Namsa jobs in Irvine, CA - 28 jobs

NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976. We are shaping the industry. NAMSA has been a key contributor to the development of the test methods that govern our industry. We have become the industry's premier provider. We provide support for clients during every step of the product development lifecycle and beyond. Come and work for an organization with the: Vision to inspire innovative MedTech solutions that advance global healthcare, improve patient lives and accelerate Client success and the Mission to deliver best-in-class global MedTech development solutions through our people, expertise and technology by adhering to our core Values: Act with integrity in everything we do. Provide best-in-class customer experiences. Develop superior talent and deliver expertise. Respond with agility and provide timely results. Embrace collaboration, diverse perspectives and ideas. Job Description: • Works on assigned studies to ensure that human subject protection is maintained, Good Clinical Practice (GCP), and applicable regulations are followed. • Coordinates and manages clinical site monitoring responsibilities for assigned studies in accordance with contractual agreements, SOPs, and applicable regulatory guidelines. • May conduct on-site and remote site qualification, site initiation, interim, and site close-out monitoring visits. • Serve as primary point of contact for site questions relating to study enrollment, conduct, and close-out issues: liaise with appropriate study team members as needed. • Communicates through verbal and written communication with site investigator and project team overall site performance, trends, deficiencies, and concerns. • Supports study start-up activities such as tracking and performing quality review of study documents, completing, and distributing site activation letters, etc. • Performs study-related training. • Manages the development and maintenance of study documents, processes and systems as assigned. • Ensures quality and completeness of central and site master files. Tracks and maintains required study documents, performs quality control review, manages renewals. • Tracks study site and over all study metrics including but not limited to enrollment, deviations, adverse events, trial master file maintenance. • Attends internal and external meetings as required. • Provides all job-related progress reports and visit documentation as required. • May support safety activities such as narrative writing, managing the CEC/DSMB, etc. • OUS: Prepares and coordinates submissions to regulatory authorities. • May perform other activities as assigned. Qualifications & Technical Competencies: • Fluency in English and local language, if different, required. • Higher education degree or equivalent education, training, and experience. • Preferred 2 years clinical trial experience. • Preferred monitoring experience. • Able to work independently once trained. • Good verbal and written communication skills. • Strong organizational skills. • Basic computer proficiency. • Understanding of clinical research processes and regulations. • Certifications such as Society of Clinical Research Associates (SoCRA) or Association of Clinical Research Professionals (ACRP) Certification preferred but not required Working Conditions: • Up to 20% travel for In-House Clinical Research Associates; up to 80% travel for Field Clinical Research Associates. • The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. • While performing the duties of this job, the employee is regularly required to talk or hear. The employee is frequently required to stand; walk; sit; use hands to finger, handle, or feel and reach with hands and arms. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, depth perception, and ability to adjust focus. • Extensive use of a computer keyboard. Pay Range Minimum: $54,400.00 Pay Range Target: $80,100.00 Pay Frequency: Annual Please Note: Individual base pay depends on various factors, in addition to primary work location, such as complexity and responsibility of role, job duties/requirements, and relevant experience and skills. NAMSA is an equal employment opportunity company. NAMSA participates in pre-employment background and drug screen processes aligned to local, state and federal laws. Fair Chance Employment Statement: At NAMSA, we are committed to providing equal employment opportunities to all qualified applicants, including those with arrest or conviction records. In accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act, we will consider qualified applicants with a criminal history. Please note that NAMSA conducts a review of criminal history after the interview process and offer acceptance. This review is conducted to ensure that there is no direct, adverse, or negative relationship between the criminal history and the material job duties of the specific position. The following is a list of material job duties for this position: • May operate equipment • Records data timely and accurately • May analyze and interpret data • Conducts studies on medical devices that have an impact on human life A criminal history that directly impacts the ability to perform these duties may result in the withdrawal of a conditional offer of employment. We believe in fair chance hiring and are committed to evaluating each applicant on a case-by-case basis.

Join Our BioTec Dental Laboratory Team! Are you ready to be part of a cutting-edge dental laboratory in the heart of innovation? BioTec Dental Laboratory, located in beautiful Irvine, CA, is seeking passionate individuals to join our dynamic team! Why BioTec? ?? Innovative Practices: At BioTec, we pride ourselves on staying ahead of the curve with state-of-the-art technologies and revolutionary techniques in dental manufacturing. Be part of a team that's setting new standards in the industry! ?? Commitment to Excellence: We are dedicated to providing the best products to our customers. Join us in our mission to enhance smiles and improve lives through precision and quality craftsmanship. ?? Employee-Centric Culture: We believe that taking care of our employees translates into exceptional care for our customers. Enjoy competitive pay, comprehensive medical benefits, paid holidays, and a simple IRA with matching to support your financial wellness. ?? Perks and More: Employee lunches to fuel your day Ongoing training and development opportunities Collaborative and vibrant work environment Opportunities for career advancement Recognition programs to celebrate your achievements What We're Looking For: Housekeeper Essential Functions: Keep facilities and common areas clean and maintained. Vacuum, sweep, and mop floors. Clean and stock restrooms. Clean up spills with appropriate equipment. Notify managers of necessary repairs. Collect and dispose of trash. Keep linen room stocked. Properly clean upholstered furniture. Other duties and responsibilities may be assigned from time to time as business needs require

The Shipping Associate is responsible for ensuring the accurate, timely, and efficient packing and shipping of dental laboratory cases to clients. This role involves coordinating with production, quality control, and customer service teams to meet shipping deadlines and maintain quality standards. The ideal candidate is detail-oriented, organized, and capable of working in a fast-paced environment to support operational excellence. Essential Functions Packing and Shipping: Accurately pack dental cases to ensure they are secure and meet shipping quality standards. Prepare and print shipping labels, ensuring correct delivery addresses and proper documentation. Verify shipping contents against invoices and work orders to confirm accuracy. Logistics Coordination: Communicate with courier services and shipping vendors to schedule pickups and track shipments. Monitor shipping schedules and update case statuses in internal systems. Troubleshoot and resolve shipping issues, including delayed or misplaced deliveries, in coordination with customer service and logistics teams. Inventory and Supplies Management: Maintain an inventory of shipping supplies, including boxes, packing materials, and labels. Notify the Logistics Manager of low stock levels and assist with reordering supplies as needed. Communication and Collaboration: Work closely with production, quality control, and customer service teams to ensure cases are prepared and shipped on time. Provide shipment tracking details to internal teams or directly to clients as requested. Process Improvement and Compliance: Follow established shipping procedures and company guidelines to ensure compliance with quality standards. Identify areas for process improvement and communicate suggestions to the Logistics Manager.

The Purchasing Coordinator plays a vital role in supporting both our lab operations and accounting functions. You'll be responsible for purchasing dental materials and supplies, managing vendor relationships, tracking inventory, and handling basic accounting tasks that align with our purchase order process. This is a hands-on position ideal for someone who thrives in a fast-paced, collaborative environment and enjoys wearing multiple hats. Key Responsibilities: Procurement & Purchase Order Management • Manage the procurement process for dental lab materials, equipment, and services • Ensure timely, accurate, and cost-effective purchasing and delivery of goods • Process and track purchase orders with precision from order entry through to delivery Vendor Relations • Develop and maintain strong, reliable supplier relationships • Negotiate pricing, terms, and resolve vendor-related issues professionally Inventory Control • Monitor inventory levels and track supply usage • Conduct and support monthly inventory audits and reconciliation • Ensure materials are stocked appropriately to support daily operations Administrative & Accounting Support • Maintain accurate records of suppliers, inventory, and pricing • Update procurement and product databases regularly • Collaborate with the accounting team to ensure order/payment alignment and invoice accuracy • Provide general administrative assistance as needed Cross-Functional Collaboration • Work closely with internal teams across operations, production, and finance • Proactively communicate procurement timelines and resolve potential bottlenecks Qualifications: • Advanced proficiency in Microsoft Excel, Word, and Outlook • Experience using QuickBooks and/or Magic Touch Software a strong plus • Strong organizational skills and meticulous attention to detail • Excellent verbal and written communication skills • Ability to manage multiple priorities and meet deadlines in a fast-paced environment • Strong negotiation and critical thinking abilities

