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THE POSITION As the Senior Manufacturing Technical Specialist - Single-Use Technology (SUT), you are an integral member of the OSUT (Oceanside Single Use Technology) team in Oceanside. In this role, you will be a vital contributor to the successful commercialization of the facility, providing technical and operational expertise to support solutions preparation, upstream, and downstream manufacturing processes. The team will work closely with the existing staff in the Oceanside stainless steel operations as well as with South San Francisco Clinical Supply Center (CSC) and other network fleet partners. The candidate will engage with customer groups, network teams and vendors seeking opportunities for collaboration, proactively communicating and presenting information and offering relevant data driven information to impact decisions. Serve as a technical contact for team, customers and vendors to consult with on new technologies and troubleshooting efforts Support troubleshooting efforts on equipment, process, automation in support of release of drug substance material Initiate and lead projects that result in implementation and/or optimization of novel methods and technique, including optimizing process performance Support on the floor operations during production campaigns, validation and/or characterization studies, and Tech Transfer activities Support and maintain biologics manufacturing analytical equipment used for in-process testing Support effective partnerships within & outside of Roche; work closely with the SSF CSC for change initiatives Develop and deploy robust knowledge sharing experiences; coach and train other team members Contribute to achieving results in other organizations across the company Enhance safety of the organization through process/equipment improvements Who you are Experience in drug substance/bulk biologics experience and single use technology (SUT) preferred Understands and has experience working with single use technologies, commercial operational experience is preferred Understanding of current GMP requirements and regulations Extensive practical and theoretical expertise in biopharmaceutical manufacturing processes and process improvements Ability to work in fast paced dynamic work environment Possess excellent interpersonal, communication and collaboration skills Strong problem solving and critical thinking skills Self-motivated, organized and capable of multitasking Behaviors, competencies, and qualities of the ideal applicant: Hardworking and fast learning individual that thrives in a high paced environment Experience in clean room environment and familiarity with cGMP and ISO/FDA/EU standards is strongly preferred Ability to think critically and work both tactically and strategically Exhibit creativity in adapting to situations, develop contingency plans, and make decisions Strong quality mindset with attention to detail and a desire to deliver service excellence Ability to work effectively with others, exhibiting a professional manner and establish constructive working relationships Qualifications / Requirements: Possess thorough knowledge and understanding of cGMPs and familiarity with FDA guidelines. Familiarity with ICH and European guidelines Demonstrate organizational, time management, delegation and leadership skills Demonstrate excellent English verbal and written communication and comprehension skills Must be able to support 24x7 operations and stand for extended periods of time Must be able to interface with computer systems to successfully operate manufacturing equipment. Experience with distributed control systems or other manufacturing automation is preferred Must be able to successfully pass all job-related tests and certifications required for working in a cGMP quality environment including but not limited to: inspections and GMP requirements to perform essential functions of the job Must re-qualify every year on all job-related training and certifications as job or qualifications require May climb upwards of 6 flights of stairs a day to maneuver within the manufacturing facility. Lifting up to 25kg may be required. The cleanroom environment requires that company provided gowning is worn. This may include plant uniform, coveralls, gloves and safety shoes. Additionally, regulations prohibit makeup, jewelry, and other personal items from entering the clean room environment. Education: Bachelors, Master's, or Ph.D. degree in Engineering or Life Sciences. Work Experience: 8+ years experience in a GMP working environment with mAb biologics drug substance background (Cell Culture/Purification) is highly desired 6+ years with MS 3+ years with PhD Relocation benefits are available for this posting. The expected salary range for this position based on the primary location of California is $91,400 (min) - $130,500 (mid) - $169,700 (max). Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below. Benefits Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants. JOB FACTS Job Sub Category Process Development Schedule Full time Job Type Regular Posted Date Nov 25th 2025 Job ID 202508-120113
