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DISCOVER We are hiring a Stockroom Clerk to join our Warehouse team! DISCOVER Are you a safety-conscious, independent worker who likes to be on-the-go? The Stockroom Clerk is responsible for safely receiving, storing, and pulling raw material for the stockroom as well as maintaining the inventory history of materials used to create our industry-leading Hot Spring® Spas, Caldera® Spas, Endless Pools®, Freeflow Spas®, and Fantasy Spas® products. This entry-level position reports to the Warehouse Supervisor and requires flexibility to work in all areas of the warehouse. YOUR RIPPLE EFFECT •Is safety a priority? Before loading or unloading trailer trucks using the Forklift and Pallet Jacks, you will need to first perform routine equipment safety and maintenance checks. •Do you have an attention to detail? You’ll be responsible for ensuring completed orders are accurate by matching paperwork with delivered material. •Do you enjoy performing hands-on work? You will keep busy by storing all raw materials, picking and pulling material based on requisitions, and transporting material from the Stockroom area to different departments in the plant. •Are you computer savvy? The Stockroom Clerk will use the computer to enter and look up purchase orders, verify that material quantities match, and occasionally perform system movements and transfers. Additionally, you may run various inventory reports. •Are you a strong communicator? We’ll look to you to perform daily cycle counts and notify appropriate individuals when stock levels are low. You will also conduct routine data entry and look up stockroom inventory as needed. •Do you focus on quality? You will help keep the stockroom maintained and organized, which helps us ensure quality and efficiency in our work. WHAT YOU BRING •High school diploma or general education degree (GED); at least 1 year of related experience and/or training; or equivalent combination of education and experience. •Computer literacy (including MS Office) with accurate data entry skills. •Forklift experience required, with willingness and ability to be certified. •Stand-up Order Picker or Turret Truck certification preferred. •ERP system experience is a plus. •Excellent communication skills with the ability to interact with all levels within the organization. •Strong ability to work independently and in a team environment. WHAT YOU’LL GET At Watkins Wellness, we believe 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. As we move beyond the COVID-19 pandemic, our newly created One Watkins Return-to-Work policy is designed to meet the needs of both our business and our employees. The One Watkins program offers remote, hybrid, and onsite employment opportunities based on business needs, employee preference, and business performance. Ultimately, our goal is to remain One Watkins, with one vision and one set of values that dictate Who We Are and What We Do, regardless of where we are physically working. 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, is Accountable, values Relationships, and is a Passionate, Goal Driven Team Player.) The employee must frequently lift and move up to 50 pounds and occasionally lift and/or move up to 75 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. Hiring Range: $17.25 - $27.11 Many factors affect actual compensation including but not limited to experience, education, skills, and geographic 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
*About Us:* LIGHT Helmets is a leader in football safety equipment, dedicated to providing top-quality helmets for all levels of play. We are currently seeking a detail-oriented and skilled individual to join our team as a Helmet Assembly Technician & Reconditioning Specialist. *Key Responsibilities:* * Assemble helmets according to company specifications and safety standards * Inspect, repair, clean, and recondition used helmets to ensure they meet safety and quality guidelines * Perform quality control checks throughout the assembly and reconditioning process * Maintain and organize tools, equipment, and workstations * Follow safety protocols and company procedures to ensure a secure working environment * Assist in inventory management of helmet components and supplies * Work collaboratively with the production team to meet deadlines and efficiency goals *Qualifications & Skills:* * Previous experience in assembly, manufacturing, or a similar technical role is preferred * Strong attention to detail and ability to work with small components * Basic mechanical skills and familiarity with hand tools * Ability to stand for extended periods and perform repetitive tasks * Understanding of safety standards and quality control procedures * Good communication skills and the ability to work in a team environment * Football experience is a plus *Benefits:* * Opportunities for training and career growth * Exciting culture with the fastest growing sports equipment company Please apply via email with your resume and a brief description why you believe you would be a good fit. Pay: $19.50 per hour Expected hours: No more than 40.0 per week Benefits: * Employee discount * On-the-job training Work Location: In person
Manufacturing Engineer II Performs a variety of manufacturing engineering activities on ocular related products including manufacturing scale up, development, and sustaining activities. Responsibilities include developing creative solutions to manufacturing problems, development and execution of process, equipment, and product validations, ensuring the proper engineering deliverables are accurately generated, generation of 3D CAD models and 2D CAD drawings for assembly tools and fixtures, test procedures, project management and leadership, and maintaining schedule. May lead manufacturing related project teams with other engineers, technicians, and manufacturing staff with a focus on meeting manufacturing requirements with technically strong, high quality, cost effective approaches. Duties shall be performed with attention to detail while supporting Glaukos’ Quality Policy and the appropriate regulatory agencies, including FDA Quality System