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Welcome to Gelson’s! For over 70 years, Gelson’s has served Southern California shoppers with an enthusiasm for food of the highest quality. Our commitment to quality, selection and exceptional service sets us apart. We strive to exceed our customers’ expectations with every visit, and we take pride in creating a positive shopping experience. Come join the Gelson’s team and help us continue our tradition of excellence in grocery retail. Why work with us: Be part of a dynamic team that values collaboration and innovation Showcase your leadership skills and make an impact on your store’s success Embrace a culture that prioritizes customer satisfaction and team excellence We are a certified “Great place to work” in California for the third consecutive year Benefits: We offer competitive union wages Employee discounts Generous union benefits and retirement plans Opportunities for career growth and development Responsibilities: As a Kitchen production team member at Gelson’s, you will play a key role in supporting the daily operations of Gelson’s kitchen department. You will prepare food products according to Gelson’s recipes and high quality standards. Your responsibilities will include, but are not limited to: Prepare and present various items including salads, sandwiches, pizzas, pasta, dressings, entrees, and all catering offerings. Prepare both salad production from scratch as well as finishing previously prepared items. You will prepare proteins, entrees, and side dishes that may include baking, frying, grilling, roasting, and steaming. You must display a clear understanding of all cooking techniques and terminologies and monitor food quality to ensure Gelson’s standards. Monitor product quality, freshness, presentation, and ensure proper rotation of merchandise in accordance with store policy. Support the kitchen department staff, ensuring a positive and collaborative work environment. Provide excellent customer service and respond appropriately in all customer interactions. Ensure compliance with company policies, procedures, and health and safety regulations. Embrace new challenges and be a flexible team player, taking on responsibilities as needed. Other duties and responsibilities as required. Qualifications: High school diploma or equivalent Previous experience in a grocery retail setting preferred. Superior knife skills and strong working knowledge of food service operations. Strong organizational and multitasking skills. Excellent communication and interpersonal abilities. Flexibility to work a varied schedule, including evenings, weekends, and holidays. Physical requirements: Continuous hand manipulation including, grasping, pushing, pulling and fine manipulation Reaching above and at shoulder level frequently Standing up to 8 hours per day Lifting and carrying up to 50 lbs. frequently Working near hazardous machinery (Slicer, mixer, knives) Walking on uneven ground (Floor mats) Exposure to dust, gas, fumes (Oven, stove) Exposure to noise (Mixers, food processor) Exposure to extremes in temperature (Deli coolers, freezer, ovens) How to Apply: Apply today and take the first step toward a rewarding career with one of Southern California’s most respected grocery chains. We are committed to fostering a friendly and inclusive work environment. Gelson’s is an equal opportunity employer and encourages individuals from all backgrounds to apply. Union pay range: $18.48 - $22.50 Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
We are hiring a Manufacturing Engineering Technician to join our Manufacturing Engineering team! DISCOVER Are you passionate about improving processes and driving efficiency? As a Manufacturing Engineering Technician, you’ll be at the heart of our production operations—helping transform ideas into reality. In this role, you’ll support engineers in implementing and optimizing manufacturing processes, tools, and equipment that keep our products moving from concept to completion. You’ll troubleshoot technical challenges, validate new technologies, and ensure every step meets our high standards for quality, safety, and performance. Your work will directly impact how we deliver exceptional products to customers around the world. YOUR RIPPLE EFFECT Do you enjoy solving problems on the production floor? Assist in troubleshooting and resolving technical issues to minimize downtime and product rejection. Are you detailed and process-driven? Help create and maintain documentation such as SOPs, Work Instructions, BOMs, and validation reports. Do you thrive in hands-on environments? Support the design and validation of tooling and equipment, including mechanical fixtures and alignment tools. Are you curious about automation and innovation? Contribute to implementing new technologies that enhance manufacturing capabilities through automation and process programming. Do you value collaboration? Work closely with engineers, vendors, and cross-functional teams to ensure quality and efficiency across the product lifecycle. Are you ready to expand your impact? Travel regularly to our Tijuana, MX locations to support manufacturing initiatives. WHAT YOU BRING Two years of experience with robotics/programming (Engineering degree not required but valued)Experience with production fabrication and assembly processesProficiency in Microsoft Office Suite (Word, Excel, PowerPoint, MS Project, Visio)Knowledge of AutoCAD and SolidWorks is a plusStrong communication skills and ability to present to peers and leadershipComfortable collaborating with vendors and working independently with minimal supervisionAbility to communicate in basic Spanish for collaboration with Spanish-speaking team members WHAT YOU’LL GET At Watkins Wellness, we believe that everyone should ‘Feel good. Live well’. We offer employees the opportunity to join a dynamic, growing industry leader with an outstanding and well-deserved reputation for leadership and commitment to our employees, customers and community. Our employees are eligible to receive exceptional health and wellness benefits, paid time off, company bonus, profit sharing, 401k match, education assistance, and much more. We are proud of the people we are and the products we make — products that make a difference to the health and well-being of others. We look for candidates that exhibit The Watkins Way (always Ethical, endeavors to be Transparent, embraces Inclusion, welcomes Diverse backgrounds and perspectives, Accommodating, believes in Work-Life Balance, puts Safety First, Accountable, values Relationships, Passionate, Team Player, and Goal Driven). The employee must frequently lift and move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, color vision, peripheral vision and depth perception. The noise level in the work environment is usually quiet. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire We offer competitive compensation determined by each individual's relevant experience, skills and education. Hiring Range: $25-$40 hr. Many factor are taken into consideration in determininig pay, including education and location Company: Watkins Manufacturing Shift 1 (United States of America) Full time Watkins (the “Company”) is an equal opportunity employer and we strive to employ the most qualified individuals for every position. The Company makes employment decisions only based on merit. It is the Company’s policy to prohibit discrimination in any employment opportunity (including but not limited to recruitment, employment, promotion, salary increases, benefits, termination and all other terms and conditions of employment) based on race, color, sex, sexual orientation, gender, gender identity, gender expression, genetic information, pregnancy, religious creed, national origin, ancestry, age, physical/mental disability, medical condition, marital/domestic partner status, military and veteran status, height, weight or any other such characteristic protected by federal, state or local law. The Company is committed to complying with all applicable laws providing equal employment opportunities. This commitment applies to all people involved in the operations of the Company regardless of where the employee is located and prohibits unlawful discrimination by any employee of the Company. Watkins is an E-Verify employer. E-Verify is an Internet based system operated by the Department of Homeland Security (DHS) in partnership with the Social Security Administration (SSA) that allows participating employers to electronically verify the employment eligibility of their newly hired employees in the United States. Please click on the following links for more information. E-Verify Participation Poster: English & Spanish E-Verify Right to Work Poster: English & Spanish
San Diego, CAManufacturing – Manufacturing /Full Time /On-Site With extensive experience in developing biologics and bioconjugates, we offer a seamless service delivered by fully integrated teams, from early discovery to commercial manufacturing. Forward-thinking and committed, we find the best solution and use the right technologies to design, develop and manufacture your products to ensure we get vital medicines to patients quickly and safely. We are dedicated to quality excellence. We are driven to get better treatments to market, efficiently and responsibly by reducing timelines and delivering the highest quality products and services. We are Abzena. More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient. As a member of the manufacturing team at Abzena, you will be responsible for executing daily task in strict compliance with manufacturing batch records, SOP’s, and Good Manufacturing Practices (GMP). You will take ownership of the production process, facility, and environment to ensure smooth operations. Additionally, you will collaborate cross-functionally with key departments, including QA, MS&T, Facilities, and others to support successful and compliant manufacturing activities and responsibilities. Responsibilities Operate under cGMP manufacturing conditions. Ensure compliance to training on all activities prior to GMP execution. Adhere to appropriate gowning procedures required for working in Class 10,000 and Class 100,000 cleanrooms. Perform operations in a bio-safety cabinet using aseptic technique and maintain asepsis of all closed container sterile processes. Ensures right-the-first-time performance of all process steps. Perform production activities including depth filtration, purification by affinity, ion exchange, and hydrophobic interaction chromatography, viral inactivation and filtration, tangential flow filtration, sterile filtration, and bulk drug substance fills. Escalate process related issues as they arise Inventory manufacturing lab supplies and ensure items are properly stocked. Participate in batch readiness activities such as general planning and coordination, material requests and transfer, and material and equipment staging. Maintain cleanroom standards for cleanliness and order Conduct activities in support of production schedules as directed by senior staff. Work effectively and efficiently in a team environment. Support multiple projects simultaneously. Crosstrain on various tasks including autoclaving of assemblies, formulation of buffers, and Downstream operations to support overall success of the Biologics group. Perform manufacturing and process development activities for projects and products in collaboration with others. Review GMP records for completeness, accuracy, and compliance on a daily basis in conformance with regulatory requirements. Review manufacturing SOPs, master batch records, specifications, and other applicable cGMP documentation. Adhere to quality standards set by regulations and Abzena policies, procedures, and mission. Operate to the highest ethical and moral standards. Adjust to a flexible work schedule including weekend work, as needed. Perform additional duties as assigned. Qualifications A minimum of 2 years of experience in a GMP pharmaceutical/biotech environment role with a technical degree or equivalent combined years of both. Demonstrate knowledge and understanding of cGMPs and how they apply to responsibilities. Experience with aseptic handling, including BSC operations to maintain the integrity of sterile systems. Knowledge of purification using column chromatography Experience using single-use technologies, such as tube welding, tube sealing, and disposable systems A proven ability to confidently compute basic arithmetic operations. Physical Requirements Ability to sit or stand for extended periods of time. Frequently lift and or move objects at least 50 pounds in weight. Ability to gown aseptically Use arms, hands and fingers to handle, feel or reach. Ability to climb, balance, stoop, kneel, crouch, or crawl. Visual abilities including near and far sight, color, peripheral vision, depth and ability to focus. $70,000 - $90,000 a year FLSA: Non-Exempt Abzena is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, and training.
