Quality assurance technician jobs in Carlsbad, CA - 830 jobs

This is an exciting opportunity to join a growing company that focuses on precise, early detection of emerging diseases. The Quality Assurance Specialist ensures products, processes, and documentation meet established quality standards and comply with applicable regulatory requirements. This role blends regulatory submissions and strategy with quality system implementation, auditing, and continuous improvement to support product approvals, market access, and patient safety. Responsibilities Develop, implement, and maintain the Quality Management System (QMS). Plan, conduct, and coordinate internal and supplier audits to ensure compliance with regulatory and accreditation standards (e.g., CLIA, CAP). Manage document control, change control, CAPA, nonconformance management, complaint handling, and MDR/Vigilance activities. Coordinate proficiency testing programs and analyze results to identify trends and improvement opportunities. Ensure all required regulatory licenses and accreditations remain current. Maintain quality documentation, SOPs, and laboratory testing procedures. Prepare, analyze, and present quality metrics and reports for management review. Train and onboard new personnel; review training documentation and monitor ongoing competency of testing staff. Maintain working knowledge of laboratory protocols, specimen processing, equipment operation and maintenance, and data analysis. Review and approve product labeling, packaging, promotional materials, and technical documentation for regulatory compliance. Monitor changes in global regulations, standards, and guidance; assess impact and recommend updates to internal processes. Partner with cross-functional teams (R&D, manufacturing, engineering, clinical, marketing) to embed quality and regulatory requirements early in product development. Lead or support management reviews, regulatory and quality training programs, and continuous improvement initiatives. Prepare, submit, and maintain regulatory filings, documentation, and reports. Coordinate with regulatory and accreditation bodies to support product approvals, certifications, and inspections. Ensure compliance with internal health and safety policies; report and address violations as required. Participate as an external auditor on College of American Pathologists (CAP) inspection teams, as required by the CAP accreditation program. Requirements And Desired Experience Bachelor's degree (required) in life sciences, biology, chemistry, engineering, pharmacy, or related field; Master's a plus 3+ years of laboratory experience, including experience with audits, compliance systems, and regulatory submissions. Strong knowledge of key regulations and standards: FDA QSR (21 CFR Part 820/211), ISO 13485/9001, EU MDR/IVDR, GMP, ICH guidelines, etc. Working knowledge of relevant regulatory frameworks Professional certification is a plus (i.e, Regulatory Affairs Certification - RAC, ASQ Certified Quality Auditor - CQA). CLS Generalist or CGMBS license preferred Proven knowledge of quality assurance terminology, software, methods, and tools. Previous experience with Laboratory Information Management Systems is preferred. Proficient in QMS software (i.e. MediaLab, TrackWise, MasterControl or similar) Strong analytical, problem-solving, and decision-making skills. Experience in compliance and/or regulatory and knowledge of laboratory standards and regulations Experience with Microsoft Office Suite; Word, Outlook, Excel Excellent written and verbal communication skills for agency interactions, technical writing, and cross-functional collaboration. Able to effectively present information and respond to questions from various stakeholders Compensation (DOE): $80,000 - $95,000 annual salary

Wildcat Discovery Technologies is dedicated to becoming the leader in battery material development, integration, and supply. By blending the production of high-performance, U.S.-made cathode active materials with advanced battery services, Wildcat creates comprehensive solutions for customers across industries. Based on 15 years of expertise, Wildcat produces innovative materials like LFP, LMFP, and DRX at its U.S. facility, optimizing battery cell performance in hundreds of successful projects. Recognized for its innovations, Wildcat was named one of the "50 Most Innovative Companies" by Technology Review magazine. The company collaborates with global leaders in the battery supply chain, spanning automotive, electronics, medical, and military applications. Role Description Wildcat Discoveries is looking for a highly motivated Engineering Technician to join our pouch cell team! Within this role, you will operate automated lithium-ion battery cell production equipment to support evaluation of novel cell designs and chemistries. This role will directly support the development of processes and fabrication of lithium-ion battery pouch cells. The work environment is demanding, fast-paced, and incredibly exciting. The ideal candidate should be ready to push their limits, as they join a world-class scientific team dedicated to developing and discovering advanced materials for lithium-ion batteries. At Wildcat, the sky's the limit - with the right attitude, work ethic, and quality of work you can blaze your own trail. Essential Functions Operate industrial mixers, aliquot raw materials, work in a fume hood and glove box. Work with flammable, moisture sensitive chemicals, in addition to working with automated process equipment that operate at a high speed, high temperature, high pressure, and vacuum. Utilize analytical equipment to ensure quality control. Operate coating and roll-to-roll process equipment for coating battery electrodes. Monitor and troubleshoot existing equipment and processes to make a product according to product specifications. Follow standard operating procedures (SOP's) and other written procedures, and maintaining accurate records of work performed. Report problems, issues and unexpected observations in a timely manner. Meet timelines and deadlines consistently. Complete production documentation, and support transfer of materials to next stage of processing. Respect others in the workplace with a professional attitude; be considerate of others with housekeeping, shared equipment; provide a safe working environment for others. Calibrate, clean, and maintain equipment in good working condition. Knowledge, Skills & Abilities Required Basic knowledge of scientific laboratory procedures, techniques, equipment and apparatus used in a chemistry laboratory. Basic knowledge of health and safety practices and precautions applicable to a chemistry laboratory. Maintain a commitment to safety, quality, and continuous improvement Ability to effectively and safely operate, adapt and maintain laboratory and manufacturing equipment. Ability to utilize computer hardware and software. Ability to keep detailed and precise records. Ability to thrive in a multi-tasking, fast paced environment Ability to communicate and work effectively and cooperatively with lab technicians, engineers, research associates and scientists. Education & Experience Bachelor's level degree or higher in a scientific or engineering field such as mechanical engineering, industrial engineering, electrical engineering, chemistry, chemical engineering Experience in semiconductor, medical devices, metallurgy, plastics, and/or lithium ion battery manufacturing is preferred Generally some exposure to working in a laboratory environment or a manufacturing environment, and working with chemicals. Familiarity with Roll-2-Roll manufacturing a plus Experience with clean rooms and/or dry rooms a plus Pilot line manufacturing experience a plus Wildcat Discovery Technologies is an equal opportunity employer. We are committed to creating an inclusive environment for all employees, free from discrimination based on race, gender, religion, disability, and other protected characteristics under FEHA. Pay range is expected to be from $26 to $33 per hour.

