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#GKOSUS Generous. Innovative. Leadership-driven. Family-oriented. Socially responsible. Founded in 1998, Glaukos Corporation is an ophthalmic pharmaceutical and medical technology company focused on developing and commercializing novel therapies for the treatment of glaucoma, corneal disorders, and retinal diseases. Our mission at Glaukos is to truly transform vision by pioneering novel, dropless therapies that can meaningfully advance the standard of care and improve the lives of patients suffering from chronic, sight-threatening eye diseases. Innovation is at the core of everything we do, and we are resolute in our commitment to challenge conventional thinking with new treatment alternatives that are supported by real science, robust clinical evidence, and an unrelenting focus on patients. Our constant pursuit of game-changing technologies that disrupt legacy treatment paradigms is encapsulated in the Glaukos mantra “We’ll Go First,” which articulates our willingness to take chances, our determination to forge new ground, and our commitment to continuous improvement in all that we do. Our company completed an initial public offering in June of 2015, and our shares are traded on the New York Stock Exchange under the ticker symbol “GKOS”. Our global headquarters is in Aliso Viejo, California with additional locations in San Clemente, California, and Burlington, Massachusetts. Glaukos Corporation is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law. All offers of employment are contingent upon the successful completion of a background check, including successfully passing a drug screen, based on the position and local regulations.
#GKOSUS Generous. Innovative. Leadership-driven. Family-oriented. Socially responsible. Founded in 1998, Glaukos Corporation is an ophthalmic pharmaceutical and medical technology company focused on developing and commercializing novel therapies for the treatment of glaucoma, corneal disorders, and retinal diseases. Our mission at Glaukos is to truly transform vision by pioneering novel, dropless therapies that can meaningfully advance the standard of care and improve the lives of patients suffering from chronic, sight-threatening eye diseases. Innovation is at the core of everything we do, and we are resolute in our commitment to challenge conventional thinking with new treatment alternatives that are supported by real science, robust clinical evidence, and an unrelenting focus on patients. Our constant pursuit of game-changing technologies that disrupt legacy treatment paradigms is encapsulated in the Glaukos mantra “We’ll Go First,” which articulates our willingness to take chances, our determination to forge new ground, and our commitment to continuous improvement in all that we do. Our company completed an initial public offering in June of 2015, and our shares are traded on the New York Stock Exchange under the ticker symbol “GKOS”. Our global headquarters is in Aliso Viejo, California with additional locations in San Clemente, California, and Burlington, Massachusetts. Glaukos Corporation is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law. All offers of employment are contingent upon the successful completion of a background check, including successfully passing a drug screen, based on the position and local regulations.
Quality Inspector *Location:* San Diego, CA *Company:* Continental Controls *Job Type:* Full-Time, Exempt Position Summary Continental Controls is seeking an experienced *Quality Inspector* with a strong background in *precision machining*. This position is responsible for inspecting machined components and assemblies to ensure compliance with engineering drawings, specifications, and customer requirements. The ideal candidate has extensive experience inspecting tight-tolerance machined parts and is proficient with precision measuring equipment. Essential Responsibilities * Perform incoming, in-process, and final inspections of precision machined components. * Read and interpret engineering drawings, blueprints, specifications, and GD&T. * Verify dimensions, tolerances, surface finishes, and material requirements. * Perform First Article Inspections (FAI) and document inspection results. * Use precision measuring equipment including calipers, micrometers, height gauges, bore gauges, pin gauges, thread gauges, and surface plate inspection equipment. * Inspect CNC-machined parts for dimensional accuracy and workmanship. * Identify, document, and disposition nonconforming material. * Work closely with Machining, Engineering, and Production to resolve quality issues. * Maintain accurate inspection records and quality documentation. * Support corrective and preventive actions and continuous improvement initiatives. Qualifications * Minimum *5 years of quality inspection experience in a precision machining environment*. * Strong understanding of CNC machining processes and machined components. * Ability to read and interpret complex engineering drawings. * Working knowledge of *GD&T (ASME Y14.5)*. * Experience performing First Article Inspections. * Proficient with precision measuring