The Position As the Senior Manufacturing Technical Specialist - Single-Use Technology (SUT), you are an integral member of the OSUT (Oceanside Single Use Technology) team in Oceanside. In this role, you will be a vital contributor to the successful commercialization of the facility, providing technical and operational expertise to support solutions preparation, upstream, and downstream manufacturing processes. The team will work closely with the existing staff in the Oceanside stainless steel operations as well as with South San Francisco Clinical Supply Center (CSC) and other network fleet partners. The candidate will engage with customer groups, network teams and vendors seeking opportunities for collaboration, proactively communicating and presenting information and offering relevant data driven information to impact decisions. Serve as a technical contact for team, customers and vendors to consult with on new technologies and troubleshooting efforts Support troubleshooting efforts on equipment, process, automation in support of release of drug substance material Initiate and lead projects that result in implementation and/or optimization of novel methods and technique, including optimizing process performance Support on the floor operations during production campaigns, validation and/or characterization studies, and Tech Transfer activities Support and maintain biologics manufacturing analytical equipment used for in-process testing Support effective partnerships within & outside of Roche; work closely with the SSF CSC for change initiatives Develop and deploy robust knowledge sharing experiences; coach and train other team members Contribute to achieving results in other organizations across the company Enhance safety of the organization through process/equipment improvements Who you are Experience in drug substance/bulk biologics experience and single use technology (SUT) preferred Understands and has experience working with single use technologies, commercial operational experience is preferred Understanding of current GMP requirements and regulations Extensive practical and theoretical expertise in biopharmaceutical manufacturing processes and process improvements Ability to work in fast paced dynamic work environment Possess excellent interpersonal, communication and collaboration skills Strong problem solving and critical thinking skills Self-motivated, organized and capable of multitasking Behaviors, competencies, and qualities of the ideal applicant: Hardworking and fast learning individual that thrives in a high paced environment Experience in clean room environment and familiarity with cGMP and ISO/FDA/EU standards is strongly preferred Ability to think critically and work both tactically and strategically Exhibit creativity in adapting to situations, develop contingency plans, and make decisions Strong quality mindset with attention to detail and a desire to deliver service excellence Ability to work effectively with others, exhibiting a professional manner and establish constructive working relationships Qualifications / Requirements: Possess thorough knowledge and understanding of cGMPs and familiarity with FDA guidelines. Familiarity with ICH and European guidelines Demonstrate organizational, time management, delegation and leadership skills Demonstrate excellent English verbal and written communication and comprehension skills Must be able to support 24x7 operations and stand for extended periods of time Must be able to interface with computer systems to successfully operate manufacturing equipment. Experience with distributed control systems or other manufacturing automation is preferred Must be able to successfully pass all job-related tests and certifications required for working in a cGMP quality environment including but not limited to: inspections and GMP requirements to perform essential functions of the job Must re-qualify every year on all job-related training and certifications as job or qualifications require May climb upwards of 6 flights of stairs a day to maneuver within the manufacturing facility. Lifting up to 25kg may be required. The cleanroom environment requires that company provided gowning is worn. This may include plant uniform, coveralls, gloves and safety shoes. Additionally, regulations prohibit makeup, jewelry, and other personal items from entering the clean room environment. Education: Bachelors, Master's, or Ph.D. degree in Engineering or Life Sciences. Work Experience: 8+ years experience in a GMP working environment with mAb biologics drug substance background (Cell Culture/Purification) is highly desired 6+ years with MS 3+ years with PhD Relocation benefits are available for this posting. The expected salary range for this position based on the primary location of California is $91,400 (min) - $130,500 (mid) - $169,700 (max). Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below. Benefits Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.
