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Dr. Bronner’s Company Culture Cool, kind, and capable employees are core to Dr. Bronner’s company culture! Our people are our greatest strength—strong and healthy relationships drive our success. Our workforce is impassioned, collaborative, engaged, and shares a commitment to diversity, inclusivity, and equity. Respect for differences in perspective and experience enriches our community with a sense of belonging. We seek to model a better, more just and caring world in how we show up for work, and how we show up for each other! “All-One!” Benefits As All-One, our employees are family. We support our employees to live their best life and to be happy and prosperous, with these benefits*: Full company-paid medical (PPO), dental, and vision for employees and dependents Annual discretionary bonus 13 paid holidays Profit-sharing plan for retirement Childcare assistance program Access to certain health services that may be limited in your state Dr. Bronner’s product discounts Education Investment Initiative Bring Your Dog to Work program Free daily vegan lunches Green Team and Toastmasters Vanpool Program Employee Giving Program *Please note that benefits are offered to eligible employees and are subject to specific terms and conditions. ______________________________________________________________________ Salary Range $89,000 - $95,000 depending on experience Location On-site position in Vista, CA. Schedule 1:00 PM to 10:00 PM Monday through Friday Responsibilities: Directs employees based on daily production needs. Assists with reviewing production orders for domestic customers and creating work schedules for production based on shipment schedules and confer with supporting department on work schedule. Ensures daily production requirements are achieved to meet customer expectations and works with leads and units to meet the demands of the department. Responsible for providing updates and support cross-departmentally related to inventory status, including the communication regarding international material with shipping and Ops Admin department to correctly reflect on ERP system. Plans, tracks, analyzes, and reports on projects/orders of varying contract type, size and complexity. Provides production/manufacturing work status reports for items such as change requests, new work item estimates, and resolution of potential schedule/work problems. Analyzes task/project schedule variances and advises management of discrepancies and anticipated problems in a timely manner. Prepares and maintains employee performance evaluations, corrective actions, performance development plans, trainings, time off requests, employee timecards and any employee related needs. Supports Production and lead manufacturing in identifying opportunities for improvements and optimization. Assists with assessing employee production needs, hiring, workflow, and termination of all assigned employees. Attends International Standards Organization (ISO), safety, production related meetings, management trainings. Assists with reviewing department budget reports and supporting with making best use of financial resources. Other duties as assigned within job scope. Qualifications: High school diploma or GED. 3-5 years of related experience with supervising and supporting a production/manufacturing team. At least 6 years in a manufacturing environment performing progressive experience in planning, budgeting, and performance measurements. Basic knowledge of Microsoft Office Programs (Word, PowerPoint, Excel, and Outlook.) We understand that not all candidates will meet every qualification and encourage all interested candidates to apply. Any combination of education and work experience that would be equivalent to the stated minimum requirements would qualify for consideration for this position. Dr. Bronner’s is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender identity or expression, sexual orientation, national origin, genetics, disability, age, marital status, sex (including pregnancy, childbirth, reproductive health decisions, breastfeeding, or related conditions), veteran status, or other basis protected by law.
San Diego, CAQuality – Quality Assurance /Full Time /On-Site With extensive experience in developing biologics and bioconjugates, we offer a seamless service delivered by fully integrated teams, from early discovery to commercial manufacturing. Forward-thinking and committed, we find the best solution and use the right technologies to design, develop and manufacture your products to ensure we get vital medicines to patients quickly and safely. We are dedicated to quality excellence. We are driven to get better treatments to market, efficiently and responsibly by reducing timelines and delivering the highest quality products and services. We are Abzena. More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient. The Quality Assurance Associate I/II, Quality Operations will ensure the site performs in a state of compliance by supporting Quality oversight activities and fostering an empowered culture of quality across manufacturing processes.The Associate will support on the floor activities, perform batch record review of buffer/medias/process records, support Deviations/ Change Controls / CAPAs and support quality workstreams as required. Responsibilities Provide hands-on QA collaboration and oversight to staff, ensuring compliance to good documentation practices, data integrity compliance, site inspection readiness SOPs, and relevant Good Regulated Practice (GxP) requirements. Work on the floor during production and help make quality decisions to ensure compliance with procedures and regulations. Perform Raw material sampling and release of utilities as and when needed by QA Raw Material team. Perform regular area walkthroughs of the manufacturing and Quality Control areas. Author minor deviations for topics that pertain to Quality Assurance Operations. Author Standard Operating Procedures (SOPs) for topics that pertain to Quality Assurance Operations. Perform batch record review for buffer / media, upstream and downstream manufacturing batch records. Perform disposition of buffer/media solutions manufactured at Abzena. Review and approve manufacturing deviations (minor), CAPAs, change controls and Standard Operating Procedures (SOPs). Support other departments as required to fulfill business needs. Comply with Abzena's policies and procedures. Communicate effectively with supervisors and colleagues. Participate effectively as a team player in all aspects of Abzena's business. Adhere to quality standards set by regulations and Abzena policies, procedures, and mission. Qualifications Minimum of B.S. degree in Life Sciences or Engineering with 2 years of experience in a GMP regulated Biopharmaceutical facility or equivalent. 1-3 years of experience in a Quality Assurance-related function. Experience overseeing manufacturing operations, batch record review and quality record. Knowledge of industry standards and regulation requirements for biologics and parenteral products in clinical development and commercial. Knowledge of GMP regulations (US, EU and ROW), good documentation practices, cGMP, 21CFR, USP and other applicable regulations, standards, and guidance. Ability to work in a cross-functional environment and resilience to a fast-paced environment. Physical Requirements Ability to stand for 3-4 hours at a time and sit for 2 to 3 hours at a time. Frequently lift and or move objects up to 30 pounds. Stand/walk during the entire length of shift. Use arms, hands, and fingers to handle, feel or reach. Ability to climb, balance, stoop, kneel, crouch, or crawl. Visual abilities including near and far sight, color, peripheral vision, depth, and ability to focus. $60,000 - $80,000 a year Please note that this range encompasses both QA Associate I and II ranges FLSA: Non-Exempt Abzena is an equal-opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, and training.
