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The Company Dexcom Corporation (NASDAQ DXCM) is a pioneer and global leader in continuous glucose monitoring (CGM). Dexcom began as a small company with a big dream: To forever change how diabetes is managed. To unlock information and insights that drive better health outcomes. Here we are 25 years later, having pioneered an industry. And we're just getting started. We are broadening our vision beyond diabetes to empower people to take control of health. That means personalized, actionable insights aimed at solving important health challenges. To continue what we've started: Improving human health. We are driven by thousands of ambitious, passionate people worldwide who are willing to fight like warriors to earn the trust of our customers by listening, serving with integrity, thinking big, and being dependable. We've already changed millions of lives and we're ready to change millions more. Our future ambition is to become a leading consumer health technology company while continuing to develop solutions for serious health conditions. We'll get there by constantly reinventing unique biosensing-technology experiences. Though we've come a long way from our small company days, our dreams are bigger than ever. The opportunity to improve health on a global scale stands before us. Meet the team: Test Lab supports Dexcom internal customers including quality, process engineering, clinical trials, and R&D by providing testing and related data to make critical product decisions. The team executes a high variety of testing which includes visual inspections, measurements, mechanical/destructive testing, and wet lab testing. Working with the Test Lab team, you can expect exposure to each of these teams and understand how Dexcom ensures a great product is made for our patients! Where you come in: You will execute a wide variety of testing in a laboratory setting and make detailed observations while performing tasks You will follow laboratory protocols, test procedures, and chemical safety guidelines You will maintain laboratory equipment, glassware, and inventory levels of consumable supplies You will assist with testing traceability by filing, recordkeeping, and entering data into datasheets and databases You will support the processing of large data sets using set programs and macros You will perform limited troubleshooting for laboratory equipment You will assist with test method validations and GRR testing You will support process qualification testing You will ideate and execute continuous improvement projects to improve the lab You will maintain 6S best practices What makes you successful: You have experience in a lab environment; should include experience in mechanical and/or wet lab testing You bring an eye for safety. Maintaining a safe environment for you and others as well as finding opportunities to improve lab safety You understand how to follow and edit written procedures for commercial use You have experience speaking effectively with large groups, customers and team members What you’ll get: A front row seat to life changing CGM technology. Learn about our brave #dexcomwarriors community . A full and comprehensive benefits program. Growth opportunities on a global scale. Access to career development through in-house learning programs and/or qualified tuition reimbursement. An exciting and innovative, industry-leading organization committed to our employees, customers, and the communities we serve. Travel Required: 0-5% Experience and Education Requirements: Typically requires a minimum of 2-4 years of related experience and a High School diploma/certificate or equivalent. Please note: The information contained herein is not intended to be an all-inclusive list of the duties and responsibilities of the job, nor are they intended to be an all-inclusive list of the skills and abilities required to do the job. Management may, at its discretion, assign or reassign duties and responsibilities to this job at any time. The duties and responsibilities in this job description may be subject to change at any time due to reasonable accommodation or other reasons. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Dexcom’s AAP may be viewed upon request by contacting Talent Acquisition at talentacquisition@dexcom.com. If you are an individual with a disability and would like to request a reasonable accommodation as part of the employment selection process, please contact Dexcom Talent Acquisition at talentacquisition@dexcom.com. Meritain, an Aetna Company, creates and publishes the Machine-Readable Files on behalf of Dexcom. To link to the Machine-Readable Files, please click on the URL provided: https://health1.meritain.com/app/public/#/one/insurerCode=MERITAIN_I&brandCode=MERITAINOVER/machine-readable-transparency-in-coverage?reportingEntityType=TPA_19874&lock=true To all Staffing and Recruiting Agencies: Our Careers Site is only for individuals seeking a job at Dexcom. Only authorized staffing and recruiting agencies may use this site or to submit profiles, applications or resumes on specific requisitions. Dexcom does not accept unsolicited resumes or applications from agencies. Please do not forward resumes to the Talent Acquisition team, Dexcom employees or any other company location. Dexcom is not responsible for any fees related to unsolicited resumes/applications. Salary: $21.49 - $32.25
