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SUMMARY Under general supervision, the Senior Manufacturing Associate, Downstream, will perform routine manufacturing activities in GMP manufacturing areas including purification and the associated sub-processes/ preparation. Operations will be performed according to Standard Operating Procedures (SOPs) and batch records. Perform manufacturing steps, execute routine batch records, and revise documents such as batch records and SOPs as needed. Drives projects and assignments and provides mentorship to associates. Flexible shift schedule and overtime may be required. JOB RESPONSIBILITIES Technical: ? Perform moderately complex tasks using defined protocols or procedures which contribute to the achievement of project milestones. ? Perform GMP manufacturing activities in assigned areas. ? Set-up, operate, maintain and clean downstream bioprocessing equipment, which includes but is not limited to chromatography systems, UF/DF and Viral filtration skids and mixers. ? Perform basic troubleshooting of bioprocess equipment. ? Perform manual cleaning and sterilization of manufacturing areas, parts and components. Compliance: ? Follow Standard Operating Procedures (SOPs), current Good Manufacturing Practices (cGMPs), plant safety guidelines and other established procedures during the manufacturing process to produce quality products. ? Accurately complete and maintain detail-oriented process-related documentation of equipment logs and batch records following the manufacturing Good Documentation Practices (GDP). ? Draft and revise SOPs and batch records. Teamwork and Communication: ? Participate in regularly scheduled team meetings to discuss ideas, troubleshoot issues, go over lessons learned and identify future projects or tasks. ? May provide mentoring and coaching to colleagues, team members, or those with similar or less experience ? Act as Lead when Specialist/Supervisor is unavailable. ? Address production issues and report any compliance related concerns to supervisor and/or management as soon as possible. ? Fosters teamwork and is expected to suggest project improvements. JOB REQUIREMENTS Education and Experience ? Advanced degree in life sciences or related discipline with 3 years of experience in the pharmaceutical or biotech industry, or equivalent education and experience. ? Bachelor's degree with 6 years of experience in the pharmaceutical or biotech industry, or equivalent education and experience. ? High School Diploma/GED with 8 years of experience in the pharmaceutical or biotech industry, or equivalent education and experience. Knowledge, Skills and Abilities: ? Downstream/Purification experience and skills in Protein Chromatography, TFF, Depth Filtration, Viral Filtration, Bulk Drug Substance Formulation, and Final Filtration. Aseptic Sampling of process pools and buffers. Buffer Preparation, Tubing assemblies and Autoclaving Operations. ? Knowledge of UNICORN and Common Control Platform (CCP) Software is preferred. ? Fundamental knowledge of current biologics regulations and cGMP for drug substance operation. ? Proficient with Microsoft Word and Excel. ? Able to work with pressurized systems, steam, and corrosive chemicals with necessary safety precautions. ? Demonstrated ability to follow and document activities in written procedures and/or logbooks. ? Detail-oriented, strong team player. ? Effective collaboration skills and the ability to work cross functionally across categories and internal stakeholders.
*La Belle Enclosures* is a high-end metal fabrication shop specializing in products for luxury residential projects. We produce refined, architectural metalwork with a strong emphasis on craftsmanship and detail. We are looking for a *skilled metal fabricator* to join our growing shop. ⸻ *Position Overview* This role is hands-on and fabrication-focused. You’ll be working primarily in the shop fabricating custom metal components, assisting with assemblies, and occasionally helping with installations. ⸻ *Responsibilities* * Fabricate custom metal components * TIG welding (Aluminum, stainless, brass experience a plus) * Cutting, drilling, tapping, grinding, sanding, and finishing * Read and follow shop drawings and measurements * Assist with mockups, assemblies, and occasional on-site installs * Maintain a clean, organized, and safety-focused workspace * Communicate clearly with the shop lead on timelines and details ⸻ *Requirements* * 2+ years experience in metal fabrication (custom work preferred) * Comfortable with TIG welding and precision fabrication * Strong attention to detail and pride in clean work * Ability to measure accurately and work independently * Reliable, punctual, and professional * Valid driver’s license *Bonus (not required):* * Brass fabrication or finishing experience * Ability to read CAD / shop drawings ⸻ *What We Offer* * Competitive hourly pay (based on experience) * Consistent work in a growing, design-focused shop * Opportunity to grow with the company * High-quality projects * Small team, respectful environment, and clear expectations Pay: $20.00 - $30.00 per hour Work Location: In person
Description: CNC Lathe Set-Up 6721 Cobra Way, San Diego, CA 92121, USA Full-time Company Description Welcome to CoreDux USA, a leading innovator in the machining industry located in the vibrant Sorrento Valley area of San Diego. As a rapidly growing company, we specialize in providing high-precision machining solutions that cater to a wide array of industries, including aerospace, automotive, medical devices, and consumer electronics. Our commitment to quality and excellence has earned us a reputation for delivering exceptional products and services to our clients. At CoreDux USA, we pride ourselves on our state-of-the-art facility, equipped with cutting-edge technology and advanced machinery, enabling us to meet the most demanding project requirements with unparalleled accuracy and efficiency. Our team of skilled professionals is dedicated to pushing the boundaries of innovation and delivering results that exceed expectations. As we continue to expand our operations, we are looking for talented and motivated individuals to join our team. We offer a dynamic work environment that fosters professional growth, collaboration, and creativity. If you're passionate about machining and eager to be part of a company that values innovation and excellence, CoreDux USA is the perfect place for you. Join us on our exciting journey and contribute to shaping the future of the machining industry! Job Description The primary function of this position is to set-up, verify, and operate CNC lathes to machine complex parts to customer requirements. 