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We are currently looking to add a Manufacturing Associate l to our team in San Diego. Responsible for maintenance and production of high quality viral and execution of assays in support of San Diego’s manufacturing activities. Able to provide experienced support on more complex projects and completes manufacturing or QC processes with guidance. Our award-winning culture is friendly, collaborative, and supportive, providing endless opportunities for individuals to learn and grow, both personally and professionally. At Microbiologics, we believe that "great vision without great people is irrelevant." That's why we are always looking for great people to join our dynamic, innovative company as we provide the highest quality biomaterials for a safer, healthier world. What can I expect in this role? In this position, you will work Monday-Friday regular day time business hours. Some key duties in this role include · Provides higher level support during manufacturing process of viruses and can successfully complete assigned processes tasks with guidance. · Able to prioritize and manage their time into an accurate daily schedule to complete assigned tasks on time. · Ensures proper documentation is maintained in a timely manner and in accordance with Quality Assurance. · Intermediate Assay Operator: HAI assay, Ab stain TCID50 assay, ddPCR, endotoxin testing, ELISA, and other standard assay service offerings. · Outstanding performance and adherence to manufacturing SOPs and other relevant SOPs to the position. · Understands how to operate in the manufacturing spaces efficiently. · Upon request, executes the creation of new procedures or forms with guidance. · Upon request, executes the writing of validation plans, execution of plans, and creation of validation reports with supervision. · Consistent and thorough completion of lab maintenance activities as assigned and supports other team members when able. · Able to thaw and maintain multiple cell lines at one time for the support of multiple contracts. · Qualified operator of the cell countess for the counting of cells (multiple cell lines). · Can consistently seed plates and flasks at the required density in support of production or QC processes. · Often (but not required for the position) is a qualified BSL-3 Operator. · Performs the training of others upon request. · Maintenance of supply and material levels to trigger re-orders and replenishments. · Can troubleshoot Lab instrumentation. Who is Microbiologics? Microbiologics is one of the fastest growing international biotechnology companies in the nation. We are the world’s leading experts and go-to collaborators in biological products and services, focused on protecting the health and safety of people around the world. For over 50 years, we have been partnering with healthcare and life science laboratories, manufacturers, and suppliers across the globe to co-create and provide biological control materials, assay services and consulting for microbiology, molecular diagnostics, and virology. Headquartered in Saint Cloud, Minnesota, we have additional facilities in California, Kentucky, and Michigan. What can we offer you? Glad you asked! We have a comprehensive benefits package that includes your standard benefits such as health and dental insurance, health savings account (company funded), life insurance, short and long-term disability, and a 401k program with a generous match to name a few. In addition, we are proud to support our team and their families by offering daycare assistance, tuition reimbursement, bonus potential, a competitive compensation and benefits package, and plenty of opportunities for training and growth. What makes you a good fit? Our goal is finding the right individual for our team – we firmly believe that the right person is someone to invest in and invite to join our family. Here is what we are looking for: Education/Experience · Bachelor’s degree in Biology, Virology, Microbiology or related field or equivalent experience required.· Previous laboratory experience preferred. · Knowledge of aseptic technique and basic laboratory facilities and equipment. · Competent in proper pipetting techniques and experience in serial dilutions, dilution factors, and calculation of final dilutions.· Basic understanding of the scientific method and scientific notation.· Strong attention to detail. If you have a passion for science, we encourage you to apply! #LI-NS1
Join us in creating exceptional products through precision assembly! Your skills will help shape innovative solutions while advancing your career in a vibrant manufacturing environment dedicated to quality and safety. *Job Summary* Join our dynamic manufacturing team as a Manufacturing Assembler, where your hands-on skills and mechanical knowledge will drive the creation of high-quality products. In this energetic role, you will be responsible for assembling components on the production line, ensuring precision and efficiency at every step. Semiconductor disciplines include Wire Bonding, Silicon Wafer Preparation, Silicon Die Attach, Plastic Encapsulation and Decapsulation, Surface Mount, and Mold Press operations. Your contributions will directly impact our ability to deliver innovative solutions to customers worldwide. If you thrive in a fast-paced environment and enjoy working with tools and machinery, this position offers an exciting opportunity to grow your manufacturing career. *Duties* * Meet production, quality, and efficiency standards. * Work under a microscope for extended periods, at times. * Read and follow detailed written as well as verbal work instructions. * Maintain a clean, organized, and efficient workspace. * Collaborate with team members on the assembly line to meet production