We’re seeking experienced Cable Assemblers to join a high-performing team working on precision electronic and mechanical assemblies. This role involves tasks such as wiring, soldering, cable harnessing, and interpreting schematics and blueprints. *Responsibilities:* * Assemble cables, harnesses, and subassemblies using hand tools and schematics * Perform soldering and compression connections * Inspect and verify quality in accordance with control procedures * Disassemble, modify, and reassemble components as needed * Maintain a clean and safe work environment * Participate in training and continuous improvement activities *Qualifications:* * High school diploma or equivalent * Minimum 3+ years of experience in cable or electronic assembly * Ability to read schematics, blueprints, and wire lists * Familiarity with tools such as soldering irons, calipers, and tape measures * Ability to obtain a DOD security clearance * IPC620 certification and soldering certification preferred * Willingness to work overtime and flexible shifts * No C2C, C2H or similar candidates will be considered. *Apply Today!* If you’re detail-oriented, quality-driven, and ready to take on a hands-on role in a dynamic environment, we’d love to hear from you. Apply now! Job Types: Temp-to-hire, Contract Pay: $24.00 - $29.00 per hour Expected hours: No less than 40 per week Benefits: * 401(k) * Dental insurance * Health insurance * Vision insurance Application Question(s): * To be eligible for a DOD security clearance, candidates must pass a drug test and background check and be a U.S. citizen. Can you confirm that you meet these requirements? * Currently, no Corp to Corp, C2H, or similar candidates will be considered. Would that be a problem for you? Experience: * Long Haul Cable Assembly: 3 years (Preferred) License/Certification: * IPC-610 Certification (Preferred) Location: * Poway, CA 92064 (Preferred) Shift availability: * Day Shift (Preferred) * Night Shift (Preferred) Work Location: In person
Become part of a team that champions wellness worldwide. CAPTEK® Softgel International is a global leader in the development and production of high-quality nutraceutical supplements. As a contract manufacturer organization (CMO), we collaborate with innovators from some of the world’s most successful brands. We are actively hiring for 2nd Shift (2:00 PM - 10:15 PM)! 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. Machine Operators • Technicians • Packaging • Inspection • Janitorial CAPTEK® is ACCEPTING APPLICATIONS for Production and Manufacturing positions. Responsibilities Include: • Operating equipment to defined standards and product requirement goals • Supporting a safe working environment by adhering to all plant safety, policies and procedures, including wearing appropriate Preventative Protective Equipment (PPE) • Conducting required quality checks on products to ensure customer satisfaction • Extensive amounts of reading, writing, and documenting • Working up to 8 hours per day in a loud/noisy, powdery, sometimes smelly environment • Must be able to perform tasks such as lifting, walking, climbing, stooping, standing, pushing and/or pulling We will hire and train candidates who are self-motivated. We promote from within and offer excellent growth opportunities for anyone looking for a career not just a job. Benefits Include: • Medical Insurance • Dental Insurance • Vision Insurance • Life Insurance • Long Term Disability • $500 Referral Bonus Program • 401k • 401k Matching • Flexible Spending Account (FSA) • Employee Assistance Program (EAP) • Tuition Reimbursement We comply with E-Verify, Background Checks and Drug Screens. Thank you for your interest in joining the CAPTEK team. You will be contacted shortly if your application is selected.
