Quality control analyst jobs in Spanish Fork, UT

• Perform cleaning of lab glassware in accordance with Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (cGMP). • Perform lab housekeeping practices. • Must work in compliance with all Company policies and procedures, including safety rules and regulations. Knowledge of the following is helpful: • Current Good Manufacturing Practices (cGMP) and other relevant regulatory requirements. • Basic chemistry laboratory practices and techniques. • Current Company policies, practices and procedures, including safety rules and regulations. Qualifications Minimum Qualifications: High School Diploma or equivalent. Related experience in pharmaceutical manufacturing laboratory is helpful. Additional Information To know more about this position, please contact: Shweta T ********************************* ************

HemaSource is looking for a detail-focused and analytical Quality Control Analyst to support the intake, evaluation, investigation, and reporting of medical device product complaints. This role directly contributes to patient safety and ensures our products meet global regulatory standards. You will be part of a highly collaborative Quality team that values accuracy, critical thinking, and a commitment to continuous improvement. If you enjoy problem-solving, working with technical data, and partnering across Quality, Engineering, and Regulatory teams, this is an excellent opportunity to grow your career in a fast-paced and mission-driven environment. You will play a vital role in supporting compliance with FDA regulations, international standards, and internal quality system requirements while helping drive improvements in product performance and customer satisfaction. Key Responsibilities Receive, review, and process medical device product complaints, ensuring accurate documentation and timely assessment. Conduct thorough complaint investigations using root-cause analysis and cross-functional input. Ensure compliance with FDA, ISO 13485, EU MDR, and internal quality system requirements. Prepare and submit required regulatory reports (MDRs, vigilance reports) within strict timelines. Analyze complaint data to identify trends and contribute to CAPA and continuous improvement efforts. Communicate clearly with internal teams and external customers regarding complaint status and findings. Maintain accurate, audit-ready records, complaint metrics, and documentation. Manage LMS activities including training assignments, system maintenance, and compliance reporting. Qualifications Bachelor's degree in Life Sciences, Engineering, or related field. 2+ years of medical device complaint handling, post-market surveillance, or quality experience. Familiarity with FDA regulations, ISO 13485, EU MDR, and quality system requirements. Strong analytical, critical-thinking, and problem-solving skills. Excellent written and verbal communication skills. Proficient with Microsoft Office; experience with QMS/ERP/complaint systems preferred. Why Join Us Opportunity to grow in Quality, Regulatory, or Technical Operations. Meaningful work that directly impacts patient safety and product quality. Supportive team environment with clear development pathways. Stable, growing company invested in compliance excellence. Physical Requirements Prolonged computer work. Ability to lift up to 10 lbs. occasionally. Who We Are: HemaSource is an innovative logistics solution partner that combines best-in-class analytics and high-quality medical product supply to specialty ambulatory clinics. Our mission is to drive customer operational efficiencies and related cost savings in high volume ambulatory care clinics. HemaSource's patented data analytics software tool and our superior customer service have enabled us to become the preferred disposables provider to the plasma collection market.

Job DescriptionSalary: MUSH is a place where driven individuals unlock their highest potential. We believe that change starts within, and as a team, we accomplish extraordinary feats. If you want to build a reputation of doing hard things well, and aspire to make the world a little healthier, MUSH may be a great place for you. Our first product line of ready-to-eat overnight oats pioneers a new category for the breakfast occasion, offering a healthy, satiating, and convenient alternative to traditional morning meals. By making healthy food more accessible, we believe that humankind can feel, think, and do better. Role Description MUSH is seeking a dynamic and open minded teammate to support our Research and Development (R&D) Team at our manufacturing facility in Salt Lake City. The successful candidate has exceptional organization and prioritization skills. General Responsibilities: Support batching for innovation and customer requests Order and maintain inventory for innovation and new ingredients Manage inventory logistics: ingredient labels, shipping boxes, ice packs, shipping labels Operate analytical instruments for QA and secondary supplier approval (pH, viscosity, water activity) Conduct internal sensory testing for secondary supplier approvals Manage formulations and ingredients in Genesis software to ensure accuracy, cost tracking, and efficiency Other duties as assigned Experience Requirements: High School Diploma or GED preferred Strong proficiency in all MS Office/Google applications Problem solving, excellent verbal and oral communication skills Ability to manage multiple priorities and consistently meet time sensitive tasks in a fast paced environment Cultural Expectations: Set an example. Hold yourself accountable to standards of excellence Teammate: know when to follow, know when to lead; always serving others Beginners Mind: provide possibilities, options, and solutions Communicator: use tact and precision to communicate ideas, issues, and feedback Self-Starter: there is no turn-key manual for success, you are helping to build one Results Driven: you demand results, but focus on the robust processes that yield them Attention to Detail: unwavering discipline with little things that make big differences Relationship Builder: customer first mentality with all internal & external counterparts Problem Solver: expect the unexpected; be agile & effective in combating issues Thrive on Adversity: our goals are lofty and our values are grounded in humility. We bite off more than we can chew and roll our sleeves up when the situation calls for it. Fun: check the fun box every day. Love what you do & do it well.