Regulations (21 CFR 820), 21 CFR 210/211 and ISO Standards (ISO 13485). Develop and Improve Manufacturing Methods and Processes Develop and improve manufacturing methods, systems, and processes to produce high quality products that are complex and broad in scope at optimal cost. Support new product development or existing product line extensions/modifications by ensuring new products or manufacturing processes are designed to facilitate ease of manufacturing and to produce quality, cost effective products with optimized yields. Provide manufacturing input during design review meetings. Provide engineering support to the manufacturing operation on routine basis. Address product and process related issues arising on the production floor including proactively identifying and solving known issues to improve yields and cost. Identify and evaluate opportunities for improvement and make specific recommendations for adoption. Perform cost analyses to reduce or optimize product costs. Write process protocols, reports, manufacturing instructions, procedures, and FMEA. Ensures compliance with GMP’s and internal protocol. Uses appropriate statistical support and Design of Experiments (DOE) when developing recommendations. Utilize establish ERP system to support manufacturing operations. Determine specific requirements of manufacturing operation in order to specify equipment, fixturing, and process parameters. Collaborate on design with suppliers to fulfill equipment and fixturing requirements. Establish and manage preventive maintenance program. Design and/or provide oversight for processes, fixtures, and tooling for associated manufacturing operations. Develop plans to evaluate process repeatability and stability through equipment qualification and process validation. Applies six sigma methodology as appropriate. How You’ll Get There: Experience: BS Mechanical Engineering or equivalent required 2+ years related experience, or a Master’s Degree and a minimum of 0-2 years of experience 2+ years of medical device or pharmaceutical experience. Experience with ocular product a plus Detail oriented with the ability to work in a clean room environment. Experience with phased new product development processes from concept through full production release. Ability to work in team environment as contributor and leader Ability to create and maintain scheduled plans while maintaining quality of engineering deliverables with guidance for engineering management. Excellent decision making/problem solving skills. Strong verbal and written communication skills. Proficient in MS Word, Excel, Statistical Software, Outlook, and MS Power Point. Ability to use MS Project (Only for level Sr and Principal). 2+ years or experience working as manufacturing engineering on complex medical device / pharma subassembly and top-level assembly builds. 2+ years of experience working with a wide range of manufacturing methods, including machined, extruded, molded and laser cut parts. 2+ years’ experience generating tooling / fixturing design to support production, Solidworks design preferred. Knowledge of cGMP and ISO regulations required. Experience with MRP a plus. Ability to interact with all departments required. Ability to coordinate activities with outside vendors. #GKOSUS
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.
General Summary: Packages finished food products at the end of the manufacturing process. Benefits and Culture We offer a competitive compensation and benefits package designed to help employees live a healthier life, build rewarding careers and save for the future. Reser's offers choices whenever possible, because we recognize the diverse and ever changing needs of our employees. Full-time employee benefits include medical, dental, vision, AD&D, life, 401(k) with discretionary match, wellness programs, paid time off, company paid holidays and a variety of voluntary benefit options. We strive to be your Employer of Choice. As one of our five cornerstones, this means that we go all-out to create an environment that shows we are committed to investing in employee growth and creating a culture of belonging where employees want to build a lasting career. Visit our website to learn more about our competitive benefit programs - https://www.resers.com/careers/#benefits Principle Duties and Responsibilities 1. Checks for correct packaging boxes and containers. 2. Ensures product date and weight are within established guidelines. 3. Seals filled product packages and boxes. 4. Examines containers, materials, and products to ensure packaging meet company specifications. 5. Removes defective products or packages from the production line. 6. Assembles product containers on an assembly line. 7. Maintains a clean and organized work area. 8. Follows company safety guidelines and Good Manufacturing Practices. 9. Regular attendance and punctuality are required due to working with people, items and equipment that are at the facility. Job Specifications 1. Production or assembly experience is preferred. 2. English/Spanish bilingual a plus. Working Conditions 1. Refrigerated food manufacturing plant. 2. The environment will be wet and cold with temperatures ranging from 25°F to 110°F. 3. Repetitive hand, wrist, and finger activities. 4. Repetitive lifting, kneeling, and bending with items in excess of 20 lbs. is required. 5. Requires walking and standing for long periods of time. 6. Production demands may require overtime and/or evening or weekend scheduling. Compensation: $17.25 per hour/non-exempt Recipe for Success Reser’s is the leading provider of fresh refrigerated deli salads, side dishes, and prepared foods for the supermarket, club store, and food service industries. Family owned and operated, Reser’s has been a proud sponsor of good times at racetracks, picnics, BBQs, music festivals, and affordable family meals since 1950. Reser’s family of brands include Reser’s American Classics, Main St Bistro, Stonemill Kitchens, and more. With more than 4,500 employees, Reser’s operates 14 facilities in the US, Mexico, and Canada and actively supports the communities it serves. 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.
