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Overview: Position Summary: The QC Technologist I is responsible for the execution of a broad range of bench test procedures used in the testing of finished goods prior to release, assisting with investigations of product performance, routine validation studies, and housekeeping within the Quality Control (QC) laboratory. The QC Technologist I maintains the documentation of approved QC Standard Operating Procedures (SOP) in compliance with applicable regulations and ISO standards. This is a temporary role lasting between 3 and 6 months, with the possibility of extension. The pay rate for this position is $19-$24/hr, depending on experience. Responsibilities: Key Accountabilities Essential Functions: Perform testing finished goods per relevant SOP. Assist with testing as required for product validation and process validation on existing products. Maintain proper laboratory housekeeping and ensure adequacy of supply levels in the QC laboratory by informing appropriate personnel of low supply levels as required. Document all finished goods test results and maintain product release records (including electronic records). Document existing product/process validation test results (including electronic records). Maintain product testing database and perform relevant statistical analyses associated with product specifications as specified in laboratory SOPs. Ensure and maintain compliance with the Company’s quality system requirements through training and adherence to policies, procedures and processes. Other duties as assigned. Qualifications: Minimum Knowledge & Experience Required for the Position: High school diploma required; Bachelor’s degree in Science or equivalent experience preferred. Phlembotomist experience required. Understanding of Good Laboratory Practices (GLP) preferred. Previous experience in a Quality Control (QC) lab and/or Quality Assurance (QA) role within regulated medical device manufacturing or In-Vitro Diagnostic device (IVD) manufacturing Phlebotomy certification a plus. Knowledge of FDA-GMP/QSR and ISO standards for quality a plus. Good written and verbal communication skills. Ability to work as part of a team. Basic skills with common laboratory techniques, such as pipetting and use of balances. Basic skills with Microsoft Office suite. Basic skills with Large Enterprise Resources Planning (ERP) and Laboratory Information Management (LIMS) systems a plus.
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. Schedule AM - 1:30 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 $18.00-19.00/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.
*To be considered*, please fill out an application on our website here: https://www.cutwaterspirits.com/join-the-crew/ Cutwater Spirits is currently hiring a *Full-Time PackagingTechnician *to join our growing team. The Production Tech I is the entry level into the production/packaging team. They work on packaging lines to completes various tasks necessary to ship finished products from Cutwater Spirits. The Production Tech I is responsible for: can-filling machinery, bottle-filling machinery, boxing machinery, pallet wrapping machinery, and other general production operations. They work as a valuable team member, and the position’s focus is on maintaining consistency and timeliness within the production function—all while maintaining high quality. This position works under the direction of the Operations Manager. *Daily Duties, Functions, and Responsibilities:* * · Work on packaging lines (canning and bottling). * · Use a forklift to move materials and finished products. * · Unload packaging materials from pallets. * · Load finished products onto pallets. * · Maintain cleanliness of the distillery warehouse. * · Follows SOPs to ensure that products are packaged consistently. * · Works closely with the Operations Manager to ensure smooth operation of packaging machinery and equipment. * · Performs daily start-up and clean-up procedures on all assigned packaging stations. * · Works with maintenance employees/personnel to assist with equipment problems and troubleshooting. * · Performs daily basic maintenance for machinery. * · Assists in the production records management. * · Works to achieve packaging/distribution short and long-term goals and metrics. * · Adheres to all safety precautions, rules and guidelines. * · May stack and palletize finished product and prepare storage. * · May manually operate all phases of packaging in the case of machinery failure/maintenance. * · Embraces and fulfills the core values and culture of Cutwater