2nd Shift (1:45pm - 10:15pm) Other responsibilities will include: Set-up of CNC lathes including calibration of cutting tools and location of work offsets for part production. Verification of CNC programs and, when required, operation of lathes. Completion of all applicable paperwork (working to ISO 9000 standards). Performance of dimensional and visual inspections for first piece and in-process manufacturing. Cleanliness of the work area and proper handling of tools, equipment, and stock to prevent damage or loss. Assist in training other machinists or in supervising machine operators. Related detail work including de-burring, modification, re-work and assembly, as needed. May require training in hazardous material handling depending on job assignment. Perform other duties as requested. Qualifications Minimum 5 years CNC job shop experience. Must work to close tolerances in a high volume environment. Must be proficient with complicated blueprints and advanced job shop mathematical calculations. Familiar with CNC programming codes and able to perform complex set-ups for prototype and production runs. Must be able to follow written instructions and to work with no supervision. Must be familiar with cutting tool feeds and speeds. Understanding of true position tolerancing and Cartesian coordinate systems. Requires frequent bending, reaching and lifting of objects weighing up to 25 lbs. This position is paying between $28-$38 per hour depending on experience. Additional Information All your information will be kept confidential according to EEO guidelines. Diversity, Equity, and Inclusion (DE&I) Statement At CoreDux USA, we are committed to fostering a diverse, equitable, and inclusive workplace. We believe that diversity in our workforce enhances creativity, innovation, and problem-solving. We strive to create an environment where every employee feels valued, respected, and empowered to bring their authentic selves to work. Equal Employment Opportunity (EEO) Statement CoreDux USA is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, sex (including pregnancy, childbirth, breastfeeding, and related medical conditions), gender, gender identity, gender expression, sexual orientation, marital status, national origin, ancestry, citizenship status, age, physical or mental disability, medical condition, genetic information, military or veteran status, or any other characteristic protected by applicable federal, state, or local laws. We are dedicated to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans in our job application procedures. Benefits: 401(k) Dental insurance Employee assistance program Flexible spending account Health insurance Health savings account Life insurance Vision insurance Long Term Disability Benefits Short Term Disability Benefits Paid Time Off Company Paid Holidays School Visitation Leave Leave for Organ / Bone Marrow Donor Diversity, Equity, and Inclusion (DE&I) Statement At CoreDux USA, we are committed to fostering a diverse, equitable, and inclusive workplace. We believe that diversity in our workforce enhances creativity, innovation, and problem-solving. We strive to create an environment where every employee feels valued, respected, and empowered to bring their authentic selves to work. Equal Employment Opportunity (EEO) Statement CoreDux USA is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, sex (including pregnancy, childbirth, breastfeeding, and related medical conditions), gender, gender identity, gender expression, sexual orientation, marital status, national origin, ancestry, citizenship status, age, physical or mental disability, medical condition, genetic information, military or veteran status, or any other characteristic protected by applicable federal, state, or local laws. We are dedicated to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans in our job application procedures. Benefits: 401(k) Dental insurance Employee assistance program Flexible spending account Health insurance Health savings account Life insurance Vision insurance Long Term Disability Benefits Short Term Disability Benefits Paid Time Off Birthday Lunches Company Paid Holidays School Visitation Leave Leave for Organ / Bone Marrow Donor Recruiters and Staffing Agencies Thank you for your interest in our job opening, but we are not engaging recruiters for this position and will not respond to recruiter/agency inquiries. Requirements: Set-up of CNC lathes including calibration of cutting tools and location of work offsets for part production. Verification of CNC programs and, when required, operation of lathes. Completion of all applicable paperwork (working to ISO 9000 standards). Performance of dimensional and visual inspections for first piece and in-process manufacturing. Cleanliness of the work area and proper handling of tools, equipment, and stock to prevent damage or loss. Assist in training other machinists or in supervising machine operators. Related detail work including de-burring, modification, re-work and assembly, as needed. May require training in hazardous material handling depending on job assignment. Perform other duties as requested. Qualifications Minimum 5 years CNC job shop experience. Must work to close tolerances in a high volume environment. Must be proficient with complicated blueprints and advanced job shop mathematical calculations. Familiar with CNC programming codes and able to perform complex set-ups for prototype and production runs. Must be able to follow written instructions and to work with no supervision. Must be familiar with cutting tool feeds and speeds. Understanding of true position tolerancing and Cartesian coordinate systems. Requires frequent bending, reaching and lifting of objects weighing up to 25 lbs.