THE POSITION A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche. The opportunity In this dynamic role, you will be responsible for producing innovative biotherapeutic medicine by interfacing with highly automated production systems and controls in cGMP manufacturing environment, and maintaining areas in high state of inspection preparedness. Responsibilities include: Cross-functional Collaboration & Coordination: Represent the department on project teams, work with technology, Facilities, Engineering, and EHS to optimize equipment performance, and provide manufacturing support to meet production goals. Process & Equipment Management: Operate, troubleshoot, clean, and sterilize systems (bioreactors, columns, UF/DF systems), prepare solutions, and monitor equipment performance using automation and facility systems. Documentation & Compliance: Ensure detailed documentation, review calculations, comply with cGMP, SOP, safety protocols, environmental guidelines, and handle process metrics to recommend improvements. Expertise & Problem-Solving: Demonstrate deep knowledge in biopharma technology, manufacturing processes, and scientific concepts; investigate and address complex issues collaboratively. Supplementary Tasks: Manage cell culture areas, perform solution preparation, clean and assemble equipment, execute automated CIP/SIP processes, and operate harvest and protein purification systems effectively. Who you are: Minimum Qualifications: You have a Degree in Life Sciences or Engineering and 5 years experience, or Associate degree and 7 years experience, or High School and 9 years experience. You have a Biotech certificate from approved program. You possess excellent oral and written communication skills demonstrated by communicating with other functions and management regarding resolving investigations and theory. You have ability to lead department and/or cross functional meetings or project Physical conditions and PPE requirements: Ability to work a flexible shift structure Expected to be on feet for 8 to 10 hours a day. May climb upwards of 6 flights of stairs a day to maneuver within the manufacturing facility. Lifting up to 25lbs may be required. Environment requires that gowning in the form of hospital scrubs, bunny suits, gloves and steel toe boots be worn. Also, no makeup or jewelry can be worn when working in the clean room environment. May work with hazardous materials and chemicals. Relocation benefits are not available for this job posting. The expected salary range for this position based on the primary location for this position of Oceanside, CA is $61,000- $94,800. Actual pay will be determined based on experience, level, 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. This position also qualifies for the benefits detailed at the link provided below. Benefits Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants. JOB FACTS Job Sub Category Manufacturing Schedule Full time Job Type Regular Posted Date Dec 4th 2025 Job ID 202512-130944
The Position A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche. The opportunity In this dynamic role, you will be responsible for producing innovative biotherapeutic medicine by interfacing with highly automated production systems and controls in cGMP manufacturing environment, and maintaining areas in high state of inspection preparedness. Responsibilities include: Cross-functional Collaboration & Coordination: Represent the department on project teams, work with technology, Facilities, Engineering, and EHS to optimize equipment performance, and provide manufacturing support to meet production goals. Process & Equipment Management: Operate, troubleshoot, clean, and sterilize systems (bioreactors, columns, UF/DF systems), prepare solutions, and monitor equipment performance using automation and facility systems. Documentation & Compliance: Ensure detailed documentation, review calculations, comply with cGMP, SOP, safety protocols, environmental guidelines, and handle process metrics to recommend improvements. Expertise & Problem-Solving: Demonstrate deep knowledge in biopharma technology, manufacturing processes, and scientific concepts; investigate and address complex issues collaboratively. Supplementary Tasks: Manage cell culture areas, perform solution preparation, clean and assemble equipment, execute automated CIP/SIP processes, and operate harvest and protein purification systems effectively. Who you are: Minimum Qualifications: You have a Degree in Life Sciences or Engineering and 5 years experience, or Associate degree and 7 years experience, or High School and 9 years experience. You have a Biotech certificate from approved program. You possess excellent oral and written communication skills demonstrated by communicating with other functions and management regarding resolving investigations and theory. You have ability to lead department and/or cross functional meetings or project Physical conditions and PPE requirements: Ability to work a flexible shift structure Expected to be on feet for 8 to 10 hours a day. May climb upwards of 6 flights of stairs a day to maneuver within the manufacturing facility. Lifting up to 25lbs may be required. Environment requires that gowning in the form of hospital scrubs, bunny suits, gloves and steel toe boots be worn. Also, no makeup or jewelry can be worn when working in the clean room environment. May work with hazardous materials and chemicals. Relocation benefits are not available for this job posting. The expected salary range for this position based on the primary location for this position of Oceanside, CA is $61,000- $94,800. Actual pay will be determined based on experience, level, 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. This position also qualifies for the benefits detailed at the link provided below. Benefits Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.
