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The Opportunity QuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing, clinical chemistry and transfusion medicine. We are more than 6,000 strong and do business in over 130 countries, providing answers with fast, accurate and consistent testing where and when they are needed most – home to hospital, lab to clinic. Our culture puts our team members first and prioritizes actions that support happiness, inspiration and engagement. We strive to build meaningful connections with each other as we believe that employee happiness and business success are linked. Join us in our mission to transform the power of diagnostics into a healthier future for all. The Role QuidelOrtho is seeking a QA Electronic Data Management System (EDMS) Specialist. The QA EDMS Specialist will be responsible for management functions as they relate to training compliance and the training process automation using the Quality Electronic Data Management System (EDMS) and/or Learning Management System (LMS). This position will be a hybrid schedule, with onsite in San Diego, CA. The Responsibilities Administer the EDMS and/or LMS including performing all functions needed to maintain workflows, overseeing the setting of passwords, establishing security rules, and creating user accounts by interfacing with QuidelOrtho or other business site network administrators to establish user identities, system security and resolving EDMS/LMS helpdesk issues. Onboarding/Offboarding Coordinate training program – Communicate with managers to identify training needs, map out development plans for teams and individuals, configure of training requirements in the EDMS/LMS, and manage training curriculums and plans. Provide general EDMS/LMS training and assistance to users on the application(s). Help users resolve “help desk” issues as needed. Facilitates the Change Control process in the configuration of training requirements Assist as required in regulatory inspection activities Perform other work-related duties as assigned The Individual Required Associate degree in Business Administration/ Management, Science or equivalent experience 1-3 years of progressively more responsible experience with quality management systems in medical device or other highly regulated industry Must have experience with an EDMS, PLM, and/or LMS system (i.e., Master Control, Veeva Vault, OpenText DMS, Windchill PLM, Pilgrim, Agilent PLM, Cornerstone, etc.) Any combination of knowledge/skill with: Microsoft Word, Excel, Access, PowerPoint, Microsoft Project, Share Point, Outlook, Visio, Adobe Acrobat, Articulate, Programming: Basic HTML, XML, SQL, Visual Basic and/or Shell scripting (NT/UNIX) Effective verbal and writing communication skills This position requires high attention to detail to assure high quality documentation Preferred: ASQ Certification Working understanding of Quality Management Systems under the following regulations: ISO 13485, FDA 21 CFR 820, European Union MDD and/or IVD Advanced skills with Master Control and/or other EDMS/LMS application(s) Key Stakeholders Internal Customers: Quality Department - Collaborating on department planning and scheduling to meet department and corporate goals and objectives. EDMS/LMS “Customers” - Assisting other departments/individuals at QuidelOrtho who need application assistance (i.e. resetting electronic signatures, log in help, etc.). Training systems “Customers” – Assisting departments/ individuals at QuidelOrtho who need training systems assistance The Work Environment: The work environment characteristics are representative of both an office, manufacturing, and work from home environment. Occasional overtime and flexible work hours to meet project deadlines. Occasional travel required. Travel may include airplane, automobile travel and overnight hotel. The Physical Demands: Position requires ability to lift up to 30 lbs. on occasion. Walking, standing, and sitting for long periods of time are routine to accomplish tasks in this role. Computer work, paperwork, on phone, doing analytical work Salary Transparency The salary range for this position takes into account a wide range of factors including: education, experience, knowledge, skills, geography, and abilities of the candidate, in addition to internal equity and alignment with market data. At QuidelOrtho, its is not typical for an individual to be hired at or near the top range for their role and compensation decisions are dependent on that facts and circumstances of each case. The salary range for this position is $49,000 to $66,000 and is bonus eligible. QuidelOrtho offers a comprehensive benefits package including medical, dental, vision, life, and disability insurance, along with a 401(k) plan, employee assistance program, Employee Stock Purchase Plan, paid time off (including sick time) and paid Holidays. All benefits are non-contractual, and QuidelOrtho may amend, terminate, or enhance the benefits provided, as it deems appropriate. Equal Employment Opportunity QuidelOrtho believes in Equal Opportunity for all and is committed to ensuring all individuals, including individuals with disabilities, have an opportunity to apply for those positions that they are interested in and qualify for without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, or any other protected characteristic. QuidelOrtho is also committed to providing reasonable accommodations to qualified individuals so that an individual can perform the duties. If you are interested in applying for an employment opportunity and require special assistance or an accommodation to apply due to a disability, please contact us at r [email protected] . #LI-HF1