instruments. * Strong attention to detail and excellent problem-solving skills. * Excellent verbal and written communication skills. * High school diploma or equivalent. Preferred Qualifications * Experience operating Coordinate Measuring Machines (CMM). * Familiarity with ISO 9001 quality management systems. * Experience with AS9102 First Article Inspection requirements. * Background in aerospace, defense, medical device, or other precision manufacturing environments. Compensation & Benefits *Salary:* *$70,000–$90,000 annually*, depending on experience and qualifications. *Benefits include:* * Company contributes *up to $450 per month* toward employee medical insurance * Dental and vision insurance * 401(k) with company match * Paid holidays * Paid vacation * Paid sick leave * Benefits available after *60 days of employment* * Opportunities for training and career advancement Why Join Continental Controls? At Continental Controls, quality is the foundation of everything we build. You'll work alongside a skilled team dedicated to manufacturing precision components that meet the highest standards for performance and reliability. If you're looking for a stable company where your expertise is valued and your work makes a difference, we'd like to hear from you. *Apply today by submitting your resume and a brief summary of your machining quality inspection experience.* Pay: $70,000.00 - $90,000.00 per year Benefits: * 401(k) * Dental insurance Work Location: In person
General Atomics Aeronautical Systems, Inc. (GA-ASI), an affiliate of General Atomics, is a world leader in proven, reliable remotely piloted aircraft and tactical reconnaissance radars, as well as advanced high-resolution surveillance systems. This position will report to a director and the candidate is responsible for managing the development and implementation of activities for operations in a manufacturing and engineering environment to meet technical requirements, production safety, quality, schedule, and cost objectives. Manages all phases of manufacturing and engineering operations for cable fabrication and PWA builds and modifications with an emphasis on laboratory concept and prototyping design cycles from plant layout to daily operations. Works closely with technical staff and management across departments to develop and implement current, annual, and long-term technical, schedule, quality, business and financial objectives for manufacturing and engineering operations. May also contribute to the development of annual and long-term objectives for the organization. typically accomplishes the objectives through subordinate management. May be responsible for decisions that impact outcomes where erroneous decisions could cause serious schedule delays and additional expenditures. DUTIES AND RESPONSIBILITIES: Manage the planning, scheduling, and activities of cable harness and PWA builds in manufacturing and engineering operations to achieve technical, business, safety, quality, and financial objectives. Act as the primary contact for manufacturing and prototyping/concept cable and PWA design activities and participate in progress planning and review sessions to discuss schedules. Ensure all operations are monitored for regulatory and safety compliance. Take a proactive approach to continuous improvement and implement lean principles. Prioritize production schedules based on product introduction, equipment efficiency, and materials supply. Ensure machinery, equipment, and tools are well maintained. Identify manufacturing issues and provide leadership in developing solutions. Provide guidance to engineering regarding design concepts and specification requirements that best utilize the facilities equipment and manufacturing techniques. Ensure manufacturing leadership and excellence is maintained by overseeing the planning, attraction, selection, retention, and development of the required management, professional, and technical talent. Provide manufacturing and technical expertise to the development of new and expansion of existing business opportunities to enhance the capabilities of the organization. Maintain the strict confidentiality of sensitive information. Responsible for ensuring all laws, regulations and other applicable obligations are observed wherever and whenever business is conducted on behalf of the Company. Responsible for ensuring work is accomplished in a safe manner in accordance with established operating procedures and practices. Additional Functions: Other duties as assigned or required. We recognize and appreciate the value and contributions of individuals with diverse backgrounds and experiences and welcome all qualified individuals to apply. Job Qualifications Typically requires a Bachelors degree in business administration, engineering or a related discipline and eleven or more years of progressively complex manufacturing and engineering prototype support experience. May substitute equivalent experience in lieu of education. Must have a detailed and comprehensive understanding of the principles, concepts, theories, and practices of manufacturing operations, as well as in-depth technical understanding of cable components and harness