Job Description We are seeking a motivated and detail-oriented Quality Control / Quality Assurance (QC/QA) Specialist with 1-3 years of construction experience to support the successful execution of quality management practices on active construction projects. The QC/QA Specialist will assist in implementing and maintaining the project quality plan, performing inspections, and coordinating quality-related documentation with in owner provided software's to ensure compliance with contract documents, codes, and industry standards. Key Responsibilities: Assist in the development and implementation of project-specific Quality Control Plans Conduct daily field inspections and audits to verify conformance with contract drawings, specifications, and industry best practices Coordinate with subcontractors and trade partners to ensure quality requirements are understood and followed Maintain and organize all QC documentation, including inspection reports, non-conformance reports, testing logs, and material certifications Track and report quality metrics and deficiencies; work with the project team to ensure timely resolution Review submittals, shop drawings, and material certifications for compliance Attend QA/QC and coordination meetings; support third-party testing and inspection agencies Support punch list generation and project turnover documentation Promote a culture of continuous improvement and quality awareness on the job site Coordinate Trade Partner compliance with applicable specification and submit documentation to client interface Inspect and receive shipments of equipment and document with in the client software Qualifications: 1-3 years of QC/QA experience in commercial, industrial, or infrastructure construction Basic understanding of construction documents and specifications Working knowledge of quality management systems, inspection techniques, and common construction codes (e.g., IBC, AWS, ASTM) Strong communication and organizational skills

Job Description Job purpose The Quality Control Assistant plays a crucial role in supporting the Food Safety and Quality Assurance (FSQA) department by performing a variety of tasks related to sampling, record-keeping, and assisting with supplier and finished goods inventory hold and release procedures. This position ensures the efficient organization and management of samples, maintains accurate records of pallet status, and provides support to the FSQA team in their daily operations and projects. Duties and responsibilities Sample Management: · Collect samples of ingredients and finished products accordingly, as needed or directed. · Prepare and deliver product samples for laboratory testing as needed · Organize and maintain sample storage area for easy access and retrieval. Record Keeping and Documentation: · Support and maintain accurate records for our Hold and Release program · Always ensure proper identification of all products, in accordance to online records and our ERP system. · Maintain proper storage and record keeping of all samples for the retention program. Quality Control Support: · Assist the FSQA team with proper tagging of dispositioned products · Support the WH team in addressing issues with damaged goods, including ingredients, or packaging materials. · Participate and lead specific projects in conjunction with the WH team. Training and Orientation: · Prepare and execute training as required by the FSQA or warehouse leadership · Conduct orientation sessions for new employees. · Responsible for following and enforcing plant GMP and safety guidelines. · Requires and supports Good Manufacturing Practices and systems within all buildings and with all employees working in production and warehouse areas Qualifications · 3 years of experience in Food Safety and Quality in food manufacturing required · Strong work ethics particularly in attendance, punctuality, safety, GMP's and attention to detail. · Must be able to read and write English proficiently, with the ability to communicate effectively, clearly and professionally within all levels of the organization · Spanish as a second language, preferred Working conditions · Ability to work in a food facility environment with conveyors, and warehouse equipment. Physical requirements · Ability to lift a minimum of 50 lbs. · Ability to stand in one area for long periods of time. · Ability to work overtime as needed. · Must be able to walk for long periods of time · Must be able to read and write English Job Posted by ApplicantPro

QC asphalt field technician will coordinate all QC testing between the paving department, our in house lab, the UDOT lab, and the third party QA/QC testing companies. Oversee the third party testing companies to ensure the proper procedures are occurring on each individual project. Will work with the paving foreman to develop specific plans and rolling patterns to help ensure compaction and smoothness. Also coordinate sampling, coring, and all scheduling in regard to the QC testing on projects.