As a Quality Programs Manager 4, you will be a key leader responsible for ensuring regulatory compliance, driving continuous improvement, and embedding industry best practices across our Quality Management System (QMS). You will lead and manage cross-functional quality and compliance initiatives, working collaboratively with stakeholders across Quality, Regulatory Affairs, R&D, Operations, Manufacturing Engineering, Supply Chain, Procurement, Marketing, and Corporate Quality to achieve organizational objectives. In this pivotal role, you will harmonize quality processes across sites and business units, define clear program objectives and metrics, and proactively manage risks. You will own quality planning documentation, champion process analysis and optimization, and play a central role in regulatory inspection readiness and response. Your leadership will foster transparent communication, program success, and a culture of excellence. Knowledge In-depth understanding of FDA Quality Management System Regulations (QMSR), ISO 13485, ISO 14971, and related medical device and IVD regulatory requirements. Proficiency in quality improvement tools and methodologies, including CAPA, Health Hazard Analysis/Assessment (HHA/HRA), Health Hazard Evaluation (HHE), MRB, and SCAR. Direct experience implementing and managing Quality Management Systems in the medical device or in-vitro diagnostic industry. Advanced knowledge of project and program management methodologies, frameworks, and best practices. Familiarity with digital quality solutions such as eQMS, analytics platforms, and project management software. Skills Proven ability to lead, harmonize, and execute complex, cross-functional quality and compliance programs across multiple divisions, sites, and regions. Strong analytical and critical thinking skills to evaluate risks, issues, and trade-offs, with the ability to make sound recommendations. Advanced project management skills, including defining scope, scheduling, resource planning, and maintaining program metrics and KPIs. Proficient in preparing and presenting data-driven insights, dashboards, and executive summaries to leadership. Exceptional organizational skills and attention to detail, with the ability to manage multiple priorities and projects. Expertise in stakeholder engagement, communications, and facilitating effective meetings (e.g., kickoffs, risk reviews, pre-inspection meetings). Experience developing and delivering training on advanced quality and regulatory topics. Behaviors Collaborative leader who builds strong partnerships across business units and functions. Proactive and strategic, anticipating risks and implementing effective mitigation strategies. Change agent who drives adoption of harmonized processes and a culture of continuous improvement. Transparent and effective communicator, able to engage stakeholders at all levels with clarity and credibility. Committed to ongoing professional development and knowledge transfer. Data-driven and focused on achieving measurable results and compliance excellence. Experience Bachelor’s degree in a technical or related field (Science, Engineering, or similar required). PMP certification or equivalent formal project/program management credential required. 10+ years of experience in Quality, Compliance, or related functions, preferably within the in-vitro diagnostic or medical device industry. Demonstrated track record of leading complex, cross-functional quality and compliance programs. Experience supporting and driving PMO and Quality improvement initiatives, including defining and refining standards, processes, and tools. Proven ability to mentor and develop quality and project management professionals. Participation in third-party QMS inspections and audit response activities.
Location: [Company Location] FLSA Status: Non-Exempt Job Summary: The Production Operator Level 1 is responsible for operating and maintaining production equipment to ensure efficient and safe manufacturing processes. This role involves performing routine tasks, monitoring equipment, and ensuring product quality. The Production Operator Level 1 will work closely with other team members to meet production goals and maintain a clean and safe work environment. Key Responsibilities: Operate and monitor production equipment to ensure efficient and safe manufacturing processes. Perform routine maintenance and cleaning of equipment. Conduct quality checks on products to ensure they meet specifications. Follow standard operating procedures and safety guidelines. Report any equipment malfunctions or safety concerns to the supervisor. Maintain accurate production records and logs. Assist with material handling and inventory management. Participate in continuous improvement initiatives to enhance productivity and efficiency. Collaborate with team members to achieve production targets. Qualifications: High school diploma or equivalent. Previous experience in a manufacturing or production environment preferred. Basic mechanical skills and ability to operate production equipment. Strong attention to detail and commitment to quality. Ability to follow instructions and work independently. Good communication and teamwork skills. Willingness to work flexible hours, including shifts and weekends. EEO Statement: [Company Name] is an equal opportunity employer committed to diversity and inclusion in the workplace. 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. This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, training, and apprenticeship. [Company Name] makes hiring decisions based solely on qualifications, merit, and business needs at the time.