We are seeking a highly skilled Production Operator/Assembler II to join our team. As a mid-level Operator/Assembler, you will be responsible for assembling and fabricating various medical devices in accordance with specific procedures and drawings in a strictly controlled environment. If you have experience in assembly work and enjoy working in a cleanroom environment, we encourage you to apply! *Responsibilities* * Perform assembly operations as directed by Lead or Supervisor * GMP, ISO and procedural compliance. * Ensuring equipment is calibrated prior to performing an operation. * Performing routine preventive maintenance on production tools and equipment * Performing more complex assembly operations (e.g. SmartFlow Cannula). * Collaborate with team members to meet weekly production goals. *Skills and Qualifications* * Utilization of microscopes, calipers, rulers, etc. * Proficiency in using power tools, hand tools, and measuring equipment * Ability to read and interpret engineering diagrams, and assembly instructions * Attention to detail and ability to perform repetitive tasks with precision * Basic computer skills for data entry and Microsoft navigation * Understanding of quality system requirements: 21 CFR 820, ISO 13485 * Ability to read and write in English *Education* * High School Diploma or equivalent Job Type: Full-time Pay: $22.00 - $27.50 per hour Application Question(s): * Are you comfortable working in an onsite setting? * Are you willing to take a drug test, in accordance with local law/regulations? Education: * High school or equivalent (Preferred) Ability to Relocate: * Carlsbad, CA: Relocate before starting work (Required) Work Location: In person
Under Quality supervision, evaluates materials and products to ensure conformance to drawing requirements, procurement specifications and approved procedures. Evaluations include dimensional, functional, cosmetic and documentation as required per applicable inspection plan. Essential Duties and Responsibilities Perform Quality Control inspections, as required per ATEC procedures Read, understand, and interpret engineering (blueprint) drawings and associated GD&T (Geometric Dimension & Tolerances) Perform mechanical, visual and functional inspection. Utilization of Micro-Vu or similar lighting inspection systems preferred Engage with respective department members to maintain best inspection practices, foster a cooperative work environment, propose improvements when inefficiencies are observed Generate, complete, and maintain quality documentation such as inspection records, non-conformance reports, deviation, and scrap forms Process non-conforming materials following established procedures, able to identify and segregate non-conforming materials, transact as required in the company ERP (SAP) Perform transactions in ERP system, as necessary to release product from Inspection Read and conform to all company policies and procedures Perform documentation evaluations Interface with other departments including, Purchasing, Shipping, Receiving, Manufacturing, and Engineering as well as Supplier representatives Assist auditors during internal audits Other duties as assigned Requirements The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Good communication skills, both verbal and written Strong organization skills and attention to detail Basic math and computer skills required Firm understanding of 21 CFR (Code of Federal Regulations), Part 820, ISO 13485, Good Documentation Practices (GDP) Firm understanding of ASTM (Association of Systems & Test Methods) standards and Heat Treat conditions per ASTM standards Experience in a controlled or regulated environment required Inspection experience with Optical Comparators, Vision Systems, hand tools Education and Experience High School Diploma or equivalent and 2-5 years of experience; experience working in a medical device industry preferred. Familiarity with quality concepts such as visual inspection and defect identification. For roles based in the United States that require access to hospital facilities, must be eligible for and maintain credentials at all required hospitals, including meeting any applicable physical requirements or vaccination requirements (including the COVID-19 vaccine, as applicable). ATEC is committed to providing equal employment opportunities to its employees and applicants without regard to race, color, religion, national origin, age, sex, sexual orientation, gender identity, gender expression, or any other protected status in accordance with all applicable federal, state or local laws. Further, ATEC will make reasonable accommodations that are necessary to comply with disability discrimination laws. Salary Range Alphatec Spine, Inc. complies with state and federal wage and hour laws and compensation depends upon candidate’s qualifications, education, skill set, years of experience, and internal equity. $22.00 to $31.00 Full-Time Hourly Salary.