RELOCATION ASSISTANCE: No relocation assistance available CLEARANCE TYPE: SecretTRAVEL: Yes, 10% of the TimeDescriptionAt Northrop Grumman, our employees have incredible opportunities to work on revolutionary systems that impact people's lives around the world today, and for generations to come. Our pioneering and inventive spirit has enabled us to be at the forefront of many technological advancements in our nation's history - from the first flight across the Atlantic Ocean, to stealth bombers, to landing on the moon. We look for people who have bold new ideas, courage and a pioneering spirit to join forces to invent the future, and have fun along the way. Our culture thrives on intellectual curiosity, cognitive diversity and bringing your whole self to work - and we have an insatiable drive to do what others think is impossible. Our employees are not only part of history, they're making history. Northrop Grumman Aerospace Systems (NGAS), Autonomous Intelligence, Surveillance, Reconnaissance & Targeting Business Unit seeks a Quality Control Technician (Inspector) 2 OR Quality Control Technician (Inspector) 3 to join our team located in San Diego, California at the Rancho Bernardo site report to the Mission Assurance organization. The selected individual will support multiple programs across the Autonomous Intelligence, Surveillance, Reconnaissance, & Targeting Business Unit. Performs analyses and tests of raw materials, packaging materials, and/or finished products from manufacturing, to ensure quality standards and compliance to customer and regulatory requirements, and tolerance specifications for the chemical or physical property. Performs a variety of qualitative tests or qualitative assays on samples, and to aid in maintenance and certification of test instruments and apparatuses to ensure compliance. Prepares and monitors quality statistics and reports. Reviews production records for conformance to procedures. Conducts non-conformance tests of manufactured, packaged or tested product. Roles and Responsibilities: Provides inspection support for production and developmental builds utilizing various inspection methods to determine acceptance of product. Types of products inspected may include piece parts, cables and harnesses, electronic units and subsystems, precision electromechanical assemblies and Ground equipment Reviews production records for conformance against engineering. Provides inspection support to Environmental test and System Integration labs Supports various types of testing (Acceptance, Electrical, Environmental, Functional and Software). Verifies test results against engineering specifications for acceptance Facilitates non-conforming process; initiates discrepancy tags against non-conforming product, collaborates with Engineering for path forward Performs assigned audits (FOE/FOD, Production Process related) Education Requirement Quality Control Technician (Inspector) 2: High School Diploma with 2 years of related experience Education Requirement Quality Control Technician (Inspector) 3: High School Diploma with 4 years of related experience Basic Qualifications Ability to obtain and maintain a DOD Secret within a reasonable period of time, as determined by the company to meet its business needs. US citizen required for clearance Must be willing to work any shift, overtime or non-standard work schedule Must be able to work around composites, epoxies, and sealants for long periods of time. Must be technically proficient in Microsoft Office Suite to include but not limited to Word, Excel, Power Point and Outlook. Must be able to perform moderately strenuous physical and repetitious work to include climbing, bending, crawling, stooping, and kneeling, lifting, working with arms overhead, leaning and laying. Must be able to lift, grip, push, pull and hold 25+ pounds. Working experience with non-conforming process Working experience interpreting drawings/specifications Working experience of using hand inspection tools Must have an active secret clearance to start Preferred Qualifications: Experience working with Avionics, Cables, and Harnesses Experience with Manufacturing Execution System (MES) including NC module Experience with TeamCenter Experience with SAP Experience with performing audits Experience working in a test environment Flexibility to support occasional short-term travel Primary Level Salary Range: $51,400.00 - $85,600.00Secondary Level Salary Range: $61,100.00 - $101,800.00The above salary range represents a general guideline; however, Northrop Grumman considers a number of factors when determining base salary offers such as the scope and responsibilities of the position and the candidate's experience, education, skills and current market conditions.Depending on the position, employees may be eligible for overtime, shift differential, and a discretionary bonus in addition to base pay. Annual bonuses are designed to reward individual contributions as well as allow employees to share in company results. Employees in Vice President or Director positions may be eligible for Long Term Incentives. In addition, Northrop Grumman provides a variety of benefits including health insurance coverage, life and disability insurance, savings plan, Company paid holidays and paid time off (PTO) for vacation and/or personal business.The application period for the job is estimated to be 20 days from the job posting date. However, this timeline may be shortened or extended depending on business needs and the availability of qualified candidates.Northrop Grumman is an Equal Opportunity Employer, making decisions without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability, or any other protected class. For our complete EEO and pay transparency statement, please visit *********************************** U.S. Citizenship is required for all positions with a government clearance and certain other restricted positions.

About Artiva: Artiva is clinical-stage, publicly-traded biotechnology company focused on developing natural killer (NK) cell-based therapies for patients suffering from devastating autoimmune diseases and cancers. Artiva's lead program, AlloNK, is an allogeneic, off-the-shelf, non-genetically modified NK cell therapy candidate designed to enhance the antibody-dependent cellular cytotoxicity effect of monoclonal antibodies to drive B-cell depletion. AlloNK is delivered in the outpatient setting with no required hospitalization. AlloNK is currently being evaluated in three ongoing clinical trials for the treatment of B-cell driven autoimmune diseases. This includes two company-sponsored trials, one in systemic lupus erythematosus for patients with or without lupus nephritis, and a basket trial across autoimmune diseases (Rheumatoid Arthritis, Systemic Sclerosis, Idiopathic Inflammatory Myopathies and Sjögren's Disease), as well as an investigator-initiated basket trial in B-cell driven autoimmune diseases. Artiva's pipeline also includes CAR-NK candidates targeting both solid and hematologic cancers. Artiva was founded in 2019 as a spin out of GC Cell, formerly GC Lab Cell Corporation, a leading healthcare company in the Republic of Korea, pursuant to a strategic partnership granting Artiva exclusive worldwide rights (excluding Asia, Australia and New Zealand) to GC Cell's NK cell manufacturing technology and programs. Artiva is headquartered in San Diego, California. For more information, visit ****************** Job Summary: This position is responsible for cGMP auditing and supplier management activities at Artiva. Duties/Responsibilities: * Perform GMP/GDP audits in accordance with the external and internal audit program. * Support GXP audits (GLP, GCP, GCLP), as necessary. * Perform Drop-In GMP Internal audits. * Create and maintain audit schedules. * Track audit responses to completion. * Oversee and maintain the supplier qualification program. * Support the creation and execution of Quality Agreements with suppliers. * Update databases, prepare metrics, identify and communicate trending and tracking of audits and related supplier management activities. * Support audits by regulatory or state agencies and partners. * Support QA review of Analytical Development and Process Development data and reports, as needed. * Follow applicable regulations, including FDA, ISO, ICH, company policies and procedures. * Support other QA department needs as identified by management. Requirements: * Bachelor's degree or a combination of relevant education and applicable job experience * 5+ years' experience in an FDA regulated industry and expert knowledge of CGMP regulations * Certified Quality Auditor credential is a plus. * Ability to adapt quickly to shifting needs and/or priorities * Able to interface well with all levels of personnel * Excellent communications skills, both written and verbal and a high degree of professionalism * Exceptional attention to detail * Flexibility to travel Why you should apply: We have a fantastic team and philosophy! We are passionate - We deeply care about our team, our science, and improving the lives of autoimmune and cancer patients. We are tenacious - we are laser-focused on our mission and undeterred in our commitment to make cell therapies broadly accessible to patients with autoimmune disease and cancer. We are innovative - pushing into new frontiers for patient benefit. We are transparent - believers in flat, accessible, and open communication paths. We are inclusive - committed to the diversity of our team and ensuring that all voices are heard. In addition to a great culture, we offer: * A beautiful facility * An entrepreneurial, highly collaborative, and innovative environment * Comprehensive benefits, including: * Medical, Dental, and Vision * Group Life Insurance * Long Term Disability (LTD) * 401(k) Retirement Plan with match * Employee Assistance Program (EAP) * Flexible Spending Account (FSA) * Paid Time Off (PTO) * Company paid holidays, including the year-end holiday week * Our recognition program, Bonus.ly, is where you can trade in points earned for things you want. If all this speaks to you, come join us on our journey! Base Salary: $100,000 - 120,000. Exact compensation may vary based on skills and experience.