fabrication, and prototype PWA builds and modifications. Needs extensive experience demonstrating a broad application of operations practices, techniques, and standards; as well as comprehensive project management and leadership skills, including organizing, planning, scheduling, and coordinating workloads to meet established deadlines or milestones. Must possess the ability to resolve unusually complex management and technical problems. Strong communication, leadership, presentation, and interpersonal skills are required. Customer focused, must be able to work on a self-initiated basis and in a team environment and able to work extended hours as required. The ability to obtain and maintain DoD Security Clearance is required. Job Category Engineering Experience Level Management Workstyle Onsite Full-Time/Part-Time Full-Time Salary Pay Range Low 100,290 Pay Range High 183,098 Travel Percentage Required 0% - 25% Relocation Assistance Provided? Yes US Citizenship Required? Yes Clearance Required? Desired Clearance Level Secret Search Jobs at | General Atomics and Affiliated Companies
General Atomics Aeronautical Systems, Inc. (GA-ASI), an affiliate of General Atomics, is a world leader in proven, reliable remotely piloted aircraft and tactical reconnaissance radars, as well as advanced high-resolution surveillance systems. This position reports to a manager in an engineering environment and is responsible for implementing work activities and maintaining schedules for a cable assembly manufacturing area. Also works with engineering staff to implement concept and prototype cable designs as well as coordinating day-to-day activities of the production process under the direction of the manager, including personnel supervision, work assignments, and coordination of the product flow through the production phase. Requires complete familiarity with and understanding of the general aspects and technical phases of the job. Interprets and executes policies and procedures and recommends modifications to operating policies. DUTIES AND RESPONSIBILITIES: Supervises assemblers and technicians in an engineering environment through all phases of production and engineering prototype/concept design cycles in accordance with established schedules. Offers guidance and coaching to manufacturing personnel. Works with engineering staff to implement technical designs and concepts. In-depth understanding of automated cable harness test equipment. Ability to troubleshoot and repair test equipment for continuous operations. Oversees the design and building of tooling needed for the production process as well as engineering concept and prototyping needs. Examines defective equipment to determine cause of malfunction and reports need for repairs. Assists test department with expeditious turnaround of repairs as required. Assists engineering staff to resolve design and documentation issues. Interfaces with planning personnel in the generation of process flows, as well as with quality assurance personnel. Analyzes work orders and blueprints to determine information such as material to be used, type of operations, and sequence of operations required. Monitors usage and supply of all production materials and tooling; reorders when necessary. Interfaces with production control to help prevent material and equipment shortages. Formulates and recommends plans, policies, procedures and schedules for the section. Seeks methods to improve product quality, repeatability and efficiency. Schedules and coordinates work assignments. Ensures accurate time charging. Inspects work in progress and finished products. Recommends measures to improve production methods, equipment performance and quality of product. Suggests changes in working conditions and use of equipment to increase efficiency of the departments. Implements configuration changes in the product and supports field upgrades and operations. Interfaces with outside vendors and sales representatives to stay current on new products and services. Participates in hiring, promoting, and training subordinate employees. Assigns, directs and reviews their work. Responsible for observing all laws, regulations and other applicable obligations wherever and whenever business is conducted on behalf of the Company. Expected to work and lead the workplace in a safe manner in accordance with established operating procedures and practices. Additional Functions Other duties as assigned or required. We recognize and appreciate the value and contributions of individuals with diverse backgrounds and experiences and welcome all qualified individuals to apply. Job Qualifications Typically requires a bachelor's degree and nine or more years of progressive professional experience in a related technical field. May substitute equivalent experience in lieu of education. Must demonstrate an extensive technical understanding of cable harness production and assembly concepts and practices, with the ability to organize, schedule, and coordinate workloads and staff to meet established milestones. Ability to obtain and maintain a DoD secret clearance is required. Job Category Engineering Experience Level Supervisory Workstyle Onsite Full-Time/Part-Time Full-Time Salary Pay Range Low 73,700 Pay Range High 128,780 Travel Percentage Required 0% - 25% Relocation Assistance Provided? Yes US Citizenship Required? Yes Clearance Required? Desired Clearance Level Secret Search Jobs at | General Atomics and Affiliated Companies
