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_Quality Assurance Associate_ *Qualifications:* * Bachelor’s degree, biology or related field preferred but not required * Familiarity with cGMP, ISO 13485 requirements, FDA, and international quality * Computer skills *Duties and Responsibilities* * Stay current with all regulatory procedures and documentation in order to maintain compliance with GMP, QSRs, FDA, ISO, CE and customer requirements. * Develop procedures and practices to optimize product quality, safety, and reliability. * Work with Production and R&D to review and optimize or develop validation protocols. * Ensure compliance of product labeling and advertising. * Examine product release lot packets and review/verify product quality for product releasing. * Document and maintain accurate records of quality assurance activities, including but not limited to lot packets, SOPs, water quality records, temperature records and other investigations. * Develop or edit QSR SOPs; Production SOPs; product design history files, Instruction for Use, etc. * Make sure all documents complying with ISO13485:2016, US FDA and MDSAP standards, and fit Epitope’s operational procedures. * Prepare quality documentation and reports by collecting, analyzing and summarizing information and trends including failed processes, stability studies, recalls, corrective actions, and re-validations. * Participate in internal audits and assessments to identify non-compliances and areas for improvement. * Participate in the validation of equipment, procedures, and systems to ensure compliance with quality standards. * Take on growing responsibilities for FDA audit, ISO surveillance audits and customer audits. * Assist in EU IVDR, FDA 510(k) and other countries product registrations. * Play a key role in daily department operation to achieve delivering quality products to customers and reach customer satisfaction. It is the policy of Epitope Diagnostics to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Epitope Diagnostics will provide reasonable accommodations for qualified individuals with disabilities. Job Type: Full-time Pay: $52,000.00 - $72,000.00 per year Benefits: * 401(k) matching * Dental insurance * Health insurance * Paid time off Work Location: In person
About Our Company MDI Advanced Systems USA Inc. was established in February 2024 as the U.S. branch of MDI (Mitsuboshi Diamond Industrial Co., Ltd., Osaka, Japan). MDI is a leading equipment manufacturer specializing in precision processing technologies, including scribing, breaking, drilling, and patterning. We provide proprietary cutting tools, laser systems, and automated equipment designed to achieve high productivity. Since 1935, we have applied patented cutting technologies to glass and other hard and brittle materials. Our equipment and tools also support multi-layered structures, including metal and organic materials. Position Overview * Job Title: Process Engineer * Job Type: Full-time * Classification: Exempt (Managerial / Professional) * Visa Sponsorship: Not available * Location: San Diego, CA 92121 – Onsite * Work Schedule: Monday–Friday (Saturday, Sunday, and holidays off) * Relocation: Candidates must be willing to relocate prior to start date * Travel: Domestic and international travel required (including Japan); travel allowance provided Job Description As a Process Engineer, you will: * Test and evaluate customer samples using our singulation (cutting/dividing) equipment * Interact closely with customers and collaborate with headquarters in Japan * Prepare detailed technical reports * Analyze and interpret test results * Travel as needed for business purposes Minimum Qualifications * Bachelor’s degree in Engineering or a related field * Entry-level candidates encouraged to apply * Ability to work onsite and travel internationally * References required after interview _Note: Relocation assistance is not provided._ Compensation * Salary: $66,560 – $85,000 per year Benefits * 401(k) Plan with Matching * Health, Dental, and Vision Insurance * Paid Time Off (PTO) and Sick Leave * Travel allowance for business trips We provide a competitive compensation and benefits package along with a flexible work schedule that supports work-life balance. Equal Employment Opportunity & Background Check MDI Advanced Systems USA Inc. is an Equal Opportunity Employer. Employment is contingent upon successful completion of a background check in accordance with applicable law. At-Will Employment Employment with MDI Advanced Systems USA Inc. is on an at-will basis. This means that either the employee or the company may terminate employment at any time, with or without cause or notice, in accordance with applicable law. Job Type: Full-time Pay: $66,560.00 - $80,000.00 per year Benefits: * 401(k) matching * Dental insurance * Health insurance * Vision insurance Ability to Relocate: * San Diego, CA 92121: Relocate before starting work (Required) Work Location: In person
Malin Space Science Systems (MSSS) is a private technology company that designs, develops and operates space camera systems for government and commercial aerospace customers and provides services in spacecraft instrument operations and space science research. As a member of our multidisciplinary space imaging systems design team, the Flight Assembly Technician is responsible for high-level assembly of prototype and spaceflight electronics under the direction of the Production Manager, utilizing applicable preferred certifications and technical expertise to run production equipment. *Essential Functions* * Assembles electronic, mechanical, optical, and cable harness assemblies by following detailed work instructions and applicable NASA and IPC workmanship standards. * Responsible for operating Surface-Mount Technology (SMT) reflow machine. * Processes and operates X-Ray machine per project guidelines. * Operates Automated Optical Inspection (AOI) machine. * Prepares and operates Parylene conformal