Summary Blue Marble Communications (a T2S company) is currently seeing to hire a Manufacturing Process Engineer (MPE) responsible for product compliance with internal and customer requirements. These span conception to completion and include planning, optimization, and management of assembly, integration and test processes in a production environment. In addition, the MPE will develop, coordinate, improve, evaluate, and maintain the quality assurance program. Prior quality assurance experience and familiarity with industry standards (e.g. J-STD-001, IPC-A-600, IPC-A-610, IPC/WHMA-A-620, ISO9001, AS9100) is required. The MPE must have an aptitude and eagerness to learn, speak up when problems arise, and follow the process. They must be a self-starter with great time management skills and very strong attention to detail. Responsibilities Work with hardware design engineers to develop test plans and procedures, both at a detailed level (individual test procedures) and high level (big picture test campaign) Manage and organize various forms of manufacturing documentation, including certificates, travelers, and test data, as well as non-conformance reports, change orders, etc. Analyze production flows and procedures, estimating time and labor requirements, and propose changes that would result in improvements to throughput, efficiency, quality, etc. Help with first-article assembly, integration, and qualification testing of electro-mechanical and opto-mechanical systems Inspect PCBs, PCBAs, machined parts, mechanical assemblies, cable assemblies, optical assemblies, and sub-assemblies, as necessary Read and confirm compliance to Assembly Drawings, Bill of Materials (BOMs), Wire List, Engineering Drawings, Change Orders, and Rework Instructions Use of calipers, go/no go gages, microscopes, torque drivers, micrometers, digital multimeters, etc. as needed for ensure product compliance Participate in design reviews and review/approve documentation change orders Recommend procedural or manufacturing process changes for continuous improvement Prepares statistical analysis reports, specifications, and other technical documents. Facilitate Manufacturing Review Boards (MRBs) and Failure Review Boards (FRBs) Interface with external customers Qualifications Bachelors Degree in Engineering preferred and a minimum of 5+ years of experience J-STD-001, IPC-A-610, and/or WHMA/IPC-A-620 certification preferred Basic understanding of Geometric Dimensioning and Tolerancing (GD&T) per ASME Y14.5 Basic Knowledge of the AS9100 Quality Management Systems Strong background in industrial or manufacturing engineering fundamentals with training in work analysis, six sigma, manufacturing processes, manufacturing systems, and/or supply chain management General knowledge of common manufacturing and test processes, procedures, and equipment. Ideal candidate would have hands-on experience with some form of hardware build & test (e.g., CNC machining, 3d printing, resin casting, etc.) Strong sense of organization and attention to detail Must be a US Person (This position has export control and security-related requirements that mandate attention to the citizenship status of any potential candidate and necessitates that the individual either be a United States Citizen, Permanent Resident of the United States, or lawfully admitted into the United States as a refugee or granted asylum by the United States Government.) About Blue Marble Communications Blue Marble Communications designs and manufactures high-performance RF, free-space optical, and network communications modules and systems for deployment onboard satellites and other space vehicles. Our current product offerings include software-defined RF, microwave, and millimeter-wave modem/transceivers; optical laser communications terminals, Ethernet routers/switches, and systems comprised of combinations of these modules. BMC embraces a modern workplace culture and inclusive environment. Compensation: 90-130k DOE T2S Solutions is an Equal Opportunity Employer/Protected Veteran/Disability
*Job Overview* We are a small custom merch shop looking for 1-2 people to run our embroidery machine and office 2-5 days a week (Night and weekend shifts are also an option.) We make high quality apparel for a range of fitness studios, national brands, as well as local businesses and entrepreneurs. This is a fun opportunity to work in a hands-on environment and learn some garment skills! Strong attention to detail and a willingness to learn are necessary, and an interest in these crafts is an advantage! *Responsibilities* *include: * * Run Embroidery Machine (hands-on training) * Other Merchandise Branding (heat press, screen transfers, etc) * General Office duties - shipping out orders, greeting customers, keeping office clean and organized * Admin - utilizing Shopify to track and update merch orders * Support inventory management by organizing materials and supplies in the warehouse * Collaborate with team members to meet daily production goals and improve workflow * Follow safety protocols and company policies at all times *Qualifications* * Experience with sewing, embroidery, or heat press machines a huge plus * Strong attention to detail and quality standards * Ability to work efficiently and proactively * Good organizational skills with the ability to manage multiple tasks simultaneously * Live within a reasonable commuting distance of North Pacific Beach, San Diego Job Types: Full-time, Part-time, Temp-to-hire, Temporary, Seasonal Pay: $22.00 - $24.00 per hour Expected hours: 15 – 35 per week Benefits: * Flexible schedule * On-the-job training Work Location: In person