targets and resolve any assembly issues promptly. * Maintain accurate documentation of work performed. *Experience* * Must be a US Citizen or legal Permanent Resident. * Must be able to read and write English * Prior manufacturing facility experience is highly preferred, demonstrating familiarity with assembly processes. * Hands-on experience with hand tools, power tools, and mechanical assembly is essential for success in this role. * Knowledge of manufacturing safety standards and procedures to ensure a safe working environment. * Ability to read technical diagrams or work instructions clearly and follow them meticulously. * Strong mechanical aptitude with an eye for detail to identify potential issues during assembly. * Comfortable working on a cleanroom assembly line environment that demands strict gowning and ESD (ElectroStatic Discharge) protocols. Pay: $23.00 - $26.00 per hour Benefits: * 401(k) * 401(k) matching * Dental insurance * Employee assistance program * Employee discount * Flexible spending account * Health insurance * Health savings account * Life insurance * Paid time off * Referral program * Vision insurance Work Location: In person
At ACON labs, we are making a difference in medical care by offering medical devices for diagnosing a variety of conditions. In addition, we are able to streamline and reduce costs for the physician and/or patient directly. Come join us in developing the latest technologies that enhance human life and be a part of our growing, dynamic company. We are looking for a Production Formulation Operator onsite at our San Diego location. This position is responsible Chemical Formulations, Equipment Operating activities, and other Production activities as assigned by supervisor in production areas to meet production goals, product quality, and cost objectives. *Some Essential Duties and Responsibilities:* * Responsible for executing complex formulations according to SOPs * Be able to identify and report on any unexpected results in a timely manner * Responsible for using equipment for the assembly and processing tasks to product semi-finished component or finished product Follow SOP to perform the assigned tasks * Check the product name, batch number, quantity, specification, according to the production order * Properly document all activities according to GMP Requirements * Adhesive to all safety and quality procedures * Accurately and timely complete of all required functions * Clean production line following safety procedures and practices and maintain a clean work environment and equipment running condition * Conduct basic quality inspection of work according to SOP and training * Complete documentation records * Collaborate with quality control, warehouse, and other staff *Education and /or Experience:* * Bachelor’s degree in a Biological or Chemical Field (or equivalent) * Experience working in a GMP Laboratory * 0 - 2 years working in a related field/industry (Preferred) *Required Knowledge, Skills and Abilities:* * Must have general knowledge of computer operation * Ability to work in a team environment * Ability to work in a fast paced environment * Ability to stand for an entire shift and have manual dexterity * Ability to perform repetitive tasks and follow manufacturing procedures * Ability to work with a safety-first culture and adhere to all safety requirements at all times. * Documentation of activities must be legible. The salary range for this position takes into account a wide range of factors including education, experience, knowledge, skills, geography, and abilities of the candidate, in addition to internal equity and alignment with market data. At ACON it is not typical for an individual to be hired at or near the top range for their role and compensation decisions are dependent on the facts and circumstances of each case. The salary range for this position is $59,000 - $75,000. ACON offers a comprehensive benefits package including medical, dental, vision, life, and disability insurance, along with a 401(k) plan, employee assistance program, paid time off (including sick time), and paid Holidays. All benefits are non-contractual, and ACON may amend, terminate, or enhance the benefits provided, as it deems appropriate. Job Type: Full-time Pay: $59,000.00 - $75,000.00 per year Benefits: * 401(k) * 401(k) matching * Dental insurance * Employee assistance program * Flexible spending account * Health insurance * Life insurance * Paid time off * Vision insurance Schedule: * Monday to Friday Application Question(s): * How many years of experience do you have working in a GMP Laboratory environment? Education: * Bachelor's (Required) Experience: * Manufacturing: 1 year (Preferred) Work Location: In person
At ACON Labs, we are making a difference in medical care by offering medical devices for diagnosing a variety of conditions. In addition, we are able to streamline and reduce costs for the physician and/or patient directly. Come join us in developing the latest technologies that enhance human life and be a part of our growing, dynamic company. We are looking for a Production Operator - Dispensing onsite at our San Diego location. This position is responsible for equipment operating activities and other Production activities assigned by supervisor in production areas to meet production goals, product quality, and cost objectives. *Some Essential Duties and Responsibilities:* * Responsible for using equipment for the assembly and processing tasks to product semi-finished component or finished product Follow SOP to perform the assigned tasks. * Check the product name, batch number, quantity, specification, according to the production order. * Adhesive to all safety and quality procedures * Accurately and timely complete of all required functions * Clean production