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*Machining Operator Level 1* Modus Advanced, Inc. *Location: *Carlsbad, CA *Pay: *$30/hour *Shift: *M-Th 7am-5:30pm *Position Overview* Join the Modus Advanced team as a Machining Operator Level 1 and play a critical role in supporting our mission to help partners accelerate the process of designing and manufacturing tomorrow's innovations. In this position, you'll operate precision CNC machines and manufacturing equipment to produce components that support life-saving medical devices, critical defense systems, and aerospace innovations. At Modus Advanced, one day matters. The precision components you'll machine often go into applications where reliability isn't just about performance—it's about protecting and saving lives. Your technical expertise and commitment to quality will directly impact our ability to deliver excellence to our customers. *Key Responsibilities* *Machine Operation and Control* ● Operate CNC machines including VMCs, HMCs, and 5-axis machining centers ● Set up and control machining processes according to specifications and work instructions ● Monitor machine operations to ensure optimal performance and quality output ● Perform routine machine maintenance and basic troubleshooting ● Adjust machine parameters as needed to maintain precision tolerances ● Follow all safety protocols and procedures during machine operation *Quality Control and Inspection* ● Perform in-process inspections using precision measuring tools and gauges ● Verify dimensional accuracy and surface finish requirements ● Identify and address quality issues promptly to prevent defective parts ● Work closely with Quality Control team to ensure parts meet specifications ● Document inspection results and maintain quality records ● Stop production when quality concerns are identified *Production Planning and Documentation* ● Interpret engineering drawings, work instructions, and router information ● Maintain accurate job traveler information and production records ● Coordinate with team members to optimize workflow and meet delivery schedules ● Participate in continuous improvement initiatives to enhance manufacturing processes ● Support development of new processes and procedures *Tooling and Fixture Management* ● Fabricate and assemble various types of tooling, jigs, and fixtures ● Modify existing tooling as required for specific applications ● Maintain cutting tools and replace as needed to ensure quality ● Organize and maintain clean, efficient work areas following 5S principles *Required Qualifications* *Education and Experience* ● Certificate in Machine Shop Technology, Machine Tool Technology/Machinist, or equivalent experience ● 1-2 years of experience in mechanical assembly preferred ● Recognized machinist apprenticeship may be required ● Ability to read, write, comprehend, and communicate in English; bilingual in Spanish preferred *Technical Skills* ● Knowledge of proper use of measuring tools, gauges, and cutting tools ● Understanding of GD&T, engineering drawings, models, and work routers ● Experience with CNC machine operation and setup ● Basic understanding of manufacturing principles and troubleshooting ● Proficiency with MS Office 365 ● Strong analytical and problem-solving abilities *Physical Requirements* ● Ability to stand for extended periods during machine operation ● Manual dexterity for handling precision components and tools ● Excellent eyesight (correction allowable) for detailed inspection work ● Ability to lift and move materials as required for production *Personal Attributes* ● Strong attention to detail and commitment to precision ● Self-motivated with ability to work independently ● Excellent communication and basic math skills ● Ethical behavior and commitment to excellence ● Ability to work on complex projects with minimal guidance ● Versatility and flexibility to adapt to changing priorities ● Strong organizational and analytical skills *What We Offer* *Comprehensive Benefits Package* ● Competitive salary commensurate with experience ● Health, dental, and vision insurance ● 401(k) retirement plan with company matching ● Paid time off and holiday pay ● Professional development opportunities ● Tuition reimbursement program *Growth Opportunities* ● Clear advancement path to Operator Levels 2, 3 and lead machinist roles ● Cross-training opportunities in other manufacturing processes ● Participation in continuous improvement initiatives ● Mentorship from experienced machinists and engineers ● Access to advanced CNC training and certifications *Work Environment* ● State-of-the-art machining center with modern CNC equipment ● Strong safety culture with comprehensive training programs ● Collaborative team environment with direct engineering support ● Opportunity to work on mission-critical projects for aerospace, defense, and