Position Summary The Quality Assurance Technician ensures food safety, quality, and compliance across all production activities. This role is critical in supporting manufacturing by identifying risks, conducting inspections, and verifying that all regulatory and Suja standards are met. This is an on-site position within a production environment and reports to the QA Supervisor. Schedule 1:00pm - 9:30pm, Tuesday- Saturday with flexibility to work overtime on Monday's Essential Duties and Responsibilities Monitor production conditions, specifications, process controls and tracking controls Monitor wash line concentrations and test ppm concentrations for sanitation bucket and floor solutions Monitor a system that will verify checks on existing production control forms and be audited on the same forms that meet all program requirements. Collect Lab retain samples Verify all CCPs on-line and take corrective actions whenever necessary to assist in determining the root cause and development of a preventative action plan Responsible for checking the pH levels, temperature and brix of each batch of juice produced and is with in product specifications Verify and document Facility Operation Inspections & Good Manufacturing Practices Enforce Good Manufacturing Practices (GMPs) throughout the manufacturing areas Perform Standard Sanitation Operational Procedures (SSOPs) verification and ATP swabs Tracks non-conforming product (Holds) Perform pre-operational inspection procedures of all production/bottling equipment and facility Verify equipment calibrations. Verify volumes, lot codes, torques & bottle weights are within product specification. Complete and enter into database all pallet tags and CCP forms for production and bottling. Record cycles and verify that all HPP settings and information is correct Perform metal mesh, magnet and sock mesh inspections Verify production lot codes, labels, mold number and packaging are within product specification Shipping and receiving verifications. Verification of all raw materials being delivered and labelled with accurate information at Receipt (product name, lots, expirations, quantity received) COA Reviewing, comparing to the specification, approving and filing the COA. Escalating or placing on hold any items that are out of compliance. Review and Verify receiving documents and logs. Monitors production conditions, specifications, process controls and tracking controls as they specifically relate to raw materials used in production. Document and maintain records for all raw materials used in the production process including disposals, usage, and pre-batching of ingredients. Materials will be logged on the appropriate batch ticket for raw material commodity of interest. Commodities include raw produce, frozen juice, frozen puree, dry ingredients and aseptic products. Inspect raw materials for deficiencies relating to appearance, texture, and/or odor before production use. Inspect incoming trailers to ensure compliance with receiving standards. Report any food safety problems to the SQF Practitioner or Department Supervisor in a timely manner so that corrective actions may be performed. Job Qualifications 1–2 years of experience in Quality Control and/or the food industry preferred Familiarity with food safety regulations is a plus Other Skills & Abilites Excellent communication skills Strong computer proficiency Sharp critical thinking and problem-solving abilities Flexible and able to adapt to change Capable of working independently with moderate supervision Comfortable in a fast-paced production setting Working Conditions This role operates in a food manufacturing environment. Frequent standing, walking, and exposure to cold or wet areas are expected. Compensation and Benefits Come thrive at Suja Life! We offer a competitive benefits package, including: Hourly Pay: $20.00 Medical, dental, vision, life insurance, and more 401(k) match to help you plan for the future Paid time off: vacation, sick days & holidays Juice benefits: yes, we keep you fueled and refreshed! #ZR #INDHP Suja Life is proud to be an equal-opportunity employer seeking to create a welcoming and diverse environment. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, ancestry, physical or mental disability, medical condition, marital status, genetics, age, or veteran status or any other applicable legally protected status or characteristic. The Company complies with all federal/local/state regulations regarding pay. 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.