Bachem is a leading, innovation-driven company specializing in the development and manufacture of peptides and oligonucleotides. With over 50 years of experience and expertise Bachem provides products for research, clinical development and commercial application to pharmaceutical and biotechnology companies worldwide and offers a comprehensive range of services. Bachem operates internationally with headquarters in Switzerland and locations in Europe, the US and Asia. The company is listed on the SIX Swiss Exchange. For further information, see www.bachem.com. A brief overview The Manager / Sr. Manager, Quality Control fulfills a critical role in the active pharmaceutical ingredient (API) manufacturing operations. This individual is responsible for managing and coordinating stability testing, raw material qualification, testing and release, and validation projects. The Manager / Sr. Manager coordinates both in-house and contract laboratory testing activities. Additionally, this individual supports the Director, Quality Control in reviewing data and reports. This role also serves to advance analytical capabilities and contributes to the development of the Quality Control department. What you will do Manage and oversee execution of QC testing including IPC, API, raw material, validation, release, EM and microbial testing Supervise QC Scientists. Provide training, day-to-day scheduling, mentoring, and coaching for QC personnel Establish and revise specifications and sampling plans for IPC, raw materials and final product Develop and optimize new and existing analytical methods for qualification and release testing Coordinate stability program and the testing to meet stability endpoints, as needed Manage IPC release activities, raw material and API release activities to meet deadlines tied to manufacturing schedules Write, review, and approve QC Standard Operating procedures (SOP’s) as needed Evaluate, recommend, and implement new analytical technologies and instrumentation for raw material, final product, In process, microbial, environmental, and water testing Investigate Out-Of-Specification (OOS) test results, write reports and implement corrective and preventive actions (CAPA) to prevent recurrences Manage external test laboratories for contract testing of raw materials and other related testing Review test data for completeness and accuracy Provide timely responses to internal and external inquiries Stay abreast of new developments in analytical technologies Contribute to improvements in laboratory operations to increase efficiency and GMP compliance Qualifications Bachelor's degree in a relevant scientific field with a minimum of 8 years’ industry experience Master's degree in a relevant scientific field with a minimum of 5 years’ industry experience (preferred) PhD in a relevant scientific field with a minimum of 2 years’ industry experience (preferred) 4-6 years’ management experience 1-3 years’ experience in managing projects (preferred) Extensive experience in GMP laboratory testing such as IPC, HPLC, GC, TLC, UV-VIS Spectrophotometer, Karl Fisher Titrator, FTIR, MS, LAL, bioburden, etc. Thorough knowledge and understanding of analytical chemistry, including USP materials testing Creativity to solve technical and compliance problems Comply with good housekeeping and safety practices Experience in writing standard operating procedures (SOP’s) and test methods Excellent written and oral communication skills Excellent computer knowledge, including Microsoft Word, Excel, Power Point and Access Ability to effectively organize, multitask, and work in a fast-paced, deadline driven work environment Ability to communicate in a proactive and solution-focused manner, including keeping management aware of potential issues Detail oriented with the ability to troubleshoot and resolve problems Ability to work independently and manage one’s time Ability to drive projects to success under time constraints Communicate effectively and ability to function well in a team environment Base salary range: Manager: $109,396 - $164,095 Sr. Manager: $133,304 - $183,293 Placement of new hires in these wage ranges is based on several factors including education, skill sets, experience, and training. Total Rewards We offer all Team Members a total rewards package including competitive pay, annual performance bonus, a generous benefit package with comprehensive Medical/Dental/Vision coverage, 401(k) plan with employer contribution, and paid vacation, personal and sick days. Corporate Social Responsibility Bachem takes responsibility for future generations by a careful handling of resources and avoiding environmental risks. We continually improve our ecological performance and develop and implement new approaches for enhancing employees’ environmental awareness. EcoVadis has awarded Bachem Gold Medal status in their assessment of Bachem. Bachem Americas is an Equal Opportunity Employer As an equal opportunity employer, we celebrate the diversity of our team and are committed to building an inclusive workplace where individuals are hired and advanced based on merit, skills, and qualifications. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status, or other legally protected status. Please note: unsolicited resumes from recruitment agencies will not be considered. Nearest Major Market: San Diego