and Purpose: Quality Assurance Technicians work individually and alongside a team to ensure the quality, integrity, and consistency of all incoming raw materials and finished products. This position will report to the QA Supervisor. Essential Functions: Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Ensure that food safety and quality requirements for processing raw material into finished flavors conform to quality standards. Communicate relevant QA information to other departments. Inspect all incoming raw materials and finished products according to specified company standards. Test raw materials to identify potential replacements. Test, approve, and release finished flavors for packaging. Document all inspections and log product samples into QC sample inventory system. Maintain work area compliance with relevant quality management systems (calibrations, certifications, etc.) through recordkeeping. Prepare samples for shipment to testing facilities. Prepare and verify finished good labels. Create labels for packaging materials. Perform shelf-life evaluation and extensions for raw materials and flavors. Organize and maintain reserve sample storage. Assist QA Supervisor in investigating returned product complaints. Complete QC line sheets. Organize and retrieve physical and digital documents upon request. Organize overruns for powder and liquid finished goods. Assist Regulatory Affairs department as needed. Additional duties as assigned. Desired Knowledge, Skills, and Abilities: Ability to effectively communicate with all colleagues, levels of management, vendors, and customers. Detail-oriented with the ability to manage concurrent projects. Working knowledge Microsoft Office and applicable standard operating procedures. Leadership and Performance Management Strong analytical and problem-solving skills Mathematical computations Physical Demands: The physical responsibilities described here must be met by an employee to successfully perform the essential functions of this job. While performing the duties of this job, the employee is frequently required to sit, stand, bend, as well as talk and hear. Specific vision abilities required by this job include close vision. Must be able to regularly use hands to handle or feel objects, tools, or controls, reach with hands and arms, and climb stairs. The position requires the ability to occasionally lift, push, or pull office and lab products and supplies up to 25 pounds. Must be capable of wearing a respirator. Working Conditions: The position works in a lab and warehouse setting. This role routinely uses standard office equipment such as computers, phones, photocopiers, filing cabinets, and fax machines, and standard lab equipment such as Kiaro printers, allergen testing kits, pipettes, scales, meters, and the GC/MS. The noise level in the work environment may often be loud. Travel: Local travel to multiple worksites within a during the business day may be required Position Type / Expected Hours of Work: This is a full-time position. Standard days of work are Monday through Thursday, 10:30 am - 9:00 pm. Hours are subject to change based on company needs. Required Education and Experience: High school diploma and 6+ months of lab experience required. Bachelor's degree in Food Science, Chemistry, or related field and one year of quality assurance experience preferred.

Insight Global is looking for a QA Technician. The Quality Assurance Technician II supports manufacturing and quality control by performing inspections, testing, and equipment calibration to ensure products meet regulatory and company standards. This role involves handling nonconformances, coordinating with calibration vendors, maintaining accurate records, and assisting with process and product validation. You'll work closely with the QC and manufacturing teams to resolve issues and drive continuous improvement. We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to ********************.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: **************************************************** Skills and Requirements 2 years of experience in quality inspection, calibration monitoring, or environmental testing in a medical device. Computer skills Strong tech writing skills Has completed NCR Experience with eQMS, ERP systems, and data entry for quality documentation (SAP, Agilent, Windchill). Proficient in using inspection and metrology tools. Working knowledge of FDA QSR (21 CFR 820), ISO 13485, ISO 14644 (Cleanrooms), and ISO 11137 (Sterilization Validation) standards.

Where Performance Meets Purpose Join a team that values excellence and innovation, at a company known for its iconic golf brands. At Acushnet Company, your background and experience contribute to creating the best products for dedicated golfers worldwide. Here, your performance has purpose. What You Will Be Doing Join Our Team as a Quality Assurance Technician! We're looking for a detail-oriented professional to support our Custom Shop Putter operations from order initiation through final quality checks. In this role, you'll ensure every custom putter meets exacting standards-verifying order accuracy, finish, stamping, paint fill, weight, loft, and lie. You'll collaborate closely with internal teams and Customer Service to resolve issues, manage inventory, and maintain seamless workflows. Additional responsibilities include overseeing Moto Monday product readiness for eCommerce, ensuring timely availability of components for photography and online sales, and providing backup support for domestic shipping. If you're passionate about precision and delivering exceptional quality, we'd love to have you on our team! What You Bring High School Diploma or equivalent required Associate degree preferred Minimum 1 year experience with tour putters, custom putters, or luxury brand products Quality control experience highly preferred Ability to stand for extended periods Lift up to 30 lbs Forklift experience preferred Strong knowledge of Scotty Cameron products and history Proficiency in Microsoft Word and Excel Detail-oriented with strong communication skills Our Commitment to You At Acushnet Company, we are committed to helping our associates thrive both personally and professionally. From the start, you and your family, including domestic partners, will benefit from a comprehensive suite of health and well-being programs. Enjoy the advantages of paid time off, an onsite fitness center, acupuncture, physical therapy, wellness coaches, and more. Our financial benefits are designed to secure your future, offering a 401k with company match, health savings accounts, and flexible spending accounts. Additionally, you'll enjoy perks like pet insurance, legal planning, education assistance, and exclusive access to our Associate Store. At Acushnet Company, your performance has purpose, and we're here to support you every step of the way. Pay Range: $41,841.00-$52,501.00 Ready to Make an Impact? Join us at Acushnet Company and be part of a team that values excellence and innovation. Interview Preparation Questions Walk me through how you would verify the accuracy of a custom putter order from start to finish. What specific details would you check, and how would you handle discrepancies? Describe a time when you had to work closely with multiple teams (e.g., Customer Service, Shipping, or Production) to resolve an issue. How did you ensure clear communication and timely resolution? EEO and Additional Statements Acushnet Company is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, age, status as a protected veteran, among other things, or status as a qualified individual with a disability. EEO Employer/Veteran/Disabled. Acushnet Company respects the intellectual property and confidential information of third parties. Our policy is that no employee or applicant shall disclose confidential information of a third party to Acushnet Company. Accordingly, please do not include any confidential information of a current or previous employer on your resume or any other materials you provide to us. Acushnet Company participates is E-Verify. Please click here for more details. Global Candidate Privacy Notice

San Diego, CA, United States Are you driven by quality, detail, and making sure issues are resolved the right way the first time? Hologic is seeking a **Quality Supply Assurance Specialist II** to support our business operations by ensuring timely resolution of quality issues while maintaining full compliance for non-conformances and associated quality records. In this role, you'll work cross-functionally to support MRB and product quality forums, guide investigations, and contribute to continuous improvement across our Quality Management System. If you enjoy working in a highly detailed, regulated environment and want to help ensure safe, reliable products reach our customers, this role is for you. Knowledge + Working knowledge of FDA Quality System Regulations and ISO 13485. + Familiarity with risk management concepts and quality workflows related to non-conformances, corrections, and corrective actions. + Understanding of Quality Systems elements such as Material Review Board (MRB), Product Quality Committee (PQC), and quality metrics. + Knowledge of ERP-based quality transactions and basic quality data reporting. Skills + Ability to review and assess non-conformance, correction, and corrective action records for accuracy, completeness, and appropriateness. + Strong facilitation skills to support and coordinate cross-functional meetings (MRB, PQC, Product Response Team). + Proficiency in Microsoft Word, Excel (including graphing and data presentation), and related office tools. + Experience working in ERP systems (strongly preferred). + Excellent oral and written communication skills, including clear technical writing for quality records and SOP support. + Ability to support investigations using quality workflows, trend queries, and other analytical tools. + Strong organizational and multitasking skills in a detail-oriented, regulated environment. Behaviors + Self-starter who works effectively with minimal supervision. + Detail-focused and diligent in maintaining compliant, accurate quality records. + Collaborative team member who enjoys partnering across departments and acting as a QA interface. + Continuous improvement mindset, actively contributing ideas to improve processes and quality system performance. + Accountable and reliable, ensuring timeliness in deliverables and follow-through on quality commitments. Experience + BA/BS degree required, or equivalent experience/certification. + **2+ years** of experience in Quality, with strong emphasis on Quality Systems and non-conformances. + Experience in an FDA-regulated environment is required. + Experience supporting external audits and regulatory body inspections is beneficial. + ASQ Certification (CQA, CQE) preferred. **Why join Hologic?** We are committed to making Hologic the destination for top talent. For you to succeed, we want to enable you with the tools and knowledge required and so we provide comprehensive training when you join as well as continued development and training throughout your career. The annualized base salary range for this role is $65,900- $103,000 and is bonus eligible. Final compensation packages will ultimately depend on factors including relevant experience, skillset, knowledge, education, business needs and market demand. **Agency and Third-Party Recruiter Notice** _Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition, Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter. All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered._ **_Hologic, Inc. is proud to be an Equal Opportunity Employer inclusive of disability and veterans._** \#LI-NT1