Position Summary To safely and effectively run equipment related to HPP/Bottling/Packaging and Pack Out. Operator 2 will demonstrate the ability to run all machines within one department e.g. All machines associated with the Bottling department. Schedules Sunday-Thursday 1:00 PM - 9:30 PM Essential Duties and Responsibilities Including but not limited to: To run all machines safely and effectively within your department including but not limited to: Fillers, HPP’s, Labelers, Case Packers, Bundlers, Sleevers, Palletizers, etc. Plan to ensure you have the correct materials, equipment, and ingredients for each day. Communicate with your Shift Lead/Supervisor/Manager to advise of any issues/concerns. Communicate well with other employees. Follow all OSHA rules regarding safe machine operation. Keep your work area clean, organized, and safe always. Keep your work area clean, organized, and safe always Adhere to SOP, SSOP, GMP, and HACCP guidelines when in the plant. Department Machine Bottling Depal GRX Unscrambler F4 F5 Shot Filler Carbonated Filler HPP HPP 1 - 2 HPP 3 - 4 Trines Sleever Packaging/Pack Out Bundlers (Dimac, KHS, SMI) Drop Packer Unscrambler Job Qualifications Experience: Preferred 3+ years’ experience working in a manufacturing/warehouse environment Other Skills: Must have strong leadership skills. Problem solver skills Other Abilities: Be able to work independently with moderate supervision Ability to think ahead. Responsibilities may require an adjusted work schedule, overtime, evening/weekend hours in order to meet deadlines. Working & Environmental Conditions You’ll work in diverse environments, including: A wet, refrigerated manufacturing facility (below 40°F) A dry warehouse (up to 85°F) Freezer storage areas (as low as –10°F) Work areas may be tight and loud, with continuous exposure to noise levels over 85 dBA. You'll be required to follow strict safety protocols and consistently wear personal protective equipment (PPE), including safety glasses, ear protection, and steel-toed shoes. The position involves repetitive tasks that must be performed safely and efficiently. Physical Demands To succeed in this role, you must be able to: Stand and walk throughout the entire shift Lift and carry up to 50 lbs continuously Push/pull up to 100 lbs with consistent motion Bend, kneel, twist, squat, and reach overhead with both arms Climb ladders and stairs, and work at heights when needed Use your hands frequently for gripping and handling materials Work near moving machinery Pass a pre-employment physical exam Why Join Suja? We’re proud to offer a competitive benefits package that supports your well-being, including: Medical, dental, vision, and life insurance Additional ancillary benefits 401(k) with company match Paid vacation, sick time, and holidays And of course, Juice Benefits! Compensation $18.00-20.00/HR #ZR #INDHP Suja Life is proud to be an equal opportunity employer seeking to create a welcoming and diverse environment. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, ancestry, physical or mental disability, medical condition, marital status, genetics, age, or veteran status or any other applicable legally protected status or characteristic. The Company complies with all federal/local/state regulations regarding pay. 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.
Company Description Who is Steico Industries? STEICO has made its name manufacturing precision tube and duct assemblies to the world's major airframe manufacturers. We manufacture tube and duct assemblies. We work with a wide variety of materials including aluminum, steel, titanium, and other alloys and produce parts of all complexities. STEICO holds accreditations with NADCAP and is certified to AS9100 and ISO14001. Our focus on responsiveness and continuous improvement regularly creates manufacturing innovation. STEICO is an integral part of our customers supply chains that include Boeing, Lockheed Martin, BAE, Northrop Grumman, Honeywell, Honda Aviation, and many others. About our parent company: Senior is an FTSE UK based international manufacturing Group with 26 operations in 12 countries. Senior designs, manufactures and markets high-technology components and systems for the principal original equipment producers in the worldwide aerospace, defense, and land vehicle and power & energy markets. We have a long history of well-respected brands and an excellent reputation in our key market sectors. Senior delivers value to its customers and shareholders via operational excellence that is underpinned by its people and processes. Senior’s experienced manpower support, effective use of raw material, and high technology enable it to deliver optimized components within a short development time and at most competitive prices. The Group is split into two divisions, Aerospace and Flexonics, servicing five key sectors. Our global values underpin what we do, and how we do it … Job Description PM Shift: Monday - Thursday 3:15PM - 1:45AM Pay: $18.00 - $19.00 an hour depending on experience, plus $1.50 shift differential Safety – Integrity – Customer Focus – Respect & Trust – Accountability – Excellence As a Fabricator you will: The Fabricator is responsible for manufacturing and preparing detail components and assemblies using general shop tools that meet the customer and STEICO drawings/specifications manufactured within the documented manufacturing processes provided by STEICO. What will my responsibilities include? Operating Chop saws for trimming of Metal tubes and ducts. Operating Manual Mills and Lathes for drilling and coping of tubes and ducts. Operating Pneumatic Tools such as die grinders, Dynabrade belt sanders and pencil grinders. Operating bench buffers, bench grinders, tube expanders and 20” disk sanders. Using hand tools such as deburring tools, and rubber mallets. Using calibrated tools such as dial calipers, depth gauges, snap gauges and height gauges. Follow company policies and procedures. Other reasonable duties as business and operational needs dictate. Qualifications What key skills and experience do I need? Communication skills Written skills Education and Experience: High School diploma / General Education Completion. Experience in custom cabinet and fine woodworking trades highly beneficial Working with aluminum, stainless steel and titanium is a plus Experience reading blueprints and using measuring devices is a plus Understanding of chop saws, manual drills and general hand tools Knowledge of grinders and sanders Manual mill and lathe knowledge Additional Information Why Join Steico Industries, Inc.? Joining Steico Industries, Inc. a company of Senior Plc. means not only a rewarding career with a tight-knit and collaborative team, but you will also enjoy a competitive compensation package that includes a market-led base salary and a comprehensive benefits package along with wellness benefits, employee recognition program, matching 401k plan, paid vacation, flexible hours, employee wellness activities, tuition reimbursement, and community involvement initiatives. Please understand that you will only be considered an applicant if you apply for a posted position directly through our Company website and meet the qualifications of the job. If you need a reasonable accommodation to apply, please contact the Steico Industries at 760-438-8015. Prior to an offer of employment, applicant employment references maybe requested. Trade Compliance Statement Access to our facilities is restricted under the International Traffic in Arms Regulations (ITAR) and/or the Export Administration Regulations (EAR) to U.S. Persons (U.S. Citizens, lawful permanent residents, U.S. Nationals, U.S. refugees, asylees, or temporary residents under amnesty provisions ), and to properly licensed foreign persons. Applicants receiving a conditional offer of employment will be required to provide information to determine whether they are subject to these regulations and, if so, to assess their country of chargeability for export control purposes. Additionally, potential employee names will be screened against the Consolidated Screening List (maintained by the United States government) to determine eligibility to receive controlled technical data. To ensure there is no unexpected delay to your start date with our Company and due to the potential need to obtain an export license, we would like to promptly assess whether such a license is needed to access our facility and/or systems. Such licenses can take several weeks/months to obtain from the U.S. Government. Our Trade Compliance department may reach out to you with a Licensing Assessment form, which we request you kindly complete and return as soon as possible. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. EOE M/F/D/V/VEVRAA Federal Contractor
****** Sign-on Bonus ***** * If you're a *multifaceted Machinist* with *advanced machining skills *and proven *expertise in setup, problem-solving, and troubleshooting* — we want to talk to you. *Join the Team at Means Engineering – Where Innovation Meets Impact* At Means Engineering, we do more than build products — we build solutions that touch lives every day. As a *vertically integrated contract manufacturer*, everything we do happens under one roof: design, prototyping, production, testing, and shipping. This streamlined approach sets us apart from the rest — and it makes for a work environment that’s fast-paced, collaborative, and deeply rewarding. *Machinist III – Key Responsibilities:* * Perform advanced-level setup and operation of milling, turning, and grinding machines. * Troubleshoot and resolve machining issues quickly and effectively. * Read and interpret blueprints, technical drawings, and job specifications. * Execute high-precision benchwork and layout activities. * Edit CNC setup sheets; suggest and implement programming or process improvements. * Inspect parts to ensure conformance to quality standards and specifications. * Accurately document work in the ERP system, including job status, time tracking, and nonconformance reports. * Collaborate with Process Engineering on new product introduction (NPI) and continuous