SUMMARY: Assembles bouquets according to recipe specifications and maintains a clean and organized work area. Ensure finished product meets construction, quantity and quality specifications provided by Table Lead. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. Ensure the correct recipe is being used. Assemble Combos/Bunches by placing flowers on conveyor according to recipe specifications. Assemble Combos/Bunches by hand according to recipe specifications. Place bouquets in sleeve according to recipe specifications. Place rubber band and floral wrap on the finished product. Unpacks flower bunches from boxes. Removes sleeves from bunches and replaces with new sleeve and UPC label. Ensure and place greeting card and floral preservative food correctly. Verify UPC label has correct information. Check bouquet quality. Count and place throw away by stem in appropriate container. Separate green debris and place all waste in appropriate containers. Maintain work area clean and organized. Must be able to meet productivity goals set by Production Manager. Other duties as assigned. QUALIFICATIONS To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Ability to work on weekends and holidays. Ability to work in a refrigerated environment 45 degrees. Ability to lift to 10lbs. Ability to follow directions. Ability to communicate effectively. Ability to work effectively and relate well with others. EDUCATION and/or EXPERIENCE Six months work related experience or training; High School preferred. LANGUAGE SKILLS Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals. Ability to write routine reports and correspondence. Ability to speak effectively before groups of customers or employees of an organization. Ability to converse in Spanish. MATHEMATICAL SKILLS Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. Ability to compute rate, ratio, and percent and to draw and interpret bar graphs. REASONING ABILITY Ability to apply common sense understanding to carry out instructions furnished in written, oral, or diagram form. Ability to deal with problems involving several concrete variables in standardized situations. PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this Job, the employee is required to frequently stand, walk, use hands to finger, handle, or feel and talk and hear, and to reach with hands and arms. The employee must frequently lift and/or move up to 10 pounds and occasionally up to 10 lbs. Specific vision abilities required by this job include close vision, distance vision, color vision and ability to adjust focus. WORK ENVIRONMENT The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this Job, the employee is regularly exposed to extreme cold, wet, and humid conditions (non-weather). Work near moving mechanical parts. The noise level in the work environment is usually moderate. December 15,2025 - December 20,2025 Availability to work weekends and overtime.
*Job Posting* *Assembler (Seasonal)* *December 15,2025 - December 20,2025* *Apply Here Directly: * * _*https://workforcenow.adp.com/mascsr/default/mdf/recruitment/recruitment.html?cid=3ca6dfee-a9c1-4e24-a942-a8e3179da5e4&ccId=9201070367831_2&lang=en_US*_ Assembles bouquets according to recipe specifications and maintain a clean and organized work area. Ensure finished product meets construction, quantity and quality specifications provided by Production Lead. *ESSENTIAL DUTIES AND RESPONSIBILITIES * * Place bouquets in sleeve according to recipe specifications. * Place rubber band and floral wrap on finished product. * Unpacks flower bunches from boxes. * Removes sleeves from bunches and replaces with new sleeve and UPC label. * Ensure and place greeting card and floral preservative food correctly. * Check bouquet quality. * Count and place throw away by stem in appropriate container. * Separate green debris and place all waste in appropriate containers. * Maintain work area clean and organized. * Other duties as assigned. *REQUIREMENTS:* * Ability to work in a refrigerated environment 35 to 45 degrees * Ability to work in a fast-paced environment. * Ability to work overtime if needed. * Ability to work on weekends when required. Monday-Friday: 5:00AM-1:30PM ; Availability to work overtime. Address: Kendal Floral Supply, 1960 Kellogg Ave, Carlsbad, CA 92008. Phone Number 760-494-3415 Job Type: Temporary Pay: From $18.00 per hour Ability to Relocate: * Carlsbad, CA 92008: Relocate before starting work (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. We have an exciting opportunity for an Internal Lead Auditor Quality Department located in Poway, CA. DUTIES AND RESPONSIBILITIES: Main point of contact for Quality Management System (QMS), procedures and work instructions. Evaluate company processes (Business and Quality Systems) for compliance with quality requirements. Record and compile audit and test results and prepare graphs, charts and reports. Assist in development of audit question/checklists. Lead AS9100 quality audits and lead a team of support auditors. Identify processes, situations, etc., where organization is meeting requirements, as well as identify opportunities for improvement. Assist audit team in developing audit schedules and reports; present audit reports to top management. Assist with follow-up audits, findings, and opportunities for improvement. Will assist with root cause analysis and implementation of corrective action and preventative action for process and product related non-conformances. Integrates and analyzes project plans to ensure milestones and delivery requirements are met, ensures that all key parties are advised. Analyzes data and situations and develops solutions with Project Managers, influences and guides on actions to be taken. Represents the organization as a primary contact for internal and external audits and corrective action responses. Assist with quality training of production personnel. Ensure compliance with AS9100 standards. Manage the maintenance of company-wide, policies, procedures, work instructions, and records, to assure the company of continuous compliance conformance with appropriate standards and regulations. Other duties as required. We recognize and appreciate the value and contributions of individuals with diverse backgrounds and experiences and welcome all qualified individuals to apply. 