Diasorin is a global leader in diagnostic solutions, pushing the boundaries of science and technology to create cutting-edge tools that improve healthcare worldwide. With a legacy spanning over 50 years, we've earned our reputation for excellence by developing innovative diagnostic assays and instruments that are trusted by healthcare providers around the world. Our broad offering of diagnostic tests and Licensed Technology solutions, made available thanks to ongoing investments in research, positions us as the player with the widest range of specialty solutions in the sector and identifies us as the "Diagnostics Specialist." Why Join Diasorin? Impactful Work: When you join Diasorin, you become part of a team that's dedicated to improving lives. Your contributions will directly impact patient care, making a meaningful difference in the world. Global Reach & Innovation: Our work transcends borders. Joining Diasorin means collaborating with colleagues from all over the world, expanding your horizons, and contributing to global healthcare solutions at the forefront of the diagnostic industry. Diverse and Inclusive Culture: We believe in the strength of diversity, and our inclusive culture reflects this commitment. We value your unique perspective and offer a supportive, collaborative environment where everyone can thrive. Join Our Team: If you're passionate about innovation, diversity, and making a positive impact on healthcare, Diasorin is the place for you. We're looking for passionate and talented individuals who are ready to embrace new challenges and drive healthcare solutions forward. Are you ready to be part of a dynamic team that's shaping the future of diagnostics? Join Diasorin and become a catalyst for change in the world of healthcare. Apply today and be a part of our exciting journey toward a healthier, more connected world. Together, we can make an impact! Job Scope Responsible for manufacturing and subassemblies, components, and/or kits. Job requirements are specific to each department - Cell Culture, Formulations, Molecular Dx, Slide Production, Disc Production, and/or Washroom. Tasks may include, but are not limited to subassembly/product, and formulation, adjustment, filtration, dispensing, packaging, seed maintenance, cell infection and harvest, antigen production, organic fixation of product, protein determination, and others as required. Tasks may require operation of various production equipment such as analytical or part counting balances, pH meters, electrical mixers, filtration apparatus, liquid or solid dispensers, 96-well ELISA plate dispensing light unit, pouch sealer, tear seal applicator, biological safety cabinets, fume hoods, UV and light microscopes, centrifuge, sonicator, tissue shearer, incubator, autoclave, protein transfer system, slide spotting apparatus and application systems. Supports all applicable regulations including but not limited to FDA, ISO, and CMD/CAS requirements. Key Duties and Responsibilities Manufacture subassemblies, components, and/or kits per documented methods. Assist in investigations to identify potential root causes of issues. Understand, comply, and support FDA and ISO regulatory requirements. Understand, comply, and support all policies and procedures. Perform lab maintenance per documented cleaning requirements. Perform inventory maintenance; replenish raw materials and supplies as required per documented procedures. Provide proper storage of raw materials, subassemblies, components, and kits. Perform equipment operation and maintenance per documented procedures; calibrate as required. Maintain product identification and traceability per SOP (Standard Operating) Procedures. Record required data on documents in accordance with GDP (Good Documentation Procedures) and SOP. Identify non-conformance and initiate required documentation. Documentation may include NCMR (Non-Conforming Material Report) or deviation report. Assist in work order closure and manufacturing specification review. Assist in special projects. Assist in other production areas/departments as needed. Perform assigned tasks in accordance with applicable Environmental Health and Safety (EHS) regulations and Company EHS policies. Perform other duties as assigned. Education Qualifications, Experience, and Qualifications Bachelor's Degree in a related field required Industry experience preferred Ability to understand documents such as safety rules, operating and maintenance instructions, and procedures manuals Ability to add, subtract, multiply, and divide. Ability to round numbers to the nearest whole number, tenths, hundredths, or thousandths. Knowledge of metric system with ability to convert units - weight (milligram, gram, kilogram, etc.), volume (milliliter, liter, etc.), and distance (centimeter, millimeter, meter, etc.). Knowledge of statistical formulas with ability to calculate mean, %cv (coefficient of variance), and percent difference Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, verbal, diagram, or schedule form Standard Working Conditions Exposed to moving mechanical parts, fumes or airborne particles, and toxic or caustic chemicals. - Frequently What we offer Salary Range The salary range for this position is $21.50/hr - $24/hr . The salary range for this role represents the numerous factors considered in the hiring decisions including, but not limited to, educations, skills, work experience, certifications, etc. Beyond base salary, Diasorin offers a competitive rewards package focused on your overall well-being. We are proud to offer a comprehensive plan of health benefits, retirement and financial wellbeing, time off programs, wellbeing support and perks. Benefits may vary by role, country, region, union status, and other employment status factors. You may also be eligible to participate in an annual incentive program. An incentive award, if any, depends on various factors, including, individual and organizational performance. Diasorin is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status, and will not be discriminated against on the basis of disability. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and Canada and to complete the required employment eligibility verification document form upon hire. Diasorin is committed to providing reasonable accommodations for qualified individuals with disabilities. If you are a US or Canada candidate and require assistance or accommodation during the application process, please contact the North America Talent Acquisition Team at ********************* or ************** to request an accommodation. The above job description is intended to describe the general content, identify the essential functions, and set forth the requirements for the performance of this job. It is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Diasorin reserves the right to modify or amend this job posting as needed to comply with local laws and regulations. Please note that offers of employment at Diasorin may be contingent upon successful completion of a pre-employment background check and drug screen, subject to applicable laws and regulations. This position is not eligible for partnership with a third-party search firm vendor without expressed, written consent from the Diasorin Human Resources Department.

Are you an experienced dental lab professional with deep knowledge in Crown & Bridge and Implant case evaluation? Are you passionate about working directly with doctors to provide real-time, technical support that improves lives one smile at a time? Join the BioTec Dental Laboratory team-where innovation meets precision, and people come first. Why You'll Love Working at BioTec: Be on the Cutting Edge At BioTec, we're not just keeping up-we're leading. Join a lab that integrates state-of-the-art digital workflows, advanced restorative materials, and a commitment to clinical excellence. Make an Impact You'll play a critical role in case consultations, offering expert guidance on complex Crown & Bridge and Implant restorations, ensuring each case is crafted with precision and care. People-First Culture We invest in YOU so you can invest in our clients. Enjoy: Competitive pay Medical, dental, vision Paid holidays Paid Time Off PTO for your Birthday Simple IRA with employer match Employee lunches Ongoing training & growth opportunities A collaborative, energetic environment ? What You'll Be Doing: As a Case Manager, you will: Serve as the clinical liaison between our lab and dental offices Evaluate and consult on Crown & Bridge and Implant cases to ensure accuracy and efficiency Offer case-specific product recommendations tailored to each doctor's needs Manage communication with dental professionals via phone and CRM Document notes, updates, and status changes for each case in our system Proactively follow up with clients and internal teams to ensure smooth execution Support case troubleshooting and ensure exceptional customer satisfaction Collaborate cross-functionally with lab techs, managers, and admin teams ? What We're Looking For: Previous dental lab or clinical experience specializing in Crown & Bridge and Implant cases Strong technical knowledge of dental restorations and materials Experience working directly with dental providers in a customer-facing role Excellent communication, organization, and follow-up skills Proficiency in case documentation and CRM use A team-first mindset with a passion for patient outcomes