At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections, where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters. The Position A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche. As a Principal Validation Engineer you will lead high-impact validation projects across equipment, facilities, and utilities within a cutting-edge regulated environment. In this role, you’ll write and execute IQ/OQ/PQ protocols, guide complex cross-functional initiatives, and apply Lean and Six Sigma principles to drive continuous improvement. You’ll work closely with cross functional stakeholders, while also mentoring junior team members and helping shape validation strategy from concept through execution. The Opportunity Writes and executes Equipment, Facility, and Utilities Installation/Operational/Performance Qualifications (IQ/OQ/PQ) protocols on a variety of facility and manufacturing process equipment and analytical testing equipment in a full Biotech upstream/downstream manufacturing plant. Qualification includes conception of qualification assessments, (basic to complex) protocol strategy, authoring protocols, execution, and final report writing. Leads and provides qualification and validation support to complex and/or multinational projects in his/her assigned area. Participates and leads project planning, qualification/validation scheduling, process updates, and experimental design. Assumes responsibility for timely completion of projects or assigned work, ensuring activities are consistent with project critical path and responding appropriately to changing priorities. Deep technical knowledge of qualification of equipment, facilities, and utilities. Conceives, plans and conducts independent qualification/validation work or project work from inception through product launch and field support, defining schedules, and applying qualification or validation strategy that is robust and agile to complete projects. Apply Program Management tools to define and monitor project timelines, ensuring timely achievement of overall project goals and establishing priorities that are in line with the overall business needs. Utilizes Continuous improvement/Lean/Six Sigma manufacturing concepts to improve processes. Provides technical advice/guidance to junior scientific staff and leads project teams to solve business problems of moderate size risk and complexity and serves as an overall role model. Serves as an expert resource to other departments (e.g., Manufacturing/Operations, Development, Quality, Regulatory Affairs, and Technical Services), provides timely response and follow-ups. Who you are You have a Bachelor's degree in an Engineering, Engineering Technology, or Life Science discipline. A Master's degree in one of these fields is preferred. You have 6+ years of relevant industry experience in Equipment and/or Facility Validation. 7+ years of experience is preferred. We will consider an equivalent combination of education and experience. A Master’s degree in Engineering may qualify with 6 or more years of experience in complex mechanical or chemical systems development and validation. Knowledge, Skills and Abilities Solid understanding in the manufacture of assays, reagents and instruments as well as Verification and Validation principles, practices and tools used in that transfer. Proven ability to work on complex problems with analysis of situations or data towards successful outcomes. Demonstrated ability to apply Lean and 6 Sigma methodology in all that you do and a passion to drive It throughout the organization Proven ability to contribute and interact productively and collaboratively with project teams. Excellent verbal communication skills required. Excellent interpersonal skills required to interact with stakeholders such as system owners, quality assurance, and auditors. Excellent technical writing skills required. Studies, protocols, reports, deviations, and non-conformances must be written in a clear, structured manner directed to reviewers in an FDA regulated environment. The candidate must be a self-starter with the ability to work with minimal supervision in a fast paced environment. The candidate must have the ability to prioritize and manage multiple projects and priorities. The candidate must be a team player, willing to help others and cross train them as necessary. Permits/ Permits/Licenses and Certifications ASQC Certified Quality Engineer is a plus ISPE Certified Pharmaceutical Industry Professional (CPIP) is a plus. Relocation benefits are available for this posting The expected salary range for this position based on the primary location of California is $83,230 -$153,400 annual. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below. Benefits Who we are GenMark is now a proud member of the Roche Group, more than 100,000 people across 100 countries are pushing back the frontiers of healthcare. As a global leader in healthcare, Roche Diagnostics offers a broad portfolio of products, tools and services that help in the prevention, diagnosis and management of diseases like HPV, HIV, hepatitis and diabetes as well as other medical conditions, such as fertility and blood coagulation. With the addition of GenMark to the Roche Group, syndromic infectious disease diagnostics is now added to the long list of disease states and conditions that the Roche Group addresses. GenMark’s ePlex true sample-to-answer system offers unique solutions to address the most significant challenges facing clinical laboratories, while supporting hospital systems to deliver patient-centered, value-based care. ePlex streamlines the diagnostic workflow from physician order entry to the final test report and is the true sample-to-answer solution designed to improve patient care, reduce costs, and increase lab efficiency. GenMark is headquartered in Carlsbad, California. GenMark is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.