Benefits: 401(k) Bonus based on performance Competitive salary Opportunity for advancement About the Role: West Coast Building Solutions Inc is looking for a skilled and experienced Cabinet Refacing Installer to join our growing team in San Diego, CA. This is a hands-on role with steady, reliable work for a craftsman who takes pride in delivering beautiful kitchen and bathroom transformations. If you love working with your hands and want to be part of a team that values quality, this is the opportunity for you. Responsibilities: Install cabinet refacing materials including veneers, rigid thermofoil (RTF), and wood overlays on existing cabinet frames Replace and install new cabinet doors, drawer fronts, and hardware Measure, cut, and fit refacing materials with precision for a clean, professional finish Prep cabinet surfaces including cleaning, sanding, and priming prior to installation Communicate professionally with homeowners on-site throughout the project Ensure job sites are kept clean, organized, and safe during and after installation Troubleshoot and resolve fitting or alignment issues as they arise Requirements: 3+ years of hands-on cabinet refacing or cabinetry installation experience required Proficiency with hand tools, power tools, and finish carpentry techniques Strong attention to detail and commitment to high-quality craftsmanship Ability to work independently and manage time effectively on job sites Professional, courteous demeanor when working in customers' homes Reliable transportation and ability to travel to job sites throughout the San Diego area Valid driver's license and clean driving record preferred About Us: West Coast Building Solutions Inc is a trusted name in home improvement across the San Diego region, specializing in high-quality cabinet refacing and remodeling services. Our customers love us for our attention to detail, reliable timelines, and the stunning results we deliver without the cost of a full renovation. Our team members enjoy steady work, a supportive environment, and the satisfaction of transforming spaces every single day.
*Job Overview* The Plasma Spray / HVOF Technician or Engineer supports thermal spray operations for aerospace components, with responsibility for process setup, execution support, quality compliance, and process improvement. This role may be filled at technician or engineer level depending on candidate experience and operational need. *Duties* * · Support plasma spray and/or HVOF coating operations in accordance with process specifications and quality requirements * · Assist with setup, monitoring, troubleshooting, and optimization of thermal spray processes * · Ensure coating application parameters are controlled and documented appropriately * · Work with engineering and quality teams on process qualification, repairs, and production support * · Contribute to safe, compliant, and efficient operation of specialized coating equipment and related processes. *Requirements* * · Diploma / Engineering in mechanical or production or manufacturing with engineer-level background relevant to thermal spray operations * · Hands-on experience with plasma spray, HVOF, or related thermal spray technologies * · Understanding of process control, coating application methods, and production support in a manufacturing environment * · Ability to troubleshoot process issues and support shop floor execution; familiarity with technical documentation and quality-driven operations. * · Aerospace MRO or aerospace manufacturing experience * · Experience supporting process qualification and special process environments * · technician- or engineer-level background relevant to thermal spray operations. Pay: $100,000.00 - $115,000.00 per year Benefits: * 401(k) * Health insurance * Relocation assistance * Vision insurance Work Location: In person
Join the Leader in Advanced CNC Manufacturing – 5th Axis At 5th Axis, we’re not just shaping parts – we’re shaping the future of manufacturing. As a world leader in automated production, advanced CNC machining, and turnkey solutions, we specialize in everything from product development and precision milling/turning to plating, assembly, and logistics. We're on a mission to push the boundaries of innovation and quality in everything we do. Are you detail-oriented, hands-on, and ready to contribute to world-class precision manufacturing? If so, we want you to join our dynamic team as an Assembly/Deburr Technician. Job Summary The Assembly/Deburr Technician plays a vital role in preparing precision components for final assembly and shipment. This position is responsible for deburring, assembling, and inspecting machined parts to ensure they meet 5th Axis’s high standards for quality and performance. A regular and predictable schedule is required. What You Will Be Doing Deburr and assemble machined components for shipment according to company