Join Our BioTec Dental Laboratory Team! Are you ready to be part of a cutting-edge dental laboratory in the heart of innovation? BioTec Dental Laboratory, located in beautiful Irvine, CA, is seeking passionate individuals to join our dynamic team! Why BioTec? ?? Innovative Practices: At BioTec, we pride ourselves on staying ahead of the curve with state-of-the-art technologies and revolutionary techniques in dental manufacturing. Be part of a team that's setting new standards in the industry! ?? Commitment to Excellence: We are dedicated to providing the best products to our customers. Join us in our mission to enhance smiles and improve lives through precision and quality craftsmanship. ?? Employee-Centric Culture: We believe that taking care of our employees translates into exceptional care for our customers. Enjoy competitive pay, comprehensive medical benefits, paid holidays, and a simple IRA with matching to support your financial wellness. ?? Perks and More: Employee lunches to fuel your day Ongoing training and development opportunities Collaborative and vibrant work environment Opportunities for career advancement Recognition programs to celebrate your achievements What We're Looking For: Technicial Advisor Essential Functions: Coordinates and performs a range of department support activities; serves as a liaison between other divisions/departments. Provides administrative support such as answering inbound telephone calls, checking on ship dates, offering information on all products, updating new account information and inputting call notes in CRM. Communicates with customers, colleagues, dental technicians, and managers in a prompt articulate manner. Complies with customer service policies and procedures and call center operational standards. Relies on extensive technical knowledge to make decisions and accomplish departmental goals. Assists customers in problem solving, planning, development, and execution of stated goals and objectives. Ensures customer retention and satisfaction. Evaluates each case thoroughly and advises doctors on which product is best for the particular case. Makes outbound calls on cases that need assistance. Maintains a day-to-day professional relationship with dental technicians and managers. Follows-up on specific requests made by doctors on particular cases. Clearly updates call notes in CRM software. Clearly updates case status, location, and work orders when changes are made. Updates case pan with proper ship date and routing slip when moving cases through the lab. Seeks advice and input from the manager when needed. Performs other related duties and projects as business needs require at direction of management.

Join Our BioTec Dental Laboratory Team! Are you ready to be part of a cutting-edge dental laboratory with a heart for innovation? BioTec Dental Laboratory, located in beautiful Irvine, CA, is seeking passionate individuals to join our dynamic team! Why BioTec? ?? Innovative Practices: At BioTec, we pride ourselves on staying ahead of the curve with state-of-the-art technologies and revolutionary techniques in dental manufacturing. Be part of a team that's setting new standards in the industry! ?? Commitment to Excellence: We are dedicated to providing the best products to our customers. Join us in our mission to enhance smiles and improve lives through precision and quality craftsmanship. ?? Employee-Centric Culture: We believe that taking care of our employees translates into exceptional care for our customers. Enjoy competitive pay, comprehensive medical benefits, paid holidays, and a simple IRA with matching to support your financial wellness. ?? Perks and More: Employee lunches to fuel your day Ongoing training and development opportunities Collaborative and vibrant work environment Opportunities for career advancement Recognition programs to celebrate your achievements What We're Looking For: If you're a dedicated individual who values innovation, takes pride in crafting top-notch dental products, and wants to be part of a team that feels like family, BioTec Dental Laboratory is the place for you! We are currently seeking a: Ceramist Essential Functions: Read and follow prescriptions and instructions given by customer and examine models or impressions to determine the design of dental products to be constructed. Fabricate, alter, or repair dental devices, such as crowns, bridges, inlays, or appliances following Standard Operating Procedures (SOP) and work instructions for specifically assigned work duties and responsibilities. Test appliances/prosthetics for conformance to specifications and accuracy of occlusion, using articulators and micrometers.The preceding functions have been provided as examples of the type of work performed by employees assigned to this job classification. Management reserves the right to add, subtract, or change the job functions. Minimum Qualifications: The requirements listed below are representative of the knowledge, skill, and ability necessary to successfully perform the essential functions of the position. Education and Experience: High school diploma or GED equivalent Experience with dental lab ceramics, including but not limited to e.Max One or more of the following required: Completion of Dental Lab Technician Trainee program Minimum of 1 year Dental Lab Technician experience required Communication Skills: Proficient English verbal and written communication skills. Ability to communicate clearly with management, and team members. Ability to communicate effectively in culturally diverse business environment. Knowledge, Skills, and Abilities: Ability to follow directions Ability to recognize the differences in color and shape Excellent eye-hand coordination and manual dexterity Ability to work in a fast-paced environment and under tight deadlines. Ability to clearly identify issues and formulate and convey solutions. Ability to prioritize and organize duties and responsibilities effectively. Ability to be reliable, dependable, and adaptable. Demonstrated effective problem-solving abilities. Physical Demands: The physical demands listed below are representative of those that must be met by an employee to successfully perform the essential functions of this position. Ability to maintain long periods of mental alertness and attention to detail while setting priorities, meeting critical deadlines, and following up on assignments. Ability to maneuver throughout Company facilities, including negotiate stairs in some locations. Ability to diagnose, analyze, and resolve issues in real-time. Ability to stand for long periods of time. Ability to interact with irate or upset employees, vendors and/or contractors. Ability to deliver quality results under high pressure deadlines in a fast-paced environment.

Introduction Werfen Werfen is a growing, family-owned, innovative company founded in 1966 in Barcelona, Spain. We are a worldwide leader in specialized diagnostics in the areas of Hemostasis, Acute Care Diagnostics, Transfusion, Autoimmunity, and Transplant. Through our Original Equipment Manufacturing (OEM) business line, we research, develop, and manufacture customized assays and biomaterials. We operate directly in 30 countries, and in more than 100 territories through distributors. Our Headquarters and Technology Centers are located in the US and Europe, and our workforce is more than 7,000 strong. Our success comes from a specific focus in these rapidly evolving diagnostic areas, our commitment to customers, and our dedication to innovation and quality. We're passionate about providing healthcare professionals the most valuable and complete solutions to improve hospital efficiency and enhance patient care. Overview Amazing Total Rewards for our Field Service Team! Generous Base Salary + Incentive Compensation Company Vehicle with Personal Use Allowance Phone & Internet Reimbursement 8% 401k Match (dollar for dollar!) Comprehensive Health Care Benefits Company paid Life Insurance Flexible Spending Account (FSA) Tuition Reimbursement Talk to your recruiter for full offerings! Position Summary: Builds and maintains relationships with customers to retain North American customer install base while performing thorough installations, repairs, preventative maintenance, and product enhancement activities on highly complex Werfen instrumentation and systems. Responsible to meet Service Delivery Key Performance Indicators while maintaining costs and achieving service revenue targets. Responsibilities Key Accountabilities Essential Functions: Provides customer support with on-site visits to perform and complete installations, cost effective repairs, preventative maintenance, and product enhancement service activities on Werfen instruments and systems. Diagnoses, analyzes, troubleshoots, and fault isolates instrument symptoms and issues to determine failure and implement thorough corrective action. Delivers a high level of customer service to build and maintain customer relationships to ensure customer retention.Acts as company liaison with customers by demonstrating the highest level of professionalism, commitment, communication, and follow-up. Escalates and communicates unresolved technical issues. Advises customers regarding the proper orientation, maintenance and troubleshooting of Werfen instruments and systems. Collaborate and communicate with all Commercial Operations colleagues such as the Sales and Applications roles, sharing customer situations, product information and lead generations. Promotes service contracts and follows-up on service contract renewal through customer relationships. Ensures compliance with all Quality, Regulatory, Service & Support policies, procedures, work instructions and records, ensuring all records are compliant, complete and accurate. Responsible for accurately documenting service activities performed in a customer service report in a timely manner. Responsible for the oversight and accuracy of assigned Service Inventory. Secondary Functions: Follows company travel/expenditure and time reporting guidelines; timely submission of expense and time reporting. Performs other duties and responsibilities as assigned by the Area Service Manager. Budget managed (if applicable) N/A Internal Networking/Key Relationships To be determined based on department needs, to include interactions such as: North America Commercial Operations Client Services World Wide Service Skills & Capabilities: The ideal candidate for this position will exhibit the following skills and capabilities: Strong Organizational and Time Management Skills | Ability to Triage & Prioritize | Work Under Pressure | Exercise Good Judgement. Ability to communicate effectively to/with a variety of audiences: customers, peers, management. Technically and process oriented. Ability to work independently, managing assigned territory with minimal direction to achieve daily goals. Ability to lift up to 50 lbs. Ability to work in a team environment, collaborate with colleagues to achieve Area(s) and National goals. Qualifications Minimum Knowledge & Experience required for the position: Education: Associates degree in Electronics, Medical Technology, Biomedical Engineering or related industry training required. Equivalent experience in lieu of a degree will be considered. Experience: Minimum of 3 years of experience in a technical/support role (industry, military and/or customer facing). Additional Skills/Knowledge: Working knowledge of personal computers and Windows Operating systems; legacy up to current version preferred. Working knowledge of Lab Information Systems and computer network connectivity a plus. Working knowledge of Microsoft Office 365 preferred. Ability to participate in rotational on-call coverage to provide support as required. Ability to work extended and flexible workdays to ensure customer interactions are resolved. International Mobility: Required: No Travel Requirements: Up to 90% travel to cover assigned territory 70% of overnight travel. Valid driver's license required. Closing If you are interested in constantly learning and being challenged on a daily basis we encourage you to submit your resume or CV. Werfen is an Equal Opportunity employer and is committed to a diverse workplace. Werfen strictly prohibits unlawful discrimination, harassment or retaliation based upon an individual's race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, mental/physical disability, medical condition, marital status, veteran status, or any other protected characteristic as defined by applicable state or federal law. If you have a disability and need an accommodation in relation to the online application process, please contact ****************************** for assistance. We operate directly in over 30 countries, and in more than 100 territories through distributors. Annual revenue is approximately $2 billion and more than 7,000 employees around the world comprise our Werfen team. ************** #LI-Remote