*Manufacturing Chemist I* *Location:* Carlsbad, CA *Schedule:* Monday – Friday (Full-Time; hours to be agreed upon between employee and People Leader) *Compensation:* $57,000 – $65,000 annual base salary (determined by experience, skills, and internal equity) *Classification:* Non-Exempt *About Lumos Diagnostics* Lumos develops, manufactures, and distributes innovative diagnostic products — delivering actionable information, in real time, at the point of care. Our Manufacturing team plays a vital role in ensuring every diagnostic product we produce is reliable, consistent, and ready to make a difference in patients’ lives. We’re proud of our culture, built on our *TEAM values*, which guide how we work and lead every day: *Take Ownership* – accountability and follow-through *Engage Openly* – communication and feedback *Act with Integrity* – ethics and compliance *Move Together* – teamwork and collaboration When you join Lumos, you’re joining a company that values curiosity, collaboration, and excellence — where your work directly contributes to improving healthcare outcomes. *About the Role* We are seeking a *Manufacturing Chemist I* to join our team in Carlsbad, CA. This hands-on role supports the development, optimization, and production of reagent and buffer formulations used in Lumos’s diagnostic products. Working under ISO 13485 and cGMP standards, the Manufacturing Chemist I bridges laboratory development and full-scale manufacturing by preparing bench-scale batches, performing analytical and stability testing, and documenting results with precision. This position is ideal for candidates early in their chemistry or life sciences career who want to gain experience in a regulated diagnostic manufacturing environment. *Key Responsibilities* * Prepare reagent and buffer formulations according to established procedures and specifications. * Conduct laboratory testing (e.g., pH, viscosity, appearance, stability) to ensure quality and consistency. * Support process transfer and scale-up activities from lab to manufacturing production. * Maintain accurate documentation of formulations, test data, and batch records in compliance with ISO 13485 and cGMP standards. * Assist in troubleshooting formulation or process issues in collaboration with Manufacturing, R&D, and Quality teams. * Follow all safety, environmental, and quality system procedures. * Maintain a clean and organized laboratory environment. *What We’re Looking For* *Minimum Qualifications* * Bachelor’s degree in *Chemistry, Biochemistry, Chemical Engineering, or related scientific discipline.* * 0–2 years of experience in formulation, analytical testing, or laboratory/manufacturing support. * Basic understanding of chemistry principles and analytical methods. * Knowledge of *ISO 13485* and *cGMP* standards preferred. * Excellent documentation and organizational skills with high attention to detail. * Ability to collaborate effectively in a team environment and communicate clearly. * Proficiency with Microsoft Office applications (Word, Excel, Outlook). *Preferred Qualifications* * Hands-on experience with reagent or buffer formulation. * Exposure to design transfer, process validation, or scale-up from lab to manufacturing. * Experience in diagnostics, medical device, or life sciences manufacturing. *Why Join Lumos Diagnostics?* * Be part of a mission-driven company improving healthcare through innovation. * Work in a culture guided by integrity, accountability, and collaboration. * Comprehensive benefits package including medical, dental, vision, life insurance, disability coverage, 401(k) with employer match, paid vacation, and holidays. * Contribute to meaningful work that directly supports patient care and product excellence. *How to Apply* To be considered for this position, please submit your resume and ensure all application questions are fully answered. Incomplete applications may not be reviewed. Job Type: Full-time Base Pay: $57,000.00 - $65,000.00 per year Benefits: * 401(k) matching * Dental insurance * Employee assistance program * Employee discount * Flexible schedule * Flexible spending account * Health insurance * Health savings account * Paid time off * Parental leave * Professional development assistance * Referral program * Tuition reimbursement * Vision insurance Application Question(s): * This is a full-time, on-site position located in Carlsbad, CA, with a Monday–Friday schedule. Are you available to work on-site during regular business hours? * The annual base salary range for this position is $57,000 – $65,000, determined by experience, skills, and internal equity. Are you comfortable with this compensation range? * Do you have 0–2 years of formulation, analytical testing, or laboratory/manufacturing experience? * Are you familiar with Good Manufacturing Practices (cGMP) or ISO 13485 requirements? * Do you have experience preparing or handling chemical reagents, buffers, or formulations in a laboratory or production setting? * Are you proficient in Microsoft Office applications (Word, Excel, Outlook) and comfortable learning new laboratory software systems? * This role involves preparing chemical solutions, reagents, and buffers according to written procedures. Do you have experience accurately measuring, mixing, or preparing chemical formulations in a laboratory environment? * Have you ever worked with pH meters, balances, or other common lab equipment used in chemical or reagent preparation? Education: * Bachelor's (Required) Ability to Commute: * Carlsbad, CA 92010 (Required) Ability to Relocate: * Carlsbad, CA 92010: Relocate before starting work (Required) Work Location: In person
Company Description Founded in 1978, California Closets has built a reputation as the leader and design authority in premium space management, delivering custom-designed organizational solutions and exceptional service. We believe home is more than just a place — it should be a source of creativity, comfort, and connection. From beautiful walk-in closets and entertainment centers to versatile pantries and home offices, we design custom storage solutions that add value to your life and home by making space for what belongs. Think of it as ‘practical magic.’ Job Description The Installation Tech installs custom designed residential storage systems and accessories using a variety of luxury materials. A successful candidate will have experience with hand and power tools, measurements and the ability to provide exceptional customer service to our clients. What We Offer: Hourly Rate from $20.00 to $20.99 DOE Health insurance PTO days, paid holidays, and sick days 401K retirement plan Transportation from Company’s location to and from customer job sites will be provided Company tools and PPE provided Day shift hours Grow your career with us – many promotional opportunities available Working with luxury products and 100% custom builds Duties and Responsibilities: Perform skilled and semi-skilled carpentry work to install custom storage systems such as closets, cabinets, offices, and other spaces in the home or commercial buildings. Utilize company-provided CAD drawingsblueprints to install systems properly and efficiently. Assemble and install systems of varying complexity. Assists in the removal and installation of materials in customer