Skilled Finish Carpenter Our company is looking for a reliable, hardworking Finish Carpenter to complete the finishing touches on trim and carpentry work for different residential construction projects. You may work on a variety of projects, including doors, cabinet installation, window installation, stairs systems, molding, hardware, paneling installations. Our ideal candidate has an aptitude for precision and can accommodate unique build requirements from clients. We prefer candidates who have prior experience or training in trim carpentry or finish carpentry. Skills and Abilities: * Bilingual a plus NOT a must (fluent in both English and Spanish) * Keen attention to detail. * Carpentry trade tools. * Must have a valid California Driver’s License and working phone * Experienced in the areas of finish carpentry, materials of construction, building systems, interdisciplinary coordination, and construction processes on buildings with a high degree of complexity and high-quality finishes is essential. * Troubleshooting and communication skills. Physical Demands: While performing the duties of this job, the employee is frequently required to sit, reach, push, pull, walk, climb, crawl, and climb ladders. The employee may also on occasion be required to lift objects up to 80 pounds. Job Type: Full-time Pay: $30.00 - $35.00 per hour Benefits: * Flexible schedule Work Location: In person
*POSITION DESCRIPTION*: FINISHING TECHNICIAN (Deburr & Polish) *IMMEDIATE, FULL-TIME POSITION for a Deburrer/Polisher for (Space industry). *_(Experienced polishing as a jeweler or nail tech OK)_ Sets-up and operates machinery and hand tools to polish metal surfaces on a variety of metal components that meets the drawing specifications. Must be local to the Temecula area, no exceptions (30-40 miles). FUNCTIONS AND RESPONSIBIITIES The following duties are common for this position. These are not to be construed as exclusive or all-inclusive. Other duties may be required as assigned. 1. Responsible for deburring & polishing metal rocket components.to meet the drawing spec: * Positions parts correctly to attain proper dimensions & finish. * Works from blue prints to achieve part finish specification using drummels, sand paper, sandblaster, tumblers, polisher ( TWISTER) and common hand tools to remove debris, smooth and polish a variety of parts to meet contour, size, and finish requirements. * Keeps workstation clean and orderly. * Verifies parts meet requirements of the work order and has understanding prior to beginning work. * Responsible for quality of the finished product. * Overtime as needed. 2. Follows ALL Company safety rules and safe work practices. 3. Performs other duties as assigned. KNOWLEDGE SKILLS AND ABILITIES REQUIRED TO PERFORM THE ESSENTIAL JOB FUNCTIONS: * Knowledge of machines and tools used to deburr and polish parts. * Can use basic inspection tools such as Micrometers, Calipers, Indicators. * Basic understanding of reading blueprints and schematics. * Relies on experience and judgement to plan and accomplish goals. * Ability to work well with hands. Job Type: Full-time Pay: $18.00 - $23.50 per hour Benefits: * 401(k) matching * Dental insurance * Health insurance * Paid time off * Tuition reimbursement Application Question(s): * Do you have good eyesight? Are you a detailed reader? * What is it that you like about Deburring and Polishing Parts? * Drug screening required.. Do you use any drug not prescribed to you?. * Are you willing to undergo a Background Check? * CAN YOU READ DRAWINGS DONE IN GD & T ? * Have you ever deburred or polished metal parts for any industry? If so, what kind of parts? * What job did you deburr or polish parts? What equipment did you use? * Have you ever worked in aerospace or space industry? What did you do? * Do you have a sense of urgency while working? * Do you like the manufacturing environment ? When and What job have you been involved in a manufacturing environment? * Do you have the finesse to do careful handwork. This job requires only taking off .0002-.0005 of an inch. Very Very small amounts of material. * Can you use measurement equipment? If so, which ones? Education: * High school or equivalent (Required) Experience: * Machine shop/Manufacturing: 1 year (Preferred) Work Location: In person
General Atomics Aeronautical Systems, Inc. (GA-ASI), an affiliate of General Atomics, is a world leader in proven, reliable remotely piloted aircraft and tactical reconnaissance radars, as well as advanced high-resolution surveillance systems. We have an exciting opportunity for a Vice President of Quality Assurance to join our Quality Assurance team in Poway, CA. As the Vice President of Quality Assurance, you will play a pivotal role in developing and executing the company’s strategic quality plan in collaboration with executive leadership and senior leaders. You will lead efforts to ensure compliance with industry standards, customer requirements, and regulatory mandates while fostering a culture of excellence across all levels of the organization. This role demands a forward-thinking leader who combines technical expertise with strategic insight to deliver impactful results. DUTIES AND RESPONSIBILITES Strategic Leadership: Drive quality initiatives that enhance operational performance and support business goals. Decision-Making Excellence: Make data-driven decisions that balance cost, schedule, risk, safety, and employee morale. Quality Culture Development: Inspire a company-wide commitment to quality and continuous improvement. EHS Oversight: Responsibility for Environmental, Health, and Safety programs. Establish quality strategies aligned with organizational goals, ensuring consistent quality across the product lifecycle. Build and lead a high-performing quality assurance team, fostering continuous improvement and operational excellence. Ensure compliance with industry standards (AS9100, CMMI), legal regulations (ITAR/EAR), and customer requirements. Spearhead quality control systems and audit protocols to monitor production processes and identify improvement opportunities. Collaborate cross-functionally to integrate quality assurance measures into all business areas. Manage the department budget to optimize resource allocation while maintaining high-quality standards. Analyze data to identify process improvement opportunities and document action plans. Develop Quality Assurance Plans for new projects and oversee their execution. Maintains awareness and communicates condition of Quality concerns to executive management. Lead and oversee complex root cause analysis and implement corrective actions to address errors. Provide key leadership skills, strong business acumen, and the ability to handle high-level difficult situations independently leading the Quality Organization. Design dashboards for quality performance reporting and drive actions across internal teams. Represent the organization in audits and inspections with regulatory bodies such as DCMA, DCAA, and certification authorities. Provides direction, mentoring and training to lower-level managers and staff in quality concepts while recruiting and retaining top talent. Protect organizational assets by ensuring compliance with information security, HR, and corporate policies. Responsible for ensuring all laws, regulations and other applicable obligations are observed wherever and whenever business is conducted on behalf of the Company. Responsible for ensuring work is accomplished in a safe manner in accordance with established operating procedures and practices. Other duties as required. We recognize and appreciate the value and contributions of individuals with diverse backgrounds and experiences and welcome all qualified individuals to apply. 