Diasorin is a global leader in diagnostic solutions, pushing the boundaries of science and technology to create cutting-edge tools that improve healthcare worldwide. With a legacy spanning over 50 years, we've earned our reputation for excellence by developing innovative diagnostic assays and instruments that are trusted by healthcare providers around the world. Our broad offering of diagnostic tests and Licensed Technology solutions, made available thanks to ongoing investments in research, positions us as the player with the widest range of specialty solutions in the sector and identifies us as the "Diagnostics Specialist." Why Join Diasorin? Impactful Work: When you join Diasorin, you become part of a team that's dedicated to improving lives. Your contributions will directly impact patient care, making a meaningful difference in the world. Global Reach & Innovation: Our work transcends borders. Joining Diasorin means collaborating with colleagues from all over the world, expanding your horizons, and contributing to global healthcare solutions at the forefront of the diagnostic industry. Diverse and Inclusive Culture: We believe in the strength of diversity, and our inclusive culture reflects this commitment. We value your unique perspective and offer a supportive, collaborative environment where everyone can thrive. Join Our Team: If you're passionate about innovation, diversity, and making a positive impact on healthcare, Diasorin is the place for you. We're looking for passionate and talented individuals who are ready to embrace new challenges and drive healthcare solutions forward. Are you ready to be part of a dynamic team that's shaping the future of diagnostics? Join Diasorin and become a catalyst for change in the world of healthcare. Apply today and be a part of our exciting journey toward a healthier, more connected world. Together, we can make an impact! Job Scope Responsible for evaluating applicable regulations and the Group standards, determining applicability to company operations. Implement procedures and policies that result in conformance with environmental, health and safety and dangerous goods regulations, and the protection of employees and the environment and the Group Standards. Assure health, safety and environmental concepts are considered into business, operations planning and decision-making processes. Support applicable regulations including ISO, Local, State, and/or Federal requirements. Job Responsibilities Evaluate the workplace, equipment and processes to ensure compliance with local, state and federal regulations and industry standards. Evaluate applicable environmental, safety, occupational health, disease control and dangerous goods transportation regulations to determine applicability to company Identify hazards and conditions that may result in personal injury or company loss, and develop methods and procedures to eliminate these hazards. Develop, implement and maintain EHS programs, procedures and policies to meet regulatory requirements/compliance and minimize loss. Maintain internal and regulatory reporting, including data collection and reporting including, but not limited to air, storm water, industrial discharge, and waste disposal. Serve as primary contact for all regulatory agencies, for inspections, permitting, and reporting. Conduct routine safety observations to ensure compliance with regulatory agencies, company environmental, health and safety policies, procedures and practices. Keep abreast of any safety, environmental or dangerous goods transportation regulations that impact the facility. Manage incident reporting, worker compensation, OSHA Occupational Illness and Injury, and CDC exposure reporting programs to minimize worker injury or disease and lower worker's compensation costs. Participate in the investigation of incidents, near misses and property damage incidents. Assist with incident investigations to identify root causes, make recommendations, and implement corrective/preventative actions. Ensure follow up is done to minimize future exposure and proper documents are maintained. Manage administrative functions to include submission of first report of injury, medical statements, and medical records to insurance carrier or administrator. Work with the insurance company, employee, and local health care providers to assure employee receives appropriate care and expedient return to work. Review research and develop manufacturing, and labeling (SDS, IFU) documents and processes to assure facility and corporate procedures and policies, and EHS regulatory requirements are met. Manage waste handling and disposal, including but not limited to hazardous waste and bio-waste, to assure proper collection, storage, transportation and final disposal of waste is in compliance with local, state and federal environmental regulations. Evaluate environmental regulations, determine applicability, and develop and implement procedures and policies to meet requirements. Evaluate waste and determine appropriate waste classification. As needed, manage analysis and method of disposal for waste to include transportation and final disposition. Manage emergency response programs to result in increased loss control in the event of an emergency. Monitor, update and improve emergency response procedures. Organize and execute emergency drills including, but not limited to medical, spill and fire. Participate in training processes that inform employees of EHS requirements and safety procedures and policies, and foster the improvement of safety understanding, lower exposure and incident rates. Manage development and delivery of safety training programs, including demonstrating the importance of conforming to EHS policies and procedures, and consequences of failing to comply. Assist in maintaining documentation of EHS training. Formally and informally encourage safe behaviors in others. Participate in formal and informal training required to increase skills to meet work expectations. Practice safe working techniques and re-enforce EHS policies and procedures. Practice leadership competencies that fosters open communication. Perform work in a safe manner consistent with health, safety and environmental policies and assume responsibility for personal safety and that of co-workers to result in a safe work environment for all employees and the protection of the environment and the community at large. Promote open channels of communication throughout the organization through continual thoughtful and open communications. Actively participate in team meetings and act as a resource to the group. Actively facilitate in sharing of information across , the organization in a way that results in good coordination of actions and decisions, and continuous improvement of results and performance. Promote through interactions an environment that supports trusting relationships and ethical leadership. Understand and utilize documentation protocols and accurately and legibly complete all documentation on time to result in a product/process history consistent with GMP and EHS requirements. Review, understand, and accurately complete in a timely fashion, documents such as procedures, forms, worksheets, and notebooks. Route, handle and/or store completed documentation appropriate for the work completed. Follow established compliance procedures designed to ensure that all regulatory requirements are met; activities may include audits, documentation, and the understanding of the requirements of agencies such as OSHA, EPA, DOT/IATA and FDA. Act as advisor to the Safety Committee, and assist in facilitating meetings or training of committee members. Perform assigned tasks in accordance with applicable Environmental Health and Safety (EHS) regulations and Company EHS policies. Perform other duties as assigned. Education and Experience Qualifications Bachelor's Degree Bachelor's in environmental, occupational health and safety or related science field such as biology, chemistry or engineering required 5+ Years related experience managing an EHS program in a manufacturing setting to include development and implementation of environmental health and occupational safety programs designed to meet and exceed applicable regulatory requirements required Good understanding of environmental, occupational health and safety, and dangerous goods regulations at local, state and federal levels (OSHA, EPA, DOT/IATA, CDC, GHS Ability to apply regulatory requirements and good practices within a manufacturing setting Proficient with MS Word, Excel and PPT. Familiarity with Google Suite Good written and verbal communication skills Ability to work with a diverse employee population and all organizational levels Strong analytical/problem solving skills, including the ability to sort out essential versus non-essential variable Ability to work independently with attention to detail Ability to manage projects with moderate supervision, including good planning, time management and organizational skills Able to read, analyze, and interpret general business periodicals, professional journals, technical procedures, and governmental regulations. Able to write reports, business correspondence, and procedure manuals. Able to effectively present information and respond to questions from various groups of managers, clients, customers, regulators, and the general public Able to work with mathematical concepts such as probability and statistical inference, and fundamentals of plane and solid geometry / trigonometry. Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations. Ability to collect and manipulate information enabling rapid analysis of trends and implications Able to define problems, collect data, establish facts, and draw valid conclusions. Able to interpret an extensive variety of technical instructions in mathematical, diagrammatic or written forms and deal with multiple abstract and / or concrete variables Flexible to change and open to constructive feedback Standard Physical Demands Is required to walk between buildings, will spend extended periods at computer keyboard inputting data and preparing reports, will stand for extended periods when performing safety inspections. - Constantly Standard Working Conditions Supervises and assists in the handling of chemical, radioactive and biological waste - Constantly Assists in the inspection and administration of the Select Agent Program for high consequence biological agents. - Constantly What we offer: Salary Range The hiring range for this position is $85,000 - $100,000 annually. The salary range for this role represents the numerous factors considered in the hiring decisions including, but not limited to, educations, skills, work experience, certifications, etc. Beyond base salary, Diasorin offers a competitive rewards package focused on your overall well-being. We are proud to offer a comprehensive plan of health benefits, retirement and financial wellbeing, time off programs, wellbeing support and perks. Benefits may vary by role, country, region, union status, and other employment status factors. You may also be eligible to participate in an annual incentive program. An incentive award, if any, depends on various factors, including, individual and organizational performance. Diasorin is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status, and will not be discriminated against on the basis of disability. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and Canada and to complete the required employment eligibility verification document form upon hire. Diasorin is committed to providing reasonable accommodations for qualified individuals with disabilities. If you are a US or Canada candidate and require assistance or accommodation during the application process, please contact the North America Talent Acquisition Team at ********************* or ************** to request an accommodation. The above job description is intended to describe the general content, identify the essential functions, and set forth the requirements for the performance of this job. It is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Diasorin reserves the right to modify or amend this job posting as needed to comply with local laws and regulations. Please note that offers of employment at Diasorin may be contingent upon successful completion of a pre-employment background check and drug screen, subject to applicable laws and regulations. This position is not eligible for partnership with a third-party search firm vendor without expressed, written consent from the Diasorin Human Resources Department.