procedures. Operate hand tools, shop equipment, and machinery safely and efficiently. Move finished products between workstations, QC, and shipping areas as needed. Perform visual inspections to verify product quality and conformance to standards. Follow written and verbal instructions to complete assigned projects accurately and on time. Record work times, quantities, and materials used for each job. Maintain a clean, organized, and safe work area—returning tools and materials to designated areas daily. Follow all company policies and safety regulations, including proper use of personal protective equipment. Report equipment issues, product discrepancies, or injuries promptly to management. Support other departments when needed and perform other related duties as assigned. What You Bring to the Table High school diploma or equivalent. Strong communication skills and a positive, service-oriented attitude. Ability to follow instructions precisely and pay close attention to detail. Proficient computer skills and the ability to learn new software. Epicor ERP experience (preferred). Previous customer service or manufacturing experience is a plus. Ability to stand for extended periods and lift up to 25 lbs. What We Offer Comprehensive Training & Career Growth Opportunities 100% Company-Paid Medical and Dental Coverage Company-Paid Life and Disability Insurance 401(k) with up to 4% Matching Generous Paid Time Off & Paid Holidays Fun, Team-Oriented Work Environment Exciting Employee Events and Bonding Activities Ready to Grow With Us? This isn’t just a job—it’s your opportunity to be part of a company that’s leading the way in advanced manufacturing and to grow with us every step of the way. At 5th Axis, growth creates opportunity: over 90% of our managers and many key team members have been promoted from within. We’re committed to developing talent and providing clear, rewarding paths for advancement. We are proud to be an equal opportunity employer that values diversity and believes everyone can make an impact. If you require accommodations during the application or interview process, please contact [email protected].
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 Join a collaborative and fast-paced manufacturing team dedicated to delivering life-changing Dexcom CGM technology to people around the world. In this role, you'll help lead daily production operations, support and mentor team members, coordinate with cross-functional groups such as Engineering and Quality, and drive continuous improvement initiatives. We are looking for someone with strong leadership, problem-solving, and communication skills who thrives in a dynamic environment and is passionate about developing people, improving processes, and ensuring operational excellence. With competitive benefits, career growth opportunities, and a mission-driven culture, you'll have the chance to make a meaningful impact every day. Where you come in: You will direct day-to-day oversight and planning of work for the manufacturing operations. You will inspect work of operators and keep documentations of yields and reject data. You will act as liaison between operator and supervisor/manager. You will execute agreed upon production plans and yields within designated area of production. You will assist supervisor/manager in scheduling resources and equipment and conduct document training You will ensure on-time equipment maintenance and calibration. You will ensure compliance to all applicable regulations to FDA, ISO, OSHA, etc. You will interact with cross-functional departments, such as Production, Engineering, and R&D, to resolve issues associated with quality, equipment, manufacturing systems, etc. You will monitor equipment performance and makes minor adjustments such as set-ups, calibrations, and alignments. You may clear minor machine difficulties and performs maintenance and repair as trained by a technician, engineer, or supervisor. What makes you successful: You should have experience in setting daily assignments and delegating tasks or projects inside and outside of normal production with both small and large teams. (6S audits, Continuous Improvement projects, Material Sorting, Smart Start meetings, etc.) You must have the ability to effectively over-see multiple projects at one time, offer feedback for improvements, implement new strategies, and communicate proposals professionally to MFG, ENG, and support teams. You should possess the ability to adapt to change, motivated to improve performance, remain calm and reserved, and maintain a proactive mindset in a high stress, fast-paced environment. You must be technically / mechanically inclined – the ability to learn and retain technical and mechanical skills. You should be effective in communication and collaboration with associates, peers, leaders, support teams / Ability to coordinate meetings and projects professionally and in a timely manner. You should have proficient skills with computer technology. You can address and resolve material concerns such as discrepancies, incorrect information, and non-conformities. You have some experience leading and motivating your fellow team members. Nice to have Microsoft Office (Excel, Word, PowerPoint) knowledge. Nice to have experience with training associates. 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 Typically requires a minimum of 6-8 years of related experience and 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 [email protected]. 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 [email protected]. 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. AI in Hiring Notice: We may use AI supported tools to help make our hiring process more efficient, consistent, and accessible for candidates around the world. All hiring decisions are made by people. Salary: $23.70 - $35.52 #DexcomUS