Description: CNC Mills Set-Up 6721 Cobra Way, San Diego, CA 92121, USA Full-time Company Description Welcome to CoreDux USA, a leading innovator in the machining industry located in the vibrant Sorrento Valley area of San Diego. As a rapidly growing company, we specialize in providing high-precision machining solutions that cater to a wide array of industries, including aerospace, automotive, medical devices, and consumer electronics. Our commitment to quality and excellence has earned us a reputation for delivering exceptional products and services to our clients. At CoreDux USA, we pride ourselves on our state-of-the-art facility, equipped with cutting-edge technology and advanced machinery, enabling us to meet the most demanding project requirements with unparalleled accuracy and efficiency. Our team of skilled professionals is dedicated to pushing the boundaries of innovation and delivering results that exceed expectations. As we continue to expand our operations, we are looking for talented and motivated individuals to join our team. We offer a dynamic work environment that fosters professional growth, collaboration, and creativity. If you're passionate about machining and eager to be part of a company that values innovation and excellence, CoreDux USA is the perfect place for you. Join us on our exciting journey and contribute to shaping the future of the machining industry! Job Description We are seeking a skilled CNC Mill Set-Up Operator to join our team. The ideal candidate will be responsible for operating computer numerical control (CNC) machines to fabricate parts and components with precision. Duties: Set-up, verify, and operate 3rd and 4th axis CNC mills to machine complex parts to customer requirements. Read and interpret blueprints to understand product specifications Monitor machine operations to detect any problems Inspect finished products for quality and adherence to specifications Perform routine maintenance on machines Qualifications Machining & Set-up: 5 years (Required) Sound knowledge of feeds, speeds, and material removal process. Familiar with CNC programming codes. Must be familiar with cutting tool feeds and speeds. Ability to set up parts independently. Understanding of true position tolerance and Cartesian coordinate systems. Must be able to follow written instructions. Experience working to close tolerances in a high-volume environment. Proficiency reading complicated blueprints. We have 2nd and 3rd shift positions with a salary range of $30-$40 per hour based on experience. Additional Information All your information will be kept confidential according to EEO guidelines. Diversity, Equity, and Inclusion (DE&I) Statement At CoreDux USA, we are committed to fostering a diverse, equitable, and inclusive workplace. We believe that diversity in our workforce enhances creativity, innovation, and problem-solving. We strive to create an environment where every employee feels valued, respected, and empowered to bring their authentic selves to work. Equal Employment Opportunity (EEO) Statement CoreDux USA is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, sex (including pregnancy, childbirth, breastfeeding, and related medical conditions), gender, gender identity, gender expression, sexual orientation, marital status, national origin, ancestry, citizenship status, age, physical or mental disability, medical condition, genetic information, military or veteran status, or any other characteristic protected by applicable federal, state, or local laws. We are dedicated to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans in our job application procedures. Benefits: 401(k) Dental insurance Employee assistance program Flexible spending account Health insurance Health savings account Life insurance Vision insurance Long Term Disability Benefits Short Term Disability Benefits Paid Time Off Birthday Lunches Company Paid Holidays School Visitation Leave Leave for Organ / Bone Marrow Donor Recruiters and Staffing Agencies Thank you for your interest in our job opening, but we are not engaging recruiters for this position and will not respond to recruiter/agency inquiries. Requirements: Duties: Set-up, verify, and operate 3rd and 4th axis CNC mills to machine complex parts to customer requirements. Read and interpret blueprints to understand product specifications Monitor machine operations to detect any problems Inspect finished products for quality and adherence to specifications Perform routine maintenance on machines Qualifications Machining & Set-up: 5 years (Required) Sound knowledge of feeds, speeds, and material removal process. Familiar with CNC programming codes. Must be familiar with cutting tool feeds and speeds. Ability to set up parts independently. Understanding of true position tolerance and Cartesian coordinate systems. Must be able to follow written instructions. Experience working to close tolerances in a high-volume environment. Proficiency reading complicated blueprints.
