensive benefits package that includes: Medical, Dental, and Vision Insurance Health Savings Account (HSA) & Flexible Spending Account (FSA) options Company Paid Life, Short-Term & Long-Term Disability Insurance 401(k) with up to 4% Company Match Four (4) weeks Paid Time Off Gym Membership Reimbursement Compensation: $63,000 to $67,000 About Quicksilver Scientific At Quicksilver Scientific, we believe in transforming health through science and innovation. Our mission is to help people live healthier, more vibrant lives with natural medicine that works. We are proud to foster a diverse, inclusive, and collaborative workplace. Ready to make a global impact? Apply today and join a team where your expertise truly matters. Quicksilver Scientific is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.

Join Amrize as a Quality Control Technician II and help construct whats next. If you're ready to put your skills to work on projects that matter - and build a career with a company that's building North America - we want to hear from you! ABOUT THE ROLE Collects samples and performs accurate quality control testing to ensure product quality. Provides verbal and/or written test results to management and production staff in a timely manner. Assists manager with customer service issues as directed. Certifies results of laboratory findings. Provides QC support on various residential and commercial projects. WHAT YOU'LL ACCOMPLISH * Demonstrates a commitment to communicating, improving and adhering to safety policies in all work environments and areas. * Ensures that all testing is conducted efficiently and consistently to ensure accurate results. * Prepare required documents with test results to be presented to production personnel and quality control management. * Maintains mix designs as required by DOT or local city/county specifications or to ensure accuracy of products used in mix. * Ensure that safety, compliance and environmental requirements are followed. * Examines laboratory samples to determine their physical properties. Uses a variety of instruments and calculations to determine conformity. Performs various tests to make certain that samples meet required standards. * Records, analyzes, certifies and prepares summaries of findings. Maintains records of test results using various databases. * Provide technical support for production. * Assist in the investigation and testing, and sampling of raw materials and finished products to help solve quality problems. * Demonstrate a commitment to communicating, improving and adhering to health, safety and environmental policies in all work environments and areas. Promote a culture of safety and exhibit these behaviors. WHAT WE'RE LOOKING FOR Education: High school diploma or equivalent Required Work Experience: 3-5 year Required Training/Certifications: State regulated or industry certifications, as required Travel Requirements: 5% Additional Requirements: * Successful candidates must adhere to all safety protocols and proper use of Amrize approved Personal Protection Equipment (PPE), including but not limited to respirators. Employees that are required to wear respirators must be clean shaven where the respirator seal meets the face in order to pass the qualitative and quantitative fit test WHAT WE OFFER * Competitive salary * Retirement Savings: Choose from 401(k) pre-tax and/or Roth after-tax savings * Medical, Dental, Disability and Life Insurance * Holistic Health & Well-being programs * Health Savings Accounts (HSAs), Flexible Spending Accounts (FSAs) for health and dependent care * Vision and other Voluntary benefits and discounts * Paid time off & paid holidays * Paid Parental Leave (maternity & paternity) * Educational Assistance Program * Dress for your day Accepting applications through 12/23/25 Amrize is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We thank all applicants for their interest; however, only those selected for an interview will be contacted. BUILDING INCLUSIVE WORKSPACES At Amrize, there is endless opportunity for you to play your part. Whether you're in a technical, managerial, or frontline role, you can shape a career that works for you. We're seeking builders, creative thinkers and innovators. Come put your expertise to work while developing the knowledge and skills to drive your career forward. With us you'll have the chance to build your ambition! Amrize North America Inc. takes pride in our hiring processes and our commitment that all qualified applicants will receive consideration for employment without regard to age, race, color, ethnicity, religion, creed, national origin, ancestry, gender, gender identity, gender expression, sex, sexual orientation, marital status, pregnancy, parental status, genetic information, citizenship, physical or mental disability, past, current, or prospective service in the uniformed services, or any other characteristic protected by applicable federal, state or local law. Amrize North America Inc, and its respective subsidiaries are Equal Opportunity Employers, deciding all employment on the basis of qualification, merit and business need. Amrize Canada Inc. is committed to the principles of employment equity and encourages the applications from women, visible minorities, and persons with disabilities. In compliance with the ADA Amendments Act (ADAAA), if you have a disability and would like to request accommodation in order to apply for a position with us, please email recruiting-accommodations@amrize.com. This email address should only be used for accommodations and not general inquiries or resume submittals. In Ontario, our organization/business is committed to fulfilling our requirements under the Accessibility for Ontarians with Disabilities Act. Under the Act, accommodations are available on request for candidates taking part in all aspects of the selection process. While we sincerely appreciate all applications, only candidates selected for an interview will be contacted.