coating machine. * Maintains detailed assembly records according to company and industry standards. * Assists hardware engineering in assembly of prototype electronics and cable harnesses, testing, troubleshooting, and mechanical integration. * Maintains all required NASA and IPC trainings and recertifications. * Performs ESD check-in on a daily basis. * Cross-trains in assembly disciplines to support all aspects of work completion. * Participates in team meetings and provides updates on work status. * Maintains work area, tools and equipment. Performs required maintenance as needed. * Prior to entering assembly, test, storage or development areas within the Camera Systems Group unescorted, receive initial and ongoing annual training in the fundamentals of Electrostatic Discharge (ESD). *Non-Essential Functions* * Travels to customers and/or vendors as required. * Performs other duties as required or requested which may become essential to this position. *Minimum Qualifications* * High-School Graduate / GED required. Some college or Trade School / ROP certification desired. * Minimum of 3 years of solder assembly experience. * Minimum of 5 years of operating experience with either SMT, AOI, Parylene or X-Ray machines. * Excellent hand soldering, cable harness assembly, mechanical assembly, documentation, organization, and communication skills. * Excellent attention to detail and ability to work closely with each member of a production team. * Must be able to read schematics and mechanical drawings and precisely follow detailed written instructions. * J-STD-001 certification is required. Space Addendum certification is preferred and is a requirement to perform the position. * Polymerics mix and application experienced preferred; will be required to obtain NASA-STD 8739.1 certification. * Must be computer literate with knowledge of MS Excel and Word. * Results-oriented, self-motivated and dependable. * Hands-on machinist experience for manufacturing test fixtures is preferred. * Ability to work outside of regular business hours. * Occasional travel to customers and/or vendors may be required. *Physical Requirements* Must be able to remain in a stationary position operating lab equipment for periods of time. Must be able to perform repetitive soldering tasks under a microscope to properly position hardware. Ability to inspect parts and assemblies under a microscope to determine product placement. Ability to work and move around in a cleanroom environment, wearing required outer garments including smock/coveralls, shoe covers, mask, goggles, hood, gloves and ESD wrist strap. Must be able to communicate clearly with a variety of people on a daily basis. Must be able to traverse spaces in and around the office, labs, and machine shop as applicable. Ability to lift and carry up to 10 lbs. as needed. Possess mental acuity at a level which will facilitate execution of complex technical instructions. Ability to practice safe driving habits while following all state safety regulations and standards.Ability to handle high stress levels in connection with multiple conflicting priorities and deadlines. High tolerance for ambiguity and shifting expectations. Ability to travel to customers and/or vendors locations. *Disclaimer* The employee must be able to perform the essential functions of the position satisfactorily and, if requested, reasonable accommodations will be made to enable employees with disabilities to perform the essential functions of their job, absent undue hardship. The Employer retains the right to change or assign other duties to this position. _MSSS is committed to providing equal employment opportunities to all individuals, regardless of any protected status, including veterans and individuals with disabilities._ Job Type: Full-time Pay: $32.00 - $34.00 per hour Expected hours: 40 per week Benefits: * 401(k) * Dental insurance * Flexible spending account * Health insurance * Life insurance * On-the-job training * Paid sick time * Paid time off * Parental leave * Vision insurance Work Location: In person
*Engineering Manager, Product Development* Location: Carlsbad, California Schedule: Full Time, Day Shift, On-Site *Position Summary* Lumos Diagnostics is seeking an Engineering Manager, Product Development to lead engineering execution supporting the FebriDx platform and future product initiatives. This is a hands-on leadership role responsible for delivering technically sound, manufacturable, and compliant engineering solutions across the product lifecycle. The Engineering Manager leads a small team of engineers while actively contributing to product and process development, ensuring alignment with business priorities, project timelines, and quality standards. This role partners closely with Product, R&D, Quality, Manufacturing, and Operations to advance product improvements, support manufacturing readiness, and strengthen engineering processes as the organization continues to scale. *Essential Duties and Responsibilities* · Lead engineering execution in support of new product development and enhancements to existing product lines · Provide technical direction to engineers to ensure solutions are feasible, manufacturable, and aligned with performance and quality requirements · Support projects from development through commercialization while maintaining accountability for engineering deliverables and timelines · Identify technical risks early and collaborate with cross-functional partners to develop mitigation plans · Participate in design reviews and support verification, validation, and documentation activities within regulated quality systems · Directly manage engineers by providing coaching, feedback, and performance management · Prioritize workload, set expectations, and ensure team members are positioned for success · Foster a collaborative and accountable team culture · Partner cross-functionally with Product, R&D, Quality, Manufacturing, and Operations to support technical execution · Support transfer to manufacturing activities including process development, yield improvement, validation, and production support · Communicate progress, risks, and recommendations clearly to stakeholders and leadership · Contribute to development and refinement of engineering best practices and processes · Support root cause analysis and corrective actions related to product or manufacturing issues · Perform other duties as assigned *Minimum Qualifications* · Bachelor’s degree in Engineering or related technical discipline such as Mechanical, Manufacturing, or similar · Five or more years of progressive engineering experience in product development or regulated environments · Prior experience leading or supervising engineers · Experience supporting cross-functional product development initiatives · Experience with design for manufacturability and process development · Experience supporting product transfer to manufacturing and production scale · Experience working within FDA or ISO 13485 regulated environments · Strong technical problem solving and execution skills · Demonstrated ability to manage competing priorities and deliver projects against timelines · Strong interpersonal skills with the ability to collaborate effectively across cross-functional teams *Compensation* Annual salary range: $140,000 to $170,000 depending on internal equity, experience, and qualifications This position is eligible for a discretionary annual performance bonus based on individual and company performance *Benefits* Comprehensive benefits package including medical, dental, vision, life insurance, and disability coverage 401(k) with employer match Three weeks of vacation accrued annually Sick time, paid holidays, and a floating holiday *About Lumos Diagnostics* Lumos Diagnostics develops, manufactures, and commercializes innovative diagnostic solutions that deliver reliable results at the point of care. Our culture is guided by our core values Take Ownership Engage Openly Act with Integrity Move Together *Work Environment* This role is primarily performed on-site in an office, laboratory, and manufacturing environment working standard day shift hours *Why Join Lumos* You will have the opportunity to lead impactful engineering initiatives, work cross-functionally, and contribute to innovative product development in a collaborative environment *Screening Question Instruction Note* All screening questions must be answered in full for consideration for this role. Incomplete applications may not be reviewed. Pay: $140,000.00 - $170,000.00 per year Benefits: * 401(k) * 401(k) 4% Match * 401(k) matching * AD&D insurance * Dental insurance * Disability insurance * Employee assistance program * Employee discount * Flexible schedule * Flexible spending account * Health insurance * Health savings account * Life insurance * Paid jury duty * Paid time off * Parental leave * Professional development assistance * Tuition reimbursement * Vision insurance Application Question(s): * How many years of progressive engineering experience do you have in product development or regulated environments? * Do you have experience working in a regulated environment such as FDA, ISO 13485, or similar quality systems? * Do you have prior experience leading, supervising, or managing engineers or technical teams? * How many years of people leadership experience do you have? * Do you have experience supporting product development from concept through commercialization? * Do you have experience with design for manufacturability and supporting transfer to manufacturing? * 9. Which of the following areas do you have hands-on experience with? • Product development engineering • Process development • Manufacturing support • Validation activities • Root cause analysis and CAPA • Automation or equipment development • None of the above * This role is a full-time, on-site position in Carlsbad, California working a day shift schedule. Are you able to meet these requirements? * 13. This role has an annual salary range of $140,000 to $170,000 depending on experience and internal equity. Are you comfortable with the offered range? Education: * Bachelor's (Required) Shift availability: * Day Shift (Required) Ability to Commute: * Carlsbad, CA 92010 (Required) Work Location: In person
Position Summary The Quality Assurance Technician ensures food safety, quality, and compliance across all production activities. This role is critical in supporting manufacturing by identifying risks, conducting inspections, and verifying that all regulatory and Suja standards are met. This is an on-site position within a production environment and reports to the QA Supervisor. Schedule 1:00 PM - 9:30 PM Sunday-Thursday, with flexibility for OT on Friday's Essential Duties and Responsibilities Monitor production conditions, specifications, process controls and tracking controls Monitor wash line concentrations and test ppm concentrations for sanitation bucket and floor solutions Monitor a system that will verify checks on existing production control forms and be audited on the same forms that meet all program requirements. Collect Lab retain samples Verify all CCPs on-line and take corrective actions whenever necessary to assist in determining the root cause and development of a preventative action plan Responsible for checking the pH levels, temperature and brix of each batch of juice produced and is with in product specifications Verify and document Facility Operation Inspections & Good Manufacturing Practices Enforce Good Manufacturing Practices (GMPs) throughout the manufacturing areas Perform Standard Sanitation Operational Procedures (SSOPs) verification and ATP swabs Tracks non-conforming product (Holds) Perform pre-operational inspection procedures of all production/bottling equipment and facility Verify equipment calibrations. Verify volumes, lot codes, torques & bottle weights are within product specification. Complete and enter into database all pallet tags and CCP