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General Atomics Aeronautical Systems, Inc. (GA-ASI), an affiliate of General Atomics, is a world leader in proven, reliable remotely piloted aircraft and tactical reconnaissance radars, as well as advanced high-resolution surveillance systems. Under minimal supervision, this position is responsible for performing a variety of non-routine and non-repetitive assembly operations on electronic and /or mechanical assemblies and subassemblies. Determines and/or follows methods and sequence of operations in performing assembly tasks such as wiring, component installation, hand soldering and cable harnessing on assembly units. Makes continuity checks on work in process and completed work. May monitor and verify quality in accordance with control procedures. This position is for the second shift. DUTIES & RESPONSIBILITIES: Assembles components, assemblies or sub-assemblies. Makes setups and adjustments holding tolerances to specifications. May perform duties as required in assembly of electronic equipment such as cables, harnesses, chassis, and printed circuit boards; or may perform mechanical assembly of panels, LRU's, batteries, and servo motors as it pertains to cable assembly. May disassemble, modify, rework, reassemble and test experimental/prototype assemblies or subassemblies according to specifications. Responsible for observing all laws, regulations and other applicable obligations wherever and whenever business is conducted on behalf of the Company. Expected to work in a safe manner in accordance with established operating procedures and practices. Completes Disposition on Nonconforming product when needed. Participates in production Integrated Process Team (IPT) Communicates/works with engineering and other support departments. Participates/runs weekly cell team meeting. Mentors team members in assigned cell. Assist team/assemblers in building and solving technical issues of cable assembly. Additional Functions: Performs 5S housekeeping and cleanup duties upon completion of assigned tasks Supports Clean-as-you-go cleanup duties during the shift. May train lower level assemblers or act as a lead and direct the work of others. Other duties as assigned or required. We recognize and appreciate the value and contributions of individuals with diverse backgrounds and experiences and welcome all qualified individuals to apply.50198 Job Qualifications: Typical requires a high school diploma or equivalent and seven or more years experience. Must be customer focused and possess: The ability to read and interpret engineering drawing and wire lists. Extensive knowledge in specialized functions. A comprehensive understanding of the general and specific aspects and technical phase of the job and their practical to complex applications to intricate problems. Good knowledge of computer operations and applications pertinent to the position. Familiarity with use of soldering and compression connection tools. Good visual perception and ability to distinguish between colors. The ability to work independently or in a team environment is essential as is the ability to work extended hours as required. Ability to obtain and maintain DoD Security clearance is required. Salary:$52,020 - $77,325Travel Percentage Required 0 - 25Relocation Assistance Provided Not Provided US Citizenship Required? YesClearance Required? Desired Clearance LevelMid-Level (3-7 years) WorkstyleOnsite
General Atomics Electromagnetic Systems (GA-EMS) designs and manufactures first-of-a-kind electromagnetic and electric power generation systems. GA-EMS’ expanding portfolio of specialized products and integrated system solutions support critical fleet, space systems and satellites, missile defense, power and energy, and process and monitoring applications for defense, industrial, and commercial customers worldwide. We are seeking a Quality Engineer Level III to support QA Compliance activities on complex Defense programs. The successful candidate will serve as a critical quality interface between engineering, program management, manufacturing, contracts and supplier quality to ensure that GA-EMS meets or exceeds all customer requirements throughout the contract lifecycle. This position is responsible for overseeing the compliance of all internal processes, products, and services with customer, regulatory, and contractual quality requirements. This role is ideal for a seasoned quality professional with strong technical acumen, extensive working knowledge of aerospace/defense quality systems, experience interpreting customer and government contract requirements, and the ability to drive compliance across multiple functional areas. DUTIES AND RESPONSIBILITIES: Perform QA Compliance activities for assigned programs throughout the full contract lifecycle (RFP through Delivery). Interface with program management, engineering, manufacturing, quality assurance, supply chain management, and contracts to ensure compliance with customer requirements. Participate in AS9100 audits, risk management activities, and support root cause analysis (RCA) and corrective/preventive action (CAPA) investigations. Ensure compliance with contractual requirements, industry standards (e.g., AS9100, ISO 9001), internal procedures, and customer specifications. Develop and analyze quality metrics to identify trends and drive continuous improvement initiatives. Track and monitor active proposals and contracts. Support the preparation and presentation of Requirements Compliance Matrix and the status of the Matrix at program reviews and customer meetings. Mentor junior quality engineers and provide technical guidance as needed. Prepares statistical analysis reports, specifications and other technical documents. Responsible for observing all laws, regulations and other applicable obligations wherever and whenever business is conducted on behalf of the Company. Expected to work in a safe manner in accordance with established operating procedures and practices. Other duties as assigned or required. We recognize and appreciate the value and contributions of individuals with diverse backgrounds and experiences and welcome all qualified individuals to apply. 51357 Job Qualifications: Typically requires a bachelor's or master's degree in engineering or related discipline and five or more years of related experience with a bachelor's degree or three or more years with a master's degree. May substitute equivalent experience in lieu of education. 6-8 years of quality engineering experience in the defense, aerospace, or high-reliability industry preferred. Experience in reading and interpreting engineering drawings, specifications, and test procedures. Strong working knowledge of AS9100, ISO 9001, and DoD/Customer quality standards and processes (e.g., MIL-STD-883, MIL-STD-973, EIA-649). Experience with root cause analysis, problem solving, and corrective/preventive action systems. Familiarity with risk management, FMEA, and configuration management principles. U.S. Citizenship required; must be able to obtain and maintain a DoD Security Clearance. Experience working with Microsoft Products (Word, Excel, Project, etc.) SAP is a plus. Able to work extended hours as required. Travel up to 25% may be required. PREFERRED QUALIFICATIONS: Current active DoD clearance (Secret or higher). Experience working directly with major defense customers Hands-on experience with quality management tools (SAP, DevonWay, Windchill, PDM, Accuris). Proficiency in interpreting engineering drawings and applying GD&T per ASME Y14.5 standards. Strong project management, interpersonal and communication skills with a collaborative, team-oriented mindset. Salary:$81,080 - $141,650Travel Percentage Required 0 - 25Relocation Assistance Provided Provided US Citizenship Required? YesClearance Required? Desired Clearance LevelMid-Level (3-7 years) WorkstyleOnsite
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.