homes. Maintain shop tools and equipment in safe working order (tools are provided). Install systems independently or with team members depending on the size of the job. Provide a high level of customer service for in-home installations. Maintain safety standards at all time. Responsible for driving to and from customer sites and operating a company-provided vehicles in a safe manner. Perform other duties and responsibilities as assigned by the supervisor. Qualifications Must maintain a valid driver's license and clean driving record High School diploma or equivalent Experience with common hand and power tools Trade or vocational school experience desirable Cabinetry or carpentry skills desirable Strong verbal and written communication and listening skills Able to walk, lift 50 pounds, reach, stoop, stand, grasp, balance, climb stairs, kneel, and crouch Additional Information Find us on Facebook, YouTube, and Instagram We are an equal opportunity employer. We E-Verify. All your information will be kept confidential according to EEO guidelines. CA Privacy Policy - California Privacy Policy - California Closets Terms and Conditions: https://www.californiaclosets.com/terms-conditions/
About Us We are a leading designer and manufacturer of subsea thrusters and propulsion systems for marine and underwater applications. Our products are engineered for reliability and performance in challenging environments, with a strong focus on quality, innovation, and precision. We operate in a low-volume, high-mix manufacturing environment where adaptability and problem-solving are key to success. Position Overview We are seeking a hands-on Production Manager to lead our electro-mechanical assembly team and ensure timely, high-quality production of our subsea thrusters and related systems. This role requires a proactive leader who can balance day-to-day operations with continuous improvement initiatives. The ideal candidate will bring strong leadership, technical expertise, and organizational skills to a dynamic environment where many products are prototypes or first-of-a-kind builds. Key Responsibilities * Team Leadership & Management * Supervise, mentor, and develop a team of ~7 assemblers and technicians. * Plan, assign, and manage daily workloads to meet production schedules and delivery targets. * Foster a culture of accountability, teamwork, and continuous improvement. * Conduct regular performance check-ins and support employee development. * Production Planning & Execution * Coordinate production priorities based on customer demand, project timelines, and resource availability. * Ensure efficient flow of materials, tools, and documentation through all stages of assembly and test. * Monitor and report on production metrics such as throughput, yield, and on-time delivery. * Process Development & Documentation * Create and maintain detailed production work instructions from engineering drawings, schematics, and models. * Develop standard operating procedures (SOPs) for assembly, integration, and testing. * Drive process improvements to enhance efficiency, quality, and repeatability. * Technical Problem Solving * Support and guide the team in troubleshooting electro-mechanical, hydraulic, and control system issues. * Collaborate closely with Engineering to resolve design and manufacturability challenges. * Lead root cause analysis and implement corrective/preventive actions for recurring issues. * Quality & Safety * Uphold high standards for workmanship, safety, and documentation. * Ensure compliance with internal quality procedures and customer requirements. * Promote a safe and organized work environment through regular audits and training. Required Skills & Experience * 5+ years of experience in production management or manufacturing supervision, ideally in low-volume, high-mix or prototype environments. * Strong background in electro-mechanical assembly, including wiring, soldering, mechanical fit-up, and testing. * Proven leadership experience with the ability to motivate, coach, and hold team members accountable. * Excellent organizational and multitasking skills to manage diverse products and priorities simultaneously. * Proficiency with computer tools, including ERP/MRP systems, Microsoft Office, and document control platforms. * Ability to interpret engineering drawings, schematics, and BOMs. * Experience with production planning, scheduling, and workflow optimization. * Strong problem-solving and troubleshooting capabilities with a hands-on approach. * Clear, professional communication skills for collaboration across departments (Engineering, Quality, Supply Chain, etc.). Preferred Qualifications * Knowledge or experience in the subsea, marine, or defense industry. * Experience with ISO 9001 or similar quality management systems. * Exposure to lean manufacturing principles or continuous improvement initiatives. * Familiarity with testing and validation of electro-mechanical systems. * Associate’s or Bachelor’s degree in Engineering, Manufacturing, or related technical discipline (or equivalent experience). Why Join Us * Opportunity to work on cutting-edge, high-performance subsea technologies. * A collaborative environment where innovation and hands-on problem-solving are valued. * Direct impact on production outcomes and product quality. * Competitive compensation and benefits package. Job Type: Full-time Pay: $80,000.00 - $110,000.00 per year Benefits: * 401(k) * Dental insurance * Flexible spending account * Health insurance * Health savings account * Life insurance * Paid time off Work Location: In person
*Quality Control Analyst* *Schedule:* Monday – Friday (Full-Time; hours to be agreed upon between employee and People Leader) *Compensation:* $75,900 – $86,200 annual base salary (determined by experience, skills, and internal equity) *About Lumos Diagnostics* Lumos develops, manufactures, and distributes innovative diagnostic products — delivering actionable information, in real time, at the point of care. Our Quality team plays a key role in ensuring every product we produce meets the highest standards of safety, accuracy, and compliance. We’re proud of our culture, built on our *TEAM values*, which guide how we work and lead every day: *Take Ownership* – accountability and follow-through *Engage Openly* – communication and feedback *Act with Integrity* – ethics and compliance *Move Together* – teamwork and collaboration When you join Lumos, you’re joining a company where quality, integrity, and teamwork drive everything we do. *About the Role* We are seeking a *Quality Control Analyst* to join our team in Carlsbad, CA. This role is responsible for performing inspections, laboratory testing, and documentation to ensure that raw materials, in-process materials, and finished products meet established specifications and quality standards. Working in a regulated ISO 13485 and FDA QSR environment, you’ll support product release activities, assist in investigations and audits, and help maintain our Quality Management System (QMS). This position requires attention to detail, analytical thinking, and a passion for continuous improvement in a fast-paced, collaborative setting. *Key Responsibilities* * Perform inspections and laboratory testing of raw materials, in-process materials, and finished products. * Generate