52514 Job Qualifications: Typically requires a bachelors degree in Business Administration or a related discipline and three or more years of progressive professional project administration experience. Equivalent professional experience may be substituted in lieu of education. Must have certification as Lead Auditor to AS9100 standards. Ability to work well unsupervised, manage conflicts, handle multiple tasks, be detail oriented and highly motivated. Ability to identify issues, analyze data and develop solutions to a variety of complex problems Strong analytical, verbal, inter-personal and written communication skills Well organized to work high volume of documents in fast-paced environment. Ability to work under the pressure of meeting deadlines and perform well in team situations. Excellent oral, written, and listening communications skills to interact with all levels of the organization. The ability to obtain and maintain DoD Security Clearance is required. Salary:$62,510 - $105,628Travel Percentage Required 0 - 25Relocation Assistance Provided Not Provided US Citizenship Required? YesClearance Required? Desired Clearance LevelMid-Level (3-7 years) WorkstyleOnsite
General Atomics Aeronautical Systems, Inc. (GA-ASI), an affiliate of General Atomics, is a world leader in proven, reliable remotely piloted aircraft and tactical reconnaissance radars, as well as advanced high-resolution surveillance systems. We are seeking a detail-oriented and experienced Quality Engineer to join our Receiving Inspection team. The ideal candidate will be responsible for ensuring that all composite parts and assemblies meet quality standards, customer requirements, and regulatory compliance. You will play a critical role in driving continuous improvement, supporting production processes, and maintaining quality systems in a fast-paced manufacturing environment. DUTIES AND RESPONSIBILITIES: Analyzes design reliability and quality to recommend process changes and enhancements. Creates or recommends design, dimensional or manufacturing process changes to improve products and reduce costs. Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment. Audits quality systems for deficiency identification and correction. Implements solutions to complex problems occurring internally and at vendor facilities. Prepares statistical analysis reports, specifications and other technical documents Interprets and adapts quality standards and government regulations. May perform incoming material/part inspection. May generate nonconformance, material rejections and corrective action reports, as well as communicating final acceptance test reports with customers. May also generate and maintain files of all quality and as-built information for each product. Responsible for observing all laws, regulations and other applicable obligations wherever and whenever business is conducted on behalf of the Company. Expected to work in a safe manner in accordance with established operating procedures and practices. Other duties as assigned or required. We recognize and appreciate the value and contributions of individuals with diverse backgrounds and experiences and welcome all qualified individuals to apply. 52509 Job Qualifications: Typically requires a bachelor's or master's degree in engineering or related discipline and five or more years of related experience with a bachelor's degree or three or more years with a master's degree. May substitute equivalent experience in lieu of education. Must be able to apply a basic understanding of inspection methods and have a basic knowledge of computer operations and applications. Must have the analytical ability required to develop solutions to routine and non-routine quality issues and the skills required to present those solutions to internal contacts. Must be detail-oriented to accurately prepare statistical reports and technical documents in support of company objectives. Must have good leadership skills to ensure project costs and schedules are maintained. Able to work extended hours as required. Salary:$81,080 - $141,650Travel Percentage Required 0 - 25Relocation Assistance Provided Not Provided US Citizenship Required? YesClearance Required? No Clearance LevelMid-Level (3-7 years) WorkstyleOnsite
Job Description: Cape Fox Concentric Methods is accepting resumes for a Radiographic Technician to provide support to our deserving Marines at Camp Pendleton. Requirements: Certified by the American Registry of Radiologic Technology (ARRT) Possess a minimum of 1 year of full-time experience within the last 3 years in a setting corresponding to the requirements. Graduate from an academic program accredited by the Joint Review Committee on Education in Radiologic Technology (JRCERT) The total hourly pay for this non-exempt position is $51.09 for up to 40 hours per week. This is comprised of a base hourly rate of $46.97 plus $4.93 per hour Health & Welfare (H&W) for up to 40 hours per week as required by the Service Contract Labor Standards (SCLS) regulations. This rate represents the company’s good faith and reasonable estimate of possible compensation at the time of posting. In addition, for eligible positions we offer a variety of benefits including specified holidays, paid leave, health insurance, dental insurance, vision insurance, life and disability insurance, tuition reimbursement, as well as 401K with company match. This job will be posted until filled or withdrawn. Duties: Perform routine diagnostic radiological procedures/services. Adhere to radiation safety policies and procedures in accordance with Radiology Department policies and procedures. Send appropriate image series to the radiologist for reading according to facility protocol. Correctly position the patient for the examination and make technical adjustments necessary for the required examination. Determine if any special patient preparation is required. Process digital images and submit for interpretation by radiologists. Document all procedures and maintain records. As