San Diego, CA Technical Operations – Manufacturing / Non-exempt Full-time / On-site Apply for this job Fate Therapeutics is looking for a highly motivated and detail-oriented Manufacturing Associate III/II to join our Manufacturing team to execute the manufacturing of iPSC-derived allogenic cell therapy products in the clean room cGMP compliant environment. The successful candidate will execute batch records, follow SOPs and perform manufacturing logistical support activities per cGMP, GDP and safety standards. The candidate will develop and apply critical skills across a variety of production activities, including but not limited to, aseptic techniques, equipment operation, product sampling and enumeration, reagent and material preparation and cell processing. The candidate will work both independently on routine activities and participate in cross-functional collaborations on more strategic and complex initiatives. This is a full-time, non-exempt position located at our corporate headquarters in San Diego, CA. Responsibilities Responsible for the execution of cell culture manufacturing activities of iPSC-based drug product from thaw of MCBs through harvested cryopreservation and quarantine of drug product closely following approved batch records and SOPs. Work in a cleanroom environment, performing aseptic processing while maintaining manufacturing environmental conditions. Accurate and timely documentation of manufacturing activities performed. Responsible for documenting deviations and reporting such deviations to department management. Assure manufacturing facility is maintained in a clean and organized state. Maintain cGMP training requirements. Engage with supply chain and materials management to ensure adequate inventory of raw materials to support planned production activities. Work independently and collaboratively on manufacturing support activities. May identify innovative solutions and support initiation of process improvements. Assist in the GMP training of others. Performs visual inspection of drug product. Qualifications Bachelor’s degree in a relevant discipline with at least 2 years of relevant experience in cell product GMP manufacturing. A High School diploma with 3+ years of relevant experience will also be considered. Experience in iPSC drug product manufacturing is a plus. Ability to read and follow manufacturing related documents including Batch Records, SOP’s, Work Instructions and Forms. Self-motivated, flexible, able to prioritize, multi-task, and work in a fast-paced and dynamic environment. Familiarity with standard cell culture methods is required. Knowledge of cGMP regulations applicable to biologics and cell therapy manufacturing is preferred. Must be team oriented and flexible, striving for team success and quality results. Visual Acuity Testing 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. Evening and weekend work may be required. 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 $30 - $37/hr 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.