What if the work you did every day could impact the lives of people you know? Or all of humanity? At Illumina, we are expanding access to genomic technology to realize health equity for billions of people around the world. Our efforts enable life-changing discoveries that are transforming human health through the early detection and diagnosis of diseases and new treatment options for patients. Working at Illumina means being part of something bigger than yourself. Every person, in every role, has the opportunity to make a difference. Surrounded by extraordinary people, inspiring leaders, and world changing projects, you will do more and become more than you ever thought possible. We're seeking a driven and talented Validation Engineer to support manufacturing operations through close collaboration with cross‑functional partners. This role is critical in defining, implementing, and maintaining validation activities that ensure robust, compliant manufacturing processes and systems. The ideal candidate brings experience in quality engineering, process development, or process engineering, and can quickly develop while working independently within a fast‑paced, team‑oriented environment. As a Validation Engineer, you will play a key role in driving overall quality performance and compliance by leading validation deliverables and activities across manufacturing systems and processes. Responsibilities: Represent the Consumable Validation group as the validation subject matter expert in manufacturing operations value streams and project teams, ensuring validation requirements and deliverables are communicated to the teams. Develop and articulate robust strategies for validation of processes and systems through development and release of holistic validation plans. In collaboration with end users, process owners, quality engineers and other team members, develop validation protocols and oversee execution of IQ, OQ, PQ for manufacturing processes and systems. Write reports summarizing results and statistics for all equipment and process validation projects. Be accountable for timely completion of all validation deliverables in accordance with manufacturing needs and project timelines. Learn and understand the applicable technology and engage in technical discussions. Provide consultation to other departments performing validation activities. Provide input for creation of requirements documents. Actively participate in creation of risk management documents such as pFMEA for systems and processes. Perform job function in compliance with the internal procedures and applicable external regulations and standards, e.g. FDA QSR, ISO-13485. Initiate and execute controlled document change requests. Execute other related tasks assigned by the supervisor. Listed responsibilities are an essential, but not exhaustive list, of the usual duties associated with the position. Changes to individual responsibilities may occur due to business needs. Experience: 1-2 years of related Validation experience in the life science industry (i.e. medical device/IVD, pharmaceutical, biotech) is preferred. Knowledge and working application of FDA and cGMP requirements. Knowledge and working application of validation principles and guidelines and industry practice, FMEA, and Risk Management. Knowledge and application of statistical techniques as a decision-making tool and practical experience in use of statistical analysis software JMP highly desirable. Knowledge and working application of standard operating procedures. Demonstrated ability to accomplish goals in collaboration with cross-functional teams. Demonstrated analytical problem-solving skills. Computer competency in MS Office. Excellent interpersonal, written, and verbal communication skills. Adaptable to fast-paced, dynamic work environment with ability to manage projects methodically. ValGenesis eVLMS and Teamcenter PLM experience is a plus. Education: Requires a bachelor’s degree or master’s degree in engineering or science. 1-2 years of related experience is preferred. The estimated base salary range for the Validation Engineer 1 role based in the United States of America is: $62,900 - $94,300. Should the level or location of the role change during the hiring process, the applicable base pay range may be updated accordingly. Compensation decisions are dependent on several factors including, but not limited to, an individual’s qualifications, location where the role is to be performed, internal equity, and alignment with market data. Additionally, all employees are eligible for one of our variable cash programs (bonus or commission) and eligible roles may receive equity as part of the compensation package. We offer a wide range of benefits as innovative as our work, including access to genomics sequencing, family planning, health/dental/vision, retirement benefits, and paid time off. We are a company deeply rooted in belonging, promoting an inclusive environment where employees feel valued and empowered to contribute to our mission. Built on a strong foundation, Illumina has always prioritized openness, collaboration, and seeking alternative perspectives to propel innovation in genomics. We are proud to confirm a zero-net gap in pay, regardless of gender, ethnicity, or race. We also have several Employee Resource Groups (ERG) that deliver career development experiences, increase cultural awareness, and offer opportunities to engage in social responsibility. 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. Illumina conducts background checks on applicants for whom a conditional offer of employment has been made. Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable local, state, and federal laws. Background check results may potentially result in the withdrawal of a conditional offer of employment. The background check process and any decisions made as a result shall be made in accordance with all applicable local, state, and federal laws. Illumina prohibits the use of generative artificial intelligence (AI) in the application and interview process. If you require accommodation to complete the application or interview process, please contact accommodations@illumina.com. To learn more, visit: https://www.dol.gov/ofccp/regs/compliance/posters/pdf/eeopost.pdf. The position will be posted until a final candidate is selected or the requisition has a sufficient number of qualified applicants. This role is not eligible for visa sponsorship.