improvement projects. * Maintains a clean, organized, and safe work environment; follows all company policies and safety *Machinist III – Requirements:* * *Minimum of 7 years* of related machining experience. * Strong English communication skills – able to understand verbal and written instructions, collaborate with team members, and actively participate in meetings and training. * Math proficiency in algebra, geometry, and trigonometry. * *Exceptional measurement skills* with the ability to work within tight tolerances. * Expertise in reading and interpreting technical drawings, specifications, and quality standards. * Ability to document quality control requirements clearly and accurately. * Solid understanding of tooling, equipment safety, and machining best practices. * A proactive mindset for addressing non-conforming operations and producing accurate, high-quality parts. *What we offer:* * Competitive compensation and benefits package (medical/dental/vision & voluntary supplemental plans) * PTO and one week of paid time off during our end-of-year holiday shutdown * 401(k) plan * Opportunities to work across diverse industries and technologies * A supportive, talented team environment * Air-conditioned with 3, 4 and 5 axis HAAS machines. * State-of-the-art equipment and clean, safe work environment Job Type: Full-time Pay: $31.26 - $40.57 per hour Expected hours: 40 per week Benefits: * 401(k) * Dental insurance * Health insurance * Life insurance * Paid time off * Referral program * Vision insurance Work Location: In person
*CNC Programmer Job Description* *Overview* We are seeking a skilled CNC operator to join our innovative team. The ideal candidate will have a strong background in programming CNC machines and a solid understanding of mechanical processes. This role involves creating precise programs for CNC equipment, ensuring high-quality production standards, and contributing to the overall efficiency of our manufacturing operations. *Responsibilities* * Develop and optimize CNC programs (V-Carve) for various cabinet designs and van layouts. * Interpret 3d parametric models with Fusion 360 for all interior van layouts. * Operate and maintain CNC machines. * Collaborate with engineering teams to fabricate parts according to specifications. * Perform materials handling tasks, ensuring proper storage and management of materials used in production. * Assemble components as required, demonstrating wood-working knowledge and expertise. * Troubleshoot programming issues and make necessary adjustments to improve production efficiency. * Ensure compliance with safety standards and maintain a clean working environment. *Skills* * Proficient in CNC operating with experience in various building processes. * Familiarity with cabinetry and associated hardware. * Mechanical knowledge with the ability to assemble and fabricate components effectively. * Experience in materials handling within a manufacturing setting. * Excellent problem-solving skills and attention to detail. * Strong communication skills for effective collaboration with team members. Here at Rogue, we build for those that seek the exceptional. Our team has a constant desire to innovate the industry. Join us as a CNC operator where your expertise will contribute significantly to our manufacturing success! Job Type: Full-time Pay: $25.00 - $35.00 per hour Benefits: * 401(k) * 401(k) matching * Dental insurance * Employee discount * Health insurance * Paid time off * Vision insurance Ability to Commute: * Carlsbad, CA 92011 (Required) Ability to Relocate: * Carlsbad, CA 92011: Relocate before starting work (Required) Work Location: In person
If you are a morning person who is interested in working in a fast-paced and dynamic bakery setting, we'd like to meet you! Ultimately, you will help our Packaging department run smoothly, ensuring timeliness, accuracy, and organization for all the product that leaves our local Carlsbad bakery. We are looking for a Packer to perform daily distribution tasks that will support our team and bakery in distributing all our freshly baked breads and pastry. *Shifts start at 3:00 am. Must be available to work weekends.* *Responsibilities* * Carefully pack baked goods into designated packaging materials while ensuring products are not damaged and maintaining consistent quality according to customer requests * Inspect product for defects or irregularities and remove any that do not meet quality standards * Use proper machinery to slice or package products according to production requirements * Maintain proper documentation and/or records * Accurately label packages with product information, including type, date, and any necessary nutritional information or barcodes * Adheres to food safety, cGMP practices and company policy at all times. * Assist in tracking inventory levels of packaging materials and finished products, reporting any shortages or discrepancies * Maintain a clean and organized work area, including cleaning packaging equipment and work surfaces as needed * Sanitation responsibilities including but not