medical device customers *Our Commitment to Excellence* At Modus Advanced, we maintain the highest standards of quality and precision. Our AS9100 and ISO 9001 certifications reflect our commitment to excellence in everything we do. As a Machining Operator Level 1, you'll be an integral part of maintaining these standards while supporting our customers' critical missions. We're looking for team members who understand that in our world, precision isn't just about meeting specifications—it's about enabling innovations that save and protect lives. Every component you machine could be the difference between success and failure in a life-critical application. Ready to join our team? Apply today and become part of a company that's accelerating tomorrow's innovations. Job Type: Full-time Pay: $30.00 per hour Benefits: * 401(k) * Dental insurance * Employee assistance program * Health insurance * Life insurance * Paid time off * Referral program * Retirement plan * Vision insurance Work Location: In person
*Responsibilities* * Operate Flexo press/ Digital Hybrid to produce jobs according to specifications. * Prepare the press for printing and die-cutting. * Load substrate, install tooling, mount plates, set print impression, and adjust the press. * Ensure that substrate, ink, and tooling meet required specifications. * Adjust ink distribution, speed, and temperature in the drying chamber. * Troubleshoot and correct print issues quickly to minimize downtime and material waste. * Perform routine maintenance, including oiling, cleaning, and minor repairs. *Requirements* * Must have proven experience operating a Mark Andy, Nilpeter, MPS, Omet, or other servo-driven narrow web press. * Team-oriented with excellent communication skills. Job Type: Full-time Pay: $25.00 - $38.00 per hour Application Question(s): * Can you operate Mark Andy, Nilpeter, MPS, Omet press ? * This job is for Second Shift 4pm-2:30 AM- Mon-Thursday. Are you Ok with this shift ? Work Location: In person
General Atomics Aeronautical Systems, Inc. (GA-ASI), an affiliate of General Atomics, is a world leader in proven, reliable remotely piloted aircraft and tactical reconnaissance radars, as well as advanced high-resolution surveillance systems. Under minimal supervision, this position is responsible for performing a variety of non-routine and non-repetitive assembly operations on electronic and /or mechanical assemblies and subassemblies. Determines and/or follows methods and sequence of operations in performing assembly tasks such as wiring, component installation, hand soldering and cable harnessing on assembly units. Makes continuity checks on work in process and completed work. May monitor and verify quality in accordance with control procedures. DUTIES & RESPONSIBILITIES: Assembles components, assemblies or sub-assemblies. Makes setups and adjustments holding tolerances to specifications. May perform duties as required in assembly of electronic equipment such as cables, harnesses, chassis, and printed circuit boards; or may perform mechanical assembly of panels, LRU's, batteries, and servo motors as it pertains to cable assembly. May disassemble, modify, rework, reassemble and test experimental/prototype assemblies or subassemblies according to specifications. Responsible for observing all laws, regulations and other applicable obligations wherever and whenever business is conducted on behalf of the Company. Expected to work in a safe manner in accordance with established operating procedures and practices. Completes Disposition on Nonconforming product when needed. Participates in production Integrated Process Team (IPT) Communicates/works with engineering and other support departments. Participates/runs weekly cell team meeting. Mentors team members in assigned cell. Assist team/assemblers in building and solving technical issues of cable assembly. Additional Functions: Performs 5S housekeeping and cleanup duties upon completion of assigned tasks Supports Clean-as-you-go cleanup duties during the shift. May train lower level assemblers or act as a lead and direct the work of others. Other duties as assigned or required. We recognize and appreciate the value and contributions of individuals with diverse backgrounds and experiences and welcome all qualified individuals to apply. 51588 Job Qualifications: Typical requires a high school diploma or equivalent and seven or more years experience. Must be customer focused and possess: The ability to read and interpret engineering drawing and wire lists. Extensive knowledge in specialized functions. A comprehensive understanding of the general and specific aspects and technical phase of the job and their practical to complex applications to intricate problems. Good knowledge of computer operations and applications pertinent to the position. Familiarity with use of soldering and compression connection tools. Good visual perception and ability to distinguish between colors. The ability to work independently or in a team environment is essential as is the ability to work extended hours as required. Ability to obtain and maintain DoD Security clearance is required. Salary:$52,020 - $77,325Travel Percentage Required 0 - 25Relocation Assistance Provided Not Provided US Citizenship Required? YesClearance Required? Desired Clearance LevelMid-Level (3-7 years) WorkstyleOnsite