line following safety procedures and practices and maintain a clean work environment and equipment running condition. * Conduct basic quality inspection of work according to SOP and training * Complete documentation records *Education and /or Experience:* * High school diploma/GED required; and * 1 year of assembly work experience in a medical device manufacturing environment. *Required Knowledge, Skills and Abilities:* * Must have general knowledge of computer operation; * Ability to work in a team environment; * Ability to work in a fast paced environment; * Ability to stand for an entire shift and have manual dexterity; * Ability to perform repetitive tasks and follow manufacturing procedures; and * Ability to work with a safety-first culture and always adhere to all safety requirements. Job Type: Full-time Pay: $20.00 - $22.00 per hour Education: * High school or equivalent (Required) Experience: * Manufacturing environment: 1 year (Required) * Assembly work in a medical device environment: 1 year (Required) 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. Under general supervision, this position is responsible for planning, preparing, issuing and controlling production schedules and coordinates with material requirements to ensure a controlled flow of approved materials timed to meet production requirements. Advises management of the status of work in progress, material availability, and potential production problems to ensure that personnel, equipment, materials and services are provided as needed. DUTIES AND RESPONSIBILITIES: Contributes to efficient operation of organization by inputting to or preparing short and long-range plans and schedules reports and providing progress follow-up and adjustment information.; develops planning activities that support schedule development; schedules, monitors performance, analyzes and reports on activities to ensure flow of material. Develops manufacturing work orders in accordance with Material Requirement Planning (MRP) planned order requirements; guides manufacturing on action(s) to be taken. Investigates and resolves manufacturing related issues; performs product assessments for part or product designs; provides input for manufacturing processes and manufacturing technologies to meet cost and schedules. Processes work orders and material transactions for non-conformance material dispositions. Interprets engineering change orders (ECO), implements dispositions affecting stock, work in progress, and NEXT assembly. Develops standard and non-standard reports; identifies issues, exceptions and variances and develops solutions to moderately complex issues; reviews processes and procedures to support business and regulatory agency requirements. Represents group with interdepartmental activity with quality, manufacturing, purchasing, engineering and inventory control. Alerts operating or project management to deviation from established norms; develops and recommends solutions to a variety of problems of moderate scope and complexity. 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. May perform physical movement of hardware as a result of processing NCR and ECO dispositions. 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. Job Qualifications Typically requires a bachelor’s degree in business administration with an emphasis in Planning, Engineering, Production Control or a related discipline and three or more years progressive experience in planning, scheduling, budgeting and performance measurement. May substitute equivalent experience in lieu of education. Must have a general understanding of manufacturing planning principles, theories and concepts as well as ability to understand accounting and manufacturing systems in a research or production environment and to learn and apply basic planning tools and techniques; and knowledge of concepts and principles of planning to develop solutions to a variety of problems. Must be customer focused and possess the ability to identify issues and interpret data including engineering drawings. Organization skills to maintain flow of work within the unit. Good interpersonal, verbal and written communication skills to interface with internal employees and to accurately document, report and present. Ability to maintain strict confidentiality of sensitive information; and knowledge of computer operations and applications and word processing and spreadsheets. Ability to work both independently and in a team, environment is essential as is the ability to work extended hours as required. Ability to obtain and maintain a DoD secret clearance is required. Job Category Manufacturing Experience Level Mid-Level (3-7 years) Workstyle Onsite Full-Time/Part-Time Full-Time Salary Pay Range Low 56,820 Pay Range High 96,015 Travel Percentage Required 0% - 25% Relocation Assistance Provided? No US Citizenship Required? Yes Clearance Required? Desired Clearance Level Secret
Company Description ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients’ lives by Overcoming Resistance In Cancer. ORIC’s clinical stage product candidates include (1) rinzimetostat (ORIC-944), an allosteric inhibitor of the polycomb repressive complex 2 (PRC2) via the EED subunit, being developed for prostate cancer, and (2) enozertinib, a brain penetrant inhibitor that selectively targets EGFR exon 20, HER2 exon 20 and EGFR atypical mutations, being developed across multiple genetically defined cancers. Beyond these two product candidates, ORIC® is also developing multiple precision medicines targeting other hallmark cancer resistance mechanisms. ORIC has offices in South San Francisco and San Diego, California. For more information, please go to www.oricpharma.com, and follow us on X or LinkedIn. Reporting to the Senior Vice President of Quality, the