forms for production and bottling. Record cycles and verify that all HPP settings and information is correct Perform metal mesh, magnet and sock mesh inspections Verify production lot codes, labels, mold number and packaging are within product specification Shipping and receiving verifications. Verification of all raw materials being delivered and labelled with accurate information at Receipt (product name, lots, expirations, quantity received) COA Reviewing, comparing to the specification, approving and filing the COA. Escalating or placing on hold any items that are out of compliance. Review and Verify receiving documents and logs. Monitors production conditions, specifications, process controls and tracking controls as they specifically relate to raw materials used in production. Document and maintain records for all raw materials used in the production process including disposals, usage, and pre-batching of ingredients. Materials will be logged on the appropriate batch ticket for raw material commodity of interest. Commodities include raw produce, frozen juice, frozen puree, dry ingredients and aseptic products. Inspect raw materials for deficiencies relating to appearance, texture, and/or odor before production use. Inspect incoming trailers to ensure compliance with receiving standards. Report any food safety problems to the SQF Practitioner or Department Supervisor in a timely manner so that corrective actions may be performed. Adhere to SOP, SSOP, GMP, and HACCP guidelines when in the plant. Regular and reliable attendance. Job Qualifications 1–2 years of experience in Quality Control and/or the food industry preferred Familiarity with food safety regulations is a plus Other Skills & Abilities Excellent communication skills Strong computer proficiency Sharp critical thinking and problem-solving abilities Flexible and able to adapt to change Capable of working independently with moderate supervision Comfortable in a fast-paced production setting Working Conditions This role operates in a food manufacturing environment. Frequent standing, walking, and exposure to cold or wet areas are expected. Compensation and Benefits Come thrive at Suja Life! We offer a competitive benefits package, including: Hourly Pay: $20.00 Medical, dental, vision, life insurance, and more Paid Parental Leave – 12 Weeks at 100% Pay 401(k) match to help you plan for the future Paid time off: vacation, sick days & holidays Juice benefits: yes, we keep you fueled and refreshed! #ZR #INDHP Suja Life is proud to be an equal-opportunity employer seeking to create a welcoming and diverse environment. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, ancestry, physical or mental disability, medical condition, marital status, genetics, age, or veteran status or any other applicable legally protected status or characteristic. The Company complies with all federal/local/state regulations regarding pay.
Category Legal, Compliance & Policy Location Mountain View, California; San Diego, California Job ID 19703 Company Overview Intuit is the global financial technology platform that powers prosperity for the people and communities we serve. With approximately 100 million customers worldwide using products such as TurboTax, Credit Karma, QuickBooks, and Mailchimp, we believe that everyone should have the opportunity to prosper. We never stop working to find new, innovative ways to make that possible. Job Overview Overview: Come join our amazing team of leaders, learners and world-class compliance professionals. We're a high-performing team that enjoys working together to accelerate innovation across the Intuit ecosystem by delivering impactful business outcomes that strengthen the Intuit brand. Intuit’s Legal, Compliance & Policy Organization (LCPO) is seeking a Staff Compliance Testing Manager with strong leadership experience working with large teams to deliver impactful business outcomes that meet our obligations to our customers, partners and regulators. This role is a hybrid role – with 3 days a week in office expectations. Responsibilities What you’ll bring This role requires a collaborative and influential leader with a strong compliance background and a proven ability to drive results in a fast-paced environment. Here's what you'll need to succeed: Leadership & Collaboration: Demonstrated ability to build trust, foster collaboration, and act as a trusted advisor to stakeholders at all levels. Adept at navigating complex situations and effectively translating feedback into action. Cultivates a “One Team” mindset demonstrating extreme ownership. Compliance Expertise: Bachelor’s Degree with 10+ years of experience in compliance, internal audit, or public accounting, preferably within the software or FinTech industry. A strong understanding of business and compliance processes, including system and IT general controls. Execution & Accountability: Proven ability to manage and prioritize multiple projects, supervise resources, and drive accountability within large teams to achieve desired outcomes.Skilled at navigating complex problems and delivering solutions that drive impactful results. Communication & Influence:Exceptional communication and influencing skills to drive decision-making with velocity; effectively conveys complex information, actively listens to understand various viewpoints, and skillfully manage conversations—including escalations—to ensure timely and informed decisions. Problem-Solving & Mentorship: A strategic thinker with strong problem-solving skills. Passionate about creating opportunities for others to learn and grow by sharing diverse perspectives and developing balanced solutions. CISA, CIA, or CAMS certification preferred. Qualifications How you will lead A highly motivated and experienced leader with a proven track record of driving results within a collaborative environment. You will be a key player to help business stakeholders strengthen and mature new and existing compliance programs and products