Spirits. * · Other duties as assigned. *Physical Conditions:* * Work takes place in cold, hot, wet, humid, and loud environment for long periods. * Requires routine lifting of 40-60 pounds. * Conducts most work in a standing position. * Requires frequent standing, walking, bending, stooping and lifting. * Requires frequent operation of a variety of warehouse machine/equipment. * Requires the ability to manipulate large quantities of bottles, packaging materials, hoses, pallets, etc. with hands. *Minimum Knowledge, Skills, and Abilities:* * Understands and employs a Safety-First approach. * Must be 21 years of age, have a valid driver’s license and safe driving record. * Ability to maintain a Food Handler’s Certification. * Detail oriented and ability to multi-task. * Ability to work independently as well as strong team orientation and ability to work with diverse group of individuals. * Technical, troubleshooting, and problem-solving skills. * Scheduling flexibility--ability to work a variety of shifts and availability on weekends and nights/overnights. * Ability to follow oral and written instructions Education and Experience: * Prior food/beverage production experience (preferred). * Prior forklift experience (preferred). * High School Diploma or equivalent required. *To be considered*, please fill out an application on our website here: https://www.cutwaterspirits.com/join-the-crew/ Job Type: Full-time Pay: $23.05 per hour Benefits: * 401(k) matching * Dental insurance * Health insurance * Paid time off Work Location: In person
THE POSITION We are seeking a dedicated QC Associate II to join our team. In this role, you will play a critical part in supporting manufacturing operations through environmental monitoring, microbiological and chemical testing, and data analysis. You will also contribute to maintaining the highest standards of good manufacturing practices (GMP) and good laboratory practices (GLP). As a QC Associate II, you'll assist in ensuring product quality by conducting routine and non-routine testing, calibrating and maintaining laboratory equipment, optimizing testing methods, and troubleshooting. You will actively support our product operations by investigating anomalies, compiling regulatory documentation, and driving process improvements, all while keeping the laboratory audit-ready and fully compliant. This is an exciting opportunity for someone who thrives in a hands-on technical environment and is eager to contribute to the success and advancement of our quality control programs. Shift information: Sun-Wed 4x10 shift, 8:00 AM - 6:30 PM The Opportunity Collect, process, and report data for samples associated with environmental monitoring and in-process testing from clinical and/or commercial manufacturing facilities. Perform microbiological and chemical testing at all levels of complexity to support manufactured products, investigations, special studies, and validations. Conduct data review, data trending, report writing, and manage laboratory maintenance. Collect and enter data into electronic systems while generating comprehensive reports. Initiate, compile, and perform laboratory investigations, including reviewing documents, conducting internal and external interviews, tracking information, and identifying root causes of issues. Apply advanced techniques to troubleshoot assay and equipment problems, evaluate and implement new techniques and technologies, and identify functional improvements for laboratory systems or technical equipment. Train team members in basic and complex laboratory processes, troubleshooting techniques, and other applications or assays as needed to support quality control activities. Serve as a liaison for daily activities and special projects within Quality Control (QC) or across functional teams. Act as a subject matter expert (SME) for assays and technical expertise areas, providing support to analysts within the department and across sites. Lead technical or project management efforts for specialized projects. Apply theories and principles from relevant scientific or technical disciplines to independently solve a variety of moderately complex problems and deliver effective solutions. All employees with jobs that require access to the Warehouse must be able to pass the Transportation Security Administration (TSA) Security Threat Assessment (STA). Ensures the integration of environmental health, safety, and security into the business processes, systems, and programs while reporting safety and environmental incidents including injuries, illnesses, and safety suggestions within one’s functional area. Fosters a positive safety culture in which no one gets hurt. Supplementary Responsibilities: Act as designee in cross-site and/or interdepartmental meetings Facilitate team meetings as required Attends department and corporate meetings Attends seminars and/or classes to enhance technical or professional skills Who you are Bachelor’s Degree in Biology, Microbiology, Biochemistry, Chemistry or other relevant discipline 5-6 years of related experience Relocation benefits are not available for this posting The expected salary range for this position based on the primary location of California is $66,200 -$122,900 annual. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below. Benefits 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 Quality Schedule Full time Job Type Regular Posted Date Oct 21st 2025 Job ID 202510-126500
The Position We are seeking a dedicated QC Associate II to join our team. In this role, you will play a critical part in supporting manufacturing operations through environmental monitoring, microbiological and chemical testing, and data analysis. You will also contribute to maintaining the highest standards of good manufacturing practices (GMP) and good laboratory practices (GLP). As a QC Associate II, you'll assist in ensuring product quality by conducting routine and non-routine testing, calibrating and maintaining laboratory equipment, optimizing testing methods, and troubleshooting. You will actively support our product operations by investigating anomalies, compiling regulatory documentation, and driving process improvements, all while keeping the laboratory audit-ready and fully compliant. This is an exciting opportunity for someone who thrives in a hands-on technical environment and is eager to contribute to the success and advancement of our quality control programs. Shift information: Sun-Wed 4x10 shift, 8:00 AM - 6:30 PM The Opportunity Collect, process, and report data for samples associated with environmental monitoring and in-process testing from clinical and/or commercial manufacturing facilities. Perform microbiological and chemical testing at all levels of complexity to support manufactured products, investigations, special studies, and validations. Conduct data review, data trending, report writing, and manage laboratory maintenance. Collect and enter data into electronic systems while generating comprehensive reports. Initiate, compile, and perform laboratory investigations, including reviewing documents, conducting internal and external interviews, tracking information, and identifying root causes of issues. Apply advanced techniques to troubleshoot assay and equipment problems, evaluate and implement new techniques and technologies, and identify functional improvements for laboratory systems or technical equipment. Train team members in basic and complex laboratory processes, troubleshooting techniques, and other applications or assays as needed to support quality control activities. Serve as a liaison for daily activities and special projects within Quality Control (QC) or across functional teams. Act as a subject matter expert (SME) for assays and technical expertise areas, providing support to analysts within the department and across sites. Lead technical or project management efforts for specialized projects. Apply theories and principles from relevant scientific or technical disciplines to independently solve a variety of moderately complex problems and deliver effective solutions. All employees with jobs that require access to the Warehouse must be able to pass the Transportation Security Administration (TSA) Security Threat Assessment (STA). Ensures the integration of environmental health, safety, and security into the business processes, systems, and programs while reporting safety and environmental incidents including injuries, illnesses, and safety suggestions within one’s functional area. Fosters a positive safety culture in which no one gets hurt. Supplementary Responsibilities: Act as designee in cross-site and/or interdepartmental meetings Facilitate team meetings as required Attends department and corporate meetings Attends seminars and/or classes to enhance technical or professional skills Who you are Bachelor’s Degree in Biology, Microbiology, Biochemistry, Chemistry or other relevant discipline 5-6 years of related experience Relocation benefits are not available for this posting The expected salary range for this position based on the primary location of California is $66,200 -$122,900 annual. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below. Benefits 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.
Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. Responsible for overseeing Bio Supplies Manufacturing Site. Goal is to ensure the quality, safety and efficacy of products drawn/manufactured by Bio Supplies and their adherence to the applicable regulations and the corresponding licenses or marketing authorizations. Responsibilities include but are not limited to: Oversee the establishment and implementation of manufacturing and quality policies to assure the compliance with the FDA and/or EC, if applicable. And other applicable regulations guidelines and practices related with the manufacture of the Bio Supplies products Oversee and ensure that each product has been manufactured and/or tested in accordance with the requirements of its license (or marketing authorization) and the principles and guidelines of the current regulations Establish Bio Supplies manufacturing site goals and objectives; track and evaluate the critical process data to recommend continuous improvement throughout the organization. Propose and Manage the budgets and investments of Bio Supplies Manufacturing site departments and facilities in order to assure the correct performance of the work in these areas and the implementation of improvements in these areas in light of technical, scientific progress and advancements. Lead staff meetings to update and direct senior management in regards to business issues occurring in the organization. Responsible to communicate Manufacturing Operations strategy to Top Management and lead Management meetings accordingly Participate in regulatory and internal inspections/audits including providing written responses as applicable for area of responsibility. Maintain current knowledge of regulatory and industry standards, trends and advancements through independent reading and training. Directly supervises the Manufacturing site Operations Management team Available to travel as needed Participates with senior management to establish strategic plans and objectives. Makes final decisions on implementation and ensures operational effectiveness. Effectively cascades functional strategy and contributes to development of organizational policies. Interacts with senior management and executives on decisions that affect business operations. Reconciles Bio Supplies leadership views to drive business results. This Job Description is intended to present the general content and requirements for the performance of this position. The description should not be construed as an exhaustive statement of duties, responsibilities or requirements. Managers and supervisors may assign other responsibilities as needed. Skills/Qualifications/Education: 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, skills, education, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Master’s Degree in Biology, Chemistry, Biochemistry, Engineering or closely related scientific/technical discipline. An equivalent combination of education and experience may be taken into consideration Minimum 10 years senior management experience, preferably in an FDA regulated environment; Project Management experience required Thorough knowledge of FDA and international regulatory, quality and cGMP regulations Demonstrated leadership skills with ability to motivate, guide, train, coach and develop subordinates Excellent verbal and written communication Must be able to read, write, and speak English Must have strong technical writing skills Strong interpersonal skills with ability to interact with all levels of personnel in a professional manner Ability to manage multiple projects, simultaneously, meet deadlines, and handle an ever changing, fast paced critical work environment Strong organizational, analytical and problem-solving skills Ability to analyze detail and perform structured decision-making daily Depending on the area of assignment, directly related experience or a combination of directly related education and experience and/or competencies may be considered in place of the stated requirements. Example: If a job level requires a Bachelor’s degree plus 4 years of experience, an equivalency could include 8 years of experience, an Associate’s degree with 6 years of experience, or a Master’s degree with 2 years of experience. Work is performed in an office environment with exposure to electrical office equipment. Frequently sits for 6-8 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Occasionally walks. Occasionally bends and twists neck. Light to moderate lifting and carrying objects with a maximum lift of 25lbs. Frequently drives to site locations, frequently travels within the United States, occasional international travel. Able to communicate complex information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Frequently interacts with others, relates sensitive information to diverse groups. Ability to apply abstract principles to solve complex conceptual issues. Performs a wide range of complex tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. For California: The estimated pay scale for the Director of Operations, Bio Supplies Manufacturing role based in Vista, California is $155,000.00 - $220,000.00 per year. #LI-CB1 Third Party Agency and Recruiter Notice: Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate. Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws. Location: NORTH AMERICA : USA : CA-Vista:USVISTA - Vista CA-995 Park Center Drive-AC Learn more about Grifols