Company: Elevate Health Sciences Quality Control Technician Time: 40 hours/week Employment Type: Full-time (Non-Exempt) SHIFT: 5:00 PM to 5:00AM Monday - Thursday (overtime as needed) will be trained on the following responsibilities, prior experience is not required. Primary Responsibilities Conducts Allergen and ATP swab tests. Complete first article verification of production runs Responsible for pulling in-process and finished good samples. Ensure GMP compliance during manufacturing process. Ensure every job matches the information provided on the batch record. Adhere to company PPE requirements as indicated, per position. Able to complete work on time and meet changing scheduling demands. Manages time and workload efficiently and prioritizes workflow effectively. Experience working in a highly regulated and compliant environment to deliver accurate results. Perform other duties as assigned by the Supervisor/Lead. Other Duties as assigned. Knowledge/Skills Requirements: Prior GMP experience. Must be able to read, write, interpret and execute written instructions, and communicate in English. Ability to multi-task and meet deadlines under pressure in a fast-paced manufacturing environment. Experience in any manufacturing field or industry is a plus. Self-motivated, pro-active. Communicate in a clear and concise manner. Work cooperatively with others. Spanish speaking is not required but a huge plus! Physical Requirements: Ability to lift up to 50 lbs. Ability to stand for duration of shift. Willingness to follow all GMP, including wearing head covers and gowns. While performing the duties of this job, the employee is regularly required to stand; walk; sit; use hands to finger, handle, or feel; reach with hands and arms; exposure to various powders, chemicals, and allergens: climb or balance; stoop, kneel, crouch, or crawl; converse and listen; taste or smell. Our Benefits & Perks: You will be part of an engaged, inclusive, global community that values family, giving back, beauty, and sustainability. We offer competitive benefits to eligible employees with comprehensive medical, vision, and dental coverage; supplemental life, voluntary short-term, and disability insurance; free access to therapists; a health savings account and 401k. You'll also be empowered to prioritize what's important to you through our vacation policy.

Full-time Description MERS Transfer of Servicing/Beneficiary Rights: Process Transfer of Servicing (TOS) and Transfer of Beneficiary (TOB) rights within MERS guidelines upon loan sale or transfer. Obtain and review daily Purchase Advices to ensure transfers are executed promptly and correctly. MERS Reconciliation & Compliance: Execute daily, weekly, and monthly reconciliations between the MERS System and the company's Loan Origination System (LOS) to identify and cure all discrepancies. Maintain documentation and files for MERS audits and annual reports, ensuring 100% compliance with MERSCORP Holdings rules and guidelines. Perform MIN-level research and resolution for any MERS-related issues or rejects/warnings. Conduct reverification of employment, income, assets, and other critical loan applications data via phone, email, and mail. QC Reverification Responsibilities: Conduct reverification of employment, income, assets, and other critical loan applications data via phone, email, and mail. Document all reverification attempts and results accurately in the loan origination system. Identify discrepancies and inconsistencies in information and escalate them to the appropriate parties for resolution ? Ensure compliance with company policies, regulatory requirements, and investor guidelines Maintain confidentiality and security of sensitive information. Communicate effectively with internal teams, borrowers, employers, and financial institutions. Assist in preparing reports on reverification activities and findings Stay up-to-date with industry's best practices and regulatory changes. Servicing Responsibilities: Perform Interim Mortgage Servicing functions per investor and agency guidelines as assigned. Requirements Qualifications: Two years of similar or related experience. Knowledge of mortgage industry regulations and compliance requirements. Excellent organizational skills. Proficient verbal and written skills to effectively communicate and provide customer service required. Excellent customer service skills, strong communication, interpersonal and problem solving skills. Excellent time management skills with an emphasis on quality. Must be self-motivated, creative and able to work in a team environment while thinking independently and sharing knowledge and ideas. Must be able to multitask between multiple projects and able to adapt to constant modification of the workflow. Ability to work independently and as part of a team. $20-24 DOE. Salary Description $20-24

We are Reckitt Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose. Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege. Research & Development In Research and Development, we're full of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working to create a cleaner, healthier world. With nine Centres of Excellence, we continually seek out new opportunities by using science, our entrepreneurial flare and our fearless innovation to develop and enhance our existing portfolio, never compromising on quality or performance. We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality. The size of our organisation means you'll have the opportunity to learn and work in different functions within R&D, giving you exposure to different disciplines, teams and environments. You will also have access to our Research and Development Academy, designed to develop our team and allow you to grow in our great organisation. About the role As an R & D Technician at Reckitt, you will thrive in our fast-paced environment alongside a team of expert scientists dedicated to ensuring product safety and efficacy. Your meticulous attention to detail will be crucial in supporting technical dossier management and analytical lab compliance. This role is not currently sponsoring visas or considering international movement at this time. Your responsibilities * Assist the R&D Analytical Lab and R&D Pilot Plant with placing purchase orders and reconciling accounts and invoices using Excel, SharePoint, and SAP. * Track stability protocols and pull samples at required time points. Route samples for required testing. * Create orders for testing at 3rd party labs where required and ship samples. * Administrate shipment of packages through UPS for the R&D group. * Regularly update the chemical inventory and lab equipment status for the R&D Analytical Lab in lab database. * Organize and maintain stores of lab consumables. * Enter analytical results from 3rd party laboratories in lab database. * Carry out administrative tasks in lab database for routine maintenance. * Organize and maintain archived analytical documentation. * Participate in lab cleanup/5S processes and activities. * Provide general clerical support by assisting with copies, scanning, and updating lists. * Assist in the preparation and maintenance of documents, spreadsheets and presentations using MS Word, Excel and Power Point. * Review analytical lab administrative process and make efficient improvements. * Diagnose and handle business issues as they arise in a logical, self-directed manner and with manager's input as needed. The experience we're looking for * High School Diploma required, Associate degree in a scientific field is a plus. * Laboratory experience preferred; familiarity with laboratory terminology. * Excellent organizational skills. Ability to apply logical thinking to solve a variety of problems. * Interpersonal skills with the ability to work in a team-oriented environment. * Proficient in English. Good verbal and written communication skills. * Ability to display a degree of flexibility regarding changing project priorities. * Knowledge with MS Office Software applications. The skills for success R&D, Product Lifecycle Management, Commercial Awareness, Business Partnership, Collaboration, Partnership building, Collaborator, Ability to challenge the status quo, Propose improvement, Accountability, Adaptability, Analytical, Formulation, Science, Chemistry. What we offer With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way. We invest in the wellbeing of our people through parental benefits, an Employee Assistance Program to promote mental health, and life insurance for all employees globally. We have a range of other benefits in line with the local market. Through our global share plans we offer the opportunity to save and share in Reckitt's potential future successes. For eligible roles, we also offer short-term incentives to recognise, appreciate and reward your work for delivering outstanding results. You will be rewarded in line with Reckitt's pay for performance philosophy. US salary ranges USD $62,000.00 - $92,000.00 Equality We recognise that in real life, great people don't always 'tick all the boxes'. That's why we hire for potential as well as experience. Even if you don't meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you. All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law. Nearest Major Market: Salt Lake City Job Segment: Counseling, Nutrition, Healthcare