The Assurance Experienced Associate will be responsible for preparing financial statements with disclosures, applying basic areas of GAAP as necessary and documenting, validating, testing, and assessing various control systems. This position may also be involved in reviews and agreed-upon procedure engagements. Job Duties: Control Environment: Applies knowledge and understanding of the collective effect of various factors on establishing or enhancing effectiveness, or mitigating the risks, of specific policies and procedures by: Identifying and considering all applicable policies, laws, rules, and regulations of the firm, regulators, or other authoritative bodies as part of engagement team Making constructive suggestions to improve client internal controls and accounting procedures Documenting and validating the operating effectiveness of the clients' internal control system GAAP: Applies knowledge and understanding of governing principles; applying these principles to client transactions; and documenting and communicating an understanding and application of these principles by: Providing support of conclusions with authoritative literature Drafting basic sets of financial statements with disclosures Researching intermediate areas of accounting and forming an initial opinion on the correct treatment independently GAAS: Applies knowledge and understanding of professional standards; application of the principles contained in professional standards; and the ability to document and communicate an understanding and application of professional standards on an engagement by: Developing and applying an intermediate knowledge of auditing theory, a sense of audit skepticism, and the use of BDO audit manuals Applying auditing theory to various client situations Documenting in line with BDO policy, identifying deviations and notifying more senior team members in order to obtain appropriate approvals Applying knowledge to identify instances where testing may be reduced or expanded and notifying more senior team members of the occurrence Contributing ideas/opinions to the engagement teams Methodology: Applies knowledge and application of BDO standards to guide effective and efficient delivery of quality services and products by: Completing all appropriate documentation of BDO work papers Ensuring assigned work is performed in accordance with BDO methodology and requirements Research: Applies methodology used to seek or maintain information from authoritative sources and to draw conclusions regarding a target issue based on the information by: Researching basic and intermediate accounting topics and forming an initial opinion on the treatment independently Other duties as required: Supervisory Responsibilities: N/A Qualifications, Knowledge, Skills and Abilities: Education: Bachelor's degree in Accounting, Finance, Economics or Statistics, required OR Bachelor's degree in other focus area and CPA certification, required Master's in Accountancy, preferred Experience: One (1) or more years of prior relevant audit experience and/or public accounting, private industry accounting or consulting/professional services experience, required License/Certifications: Eligible to sit for the CPA exams upon starting employment required and actively pursuing completion of the exams, required CPA, preferred Software: Proficient with the Microsoft Office Suite, preferred Experience with assurance applications and research tools, preferred Language: N/A Other Knowledge, Skills & Abilities: Basic understanding and experience planning and coordinating the stages to perform an audit of a basic public and/or private company Ability and willingness to travel, as needed Knowledge of internal accounting controls and professional standards and regulations (GAAP, GAAS, Sarbanes-Oxley, etc) Strong verbal and written communication skills with the ability to adapt style and messaging to effectively communicate with professionals at all levels both within the client organization and the firm Ability to successfully multi-task while working independently and within a group environment Solid analytical and diagnostic skills and ability to break down complex issues and implementing appropriate resolutions Ability to of work in a demanding, deadline driven environment with a focus on details and accuracy Solid project management skills Individual salaries that are offered to a candidate are determined after consideration of numerous factors including but not limited to the candidate's qualifications, experience, skills, and geography. California Range: $83,000 - $90,000 Colorado Range: $75,000 - $80,000 Illinois Range: $76,000 - $82,000 Maryland Range: $72,000 - $78,000 Minnesota Range: $70,000 - $74,000 NYC/Long Island/Westchester Range: $75,000 - $80,000 New Jersey Range: $76,500 - $83,000 Ohio Range: $70,000 - $78,000 Washington Range: $80,000 - $85,000

5th Axis is the world leader in automated production, manufacturing, and machining. We are a turn-key solution provider with a focus on product development, milling, turning, assembly, plating, Are you a creative thinker who loves turning ideas into reality? Ready to tackle exciting challenges and design the future? Join our team of forward-thinkers and shape groundbreaking solutions in an environment that rewards your expertise and passion! As an Automation Maintenance and Quality Technician, you will play a crucial role in ensuring the efficient operation of our automation systems, maintaining high-quality production standards, and contributing to the overall success of our manufacturing processes. Please note: This position requires to work an alternating weekend schedule. What You Will Do: Perform routine maintenance tasks on CNC machines and automation systems. Clean and maintain the robot, including emptying chips, cleaning, and replacing coolant as needed. Ensure that all equipment is in proper working condition for continuous production. Monitor production processes and make necessary adjustments to maintain efficiency and quality. Perform routine quality checks to ensure parts are within tolerance. Inspect finished parts using micrometers, calipers, and other precision measuring tools. Compare finished parts to blueprints to ensure they meet specified standards. Document and report any deviations or quality issues. Unload and reload materials in the robot to facilitate continuous production. Safely handle and transport materials as required. Maintain detailed records of maintenance activities, production data, and quality control checks. Report any equipment malfunctions, maintenance needs, or quality concerns to the supervisor. Assist with material management as needed Adherence to safety protocols and practices Perform other duties as assigned. Do you have: High school diploma or equivalent; technical certification or degree in a related field is a plus. Proven experience operating CNC machines for at least 2 years. Proficiency in using micrometers, calipers, and other precision measuring tools. Strong blueprint reading skills and the ability to interpret technical drawings. Attention to detail and a commitment to maintaining high-quality standards. Knowledge of robotics and automation technology is advantageous. Excellent problem-solving and troubleshooting skills. Strong communication skills and the ability to work effectively within a team. Basic computer skills for data entry and equipment control. Adherence to safety protocols and practices. Able to use proper tools such as calipers, gauge, pins and micrometers. Knowledgeable using test indicators. Ability to understand setup sheets. Basic knowledge of programs. Basic knowledge of G&M codes. Basic tooling knowledge. Ability to maintain a safe and clean working environment while adhering to company policies, quality policies, and industry standards. Detail oriented, organized, and able to demonstrate a high sense of urgency. What We Offer: Training and room to grow We pay 100% of our employees' costs toward medical, and dental. Company sponsored life and disability Insurance 401K with up to 4% matching Paid holidays Generous Paid Time Off accrual Pleasant non-corporate environment Fun team bonding events Are You Ready to Join Us? Hyper-growth means hyper opportunities for everyone on our team! At our company, we believe in growing talent from within, providing clear paths for advancement across all roles. Over 90% of our managers and countless others in key positions were promoted internally. If you're ready to grow with us, join our team and discover where your potential can lead! 5th Axis believes that everyone can make an impact, and we are proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex, race, creed, color, gender, religion, marital status, domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition, sexual orientation, pregnancy, military or veteran status, citizenship status, and genetic information. If you require an accommodation to complete the application or the interview process, please contact *******************