51326 Job Qualifications: Bachelor’s degree in Engineering, Quality Management, or a related field; advanced degree preferred. 15+ years of leadership experience in quality assurance, particularly in aerospace, defense, or manufacturing industries. Must have a broad hardware and software background and understanding of applicable disciplines outside primary areas of expertise; and the ability to solve complex management and technical problems. Must possess excellent interpersonal skills, strong analytical and planning skills, and well-developed communication, writing and presentation skills. Expertise in advanced metrology, non-destructive inspection, and compliance frameworks such as AS9100 and CMMI. Proven ability to lead large teams, manage complex projects, and collaborate across departments. Strong business acumen, strategic thinking, and ability to navigate high-level challenges. Trusted by regulatory agencies and respected by internal stakeholders for technical expertise and leadership. Requires some travel Ability to obtain and maintain a security clearance. May be subject to a security investigation and must meet eligibility requirements for access to classified information. U.S. Citizenship is required. Preferred Qualifications Extensive experience in quality assurance, process improvement, and strategic planning. Proven managerial expertise and a deep understanding of GA-ASI’s business areas. A track record of leading complex initiatives that deliver measurable success. Salary:nullTravel Percentage Required 0 - 25Relocation Assistance Provided Provided US Citizenship Required? YesClearance Required? Desired Clearance LevelExecutive WorkstyleOnsite
Why work for PCI Pharma Services? At PCI, we have an uncompromising focus on providing quality and operational excellence and providing the industry leading customer experience. Our people make all of this happen, so providing an industry leading experience for our people is equally as important. By creating an authentic culture of purposeful work, we aspire to be an interesting and fulfilling place for talented individuals to grow careers. We live a philosophy of intentional learning combined with real-life experience supported by a fair and competitive rewards program. We are individuals, teams and a company that believes in our purpose and our approach is simple, the people who work at PCI fuel our business; we don’t say no, we figure out how. Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. Job Details: The QA Associate I is responsible for performing a wide variety of routine and semi-routine activities pertaining to assuring compliance with Quality Assurance (QA) requirements and applicable regulatory requirements. The QA Associate I promotes a cGMP environment and collaborates with internal team members to ensure adherence to specifications, processes, and procedures. The QA Associate I performs documentation review and ensures completeness and accuracy of information contained in all documents, document files, databases, and documentation systems. Understanding and execution of basic cGMP and GDP principles is required. Responsibilities: Performs cGMP documentation/data review (e.g. logbooks, cleaning logs, sterilization records, stability reports, buffer batch records. QMS process support for change controls and quality investigations. Performs AQL inspection of final filled product. Performs area line clearance operations in support of manufacturing operations. Provides QA oversight and performs real time, on-the-floor documentation review during manufacturing operations. Generate labels for cGMP use. Reviews, approves, and reconciles labels for cGMP use. Sterile gown qualified to support cGMP activities in sterile suites. Assists in the review and data entry of Calibration and Preventative Maintenance records. Assists in the review of equipment and facility related Change Control documentation. Maintains equipment files and archives. Regular and reliable attendance on a full time basis [or in accordance with posted schedule]. Responsible for exhibiting professional behavior with both internal and external business associates that reflects positively on the company and is consistent with the company’s policies and practices. Embodies PCI Pharma Services cultural values and aligns daily actions with department goals and company culture. Requirements: High School Diploma or equivalent required. Bachelor’s degree in a Life Sciences discipline preferred Zero to two (0-2) years of relevant experience in documentation, QA, or equivalent. Knowledge of cGMP regulations and good documentation practices preferred. Experience with Computerized Maintenance Management Software (CMMS) preferred. Demonstrated ability to follow detailed directions in a laboratory environment preferred. Ability to work independently, within prescribed guidelines, and as a team member. The base hourly range for this position is $21.69 - $24.40 USD plus annual performance bonus eligibility. Final offer amounts are determined by multiple factors including and not limited to specific and relevant experience, credentials, geography and subject matter expertise. Join us and be part of building the bridge between life changing therapies and patients. Let’s talk future For Los Angeles applicants, we abide by the Fair Chance Initiative for Hiring. Learn more about the policy here: FCIHO Equal Employment Opportunity (EEO) Statement: PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. At PCI, Equity and Inclusion are at the core of our company’s purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity – at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture. #LI-KC1 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.