Job DescriptionSalary: $20 - $22 DOE This is a full time, non-exempt position. This individual is responsible for completion of activities related to the Quality system. This position regularly interacts and/or collaborates with other departments within BioFire in the execution of their duties. Position follows standard work practices and procedures, and must operate in accordance with FDA, OSHA, ISO, and applicable government regulations and standards. This individual will collect, organize, monitor, and distribute information related to Quality and process improvement functions, possibly including but not limited to compliance to and documentation of Quality Management standards. Typically generates reports using computer skills and distributes those reports to various users in the organization. This individual will follow established procedures to complete tasks within the Quality system. Other responsibilities include assisting with other activities related to the Quality system. This position requires intermediate computer skills, and good attention to detail. After training has been completed, this individual is expected to work independently or cooperatively in the completion of tasks assigned by their direct supervisor. Principal Job Duties and Responsibilities: Perform all work in compliance with company policy and within the guidelines of BioFires Quality System. Maintains records that comply with regulatory requirements, Good Manufacturing Practices and Standard Operating Procedures. Provides support to all aspects of the Quality System; provides assistance in other Quality Department duties and projects as assigned. Must be able work in a clean-room environment. Performs Functional QC and analysis for all manufactured products, prepares and/or reviews process reports and data. Provides support to all aspects of the Quality System; provides assistance in other Quality department duties and projects as assigned. Training and Education: High School Diploma or equivalent Good computer skills, including proficiency in MS Word, Excel, and PowerPoint. Requires basic laboratory skills, and experience working in a biotech/scientific laboratory setting (i.e. use of pipettes, measurements) Experience: 1-2 years of experience in applicable industry ( g ., ISO 9001, ISO 13485 or GMP) At least one year of laboratory work experience is preferred AS degree in a Biology or Chemical Science may substitute for demonstrated basic laboratory skills (i.e. use of pipettes, measurements) and good computer skills, including proficiency in MS Word and Excel) Benefits: Medical Dental Vision 401k - company match of 5% regardless of participation and up to a total of 9.5% company match if contributing 4 Weeks of PTO 9 Paid Holidays Paid Winter Break from the work week between December 24 thru December 31 Participation in Company's Wellness Program (discounted medical premiums) Multiple Company Sponsored Events Each Year (catered breakfast/lunch, holiday parties, snacks) Stimulating work environment Convenient location near I-15 and Trax Station Free Parking Our EEO Policy BioFire Defense is an equal opportunity employer (M/F/D/V). We recruit, employ, train, compensate, and promote without regard to race, religion, creed, color, national origin, age, gender, sexual orientation, marital status, disability, veteran status, or any other basis protected by applicable federal, state or local law. BioFire Defense complies with applicable state and local laws governing non-discrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including, but not limited to, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow. Job Description Summary To ensure that Quality Control (QC) procedures are conducted in compliance with standards of Good Manufacturing Practices, thereby providing continuous support to our product quality and customer service performance in the SLC factory. Scope / Dimensions of Role : Delivery of accurate and reliable QC processes (e.g. analysis) to support the targets and needs of the business. Challenging and passionate about Quality, taking responsibility and ownership for compliant processes that continually improve. Responsibilities / Accountabilities : Conducting analysis in accordance with relevant Good Manufacturing & Control Laboratory Practices To ensure that analytical chemistry results are checked, approved, recorded and available for inspection To ensure that equipment used is maintained and calibrated to appropriate standards. To understand and follow all necessary Health & Safety systems and ensure that work is consistent with safe working practices. To provide effective application of analytical investigations, non-conformance reporting and change management within QC as defined in SOPs. To have responsibility for adherence and timely completion of quality systems processes (e.g. OOS/QDR/CC) in line with current SOP's. To ensure that effective CAPA are appropriately implemented. To ensure that audit readiness is maintained at the agreed level. To maintain high standards of laboratory housekeeping in his or her work area. To maintain and support the laboratory quality systems. To ensure daily workloads are completed in timely manner. Key Challenges: Working in a highly regulated and compliant environment to deliver accurate results. Delivering output in an efficient manner against focused lead times. Providing clear and effective communication throughout the supply chain. Offering a dynamic and flexible attitude to facilitate a fast-moving operation Skills and Competencies : For most positions there is a competency matrix developed. The required functional skills are defined and should be used for the evaluation of candidates for this role Competency / Area Skill Level Supply Excellence Analytical Skills & Decision Making Offers accurate working practices and delivery of reliable results. Reviews and reports data, highlighting spurious incidences (e.g. Trending) Contributes to investigations and offers conclusions to support management in decision-making MS Office Skills Personal Attributes : Good communication skills with the ability to present information in a clear and concise manner. High level of accuracy in working practices with close attention to detail. Ability to integrate cross-functionally to support customer service and investigations. The business language is English, therefore fluency in English is essential and fluency in local languages advantageous In line with core values, the candidate will be achievement focused and able to work in a direct and often pressurized environment. Entrepreneurial skills in terms of innovation and problem solving are key along with tenacity, tough-mindedness and ability to influence and demonstrate strong team working abilities and commitment. Qualifications Professional Qualifications/ Experience Requires a Bachelor's degree in Chemistry or related field or an equivalent combination of education and experience. Requires basic understanding of HPLC or ICP and other scientific instrumentation. Excellent organizational and communication skills with ability to work cross functionally. LIMS and/or other data systems experience a plus. Ideally experience in food, dietary supplements or pharmaceutical GMP/GLP Ability to work on own initiative in an accurate and reliable manner Additional Information All your information will be kept confidential according to EEO guidelines. With Regards, Abhishek Singh 650-399-0881 Clinical Recruiter Integrated Resources, Inc.