Job DescriptionSalary: $25 - $30/hr Ready to Transform Your Career? Join SpiTrex 3D! Are you looking to be part of a dynamic team in the cutting-edge world of additive manufacturing? Do you thrive in a fast-paced, growing environment that blends high technology and USA manufacturing? If so, we have the perfect opportunity for you! We are a leading additive manufacturing company located in vibrant Carlsbad, California. Our innovative solutions are revolutionizing the industry, and we're seeking a talented Quality Assurance Associate to join our growing team. Imagine a workplace where your growth knows no bounds - where data drives success, and your career flourishes. We believe SpiTrex 3D is a workplace like no other. It is a place to be challenged, explore your curiosity, and grow your career. Job Overview: As a Quality Assurance Associate at SpiTrex 3D, you will play a crucial role in ensuring the highest standards of quality for our 3D printed products and services. Your focus will be on supporting and organizing critical Master Batch Records (MBRs) and Certificates of Conformances while supporting quality control activities such as with data entries (ERP System), lean manufacturing/scheduling, record archiving, documenting training records, and supporting change controls. Essential Functions: Company Culture and Mission: Consistently apply core values (Integrity, Impact, Dedication) to your decision-making process and interactions with others. Uphold and contribute to the companys quality policy commitment. Master Batch Records: Prepare master batch record job folders for new production builds Support and organize records and data entries to allow for approvals in a timely manner with an accurate compilation of product Master Batch Records, which include Certificates of Conformance. Assist in verifying manufacturing scheduling to ensure that all quality activities are occurring at or ahead of schedule. Using Microsoft Word, Excel, and JobBoss2 document and record data entries in cooperation with handwritten records. Review executed records for compliance, ensuring completeness of all necessary testing and documents across various processes as needed Quality Control Records: Archive, physical retains, printed records, and electronic records with scanning, filing, and sorting per quality standards. Ensure product processes adhere to established quality standards and guidelines. Support data collection and monitor data throughout the production process where needed. Defect Detection/nonconformances: Collaborate and support the identify and document defects, nonconformances, or deviations from quality standards. Work closely with quality leadership and production teams to address and resolve quality issues promptly. Support corrective actions to prevent recurrence of defects as needed. Training and Education: Stay updated on industry trends, quality standards, and regulations as needed. Support the maintenance of training records and training matrixes. Shipping Receiving: Assist with front office incoming receiving and outgoing shipments for both products and supplies. Assist in developing and performing quality checks and documentation for incoming materials. Communication Effectively communicate quality related information to supervisors, colleagues, and other relevant stakeholders. Compliance Comply with ISO 13485 Quality Management System, FDA 21 CFR Part 820 Quality System Requirements (QSR), and medical device industry requirements. Assist in the implementation of the quantity management system. Other work-related tasks as assigned. Competency: Understanding of quality control principles and inspection techniques. Strong understanding of GMPs and GDP for production and generation of batch records. Basic familiarity with mechanical testing and materials characterization. Excellent organizational skills. Basic ability to read and interpret engineering drawings and specifications. Problem-solving and troubleshooting skills. Organizational and time management skills. Very strong attention to detail. Strong commitment to safety and quality assurance. Effective communication and interpersonal skills to work with cross-functional teams. Education and Experience: Associate degree in related field and/or 18 months-4 years experience preferred. Experience in quality control in the medical device industry, aerospace, or automotive industry preferred. Experience with mechanical testing and materials characterization preferred. Benefits Include: Medical, Vision and Dental Insurance Short Term Disability 401(k) plus match Vacation days Paid holidays

We're looking for people who put their innovation to work to advance our success - and their own. Join an organization that ensures a more secure world through connecting and protecting our customers with inventive electrical solutions. Experience the opportunity to excel in a role that sets you on a path to becoming a quality engineering expert. At nVent Management Company, we are committed to nurturing your ambition, ensuring you can develop your skills in an environment dedicated to flawless execution and world-class standards. As a Quality Technician, you will gain invaluable experience and contribute to our mission of achieving exceptional quality. You will: Shift: Weekend (Fri/Sat/Sun 6:00 am - 6:00 pm) * Lead root cause problem-solving activities aimed at enhancing internal and external quality levels. * Perform process validations, in-process inspections, and quality monitoring of manufacturing processes and products. * Support design, manufacturing, and quality engineering functions through data collection, analysis, product reviews, and process capability assessments. * Develop and adhere to Quality Management Systems (QMS) objectives, and train personnel to align with QMS standards. * Conduct internal ISO standard audits and provide necessary audit support. * Prepare formal documented First Article Inspection (FAI) reports for both customer and internal use. * Identify and apply suitable measuring tools and equipment to confirm dimensional and functional requirements. * Communicate effectively across various departments such as Operations, Supply, Manufacturing Engineering, Design, Quality, Customer Service, Production Planning, and Logistics. * Lead or assist in maintaining the calibration status of inspection, test, and measurement equipment. * Perform other related duties as assigned. * No corrective actions or performance improvement plans within six (6) months of the job posting opening date. * No decision making leaves within 12 months of the job posting opening date. * Most recent performance rating achieves or higher. * Successfully completed six (6) months in current job bid classification OR current career advancement classification. Requirements: * High school diploma or equivalent experience. * American Welding Society (AWS) Certification as Certified Welding Inspector preferred. * Proficiency in reading blueprints; knowledge of Geometric Dimensioning and Tolerancing (GD&T) is a plus. * Interest in academic and career development preferred. * Minimum of 2 years of experience in quality. * Preferable experience with precision metal fabrication measurement tools and techniques. * Strong knowledge of charting and process control methods. * Familiarity with Quality Management Systems (QMS) is preferred. WE HAVE: * A dynamic global reach with diverse operations around the world that will stretch your abilities, provide plentiful career opportunities, and allow you to make an impact every day * nVent is a leading global provider of electrical connection and protection solutions. We believe our inventive electrical solutions enable safer systems and ensure a more secure world. We design, manufacture, market, install and service high performance products and solutions that connect and protect some of the world's most sensitive equipment, buildings and critical processes. We offer a comprehensive range of systems protection and electrical connections solutions across industry-leading brands that are recognized globally for quality, reliability and innovation. * Our principal office is in London and our management office in the United States is in Minneapolis. Our robust portfolio of leading electrical product brands dates back more than 100 years and includes nVent CADDY, ERICO, HOFFMAN, ILSCO, SCHROFF and TRACHTE. Learn more at ************** * Commitment to strengthen communities where our employees live and work * We encourage and support the philanthropic activities of our employees worldwide * Through our nVent in Action matching program, we provide funds to nonprofit and educational organizations where our employees volunteer or donate money * Core values that shape our culture and drive us to deliver the best for our employees and our customers. We're known for being: * Innovative & adaptable * Dedicated to absolute integrity * Focused on the customer first * Respectful and team oriented * Optimistic and energizing * Accountable for performance * Benefits to support the lives of our employees Pay Transparency nVent's pay scale is based on the expected range of base pay for this job and the employee's work location. Employee pay within this range will be based on a combination of factors including knowledge, skills, abilities, experience, education, and performance. Where federal, state, or local minimum wage requirements exist, employee pay will comply. Compensation Range: $23.90 - $44.40 Per Hour Depending on the position offered, employee may be eligible for other forms of compensation, such as annual incentives. Benefit Overview At nVent, we value our people and their health and well-being. We provide a broad benefits package with meaningful programs for eligible full-time employees that includes: * Medical, dental, and vision plans along with flexible spending accounts, short-term and long-term disability benefits, critical illness, accident insurance and life insurance. * A 401(k) retirement plan and an employee stock purchase plan - both include a company match. * Other supplemental benefits such as tuition reimbursement, caregiver, personal and parental leave, back-up care services, paid time off including volunteer time, a well-being program, and legal & identity theft protection. At nVent, we connect and protect our customers with inventive electrical solutions. People are our most valuable asset. Inclusion and diversity means that we celebrate and encourage each other's authenticity because we understand that uniqueness sparks growth.