THE POSITION A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche. The Opportunity We are hiring QC Associate I to join our team, focusing on microbiology testing support. In this role, you will be responsible for: Core Responsibilities: Collect, process, analyze, and report data for samples associated with utilities, environmental monitoring (EM), cleaning validation/verification samples, and product samples. Execute and document routine and non-routine testing to support data generation, including bioburden, endotoxin, TOC, conductivity, and other general techniques according to established procedures. Compliance and Quality System Adherence: Apply advanced knowledge of GMP, GDP, and Data Integrity ALCOA principles daily. Ensuring compliance with GMP requirements through accurate testing, detailed documentation, and timely reporting of all results. Follow established safety and environmental guidelines and maintain the laboratory in an inspection-ready state (e.g.,5S implementation) Equipment Maintenance and Readiness: Maintain laboratory equipment and ensure proper calibration and documentation. Technical Support and Troubleshooting: Perform basic troubleshooting of microbiological and chemical assays and provide initial support for instrument issues to minimize downtime. Materials and Inventory Management: Manage laboratory supplies by performing inventory checks and stocking supplies as needed (e.g., media, reagents). Investigation and Data Review: Assist in data trending and data review for conformance to specifications/limits. Identify and escalate OOS, OAL, or atypical results. Support laboratory investigations, deviations, and CAPAs as needed. Training and Cross-Functional Liaison: Complete required onboarding and ongoing GMP/laboratory training within established timelines. Maintain training compliance and qualifications for all assigned methods and tasks. Assist in training and mentoring others in basics to complex laboratory tasks and troubleshooting techniques, as applicable. Participate in cross-training across microbiology and chemistry testing to support operational flexibility. Serve as a liaison for daily activities and special projects within QC or cross-functionally. Independent Execution: Demonstrate the ability to work independently with little supervision and provide support for the execution of studies and protocols as needed Who you are You possess a Bachelor’s degree in Chemistry, Biochemistry, or a related scientific discipline with 3-4 years of experience in GMP-regulated laboratory. Knowledge, Skills, and Abilities Strong attention to detail and data integrity mindset Good understanding of aseptic techniques and cleanroom practices. Work in office and laboratory environments. May work in the clean room environment that requires gowning and no make up or jewelry May work in the clean room environment where it is loud due to different equipment operating Work in office and laboratory environments GMP Execution & Compliance: Experience working in a GMP environment with the ability to read and follow Standard Operating Procedures (SOP) precisely. Possesses knowledge of laboratory safety procedures and basic experience supporting quality events. Data & Systems Proficiency: Proficiency with laboratory electronic systems, including LIMS and Microsoft Office. Agile Teamwork & Organization: Demonstrates excellent organizational skills and the ability to be agile and work independently in a fast-paced environment. Ability to adapt and work across multiple functional areas (cross-trained environment). Ability to manage multiple tasks and meet timelines. Quality Mindset & Communication: Excellent interpersonal, written, and verbal communication skills. Possesses a continuous improvement mindset and basic experience supporting audit or inspection activities. May be required to work overtime, some evenings and weekends Physical & Work Environment Requirements Must be able to stand, walk, and use laboratory equipment for extended periods. Ability to lift up to 35 lbs and wear necessary personal protective equipment (PPE). Work is performed in a cGMP-regulated manufacturing facility. Work in the laboratory and with instruments that may involve exposure to hazardous chemicals (corrosive, toxic, flammable, etc) Relocation benefits are available for this posting The expected salary range for this position based on the primary location of California is $52,600 - $80,000 Annual. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below. Benefits Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants. JOB FACTS Job Sub Category Quality Schedule Full time Job Type Regular Posted Date Apr 7th 2026 Job ID 202604-108498
The Position A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche. The Opportunity We are hiring QC Associate I to join our team, focusing on microbiology testing support. In this role, you will be responsible for: Core Responsibilities: Collect, process, analyze, and report data for samples associated with utilities, environmental monitoring (EM), cleaning validation/verification samples, and product samples. Execute and document routine and non-routine testing to support data generation, including bioburden, endotoxin, TOC, conductivity, and other general techniques according to established procedures. Compliance and Quality System Adherence: Apply advanced knowledge of GMP, GDP, and Data Integrity ALCOA principles daily. Ensuring compliance with GMP requirements through accurate testing, detailed documentation, and timely reporting of all results. Follow established safety and environmental guidelines and maintain the laboratory in an inspection-ready state (e.g.,5S implementation) Equipment Maintenance and Readiness: Maintain laboratory equipment and ensure proper calibration and documentation. Technical Support and Troubleshooting: Perform basic troubleshooting of microbiological and chemical assays and provide initial support for instrument issues to minimize downtime. Materials and Inventory