directed, perform system calibrations and quality control tasks according to the manufacturer and facility policy. Recognize artifacts and equipment errors and notify designated Government personnel of outlying values. Initiate repair call procedures for equipment malfunctions by notifying designated Government personnel. Report problems to the Biomedical Repair Section and record the problem condition in the trouble call logbook. Observe and report to the radiologist any symptoms which have direct bearing on the patient's condition as a result of adverse reaction to contrast media and inform the radiologist of any condition requiring his/her attention. Cape Fox Corporation, its subsidiaries, and affiliates provide equal employment opportunities to all persons and prohibit employment decisions on the basis of race, religion, color, creed, national origin, sex, age, disability, political affiliation, protected veteran status, or sexual orientation, or any other characteristic protected by federal, state, or local law. Cape Fox Corporation, its subsidiaries, and affiliates offer preference to Cape Fox Corporation Shareholders, descendants, and other Native Americans pursuant to Public Law 100-241.Recognize the need for and institute the necessary emergency measures for situations where a person requires resuscitation procedures due to cardiac or respiratory arrest. Job Requirements: Degree: Certificate. Education: Graduate from an academic program accredited by the Joint Review Committee on Education in Radiologic Technology (JRCERT). Certification: Certified by the American Registry of Radiologic Technology (ARRT) Experience: One year of experience as a radiologic technologist.
About Axillon Aerospace Axillon Aerospace is a leading provider of complex, highly engineered composite and polymer solutions for demanding commercial and defense applications. We are comprised of six, purpose-built centers of excellence throughout the USA and Mexico, each strategically focused on serving specific markets across aerospace engines and airframes, as well as munitions, radomes, antennas and fuel containment. Learn more at axillonaerospace.com. Job Designation The Quality Engineer 2 provides a range of expertise to ensure that the products are free of flaws, and function as designed. Participates in assuring high reliability and proper performance per product requirements. Job Core Responsibilities Fosters compliance to internal and external requirements on the assigned program(s) by means of addressing issues preventing from meeting requirements Works with customer(s) to request approval of products deviating from approved processes and requirements Leads APQP/PPAP package generation, including orchestrating the development and update of the package items Reviews and approves changes to the planning, work instructions, procedures and product acceptance Reviews and creates inspection forms, records, techniques and procedures for accuracy and relevance and provide changes when necessary Defines and conducts both systematic/methodical and random/arbitrary tests to ensure proper performance of products Leads MRB team to assess defect severity and occurrence, providing input on internal product disposition Analyzes cause for defects and provide opportunities for improvement activities while monitoring process capabilities Leads and performs root cause analysis initiatives for process related concerns Provides technical and regulatory expertise for a range of quality assurance testing and inspection activities associated with product development and manufacturing Performs internal audits of the operation process using inspection results and statistical techniques to provide timely, accurate process and product analysis Analyzes audit results and determines proper corrective and preventive action Performs review and release of products, engaging customer representatives as required, and completing the shipping paperwork Performs First Article Inspections for changes to fit, form, or function to the products Consistent exercise of independent judgment and discretion in matters of significance Regular, consistent and punctual attendance is required. May need to work nights and weekends, variable schedule(s) and additional hours as necessary Job Specifications Education : Post-secondary degree in Engineering Years Experience : 3 - 5 years of relevant experience Skills : Knowledge of complex Quality Engineering processes and regulatory requirements Excellent ability to apply a systematic and analytical approach to problem solving Advanced knowledge and ability to apply core concepts of engineering and statistical process control Ability to interpret internal/external business challenges and make recommendations for improvements to products, processes or services Ability to explain a range of complex technical information and options to overcome challenges Demonstrated analytical skills to proactively identify and solve problems: 6 sigma certification and applied experience a plus Effective interpersonal, verbal and written communication skills to drive tasks to completion Please note that the salary range information is only applicable for California. Compensation is based on a variety of factors, candidate experience, qualifications, location as well as market and business considerations. Pay Range: $95K-$110K. Axillon is an Equal Opportunity Employer. Axillon is committed to ensuring equal employment opportunities for all job applicants and employees. Employment decisions are based upon job related reasons regardless of race, ethnicity, color, religion, sex, sexual orientation, age, national origin, disability, gender identity, genetic information, veteran status, or any other status protected by law. This position requires 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.