Under the direction of the Quality Assurance Manager, the Quality Inspector will maintain quality standards by approving incoming materials, in-process production, finished products, and recording the results. Essential Job Functions (primary duties and outputs of position) Inspect at receiving and in-process inspection. Complete operation sheet with stamping and dating for controlled production. Maintain lot traceability. Interpret production schematics, specification and/or blueprints. Perform final inspection of complex assemblies or first article inspection. Administer prescribed inspection procedures, set up and checks. Perform visual inspections on production bench-assembled components and subassemblies for conformance. Predetermine electrical and/or mechanical standard, specification or tolerances. Maintain gauges in working order. Provide training to other employees. Safety Follow safe work practices, participate in safety training as required, and report any unsafe condition or accident. Quality Employees are responsible to understand and support the quality policy and the appropriate elements of the quality management system for their areas of work, reduce, eliminate, and prevent quality deficiencies including escapes. Initiate action to prevent the occurrence of nonconformities related to product, process, and quality system. All employees have the responsibility and authority to identify quality deficiencies, elevate any concerns for action within or related to our quality system and processes. Communication Communicate effectively in English, both verbally and in writing. Maintain effective and constructive working relationships with others both internally and externally. Prepare effective reports and presentation of departmental information. Requirements Education/Work Experience Requirements Must have high school diploma or GED. 3 or more years' experience in manufacturing QA inspection. Must be able to operate standard inspection devices and/or elementary testing equipment. Able to test subassemblies. Ability to read and understand wiring diagrams; schematics, blueprints. Ability to read and interpret drawings and follow verbal and written job instructions. Able to pass IDC-J-STD-001 on IPC A610. Experience working in a controlled environment where lot traceability is required. Computer experience (using Excel) for data collection. Physical/Travel Requirements This position requires bending, walking, and standing, typing and lifting a maximum of 25 lbs. No travel required. Salary Description $20-25/Hour

Responsible for reviewing digital files, proofs, and overlays to ensure content is built to required specifications and precise to established internal expectations, documented tolerances, print industry standards, procedures and/or published direction. Evaluate and review cards, provide direction for print accuracy or improvement. Quality Control is an extension of Prepress Production and works closely with a variety of internal departments to ensure quality and fiscal responsibility. ESSENTIAL DUTIES AND RESPONSIBILITIES The following statements are intended to describe the general nature of the level of work being performed by an individual assigned to this job. Other duties may be assigned. Review print design engineering, product content, printability and make recommendations to ensure quality standards are attained. Assessed delivered information and implementation of direction received from designated Lead, Project Manager(s), Marketing, Legal, Design, Sports & Entertainment, Operations and written documentation from mechanicals, briefs, and costing documentation. Ensure the highest possible quality of files produced within lithographic pre-production environment. Quality Control Technician(s) will maintain a global view of these production procedures and make on-going recommendations to ensure tolerances are maintained and quality product files produced. Effective communication skills required demonstrate close mindfulness with organized practices. Responsible for interacting daily with Digital Operations Team Lead, Project Manager(s), Prepress Production personnel and Designers.' Support and adhere to internal Creative Departmental procedures and requirements to include but not limited to, assisting Prepress Production during production heavy cycles. Proficiency in the following software or systems: Adobe Creative Suite, MS Office, and Excel. Hands-on, energetic and motivated self-starter with the ability to work additional hours as required. INTERACTION This position will interact closely with the Director of Creative, Digital Operations Production Manager, Project Managers, Prepress Production, Designers, and other internal personnel. EDUCATION/YEARS EXPERIENCE High School Diploma or equivalent. College Degree with an emphasis in Graphic Arts a plus. 1-2 years of experience in Prepress or related area, publishing, or relevant duties. Knowledge of Kodak Prinergy is a plus. REQUIREMENTS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. KNOWLEDGE, SKILLS AND ABILITIES Present understanding of Prepress and Print Industries' standards, competent knowledge of established production tolerances. Familiarity with the 4/c process, to include, but not limited to: spot colors, varnish, foil, die cuts, deboss and/or embossing. Imposition software skills with a basic understanding of file standards for print production (bleed, trapping, color separation, resolution, etc.). Minimally an intermediate knowledge of Mac and applied software with verified results, fundamental knowledge of ripping and trapping of digital files through a Prinergy Workflow. The qualified applicant must possess acceptable computer skills; a working knowledge of Adobe Creative Suite is a plus. Additionally, basic to intermediate proficiency in the following software: Microsoft Word, Excel, and Outlook. Strong oral and written communication skills demonstrate close mindfulness with organized practices. Ability to articulate clearly with internal partners and not be afraid to ask questions. Effective organizational skills with the ability to manage multiple, high priority projects with dedicated attention to detail. Demonstrated ability to read, comprehend written instructions and follow pre-established guidelines. Utilize technology and maximize efficiency: Maintain education and ability of innovative techniques, technologies, and software capabilities. On an on-going basis, ensure we are maximizing our technology resources and making recommendations for improvements. Excellent interpersonal, problem solving and troubleshooting skills. Professional demeanor; collaborator orientation. Ability to perform duties under minimal supervision while exercising reasonable discretion and independent judgment. Manage time effectively, prioritizing duties and meeting deadlines. Ability to maintain flexible work hours. Work hours are mostly consistent, but production requirements require flexibility. Knowledge of the following areas would be desirable: NHL, Football and Basketball, and/or historical knowledge of pop culture, including comics and films spanning a multitude of trends. Hands-on, energetic and motivated self-starter