Sr. Director of Quality will lead provide quality oversight of clinical development and manufacturing programs. This individual will lead the Chemistry, Manufacturing, and Controls (CMC) QA team and provide end-to-end development to manufacturing support for clinical stage programs and will develop systems to commercialize late-stage assets. This position will design, develop, and implement clinical and commercial quality strategies to ensure appropriate compliance to applicable regulatory regulations. The successful candidate will work closely with Technical Operations, Regulatory Affairs, and third-party Contract Development and Manufacturing Organizations (CDMOs) and will be responsible for all levels of studies, ranging from simple to complex and requires an in-depth understanding of GMPs, global Health Authority requirements, program management, quality systems, validation, and data integrity. Strong cross-functional team leadership and project management skills are essential requirements of the role. Job Description Ensure compliance with all applicable local and global drug regulations. Oversee Quality CMC functions with oversight and authority over batch disposition, manufacturing, packaging, labeling and testing activities to ensure product quality and timely release of materials and products. Provide hands-on leadership to effectively facilitate quality functions related to batch disposition, investigations, process and analytical data review, supply distribution and risk management. Serve as a point of contact for complex or high-risk quality issues and decisions. Identify and manage quality risks across the product life cycle, recommend and support mitigation strategies. Operate closely with ORIC technical operations team, Contract Manufacturing Organizations (CMOs), contract testing laboratories, and distribution sites to facilitate quality review of process/analytical data and reports, ensuring technical rigor and phase appropriate compliance to support program decisions. Work cross-functionally with Regulatory Affairs to ensure timely and accurate review of submissions. Operates closely with clinical program teams and serves as an active participant in clinical development meetings ensuring continuous quality support. Develop performance-based quality metrics and trend analyses to drive continuous improvement. Perform and present Annual Product Reviews for late-stage programs. Lead, mentor and develop a high-performing Quality team effectively scaling the team to support clinical into commercial programs. Serve as Chair or primary Quality member in various governance committees including ORIC’s Stability Review Board, Material Review Board and Change Review Board Represent ORIC Quality in CDMO meetings, regulatory authority interactions, strategic leadership meetings as needed. Demonstrate a high level of adaptability in dynamic and fast-paced environments. This includes the ability to adjust strategies, workflows, and priorities in response to changing business needs, technologies, and stakeholder expectations. Develop new functional, late phase, commercial ready SOPs, Policies/Plans as necessary. Qualifications Bachelor’s or Master’s degree in Chemistry, Biology, or a related scientific discipline 15+ years of relevant experience in Quality Assurance and/or Quality Control in the pharmaceutical industry. 7+ years of prior senior leadership experience. Deep hands-on knowledge in ICH, GMP, and regulatory guidance relevant to new drug development and commercialization. Experience with preparing for commercial stage operations and regulatory interactions preferred. Experience over a broad set of Quality Assurance functions with extensive knowledge of industry best practices and trends. Ability to understand business objectives and how they translate into quality priorities. Demonstrated ability to develop a vision for Quality functions as it transitions through the phases of drug development to commercialization. Demonstrated success in working with and managing CDMOs and external partners using succinct and thorough communication skills. Demonstrated ability to work independently and efficiently in a collaborative, fast-paced, integrated, multidisciplinary team environment that includes external partners. Proven ability to manage multiple priorities and deliver high-quality work. Demonstrated initiative, ownership, problem identification, problem solving, and analytical and strategic thinking skills. Demonstrated ability to quickly adapt and find creative solutions to ensure deliverables are met. Results driven, collaborative leader with proven ability to perform in a fast-paced environment with a high attention to detail and demonstrated ability to manage and prioritize multiple competing tasks Excellent verbal and written communication skills, with the ability to build productive long-term team relationships at all levels of supplier organizations, including with senior executives Skilled at managing autonomous, high-performing professionals who value flexibility, while ensuring alignment, collaboration, and delivery of results. Additional Information The anticipated salary range for candidates who will work on-site at our San Diego location is between $220,000-$270,000. The final wage offered to a successful candidate will be dependent on several factors that may include, title, type and length of experience within the role, type and length of experience within the industry, education, geography, and other job-related factors. ORIC Pharmaceuticals, Inc. is an equal opportunity employer. ORIC does not discriminate based on race, color, religion, gender, sexual orientation, gender identity, age, national origin, disability status, protected veteran status, or any other legally protected characteristics.