Biotec Dental Laboratory is a leader in innovative dental solutions, committed to providing high-quality restorations and cutting-edge technology to dental professionals. We are seeking a Marketing Intern to support our growing marketing initiatives and gain valuable hands-on experience in a fast-paced, collaborative environment. What You'll Do: Tradeshow & Event Coordination: Assist in planning and executing industry conferences, learning events, and tradeshows. Social Media Management: Create engaging content to enhance brand awareness and audience engagement across LinkedIn, Instagram, and Facebook. Marketing & Fee Schedule Updates: Assist in updating fee schedules and marketing materials to ensure accuracy and consistency. Campaign Development: Collaborate with the team on promotional campaigns and outreach initiatives. Market Research: Conduct industry research and gather insights to support strategic marketing decisions. Why Join Us? Gain real-world marketing experience in a growing, innovative company. Work closely with experienced professionals in dental technology and marketing. Enhance your skills in event planning, social media management, and strategic marketing. Receive college credit for your internship experience. ?? Ready to launch your marketing career? Apply now and be part of a team that's shaping the future of dental technology!

Diasorin is a global leader in diagnostic solutions, pushing the boundaries of science and technology to create cutting-edge tools that improve healthcare worldwide. With a legacy spanning over 50 years, we've earned our reputation for excellence by developing innovative diagnostic assays and instruments that are trusted by healthcare providers around the world. Our broad offering of diagnostic tests and Licensed Technology solutions, made available thanks to ongoing investments in research, positions us as the player with the widest range of specialty solutions in the sector and identifies us as the "Diagnostics Specialist." Why Join Diasorin? Impactful Work: When you join Diasorin, you become part of a team that's dedicated to improving lives. Your contributions will directly impact patient care, making a meaningful difference in the world. Global Reach & Innovation: Our work transcends borders. Joining Diasorin means collaborating with colleagues from all over the world, expanding your horizons, and contributing to global healthcare solutions at the forefront of the diagnostic industry. Diverse and Inclusive Culture: We believe in the strength of diversity, and our inclusive culture reflects this commitment. We value your unique perspective and offer a supportive, collaborative environment where everyone can thrive. Join Our Team: If you're passionate about innovation, diversity, and making a positive impact on healthcare, Diasorin is the place for you. We're looking for passionate and talented individuals who are ready to embrace new challenges and drive healthcare solutions forward. Are you ready to be part of a dynamic team that's shaping the future of diagnostics? Join Diasorin and become a catalyst for change in the world of healthcare. Apply today and be a part of our exciting journey toward a healthier, more connected world. Together, we can make an impact! Job Scope The Account Executive is responsible for driving revenue growth, new account acquisition, and adoption of Diasorin's non-acute Point-of-Care (POC) portfolio across a defined territory. The role operates in a hybrid sales model, selling through distribution partners while directly engaging and influencing clinical end-users in physician office labs (POLs), urgent care, retail health, and pharmacy settings. This position requires strong diagnostic sales expertise, distributor-management capability, technical aptitude in molecular/rapid testing, and disciplined territory execution to support Diasorin's expansion in the non-acute POC market. ***Territory includes California-South (Los Angeles, San Diego, Orange County). Candidate must reside in Los Angeles or Orange County.*** Key Duties and Responsibilities Territory & Account Management • Execute a disciplined sales process including prospecting, pipeline development, account planning, and quarterly business reviews. • Drive adoption of Diasorin's non-acute POC portfolio through product demonstrations, workflow discussions, and value-based selling. • Achieve or exceed revenue targets, quota attainment, trial-to-conversion metrics, and territory growth objectives. • Manage large geographies effectively while prioritizing high-value opportunities. Distributor & Channel Partner Leadership • Build, coach, and support national and regional distributor partners (e.g., McKesson, Cardinal, Medline, Henry Schein). • Conduct joint sales calls, ride-alongs, distributor training, and business reviews to accelerate pull-through. • Support distributor pipeline development, opportunity qualification, and territory execution. • Monitor distributor KPIs and collaborate to address performance gaps or conflicts. Customer Engagement & Clinical Insight • Engage confidently with Lab Directors, Medical Directors, nursing leadership, office managers, and clinical teams. • Deliver customer training, workflow optimization discussions, in-services, and onboarding support. • Translate technical assay benefits into clinical outcomes, operational efficiency, and financial ROI. • Maintain understanding of clinical workflows, CLIA-waived environments, and relevant quality metrics. Technical & Molecular Aptitude • Communicate molecular diagnostics concepts including assay performance, sensitivity/specificity, workflow advantages, and instrument differentiation. • Support new product launches, promotional initiatives, and regional marketing activities. Operational Excellence • Maintain accurate CRM data, forecasting, pipeline quality, activity reporting, and expense compliance. • Track KPIs including sales calls, demos, distributor activations, trials, conversions, and revenue per account. • Participate in trade shows, regional events, distributor meetings, and team trainings as needed. Education, Experience and Qualifications • Bachelor's degree required; scientific or business-related field preferred. • 3-7+ years of field sales experience in clinical diagnostics, point-of-care testing, molecular diagnostics, medical devices, or lab equipment. • Proven success selling through distribution partners in non-acute settings (POLs, urgent care, outpatient clinics, PCP offices, retail health, pharmacy-based care). • Demonstrated ability to meet or exceed quota in a technical, consultative sales environment. • Familiarity with molecular testing platforms (PCR/NAAT) or related rapid/respiratory diagnostic modalities. • Strong communication and presentation skills with clinical and administrative decision makers. • Ability to simplify complex scientific concepts for clinical audiences. • Strong organization, accountability, and territory management capability. • Valid Drives License is required Preferred Qualifications • Experience launching new diagnostic or molecular platforms in competitive markets. • Knowledge of CPT coding, reimbursement dynamics, CLIA regulations, and workflow optimization. • Existing relationships with key distributor representatives in the region. • Experience managing multi-state territories. What We Offer The hiring range for this position is $110,321 - $149,258 annually and incentive compensation eligible. The salary range for this role represents the numerous factors considered in the hiring decisions including, but not limited to, educations, skills, work experience, certifications, etc. Beyond base salary, Diasorin offers a competitive rewards package focused on your overall well-being. We are proud to offer a comprehensive plan of health benefits, retirement and financial wellbeing, time off programs, wellbeing support and perks. Benefits may vary by role, country, region, union status, and other employment status factors. You may also be eligible to participate in an annual incentive program. An incentive award, if any, depends on various factors, including, individual and organizational performance. Diasorin is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status, and will not be discriminated against on the basis of disability. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and Canada and to complete the required employment eligibility verification document form upon hire. Diasorin is committed to providing reasonable accommodations for qualified individuals with disabilities. If you are a US or Canada candidate and require assistance or accommodation during the application process, please contact the North America Talent Acquisition Team at ********************* or ************** to request an accommodation. The above job description is intended to describe the general content, identify the essential functions, and set forth the requirements for the performance of this job. It is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Diasorin reserves the right to modify or amend this job posting as needed to comply with local laws and regulations. Please note that offers of employment at Diasorin may be contingent upon successful completion of a pre-employment background check and drug screen, subject to applicable laws and regulations. This position is not eligible for partnership with a third-party search firm vendor without expressed, written consent from the Diasorin Human Resources Department.