Build Your Career. Build America's Future. Vulcan Materials Company is the nation's largest producer of construction aggregates and a major producer of aggregates-based construction materials including asphalt and ready-mixed concrete. When you join Vulcan, it's more than starting an exciting career - you get to make a difference for millions of people every day across the country. When you join Vulcan, you join a dynamic culture in which career development is encouraged, excellence is rewarded, and diversity is valued. No matter the role or the location across the country, every member of the Vulcan team lives through the Vulcan Way: doing the right thing, the right way, at the right time. We're Coming Back Together To Be Together 100% In Office & Onsite At Vulcan Materials, we believe that the heart of our success lies in the strength of our engagement, our connection, and our commitment to developing our people. We are excited to restore the collaborative in-person environment that fuels our innovation and growth. This move is not just about being physically present; it's about reigniting the spirit that comes from face-to-face interactions, fostering a collaborative, inclusive culture where every voice is heard and everyone thrives. What You'll Do: Ensure Quality Control. Conduct routine testing of in-process materials, raw materials, environmental samples, and finished materials to ensure quality control of products at the point of production, shipping, and arrival upon the job site. Adhere to testing methods, including American Society for Testing and Materials (ASTM), American Association of State Highway and Transportation Officials (AASHTO) and Department of Transportation (DOT). Document and Report Information. Complete all required reports in a timely and accurate manner, interpreting, documenting, and storing the results. Communicate test results in a timely manner to the supervisor and properly document in a database. Maintain Lab Standards. Ensure housekeeping standards are maintained in and around the lab. Troubleshoot problems and review basic product specifications. Inspect, calibrate, and maintain testing equipment periodically. Monitor Stockpile. Inspect stockpiles, materials sources, and truckloads at plant sites. Monitor the daily construction of the stockpile to ensure that segregation and contamination is kept to a minimum or eliminated. Notify management immediately if contamination is identified. Inspect Equipment and Structures. Conduct routine inspections of the plant equipment in order to ensure safe, reliable, and compliant operations to maximize production and minimize interruptions. Additional Responsibilities. Other duties as assigned. Skills You'll Need: Experience. Prior training or experience in the materials testing field is preferred. Knowledge of general principles and practices of aggregate production is preferred. Travel. This role requires travel to various sites throughout Southern California. Must be willing to drive to these sites when needed and have a valid Driver's License. Safety Knowledge. Must display knowledge and awareness of construction and mining site hazards. Math Skills. Must possess good math skills and demonstrate the ability to perform simple to moderately complex arithmetic calculations. Technology Skills. Must have the ability to use computerized equipment and technology. Must be proficient in Microsoft Office Suite, Google, Oracle Business Environment, and other software packages relevant to the position. What You'll Like About Us: Great Company Culture. Our people share a competitive drive for excellence in an environment of trust, teamwork, open-mindedness and communication. Safe. Industry leader in health and safety standards. We are committed to creating a safe work environment and protecting all employees and customers. Meaningful Work. What sets up apart is the work we do impacts daily lives - and every employee contributes. Our aggregates produced are used to build roads, schools, hospitals, airports, and housing throughout the United States. Health Benefits. Medical, Dental, Vision programs, plus much more. Rest and Relaxation. Paid vacation, personal floating days, and paid holidays. Prepare for the Future. 401(k) with company match and contribution. Training and Development. We see our development programs and helping our employees meet their goals as a key part of our business. Salary Range: the base salary range for this role is between $27.00 to $30.00 per hour. This range is not inclusive of our discretionary bonus or equity package. When determining a candidate's compensation, we consider a number of factors, including skillset, experience, job scope, and current market data. Vulcan Materials Company is committed to employing a diverse workforce. You will receive consideration without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, gender expression, veteran status, or disability. You also have the right to be free from discrimination for medical needs arising from pregnancy, childbirth, or related medical conditions. NOTICE TO TEMPORARY STAFFING AGENCIES, PLACEMENT SERVICES AND PROFESSIONAL RECRUITERS Vulcan Materials Company has an internal recruiting department. Please review our policy as it relates to the use of temporary staffing agencies, placement services and professional recruiters.

About Axillon Aerospace Axillon Aerospace is a leading provider of complex, highly engineered composite and polymer solutions for demanding commercial and defense applications. We are comprised of six, purpose-built centers of excellence throughout the USA and Mexico, each strategically focused on serving specific markets across aerospace engines and airframes, as well as munitions, radomes, antennas and fuel containment. Learn more at axillonaerospace.com. Job Designation The Quality Technician supports the quality department and site manufacturing operations by ensuring the correctness of documentation and quality submittals to the customers, as well as supporting Quality Engineering activities pertaining to product flow and compliance. Job Core Responsibilities Non-conformance: When there are non-conformances identified, the quality technician ensures correctness and validates the non-conformance. Works with manufacturing engineers to establish the correct disposition and corrective actions for any non-conformances identified. Serves as the focal point to the customer when submitting non-conformances and quality notifications to gain approval from the customer. Ensures quality records are maintained per customer requirements. Product flow: Supports production by ensuring on time delivery is achieved. Ensures correctness of production travelers to prevent escapes. Conducts electronic disposition transactions through site Quality Database system. Maintains reports & records for all aspects of Material Review Board process. Supports Quality Engineers in the creation of Corrective Action Documentation. Performs visual inspections of parts to sort non-conformances and document/review documentation of non conformance. Documents production issues for communication and resolution. Develops, coordinates, implements, updates, monitors, and assures compliance with site quality policies and procedures, through audits. Job Specifications Education: A Secondary Certificate/High School Diploma or equivalent combination of relevant education and work experience that will allow successful performance of job expectations. Years' Experience: 2-6 years of relevant experience Skills: High school graduate or equivalent. College Degree Preferred. Excellent math skills. Exceptional attention to detail. Ability to read blueprints, apply GDT and understand industry and customer specifications. Proficiency in use of standard measuring tools such as micrometers, calipers, height gauges, electronic calculators, etc. Experience working in a quality inspection role in manufacturing. Aerospace industry preferred. Please note that the salary range information is only applicable for California. Compensation is based on a variety of factors, candidate experience, qualifications, location as well as market and business considerations. Pay Range: $31.00/hour- $35.00/hour. Axillon is an Equal Opportunity Employer. Axillon is committed to ensuring equal employment opportunities for all job applicants and employees. Employment decisions are based upon job related reasons regardless of race, ethnicity, color, religion, sex, sexual orientation, age, national origin, disability, gender identity, genetic information, veteran status, or any other status protected by law. This position requires use of information which is subject to the International Traffic in Arms Regulations (ITAR). All applicants must be U.S. persons within the meaning of ITAR. ITAR defines a U.S. person as a U.S. Citizen, U.S. Permanent Resident (i.e. 'Green Card Holder'), Political Asylee, or Refugee.

ADARx is seeking a qualified and highly motivated individual at the QA Associate III level to join the Quality Assurance (QA) group. This is a key role within the QA group and offers exciting opportunity for the successful candidate to make major contributions to the development, implementation and maintenance of the Quality Management System (QMS) at ADARx. This role will collaborate closely with CMC and Clinical functions at ADARx to ensure that quality practices, procedures, standards and systems are established and followed to maintain compliance to applicable cGxP regulations. Essential Responsibilities: Assist in the development, implementation, improvement and maintenance of ADARx's overall Quality Management System (QMS). Support the implementation of an electronic Quality Management System (eQMS) and act as the administrator to ensure proper configuration and usage of the system. Provide training and support to eQMS users. Provide QA support and oversight to internal staff and suppliers to ensure compliance with SOPs and relevant cGxP requirements. Manage the Document Control process for creating or revising controlled documents following internal procedures. Manage the training program and ensure all GxP related personnel receive appropriate training. Maintain and update training files and training curricula. Support the development of QA-related training materials and provide QA process training to new and existing employees. Author, review, and approve Quality System records, including deviation, CAPA, change records, etc. Author, review, and approve controlled documents for QA and other functional areas. Conduct and support supplier qualification activities, including issuance and review of quality questionnaires, supplier audits, and review of quality agreements. Manage supplier files and the approved supplier list to ensure they are accurate and up-to-date. Support internal audits, including planning, risk assessment, scope, audit program development, fieldwork, reporting and action follow-up. Collect and summarize Key Quality Indicator (KQI) metrics for review to identify trends. Support the preparation and hosting of regulatory inspections and external audits. Proactively identify gaps/risks and propose solutions to support continuous improvement. Essential Physical Characteristics: Reasonable accommodation(s) may be made to enable qualified individuals with disabilities to perform the essential functions of a job, on a case-by-case basis. On-Site Protocol: Physical presence at the ADARx Pharmaceuticals worksite is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture. Qualifications: BS/MS degree in a related scientific or technical discipline 6+ years of experience in the biotech/pharmaceutical industry 4+ years of experience in the QA function in a cGxP environment Strong understanding of cGMP and ICH regulations and guidance Demonstrated experience in development and implementation of quality processes, procedures and systems Prior experience using an eQMS is required Preferred Qualifications Previous experience in a GMP QC lab or manufacturing environment preferred GCP experience a plus Experience in implementation and/or administration of an eQMS is a plus Required Key Attributes: Must be able to work independently with supervision as needed. Must be collaborative, work well with other team members in a matrix team environment. Excellent written and verbal communication skills are essential for this role. Strong organizational skills with attention to detail and accuracy. Ability to maintain a high level of confidentiality and exercise discretion. Adaptable / Flexible - willing and able to adjust to multiple demands and shifting priorities as well as an ability to meet day-to-day challenges. Understand project timelines and deliverables and plans/coordinate project work accordingly with departmental, functional, and external stakeholders. Compensation: This is a full-time position, Monday-Friday. Pay is commensurate with experience. Equity-based compensation Performance-based bonuses 401(k) with Company Match Medical, Dental, Vision Flexible Spending Account Life Insurance Employee Assistance Program Employee Discounts Gym Membership Paid Vacation Paid Holidays Paid Sick, Jury Duty, Bereavement Work Authorization: United States (Required) Background Check As a condition of employment, you must successfully complete all post-offer, pre-employment requirements, including but not limited to a background check. Company Overview: ADARx Pharmaceuticals, Inc., (the “Company” or “ADARx”) located in San Diego, is a late-clinical stage biotechnology company committed to turning cutting-edge science into life-saving therapeutics. ADARx has developed proprietary RNA targeting platforms and technology for silencing or editing target mRNA. ADARx has a growing pipeline of RNA targeting therapeutics for treating diseases across a range of therapeutic areas including genetic, cardiometabolic, complement-mediated diseases and central nervous system. ADARx currently has multiple active programs in development with the lead candidate in the clinic. We are well-financed by a syndicate of highly regarded investors. ADARx Pharmaceuticals is an EEO employer committed to an exciting, diverse, and enriching work environment. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. Disclosure Statement The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual target bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, type and length of experience within the industry, and other job-related factors permitted by law. Total Compensation includes base salary; benefits: medical, vision, and dental insurance; life insurance; 401(k) matching program; paid time off; paid holidays; Employee Assistance Program; and other employee benefits. This role may also be eligible for short-term or long-term incentive compensation, including but not limited to cash bonuses. Following a conditional offer of employment, satisfactory completion of a background check (including criminal records check) is required prior to beginning employment. Any offer of employment may be rescinded if the background check reveals disqualifying information, and/or it is discovered that the candidate knowingly withheld or falsified information. Failure to satisfactorily complete the background check may affect the continued employment of a current NAI employee who was conditionally offered the position.