Overview: We are currently seeking a Dog Food Production and Sanitation Worker to join our team. As a Sanitation Worker, you will play a crucial role in maintaining cleanliness and sanitation standards within our facility. This is a physically demanding position that requires attention to detail and the ability to work in a fast-paced environment. Hours are Monday-Friday from 2:00pm to 10:30pm with two paid 10 min. rest breaks, and an unpaid lunch 30 minute lunch. You will also be assisting in producing human-grade dog food. Non-Negotiables: * Be here on time. * Be reliable every day. * Be safe and follow SOPs — no shortcuts. *Primary Responsibilities:* * Set up for pet food production runs * Assist in all aspects of production * Pack and ship finished product onto pallets and load into frozen storage areas * Assist with shipping and receiving of ingredients, equipment, and pet food product * Follow food safety and quality control protocols * Utilize and operate machinery, equipment, and cleaning tools * Adhere to safety guidelines and use personal protective equipment (PPE) when necessary * Clean and sanitize production areas, including equipment, floors, walls, and surfaces * Follow established cleaning procedures and protocols * Maintain cleanliness of restroom facilities. * Maintain inventory of supplies and notify supervisor when reordering is necessary * Perform routine inspections to identify any maintenance or repair needs * Dispose of waste and recyclable materials properly * Collaborate with team members to ensure efficient workflow and timely completion of tasks *Preferred skills:* * Experience in commercial or industrial cleaning * Kitchen or food manufacturing experience * Knowledge of sanitation practices and procedures * Ability to perform heavy lifting and physical tasks for extended periods of time * Familiarity with warehouse or food production environments * Strong attention to detail and ability to follow instructions accurately * Excellent time management skills to prioritize tasks effectively *Physical requirements:* * Ability to Lift: Frequently lift up to 40 pounds or more; occasionally lift up to 80 pounds, including bags of ingredients and finished products. * Stamina: Stand for extended periods (8-12 hours) and perform repetitive tasks. * Mobility: Navigate through production areas, including bending, squatting, and walking on varied surfaces. * Manual Dexterity: Operate machinery and hand tools with precision; ability to perform fine motor tasks. * Visual Acuity: Ability to see details and distinguish colors for quality control and labeling. * Hearing Ability: Hear machinery sounds and alarms in a loud environment for safety monitoring. * Balance and Coordination: Maintain stability while performing tasks in a fast-paced environment. * Adaptability: Tolerance for varying temperatures, humidity, and exposure to dust and allergens. * Strength and Endurance: Ability to engage in physically demanding activities, including pushing and pulling equipment. * Hand-Eye Coordination: Effectively manage tasks requiring coordination between vision and hand movements. * Tolerance for Noise: Ability to work in an environment with loud machinery, wearing appropriate hearing protection as needed. * Machinery Operation: Work with various types of machinery and equipment, which may be sharp, heavy, and require specific training for safe use. *Additional requirements:* * Must be able to reliably commute to Vista, California (92081) * Hold an active food handler’s certification prior to employment, or will be required to become certified upon employment We offer competitive pay rates and opportunities for career growth within our organization. If you are a dedicated individual with a strong work ethic and a commitment to maintaining cleanliness and sanitation standards, we encourage you to apply for the position of Sanitation Worker. Bonus - Friendly environment - We have two friendly office dogs - Free or discounted dog food for you and your family Job Type: Full-time Pay: $20.00 - $21.00 per hour Expected hours: 40 per week Benefits: * Paid time off Application Question(s): * This job starts at 2:00PM Can you reliably be here every day on time? * If you knew you were going to be late, what would you do? * This job requires standing for long shifts doing repetitive tasks. Are you okay with that? * We have a zero-tolerance policy for drugs or alcohol at work. Can you follow that? * Why are you interested in this position? Shift availability: * Night Shift (Required) Ability to Commute: * Vista, CA 92081 (Required) Work Location: In person
Quality Assurance Inspector I Monday - Friday, 8:30am - 5:00pm About Us At Argen, we’re in the business of creating healthy, confident smiles one case at a time. Argen is a global leader in dental manufacturing with headquarters in San Diego, CA, subsidiaries in Canada, Germany, UK, and China, and sales in 105 countries worldwide. We have a team of 400 Awesome team members. Founded more than 50 years ago as a precious metals company in South Africa, Argen has grown to become the largest dental zirconia manufacturer in North America, largest dental alloy provider worldwide, and leader in digital dentistry solutions with a product offering that span fixed, removable, ortho, implants, and equipment. Our 140,000 square foot manufacturing center houses more than 150 3D printing and milling machines and operates six days a week. Argen’s products are held to the highest