*Job Title: Laborer* *Location: Escondido, CA 92029* *1st Shift: * *4:00am - 12:30pm (M-F) * *Temp to Hire* *Description:* * This position requires 0-3 Years of experience. * The Production Worker primarily works in the outside production area of the AmeriGas Cylinder Exchange facility. * The employee is responsible for the processing of cylinders (20 lb. barbecue grill cylinders). *Key Responsibilities:* * Follow all company safety procedures and model a strong commitment to safety. * Sort, inspect, clean, paint, label, and refill empty propane cylinders. * Maintain consistent quality standards for cylinder processing. * Load filled cylinders onto trucks for shipment. * Stand and walk 8–12 hours per shift; lift to 50 lbs. repeatedly. * Perform general housekeeping duties to maintain a safe work environment. * Work collaboratively with the production team and demonstrate continuous improvement. * Ability to work in a fast-paced environment. * Capability to obtain state licensing and forklift certification. *Requirements:* * High School diploma or equivalent required. * Manufacturing experience preferred. *Key words: (Warehouse, Manufacturing, Production Worker, Cylinder, Exchange, Propane, Barbeque Grill, Safety Procedures, PPE, Sort, Inspect, Clean, Paint, Label, Refill, Quality Standards, Load, Unload , Teamwork, Production, Stand, Walk, Lift 50 pounds, General Housekeeping, Mechanical Aptitude, Computer Knowledge, Forklift Certified, Forklift Certification)* *#REQNon-IT* Job Type: Contract Pay: $18.00 per hour Work Location: In person
Overview We have an immediate opportunity for a Group Manager – Quality Management System (QMS) to lead the design, implementation, and continuous improvement of our enterprise-wide Quality System in San Diego, CA. You will be part of the Operational Excellence and Continuous Improvement team, responsible for embedding a culture of data-driven quality, coaching excellence, and customer obsession across Intuit’s Customer Success, Partner Operations, and Sales organizations. In this role, you will define and operationalize the Quality Management System (QMS) strategy that drives measurable improvements in Service Quality, customer outcomes, and business performance. You will work closely with cross-functional stakeholders, including Operations, Technology, Data Science, and Change Management, to scale consistent, explainable, and automated quality standards across global contact center operations. Responsibilities Lead the design, deployment, and continuous evolution of the Quality Management System (QMS) across all business units and partner sites. Establish a unified quality governance model integrating AI-based scoring, human audit frameworks, and coaching feedback loops. Partner with Product and Technology teams to define system requirements, guide QMS platform enhancements, and ensure seamless data integration and reporting. Develop and maintain the Quality Policy, Standards, and Procedures that underpin service excellence and compliance. Define and track key quality performance indicators (KPIs) such as Service Quality Score (SQS), Critical Error Rate, and Coaching Effectiveness, ensuring alignment with customer and business outcomes. Drive process optimization and corrective action plans based on quality insights, focusing on root cause elimination and sustainable improvement. Build internal capability through quality leadership coaching, calibration sessions, and certification of Quality Leaders and Coaches. Partner with Operational Excellence and Learning teams to embed QMS principles into daily management, problem-solving, and performance routines. Ensure compliance with internal and external standards and lead readiness for any quality-related audits or reviews. Cultivate a culture of continuous improvement and accountability across operations, promoting ownership, advocacy, and expertise at every level. Qualifications Bachelor’s degree in Business Operations, Quality Management, Engineering, or equivalent work experience; Master’s preferred. Lean Six Sigma Black Belt (LSSBB) or equivalent certification required. Proven experience designing, deploying, and running Quality Management Systems within large-scale, global contact center or customer success environments. Strong understanding of technology platforms, data architecture, and AI-based quality systems; able to translate operational needs into technical requirements. Experience collaborating with Tech, Data, and Product teams to develop automation and quality analytics capabilities. Demonstrated success leading cross-functional quality improvement programs with measurable business impact. Strong facilitation and stakeholder management skills; able to influence at all organizational levels. Deep understanding of Continuous Improvement, Root Cause Analysis, and Process Control methodologies. Familiarity with ISO 9001, COPC, or equivalent quality frameworks is highly desirable. The experience you need to excel in the role: 7–10 years of