Job Description Federal Construction Professionals - QCM, Superintendent, PM Use the link below to Apply! https://hiring.elitercservices.com/fcc-2046 Elite Recruiting and Consulting Services, SDVOSB, is building an ongoing pipeline of experienced Federal construction professionals for upcoming NAVFAC, USACE, and Guard projects nationwide. If you have worked on military bases or federal vertical or horizontal projects, we want to connect. We support primes preparing for new phases, new awards, and upcoming mobilizations. Roles We Are Currently looking for Quality Control Manager Construction Superintendent Project Manager Types of Projects Access control facilities Barracks and housing Aircraft hangars HVAC and MEP upgrades Ranges and training facilities Renovations on Air Force, Army, Marine Corps, and Guard installations What Helps You Stand Out NAVFAC or USACE project experience CQM certification EM 385 1 1 OSHA 30 Secret or Top-Secret clearance Ability to travel Strong documentation and coordination skills How to Apply Complete our Federal Construction Candidate Form for fastest review Use the link below to apply! https://hiring.elitercservices.com/fcc-2046 We will reach out as soon as your experience matches an upcoming federal project. Veterans are encouraged to apply.

Salt Lake City Regular MERIEUX NUTRISCIENCES As a trusted partner, our Public Health mission is to make food systems safer, healthier and more sustainable. Throughout our global network in 27 countries, we offer to our customers a wide range of testing and innovative solutions dedicated to preventing health risks related to food, environment and consumer goods. External growth has been a key pillar of our history with more than 40 acquisitions completed in the last 10 years. If you want to contribute to an inspiring long-term purpose, to be part of a fast growing company on a high-value market with significant build-up opportunities, and to grow in an entrepreneurial and warm environment, join us! YOUR DAY TO DAY LIFE We are looking for a Chemist 1 in 1945 Fremont Drive, Salt Lake City, UT 84104 USA. Your mission will be to: The incumbent is responsible for performing chemical analysis on food/pharmaceutical samples. The incumbent analyzes the concentration of certain components in food samples. The incumbent must accurately prepare and process the samples to obtain the needed results. * Analyses w/Extractions (Cholesterol, FAP, ICP, MOJO, FFA, etc.) * Ensure that proper analysis methods are conducted on the appropriate samples. Maintain chemistry quality control records and procedures for each test. * Extract desired components from samples with appropriate processes such as distillation, solvent extraction and acid digestion, so that concentrations can be determined. * Calculate the concentration of components present in samples and post results. * Wash glassware as needed and prepare samples as needed. * Prepare standards or reagents that are needed for the analysis procedure. * Maintain knowledge of Laboratory Information Management System (LIMS) required to complete job responsibilities. * Maintain clean laboratory by washing countertops, sweeping floors, storing analysis materials, etc. * Initiate and investigate customer complaint and non conformances Determine root cause and corrective action * Review batches and respond to out of specification results or questionable data. * Maintain equipment records in appropriate software systems. Meet the housekeeping schedule on time. * This position has the responsibility and authority to identify departures from the quality system or test procedures and document such observations in accordance with the prescribed non conformance system and the supervisor is notified. * Responsibility to support laboratory management in the implementation maintenance and improvement of the management system. * Adhere to all safety policies. * Perform other related tasks as needed YOUR PROFILE A basic knowledge of instrumentation and theory including HPLC, GC, ICP and AA is helpful. Basic knowledge of food science is helpful to analyze the chemical content of samples. Associates degree required, Bachelors preferred. Required skills: One - two years experience. This position requires a general knowledge of chemistry to perform analyses. A general knowledge of the Laboratory Information Management System and Laboratory Instrument Data systems are required to process client data. The incumbent needs a broad knowledge of analytical chemistry to perform analysis procedures. Manual