and document non-conformance reports and support investigations. * Maintain quality metrics, data analysis, and trending to monitor product and process performance. * Participate in internal and external audits and regulatory inspections. * Assist in supplier quality monitoring and documentation review for accuracy and compliance. * Support complaint investigations and CAPA activities as assigned. * Contribute to the continuous improvement of the Quality Management System (QMS). *What We’re Looking For* *Minimum Qualifications* * Bachelor’s degree or equivalent relevant experience. * 2–4 years of quality control or laboratory experience in a regulated environment (medical device, biotech, or life sciences). * Strong understanding of cGMP, ISO 13485, and FDA Quality System Regulations. * Excellent documentation skills and attention to detail. * Proficiency with Microsoft Office and general lab or database software. * Strong organizational and communication skills. *Preferred Qualifications* * Experience supporting CAPA, internal audits, validation, or supplier quality processes. * ASQ certifications (CQI, CQA, or similar) are a plus. *Why Join Lumos Diagnostics?* * Be part of a mission-driven company improving healthcare through innovation. * Work in a culture guided by integrity, accountability, and collaboration. * Comprehensive benefits package including medical, dental, vision, life insurance, disability coverage, 401(k) with employer match, paid vacation, and holidays. * Contribute to meaningful work that directly supports patient care and product excellence. *How to Apply* To be considered for this position, please submit your resume and ensure all application questions are fully answered. Incomplete applications may not be reviewed. Job Type: Full-time Base Pay: $75,900.00 - $86,200.00 per year Benefits: * 401(k) matching * Dental insurance * Employee assistance program * Employee discount * Flexible schedule * Flexible spending account * Health insurance * Health savings account * Life insurance * Paid time off * Parental leave * Professional development assistance * Referral program * Tuition reimbursement * Vision insurance Application Question(s): * Do you have 2–4 years of quality control or laboratory experience in a regulated environment such as medical device, biotechnology, or life sciences? * Do you have experience performing quality control inspections, analytical testing, or in-process evaluations under cGMP or ISO-regulated conditions? * Are you familiar with ISO 13485, ISO 9001, or FDA Quality System Regulations (QSR)? * Are you proficient in Microsoft Office applications (Word, Excel, Outlook) and comfortable learning laboratory software or databases? * Have you previously worked in a regulated ISO 13485 or FDA-controlled laboratory or manufacturing environment? * Are you experienced in maintaining accurate documentation and following Standard Operating Procedures (SOPs)? Education: * Bachelor's (Required) Ability to Commute: * Carlsbad, CA 92010 (Required) Ability to Relocate: * Carlsbad, CA 92010: Relocate before starting work (Required) Work Location: In person
With extensive experience in developing biologics and bioconjugates, we offer a seamless service delivered by fully integrated teams, from early discovery to commercial manufacturing. Forward-thinking and committed, we find the best solution and use the right technologies to design, develop and manufacture your products to ensure we get vital medicines to patients quickly and safely. We are dedicated to quality excellence. We are driven to get better treatments to market, efficiently and responsibly by reducing timelines and delivering the highest quality products and services. We are Abzena. More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient. As a member of the manufacturing team at Abzena, you will be responsible for executing daily task in strict compliance with manufacturing batch records, SOP’s, and Good Manufacturing Practices (GMP). You will take ownership of the production process, facility, and environment to ensure smooth operations. Additionally, you will collaborate cross-functionally with key departments, including QA, MS&T, Facilities, and others to support successful and compliant manufacturing activities and responsibilities. Responsibilities Operate under cGMP manufacturing conditions. Ensure compliance to training on all activities prior to GMP execution. Adhere to appropriate gowning procedures required for working in Class 10,000 and Class 100,000 cleanrooms. Perform operations in a bio-safety cabinet using aseptic technique and maintain asepsis of all closed container sterile processes. Ensures right-the-first-time performance of all process steps. Perform production activities including depth filtration, purification by affinity, ion exchange, and hydrophobic interaction chromatography, viral inactivation and filtration, tangential flow filtration, sterile filtration, and bulk drug substance fills. Escalate process related issues as they arise Inventory manufacturing lab supplies and ensure items are properly stocked. Participate in batch readiness activities such as general planning and coordination, material requests and transfer, and material and equipment staging. Maintain cleanroom standards for cleanliness and order Conduct activities in support of production schedules as directed by senior staff. Work effectively and efficiently in a team environment. Support multiple projects simultaneously. Crosstrain on various tasks including autoclaving of assemblies, formulation of buffers, and Downstream operations to support overall success of the Biologics group. Perform manufacturing and process development activities for projects and products in collaboration with others. Review GMP records for completeness, accuracy, and compliance on a daily basis in conformance with regulatory requirements. Review manufacturing SOPs, master batch records, specifications, and other applicable cGMP documentation. Adhere to quality standards set by regulations and Abzena policies, procedures, and mission. Operate to the highest ethical and moral standards. Adjust to a flexible work schedule including weekend work, as needed. Perform additional duties as assigned. Qualifications A minimum of 2 years of experience in a GMP pharmaceutical/biotech environment role with a technical degree or equivalent combined years of both. Demonstrate knowledge and understanding of cGMPs and how they apply to responsibilities. Experience with aseptic handling, including BSC operations to maintain the integrity of sterile systems. Knowledge of purification using column chromatography Experience using single-use technologies, such as tube welding, tube sealing, and disposable systems A proven ability to confidently compute basic arithmetic operations. Physical Requirements Ability to sit or stand for extended periods of time. Frequently lift and or move objects at least 50 pounds in weight. Ability to gown aseptically Use arms, hands and fingers to handle, feel or reach. Ability to climb, balance, stoop, kneel, crouch, or crawl. Visual abilities including near and far sight, color, peripheral vision, depth and ability to focus. FLSA: Non-Exempt Abzena is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, and training.