Master Fabricator [Independent Contractor] *Location:* San Diego, California, on-site position *Type:* Independent Contractor *Schedule: *Flexible, project-dependent *Compensation: *Fixed pay per set of orders (details provided upon inquiry) *About Us:* We’re a growing van conversion company specializing in DIY kits that help our customers build out their dream adventure vans. Our team designs and manufactures precision-cut components using CNC routers and CNC plasma tables, then packages them for safe, efficient shipment to DIY van builders across the country. Additionally, we install kit components into client vans on site at our shop. *About the Role:* We are seeking a Master Fabricator with a broad range of hands-on skills to assist in all aspects of campervan conversions. They will create custom aluminum and composite components for campervan builds, including structural and aesthetic elements. They will handle the hands-on assembly and installation of cabinetry, flooring, and other components inside the van builds. They ensure each component fits perfectly and is securely installed. *Responsibilities:* * Cut, prep & weld aluminum parts, frames & accessories * Assist with carpentry, electrical, plumbing, and fabrication tasks * Install cabinets, panels, flooring, and furniture inside the vans. * Follow blueprints and CAD drawings to maintain accuracy. * Assist the Electrical & Plumbing Specialists in system installation as needed. * Collaborate with electrical & plumbing teams to ensure fit and function of all components * Build and install roof racks, bumpers, storage solutions, and more * Collaborate with designers and other trades to ensure integration * Maintain high standards of safety and quality, and a clean & efficient workspace * Provide input on design improvements and fabrication techniques * Perform general assembly, finishing, and troubleshooting * Adapt to changing project needs and timelines *Qualifications:* * 3+ years’ experience in construction, metal fabrication, welding or related trades * Broad skill set across carpentry, electrical, plumbing, and/or metalwork * Experience with MIG, TIG, and stick welding is a plus * Experience in woodworking, metal fabrication, or general construction. * Strong attention to fit, finish, and detail. * Willingness to learn and take on new challenges * Ability to read and interpret technical drawings * Strong problem-solving skills and creativity * Own tools and reliable transportation * Valid California driver’s license and proof of insurance *What We Offer:* * *Diverse Projects:* Work on a variety of custom campervan builds, each with unique challenges and opportunities to showcase your skills. * *Competitive Pay:* We offer competitive project-based compensation, commensurate with your experience and expertise. * *Flexible Schedule:* We offer project-based work that fits your schedule * *Collaborative Environment:* Join a team of skilled and passionate professionals dedicated to creating high-quality campervans. * *Growth Opportunities:* Expand your skills and knowledge through diverse projects and collaboration with experienced specialists. * *Opportunity to Contribute:* Play a key role in creating unique and functional campervans that enable adventure and exploration. * *Autonomy:* Work independently and take ownership of your projects, while still having access to support and resources when needed. * *Project Variety:* Opportunity to work on different types of vans and conversion styles, keeping the work interesting and challenging. * *Reputation:* Be part of a company known for quality and innovation in the campervan conversion industry. * *Streamlined Processes:* We strive to provide clear project scopes, efficient communication, and timely payments. Job Types: Part-time, Contract Pay: $25.00 - $35.00 per hour Benefits: * Employee discount * Professional development assistance Work Location: In person
Description: Your Impact: You will be an integral part of a friendly Quality Assurance Team that is dedicated, agile, and collaborative. In this role, you will work on-site directly with all GMP related functional teams that are committed to delivering quality products to our clinical patients. Your talents and expertise will directly contribute to the passion to develop innovative therapies with the capacity to cure. You will learn and advance in your career as this group is forward-thinking and fully supportive of career development. If you are an individual that is driven to make a difference, have a strong work ethic, and you want to be a part of an exciting bigger picture, the Quality Assurance team welcomes you! Position Summary: We are seeking an exceptional candidate to join our Quality team in San Diego, CA. The Manufacturing Quality Assurance Associate candidate will have Manufacturing Quality Assurance (MQA) related responsibilities to ensure Poseida’s starting materials and Clinical products meet cGMP