AleSmith Brewing Company is dedicated to creating the world’s highest quality beer while promoting an understanding and appreciation of craft beer and its styles and traditions to those we faithfully call our customers. We operate at the highest level of integrity and display excellence in all we do, from brewing to collaborating with each other and the organizations of our craft, and most of all, to the way we treat our customers. Job purpose The *Packaging Assistant* will assist in all packaging operations, including cleaning, maintaining all Packaging equipment, and keeping warehouses and supplies organized. Also, to assist with regular brewery and packaging equipment maintenance while following safety procedures and Company SOP’s (Standard Operating Procedures). Duties and responsibilities Include the following. Other duties may be assigned. * Assists with setup, cleaning, and operation of packaging machinery * Places packages in boxes, applies carriers, and stacks finished product * Operates forklift to move pallets around warehouse * Assists with conducting inventory and related documentation * Operates keg washing machine to wash and sanitize kegs * Assists in the troubleshooting, repair and preventative maintenance of brewery equipment * Performs general cleaning duties, such as cleaning floors, drains, packaging equipment, and all packaging areas * Assist in the transition of duties and communication between shifts * Participate in continuing education related to brewery and packaging operations, and safety and regulatory requirements * Assist in resolving customer issues and ensure customer satisfaction while maintaining the integrity of the Company * Follows all safety procedures and SOP’s and wear safety, personal protective equipment (PPE) Qualifications 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 accommodations may be made to enable individuals with disabilities to perform the essential functions. * Must be at least 21 years of age * Ability to work some evenings, nights, weekends, and holidays * Proficiency in communication, including verbal and written skills * Ability to work with hazardous cleaning chemicals * Ability to routinely lift, push and pull 55 lbs * Ability to stand and walk for up to 10 hours a day * Be motivated, hard-working, safety-minded and innovative with a commitment to representing and enjoying the culture and success of AleSmith * Be an exceptional team player with the ability to work independently as well * Ability to stay organized and follow checklists, departmental guidelines and SOP’s AleSmith Brewing Company provides equal employment opportunities to all employees and applicants for employment regardless of race, color, religion, gender, sexual orientation, gender identity or expression, national origin, ancestry, age, genetic information, marital status, pregnancy, medical condition, physical disability, mental disability, veteran status or any other characteristic protected by state or federal law. Job Type: Full-time Pay: $19.00 per hour Benefits: * 401(k) * 401(k) matching * Dental insurance * Employee assistance program * Employee discount * Health insurance * Life insurance * Paid time off * Referral program * Retirement plan * Vision insurance Work Location: In person
*ABOUT GALLANT* Gallant is the leader in veterinary regenerative medicine on a mission to bring transformational “ready-to-use” stem cell therapies to pets everywhere that treat the root cause of disease. With five high value clinical stage programs in development and a platform that is generating additional therapies, the company is positioned for their first FDA conditional approval in 2026, bringing a new class of therapies to animal health. Gallant is a privately-held company and backed by top venture capital firms BOLD Capital, Digitalis Ventures, Hill Creek Partners and NovaQuest, and recently completed our Series B financing. We have onsite GMP manufacturing, R&D and offices headquartered in La Jolla, CA. We offer a competitive base salary, generous health benefits, stock compensation, PTO, and virtual work environment as needed. We are a tight, incredibly smart and passionate team, deeply committed to our vision to bring “ready-to-use” stem cell therapies to pets worldwide. *Cell and Gene Therapy Products for Veterinary Medicine * *Position Summary * The QC Analyst will perform hands-on Quality Control testing and laboratory activities for our pet-specific cell and gene therapy programs. Reporting to the