*Garage Remodel Installer* *About Us* The Garage Company transforms ordinary garages into high-end, functional spaces. We take pride in quality craftsmanship, professionalism, and teamwork. *Position Summary* We’re looking for a reliable, hard-working *Installer* to join our team. Experience in construction or installation is helpful but not required — we’ll provide full training. If you’re motivated, detail-oriented, and enjoy hands-on work, this is a great opportunity to grow with a reputable company. *Responsibilities* * Install cabinets, flooring, and storage systems. * Safely handle materials and tools. * Work with teammates to complete projects on schedule. * Maintain a clean and safe job site. * Follow all safety and quality standards. *Qualifications* * Construction or remodeling experience is a plus. * Dependable, positive, and eager to learn. * Able to lift and move materials as needed. *Why Join Us* * Competitive pay and steady work. * Full training provided. * Supportive, professional environment. *Apply today to join The Garage Company team.* Job Types: Full-time, Part-time Pay: $17.00 - $24.00 per hour Work Location: In person
Company Description Protec Arisawa is the global leader in the design and manufacturing of FRP (Fiber Reinforced Plastic) Pressure Vessels for membrane filtration systems. With over 40 years of experience in filament winding and three production sites on three different continents, Protec Arisawa is renowned for its cutting-edge technology and high-quality pressure vessels. Our commitment to quality and innovation makes us the supplier of choice for many industries worldwide. Role Description This is a full-time, on-site role for a Senior Quality Engineer located in Vista, CA. The Sr. QA Engineer will be responsible for overseeing quality control processes, ensuring product quality, and managing quality assurance activities. Day-to-day tasks include maintaining quality standards, performing inspections, implementing quality management systems, and identifying areas for improvement. The role also involves collaborating with cross-functional teams to ensure compliance with industry standards and regulatory requirements. PAA is certified by the American Society of Mechanical Engineers (ASME), Code Section X. This certification requires strict quality requirements in manufacturing and documentation processes. The Sr. QA Engineer ensures that all department functions support and meet the requirements of the company’s quality plan and those of the ASME, Code Section X. Duties & Responsibilities Responsible for product quality, ensuring that standard operating procedures are followed and adhered to at all times. Manages departmental performance measures, including visual controls and provides regular progress reports to management and training to manufacturing personnel. Prepares and maintains Quality Manual & process procedures. Ensures company-wide compliance with requirements of ASME Code Section X while maintaining record documentation compliance with ASME. Helps in the selection and monitoring of vendors to ensure quality, code compliance and the proper documentation. Performs other duties as assigned. Qualifications Bachelor’s degree in Engineering, Quality Management, or related field and a minimum of six (6) years progressive experience in manufacturing and Quality Control, or equivalent combination of education and experience. Must be familiar with lean manufacturing methodologies and Six Sigma continuous improvement. Experience in Product Quality and Quality Management Strong analytical and problem-solving abilities Excellent attention to detail and organizational skills Ability to work collaboratively with cross-functional teams Proficient on Microsoft Office 365, Email, One Drive, Teams, SharePoint, Business Central The ability to travel, both domestically and internationally, as needed.
Since 1980, NAI has been a leader in nutritional health, bringing whole food-based supplements to a global population. NAI is a leading expert and manufacturer of dietary supplements. We are involved in every facet of the industry, including research, development, manufacturing and marketing and advocacy. As a company, we continue to grow with manufacturing locations in Vista and Carlsbad, CA. We are looking for seasoned and entry level candidates that are interested in working for a great company with opportunities to grow, competitive pay and benefits. Shift: 2nd, 3:15 PM to 11:45 PM Summary Primarily responsible for duties associated with the packaging operation to include machine monitoring, finished product packaging inspections, manual assembly, and pack-outs. Essential Duties & Responsibilities Follows department procedures, batch record instructions and cGMP guidelines always Follows verbal instructions and direction from Line Lead, Department Lead, Supervisor or Manager or other authorized personnel Operates packaging equipment and makes any necessary adjustments as needed to meet expected efficiency Responsible for first level quality control of product through in-process monitoring and/or visual inspections Performs various types of manual pack-outs, such as bottle packing, consumers, reworks, cleaning etc. Performs disassembly and reassembly of equipment to include washing and sanitization of equipment, main packaging room, floors, walls, etc. Performs