Since 1980, NAI has been a leader in nutritional health, bringing whole food-based supplements to a global population. NAI is a leading expert and manufacturer of dietary supplements, and we are involved in every facet of the industry, including research, development, manufacturing and marketing and advocacy. As a company, we continue to grow with manufacturing locations in Vista and Carlsbad, CA. We are looking for seasoned and entry level candidates that are interested in working for a global company with opportunities for growth, development, competitive pay and benefits. 3rd Shift 11:00 PM to 7:00 AM Summary Primarily responsible to produce blends as required in order to satisfy quality, manufacturing and customer requirements. This position represents a critical process in the production cycle and attention to detail is a requirement. Essential Duties & Responsibilities Under general supervision, performs duties associated with processing technologies in manufacturing operations involved with blending or mixing of ingredients. By end of orientation period, must be able to competently and safety operate equipment associated with blending operations. Follows batch record instructions, Standard Operating Procedures, and training manuals. Accurately completes required paperwork and documentation, including basic math calculations such as % yield and tare weight. Monitors and inspects product quality during processing. Disassembles, cleans, sanitizes, and reassembles equipment. Able to adjust functional parts and instrument controls. Reports process or equipment problems to supervisor; performs minor or basic troubleshooting. Cleans and maintains processing rooms and equipment. Attends all company training sessions. Meets performance standards for quality, productivity, reliability, initiative, safety, and work relationships. Carries out all responsibilities in compliance with the organization’s policies, procedures, and state, federal, and local laws. Fully complies with current Good Manufacturing Practices (cGMP’s) and health and safety regulations. Other Duties Operation of auxiliary equipment such as Fitzmill and screeners when required during the process. Verifies and checks off all materials against batch record before loading blender. Loading of raw materials into blenders and unloading when batches are blended. Weigh drums of blended material and record weights on batch record. Completes any paperwork necessary (e.g., batch records (yields), drum labels, etc.) Clean blenders after processing and maintain a clean and organized work area. Other duties as required. May be required to assist in other departments to support workload. Qualifications Required: High school diploma or GED At least one year of manufacturing/packaging work experience; knowledge of cGMP’s preferred. Ability to speak, read, write and understand English fluently. Must have neat and legible handwriting and be highly accurate in recording on process documents. Must have good math computation skills and able to use a calculator. Knowledge of and competency with using metric measurements. Ability to execute the established procedures required in the Blending process. Must have mechanical aptitude and be able to react to machine and equipment requirements. Must be able to work well as a team member with all departments within the company. Physical Demands While performing the duties of this job, the employee is regularly required to walk; use hands or fingers, handle, or feel; reach with hands and arms; stoop and kneel; talk and hear. The employee is frequently required to sit and stand. Specific vision abilities required by this job include close vision, color vision, peripheral vision, depth perception, and the ability to adjust and focus. Lifting requirement: Up to the maximum safety-recommended 50 pounds The physical demands are representative of those that must be met by employee to successfully perform the essential functions of this job. Reasonable accommodations may be made upon request to enable individuals with qualified disabilities to perform the essential functions of the job. Benefits Medical plan options - Two HMO and one PPO Dental, vision, life insurance and other voluntary benefit options. 3 weeks' vacation and 11 paid holidays 401k including company matching and profit sharing $1,000 Employee Referral Bonus Quarterly employee lunches, Employee of the Month and other recognition programs Opportunities for advancement Comprehensive training Tuition Reimbursement and more! NAI is an Affirmative Action/Equal Opportunity Employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, physical or mental disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. Upon a conditional offer of employment, a satisfactory completion of a background check (including criminal records check) with submission and passing a pre-employment post offer drug test is required prior to beginning employment. Any offer of employment may be rescinded if the background check reveals disqualifying information, and/or it is discovered that the candidate knowingly withheld or falsified information. Failure to satisfactorily complete the background check may affect the continued employment of a current NAI employee who was conditionally offered the position. Upon successful completion of the background check process, we will determine the date when your employment begins. NAI utilizes E-Verify to electronically verify employment eligibility. Monday through Friday 11:00pm to 7:30am
Since 1980, NAI has been a leader in nutritional health, bringing whole food-based supplements to a global population. NAI is a leading expert and manufacturer of dietary supplements. We are involved in every facet of the industry, including research, development, manufacturing and marketing and advocacy. As a company, we continue to grow with manufacturing locations in Vista and Carlsbad, CA. We are looking for seasoned and entry level candidates that are interested in working for a great company with opportunities to grow, competitive pay and benefits. Summary Primarily responsible for the duties associated with the preparation process, weighing of raw materials and checking/verifying weights being performed in the Weighing operation. Essential Duties and Functions: Under general supervision, performs duties associated with weighing, or dispensing raw materials used for manufacturing operations. By end of orientation period, must be able to competently and accurately process batch orders. Follows batch record instructions, Standard Operating Procedures, and training manuals. Accurately completes required paperwork and documentation, including basic math calculations such as % yield and tare weight. Monitors and inspects product quality during processing. Disassembles, cleans, sanitizes, and reassembles equipment. Able to