Management: Manage laboratory supplies by performing inventory checks and stocking supplies as needed (e.g., media, reagents). Investigation and Data Review: Assist in data trending and data review for conformance to specifications/limits. Identify and escalate OOS, OAL, or atypical results. Support laboratory investigations, deviations, and CAPAs as needed. Training and Cross-Functional Liaison: Complete required onboarding and ongoing GMP/laboratory training within established timelines. Maintain training compliance and qualifications for all assigned methods and tasks. Assist in training and mentoring others in basics to complex laboratory tasks and troubleshooting techniques, as applicable. Participate in cross-training across microbiology and chemistry testing to support operational flexibility. Serve as a liaison for daily activities and special projects within QC or cross-functionally. Independent Execution: Demonstrate the ability to work independently with little supervision and provide support for the execution of studies and protocols as needed Who you are You possess a Bachelor’s degree in Chemistry, Biochemistry, or a related scientific discipline with 3-4 years of experience in GMP-regulated laboratory. Knowledge, Skills, and Abilities Strong attention to detail and data integrity mindset Good understanding of aseptic techniques and cleanroom practices. Work in office and laboratory environments. May work in the clean room environment that requires gowning and no make up or jewelry May work in the clean room environment where it is loud due to different equipment operating Work in office and laboratory environments GMP Execution & Compliance: Experience working in a GMP environment with the ability to read and follow Standard Operating Procedures (SOP) precisely. Possesses knowledge of laboratory safety procedures and basic experience supporting quality events. Data & Systems Proficiency: Proficiency with laboratory electronic systems, including LIMS and Microsoft Office. Agile Teamwork & Organization: Demonstrates excellent organizational skills and the ability to be agile and work independently in a fast-paced environment. Ability to adapt and work across multiple functional areas (cross-trained environment). Ability to manage multiple tasks and meet timelines. Quality Mindset & Communication: Excellent interpersonal, written, and verbal communication skills. Possesses a continuous improvement mindset and basic experience supporting audit or inspection activities. May be required to work overtime, some evenings and weekends Physical & Work Environment Requirements Must be able to stand, walk, and use laboratory equipment for extended periods. Ability to lift up to 35 lbs and wear necessary personal protective equipment (PPE). Work is performed in a cGMP-regulated manufacturing facility. Work in the laboratory and with instruments that may involve exposure to hazardous chemicals (corrosive, toxic, flammable, etc) Relocation benefits are available for this posting The expected salary range for this position based on the primary location of California is $52,600 - $80,000 Annual. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below. Benefits Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.
We are a 30-year old company seeking long-term dedicated Mechanical Assemblers. *Job Description:* As a member of the team, the Mechanical Assembler will work closely with the Assembly Lead to ensure all machine automation, custom machinery, and minimum builds are properly manufactured to Accutek's high standards and quality assurance to ensure that Accutek equipment is built in accordance with customer requirements. This position will build assemblies and sub-assemblies per BOM and manufacturing instructions using basic hand tools to small power tools and by following industrial schematics. This position will assist the Lead in completing and updating the Compartment Binder, BOMs, and manufacturing documentation. This position is responsible for the quality of machines, training of employees and customer service when needed. This position will also assist in assembly, assembly preparation, troubleshooting, applications testing, assembly documentation and technical support. *Job Duties:* * Responsible for activities day-to-day activities associated with assembly of machinery that include but not limited components, sub-assemblies, machine assemblies, final assembly, soft plumbing, paint, and decoration in a timely and accurate completion of all work in the highest quality. * Responsible for maintaining a clean, organized work area while maintaining good safety practices. Ensure proper safety standards outlined by the engineer are being followed. * Responsible for safety and security of all tools issued or owned. * Responsible for the following and using the preventative maintenance schedule set forth by the Production Manager. * Assist the Production Manager in developing and maintaining the procedures used to assemble machinery. *Job Qualifications:* * Mechanical aptitude with the ability to use hand tools and tape measure accurately is a must. * Ability to lift 50lbs is required. * Ability to learn and understand technical information related to our products offered. * Ability to analyze situations and react in a timely manner. * Skilled in recording, compiling, and organizing information efficiently and accurately. * Good interpersonal skills, including discipline, teamwork, and training. * Human relations skills based in communication, leadership, and delegation experience. * Strong verbal and written communication skills. *Benefits:* We have a full benefits package including: · Paid Holidays and Vacation · Health Benefits · 401k *Company Information:* As a leading global company in providing packaging machinery, and packaging solutions to business and industry, Accutek specializes in providing dependable and affordable product to our end users ranging from single semi-automatic to fully automatic and integrated production lines. Accutek has experienced increased sales every year through acquisition, market penetration, and organic growth. If you are motivated, want to excel and grow, work for a stable company that wants you to succeed - then this position is for you! Please send your resume and salary requirements to the Human Resource Dept. (No Phone Calls Please.) Pay: From $18.00 per hour Benefits: * 401(k) * Dental insurance * Health insurance * Life insurance * Paid time off * Vision insurance People with a criminal record are encouraged to apply Work Location: In person