dexterity is needed to pipet samples where required. Analytical skills are necessary for completion of tasks within the department. Work Environment: The incumbent works in a laboratory setting with proper lighting and temperature control. Occasional exposure to laboratory fumes, chemicals, and materials will occur when in the laboratory. Safety equipment of gloves, laboratory coat and eyeglasses may need to be worn depending on the testing process. The incumbent may use the autoclave daily to complete the analysis process. Continuous lifting of analysis materials weighing up to 50 pounds are necessary to transport media materials. The incumbent can expect extended time spent in a standing position. The incumbent should be able to detect slight variation in shades of colors. WHY JOIN US? * Because you would contribute to an inspiring Public Health purpose, supported by long-term and visionary shareholders. * Because you would have an impact on our strategic pillars that build on 50 years of experience and expertise. * Because you would be part of a community of an enthusiastic and skilled group of people who love co-building together and serving a purpose bigger than them. * Because you would be welcome as you are, in a diverse and open-minded environment that is rich in our singularities and differences. * Because you would grow in an international group of more than 8200 fantastic team members, with plenty of opportunities to learn and share. Ready for the journey? To apply please click on 'Apply now' button

Full-time Description Accurately reads, understands, follows, and updates required process data and reports. Completes tasks and training/qualifications as assigned. Follows good housekeeping and cleanliness protocols within department. Reviews procedures and provides input to make logical updates. Requirements Assist day-to-day production floor tasks Follow instructions from supervisors and leads Perform basic material handling duties Maintain a clean and safe work environment Inspect materials or products for quality Support overall workflow to help meet production goals Skills Required Attention to detail - ensure accuracy in all task Strong listening skills - able to follow instruction clearly Fast learner - quickly adapts to new tasks and processes Dedication to quality - committed to producing high-quality work Experience Required 0-3 years Physical/Environmental Demands Able to sit, walk, stand, etc. for prolonged periods of time Able to lift up to 25 lbs., on occasion Able to work in dusty, noisy areas and wear appropriate PPE such as eye protection, ear plugs, latex or nitrile gloves, etc. Education/Knowledge Required Able to read, write, speak English. Able to use microscope, calculator, Microsoft Excel

Job DescriptionSalary: Quality Control Technician | Join Our Innovative Team at MZ Packaging LLC About Us: Join our dynamic team at MZ Packaging LLC, where we are committed to excellence and innovation. We are looking for a dedicated Quality Control Technician to ensure our products meet the highest standards of quality and safety. Key Responsibilities: Conduct regular inspections and tests on products to ensure compliance with quality standards. Document and report any quality issues and collaborate with the production team to resolve them. Maintain and calibrate testing equipment to ensure accuracy. Assist in the development and implementation of quality control procedures. Analyze data and generate reports to track quality performance. Participate in continuous improvement initiatives to enhance product quality. Qualifications: High school diploma or equivalent; a degree in a related field is a plus. Proven experience in quality control or a similar role. Strong attention to detail and excellent analytical skills. Ability to work independently and as part of a team. Proficiency in using quality control software and tools. Excellent communication and documentation skills. Why Join Us? Competitive salary and benefits package. Full-time position with first shift, but some second shift work may be required. Opportunities for professional growth and development. A supportive and collaborative work environment. Be part of a company that values innovation and quality. #QualityControl #QualityControlTechnician #SaltLakeCityJobs #FullTimeJob #CompetitiveSalary #JobOpening #CareerOpportunity #JoinOurTeam #QualityAssurance #ManufacturingJobs For more information about our company, visit our website at [**********************************************************