adjust functional parts and instrument controls. Reports process or equipment problems to supervisor; performs minor or basic troubleshooting. Cleans and maintains processing rooms and equipment. Attends all company training sessions. Meets performance standards for quality, productivity, reliability, initiative, safety, and work relationships. Carries out all responsibilities in compliance with the organization’s policies, procedures, and state, federal, and local laws. Fully complies with current Good Manufacturing Practices (cGMP’s) and health and safety regulations. Other Duties Responsible for checking the accuracy of scales at the beginning of each shift. Weighs raw materials into drums. Inputs amount of materials being weighed into computer. Performs weight checks as needed. Completes any paperwork necessary e.g., batch records, material prepping sheet, etc. Maintain a clean working environment in Production area. Other duties as required. May be required to assist in other departments to support workload. Qualifications High school diploma or GED; English literacy At least one year of manufacturing experience related to solid dosage technology; knowledge of cGMP’s preferred. Basic math computation skills using a calculator are required. The ability to speak, read, write, and understand English- verbal and written instructions, SOP's and batch records. Mechanical aptitude as demonstrated by to dissemble and reassemble machine for cleaning. Physical Demands While performing the duties of this job, the employee is regularly required to walk; use hands to finger, handle, or feel; reach with hands and arms; stoop and kneel; talk and hear. The employee is frequently required to sit and stand. Specific vision abilities required by this job include close vision, color vision, peripheral vision, depth perception, and the ability to adjust and focus. Lifting requirement: Up to the maximum safety-recommended 50 pounds The physical demands are representative of those that must be met by employee to successfully perform the essential functions of this job. Reasonable accommodations may be made upon request to enable individuals with qualified disabilities to perform the essential functions of the job. Work Environment Mainly manufacturing facility where exposed to computerized equipment, moving mechanical parts, forklifts, heavy pallets, moderate to loud noise level, and air-borne dust and powders. While working, will be required to wear various personal protective equipment (e.g., clothing, hair net, face mask, gloves, goggles, etc.). Benefits: Medical plan options – Two HMO and one PPO Dental, vision, life insurance and other voluntary benefit options. 3 weeks’ vacation and 11 paid holidays 401K including company matching and profit sharing $1,000 Employee Referral Bonus Quarterly employee lunches, Employee of Month and other recognition programs Opportunities for advancement Comprehensive training Tuition Reimbursement and more! NAI is an Affirmative Action/Equal Opportunity Employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, physical or mental disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. Following a conditional offer of employment, satisfactory completion of a background check (including criminal records check) is required prior to beginning employment. Any offer of employment may be rescinded if the background check reveals disqualifying information, and/or it is discovered that the candidate knowingly withheld or falsified information. Failure to satisfactorily complete the background check may affect the continued employment of a current NAI employee who was conditionally offered the position. 7 AM to 3:30 PM, Monday - Friday
Summary The Production Associate is responsible for plant operations and activities including shipping, receiving, packing, inventory, shipments and completing checks on equipment and products to ensure quality of production. The position is entry level and is expected to acquire skills and knowledge to perform advanced work through training and development. Position promotion levels will be commensurate with experience and cross training. Essential Duties and Responsibilities – general operations responsibilities that may include the following: Check and maintain stock levels, dispose of damaged or defective stock and communicate to supervisors. Check inbound and outbound freight for spec, location fill loads for correct DOT and valves. Load/Unload trucks via forklift - CDL required for forklift operation. Inspect product for compliance, quality assurance and proper markings, checking valves and pressure on inbound loads. Operate hand grinder, recovery and reclaim equipment and as required perform routine maintenance on equipment. Communicate with internal logistics team and coordinate with laboratory technicians on product specification quality controls. Perform hydrostatic testing on cylinders and complete testing logs. Filling and packaging refillable gas cylinders. Preparation and painting of cylinders. Packaging, pulling and processing orders – strapping, stickers, paperwork, pictures. Pulling orders – using forklift and/or pallet jack, palletizing, staging for shipment and entering orders on data entry processing system. May operate up 4 automated packing stations at a time. Record transactions in company proprietary systems/software. Research issues from orders and repair. Committed to safety at all times. Other duties may be assigned. Supervisory Responsibilities – This position has no supervisory responsibilities. FLSA designation – given technical roles and responsibilities and absence of a supervisory role this position has been determined to be non-exempt under FLSA standards. Education and Experience Ability to communicate in standard business style and grammar. Ability to work in different areas as needed. Ability to follow directions accurately. Computer skills a plus, but not required. Experience in working with hazardous / non-hazardous material. Experience with compressed gases a plus, but not required Proven working experience as a warehouse worker. High School Diploma or G.E.D. Basic math skills required. Thorough understanding of plant policies and procedures. Certificates, Licenses, Registrations - operator’s license required for forklift Physical Demands / ADA requirements Ability to perform work during prolonged standing for up to 8 hours; frequent bending, crouching, reaching, grasping, feeling and repetitive motion also required. Ability to perform functions during occasional climbing, kneeling, crawling, pushing, pulling and finger activities. Extensive movement of cylinders and some lifting between 30lbs-100lbs. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The standard working schedule is Monday through Friday, from 6:00 a.m. to 2:30 p.m., with occasional Saturdays as needed.