MAST is seeking a Process Engineering Intern who is an undergraduate student or recent graduate who will learn the inner workings of an engineering-oriented company that focuses on innovation in the Aerospace industry. STM specializes in the production of electrically conductive materials and textiles that services Aerospace, Defense (e.g. Lockheed Martin, Northrup Grumman), Medical, Telecommunications and many other industries. The Summer 2026 internship program will begin June 1st and run approximately 12–16 weeks, with anticipated end dates between August 28th and September 18th depending on availability. Interns will work 20–30 hours per week (minimum 20, maximum 30), Monday through Friday, with flexible scheduling. About MAST: MAST Technologies is an industry leader in advanced RF and EMI absorbing materials. We create engineered solutions that support mission-critical defense and aerospace applications worldwide. Our employees contribute directly to cutting-edge innovation and enjoy a collaborative environment focused on quality, technical excellence, and continuous improvement. Job Accountabilities: Equipment Qualification: Assist with the qualification planning and associated testing of new capital equipment Process Development: Assist with the development of process parameters of new equipment Product Development: Assist NPI engineers with the development of new products and associated testing Documentation: Generate standard work, training, and other equipment documentation. Document trials, test plans, and test results of new product development Drawings: Create detailed engineering drawings with industry-standard CAD tools (e.g. Solidworks) Documentation / Specs Research: Create, review, interpretate, and maintain project documentation and technical specifications Configuration Control Board (CCB) & Engineering Requests (ER): assist the design team in collecting necessary data to conclude a CCB & ER process Perform other duties and projects as assigned or requested Job Specifications: Education: A Secondary Certificate/High School Diploma/GED and at least two years of schooling pursuing a Bachelor's or degree in aerospace, mechanical or structural engineering Years’ Experience: 0-2 years of relevant work experience that will allow successful performance of job expectations Skills: Strong attention to detail, good organizational skills and the ability to prioritize with changing situations Experience with solid modeling software Good interpersonal, written and verbal communication skills to drive tasks to completion Working knowledge of Microsoft Office Suite Benefits: MAST is an Equal Opportunity Employer Veterans/Disabled - Affirmative Action Employer. This position requires the 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.
As a Quality Assurance Specialist 3 within our Regulatory and Quality - Diagnostics team, you will be integral to ensuring the highest standards of compliance and operational excellence in our laboratory environment. Reporting to the Senior Manager, Quality Assurance, you will drive quality initiatives and maintain robust Quality Management Systems (QMS) that meet state, federal, and accrediting body requirements—including California, CLIA, CAP, and NYSDOH. Knowledge In-depth understanding of Quality Management System (QMS) requirements and regulatory frameworks such as CLIA, CAP, NYSDOH, and state/federal regulations. Advanced knowledge of managing deviations, non-conformances, complaints, and Corrective and Preventive Actions (CAPA). Familiarity with Laboratory Developed Tests (LDTs) in CAP-accredited and CLIA-certified environments. Working knowledge of risk assessments, compliance audits, and quality improvement processes. Experience with MediaLab and medical device quality system regulations is a plus. Skills Demonstrated ability to develop, implement, and enhance QMS for ongoing compliance with regulatory standards. Proficient in administering quality programs such as audit, CAPA, change control, document control, and complaints management. Skilled in processing complex quality records and higher-level CAPA records with minimal supervision. Competence in reviewing validation records, equipment documentation, MLR materials, and change control documents for accuracy and compliance. Strong analytical skills to trend, maintain, and report department metrics and drive process improvement initiatives. Ability to lead and provide training on quality processes and procedures. Excellent verbal and written communication and presentation skills. High proficiency in Microsoft Suite; experience with MediaLab preferred. Strong organizational skills, attention to detail, multitasking, and time management in a fast-paced environment. Self-motivated, able to work independently and as a cross-functional team member. Behaviors Champion a proactive quality culture through effective training, communication, and ongoing quality awareness. Serve as a role model for ethical conduct, adhering to company policies, the Code of Business Conduct, and all applicable regulations. Proactive in identifying opportunities for process improvement and executing improvement projects. Highly detail-oriented, accountable, and committed to error-free performance. Collaborative and communicative, facilitating adherence to quality requirements and supporting cross-departmental initiatives. Experience & Education Bachelor’s degree in life sciences, physical sciences, engineering, or other technical field required. 5–8 years of experience in Quality Assurance/Systems. Experience investigating and resolving nonconforming events, deviations, and complaints. ASQ Certification or equivalent experience preferred. Experience in medical device quality system regulations is a plus. Completion of on-the-job training including HIPAA and safety procedures. 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 $86,400-$135,100 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