*Responsibilities and Duties* · Lab works, including grind powders, cutting electrode, weighting electrode, calendaring electrode, etc. · Use your attention to detail to identify issues with equipment/materials, and help improve material/electrode processing steps · Follow SOPs to increase efficiency · Record work and keep data updated in an online database · Maintain a tidy and effective work area · Work collaboratively with other technicians, engineers, and scientists and effectively communicate results to troubleshoot, correct, and prevent issues · Execute small development projects in collaboration with scientists and engineers. *Knowledge and Skills Requirements* · Thrive in a fast-paced research and development environment working with multidisciplinary team and scientists · Laboratory experience that includes hands-on bench-top chemical handling and preparation · Two years of work experience in a fast-paced lab or manufacturing environment requiring high accuracy execution of processes or experiments; or 2 years of a technical degree. · Excellent organization and meticulous record-keeping skills · Proficiency with MS Office applications, particularly Excel and Outlook · Contribute to team efforts by accomplishing related results as needed · Able to read, comprehend, and perform standard operating procedures and work instructions *Physical Requirements and Working Conditions* · Ability to perform work using fume hoods on a daily basis with use of fine motor skills for extended periods of time, standing, reaching and twisting motions · Repetitive use of hands - light to forceful handling of material · Pass a respirator fit test and be able to wear respiratory protection on a daily basis · Wear personal protective equipment including, but not limited to, a lab coat, gloves, safety glasses, and steel toe safety shoes · Move items up to 50 lbs with the assistance of lift equipment and carts Job Type: Full-time Pay: $20.00 - $23.00 per hour Benefits: * 401(k) * 401(k) matching * Dental insurance * Health insurance * Paid time off * Parental leave * Vision insurance Work Location: In person
Become part of a team that champions wellness worldwide. CAPTEK® Softgel International is a global leader in the development and production of high-quality nutraceutical supplements. As a contract manufacturer organization (CMO), we collaborate with innovators from some of the world’s most successful brands. Summary: Quality Assurance Manager is responsible for the whole oversight of the Quality Assurance, and floor quality at both manufacturing and packaging sites. They are to appropriate, delegate, and review Quality Assurance operations and related tasks to ensure company's full Quality Assurance support as well as quality operational guidance and training to subordinate staff and other departments within the organization. They will need to ensure the quality assurance group in properly evaluating floor process quality systems and controls, investigations and dispositions, and any other quality needs to drive to quality product manufacture, processes, and systems. The individual will need to continually review and uphold company policies, procedures, and quality requirements required in the dietary supplement industry. Essential Duties and Responsibilities: • Manages all QA Supervisors, Assistant Supervisors, Leads, Technicians, and Document Control Specialists in both manufacturing and packaging facilities. This may include, but is not limited to, scheduling and coordinating work assignments for the department/shifts, along with planning and setting QA department goals and objectives, and respectively coordinating and directing QA department activities. • Per compliance to cGMP, Captek SOPs, and training, thoroughly reviews and verifies Quality Assurance systems and operations within the department and in application at floor, driving facilities' organizational quality. • Conduct departmental adherence, task, and/or job performance reviews which include developing and managing metrics to track and drive facilities' quality performance, respective appropriate actions for negative trend remediation, and for continual improvement. • Represents Captek's Quality Assurance operations as needed in customer and regulatory audits, meetings, qualifications, subsequent CAPA’s and/or any other such required instances. • As