Manager, Quality Control, this laboratory-based role will execute phase-appropriate QC assays and procedures that ensure full compliance with current Good Manufacturing Practices (cGMP) and applicable veterinary regulatory requirements. The ideal candidate will bring strong technical expertise in analytical, microbiological, and environmental testing for cell and viral-vector manufacturing, combined with meticulous attention to detail and a pragmatic, compliant approach suitable for both early clinical and late-stage commercial readiness. This is a key individual-contributor role that will support quality culture and enable rapid, compliant advancement of our novel therapies for pets. *Key Responsibilities* * Execute in-process, release, and stability testing programs (identity, purity, potency, safety, sterility, endotoxin, bioburden, and microbial testing) for stem cell and viral-vector based products in accordance with cGMP, SOPs, and FDA CVM guidance. * Perform laboratory testing to support raw material inspection process in accordance with USP standards for release of ancillary raw materials. * Perform environmental monitoring and compile reports summarizing observed trends (viable/non-viable particle counting, surface and air sampling) in ISO-classified cleanrooms and support media fill programs and sterility assurance activities. * Accurately document all testing activities, results, and observations in laboratory notebooks, electronic systems, batch records, and certificates of analysis. * Assist in the investigation of out-of-specification (OOS) results, laboratory deviations, and environmental excursions; support implementation of corrective and preventive actions (CAPA) as assigned. * Support QC method qualification, validation, and transfer activities for advanced therapy products. * Prepare and maintain QC reagents, standards, controls, and laboratory inventory; perform routine equipment calibration and maintenance. * Assist in performing monthly laboratory inventory counts ensuring accuracy and timely reporting to Purchasing and Inventory Management personnel. * Collaborate cross-functionally with Manufacturing, Process Development, Quality Assurance, and Regulatory Affairs teams to ensure timely delivery of compliant QC data for batch disposition and regulatory submissions (e.g., FDA Center for Veterinary Medicine (CVM) Investigational New Animal Drug (INAD) applications and eventual New Animal Drug Applications (NADA). * Participate in internal audits, supplier/CMO testing oversight activities, and regulatory inspection readiness as required. * Perform risk assessments and support mitigation strategies for QC testing and stability activities per ICH Q9 and FDA guidance. * Stay current with evolving FDA CVM, USP, ICH, and international guidelines specific to QC testing of veterinary advanced therapies. * Support continuous improvement initiatives, process optimizations, and adherence to quality management systems (QMS). *Required Qualifications* *Education* * Bachelor’s degree in scientific discipline (Biology, Microbiology, Chemistry, or related field) required. Master’s degree is a plus but not required. *Experience* * 2–5 years of hands-on Quality Control or analytical laboratory experience in the biopharmaceutical industry, with direct exposure to cell therapy, gene therapy, or complex biologics testing preferred. * Demonstrated experience performing GMP-compliant analytical and microbiological testing, environmental monitoring, and sterility assurance activities in a cleanroom environment. * Familiarity with cell-based potency assays, flow cytometry, qPCR, ELISA, or compendial microbiological methods is highly desirable. * Experience supporting QC for autologous or allogeneic cell products and/or viral-vector gene therapies is a plus. *Skills & Competencies* * Working knowledge of U.S. GMP regulations (21 CFR Parts 210/211), USP compendial methods, ICH guidelines, and risk-management principles as they apply to QC operations. * Strong attention to detail, organizational skills, and ability to execute detailed SOPs while maintaining high standards of data integrity in a fast-paced biotech setting. * Excellent written and verbal communication; able to clearly document results and contribute to team discussions. * Passion for animal health and a collaborative, positive, team-oriented mindset. *Preferred Qualifications* * Direct experience with veterinary biologics or FDA CVM-regulated products. * Previous work in a startup or small-biotech environment. * Professional certifications or aseptic processing/sterile manufacturing training are advantageous but not required. *Most Important Qualities:* * Strong communication skills, both written and verbal * Easily adapts to change, enjoys a dynamic environment * Willingness to learn * High integrity, genuine * Entrepreneurial spirit * Remarkable discipline and organization * Great attention to detail * High speed of execution * Strong work ethic * Resourcefulness, ability to get things done on your own despite obstacles * Ability to receive and incorporate feedback * Passion for service * Great at conflict resolution * Consistently positive attitude * Loves pets! *Work Environment* This is a full-time, on-site position based at our cGMP manufacturing facility. This role requires hands-on presence in the QC laboratory and on the manufacturing floor during production campaigns, including occasional off-shift or weekend support as dictated by the manufacturing and testing schedule. All duties will be performed in strict compliance with FDA regulations related to the manufacture of cell and gene therapy products for veterinary medicine, including current Good Manufacturing Practice (cGMP) and CVM-specific guidance. The QC Analyst plays a critical role in ensuring the safe, complaint, and reliable production of advanced veterinary therapies. *Job Type*: Full-Time We are an equal opportunity employer committed to advancing safe and effective veterinary cell and gene therapies in full accordance with FDA/CVM standards. Pay: From $70,000.00 per year Benefits: * 401(k) * 401(k) matching * Dental insurance * Health insurance * Life insurance * Paid time off * Vision insurance Application Question(s): * Tell us why you think you are a good fit for this role. Work Location: In person
Additional Location(s): N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions. About This Role: The Process Technician role will be responsible for Catheter production line support, troubleshooting, preventative maintenance activities, and fabrication of tooling. This role collaborates cross-functionally with Quality, Engineering, and Maintenance teams to support continuous improvement and compliance with regulatory standards. Troubleshoots mechanical, electrical, and process issues in real-time to minimize downtime and maintain production flow. Your Responsibilities will Include: Apply critical thinking to solve complex problems and ask insightful questions, even without being a subject matter expert. Collaborate with Engineering to ensure manufacturing processes are optimized for scalability and efficiency. Manage and organize equipment and spare parts inventory to support uninterrupted production. Maintain accurate documentation for equipment, including manuals, service records, and change orders. Complete qualifications for new and existing equipment. Perform routine preventative maintenance on manufacturing equipment to minimize downtime. Contribute to process improvement projects aimed at enhancing product quality, reducing scrap and rework, lowering costs, and boosting performance. Identify and troubleshoot process related issues, implementing corrective actions to maintain production standards. Analyze scrap data to determine root causes and drive improvements through operator training and process control enhancements. Demonstrate deep process knowledge and provide hands-on guidance and training to production operators. Support daily production activities to ensure timely delivery of high-quality products. Assist in scaling equipment and processes from prototype development through pilot runs to full-scale manufacturing. What We’re Looking For In You: Minimum Qualifications High school diploma or equivalent. Required Experience: Minimum of 3 years of hands-on experience in low or high volume production environments. Proven ability to troubleshoot and maintain manufacturing equipment to ensure optimal performance. Demonstrated commitment to safety protocols, including proper use of lab safety equipment. The candidate should have good organizational skills, personal skills, and a strong follow-through “can do” attitude. Follows instructions, responds to management direction. Ability to physically handle small, delicate parts. Ability to read and understand work instructions, process guidelines, visual workmanship standards, and technical drawings. Preferred Qualifications Experience in manufacturing catheter or fiberoptic products is highly desirable. Prior experience with microscope-based inspection and medical device assembly. Skilled in performing in-process inspections to ensure product quality and adherence to workmanship standards for medical devices. Requisition ID: 632561 Minimum Salary: $ 44304 Maximum Salary: $ 75296 The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) – see www.bscbenefitsconnect.com—will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above. Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements). Compensation for exempt, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements). For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability. Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life by providing a broad range of high-performance solutions that address unmet patient needs and reduce the cost of healthcare. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological, neurological and urological diseases and conditions. Learn more at www.bostonscientific.com and follow us on LinkedIn. Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class. Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination. Among other requirements, Boston Scientific maintains specific prohibited substance test requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement. The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law.