and here is how you'll make an impact: Strategic Collaboration: Collaborate with program owners, subject matter experts, and legal teams to gain a deep understanding of the regulatory landscape and compliance requirements governing our programs and products. Risks and Controls Matrix Design: Lead the development of risk and control matrices by partnering with stakeholders to align on requirements and scope to develop risks, controls and test procedures. Compliance Maturity Evaluation: Evaluate the design and operationalization of controls and assign compliance maturity score and issue rating based on test results, and conduct root cause analyses where necessary, using data-driven and risk-based strategies. Influence & Driving One Team Results: Partner with stakeholders to prioritize and implement impactful recommendations that strengthen our programs and products and effectively align diverse perspectives to drive initiatives forward. Effective Communication & Reporting: Create and deliver high-quality deliverables, including executive summaries, reports, presentations and workpapers that simplifies complex information to diverse audiences. Present findings and recommendations to senior management and stakeholders, ensuring clarity, understanding, and alignment. Cross-Functional Partnership: Build strong relationships with cross-functional stakeholders, including Internal Audit, Finance, Legal & Compliance, Business, Risk, Security, and Technology teams, to drive reviews, remediation efforts, and process improvements. Continuous Improvement: Actively lead, contribute and participate in strategic initiatives and projects driving departmental goals to scale and move with velocity while staying abreast of industry and regulatory changes. Intuit provides a competitive compensation package with a strong pay for performance rewards approach. This position may 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: Mountain View $159,000-$215,000 San Diego $142,000- 192,500
Summary Help reimagine cancer care by shaping how our Radioligand Therapies (RLT) reach more patients—safely, reliably, and faster. At Novartis, we’re pioneering the future of treatment through the fusion of nuclear medicine and precision oncology Primary responsibilities for this position include performing tasks associated with in-coming material, in-process and release testing and reviewing laboratory data, coordinating the team/lab under its responsibility. Communicating with internal and external partners for the Quality Control organization. Supports site as technical expert in related field. This role will support manufacturing operations which will require shift work and scheduling which will require weekend work. Location: Carlsbad #CA-Onsite This role is located on-site in Carlsbad, CA. Novartis is unable to offer relocation support for this role; please only apply if this location is accessible for you. About the Role Key Responsibilities: · Management of QC Analytical activities in line with site objectives. Coordination of departmental Operational activities. Track team metrics and ensure KQI /KPI meet requirements. · Coordination of departmental Operational activities · Initiate and drive local hiring process. · Lead OpEx Projects. · Investigation of Deviation, OOx, Complaints. · Define and implement CAPAs. · Support transfer Projects and validation studies. · Track team metrics and ensure KQI /KPI meet requirements. · HSE incidents reporting and action follow up. · New equipment commissioning Support (OQ, PQ). · Resource and capacity (people and equipment) planning and workload management. · Performance and leadership support of QC Analytical team · Ensure availability of equipment, chemicals and consumables, as appropriate. · SOP review and revision. · Ensure training according to cGxP requirements. · Management of documentation and methods according to cGxP. · Exception management. · Ensure DI and compliance with cGxP and all regulatory requirements. · Leadership in GxP audits and fulfillment of internal/external audit and inspection plans. · Equipment qualification review /release. · Ensure Methods and Procedures are up to date. · Ensure qualification /calibration status of analytical equipment. · Microbiological testing review and approval. Work Experience: · Analytical Validation · Corrective and Preventive Action (CAPA) Knowledge · Deviation Management · Equipment Calibration Management · Equipment Qualification Management · Good Manufacturing Practices (cGMP) · Audit & Inspection Management · Quality Control · Quality Management Systems · Quality Control Microbiology · Stability Management · Laboratory Excellence · SOP (Standard Operation Procedure) Management · KPI Reporting · Laboratory Excellence Education and Knowledge: · Bachelor's degree in Chemistry, Biology, or other relevant scientific discipline · Minimum of 5 years of work experience in Quality Control of pharmaceutical products, preferably radiopharmaceuticals · 2 years of experience in a people manager role · Experience in managing a cGMP laboratory · Knowledge of following analytical methods/equipment: HPLC, iTLC, Endotoxin, Bioburden, pH, NVP and viable particle counters · Knowledge of FDA regulations regarding the manufacturing of radiopharmaceuticals · Applied knowledge of GXP and EP/USP guidelines The salary for this position is expected to range between $114,000 and $211,900/year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB) EEO Statement: The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. Accessibility & Reasonable Accommodations The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to [email protected] or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Division Operations Business Unit Production / Manufacturing Location USA State California Site Carlsbad Company / Legal Entity U469 (FCRS = US469) AAA USA Inc. Functional Area Quality Job Type Full time Employment Type Regular Shift Work No VIDEO