Carnegie provides innovative, high-performance product solutions to the architecture and design community. We embrace collaboration with like-minded creative partners and demonstrate that great design can thrive without negatively impacting the planet. For 75 years, Carnegie has been committed to being forever PVC-free, developing the first plant-based textile, Xorel™. Carnegie continues to be recognized as the industry’s first textile company in our market to be a certified B Corp. *Mission of the Job:* We are seeking a skilled Assembler, ideally with a textiles background, to support the Production Department by assembling products with a high level of attention to detail and ensuring all specifications are met with consistent quality. This role is responsible for the assembly and fabrication of all current in-house Kirei products using hot glue and assembly templates. The Manufacturing Assembler also supports other departments by assisting with sampling, marketing, and sales support materials. *This role is a six-month temporary position with the opportunity for conversion to a permanent role following review at the conclusion of the six-month period*. *Key Duties and Responsibilities:* *Product Assembly* * Assembles and fabricates of all current Kirei products using hot melt glue, fastener sand/or other adhesives/substrates as assigned. * Kitting, assembling, and packing of samples, marketing, and sales support materials. * Ensures quality control along each step of material handling, storage, and assembly * Provides support to warehouse for handling, transferring, and packaging based on workload and type of product * Responsible for the organization, maintenance, and general cleaning of the assembly area * Adheres to all safety regulations *Skills Needed for Success:* * *Attention to Detail *- Does not let important details slip through the cracks or derail a project. * *High Standards* - Expects personal performance and team performance to be nothing short of the best. * *Efficiency*-Able to produce significant output with minimal wasted effort * *Creativity/Innovation* *- *Generates new and innovative approaches to problems. * *Teamwork* - Reaches out to peers and cooperates with supervisors to establish an overall collaborative working relationship. *Experience, Skills, Qualifications:* * High School Diploma required * 1-2 years experience working in a production facility * Proficient in G Suite and Microsoft Office * Highly organized * Ability to work independently and on a team * Desire for growth * Capable of operating machinery and tools in a safe manner * Ability to work with hands effectively * Ability to be trained in production procedures * Ability to read and interpret written information as well as verbal instructions * Capable of lifting up to 50 pounds * Must be legally authorized to work in the United States Work Location: Onsite * Miramar 92126- Reliably commute daily or planning to relocate prior to start date. Job Type: Full-time Pay: $20.00 per hour Experience: * Fabrication: 2 years (Required) Ability to Commute: * San Diego, CA 92126 (Required) Work Location: In person
Work Schedule Standard (Mon-Fri) Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Laboratory Setting, Loud Noises (Equipment/Machinery), Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products etc.) Job Description About Thermo Fisher Scientific At Thermo Fisher Scientific, you’ll do meaningful work that makes a real-world impact. Our Mission is to enable our customers to make the world healthier, cleaner and safer. We support our colleagues with the tools, resources, and opportunities to grow their careers while advancing solutions that address global challenges—from improving human health to protecting our environment. What You’ll Do As a Sr. Staff Manufacturing Engineer, you will lead and contribute to complex technical initiatives that support advanced manufacturing operations. This role plays a critical part in driving innovation, operational excellence, and compliance within a regulated environment. You will work with automation systems, process control platforms, and manufacturing technologies while partnering across functions to design, implement, and optimize processes—from concept through validation and handover. Key Responsibilities Lead and contribute to engineering projects involving manufacturing equipment, automation systems, and process improvements Design and implement solutions to improve process efficiency, reliability, and compliance Support installation, qualification, and validation of manufacturing equipment and systems Collaborate with R&D, Quality, and Operations to resolve technical challenges and support production needs Develop and maintain engineering and validation documentation (e.g., URS, FRS, IOQ protocols) Ensure adherence to cGMP requirements and data integrity standards Support capital projects, including planning, execution, and budget tracking Troubleshoot and resolve complex equipment, automation, and process issues Provide technical guidance and mentorship to junior engineers Minimum Qualifications Advanced degree with 6+ years of experience, or bachelor’s degree with 8+ years of experience in pharmaceutical, biotech, or other regulated manufacturing environments Degree in Engineering (Chemical, Mechanical, Electrical, Automation, or related field preferred) Experience with manufacturing automation and control systems (e.g., PLCs, SCADA, or DCS platforms) Experience working in cGMP-regulated environments Demonstrated experience implementing process improvements in a manufacturing setting Experience with engineering documentation and validation practices Strong problem-solving and analytical skills Ability to collaborate effectively across cross-functional teams Clear written and verbal communication skills Preferred Qualifications Experience with Rockwell/Allen-Bradley, FactoryTalk, or DeltaV systems Experience with capital project execution in a manufacturing environment Familiarity with AutoCAD, MS Project, or Visio Experience supporting audit readiness and data integrity practices Demonstrated ability to mentor or guide other engineers Why Join Thermo Fisher Scientific? You’ll be part of a team that values innovation, integrity, intensity, and involvement, where your work directly contributes to advancing science and improving lives. Compensation and Benefits The salary range estimated for this position based in California is $143,000.00–$214,475.00. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes: A choice of national medical and dental plans, and a national vision plan, including health incentive programs Employee assistance and family support programs, including commuter benefits and tuition reimbursement At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards
We are looking for a reliable and experienced GMP Cleaner to maintain cleanliness and hygiene standards within the pharmaceutical manufacturing environment. They ensure that all areas comply with regulatory requirements and uphold stringent cleanliness protocols to guarantee product safety and quality. Pay: $18.50/hr The pay listed is the hourly range or the hourly rate for this position. A specific offer will vary based on applicant’s experience, skills, abilities, geographic location, and alignment with market data. ABM offers a comprehensive benefits package. For information about ABM’s benefits, visit ABM Employee Benefits | Front Line Team Members | (Programa de Beneficios de ABM) Shift: Sat - Sun 7am - 3:30pm, Tues, Wed & Fri 2pm - 5pm, Mon & Thurs off • Cleaning and Sanitization: Execute thorough cleaning and sanitization procedures for designated GMP areas including production rooms, laboratories, equipment, and common areas according to established protocols and schedules. • Compliance Assurance: Adhere strictly to GMP guidelines and regulatory standards while performing cleaning activities to ensure compliance with industry regulations and company policies. • Documentation and Reporting: Maintain accurate records of cleaning activities, including completion logs, sanitation checklists, and any deviations encountered during cleaning processes. Report any issues or discrepancies promptly to the appropriate personnel. • Equipment Maintenance: Assist in the maintenance and upkeep of cleaning equipment and tools to ensure their proper functioning and availability when required. Report any equipment malfunctions or deficiencies for timely resolution. • Safety and Hazard Awareness: Demonstrate a strong commitment to safety by following established safety protocols and utilizing appropriate personal protective equipment (PPE) during cleaning operations. Identify and report any potential safety hazards or concerns in the work environment. • Team Collaboration: Collaborate effectively with other departments and personnel, including manufacturing staff, quality assurance personnel, and supervisors, to coordinate cleaning activities and address any cleaning-related issues or requirements. • Continuous Improvement: Proactively contribute to the enhancement of cleaning processes and procedures by providing feedback, suggesting improvements, and participating in training sessions or workshops related to cleaning techniques, GMP standards, and regulatory updates. Required: • Must be 18 years of age or older • Must be fluent in English • 1-3 year(s) of cleaning experience Preferred Qualifications: • Previous experience in cleaning within a GMP-regulated environment, preferably in the pharmaceutical or healthcare industry. • Familiarity with GMP guidelines and regulatory requirements related to cleanliness and sanitation. • Strong attention to detail and ability to follow strict protocols and procedures. • Good communication skills and the ability to work effectively both independently and as part of a team. • Willingness to work flexible hours and adapt to changing priorities or cleaning schedules as needed About Us ABM (NYSE: ABM) is one of the world’s largest providers of facility services and solutions. A driving force for a cleaner, healthier, and more sustainable world, ABM provides essential services and forward-looking performance solutions that improve the spaces and places that matter most. From curbside to rooftop, ABM’s comprehensive services include janitorial, engineering, parking, electrical and lighting, energy and electric vehicle charging infrastructure, HVAC and mechanical, landscape and turf, and mission critical solutions. ABM serves a wide range of industries – from commercial office buildings to universities, airports, hospitals, data centers, manufacturing plants and distribution centers, entertainment venues and more. Founded in 1909, ABM serves over 20,000 clients, with annualized revenue approaching $8 billion and more than 100,000 team members in 350+ offices throughout the United States, United Kingdom, Republic of Ireland, and other international locations. For more information, visit http://www.abm.com. ABM is proud to be an Equal Opportunity Employer qualified applicants without regard race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran or any other protected factor under federal, state, or local law. ABM is committed to working with and providing reasonable accommodation to individuals with disabilities. If you have a disability and need assistance in completing the employment application, please call 888-328-8606. We will provide you with assistance and make a determination on your request for reasonable accommodation on a case-by-case basis. ABM participates in the U.S. Department of Homeland Security E-Verify program. E-Verify is an internet-based system used to electronically confirm employment eligibility. ABM is a military-friendly company proudly employing thousands of men and women who have served in the U.S. military. With ABM, you’ll have access to a world-class training program and ample opportunities to use the skills you developed while serving our country. Whether you’re looking for a frontline or professional position, you can find post-military career opportunities across ABM. ABM directs all applicants to apply at http://www.abm.com/ ABM does not accept unsolicited resumes.
Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Leica Biosystems, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. At Leica Biosystems, we’re not just shaping the future of cancer diagnostics — we’re transforming lives. Our mission of “Advancing Cancer Diagnostics, Improving Lives” is the driving force behind everything we do. As a global leader with the most comprehensive portfolio spanning from biopsy to diagnosis, we empower clinicians with innovative, reliable solutions so they can give patients timely, accurate answers when they need them most. When you join Leica Biosystems, you’re not just taking a job; you’re becoming part of a passionate team that knows every moment matters when it comes to cancer. You’ll help develop diagnostic solutions that turn anxiety into answers, and aid the acceleration of next-generation, life-changing therapies. Surrounded by a diverse and collaborative global community, you’ll be inspired each day to stretch, grow, and make an impact. Learn about the Danaher Business System which makes everything possible. The Senior Inspector, Quality Control is responsible for the testing and inspection of products at specified stages (incoming, in-process and final acceptance) to ensure product meet specifications. Responsible for conducting process validations as required by validation protocols and procedures. This role is also responsible for planning and conducting independent internal audits to assess compliance with Quality Management System and applicable regulations. In addition, prepare and distribute reports of observations to management team. Provide consultation and training in interpretation of regulation and procedures to production and quality personnel. This position reports to the Senior Manager, Quality Assurance (Deputy Management Representative) and is part of Quality Assurance and Regulatory Compliance team located in Vista and will be an on-site role. In this role, you will have the opportunity to: Perform comprehensive inspections and testing Ensure calibration, quality control, and nonconformance management Support quality systems, audits, and training The essential requirements of the job include: High school diploma required, associate degree in a technical field preferred. More than 5 years of quality control or inspection experience in medical devices or regulated manufacturing. Exceptional attention to detail, accuracy, analytical ability, documentation skills, and time‑management. Travel, Motor Vehicle Record & Physical/Environment Requirements: Travel expectations for this role are low (<10%). Overnight travel may be required. This position will require travel by car and flying in and out of airports with possible long wait times. Ability to lift, move or carry equipment up to 35lbs. While performing the duties of this job, the employee is occasionally required to walk, sit, stand, use hand to finger, handle or feel objects; reach with hands and arms; balance, stoop, bend, talk and hear. The role requires the ability to sit or stand for extended periods and perform fine motor tasks with delicate components. Specific vision abilities required by the job include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus. It would be a plus if you also possess previous experience in: Experienced in calibration, metrology, and equipment maintenance. Knowledgeable of ISO 13485, 21 CFR 820, and related regulatory standards. Strong problem-solving including identifying issues proactively and developing effective, compliant solutions Leica Biosystems, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info. The hourly range for this role is $28.00 - $30.00 an hour. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future. This job is also eligible for bonus/incentive pay. We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law. Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit www.danaher.com.
Location: 8515 Miralani Dr, San Diego, CA 92126 Schedule: Monday–Friday, 4:00am - 12:30pm What You’ll Do: As a Manufacturing Associate I, you’ll play a key role in producing high-quality standard and custom medical devices. You’ll work in a collaborative team environment, following strict GMP standards, SOPs, and customer specifications to ensure product excellence. Key Responsibilities: Operate and maintain manufacturing equipment per work instructions Perform visual inspections and identify nonconforming materials Complete production records and training documentation Support cross-functional manufacturing tasks for operational flexibility Maintain a clean, safe, and compliant work environment ✅ What You Bring: High school diploma or equivalent 1+ year of manufacturing experience preferred Experience with 3D printing and machine operations Manual dexterity and attention to detail Strong teamwork and communication skills Familiarity with Good Manufacturing Practices (GMP) Why You’ll Love Working at Argen: Competitive medical, dental, and vision plans 401(k) with employer match Generous PTO and paid holidays Employee events and wellness programs Discounts on travel, entertainment, and more About Argen: With over 500 employees and more than 50 years of innovation, Argen is the largest dental zirconia manufacturer in North America and a global leader in dental alloys and digital dentistry. Our 140,000 sq. ft. facility in San Diego houses over 150 3D printing and milling machines, operating six days a week to support our mission: helping dental labs succeed.