requirements. This role reports to the Senior Quality Assurance Specialist. Responsibilities include but are not limited to: Effectively communicate and collaborate with internal Quality Assurance, Manufacturing, Quality Control, Procurement, and Facilities teams Review executed production batch records and associated testing data to ensure the records meet cGMP expectations Participate in QA team meetings Supports the use of and maintains Quality trackers as assigned Participate in the creation, revision, and review of basic SOPs, Forms, Work Instructions and other controlled documents within the QMS, as requested Qualify for and perform clean room (ISO classified) gowning for all QA on-the-floor support activities for internal manufacturing processes Perform QA line clearance activities Perform duties related to the raw material program, and other MQA support activities as assigned Identify opportunities for improvement within the assigned roles and responsibilities and take initiative to communicate and drive positive change Complete other Quality Assurance based activities as assigned Align daily actions with department goals and company culture Drive the spirit of teamwork across all functions by supporting a team approach with focus on our patients being the top priority Fosters and embraces an environment of teamwork, accountability and responsibility that supports the manufacture of a quality product Requirements: Requirements, Knowledge, Skills and Abilities: A minimum of a Bachelor’s degree in life sciences or a related field with a minimum of 2 years of relevant experience, GMP/GxP experience preferred (an equivalent combination of education and experience may be considered) Knowledge of cGMP of FDA, ICH and EU regulations Controlled document review and /or batch release experience preferred Basic understanding of Deviations, CAPAs and Change Control processes Detail oriented with strong written and verbal communication skills Basic computer skills in Excel, PowerPoint, and word processing Ability to work independently, within prescribed guidelines, and as a team member Demonstrated ability to work effectively in a dynamic, complex and fast-paced team environment Ability to support a flexible work schedule to accommodate the Manufacturing schedule Must be able to achieve and retain cleanroom (ISO classified) gowning qualified status Must be physically capable to lift 20 pounds and stand for periods up to 2 hours Manufacturing Quality Assurance Associate Pay Rate: $27.13/hour to $50.38/hour The final pay offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type, and length of experience with the industry, education, geographic location, etc. Who We Are and What We Do Poseida Therapeutics was acquired by Roche in early 2025 and is now part of the Roche Group. Poseida is a clinical-stage biopharmaceutical company advancing differentiated allogeneic cell therapies and genetic medicines with the capacity to cure. The Company's approach is based on its proprietary genetic editing platforms, including its non-viral DNA Delivery System, Cas-CLOVER™ Site-Specific Gene Editing System, Booster Molecule and nanoparticle gene delivery technologies, as well as in-house GMP cell therapy manufacturing. Our people are as important as our cutting-edge technology. That’s why we invest in offering excellent career development opportunities to our employees, as well as highly competitive compensation and comprehensive benefits. We are committed to giving employees the resources they need to thrive, personally and professionally. Within the Roche organization, a healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact. Let’s build a healthier future, together. Recruitment Fraud Alert Alert: Beware of Employment Scams Poseida Therapeutics, Inc. has received reports of employment-related scams. These scams have appeared in forms of false job advertisements and/or unsolicited contacts via communication/chat platforms, phone, email or text from individual(s) claiming to be or represent Poseida’s Human Resources team. Be advised that Poseida Therapeutics does not extend unsolicited employment offers. Furthermore, Poseida Therapeutics does not request payment information or charge prospective employees with any fees during the recruitment process. If you would like to pursue employment opportunities with Poseida Therapeutics, Inc., please visit our official careers website https://poseida.com/careers-culture/ or official Poseida Therapeutics LinkedIn page. Job postings that do not link directly to our careers website or official Poseida LinkedIn page are not legitimate and might be fraudulent. You may report fraudulent job advertisements or contacts via our Contact Us page at https://poseida.com/contact-us/ and select the subject “Careers.” If you have been defrauded or suspect identity theft as a result of an employment scam, please contact your local law enforcement agency for guidance.