limited to washing dishes * Work closely with other bakery staff to ensure smooth operations and timely packaging of products * Follow all safety and hygiene regulations as set by the company and relevant authorities * May involve early mornings, late nights, holidays, and/or weekend shifts depending on the bakery needs * Maintain food handlers permit, provided by the company *Skills* * Strong attention to detail and quality * Great collaboration and teamwork skills * Professional demeanor with positive communication skills * Excellent organizational, time management, and multitasking skills * Must be able to demonstrate timeliness, reliability, and accountability. * Good basic math skills and the ability to spot numerical errors * Hands-on experience with MacOS, Gmail, and Google Drive a plus * Ability to work under pressure (time constraints) and multi-task *Physical Requirements * * Must be able to stand, walk, sit, lift, reach with hands and arms, stoop, kneel, and/or crouch for extended periods. * Requires lifting, carrying, pushing, and pulling up to frequently lift 15 lbs. and occasionally lift up to 50 lbs. Job Type: Full-time Pay: $17.00 - $17.50 per hour Benefits: * Dental insurance * Employee discount * Health insurance * Paid time off * Referral program * Retirement plan * Vision insurance Ability to Commute: * Carlsbad, CA 92010 (Required) Work Location: In person
Temp-to-Hire Location: 8515 Miralani Drive, San Diego, CA 92126 Schedule: Monday–Friday, 2:30 pm - 11:00 pm What You’ll Do: As a Manufacturing Associate I, you’ll play a key role in producing high-quality standard and custom medical devices. You’ll work in a collaborative team environment, following strict GMP standards, SOPs, and customer specifications to ensure product excellence. Key Responsibilities: Operate and maintain manufacturing equipment per work instructions Perform visual inspections and identify nonconforming materials Complete production records and training documentation Support cross-functional manufacturing tasks for operational flexibility Maintain a clean, safe, and compliant work environment ✅ What You Bring: High school diploma or equivalent 1+ year of manufacturing experience preferred Experience with 3D printing and machine operations Manual dexterity and attention to detail Strong teamwork and communication skills Familiarity with Good Manufacturing Practices (GMP) Why You’ll Love Working at Argen: Competitive medical, dental, and vision plans 401(k) with employer match Generous PTO and paid holidays Employee events and wellness programs Discounts on travel, entertainment, and more About Argen: With over 500 employees and more than 50 years of innovation, Argen is the largest dental zirconia manufacturer in North America and a global leader in dental alloys and digital dentistry. Our 140,000 sq. ft. facility in San Diego houses over 150 3D printing and milling machines, operating six days a week to support our mission: helping dental labs succeed. Mon-Fri 2:30pm-11:00pm
*About us* Survival Systems International Inc. is an innovative lifeboat manufacturing company with over 50 years manufacturing life boats systems and 30 years actively supporting the aerospace community. Job Title: Painter Assistant/ Sandblaster Reports To: Production Manager FLSA Status: Non-Exempt Basic Function Operate blast booth and assist with painting or coating tasks after successful removal of unwanted substances from surface(s). Apply prime, paint and/or coatings to detail parts, subassemblies, and assemblies with substrates such as metal, foam, and plastic using brush, roller and spray-painting/coating techniques and equipment. Responsibilities 1. Remove dirt, paint, grease, and other built-up material from surfaces. 2. Set up and operate a blast booth or similar equipment. 3. Load and unload the blast cabinet. 4. Assist with painting or coating as needed. 5. Apply and remove non-skid materials as needed. 6. Set up, operate, and maintain spray guns, pressure pots and other painting/coating equipment. * 7. Determine correct preparation and prepare surfaces to be painted/coated to insure proper adhesion of the primer, paint, and/or coating used. * 8. Apply primer, paint, and/or coatings to interior and exterior of parts, subassemblies, and assemblies. Work to close tolerances in the application of all materials. * 9. Locate by use of simple arithmetic, customer specification and blueprints; decals, insignia and color break areas. 