Job Title – Quality Assurance Intern Location – Solana Beach, CA LENZ Therapeutics is a pharmaceutical company focused on the commercialization of VIZZ® (aceclidine ophthalmologic solution) 1.44%, the first and only FDA-approved aceclidine based eye drop for treating presbyopia, a condition impacting an estimated 1.8 billion people globally and 128 million people in the United States. LENZ is commercializing VIZZ® in the United States and continues to establish licensing partnerships internationally to provide access to VIZZ globally. The company is headquartered in San Diego, California. If you are a college student or new graduate, our Summer Intern Program offers the opportunity to gain invaluable firsthand work experience in an area related to your academic field of study or interest. Join us for 8-12 weeks from late May to August, to experience a structured and mutually beneficial learning experience along with LENZ’s unique environment and culture. Join LENZ Therapeutics as an intern and be part of a team that believes we are better together. You will work alongside supportive, driven colleagues who are all in on our mission and committed to helping you learn and grow. This role is based on site in our Solana Beach office Monday–Thursday, with remote work on Fridays. We provide lunch onsite and come together each day, creating a collaborative, energetic environment where curiosity, ingenuity, and teamwork thrive. Overall Purpose: We are seeking a Quality Assurance Intern to gain hands-on exposure to pharmaceutical quality systems and cross-functional operations. This role provides a meaningful learning experience by supporting quality system organization, participating in team meetings, observing quality operations, and assisting with general quality initiatives. The intern will work closely with the Quality Systems team and gain insight into how a regulated pharmaceutical environment operates. This role reports to the Director, Quality. Key Responsibilities of the Role: Assist with organizing and maintaining quality documentation within Ennov and SharePoint to support efficient workflows Support administrative and operational tasks related to quality systems, ensuring data and document accuracy Participate in cross-functional team meetings to gain insight into quality operations and collaborative decision-making Shadow Quality Systems activities to learn about regulatory practices, GxP principles, and operational standards Help track, compile, and organize quality metrics or other relevant documentation Contribute to team initiatives that support process improvements, system organization, or operational efficiency Academic Credit: If an internship is associated with academic credit: The intern is responsible for coordinating credit requirements with their institution. LENZ may complete required evaluations or documentation, as appropriate. Academic credit does not replace compensation unless the internship qualifies as unpaid under California law. Physical Demands and Work Environment Onsite in Solana Beach, CA Monday to Thursday (remote Fridays). Typically works in an office environment. May, on a continuous basis, sit at desk for a long period of time, intermittently answer telephone and write or use a keyboard to communicate through written means. Some walking and lifting up to 20 lbs. may be required. The noise level in the work environment is usually low to moderate. Must be flexible to work varying schedules and hours as needed. Frequent out-of-town travel may be required. The physical demands described above are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Mission Statement: LENZ employees are united in a mission to improve and sustain vision. We are passionate and creative about applying scientific innovation to meet the needs of the millions of people worldwide who suffer from Presbyopia and other ophthalmic maladies. We focus on the development and commercialization of new therapies to bring our mission to life for patients every day. Hourly Rate Pay is $20/hr. Schedule can be up to 40 hours per week. Additional Details: Internships are temporary and typically last 8–12 weeks (start and end dates will be clearly defined in writing in the offer letter). Internships do not guarantee future employment. Required Skills: Currently pursuing or recently completed a degree in life sciences, engineering, or related field Strong attention to detail and excellent organizational skills Ability to manage multiple tasks and prioritize effectively in a dynamic environment Proficiency in Microsoft Office (Excel, Word, PowerPoint) Strong written and verbal communication skills Experience with document management systems (e.g., SharePoint) is a plus Program Requirements: Cumulative 3.0 GPA or above; college transcript required. Currently enrolled in or newly graduated from an accredited college/university. Legally authorized to work in the U.S. At least 18 years of age prior to the scheduled start date. Must complete an application and provide a cover letter expressing interest and indicating best department to further learning goals. Must successfully pass a background check prior to the program start date. Onboarding will be provided. Successfully pass all compliance modules. Final presentation on learning during last week of the program.
Production Specialists are responsible for activities associated with the manufacturing of specialty resins and additives. They handle a variety of chemicals, record information and observations relating to the chemical reaction process, troubleshoot issues with equipment, and assist in process improvement initiatives and the work plan development process. _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._ · 2-year degree in chemistry (or higher) is preferred · 2+ years of experience in bulk chemical manufacturing is preferred · High School diploma or GED · Ability to perform simple mathematical calculations using a calculator · Ability to accurately read and take measurement · With limited supervision, perform manufacturing of established products via the use of Operator Checklists (OCLs) utilizing basic chemical handling and manufacturing skills · Accurately and legibly record information related to the manufacturing operation · Perform limited in-process inspection tests in support of the manufacturing operation · Participate in the management of on-site hazardous waste activities · Continuously consider personal and site-wide safety requirements · Respond to chemical-related incidents, including spills, accidents, and emergencies, and participate in investigations to identify root causes and prevent future incidents · Contribute to continued improvement of the DMI quality management system (based on ISO9001:2015) _The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job._ _Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. _ · Stand or walk for long periods of time; sit; use fingers to make small equipment adjustments; reach with hands and arms; and talk or hear. · The employee must regularly lift and/or move items up to 55 pounds and occasionally lift and/or move up to drum quantities using supplied equipment. · Specific vision abilities required by this job include close vision, distance vision, ability to adjust focus, and the ability to distinguish color change. _While performing the duties of this job, the employee;_ · Will handle hazardous chemicals · May be exposed to fumes or airborne particles · Is required to wear the appropriate PPE equipment while handling, mixing, transporting, and packaging chemicals and materials · Will occasionally be in environments with moderate to high noise levels Job Type: Full-time Pay: $25.00 - $35.00 per hour Benefits: * Dental insurance * Health insurance * Paid time off * Retirement plan * Vision insurance Work Location: In person