standards of quality, and are FDA 510(k) cleared, ISO 13485 certified, and MDSAP compliant. Argen embodies a culture of innovation, continuous improvement, and LEAN practices in support of our mission to help our dental laboratory customers succeed. About the Opportunity The Quality Assurance Inspector I plays a pivotal role in ensuring the quality and integrity of Argen products. Inspects works in-process and finished goods in manufacturing areas to ensure conformance as defined by ISO 13485:2016, FDA regulated standards, customer specifications, Argen requirements, and applicable procedures. In this role, the successful candidate will: Provides in-process/final inspection and testing as required. Performs visual inspections of finished products. Participates in internal assessments and audits as required. Maintains proper inspection and test records. Assures that non-conforming material has been properly identified. Advises the responsible production personnel of the acceptability of products or materials based on results of testing and/or inspection. Provides solutions to technical problems and assists on special projects. Maintains lot traceability, log sheets, and good housekeeping practices at all times. Maintains a working knowledge of safety policies and regulations to ensure duties of self and others are performed in a safe manner. Ensure that lab cleanliness and safety standards are maintained. Performs thorough inspections during and after the production process to ensure product quality and compliance with standards. Verifies that all product labeling is accurate, compliant, and meets regulatory requirements. Ensures that production lines are properly cleared and prepared for the next production run, maintaining cleanliness and order. Examines and validates DHRs to ensure all documentation is complete, accurate, and in compliance with regulatory and company standards. Other duties as assigned. What does it take to be successful? High school diploma or equivalent required. Previous experience working in a GMP facility a plus. 8 hours of Quality Training (PTC) required. Strong attention to detail. Knowledge of basic arithmetic and application to solve problems. Knowledge of raw materials, production processes, quality control, costs, and other techniques for maximizing the effective manufacture and distribution of goods. Knowledge of computer skills, administrative and office procedures and systems. Communicating effectively in writing as appropriate for the needs of the audience. Technical skills and ability to understand drawings, artworks and procedures. Talking to others to convey information effectively. Perform duties with the highest regard for safety and quality. Ability to understand and follow site protocols, policies and procedures Must be flexible, forward- thinking, motivated, and have the ability to act independently. Ability to prioritize tasks and meet deadlines. Problem-solving skills. Ability to learn technical concepts by reading work instructions and standard operating procedures and completing on-the-job training. Knowledge of cGMP regulations ISO 13485, 21CFR Part 820, CMDR SOR/98-282, 93/42/EEC, RDC 16 2013, MHLW MO 169 and TG(MD)R Sch3 preferred. Our Awesome Benefits! Working for a growing innovative company like Argen means exciting opportunities for training and learning, career development and advancement from only the best in the dental industry. With all that hard work, Argen is committed to ensuring the welfare of its employees and provides an amazing benefit package that includes: Health Plans Dental Plans Vision Plan 401k with Employer Match Paid Time Off and Paid Holidays Employee Events Wellness Programs Discounts for home, travel, entertainment, relaxation that includes Mobile phone service, Technology, Airline and Hotel, Theater/Theme Park tickets, Restaurants and so much more! EOE/M/F/Vet/Disabled VEVRAA Federal Contractor
Description:*SUMMARY* The role of a Manufacturing Associate I is crucial in maintaining the efficiency and effectiveness of the production process. They actively participate in meeting production targets and deadlines, which is essential in ensuring that the company can accurately and timely deliver customer orders. *ESSENTIAL JOB FUNCTIONS* * Monitor machinery and equipment used in manufacturing, such as molded parts, to ensure products are made to specification. * Remove the parts from the machine manually. * Conduct visual inspections of the parts to check for pre-prescribed defects. * Document inventory and quality management production data, including quantities produced, defects identified, and materials used. * Correct certain defects, such as flash, using general tools based on engineering and quality feedback. * Assemble subcomponents of products, following detailed assembly instructions. * Package finished products for shipping, including labeling and preparing items according to customer orders. * Maintain a clean and safe work environment by adhering to safety protocols and cleaning schedules. * Participate in team meetings to discuss production goals and continuous improvement strategies and address concerns about the manufacturing process. * Available to cover for other associates during their lunch and break times. _*Other duties as required in support of the department and the company*_ *SUPERVISOR RESPONSIBILITIES* This role is purely as an individual contributor. Requirements:*QUALIFICATIONS* To succeed in this job, an individual must satisfactorily perform each essential job function. The requirements below represent the required knowledge, skill, and ability. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. *EDUCATION and EXPERIENCE* * A high school diploma or equivalent, e.g., vocational training, is required. * Familiarity with standard manufacturing practices and equipment preferred. * Experience in quality assurance (QA) and regulatory compliance preferred. * Experience in basic troubleshooting of manufacturing processes preferred. * Experience in the medical industries or molding businesses preferred. *LANGUAGE REQUIREMENTS* * Excellent verbal and written communication skills in English. * Conversational in any other language preferred. *MATHEMATICAL SKILLS* * Basic arithmetic: add, subtract, multiply, and divide whole numbers. *JOB SKILLS* * Familiar with Microsoft Office tools and SharePoint basics, eager to learn and expand proficiency. * Basic knowledge of Continuous Improvement, Lean Manufacturing, and the 5S Methodology. * Able to identify process deviations and product defects. * Able to effectively allocate resources to ensure timely product delivery that meets the required specifications. * Ability to set up, operate, and maintain equipment to ensure output meets established quality standards. * Dependable and willing to work overtime when necessary. *PHYSICAL DEMANDS* The employee will regularly engage in activities such as using hands to finger, handle, or feel and communicating verbally. Additionally, the employee will frequently need to reach with hands and arms while standing and walking as part of the role. Occasional lifting and movement of objects weighing up to fifty (50) pounds may be required. This position also demands specific vision capabilities, including close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus. According to ADA regulations, reasonable accommodation will be provided to ensure that individuals with disabilities can perform the job's essential functions. *WORK ENVIRONMENT* A work environment in a plant is the physical and social setting where goods production occurs. Depending on the type of product, process, and plant, the work environment may vary in terms of noise, temperature, safety, and demand. Common characteristics of a work environment in a plant are the use of machinery and exposure to hazards such as chemicals, heat, dust, or noise, with a culture of teamwork, communication, and continuous improvement. *ENVIRONMENTAL POLICY* Providien Thermoforming is dedicated to identifying and reducing the environmental impact of its operations, activities, and products. We are committed to complying with all applicable laws and other environmental regulatory requirements. We are also committed to preventing pollution and improving our environmental performance in all our global operations. This will be achieved through a comprehensive Environmental Management System that provides the framework for setting and reviewing Providien Thermoforming’s environmental objectives and targets. *PERSONAL PROTECTIVE EQUIPMENT REQUIREMENTS* * ASTM F–2412–2005, ANSI Z41–1999, or ANSI Z41–1991 rated safety toe shoes in specific areas. * Clear ANSI Z87.1 safety-rated glasses in specific areas. * Hearing protection in specific locations. * Ability to compile with JSA in specific areas. *TRAVEL* Travel is not required for this position. * SALARY INFORMATION* According to several states' laws, this position's salary range falls between *$17.25* and *$19.25* hourly/annually. However, this salary information is merely a general guideline. When extending an offer, Providien Thermoforming considers various factors such as the position's responsibilities, scope of work, candidate's work experience, education/training, essential skills, internal pay equity, and market considerations. Expected hours: 40 per week Benefits: * 401(k) * 401(k) 5% Match * 401(k) matching * Dental insurance * Employee assistance program * Employee discount * Flexible spending account * Health insurance * Health savings account * Life insurance * On-the-job training * Paid time off * Parental leave * Professional development assistance * Tuition reimbursement * Vision insurance Work Location: In person
San Diego, CA Technical Operations – Manufacturing / Exempt Full-time / On-site Apply for this job Fate Therapeutics is seeking a motivated and execution-driven Manager/Senior Manager to support GMP manufacturing operations of iPSC-derived allogenic cell therapy products. As an integral part of the Manufacturing Team, this role is responsible for overseeing operational execution in addition to managing manufacturing quality events including deviations, CAPAs, and other required change actions. This individual will play a pivotal role in defining and executing the company's operational strategy to enable the execution of a sustainable, scalable and GMP compliant manufacturing process. Accordingly, this role will require proven leadership abilities to drive meaningful communication, collaboration and coordination both internally within the Manufacturing department as well as cross-functionally across all levels of the organization. This is a full-time, exempt position located at our corporate headquarters in San Diego, CA. Responsibilities Responsible for overseeing end-to-end GMP production of iPSC-based drug product from media preparation and thaw of MCB’s through harvest and cryopreservation of drug product. Work effectively with other