Job Description Quality Control Inspector | Salt Lake City, UT Nexeo HR is hiring Quality Control Inspectors to join a leading manufacturing and production company in Salt Lake City, UT. This role is ideal for detail-oriented individuals who enjoy working in a fast-paced manufacturing environment with opportunities for long-term career growth. As a Quality Control Inspector, you will play a key role in ensuring quality assurance and compliance by performing visual and mechanical inspections, verifying materials and assemblies, and using precision tools to confirm product accuracy. Candidates with experience in quality control, inspection, or manufacturing are encouraged to apply. Responsibilities • Perform mechanical and visual inspections of raw materials, components, and sub-assemblies according to inspection plans, blueprints, and specifications • Use precision measurement tools such as microscopes, calipers, and micrometers to perform accurate quality checks • Document inspection results in compliance with quality assurance and manufacturing standards • Support document control processes, including scanning, archiving, and preparing records for shipment • Maintain compliance with FDA regulations, ISO standards, and company quality procedures • Assist with special projects, audits, and process improvements as needed Qualifications • Basic computer proficiency for documenting inspections and accessing quality systems • Strong written and verbal communication skills to interpret work instructions and collaborate with team members • Ability to read and interpret engineering drawings and technical specifications • Familiarity with FDA regulatory standards, ISO 13485, or medical device manufacturing preferred • Strong attention to detail and ability to perform repetitive inspection tasks with accuracy • Manual dexterity and ability to operate standard office and inspection equipment • Ability to sit for extended periods while entering/analyzing data • Must occasionally lift up to 25 lbs Pay Rate $19-$21 per hour Job Type Full-Time Shift/Schedule Day Shift: 6:30 AM - 6:30 PM (rotating schedule) Swing Shift: 6:30 PM - 6:30 AM (rotating schedule) Nexeo Benefits •Medical, Dental, Vision, Limited Life, Short-Term Disability. •Refer a Friend Bonus | Other Financial Incentives (Bonuses). •Weekly Pay | Direct Deposit | Rapid Pay Card. •Hassle-Free Job Search: A Nexeo Recruiter is always available to assist you. Questions? Call or Text our office today! With 100+ jobs available, we're sure to find a job for you. 1745 W 7800 S, West Jordan, UT 84088 (P) (801) 305-1300 Nexeo provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability, sexual orientation, or genetics. In addition to federal law requirements, Nexeo complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. Nexeo expressly prohibits any form of workplace harassment based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. Quality Control Inspector | Manufacturing Quality Assurance | Mechanical Inspection Specialist | Visual Inspection Technician | Precision Measurement Tools Operator | Micrometer and Caliper Inspection | Medical Device Quality Control | FDA Compliance Specialist | ISO 13485 Inspector | Raw Material Inspection | Sub-Assembly Quality Assurance | Blueprint and Specification Reading | Quality Assurance Technician | Document Control and Archiving | Manufacturing Inspection Professional INDWJ

Job Description Job Title: Product Control - AWM Public Performance Analyst Employment Terms: This role is an 8-week internship with the opportunity to transition to full-time employment Internship and full-time employment are both fully in-office Hours: Monday-Friday, 8:00am-4:00pm Target Start Date: May 4, 2026 Estimated Salary: $60,000/year Must be legally authorized to work in the United States, without the need for sponsorship now or in the future Essential Tasks - In this job, you will: Perform analytical review and reporting of performance returns against benchmarks, targets and estimates along with analysis of variances Performance oversight including critical review of significant account P&L and performance with portfolio managers and senior management Report on performance across a variety of GSAM strategies to senior management Work with the performance team on strategic initiatives to enhance the daily performance process and workflow Maintain control procedures around the performance process and management reporting General Skills and Abilities - In this job you will demonstrate: Strong interpersonal and communication skills (oral and written) Strong analytical and organizational skills The ability to work in a team environment The ability to take initiative and work efficiently Strong work ethic with a keen attention to detail Digital/Technical Skills - In this job you will demonstrate: Intermediate data management skills using Microsoft Excel (such as transferring information, using formulas such as VLOOKUP, and creating charts/graphs and pivot tables) Education/Knowledge - In this job you need to have: Bachelor's degree in any discipline A degree in Accounting or Finance is nice to have but not required CPA, CFA or other relevant industry certification is nice to have but not required Social Interaction - The following types of communication and interaction are required to perform the job successfully: Oral communication: Hourly Email communication: Hourly Instant messaging: Hourly Telephone communication: Daily Video communication: Hourly (Camera on is preferred when presenting) Interacting with supervisors: Daily Interacting with peers: Hourly Job Stressors - Employees sometimes find the following stressful about this job: Managing tight project timelines Working with multiple systems Adapting to changing technology which can affect daily interactions Varying workloads from day-to-day Job Motivators - Employees tend to find the following motivating or rewarding: Working in an inclusive environment with strong company culture This role provides flexibility and promotes healthy work-life balance The opportunity to work with an incredibly supportive team Access to great internal training resources On site wellness offerings, e.g. fitness center Candidate Assessment - To be considered for this role, compatible applicants: Will complete a Candidate Profile May complete a short work sample exercise Will be invited to participate in a Structured Candidate Meeting with the hiring manager(s) Workplace Support: Specialisterne and our employer partners are committed to providing inclusive onboarding experiences and supporting new employees as they learn on the job All new hires continue to liaise with a Specialisterne Workplace Support Specialist throughout the duration of the internship **Beware of scams and fraudulent job postings. Specialisterne only accepts applications through our careers page at ********************************************* Powered by JazzHR vPT2UUhqIG