Malin Space Science Systems (MSSS) is a private technology company that designs, develops and operates space camera systems for government and commercial aerospace customers and provides services in spacecraft instrument operations and space science research. As a member of our multidisciplinary space imaging systems design team, the Flight Assembly Technician is responsible for high-level assembly of prototype and spaceflight electronics under the direction of the Production Manager, utilizing applicable preferred certifications and technical expertise to run production equipment. Essential Functions Assembles electronic, mechanical, optical, and cable harness assemblies by following detailed work instructions and applicable NASA and IPC workmanship standards. Responsible for operating Surface-Mount Technology (SMT) reflow machine. Processes and operates X-Ray machine per project guidelines. Operates Automated Optical Inspection (AOI) machine. Prepares and operates Parylene conformal coating machine. Maintains detailed assembly records according to company and industry standards. Assists hardware engineering in assembly of prototype electronics and cable harnesses, testing, troubleshooting, and mechanical integration. Maintains all required NASA and IPC trainings and recertifications. Performs ESD check-in on a daily basis. Cross-trains in assembly disciplines to support all aspects of work completion. Participates in team meetings and provides updates on work status. Maintains work area, tools and equipment. Performs required maintenance as needed. Prior to entering assembly, test, storage or development areas within the Camera Systems Group unescorted, receive initial and ongoing annual training in the fundamentals of Electrostatic Discharge (ESD). Non-Essential Functions Travels to customers and/or vendors as required. Performs other duties as required or requested which may become essential to this position. Minimum Qualifications High-School Graduate / GED required. Some college or Trade School / ROP certification desired. Minimum of 3 years of solder assembly experience. Minimum of 5 years of operating experience with either SMT, AOI, Parylene or X-Ray machines. Excellent hand soldering, cable harness assembly, mechanical assembly, documentation, organization, and communication skills. Excellent attention to detail and ability to work closely with each member of a production team. Must be able to read schematics and mechanical drawings and precisely follow detailed written instructions. J-STD-001 certification is required. Space Addendum certification is preferred and is a requirement to perform the position. Polymerics mix and application experienced preferred; will be required to obtain NASA-STD 8739.1 certification. Must be computer literate with knowledge of MS Excel and Word. Results-oriented, self-motivated and dependable. Hands-on machinist experience for manufacturing test fixtures is preferred. Ability to work outside of regular business hours. Occasional travel to customers and/or vendors may be required. Physical Requirements Must be able to remain in a stationary position operating lab equipment for periods of time. Must be able to perform repetitive soldering tasks under a microscope to properly position hardware. Ability to inspect parts and assemblies under a microscope to determine product placement. Ability to work and move around in a cleanroom environment, wearing required outer garments including smock/coveralls, shoe covers, mask, goggles, hood, gloves and ESD wrist strap. Must be able to communicate clearly with a variety of people on a daily basis. Must be able to traverse spaces in and around the office, labs, and machine shop as applicable. Ability to lift and carry up to 10 lbs. as needed. Possess mental acuity at a level which will facilitate execution of complex technical instructions. Ability to practice safe driving habits while following all state safety regulations and standards.Ability to handle high stress levels in connection with multiple conflicting priorities and deadlines. High tolerance for ambiguity and shifting expectations. Ability to travel to customers and/or vendors locations. Disclaimer The employee must be able to perform the essential functions of the position satisfactorily and, if requested, reasonable accommodations will be made to enable employees with disabilities to perform the essential functions of their job, absent undue hardship. The Employer retains the right to change or assign other duties to this position. View MSSS Benefits MSSS is committed to providing equal employment opportunities to all individuals, regardless of any protected status, including veterans and individuals with disabilities. Reasonable accommodations will be provided to individuals who are unable to use this online system due to a disability. To request a reasonable accommodation, please contact [email protected]
Job Title: PLANT PALLETIZER Location(s): San Marcos - At this time, we are only considering local candidates who are legally authorized to work in the United States. Relocation assistance is not available for this position Work Schedule: Monday-Friday, 5am-1:30pm, Occasional Weekends Hours Per Week: 40+ hours; Full Time Job Duties: The Plant Palletizer - receives dairy products from the milk processing plant and assembles containers in the refrigerated warehouse on pallets according to specific type, size and category. Must be able to work a flexible schedule. Assists machine operators. Requires using hands to grip a metal case hook for repetitive pulling/pushing of heavy stacks of milk weighing up to 330lbs across diamond plate platform; must be physically able to lift up to 75lbs on occasion. May work on the empty case dock moving stacks of empty cases as needed. Work is conducted in a cold environment which averages 35 degrees Fahrenheit. May work outdoors. Provides quality control, housekeeping and other duties as assigned. Requires the ability to speak and understand