professional experience leading Quality or Operational Excellence programs in a complex, multi-site or global organization. Proven track record deploying QMS frameworks that integrate human auditing with technology-driven quality monitoring. Experience driving measurable improvements in Customer Satisfaction, Issue Resolution, and Compliance metrics. Strong partnership skills with Technology, enabling automation, systemization, and continuous measurement of quality performance. Ability to coach and develop leaders in adopting data-driven quality management practices. Intuit provides a competitive compensation package with a strong pay for performance rewards approach. This position will be eligible for a cash bonus, equity rewards and benefits, in accordance with our applicable plans and programs (see more about our compensation and benefits at Intuit®: Careers | Benefits). Pay offered is based on factors such as job-related knowledge, skills, experience, and work location. To drive ongoing fair pay for employees, Intuit conducts regular comparisons across categories of ethnicity and gender. The expected base pay range for this position is: Southern California $190,000-257,000
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. Starting Wage $33.63 hourly, plus 10% shift differential Location On-site position in Vista, CA. Schedule 1:15 PM to 9:55 PM Monday through Friday Responsibilities: Mixes, tabulates, and processes raw materials with attention to detail in ensuring formulas and batch records are completed in a timely manner. Operate HMI/SCADA control panels to control and monitor vegetable oil refining processes and bar base noodle production for soap manufacturing. Uses a strong understanding of vegetable oil refining process to operate refining, bleaching, and deodorization production processes. Assists with taking in line samples and analyzing samples using in-house lab equipment as part of multiple process feedback loops. Monitors utility equipment boilers, cooling towers and chillers carrying out water chemistry testing procedures regularly and report any defects to lead/supervisor. Accurately enter production data, material usage, batch records, and process readings, ensuring traceability and real-time reporting. Ensures that record batching and testing information is performed consistently and accurately, as directed by shift leader. Prepare, blend, and stage raw materials, including oil additives, citric acid solutions, and brine solutions, following approved formulations, batching instructions, and safety guidelines. Raw material managing, connecting shipping containers and ISO containers to steam hoses, handling oils and raw materials using appropriate pumps, hoses, and equipment while maintaining housekeeping and contamination controls. Uses an understanding of bar base saponification and drying processes, and modern industrial controls to saponify vegetable oils and dry the slurry into bar noodles for in-house pressing operation. Uses in-house testing equipment to control saponification and drying processes, as directed by shift leader. Reports any problems or issues to the Lead operator regarding the operation. Maintain accurate operating logs, inspection records, and shift handover communications. Perform basic troubleshooting working with hand tools and coordinate with maintenance for repairs, isolations, and equipment change-outs by creating work orders using maintenance management computer programs. Support troubleshooting activities by identifying process deviations, equipment issues, or quality concerns and communicating findings to supervisors, maintenance, and QA. Perform routine field rounds to inspect operating equipment, verify instrument readings, and identify abnormal conditions or deviations. Carries out housekeeping duties ensuring a safe and clean workspace is maintained. Performs minor maintenance and repair assignments as directed requiring the knowledge and familiar use of hand and electrical tools. Occasionally it is asked to assist other production departments as business needs dictate. Expected to attend training classes as business needs arise typically HAZWOPR, Confined space, fire extinguisher use, FIRST AID AED CPR, stormwater control, and any internal training requirements. Understands and follows Standard Operating Procedures (SOPs) and Work Instructions (WIs). Other duties as assigned within job scope. Qualifications: High school diploma or equivalent. 2 years of relative experience in refining or similar operations with industrial equipment including pumps, valves, steam lines, conveyors, and controls. Knowledge of Microsoft Office Programs (Word, PowerPoint, Excel Outlook). Must possess/obtain forklift and pallet jack certifications. Additional in-house safety certifications must be completed. Any combination of education and work experience that would be equivalent to the stated minimum requirements would qualify for consideration of 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.