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 Position Summary: The QC Technologist III is responsible for the execution of a broad range of bench test procedures used in raw material qualification, the testing of finished goods prior to release, the investigations of product performance, and for conducting routine validation studies, as well as assisting with routine maintenance of the Quality Control (QC) laboratory. The QC Technologist III works with cross-functional teams to resolve product performance issues and maintenance of QC Standard Operating Procedures (SOP) in compliance with applicable regulations and ISO standards. Additionally, QC Technologist III supports investigations and assists in trending and statistically analyzing finish product testing data. This is a temporary role lasting between 3 and 6 months, with the possibility of extension. The pay rate for this position is $29-$34/hr, depending on experience. Responsibilities Key Accountabilities Essential Functions: Perform and organize testing of biological raw materials and finished goods per relevant SOP with minimal supervision; subject matter expertise in at least one product line. Assist with planning of method, product and process validations on existing products; perform and organize testing as needed. Perform testing and prepare reports as required for environmental monitoring or investigation of out-of-specification results, as required. Perform testing and assist with preparation of reports for various special projects as deemed necessary by technical review team. Responsible for tracking relevant trends. Maintain proper laboratory housekeeping and supply levels in the QC laboratory, including submission of purchase requisitions and inventory adjustments. Document all test results and maintain product release records (including electronic records). Document existing product/process validation test results (including electronic records). Maintain product testing database and perform relevant statistical analyses associated with product specifications as specified in laboratory SOPs. As required, coordinate and assist with investigation and resolution of complaints, non-conforming material and product performance issues. Submit complex change orders to update procedures as required. As required, work cross-functionally to investigate and resolve issues deriving from finish product testing. Ensure and maintain compliance with the Company's quality system requirements through training and adherence to policies, procedures and processes. Other duties as assigned. Qualifications Minimum Knowledge & Experience Required for the Position: High school diploma required; Bachelor's degree in Science or equivalent experience preferred. A minimum of four (4) years previous Quality Control lab (QC) and/or Quality Assurance (QA) experience required; previous experience within a regulated medical device manufacturing or In-Vitro Diagnostic Device (IVDD) strongly preferred. Thorough understanding of Good Laboratory Practices (GLP) required. Practical experience with laboratory controls, internal audits, and lab training/maintenance. Phlebotomy certification a plus. Knowledge of FDA-GMP/QSR and ISO standards for quality. Excellent written and verbal communication skills. Ability to work independently and as part of a team. Proficiency with common laboratory techniques, such as pipetting and use of balances. Proficiency with Microsoft Office suite. Proficiency with Large Enterprise Resources Planning (ERP) and Laboratory Information Management (LIMS) systems preferred. 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. **************

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 Position Summary: The QC Technologist III is responsible for the execution of a broad range of bench test procedures used in raw material qualification, the testing of finished goods prior to release, the investigations of product performance, and for conducting routine validation studies, as well as assisting with routine maintenance of the Quality Control (QC) laboratory. The QC Technologist III works with cross-functional teams to resolve product performance issues and maintenance of QC Standard Operating Procedures (SOP) in compliance with applicable regulations and ISO standards. Additionally, QC Technologist III supports investigations and assists in trending and statistically analyzing finish product testing data. This is a temporary role lasting between 3 and 6 months, with the possibility of extension. The pay rate for this position is $29-$34/hr, depending on experience. Responsibilities Key Accountabilities Essential Functions: Perform and organize testing of biological raw materials and finished goods per relevant SOP with minimal supervision; subject matter expertise in at least one product line. Assist with planning of method, product and process validations on existing products; perform and organize testing as needed. Perform testing and prepare reports as required for environmental monitoring or investigation of out-of-specification results, as required. Perform testing and assist with preparation of reports for various special projects as deemed necessary by technical review team. Responsible for tracking relevant trends. Maintain proper laboratory housekeeping and supply levels in the QC laboratory, including submission of purchase requisitions and inventory adjustments. Document all test results and maintain product release records (including electronic records). Document existing product/process validation test results (including electronic records). Maintain product testing database and perform relevant statistical analyses associated with product specifications as specified in laboratory SOPs. As required, coordinate and assist with investigation and resolution of complaints, non-conforming material and product performance issues. Submit complex change orders to update procedures as required. As required, work cross-functionally to investigate and resolve issues deriving from finish product testing. Ensure and maintain compliance with the Company's quality system requirements through training and adherence to policies, procedures and processes. Other duties as assigned. Qualifications Minimum Knowledge & Experience Required for the Position: High school diploma required; Bachelor's degree in Science or equivalent experience preferred. A minimum of four (4) years previous Quality Control lab (QC) and/or Quality Assurance (QA) experience required; previous experience within a regulated medical device manufacturing or In-Vitro Diagnostic Device (IVDD) strongly preferred. Thorough understanding of Good Laboratory Practices (GLP) required. Practical experience with laboratory controls, internal audits, and lab training/maintenance. Phlebotomy certification a plus. Knowledge of FDA-GMP/QSR and ISO standards for quality. Excellent written and verbal communication skills. Ability to work independently and as part of a team. Proficiency with common laboratory techniques, such as pipetting and use of balances. Proficiency with Microsoft Office suite. Proficiency with Large Enterprise Resources Planning (ERP) and Laboratory Information Management (LIMS) systems preferred. 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. **************