English. Physical Demands: While performing the duties of this Job, the employee is regularly required to use hands to finger, handle, or feel; talk or hear and taste or smell. The employee is constantly required to stand; walk; reach with hands and arms; climb or balance and stoop. The employee must regularly push, pull; lift and/or move up to 75 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. Work Environment: While performing the duties of this Job, the employee is regularly exposed to cold, wet and/or humid conditions; moving mechanical parts; and the noise level in the work environment is usually moderate. APPLY ONLINE AT: www.HollandiaDairy.com/Careers. Applicants who are unable to use the online system due to a disability should call the HR department to request an accommodation. Benefits: Starting on day one, excellent medical, dental, vision, employer paid for long-term disability, life insurance (free up to $50k); various additional options to choose from Flexible Benefits account (FSA) for medical and dependent care Generous PTO (Paid Time Off) allowances and holiday pay 401(k) plan with employer matching Advancement and growth opportunities Fun employee and family events Employee gifts on birthdays & milestone anniversaries Safety bonuses and raffles Employee assistance program Hollandia Dairy is an Equal Employment Opportunity/Affirmative Action/Minority/Female/Vets/Disability/Sexual Orientation/Gender Identity Employer
SPEED & SPIRIT is what we look for in our candidates, defined by some simple values that inspire us to BE DRIVEN in our performance, BE VIBRANT in our sporting legacy, BE TOGETHER in our team spirit, and BE YOU to let our individual talent and experience shine. Applying for a job at PUMA is easy. Simply click APPLY ONLINE and follow the steps to upload your application. At PUMA, every application is reviewed by real people who are committed to fairness, transparency, and equal opportunity - no matter your background, identity, or experience. To ensure our process stays true to these values, no automated systems or AI tools are used to make hiring decisions. Every decision is made by real people -with real judgment and accountability. We may use functions supported by Artificial Intelligence (AI) to carry out isolated organizational steps, such as scheduling interviews. These functions have no influence on decisions in the application process. We believe in creating spaces where everyone is welcome, celebrated, and empowered to contribute authentically. Because at PUMA, whoever wants to play, can play. Your mission Develop all components and assembled clubs in a timely matter, validate and approve all product from sample phase all the way to production release of finished golf club and club components. Responsible for various aspects of product development from Beta phase to mass production to ensure products are ready to be commercialized. Knowledge of golf club manufacturing methods. Ability to take on all key manufacturing processes to maximize output and minimize bottleneck. Work in a collaborative environment with various internal (Cobra) and external (suppliers) partners. Responsible for working with suppliers to qualify new products through Pilot Run; be the owner to ensure all manufacturing processes can meet cost/quality/capacity requirements to support overall business objectives. Set up product standards, quality criteria and limits on all commercialized products with various product construction and designs. Execute testing and analysis on products to pass testing criteria and performance target. Initiate and qualify new suppliers and new methods of manufacturing on all club components to support business goals. Ownership of production “component specifications”, “cosmetic specifications”, and “club assembly specifications.” Conduct and own build trials at key assembly locations. Travel to Asia and Mexico based suppliers to manage development of new projects. Lead continuous improvements in our critical manufacturing processes in the supplier base manufacturing environment. Review current processes and procedures and lead continuous process improvement project team. Process Ownership – understand critical process setting, track performance metrics, and understand key cost drivers involved in critical manufacturing processes. Direct and work with Asia Team members on any development/process/quality concerns. Your talent 2-4 years of managing product development experience. 2+ years of experience working with suppliers based in Asia Bachelor's degree in mechanical or industrial engineering or demonstrated successful equivalent work experience. Fundamental knowledge of tooling and various other manufacturing processes (investment casting, forging, stamping, painting, etc.) Knowledge/experience with injection molding processing and tooling (Ex. compression molding processing and tooling, composite material processing and tooling). Statistical Process Control experience Strong project management skills Working knowledge of a CAD system, specifically NX (Specification drawing) Proficiency in MS Office (Word, Excel, PowerPoint, etc.) Strong documentation skills and experience Ability to travel internationally and domestically. The Hiring range base pay for this position is $70,304 - $91,900 + Bonus + Benefits (Benefit Summary Corporate) Pay may vary depending on job-related knowledge, skills, and experience Our principles PUMA provides equal opportunities for all job applicants, regardless of race, color, religion, national origin, sex, gender identity or expression, sexual orientation, age, or disability. Equality for all is one of the core principles at PUMA and we do not tolerate any form of harassment or discrimination. PUMA is a global sports brand creating footwear, apparel, and accessories that inspire athletes and everyday movers. The PUMA Group owns PUMA, Cobra Golf, and stichd, operates in 120+ countries, and has around 22,000 employees worldwide.