At Glanbia Nutritionals Inc., our portfolio centers on dairy and non-dairy nutritional ingredients. We co-innovate and deliver ingredient solutions and precision premixes for use in the mainstream food and beverage, infant and clinical, and functional nutrition markets. We are the number one provider of whey-based nutritional ingredients globally and the number one producer of American-style cheddar cheese. Our protein systems have transformed the bar and beverage categories — bringing increased levels of protein, cleaner labels and greater product functionality to market. We have a direct presence in 21 countries, with manufacturing facilities in the US, Germany and China, and international sales and technical offices around the world. Job Summary Responsible for the preparation, production and packaging of blend material. Provides assistance to the operator and fills in for basic operator duties as assigned. Maintain blend equipment and production area cleanliness. Must complete all applicable SOP and QA trainings. Compensation for roles at Glanbia varies depending on a wide range of factors including but not limited to the specific office location, role, skill set and level of experience. Glanbia provides a reasonable range of compensation for roles that may be hired in California. This range may not be applicable to other locations. The hourly rate for California based employees for this role is $21.12/hour + ($1.00 Shift Differential). Benefits Include: Medical, Dental, Vision, Prescription Drug Coverage, FSA, HSA, Life & Disability Insurance, Paid Time Off and 6% 401K match! Essential Functions Box Room duties - tape boxes, insert foil/plastic liners, apply labels to boxes Label bags, Zip tie liners, Tape filled boxes, Palletize boxes Hand clean separators, air flows, heat sealers, conveyors, scales, metal detectors Clean drains Prepare cell for wash - cover electronics, remove scan gun, apply appropriate LOTO Able to identify status of equipment and cell Operate hand jack and power jack (certified) Inspection of raw material and /or fill IBC Gather tools and supplies from tool room for blends or wash Operate conveyor metal detector, includes HACCP metal checks Basic Sampling / Aseptic Sampling Scale Check Scan in blends to NOAX Manufacturing and Inspection Cell Release Discharge blenders out of separator (not at line speed) Seal foil and plastic liners Able to assist the operator with all blending, milling, packing tasks Identify ingredient name, lot number and item number Operate High Pressure washer and Foamer Read and understand sequence of steps on BPR Screen, blend and package a variety of amino acids, vitamins and minerals, including those which are allergenic. Responsible for following the procedures for the preparation of blends and final blend product. Proper cleaning, blending, packaging and material inspection per Standard Operating Procedures. Proper cleaning of manufacturing equipment and production floor. Assist with routine maintenance on manufacturing equipment as requested by the Operator. Regular attendance is an essential function of this position. Following and living Glanbia values: Showing Respect, Winning Together, Finding a Better Way, Performance Matters, and Customers Champion. Each employee shall comply with occupational safety and health standards and all rules, regulations, and orders issued pursuant to the Occupational Safety and Health Act which are applicable to his/her own actions and conduct. Complies with all applicable food safety regulations and mandates Additional Functions Perform other duties as assigned Qualifications High School Diploma or GED preferred. Ability to work with amino acids, vitamins and fine chemicals in powder and liquid form as well as allergen products. Ability to follow direction and work with Standard Operating Procedures. Must be able to work flexible hours to include overtime and weekends on short notice Clear command of the English language both verbal and in writing. Basic computer knowledge. Typical Physical Activity Physical Demands The physical demands described represent those that must be met by an employee and the work environment characteristics are those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. · Regularly involves talking or listening, sitting, and the use of hands and fingers. · Regularly involves going up and down stairs. · Frequently involves reaching with hands and arms, standing and walking. · Occasionally involves crouching, stooping, kneeling and/or climbing or balancing. Physical Requirements Must be able to lift and carry items weighing up to 55 pounds. Manual dexterity sufficient to reach/handle items, works with the fingers, and perceives attributes of objects and materials. Involves moderate physical activity performing non-strenuous daily activities of a primarily administrative nature. Should be able to identify and distinguish colors, see clearly at 20 inches or closer and 20 feet or more, observe an area that can be seen up and down or to the left and right while eyes are fixed on a given point, judge distances and spatial relationships, and adjust the eye to bring an object into sharp focus. Typical Environmental Conditions May be exposed to moderate noise levels (i.e. office equipment, light traffic). May be exposed to moderate to high noise levels (i.e. production equipment, forklifts, heavy traffic). May be exposed to humidity, intense heat and cold, outdoor weather conditions, and fumes and toxic chemicals. May work in areas with mechanical moving parts, above ground with risk of fall, or areas with risk of electrical shock. Travel Requirements N/A Disclaimer Must perform the essential duties and responsibilities with or without reasonable accommodation efficiently and accurately without causing significant safety threat to self or others. The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and/or skills required of all personnel so classified. At Glanbia, we celebrate diversity, because we know that our individual strengths make us stronger together. We welcome and encourage interest from a wide variety of candidates, and we will give your application consideration, without regard to race, color, religion, sex, sexual orientation, gender perception or identity, national origin, age, marital status, protected veteran status, or disability status. At Glanbia our culture will celebrate individuality, knowing that together we are more.