Applied Composites (AC) is seeking a Production Assembler 1 to perform a range of routine assembly operations of small parts or components, under well-defined instructions and in accordance with company policy and safety procedures. This individual uses light powered electrical or mechanical tools, including hand tools, in the construction of subassemblies. Works with the assembly team to sandblast parts with minimal efforts, fit and align and/or adjust parts to meet specifications and requirements, some prep of composite parts for paint department necessary. Must be able to work with shop tools and equipment used in composite layup and assembly. About AC: Come and join the Applied Composites team. We are a leading provider of complex composite components, assemblies, engineering and tooling to the aerospace, defense and space system markets. Our employees are treated with respect and given the support, knowledge, and resources they need to thrive. If you are looking for a company that values and develops its employees while offering engaging work, Applied Composites may be the place for you. Job Accountabilities: Ability to use basic shop tools such as sanders, grinders and drill motors Ability to use basic measuring devices such as calipers, scale and micrometers to verify dimensions Ability to document the materials used in the process to maintain traceability Ability to do accurate work at a fast-pace Ability to sandblast parts with minimal scrap or errors Familiarity with standard shop practices in the aerospace industry Must be able to wear the necessary Personal Protective Equipment (PPE) to work with chemicals Familiarity with LEAN manufacturing principles Demonstrates all safety policies and procedures Other responsibilities as assigned Job Specifications: Education: A Secondary Certificate/High School Diploma or equivalent combination of relevant education and work experience that will allow successful performance of job expectations Years’ Experience: 0-2 years of relevant work experience Skills: Good mechanical aptitude Able to operate a variety of hand tools and light machinery Capable of performing basic mathematics Ability to read and interpret company documents, such as safety rules, operating/manufacturing instructions, policies and procedures Good manual dexterity required to work with small parts Able to problem-solving using existing procedures to perform straightforward tasks Effective oral, written and interpersonal skills Experience in laminating Carbon Fiber, Fiberglass, Kevlar, or other composite material preferred Benefits: At Applied Composites, we recognize how important your career and benefits are to you and your family. We offer a full suite of benefits including medical, dental, vision, short and long-term disability coverage, accident insurance, critical illness insurance, basic and supplemental life insurance, employee assistance plan, retirement savings and matching, tuition reimbursement and other developmental opportunities. We are committed to supporting the way you live and work. AC is an Equal Opportunity Employer Veterans/Disabled - Affirmative Action Employer. This position requires the use of information which is subject to the International Traffic in Arms Regulations (ITAR). All applicants must be U.S. persons within the meaning of ITAR. ITAR defines a U.S. person as a U.S. Citizen, U.S. Permanent Resident (i.e. 'Green Card Holder'), Political Asylee, or Refugee. 9/80 Schedule - 1st Shift
*Job Overview* CNC Set Up and Machine Operator is responsible for operating 3-5 axis CNC milling machines according to the specified setup sheets to produce the highest quality parts in the most efficient manner while meeting the drawing/planning specification /requirements. This position requires multi-axis CNC experience, strong mechanical aptitude, the ability to work with minimum supervision, and a desire to work in a creative hands-on environment. *Responsibilities and Duties* * Complete machine set-ups without the need for outside supervision/assistance. * Responsible for all phases of part machining, including job set-up to achieve first article acceptance and production run. * Must understand CNC machine origins, how to set them and how to adjust them. * Must understand CNC machine tool offsets, length and radius, and how to adjust them. * Perform and maintain accurate in-process quality inspection and records. * Identify and recommend process improvements that reduce part quality variation. * Input data into visual management forms and convey results to management. * Continuously improve processes, procedures, and eliminate waste. * Perform other related duties as assigned. * Must be able to fill out all paperwork related to the job at hand. *Qualifications* * Five (5) years experience with all phases of CNC Mill equipment operation, 4 or 5 Axis preferred. * Must be able to perform job setups including all variables involved. * Must have complete knowledge of G-code, M-code, Origins, Offsets. * Must have complete knowledge on how to adjust Offsets and variables during a cycle. * Skilled in the use of dial indicators, calipers, gauges, and plate inspection methods for fixture pick-up, first article and in-process inspection of precision machined parts. * Understanding of machine tool clearances, fixture offsets, and cutting tool offsets. * Knowledge of cutting tool feeds, speeds, and tool life usage. * Ability to follow verbal instructions and interpret blue print and quality requirements. * Ability to lift a maximum of 50 lbs (over 25 lbs with assistance). * Experience with AS9100, 5S, Lean, Six Sigma, Fagor controllers, and MasterCam a plus. First shift: 7:00AM to 3:30PM Job Type: Full-time Pay: $22.00 - $32.00 per hour Benefits: * 401(k) * Dental insurance * Flexible spending account * Health insurance * Life insurance * Paid time off * Referral program * Vision insurance Application Question(s): * Do you have at least 5 years of experience with all phases of CNC Mill equipment operation (4 or5 Axis preferred)? * Reliability and consistent attendance are vital to this role. Are you able to consistently arrive on time and maintain excellent attendance? * Which shift schedule are you applying for? (1st: 7am-3:30pm, 2nd: 1pm-9:30pm) Work Location: In person