groups including Quality Assurance, Supply Chain, Quality Control, MSAT, Process Development, and Facilities. Coordinate with applicable departments to manage Deviations, CAPAs, Continuous Improvements, Impact Assessments and Change Actions. Assure manufacturing facility is maintained in an inspection-ready state at all times. Engage with Materials Management and Planning and Sourcing teams to assure adequate inventory of raw materials to support planned production activities. Project management utilizing tools including but not limited to SmartSheet and Microsoft Office tools. Assure manufacturing staff meet and maintain cGMP training requirements. Develop personnel schedules to allow effective execution of manufacturing activities. Review and approve applicable manufacturing-related documentation. Lead authorship and review process of SOPs and GMP BRs. Identify potential process improvements for Manufacturing and design appropriate experiments to evaluate and implement those changes. May hire, oversee, train, and motivate team members, ensuring that team goals are met efficiently. Qualifications Bachelor’s or Master’s degree in a relevant discipline with 6+ years of Life Science GMP Manufacturing experience is required. A strong manufacturing administration background specifically related to tech transfer of aseptically produced cell products is preferred. A strong emphasis on quality event management and process improvement for manufacturing operations Ability to create, read, review, and edit manufacturing related documents including Batch Records, SOP’s, Work Instructions and associated forms. Self-motivated, flexible, able to prioritize, multi-task, and work in a fast-paced & dynamic environment. Experience leading projects and managing teams is required. Working Conditions Subject to extended periods of sitting and standing, vision to monitor, and moderate noise levels. Will require working with cells and cell lines of human and/or animal origin. Will require working with hazardous materials. Will require work in controlled and cGMP Manufacturing environments requiring special gowning. Compensation The salary offer will be based on a variety of factors, including level, experience, qualifications, internal equity, and location. Fate offers a competitive employment package that includes an annual bonus, equity, and a generous benefits package. The anticipated salary range for this role is $110,000 - $150,000. The preceding job description indicates the general nature and level of work performed by employees within this classification. Additional and incidental duties related to the primary duties may be required from time to time. Equal Employment Opportunity Fate Therapeutics, Inc. is an equal opportunity employer. We value diversity and are committed to creating an inclusive environment for all employees. Privacy Notice To learn about how Fate collects and uses job application information, please visit Fate's online Privacy Notice. About Fate Therapeutics, Inc. Fate Therapeutics is a clinical-stage biopharmaceutical company dedicated to bringing a first-in-class pipeline of induced pluripotent stem cell (iPSC)-derived cellular immunotherapies to patients with cancer and autoimmune diseases. Using its proprietary iPSC product platform, the Company has established a leadership position in creating multiplexed-engineered iPSC lines and in the manufacture and clinical development of off-the-shelf, iPSC-derived cell products. The Company’s effector cell pipeline includes multiplexed-engineered, iPSC-derived natural killer (NK) cell and T-cell product candidates, which incorporate novel synthetic controls of cell function, such as chimeric antigen receptors (CARs) to target tumor-associated antigens and are intended to deliver multiple mechanisms of therapeutic importance to patients including in combination with well-established cancer therapies. Fate Therapeutics is headquartered in San Diego, CA. For more information, please visit www.fatetherapeutics.com. Recruitment Fraud Alert Recently, we have been made aware of unauthorized individuals falsely presenting themselves as Fate Therapeutics employees or recruiters as part of online scams or phishing attempts. Impersonators may use the Fate Therapeutics name and logo, as well as employee names and job titles, to gain a job seeker’s personal or banking information or to request payment as a condition of being considered for a position at the company. Fate Therapeutics and its employees are not involved in these scams. Here are a few things to be aware of to help identify recruitment fraud: - Our Talent Acquisition team only corresponds from our @fatetherapeutics.com domain. - At no stage in our hiring process will we require payment or ask you to make deposits in your bank account. - We will only ask for personal information when applying for a position via our Careers page or thereafter. - We will never ask you to contact third parties to complete an application or be considered for a job. - At no stage during our hiring process will we ask you to click a link to begin a one-way video interview. - We do not use Google Hangouts, WhatsApp, or other third-party messaging platforms to recruit candidates or conduct interviews. Please exercise caution. If something feels off about your interactions, we encourage you to contact us at [email protected] to confirm the authenticity of the message. Your security is important to us, and we appreciate your vigilance.