tasks associated with the preparation of the packaging lines, such as issuing and verifying materials to the packaging batch record/line Meets performance standards for quality, productivity, reliability, initiative, safety, and work relationships Attends department and company meetings Other Duties Complies with the organization’s policies and procedures as well as state, federal and local laws Fully complies with current Good Manufacturing Practices (cGMP) and health and safety regulations Other duties as assigned Qualifications English literacy (be able to effectively communicate in English) Basic math skills; must be able to use a calculator and compute basic math equations Basic Mechanical aptitude Preferred: Knowledge of cGMP’s and/or 1 year work experience in a packaging or manufacturing environment Physical Demands The physical demands are representative of those that must be met by employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. Position requires the ability to stoop, bend over, reach, and manipulate objects repetitively while standing for extended periods of time. Must be able to lift to 30 lbs following the company's safety policy Occasionally it may require lifting >50 lbs. using assistance and following the company's safety policy Excellent eyesight and general physical health is required Ability to physically respond quickly to developments on the production line. Training Must complete all required cGMP and EH&S Training Curriculum to include additional training in accordance to federal and state standards May be required to train new packaging personnel or temporary employee on packaging process Must attend all department training sessions/meetings Benefits: Medical plan options – Two HMO and one PPO Dental, vision, life insurance and other voluntary benefit options. 3 weeks’ vacation and 11 paid holidays 401K including company matching and profit sharing $1,000 Employee Referral Bonus Quarterly employee lunches, Employee of Month and other recognition programs Opportunities for advancement Comprehensive training Tuition Reimbursement and more! NAI is an Affirmative Action/Equal Opportunity Employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, physical or mental disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. Following a conditional offer of employment, satisfactory completion of a background check (including criminal records check) is required prior to beginning employment. Any offer of employment may be rescinded if the background check reveals disqualifying information, and/or it is discovered that the candidate knowingly withheld or falsified information. Failure to satisfactorily complete the background check may affect the continued employment of a current NAI employee who was conditionally offered the position.
Leading medical device components manufacturer has immediate openings for experienced CNC Swiss Machine Operators to join their team. Operates automated CNC machinery such as Swiss machines and related equipment to fabricate precision metal parts by performing the following duties. PRINCIPAL ACCOUNTABILITIES * Reads and interprets blueprints to maintain dimensions within tolerances of precision machined parts. * Able to troubleshoot and resolve most machine operation issues without assistance and able to perform basic machine set ups. * Reads and interprets Process Sheets to ensure parts are manufactured in accordance with standard processing requirements. * Maintains machine specific tools and consumables to ensure effective operation of equipment * Ensures high quality of parts by closely monitoring and adjusting operation of machine and/or tooling while regularly inspecting parts for conformance to requirements. * Ability to quickly detect and correct minor malfunctions or out-of-tolerance machining. * Performs secondary bench operations as required, which includes but is not limited to inspection, harperization, de-burring, and cleaning of parts. * Maintains lot traceability, work orders/travelers, and good housekeeping practices at all times. * Quickly raises any machining or quality issues with appropriate supervision or engineering support. * Ability to learn and work on a wide variety of part numbers and/or departments. * Participates in local programs and initiatives to improve EHS performance. * Accurately records daily production and provides detailed handover. * May suggest areas for improvement to the production process e.g. complete kaizen suggestions and participate in 5 Why investigation problem solving analysis. QUALIFICATIONS/ KNOWLEDGE/ EXPERIENCE (TECHNICAL/ PROFESSIONAL KNOWLEDGE & SKILLS COMPETENCY) * High school diploma or equivalent and/or vocational training preferred * Minimum of 1-3 years of CNC type machining work experience with demonstrated ability or related technical certificate program. * Ability to operate CNC type machines at a high level of precision, and utilize micrometers, optical comparator, and other related equipment with optimal accuracy. * Ability to operate machinery such as: bench grinder, mill, lathe, laser or other related manufacturing machinery. * Ability to use in process inspection tools. * Ability to occasionally lift 10 – 20 pounds. * Employee stands, sits and walks frequently. * Frequently required to reach with both hands and arms and occasionally stoop, kneel, or crouch. * Specific vision abilities required by this job include close vision, peripheral vision, depth perception, and the ability to adjust focus * Direct experience with Swiss manufacturing is highly preferred Shifts available: 2nd shift: 2:00 pm - 10:30 pm (2 openings) Pay: $22/hr + 10% shift diff = *$24.20/hr+ $$ Bonus* Join our team today and contribute your expertise as we continue to deliver exceptional products in the medical device industry through precision machining! Job Type: Full-time Pay: $24.20 per hour Benefits: * Health insurance Work Location: In person