The Staff Manufacturing Engineer provides manufacturing engineering leadership supporting the development, commercialization, and production of medical devices. This role oversees a portfolio of products manufactured primarily by contract manufacturers and drives improvements in cost, lead time, manufacturability, and overall operational performance. The position collaborates cross-functionally with Product Development, Sustaining Engineering, Quality, Supply Chain, and external manufacturing partners to ensure robust manufacturing processes and scalable production. Essential Duties and Responsibilities Operate as a primary manufacturing technical resource for product development and lead manufacturing initiatives focused on cost reduction, lead time improvement, yield enhancement, and process robustness at contract manufacturers. Define and drive manufacturing strategies across the product portfolio to improve cost, scalability, and operational performance. Support the identification, technical evaluation, and relationship management of external manufacturing partners for complex medical devices. Lead technical design reviews and specification transfer from R&D to internal and external suppliers, ensuring cost-effective manufacturability and inspection through DFM, DFI, and DFA principles. Serve as the technical authority for design transfer and new product introduction (NPI), ensuring successful transition from development to production. Lead manufacturing process development and validation activities (IQ/OQ/PQ) for new and existing products. Partner with internal teams and external suppliers to resolve manufacturing issues and drive improvements in process capability, yield, and throughput. Establish technical standards within the engineering organization and mentor junior engineers. Lead and participate in Failure Mode and Effects Analysis (FMEA) to mitigate risks to product quality and patient safety. Lead investigations into nonconformances and implement corrective and preventive actions (CAPA). Analyze manufacturing data to identify trends and drive continuous improvement initiatives. Develop and maintain work instructions and documentation for manufacturing processes. Other duties as assigned. Requirements The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Strong knowledge of manufacturing processes (e.g., machining, injection molding, fabrication, secondary/finishing operations, and assembly) and their application in the production of medical devices. Strong knowledge of quality systems, inspection standards, equipment, and best practices. Strong experience with the creation, review, and analysis of engineering design specifications and the application of Design for Manufacturability (DFM), Design for Inspection (DFI), and Design for Assembly (DFA). Proficient with CAD software (e.g., SolidWorks). Strong analytical thinking and problem-solving skills, with the ability to communicate technical concepts clearly to both technical and non-technical audiences. Demonstrated success working cross-functionally with R&D, Quality, Regulatory, Marketing, and Operations teams. Strong knowledge of engineering materials and their applications, particularly metals and plastics used in medical device manufacturing, with preferred knowledge of composite materials. Demonstrated ability to manage multiple projects and priorities in a fast-paced environment. Strong knowledge of FDA regulations and quality standards (21 CFR Part 820, GMP, ISO 13485, ISO 9001, ISO 14971). Highly proficient with statistical methods and quality tools such as SPC, Gage R&R, and Design of Experiments (DOE). Demonstrated experience working with contract manufacturers and suppliers to develop, validate, and improve manufacturing processes. Expert knowledge in the interpretation and application of Geometric Dimensioning and Tolerancing (GD&T). Strong verbal, written, and organizational communication skills with the ability to operate effectively in a dynamic environment. Required to travel domestically up to 20% annually. Potential for international travel. Education and Experience Bachelor's degree in Engineering (Mechanical/Manufacturing, or related field) 10+ years of experience in manufacturing or development engineering, preferably within the medical device industry. Lean / Six Sigma Black Belt or Master Black Belt certification preferred (or in progress). For roles based in the United States that require access to hospital facilities, must be eligible for and maintain credentials at all required hospitals, including meeting any applicable physical requirements or vaccination requirements (including the COVID-19 vaccine, as applicable). ATEC is committed to providing equal employment opportunities to its employees and applicants without regard to race, color, religion, national origin, age, sex, sexual orientation, gender identity, gender expression, or any other protected status in accordance with all applicable federal, state or local laws. Further, ATEC will make reasonable accommodations that are necessary to comply with disability discrimination laws. Salary Range Alphatec Spine, Inc. complies with state and federal wage and hour laws and compensation depends upon candidate’s qualifications, education, skill set, years of experience, and internal equity. $150,000 to $170,000 Full-Time Annual Salary