Security National is seeking a detail-oriented and analytical Internal Controls Analyst to join our Internal Audit team. The Internal Controls Analyst will play a key role in maintaining and enhancing the company's internal control environment by developing and executing test sheets, performing control testing, and assisting with process documentation. The ideal candidate will have a strong background in accounting or business, familiarity with financial statements, excel at communication and relationship building, and experience working with the BlackLine reconciliation platform. Essential Duties and Responsibilities: * Develop, maintain, and execute internal control test sheets to assess the effectiveness of key controls across financial processes. * Perform internal controls testing, document findings, and provide recommendations for remediation and process improvement. * Collaborate with accounting, finance teams, and senior leadership to ensure compliance with internal control requirements and corporate policies. * Assist in the evaluation of financial statements and supporting documentation to validate control performance. * Maintain organized and accurate testing documentation for internal and external audit purposes. * Support the implementation and ongoing maintenance of BlackLine account reconciliations and control workflows. * Assist in periodic control walkthroughs and risk assessments. * Participate in control improvement initiatives and special projects as assigned. Requirements Education and/or Work Experience Requirements: * Bachelor's degree in Accounting, Finance, Business Administration, or a related field required. * Minimum 3 years of relevant experience in accounting, audit, or internal controls. * Experience preparing, analyzing, and interpreting financial statements. * Prior experience with BlackLine or similar reconciliation software strongly preferred. * Excellent Microsoft Office skills with a focus on Excel proficiency. * Excellent analytical skills, combined with impeccable business judgement. * Self-directed, energetic, intellectually curious. * Superior analytical and problem-solving skills. * Effective verbal and written communication skills. * Team player who is comfortable working in a dynamic environment. 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. * Ability to maintain regular, punctual attendance consistent with the ADA, FMLA and other federal, state and local standards. * Must be able to occasionally lift and carry up to 15 lbs. * Must be able to talk, listen and speak clearly on telephone. * Must be able to sit for prolonged periods at a desk, while working on a computer.

Job Description HemaSource is looking for a detail-focused and analytical Quality Control Analyst to support the intake, evaluation, investigation, and reporting of medical device product complaints. This role directly contributes to patient safety and ensures our products meet global regulatory standards. You will be part of a highly collaborative Quality team that values accuracy, critical thinking, and a commitment to continuous improvement. If you enjoy problem-solving, working with technical data, and partnering across Quality, Engineering, and Regulatory teams, this is an excellent opportunity to grow your career in a fast-paced and mission-driven environment. You will play a vital role in supporting compliance with FDA regulations, international standards, and internal quality system requirements while helping drive improvements in product performance and customer satisfaction. Key Responsibilities Receive, review, and process medical device product complaints, ensuring accurate documentation and timely assessment. Conduct thorough complaint investigations using root-cause analysis and cross-functional input. Ensure compliance with FDA, ISO 13485, EU MDR, and internal quality system requirements. Prepare and submit required regulatory reports (MDRs, vigilance reports) within strict timelines. Analyze complaint data to identify trends and contribute to CAPA and continuous improvement efforts. Communicate clearly with internal teams and external customers regarding complaint status and findings. Maintain accurate, audit-ready records, complaint metrics, and documentation. Manage LMS activities including training assignments, system maintenance, and compliance reporting. Qualifications Bachelor's degree in Life Sciences, Engineering, or related field. 2+ years of medical device complaint handling, post-market surveillance, or quality experience. Familiarity with FDA regulations, ISO 13485, EU MDR, and quality system requirements. Strong analytical, critical-thinking, and problem-solving skills. Excellent written and verbal communication skills. Proficient with Microsoft Office; experience with QMS/ERP/complaint systems preferred. Why Join Us Opportunity to grow in Quality, Regulatory, or Technical Operations. Meaningful work that directly impacts patient safety and product quality. Supportive team environment with clear development pathways. Stable, growing company invested in compliance excellence. Physical Requirements Prolonged computer work. Ability to lift up to 10 lbs. occasionally. Who We Are: HemaSource is an innovative logistics solution partner that combines best-in-class analytics and high-quality medical product supply to specialty ambulatory clinics. Our mission is to drive customer operational efficiencies and related cost savings in high volume ambulatory care clinics. HemaSource's patented data analytics software tool and our superior customer service have enabled us to become the preferred disposables provider to the plasma collection market. Job Posted by ApplicantPro