Production & Shipping Specialist [Independent Contractor] *Location:* San Diego, California, on-site position *Type:* Independent Contractor *Schedule: *Flexible, project-dependent *Compensation: *Fixed pay per set of orders (details provided upon inquiry) *About Us* We’re a growing van conversion company specializing in DIY kits that help our customers build out their dream adventure vans. Our team designs and manufactures precision-cut components using CNC routers and CNC plasma tables, then packages them for safe, efficient shipment to DIY van builders across the country. We’re looking for a hands-on Production & Shipping Specialist who enjoys working in a shop environment, takes pride in quality work, and can follow instructions while still using their own judgment to solve problems. This is a project-based independent contractor role, ideal for someone seeking flexible work with clear deliverables. *What You’ll Do* *Post-Processing & Finishing (CNC Components)* * Inspect and clean up wood and aluminum parts coming off the CNC router and CNC plasma table * Deburr, sand, and smooth edges to meet quality standards * Perform basic fitting checks to ensure parts meet specifications * Label, organize, and stage components for packing *Packing & Shipping* * Pick and pack DIY kit orders according to packing lists and work instructions * Build, modify, and reconfigure pallets to securely hold kit components * Wrap and band pallets for safe transport * Prepare orders for shipment (apply labels, documentation, etc.) * Work with the team to optimize packing layouts and reduce damage/returns *General Shop & Team Support* * Use basic shop tools (drills, impact drivers, sanders, grinders, saws, etc.) safely and effectively * Maintain a clean, organized work area and contribute to overall shop organization * Follow written instructions, drawings, and checklists while applying critical thinking when things don’t match or need adjustment * Communicate clearly with the production team about issues, shortages, or quality concerns *What We’re Looking For* *Required Skills & Experience* * Comfortable working with *wood and aluminum*, including basic measuring and layout * Experience with *basic shop tools* (e.g., drills, sanders, grinders, saws, hand tools) * Ability to *follow detailed instructions, diagrams, and packing lists* * Strong *attention to detail* and pride in quality work * Ability to use *critical thinking* when something looks off, is missing, or needs improvement—and speak up * Physically able to lift and move packages and materials (typically up to [50 lbs]) and be on your feet most of the day * Reliable, punctual, and able to work both *independently* and as part of a small team * *Must be able to work as an independent contractor* and manage project timelines effectively. *Nice-to-Haves (Not Required)* * Experience in a woodworking, metalworking, fabrication, or shipping/warehouse environment * Familiarity with CNC-produced parts or manufacturing processes * Experience building pallets, crating, or freight preparation * Interest in vans, camping, or DIY projects *What We Offer:* * *Diverse Projects:* Work on a variety of custom campervan builds, each with unique challenges and opportunities to showcase your skills. * *Competitive Pay:* We offer competitive project-based compensation, commensurate with your experience and expertise. * *Flexible Schedule:* We offer project-based work that fits your schedule * *Collaborative Environment:* Join a team of skilled and passionate professionals dedicated to creating high-quality campervans. * *Growth Opportunities:* Expand your skills and knowledge through diverse projects and collaboration with experienced specialists. * *Opportunity to Contribute:* Play a key role in creating unique and functional campervans that enable adventure and exploration. * *Autonomy:* Work independently and take ownership of your projects, while still having access to support and resources when needed. * *Project Variety:* Opportunity to work on different types of vans and conversion styles, keeping the work interesting and challenging. * *Reputation:* Be part of a company known for quality and innovation in the campervan conversion industry. * *Streamlined Processes:* We strive to provide clear project scopes, efficient communication, and timely payments. Job Types: Part-time, Contract Pay: $20.00 - $28.00 per hour Expected hours: 10 – 30 per week Benefits: * Employee discount * Flexible schedule * Opportunities for advancement * Professional development assistance Work Location: In person