*Overview* We are looking for a dedicated and detail-oriented Packaging Operator to join our fast moving team. The ideal candidate will play a crucial role in the packaging process, ensuring that products are packaged according to company standards and regulatory guidelines. This position requires attention to detail, time management, as well as the ability to work effectively in a warehouse environment in close proximity to others. *Responsibilities* * Wash and fill kegs, ensuring compliance with quality standards. * Pack out on canning line. * Follow all safety protocols and maintain a clean and organized work environment. * Collaborate with team members to meet production goals and deadlines. * Maintain accurate records of production activities in accordance with company policies. * Operate and maintain packaging machinery, ensuring optimal performance and efficiency. *Qualifications* * No brewery experience required, entry level position with all necessary training provided. * Basic understanding of canning and kegging. * Familiarity with safety in a brewery environment. * Experience operating forklifts is a plus not necessity, supplemental training provided. * Must be able to comfortably lift 50 pounds regularly and safely. * Physically and mentally fit to do repetitive work. * Ability to use hand tools proficiently for assembly and fabrication tasks. * Excellent attention to detail with strong organizational skills. * Ability to work independently as well as part of a team in a fast-paced environment. If you are passionate about beer, work hard, and meet the qualifications outlined above, we hope you apply for this exciting opportunity with room for growth! Job Type: Full-time Pay: $18.00 - $20.00 per hour Benefits: * Dental insurance * Employee discount * Health insurance * Paid sick time * Paid time off * Vision insurance Ability to Commute: * San Diego, CA 92121 (Required) Work Location: In person
*The Position:* The *Quality Administrator *is tasked with assisting in quality, inventory, and customer service administrative functions while supporting daily lab operations, case management, and training initiatives. *The Company:* Advanced Test Equipment Corporation is a leading provider of test and measurement equipment based in San Diego and is known for the great care we take with clients and employees alike. *Benefits*: ATEC provides a generous and competitive benefits package to meet you and your family’s needs. It includes medical, dental, vision, life, disability, FSA, 401k with match, sick time, and PTO. *Requirements:* * Minimum of 2 year quality and customer service experience preferred * ISO 9001 or ISO 17025 background. * Strong attention to detail, communication, and data entry skills * Strong ability to multitask *Responsibilities:* * Maintains and organizes quality documentation, including standard operating procedures (SOPs), quality manuals, policies, and compliance records, ensuring accuracy and accessibility. * Performs case management activities, including closing cases, updating notes, ensuring accuracy in spreadsheets/CRM, and maintaining handling time metrics. * Supports inventory processes (restock, cycle count, scrap, accessory kit verification), ensuring compliance with WKIs and SOPs. * Assists in inventory audits, address discrepancies, and maintain accurate inventory records. Track stock levels to ensure inventory availability. * Compiles and analyze survey feedback (e.g., SurveyMonkey) to generate actionable insights for improving processes and customer satisfaction. * Organizes and maintains the parts room, ensuring bins are completed, items are labeled correctly, and records are updated in GP/CRM. * Documents and escalates technical or case-related issues to relevant teams as needed. * Assists with incoming calls by responding to customer inquiries and concerns in a timely and professional manner. Collaborate with internal teams to address issues and enhance customer experience. * Performs CRM data updates related to customers to ensure accurate and up-to-date information. * Assist with first-level technical support for product or service-related issues, ensuring continuous follow-up until case closure with customer satisfaction, and overseeing the completion of billing tickets, RMAs, and other necessary tasks. * Coordinates and participates in internal and external quality audits, ensuring compliance with quality standards. Track audit findings and assist in implementing corrective actions. * Maintains accurate and organized records to support the QMS, including order process dashboards, in-service lists, and work order verifications. * Facilitates the change control process by tracking change requests and ensuring proper approvals are obtained before implementation by tracking CRs, updating WKIs, and ensuring proper approvals are obtained before release. * Identifies and implements process improvements to enhance operational efficiency, ensuring continuous quality improvement. * Maintains key quality metrics and provide regular reports on quality performance. *Our Work Environment:* * Fast paced and dynamic environment with a focus on achieving results. * Collaborative team setting with a strong emphasis on innovation and continuous improvement. * Resources for personal and professional development. * Work/life balance. * Comfortable and accessible. Job Type: Full-time Pay: $25.00 - $30.00 per hour Benefits: * 401(k) * 401(k) matching * Dental insurance * Employee assistance program * Employee discount * Health insurance * Life insurance * Paid time off * Referral program * Tuition reimbursement * Vision insurance Education: * Bachelor's (Required) Experience: * Quality audits: 2 years (Preferred) * Quality improvement: 2 years (Preferred) * Quality assurance: 2 years (Preferred) Ability to Commute: * San Diego, CA 92121 (Required) Work Location: In person