Production Manger At Lighteum Medical, we pride ourselves on being more than just a place of work. We are a vibrant, innovative team committed to making a difference in the world of medical device components by enhancing the lives of patients worldwide by delivering innovative, high-quality medical components to the MedTech industry. Be a part of a team dedicated to playing a role in creating solutions that make a real impact. Your work will contribute to improving lives. We offer a comprehensive benefits package designed to support our associates’ well-being. Our health and wellness benefits feature comprehensive medical, dental, and vision insurance. To promote financial security, we also provide a 401(k) plan with a generous company contribution and match, flexible spending accounts, and life and disability insurance. Our paid time off policy is generous, including PTO, sick leave, and paid holidays. Be a part of our team today! Production Manager Salary Range: $120,000 - $130,000 Base + Bonus Job Purpose Responsible for planning and directing all aspects of production activities in the designated areas in San Diego to manufacture high-quality components at optimum cost and in accordance with customer requirements. Principal Accountabilities Responsible for overseeing and managing optimization of manufacturing efficiencies. Plan and coordinate production activities to obtain optimum utilization of personnel, direct materials, and equipment to meet department targets (OTD/CM, etc.) Advises Management of new developments that may affect profit, schedule, costs, customer relations, and/or inter-departmental relations. Set appropriate expectations of labor scheduling requirements against expected production output. Plan and prioritize production activities to minimize downtimes and disruptions to manufacturing schedules. Leads and manages front-line production supervisors. Responsible for coaching and developing front-line supervisors to achieve high-performing teams. Responsible for timely performance feedback and annual reviews. Exercise strong judgment in managing production levels, setting operational priorities, overseeing processes, and resolving employee‑related matters Maintains a working knowledge of new technologies which may improve operations and develop recommendations accordingly. Drive measurable process improvements through hands‑on use of Lean, Six Sigma, and DMAIC methodologies. Able to support and lead Kaizen and lean projects within the area of responsibility. Manages processes in a changing environment and acts as a change champion to influence positive outcomes. Champions a proactive safety culture by modeling safe behaviors, reinforcing safety expectations, and ensuring all team members follow established safety standards. Collaborates and works closely with other functional areas such as Quality, Supply Chain, Engineering, Facilities, HR, etc. Other duties may be assigned. Qualifications / Knowledge / Experience Associates' or Bachelor’s degree in Business Administration, Operations Management or a related field. 5-7 years of progressive experience in a manufacturing environment, preferably servicing the Medical Device Industry. Minimum of three (3) years of experience in a supervisory or managerial capacity/role. Proven ability to lead teams, manage change, and deliver measurable improvements in throughput, cost, quality, safety, and overall operational performance. Working practical knowledge in progressive management technologies such as Lean Manufacturing, JIT, MRP, and ERP. Demonstrated Continuous Improvement (CI) experience with hands-on application of Lean, Six Sigma, and the DMAIC methodology. Strong understanding of safety regulations (OSHA), quality systems such as ISO, and operational KPI management including OEE, FPY, and OTD. Lean Six Sigma Certification. Proficient in Microsoft Office 365 applications. Familiarity with IFS ERP. Prolonged periods of standing and walking through the site. Prolonged periods of sitting at work working on computers. Occasionally lift of 25 pounds at a time. Visual acuity and manual dexterity to inspect products and machinery. Lighteum Medical is an Equal Opportunity Employer and encourages applications from qualified candidates regardless of sex, race, disability, age, sexual orientation, marital status, religion, belief, or any status protected by federal, state, or local law. If you require a reasonable accommodation to apply or participate in the interview process, please contact [email protected].
How will you make an impact? The Lead Manufacturing Technician , based in San Clemente, CA will be responsible for the completion of the scheduled production and management of preventative maintenance. The Lead will ensure proper documentation (cGMP and GDP), open/close jobs in MRP system, and provide feedback and updates to Management and Engineering. This position will also prepare components, build assemblies, and bulk drug formulations. All activities will be performed with good documentation practices (GDP) in accordance with current good manufacturing practices (cGMPs) and quality system regulation (QSR) medical device good manufacturing practices (GMP) requirements. Additional tasks will include performing the following: Filing, capping, and crimping operations Packaging and labeling operations Sampling Visual inspections Documentation and data input into materials requirement planning (MRP), Batch Records (BRs), and Device History Record (DHR) Track clean room, environmental chambers, and equipment preventive maintenance (PMs) What will you do? Manage the operation schedule, project schedule, and adjusts the schedule and resources accordingly Supervise production technician(s) to optimize quality and output Ability to perform all activities outlined for a Manufacturing Technician as needed Verify all documentation is followed and completed accurately (cGMP, QSR, and GDP) Manages Oracle to open and close jobs Manages inventory requests and reconciliation for accuracy Revise documentation to ensure accuracy and compliance Communicate feedback to engineering on Non-Standard Build Requests, Validation builds, Clinical builds, etc. How will you get here? To be successful in this role, you will need to have the following: Industry (medical device, pharmaceutical, and/or biotechnology) and educational experience. 8 – 10 years’ experience with high school diploma 6 – 8 years’ experience with associate degree in science or engineering 4 - 6 years’ experience with bachelor’s degree in science or engineering It is highly desirable to have experience working in and maintaining a clean room in accordance with GDP, cGMPs, and QSR standards. #GKOSUS