necessary, thoroughly reviews completed and/or prepared Quality Assurance documentation and dispositions or endorses appropriately upon verification of documentation as accurate, true, and complete. • Authors and/or reviews Quality Assurance related SOPS, while ensuring proper adherence to by subordinate Quality Control staff. • Perform and/or coordinate training of department personnel as needed, while developing, interpreting, and implementing policies and procedures for the area of responsibility. • Leads cross-functional teams on projects as pertaining to quality and process control initiatives, investigations, policies and/or procedures writing/review, best practices, and/or corrective and preventative action plans. • Assist QA Supervisors for interviewing and hiring QA personnel. • Analyze quality data and make recommendations for improvement, participating in development, interpretation, and implementation of policies and procedures for the area of responsibility. • Initiate disciplinary actions and investigates incidents when required, as appropriate. • Maintains a strong conceptual understanding of the processes, procedures, and quality requirements required of our operations. Provides staff with respective guidance and support. • Assures facilities' compliance with quality requirements, exemplifying adherence to all safety, cGMP, and Captek's Standard Operating Procedures and Policies, particularly, while keeping accountability of staff to the same. • Manages all Captek sites on the use of electronic QMS systems (QCB/MasterControl). • Adhere to HACCP and Food Safety. • Must have the ability to be flexible, handle and support multiple projects simultaneously and adjust personal style to adapt to increased business pressures, and work well under pressure while performing all tasks in an accurate, complete, timely, and appropriate manner. • Must have the ability to communicate effectively inter-and intra- departmentally on matters as pertaining to QA. • Perform other related quality and compliance duties as assigned Vice President of Quality, Regulatory Affairs & Technical Services. Qualifications: • Minimum of 10 years relevant work experience with 5 years in a Supervisory and/or Managerial role • Experience managing and scheduling a shift of five (5) or more employees • Experience in training personnel. Education/Experience: • Minimum Bachelor's degree in health science or related discipline. Master's degree preferred. Equivalent combination of education, experience, background, and assessed aptitude and capacity. • Deep working knowledge of cGMPs and FDA regulations. • ASQ CQA, PCQI and/or CHA certification preferred. Work Environment: The work environment characteristics described here are representative of 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. While performing the duties of this job, the employee is occasionally exposed to work near moving mechanical parts; fumes, or airborne particles and risk of electrical shock. The noise level in the work environment is usually moderate. Physical Demands: 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. Physical demands require sitting for extended periods of time, walking, bending, reaching, carrying, and occasionally lifting and/or moving objects up to 25 pounds. Specific vision abilities required by this job include Close vision, Peripheral vision, and the ability to adjust focus. While performing the duties of this job, the employee is occasionally required to use hands to finger, handle, or feel; reach with hands and arms; climb or balance; stoop, kneel, crouch, or crawl and talk or hear. CAPTEK is an equal employment opportunity employer. In order to provide equal opportunities to all individuals, employment decisions will be based on merit, qualifications, and abilities, not on any mental or physical disability. We comply with the law regarding reasonable accommodation for disabled employees and applicants. We do not discriminate on the basis of actual or perceived race, color, national origin, ancestry, sex (which includes pregnancy, childbirth, breastfeeding and medical conditions related to pregnancy, childbirth or breastfeeding), reproductive health decisions, gender, gender identity, gender expression, religious creed, disability (mental and physical) including HIV and AIDS, medical condition (cancer and genetic characteristics ), genetic information, age, marital status, sexual orientation, military and veteran status, or any other characteristic protected by federal, state or local law. Our management team is dedicated to this policy with respect to recruitment, hiring, placement, promotion, transfer, training, compensation, benefits, employee activities and general treatment during employment. Thank you for your interest in joining the CAPTEK team. You will be contacted shortly if your application is selected.