10. Perform rework, final touchup and feathering to the same level of difficulty as other work described herein. * 11. Maintain AS9100 quality standards per Survival Systems International’s Quality Manual. * 12. Perform other related duties as assigned. *Qualifications:* To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. *Language Ability:* Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to effectively present information and respond to questions from managers and company employees. *Math Ability:* Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. Ability to apply concepts such as fractions, percentages ratios and proportions to practical situations. *Reasoning Ability:* Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form. *Computer Skills:* To perform this job successfully, an individual should have knowledge of time keeping manufacturing software and database software. *Education/Experience:* High school diploma or general education degree (GED); and two to four years related sandblasting experience and/or training; or equivalent combination of education and experience. Minimum of two years’ experience with power tools. Minimum of two years’ experience with plastic and metal. *Equipment:* Capable of using hand, power, mechanical tools and power testing equipment. *Knowledge, Skills and Other Abilities:* · Ability to read blueprints *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. While performing the duties of this job, employee must have physical stamina and is regularly required to use hands; and reach with hands and arms. The employee is frequently required to stand; sit; stoop; walk; and talk or hear. The employee is occasionally required to kneel; stoop; crawl; climb or balance; and smell. The employee must occasionally lift and/or move up to 25 pounds. *Vision Requirements:* Close Vision (clear vision at 20 inches or less) Depth Perception (three-dimensional vision, ability to judge distances and spatial relationships) Ability to Adjust Focus (ability to adjust the eye to bring an object into sharp focus) *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 employee must wear proper PPE and the employee is frequently exposed to work near moving mechanical parts and fumes or airborne particles. Occasionally exposed to work in wet or humid conditions, high places, near toxic or caustic chemicals, outdoor weather conditions. Job Type: Full-time Pay: $20.00 - $25.00 per hour Expected hours: 30 – 40 per week Benefits: * 401(k) * Dental insurance * Employee assistance program * Flexible spending account * Health insurance * Life insurance * Paid time off * Vision insurance Experience: * painting metal parts: 3 years (Required) * blasting metal parts: 5 years (Required) Shift availability: * Night Shift (Required) Ability to Commute: * Valley Center, CA 92082 (Required) Work Location: In person
*Overview* We are seeking a dedicated and detail-oriented Packager to join our team. The ideal candidate will play a crucial role in ensuring that products are packaged efficiently and accurately, ready for distribution. This position requires a keen eye for detail and the ability to work effectively in a fast-paced warehouse environment. *Responsibilities* * Operate hand tools and power tools to assemble packaging materials as required. * Ensure products are correctly packaged according to specifications, maintaining quality standards. * Perform routine inspections of packaging equipment and report any issues to management. * Collaborate with team members to meet production goals and deadlines. * Maintain a clean and organised work area, adhering to health and safety regulations. * Assist in inventory management by keeping track of packaging supplies and materials. *Requirements* * Mechanical knowledge is essential for operating various packaging machinery. * Proficiency with hand tools and power tools is required for assembly tasks. * Previous warehouse experience is advantageous, providing familiarity with fast-paced environments. * Strong attention to detail to ensure quality control during the packaging process. * Ability to work well both independently and as part of a team, demonstrating effective communication skills. If you are enthusiastic about contributing to our packaging operations and possess the necessary skills, we encourage you to apply for this exciting opportunity! Job Types: Contract, Temporary Pay: $18.00 - $19.00 per hour Expected hours: 40 per week Work Location: In person
Corporate Overview Argonaut Manufacturing Services Inc. is a contract manufacturing organization (CMO) headquartered in Carlsbad, CA. The company is dedicated to serving highly innovative companies in the biopharmaceutical and molecular diagnostics industries. Argonaut is a full service, cost-effective partner, providing complete solutions in the areas of formulation, filling and final kitting of reagents and consumables. Argonaut provides quality and regulatory expertise to assure the highest in quality manufacturing and supply chain excellence. Benefits and Pay Range Benefits for this position, subject to applicable eligibility requirements. Medical Insurance Dental Insurance Vision Insurance Company Paid Life Insurance 1X annual Salary Voluntary Life Insurance Long-Term Disability Insurance and Short-Term Disability Insurance Flexible Spending Account and Health Saving Account 401(K) Retirement Plan 14 Days of Paid Time Off 10 Paid Holidays Annually The pay range for this position is between $27.00 - $32.00 per hour. Factors which may affect starting pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate. Position and Scope The purpose of this position is to assist in establishing and managing