Position Summary The Quality Assurance Technician ensures food safety, quality, and compliance across all production activities. This role is critical in supporting manufacturing by identifying risks, conducting inspections, and verifying that all regulatory and Suja standards are met. This is an on-site position within a production environment and reports to the QA Supervisor. Schedule 1:00pm - 9:30pm, Tuesday- Saturday with flexibility to work overtime on Monday's Essential Duties and Responsibilities Monitor production conditions, specifications, process controls and tracking controls Monitor wash line concentrations and test ppm concentrations for sanitation bucket and floor solutions Monitor a system that will verify checks on existing production control forms and be audited on the same forms that meet all program requirements. Collect Lab retain samples Verify all CCPs on-line and take corrective actions whenever necessary to assist in determining the root cause and development of a preventative action plan Responsible for checking the pH levels, temperature and brix of each batch of juice produced and is with in product specifications Verify and document Facility Operation Inspections & Good Manufacturing Practices Enforce Good Manufacturing Practices (GMPs) throughout the manufacturing areas Perform Standard Sanitation Operational Procedures (SSOPs) verification and ATP swabs Tracks non-conforming product (Holds) Perform pre-operational inspection procedures of all production/bottling equipment and facility Verify equipment calibrations. Verify volumes, lot codes, torques & bottle weights are within product specification. Complete and enter into database all pallet tags and CCP forms for production and bottling. Record cycles and verify that all HPP settings and information is correct Perform metal mesh, magnet and sock mesh inspections Verify production lot codes, labels, mold number and packaging are within product specification Shipping and receiving verifications. Verification of all raw materials being delivered and labelled with accurate information at Receipt (product name, lots, expirations, quantity received) COA Reviewing, comparing to the specification, approving and filing the COA. Escalating or placing on hold any items that are out of compliance. Review and Verify receiving documents and logs. Monitors production conditions, specifications, process controls and tracking controls as they specifically relate to raw materials used in production. Document and maintain records for all raw materials used in the production process including disposals, usage, and pre-batching of ingredients. Materials will be logged on the appropriate batch ticket for raw material commodity of interest. Commodities include raw produce, frozen juice, frozen puree, dry ingredients and aseptic products. Inspect raw materials for deficiencies relating to appearance, texture, and/or odor before production use. Inspect incoming trailers to ensure compliance with receiving standards. Report any food safety problems to the SQF Practitioner or Department Supervisor in a timely manner so that corrective actions may be performed. Ability to understand and follow verbal and written instructions related to safety, equipment operation, and daily work assignments. Adhere to SOP, SSOP, GMP, and HACCP guidelines when in the plant. Ability to understand and follow verbal and written instructions related to safety, equipment operation, and daily work assignments. Regular and reliable attendance. Job Qualifications 1–2 years of experience in Quality Control and/or the food industry preferred Familiarity with food safety regulations is a plus Other Skills & Abilities Excellent communication skills Strong computer proficiency Sharp critical thinking and problem-solving abilities Flexible and able to adapt to change Capable of working independently with moderate supervision Comfortable in a fast-paced production setting Language Skills: Ability to communicate, read, listen, and understand English. Bilingual is a plus. Working Environment Regular exposure to wet, cold manufacturing environments (temperatures as low as 35°F) Occasional exposure to dry warehouse spaces or freezer conditions (down to -10°F) Frequent exposure to high noise levels (above 85 dBA) Requires use of PPE including safety glasses, ear protection, gloves, and steel-toed footwear Physical Requirements Ability to stand and walk for the full duration of the shift Must be able to frequently lift/move hoses, equipment, and chemical containers weighing up to 50 lbs Ability to push/pull up to 100 lbs with continuous motion Must be able to bend, kneel, squat, climb stairs/ladders, and reach overhead regularly Must have sufficient hand strength and manual dexterity to operate sanitation tools and machinery Must be able to pass a pre-employment physical Compensation and Benefits Come thrive at Suja Life! We offer a competitive benefits package, including: Hourly Pay: $20.00 Medical, dental, vision, life insurance, and more Paid Parental Leave – 12 Weeks at 100% Pay 401(k) match to help you plan for the future Paid time off: vacation, sick days & holidays Juice benefits: yes, we keep you fueled and refreshed! #ZR #INDHP Suja Life is proud to be an equal-opportunity employer seeking to create a welcoming and diverse environment. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, ancestry, physical or mental disability, medical condition, marital status, genetics, age, or veteran status or any other applicable legally protected status or characteristic. The Company complies with all federal/local/state regulations regarding pay.