Become part of a team that champions wellness worldwide. CAPTEK® Softgel International is a global leader in the development and production of high-quality nutraceutical supplements. As a contract manufacturer organization (CMO), we collaborate with innovators from some of the world’s most successful brands. Summary: This individual will successfully manage all preventative maintenance and repair activities to effectively support plant operations. This individual will also coordinate and direct the design, planning, construction, maintenance, and alteration of equipment, machinery, buildings, and other-facilities by performing the following duties personally or through subordinates. Essential Duties and Responsibilities: • Maintenance: The Maintenance Manager's duty includes the maintenance, cleaning, and sanitation of the manufacturing areas, general building and office areas. The focus for this role will be establishing a robust preventative maintenance program focused on maximizing equipment uptime and extending asset life. The Maintenance manager is required to understarid the basic knowledge of building construction such as wiring, basic plumbing works etc. • Planning, Directing, budgeting and coordinating: Plan, direct, coordinate the activities of a single facility or several small facilities within the organization; required to hire the needed personnel for carrying out the above mentioned activities. • Preparing and maintaining annual budgets of the facility: Prepare budget that is required for usage of the facilities for the smooth running of the organization; required to approve and authorize budgeted expenditures for operating expenses up to authorized levels. Effectively control and maintain the department's spare parts inventory. • Administrative Duties: Oversee a team of employees from several different areas that include maintenance and janitorial personnel, as well as independent contractors. • Ensure all machinery is up to acceptable working standards • Assess current maintenance work processes, to optimize efficiency • Use data analysis to help prepare for and prevent future problems • Create and implement measures to minimize breakdowns and repairs (performing quality checks of all machinery, tools, equipment etc.) • Troubleshoot problem areas and create a clear plan of action for permanently resolving the problem • Oversee repairs and manage quality of work • Train new employees in maintenance work processes and procedures • Create a work environment with safety as a high priority • Perform evaluations of employees to ensure quality of work • Record ancrtrack daily progress/error reports • Maintain vendor relationships and order new materials as needed • Create and adhere to maintenance budgets • Perform evaluations of employees to ensure quality of work • Record and track daily progress/error reports • Maintain vendor relationships and order new materials as needed • Create and adhere to maintenance budgets • Enforce all health and safety rules and regulations according to state/federal laws and company protocol (e.g., Lockout/Tagout, Arc Flash, GMP's and OSHA) Educational Qualification: • Bachelor's Degree in Engineering or related field required. Experience Qualifications: • Requires at least 4 years' experience in a maintenance management or similar role, dietary supplement or food industry preferred. • An equivalent combination of work experience and education will be considered for the above. Required Skills: • Proven experience as maintenance manager or other managerial role • Experience in planning maintenance operations • Solid understanding of technical aspects of plumbing, carpentry, electrical systems etc. • Working knowledge of facilities machines and equipment • Ability to keep track of and report on activity • Excellent communication and interpersonal skills • Outstanding organizational and leadership abilities • Ability to manage complex and varied projects and workloads • Customer and client management skills, • Technical knowledge in construction methods, architectural and engineering drawings, • Project management skills, • Experience with Computerized Maintenance Managements Systems (CMMS) • Travel as required to support business needs Supervisory Responsibilities: • There are supervisory duties; up to 16 direct reports. Work Environment: The work environment characteristics described here are representative of 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. While performing the duties of this Job, the employee is regularly exposed to fumes or airborne particles. The employee is frequently exposed to work near moving mechanical parts and work in high, precarious places. The employee is occasionally exposed to toxic or caustic chemicals; outdoor weather conditions; extreme cold (non-weather); extreme heat (non-weather) and risk of electrical shock. The noise level in the work environment is usually loud. Physical Demands: 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. The employee must regularly lift and /or move up to 100 pounds, frequently lift and/or moveiiip to 50 pounds and occasionally lift and/or move more than 100 pounds. Specific vision abilities required by this job include Close vision, Distance vision, Peripheral vision, Depth perception and Ability to adjust focus. While performing the duties of this Job, the employee is regularly required to stand; walk; use hands to finger, handle, or feel; reach with hands and arms; climb or balance; stoop, kneel, crouch, or crawl; talk or hear and taste or smell. The employee is occasionally required to sit. CAPTEK is an equal employment opportunity employer. In order to provide equal opportunities to all individuals, employment decisions will be based on merit, qualifications, and abilities, not on any mental or physical disability. We comply with the law regarding reasonable accommodation for disabled employees and applicants. We do not discriminate on the basis of actual or perceived race, color, national origin, ancestry, sex (which includes pregnancy, childbirth, breastfeeding and medical conditions related to pregnancy, childbirth or breastfeeding), reproductive health decisions, gender, gender identity, gender expression, religious creed, disability (mental and physical) including HIV and AIDS, medical condition (cancer and genetic characteristics ), genetic information, age, marital status, sexual orientation, military and veteran status, or any other characteristic protected by federal, state or local law. Our management team is dedicated to this policy with respect to recruitment, hiring, placement, promotion, transfer, training, compensation, benefits, employee activities and general treatment during employment. Thank you for your interest in joining the CAPTEK team. You will be contacted shortly if your application is selected.
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/