Description: About the Company Biolinq is a venture-backed digital health company developing a wearable biosensor platform that measures biomarkers important to the management of many clinical conditions including diabetes. This dynamic role is a part of a team of engineers and scientists developing a novel intradermal biosensor technology and the associated software data extraction and rendering SDK that will transform the way people manage their metabolic health. Job Purpose Responsible for completing the activities in the manufacturing area to meet daily production schedule and product quality requirements. Duties and Responsibilities • Adherence to established procedures. Operate hand tools, equipment, and fixtures. Feed materials for processing • Adjust settings, perform minor troubleshooting. Work with team to identify procedural improvements to existing documents • Execute line clearance for respective process or area prior to production lot start. Confirm use of correct equipment prior to build start. Monitor adherence to line clearance practices within assigned area with continuity checks on work in progress and completed • Demonstrated proficiency across designated workflow or set of processes • Ability to execute more complex processes involving computer software, data analysis, prepared solutions • Effectively meet target output metrics. Demonstrated speed of delivery • Consistently exceeds yield and performance targets • Participation in meeting to review performance, schedule, and identify obstacles to meet daily targets. Responsible for daily completion and progress reporting for designated workflow • Maintain assigned area in a well-organized and clean manner. Adhere to 5S practices. Complete 5S daily checklist. Help identify areas of improvement for 5S • Perform cycle counts to monitor inventory levels in manufacturing area. Support lead or supervisor with material replenishment of production supplies • Adherence to attendance and tardiness expectations. Communicate absences within a reasonable timeframe • Collect process data used to perform routine analysis for supervisor or quality review. Assists lead or supervisor with gathering applicable production data in order to update daily metrics and understand performance. Enters data into manufacturing logs • Cross training to peripheral manufacturing processes outside of assigned area • Immediately notify lead or supervisor when non-conformance is identified. Complete non-conformance investigations for minor documentation issues. Aids in root cause analysis and recommends corrective actions • Participation and execution responsibilities for some problem-solving efforts. Complete A3 as the main owner with some direction or assistance from supervisor, engineer, or technician • Escalation of questions or issues to team lead or supervisor for timely response. Provide initial support to team based on previous experience with issues observed • Proactively identify improvements to productivity or safety. Regularly communicate feedback and suggestions to supervisor or support team. • Completion of abnormality/escalation cards for identified opportunities, risks, or needs in manufacturing area. Frequently communicate feedback to the rest of the team. Collaborate with engineering or support team to identify the appropriate long-term solutions for recurring minor issues • Complete training prior to performing tasks. Participate in training, onboarding, and supervision of new associates. • Confirm physical quantity of accepted and rejected sensors for assigned processes and document on DHR. Requirements: Qualifications • High school diploma or GED • Minimum 5 years of experience, Wet lab experience (preferred) • Information exchanged is generally non-complex. Has contact with employees at other levels within the company who are supporting manufacturing. • Communicates effectively in written and verbal format. • Ability to handle delicate materials and do precision manual work in manufacturing • Basic experience with Microsoft Office tools (preferred) • Communicate status of work if handing off prior to or returning from breaks or next day or work • Demonstrates consistent character of respect • Completion of build documentation in timely manner. Ability to work in a fast-paced and dynamic environment • Strong quality-orientation with attention to detail and a desire to deliver service excellence. Initiative to review daily build plan and own assigned work • Ability to come up to speed quickly • Ability to work within a team • Flexible, reliable, and adapts well to change • Continuous improvement mindset • Demonstrates root-cause problem solving to identify and perform troubleshooting Working Conditions General Office, Laboratory, and Cleanroom environments Expected travel less than 10% Physical Requirements While performing the duties of this job, the employee is regularly required to stand; walk; sit; use hands to handle or feel; reach with hands and arms; climb or balance; stoop, kneel, crouch, see, talk or hear in a standard office environment. Employee may occasionally lift/or move up to 15 pounds. BENEFITS Medical, dental, vision, health savings account, flexible spending account, life and long-term disability insurance, 401(k) plan, holidays, and PTO. At Biolinq we fully subscribe to the principles of Equal Employment Opportunity. It is our policy to provide employment, compensation, and other benefits related to employment based on qualifications, without regard to race, color, religion, national origin, age, sex, veteran status, genetic information, disability, or any other basis prohibited by federal, state or local law. In accordance with requirements of the Americans with Disabilities Act and applicable federal, state and/or local laws, it is our policy to provide reasonable accommodation upon request during the application process to applicants in order that they may be given a full and fair opportunity to be considered for employment. As an Equal Opportunity Employer, we intend to comply fully with applicable federal, state and/or local employment laws and the information requested on this application will only be used for purposes consistent with those laws. To the extent required by applicable law, The Company maintains a smoke- free workplace. As part of our efforts to ensure fair and equal pay based on merit, Biolinq supports pay transparency internally and during the recruitment process. The U.S. base salary range reasonably expected to be paid for this role is: $21.00 to $23.00 per hour. We may ultimately pay more or less than the posted range. Actual compensation packages are commensurate with experience and based on a variety of factors that are unique to each candidate including, but not limited to: skill set, depth of experience, education, certifications, and specific work location. The range displayed reflects the minimum and maximum target for new hire salaries for the job across the U.S. The total compensation package for this position may also include an annual performance bonus and/or other applicable incentive compensation plans. Biolinq also offers a comprehensive package of benefits including paid time off (vacation, holidays, sick time, parental leave), medical/dental/vision insurance, and 401(k) to eligible employees, subject to the terms and conditions of the applicable plans and any written agreement between the parties. Your recruiter can share more about the total compensation package during the hiring process. Please note: The information contained herein is not intended to be an all-inclusive list of duties and responsibilities of the job, nor are they intended to be an all-inclusive list of the skills and abilities required to do the job. Management may, at its discretion, assign or reassign duties and responsibilities to this job at any time. The duties and responsibilities in this job description may be subject to change at any time due to reasonable accommodation or other reasons. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions. An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. If you are an individual with a disability and would like to request a reasonable accommodation as part of the employment selection process, please contact Biolinq Talent Acquisition at [email protected]