Diasorin is a global leader in diagnostic solutions, pushing the boundaries of science and technology to create cutting-edge tools that improve healthcare worldwide. With a legacy spanning over 50 years, we've earned our reputation for excellence by developing innovative diagnostic assays and instruments that are trusted by healthcare providers around the world. Our broad offering of diagnostic tests and Licensed Technology solutions, made available thanks to ongoing investments in research, positions us as the player with the widest range of specialty solutions in the sector and identifies us as the "Diagnostics Specialist." Why Join Diasorin? Impactful Work: When you join Diasorin, you become part of a team that's dedicated to improving lives. Your contributions will directly impact patient care, making a meaningful difference in the world. Global Reach & Innovation: Our work transcends borders. Joining Diasorin means collaborating with colleagues from all over the world, expanding your horizons, and contributing to global healthcare solutions at the forefront of the diagnostic industry. Diverse and Inclusive Culture: We believe in the strength of diversity, and our inclusive culture reflects this commitment. We value your unique perspective and offer a supportive, collaborative environment where everyone can thrive. Join Our Team: If you're passionate about innovation, diversity, and making a positive impact on healthcare, Diasorin is the place for you. We're looking for passionate and talented individuals who are ready to embrace new challenges and drive healthcare solutions forward. Are you ready to be part of a dynamic team that's shaping the future of diagnostics? Join Diasorin and become a catalyst for change in the world of healthcare. Apply today and be a part of our exciting journey toward a healthier, more connected world. Together, we can make an impact! Job Scope The Supplier Quality Manager is responsible for developing and managing the supplier quality program within an in vitro diagnostics (IVD) manufacturing environment. This role ensures that suppliers of raw materials, components, and services meet applicable regulatory requirements (FDA 21 CFR Part 820, ISO 13485, IVDR) and company quality standards. The Supplier Quality Manager partners with Procurement, Manufacturing, R&D, and Regulatory Affairs to drive supplier qualification, audits, continuous improvement, and compliance. Duties and Responsibilities Develop, implement, and maintain the supplier quality management program. Manage and conduct supplier audits in accordance with FDA, ISO 13485, MDSAP, and IVDR requirements. Qualify and approve new suppliers, materials, and services for use in IVD manufacturing. Manage supplier corrective actions (SCARs) and ensure timely resolution of quality issues. Assign and Manae Supplier Quality Scorecard assessments Collaborate with Procurement and R&D during supplier selection and qualification. Review and approve supplier change notifications. Monitor supplier performance metrics and drive continuous improvement initiatives. Ensure supplier compliance with product, regulatory, and contractual requirements. Act as SME during regulatory inspections for supplier management topics. Manages Regular Supplier Review Board Meetings (global) Lead risk assessments for suppliers and support overall supply chain risk management. Other duties as assigned Knowledge, Experience and Qualifications Bachelor's degree in Engineering, Life Sciences, or related field required. Master's degree preferred. 7+ years of experience in Quality Assurance within IVD or medical device manufacturing. 3+ years of experience in supplier quality management or related role. Proven experience leading audits (internal and external). Experience with FDA 21 CFR 820, ISO 13485, IVDR, and ISO 14971 risk management. Training, Skills and Certifications • Strong knowledge of supplier quality principles, auditing, and risk management. • Thorough knowledge of FDA regulations and cGMP guidelines. ISO 13485, IVDR. • Excellent problem-solving and root cause analysis skills. • Highly organized with proven time-management skills • Strong communication and negotiation skills with suppliers and internal teams. • Proficiency with electronic Quality Management Systems (eQMS). • ASQ certifications (CQA, CQE, or equivalent) preferred. The hiring range for this position is $120,000-$140,000 annual base salary. The salary range for this role represents the numerous factors considered in the hiring decisions including, but not limited to, educations, skills, work experience, certifications, etc. Beyond base salary, Diasorin offers a competitive rewards package focused on your overall well-being. We are proud to offer a comprehensive plan of health benefits, retirement and financial wellbeing, time off programs, wellbeing support and perks. Benefits may vary by role, country, region, union status, and other employment status factors. You may also be eligible to participate in an annual incentive program. An incentive award, if any, depends on various factors, including, individual and organizational performance. Travel Requirements 25% Travel may be required 5% International travel may be required Diasorin is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status, and will not be discriminated against on the basis of disability. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and Canada and to complete the required employment eligibility verification document form upon hire. Diasorin is committed to providing reasonable accommodations for qualified individuals with disabilities. If you are a US or Canada candidate and require assistance or accommodation during the application process, please contact the North America Talent Acquisition Team at ********************* or ************** to request an accommodation. The above job description is intended to describe the general content, identify the essential functions, and set forth the requirements for the performance of this job. It is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Diasorin reserves the right to modify or amend this job posting as needed to comply with local laws and regulations. Please note that offers of employment at Diasorin may be contingent upon successful completion of a pre-employment background check and drug screen, subject to applicable laws and regulations. This position is not eligible for partnership with a third-party search firm vendor without expressed, written consent from the Diasorin Human Resources Department.