a microbiology program that oversees aseptic fill/finish activities, environmental monitoring, gowning qualification, and the establishment of compendial microbiology assays that include endotoxin, bioburden, and sterility. The position is responsible for ensuring all activities are performed within an appropriate level of cGMP compliance. Previous experience with aseptic filling operations and controls and drug product process validation is highly desired. This role is 100% On-Site, Monday - Friday 8 hours/day (excluding lunch break). Overtime, weekends and holidays may be required. Flexible start time between 6:00am and 9:00am with a consistent schedule. Exceptions to the schedule must be approved by the manager in advance. Responsibilities and Duties Serve as a subject matter expert (SME) for Microbiological assays and methods during internal/external audits, risk assessments, investigations, and client visits Supports assay transfer, qualification, and validation activities for microbial based assays or clients' specific methods Author, revise, and review Quality Control (QC) standard operating procedures (SOPs) and assay qualification protocols and reports Perform analysis on in-process samples, APIs, raw materials, and stability samples using existing methods Perform routine and non-routine environmental monitoring (EM) of GMP and GLP manufacturing facilities for total particulates, air viables, and surface viables. Initiate and participate in the investigation of environmental monitoring excursions and assesses potential impact on product quality Support a Gowning Qualification Program for all manufacturing and QC personnel Perform routine monitoring of pharmaceutical water and gas systems Perform Bioburden, Growth Promotion, Endotoxin, Gram Stain, Microscopy, TOC, Conductivity, and Nitrates testing Maintain QC lab equipment and provide assistance, as needed, during equipment and facility qualification activities Assist in trending EM data and generate quarterly and yearly reports Participate in inspection readiness activities Interact closely with other departments to ensure efficient, compliant, and timely execution of project activities Provide assistance as needed to maintain a functioning QC Laboratory, including material ordering, inventory control, general housekeeping, and other duties Assist in investigation and review of GMP quality events, including but not limited to deviations, non-conformances, and audit findings Operate at a consistent and exemplary level of efficiency, producing high quality and accurate results with a client driven focus Safely operate laboratory equipment in accordance to established practices and SOPs Assist in training of additional team members Under minimum supervision, support special projects as needed Operates to the highest ethical and moral standards. Adheres to quality standards set by regulations and Argonaut Manufacturing Services policies and procedures Communicates effectively with supervisors, staff, and clients Participate in projects within a team and as an individual Support continuous improvement projects related to QC Multi-task, prioritize workload, document properly and interpret data accurately Follow laboratory safety requirements to promote a safety-first culture Requirements and Qualifications Combination of Undergraduate courses and on-the-job experience in Microbiology or a related discipline (e.g., biology, chemistry, or biological sciences) Minimum three (3) years' experience in Quality Control and environmental monitoring of GMP facilities High intelligence and problem-solving skills Excellent oral and written communication and listening skills High level of personal and professional integrity and trustworthiness with a strong work ethic and the ability to work independently with minimal direction Experience in a growth-oriented, cGMP contract manufacturing organization with a focus on compliant execution of business is preferred General knowledge of one or more of compendial methods such as: Bioburden, Endotoxin, Growth Promotion, Sterility, and other microbiological methods Knowledge in environmental excursion investigations, root cause analysis, out of specifications, and knowledge of cleanroom practices is preferred Direct experience with endotoxin, bioburden, and growth promotion methodologies. Experience in sterility testing is highly desired. Experience with transfers and qualification/validations of large molecule focused analytical methods Must have experience with Microsoft Office applications Experience with quality software and 21 CFR 11 applications preferred Argonaut Manufacturing Services, Inc. is proud to be an equal opportunity employer committed to providing employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age or disability, or any other class protected by Federal, State or local laws. Argonaut complies with all employment eligibility verification requirements of the Immigration and Nationality Act and all must have the authorization to work in the US.
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.