*Overview* Buddha Teas is a fast growing tea compay located in Carlsbad. We are seeking a skilled, highly motivated Machine Operator to join our team. The ideal candidate will have experience in operating and maintaining a tea machine in a manufacturing environment. *Duties* - Operate and monitor machine - Set up machinery for operation - Perform routine maintenance on equipment - Inspect parts with precision and measuring tools - Ensure machines are producing quality products - Follow safety protocols at all times - Other duties as assigned *Qualifications* - Experience in machine operation - Knowledge of Materials handling and machining processes *Requirements* -A positive attitude and desire to be part of a team -The ability to stand for long periods of time while operating equipment -Good written and verbal communication skills and a desire to be detail oriented -The ability to work within prescribed guidelines and follow detailed directions -The initiative to work independently -Experience with machine operations, data entry, inventory systems, and stocking is helpful but not necessary *Where and when you’ll work* Buddha Teas is located in Carlsbad, CA. Hours: 40 hours per week. Monday through Thursday Working hours: 7-5:30 M-TH *What we offer* - Training as required - Friendly, casual work environment - Weekends off! - Full kitchen/break room available to all employees - Occasional employee potlucks and other fun activities *Starting salary range and benefits* - Positions pay $18-$22 based on experience and skillset - Paid holidays! - Health, Dental, and Vision benefits available *Hiring process and timeline* To apply, please send resume through Indeed. *About Us* Buddha Teas believes that a proper cup of tea provides a nourishing experience that satisfies the soul while pleasing the senses. We strive to deliver a delightful and vast array of additive-free options, which includes herbal, green, white, and black teas, as well as uniquely crafted blends. Our mission is to supply our tea drinkers with the highest quality teas available, while maintaining an affordable price point. In this way, we can offer everyone who seeks a truly excellent cup of tea the experience they desire. Join our team as a Machine Operator and be part of a dynamic manufacturing environment where your skills will be valued and developed. Job Type: Full-time Pay: $18.00 - $22.00 per hour Expected hours: 40 per week Benefits: * Dental insurance * Health insurance * Life insurance * Paid time off * Vision insurance Work Location: In person
*Title: Manufacturing - Materials Planner 2* *Location: San Diego, CA* *Duration: 12 Months* The GOPS team is continuously working to build our products Better, Faster, Cheaper. The team in San Diego is looking for an experienced Production Planner for the manufacturing of the Filmetrics product line. About you: * Candidate should be process oriented and results-driven and should enjoy a challenging and fast-paced environment. * Demonstrated aptitude to learn new concepts and norms quickly. * Ability to work under frequently changing priorities and deadlines, while keeping a keen awareness of the impact on other areas of the organization. * Demonstrated high attention to detail - perfectionists are encouraged to apply! * Ability to work well with cross-functional teams as well as independently. * Key duties include: * Work closely with Master Scheduling to understand build plan positioning, changes and required flexibility. * Planner must understand manufacturing capacity and allocate as required to meet build plan commitments. * Determines material requirements from production schedules and coordinates the efficient movement of materials with purchasing, production, and engineering in a dynamic, fast-paced environment. * Plans, schedules, and monitors the movement of material through the production cycle in a short lead-time, high mix manufacturing setting. * Work closely with purchasing to understand incoming material status and risk. * Track shortages and run shortage meetings with procurement team. Highlight to management critical part shortages that will jeopardize ship schedule. Job complexity:Requirements: * Uses skills as a seasoned, experienced professional with a full understanding of industry practices and company policies and procedures. * Resolves a wide range of issues in imaginative as well as practical ways. * Works on problems of diverse scope where analysis of data requires evaluation of identifiable factors. * Demonstrates good judgment in selecting methods and techniques for obtaining solutions. * Interacts with senior internal personnel. * Bachelor's degree with a minimum of 5 years related work experience. * Experience with SAP and MS Excel Job Type: Contract Pay: $30.00 - $35.00 per hour Expected hours: 40 per week Work Location: In person