Diasorin is a global leader in diagnostic solutions, pushing the boundaries of science and technology to create cutting-edge tools that improve healthcare worldwide. With a legacy spanning over 50 years, we've earned our reputation for excellence by developing innovative diagnostic assays and instruments that are trusted by healthcare providers around the world. Our broad offering of diagnostic tests and Licensed Technology solutions, made available thanks to ongoing investments in research, positions us as the player with the widest range of specialty solutions in the sector and identifies us as the "Diagnostics Specialist." Why Join Diasorin? Impactful Work: When you join Diasorin, you become part of a team that's dedicated to improving lives. Your contributions will directly impact patient care, making a meaningful difference in the world. Global Reach & Innovation: Our work transcends borders. Joining Diasorin means collaborating with colleagues from all over the world, expanding your horizons, and contributing to global healthcare solutions at the forefront of the diagnostic industry. Diverse and Inclusive Culture: We believe in the strength of diversity, and our inclusive culture reflects this commitment. We value your unique perspective and offer a supportive, collaborative environment where everyone can thrive. Join Our Team: If you're passionate about innovation, diversity, and making a positive impact on healthcare, Diasorin is the place for you. We're looking for passionate and talented individuals who are ready to embrace new challenges and drive healthcare solutions forward. Are you ready to be part of a dynamic team that's shaping the future of diagnostics? Join Diasorin and become a catalyst for change in the world of healthcare. Apply today and be a part of our exciting journey toward a healthier, more connected world. Together, we can make an impact! Job Scope Conduct and manage Calibration and Preventative Maintenance for equipment assets to ensure on-time completion. Prepare for and assist in audit activities. Generate trends, Non-conformances, temporary changes and change plans. Set goals and align metrics to business strategies. Key Duties and Responsibilities Oversee, perform, and document calibration and preventative maintenance procedures needed to result in equipment that is in good working condition, in accordance with corporate policies and in compliance with standards. Maintain asset management system to ensure updated and current tracking of equipment assets. Provide input into the development of preventative maintenance and calibration requirements for new and existing equipment assets. Schedule vendors to conduct repairs, perform preventative maintenance and calibrations on equipment. Coordinate contracts for equipment preventative maintenance, calibration and repair to assure contract agreements and work quality standards are met. Generate trending of on-time and past-due preventative maintenance and calibrations. Communicate and report quality performance data. Provide input into preventative action plans in setting goals and alignment metrics to business strategies. Maintain physical equipment asset files. Ensure all equipment is entered into the asset management system in a timely manner and that the calibration/preventative maintenance schedules are effective when equipment is activated. Control, storage and preservation of in-house calibration standards so that the accuracy and fitness for use are maintained. Ensure calibration procedures and forms are current and up-to-date, revising when necessary. Prepare for and assist in both external and internal audit activities. Assist with ongoing continual improvement projects. Comply with CFR 820.21 and ISO 13485 requirements for calibration. Updates procedures as necessary to ensure compliance with the most recent standard. Generate NCRs, temporary change notices and change plans as necessary. Procuring supplies and services, when needed. Other special projects and duties at the discretion of the manager Education, Experience, and Qualifications Bachelor's degree in related industry is preferred. 2-5+ years of experience within a Quality Assurance/Engineering or Metrology Organization is preferred. Knowledge of: Modern office practices and procedures Personal computer hardware and equipment MS Word and Excel; knowledge of Google Suite Strong knowledge of quality management systems, specifically a major preference. Ability to: Work and communicate effectively with a wide range of co-workers in a cooperative manner. Plan and manage time well. Maintain a high level of initiative, effort and commitment. Work with minimal supervision. Demonstrate responsible behavior and attention to detail. Align behavior with the needs, priorities and goals of the organization. What we offer Receive a competitive salary $23.00 - $26.00 per hour and benefits package as you grow your career at DiaSorin. Join our team and discover how your work can impact the lives of people all over the world. Diasorin is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status, and will not be discriminated against on the basis of disability. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and Canada and to complete the required employment eligibility verification document form upon hire. Diasorin is committed to providing reasonable accommodations for qualified individuals with disabilities. If you are a US or Canada candidate and require assistance or accommodation during the application process, please contact the North America Talent Acquisition Team at ********************* or ************** to request an accommodation. The above job description is intended to describe the general content, identify the essential functions, and set forth the requirements for the performance of this job. It is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Diasorin reserves the right to modify or amend this job posting as needed to comply with local laws and regulations. Please note that offers of employment at Diasorin may be contingent upon successful completion of a pre-employment background check and drug screen, subject to applicable laws and regulations. This position is not eligible for partnership with a third-party search firm vendor without expressed, written consent from the Diasorin Human Resources Department.

Diasorin is a global leader in diagnostic solutions, pushing the boundaries of science and technology to create cutting-edge tools that improve healthcare worldwide. With a legacy spanning over 50 years, we've earned our reputation for excellence by developing innovative diagnostic assays and instruments that are trusted by healthcare providers around the world. Our broad offering of diagnostic tests and Licensed Technology solutions, made available thanks to ongoing investments in research, positions us as the player with the widest range of specialty solutions in the sector and identifies us as the "Diagnostics Specialist." Why Join Diasorin? Impactful Work: When you join Diasorin, you become part of a team that's dedicated to improving lives. Your contributions will directly impact patient care, making a meaningful difference in the world. Global Reach & Innovation: Our work transcends borders. Joining Diasorin means collaborating with colleagues from all over the world, expanding your horizons, and contributing to global healthcare solutions at the forefront of the diagnostic industry. Diverse and Inclusive Culture: We believe in the strength of diversity, and our inclusive culture reflects this commitment. We value your unique perspective and offer a supportive, collaborative environment where everyone can thrive. Join Our Team: If you're passionate about innovation, diversity, and making a positive impact on healthcare, Diasorin is the place for you. We're looking for passionate and talented individuals who are ready to embrace new challenges and drive healthcare solutions forward. Are you ready to be part of a dynamic team that's shaping the future of diagnostics? Join Diasorin and become a catalyst for change in the world of healthcare. Apply today and be a part of our exciting journey toward a healthier, more connected world. Together, we can make an impact! SUMMARY Responsible for evaluating and optimizing manufacturing, QC, R&D and CAPA processes to improve product consistency and to increase productivity. Responsible for reviewing, performing, and documenting validations for new and existing products. Supports all applicable regulations including but not limited to FDA, ISO, IVDD, and IVDR requirements. ESSENTIAL DUTIES & RESPONSIBILITIES · Review of design, manufacturing, purchasing, and test documentation to ensure quality requirements are fulfilled. · Review specifications, operation instructions, sheets, process procedures, test procedures, inspection and test analysis. · Provide leadership in and employ advanced quality planning techniques (FMEA, Capability Studies, Measuring and Test Equipment Studies, Product Validation and Reliability Test) · Assist in determining process/equipment capabilities. · Assist in the development process flow diagrams and perform gap analyses on current controls versus required controls. · Investigate the root cause of external and internal non-conforming products. · Assist in corrective and preventive actions and verifications of effectiveness such as actions for customer complaints, internal audits, and internal and external suppliers non-conformance. · Perform assessments for process-related risks. · Assist in the development of inspection procedures and justified sample plans. · Gather, analyze, and report data reflecting status of product and process and provide recommendation to improve. · Support new product development and growth. Represent quality on new product development teams with guidance from more senior quality engineers or management. · Participate in improvement and lean projects. · Performs internal audits · Responsible for performing assigned tasks in accordance with the company's quality policies and procedures per the applicable quality management system regulations as defined in the Quality Manual. · Responsible for performing assigned tasks in accordance with applicable Environmental Health and Safety (EHS) regulations and Company EHS policies. Violations of EHS regulations or policies will be handled in accordance with the established Company disciplinary process. · Perform other duties as assigned Diasorin is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status, and will not be discriminated against on the basis of disability. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and Canada and to complete the required employment eligibility verification document form upon hire. Diasorin is committed to providing reasonable accommodations for qualified individuals with disabilities. If you are a US or Canada candidate and require assistance or accommodation during the application process, please contact the North America Talent Acquisition Team at ********************* or ************** to request an accommodation. The above job description is intended to describe the general content, identify the essential functions, and set forth the requirements for the performance of this job. It is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Diasorin reserves the right to modify or amend this job posting as needed to comply with local laws and regulations. Please note that offers of employment at Diasorin may be contingent upon successful completion of a pre-employment background check and drug screen, subject to applicable laws and regulations. This position is not eligible for partnership with a third-party search firm vendor without expressed, written consent from the Diasorin Human Resources Department.

NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976. We are shaping the industry. NAMSA has been a key contributor to the development of the test methods that govern our industry. We have become the industry's premier provider. We provide support for clients during every step of the product development lifecycle and beyond. Come and work for an organization with the: Vision to inspire innovative MedTech solutions that advance global healthcare, improve patient lives and accelerate Client success and the Mission to deliver best-in-class global MedTech development solutions through our people, expertise and technology by adhering to our core Values: Act with integrity in everything we do. Provide best-in-class customer experiences. Develop superior talent and deliver expertise. Respond with agility and provide timely results. Embrace collaboration, diverse perspectives and ideas. Job Description: • May perform various testing independently in accordance with SOPs and utilizing applicable work instructions, standards or guidelines. • Performs routine calculations and may participate in analyzing and interpreting results. • Maintain all test equipment and supplies for various testing • Clean glassware and prepare reagents for use in laboratory testing. • Perform routine disposal of laboratory waste including disposal of test articles. • Assist with making solutions and preparing reagents. • Assist in the preparation of items for testing. • Monitor raw materials and final finished media for conformance with applicable material specifications and SOPs. • May be responsible for extractions, which may include: test article and control preparation, animal holding and preparation and solution preparation. • May be responsible for chain of custody, delivery of samples, filing and sample distribution/shipping. • Accurately collect and record raw data in logbooks and on worksheets. • Maintain clean workspace, testing supplies, and equipment • May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms as applicable and in accordance with criteria outlined in Standard Operating Procedures. • May be required to operate specified laboratory equipment as applicable. • Maintains an efficient workflow process relative to sample prioritization. • Other duties as assigned. Qualifications & Technical Competencies: Principal Duties and Responsibilities Schedules and oversees daily operations of assigned laboratory area. Monitors work, coordinates resources, and communicates with other functional areas within NAMSA to address client expectations. May perform various testing independently in accordance with SOPs and utilizing applicable work instructions, standards or guidelines. Performs routine calculations and may participate in analyzing and interpreting results. Maintains all test equipment and supplies for various testing and may assist with procurement of test equipment. Clean glassware and prepare reagents for use in laboratory testing. Perform routine disposal of laboratory waste including disposal of test articles. Assist with making solutions and preparing reagents. Assist in the preparation of items for testing. May have direct client contact as needed. Monitors raw materials and final finished media for conformance with applicable material specifications and SOPs and resolve issues and non-conformances. May be responsible for extractions, test article and control preparation, animal holding and preparation and solution preparation. May be responsible for chain of custody, delivery of samples, filing and sample distribution/shipping. Accurately collect and record raw data in logbooks and on worksheets. Maintain clean workspace, testing supplies, and equipment May be responsible for checking laboratory equipment, being on-call and respond to continuous monitoring alarms in accordance with criteria outlined in Standard Operating Procedures. May be required to operate autoclave, depyrogenation oven or other specified laboratory equipment as applicable. Other duties as assigned. Qualifications and Skills High School diploma or equivalent required and at least 4 years of experience, or Bachelor degree and 1 year of experience. Sound judgment with effective decision making skills and the ability to solve problems or escalate as needed Technical Competencies Awareness of applicable guidelines and regulations including, but not limited to USP, ISO, CTFA, FSA. Knowledge of metric system, NAMSA GLP and/or GMP testing, scientific applications, experimental design, and data evaluation. Ability to work in GLP/GMP environment. **Pay range- $24.00- $28.00/hr** Working Conditions The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Requires maintaining physical condition necessary for walking, standing, or sitting for prolonged periods of time. Extensive use of computer keyboard; operate computer equipment. Working Conditions: • The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. • Requires maintaining physical condition necessary for walking, standing, or sitting for prolonged periods of time. • Extensive use of computer keyboard; operate computer equipment. Pay Range Minimum: $17.79 Pay Range Target: $28.00 Pay Frequency: Hourly Please Note: Individual base pay depends on various factors, in addition to primary work location, such as complexity and responsibility of role, job duties/requirements, and relevant experience and skills. NAMSA is an equal employment opportunity company. NAMSA participates in pre-employment background and drug screen processes aligned to local, state and federal laws. Fair Chance Employment Statement: At NAMSA, we are committed to providing equal employment opportunities to all qualified applicants, including those with arrest or conviction records. In accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act, we will consider qualified applicants with a criminal history. Please note that NAMSA conducts a review of criminal history after the interview process and offer acceptance. This review is conducted to ensure that there is no direct, adverse, or negative relationship between the criminal history and the material job duties of the specific position. The following is a list of material job duties for this position: • May operate equipment • Records data timely and accurately • May analyze and interpret data • Conducts studies on medical devices that have an impact on human life A criminal history that directly impacts the ability to perform these duties may result in the withdrawal of a conditional offer of employment. We believe in fair chance hiring and are committed to evaluating each applicant on a case-by-case basis.

BioTec Dental Laboratory is seeking a knowledgeable and solutions-driven IT Administrator to oversee and maintain the company's technical infrastructure. This role is responsible for managing hardware, software, networks, security systems, and day-to-day technical support across the laboratory. The ideal candidate is detail-oriented, proactive, and experienced in supporting a fast-paced, high-precision environment where system uptime and data accuracy are essential. Key Responsibilities Systems & Network Administration Maintain, configure, and troubleshoot all computer systems, servers, LAN/WAN networks, printers, scanners, and specialized dental lab equipment. Manage user accounts, permissions, and access within various systems and applications. Monitor network performance and ensure reliability, security, and minimal downtime. Software & Application Support Install, update, and support dental lab software platforms (e.g., CAD/CAM systems, 3D printing interfaces, case management systems). Ensure integrations between lab software and client systems operate smoothly. Provide technical support and training to staff on hardware and software use. Cybersecurity & Data Protection Implement and maintain cybersecurity policies, firewall settings, antivirus software, and data encryption. Conduct routine backups and ensure proper storage, recovery, and protection of sensitive patient and client information. Monitor systems for security breaches, vulnerabilities, and unauthorized access. Equipment Management Maintain inventory of all IT assets and ensure timely upgrades or replacements. Coordinate repairs or vendor support for specialized dental equipment and technology. Support the setup and maintenance of 3D printers, milling machines, scanners, and related systems. IT Support & Troubleshooting Serve as the primary point of contact for all technical issues, providing timely resolution. Document processes, updates, troubleshooting steps, and system changes. Train new hires on equipment, systems access, and IT protocols.

Join Our BioTec Dental Laboratory Team! Are you ready to be part of a cutting-edge dental laboratory in the heart of innovation? BioTec Dental Laboratory, located in beautiful Irvine, CA, is seeking passionate individuals to join our dynamic team! Why BioTec? ?? Innovative Practices: At BioTec, we pride ourselves on staying ahead of the curve with state-of-the-art technologies and revolutionary techniques in dental manufacturing. Be part of a team that's setting new standards in the industry! ?? Commitment to Excellence: We are dedicated to providing the best products to our customers. Join us in our mission to enhance smiles and improve lives through precision and quality craftsmanship. ?? Employee-Centric Culture: We believe that taking care of our employees translates into exceptional care for our customers. Enjoy competitive pay, comprehensive medical benefits, paid holidays, and a simple IRA with matching to support your financial wellness. ?? Perks and More: Employee lunches to fuel your day Ongoing training and development opportunities Collaborative and vibrant work environment Opportunities for career advancement Recognition programs to celebrate your achievements What We're Looking For: CAD/CAM Technician Essential Functions: Read prescriptions and specifications received from dentist. Knowledge and comfortability with computers. Operate the computer-aided design & computer-aided manufacturing steps for the designing process, including scanning, loading and creating files. Operate software for nesting designs to be processed throughout the milling / printing process. Load information into the computer, such as patient name, pan number, type of crown, shade. Follow all required steps, to insure consistent, accurate results. Review final work to confirm that quality standards have been met. Clean work area daily. All other duties as assigned.

The Logistics Associate is responsible for ensuring efficient and accurate coordination of cases and materials within the laboratory, supporting production and customer service needs. This position involves data entry, digital communication, troubleshooting, and updating critical logistics information to meet production and delivery demands. The ideal candidate thrives in a fast-paced environment, is highly detail-oriented, and can navigate complex systems while maintaining excellent communication across multiple teams. Essential Functions Data Entry and Documentation: Process work orders, update production spreadsheets, and maintain accurate records in relevant systems. Reference fee schedules for invoicing and update shipment and delivery information as required. Digital Communication: Engage with various digital platforms, including customer portals, Slack, and CRM systems, to ensure seamless communication between teams and with customers. Extract, manage, and share digital files as necessary. Case Coordination and Troubleshooting: Update shipping dates based on production demands and ensure on-time delivery. Locate cases on the production floor and troubleshoot issues in coordination with customer service, scheduling, and production management teams. Product and Process Knowledge: Maintain familiarity with product codes for all product lines and reference this information to support logistics and production processes. Stay up-to-date with laboratory workflows and production schedules to align logistics activities with operational goals. Physical and Operational Requirements: Stand on feet for long periods while navigating between multiple floors via stairs to support case tracking and logistics activities. Operate effectively in a fast-paced, dynamic environment with shifting priorities.