At PwC, our people in business application consulting specialise in consulting services for a variety of business applications, helping clients optimise operational efficiency. These individuals analyse client needs, implement software solutions, and provide training and support for seamless integration and utilisation of business applications, enabling clients to achieve their strategic objectives. As a Salesforce consulting generalist at PwC, you will possess a broad range of consulting skills and experience across various Salesforce applications. You will provide consulting services to clients, analysing their needs, implementing software solutions, and offering training and support for effective utilisation of Salesforce applications. Your versatile knowledge will allow you to assist clients in optimising operational efficiency and achieving their strategic objectives. Growing as a strategic advisor, you leverage your influence, expertise, and network to deliver quality results. You motivate and coach others, coming together to solve complex problems. As you increase in autonomy, you apply sound judgment, recognising when to take action and when to escalate. You are expected to solve through complexity, ask thoughtful questions, and clearly communicate how things fit together. Your ability to develop and sustain high performing, diverse, and inclusive teams, and your commitment to excellence, contributes to the success of our Firm. Examples of the skills, knowledge, and experiences you need to lead and deliver value at this level include but are not limited to: Craft and convey clear, impactful and engaging messages that tell a holistic story. Apply systems thinking to identify underlying problems and/or opportunities. Validate outcomes with clients, share alternative perspectives, and act on client feedback. Direct the team through complexity, demonstrating composure through ambiguous, challenging and uncertain situations. Deepen and evolve your expertise with a focus on staying relevant. Initiate open and honest coaching conversations at all levels. Make difficult decisions and take action to resolve issues hindering team effectiveness. Model and reinforce professional and technical standards (e.g. refer to specific PwC tax and audit guidance), the Firm's code of conduct, and independence requirements. As part of the Salesforce Consulting team you will lead the development and implementation of Salesforce technology-enabled solutions that address client needs. As a Senior Manager you will set the strategic direction, drive business growth, and maintain impactful executive-level client relations while mentoring the next generation of leaders. This role requires a visionary approach to problem-solving and the ability to cultivate potential within teams, delivering innovative solutions in a fast-paced environment. Responsibilities - Cultivate innovative problem-solving approaches in a dynamic environment - Deliver solutions that meet client needs - Promote collaboration and knowledge sharing across teams - Uphold the firm's standards of integrity and excellence What You Must Have - Bachelor's Degree -7 years of experience What Sets You Apart - Preferred field(s) of study: Computer and Information Science or Management Information Systems - One or more Salesforce.com certifications : Certified Administrator, Certified Developer, or Certified Sales/Service/Salesforce Industries - Demonstrating thought leadership in Salesforce technology solutions - Leading teams to develop client proposals and solutions - Developing and sustaining client relationships through networking - Preparing and presenting thorough and clear presentations effectively - Performing software configuration and coding in Salesforce.com - Leading Salesforce Industry engagements successfully - Working knowledge of Agile and SAFe environments Learn more about how we work: https://pwc.to/how-we-work PwC does not intend to hire experienced or entry level job seekers who will need, now or in the future, PwC sponsorship through the H-1B lottery, except as set forth within the following policy: https://pwc.to/H-1B-Lottery-Policy. As PwC is an equal opportunity employer, all qualified applicants will receive consideration for employment at PwC without regard to race; color; religion; national origin; sex (including pregnancy, sexual orientation, and gender identity); age; disability; genetic information (including family medical history); veteran, marital, or citizenship status; or, any other status protected by law. For only those qualified applicants that are impacted by the Los Angeles County Fair Chance Ordinance for Employers, the Los Angeles' Fair Chance Initiative for Hiring Ordinance, the San Francisco Fair Chance Ordinance, San Diego County Fair Chance Ordinance, and the California Fair Chance Act, where applicable, arrest or conviction records will be considered for Employment in accordance with these laws. At PwC, we recognize that conviction records may have a direct, adverse, and negative relationship to responsibilities such as accessing sensitive company or customer information, handling proprietary assets, or collaborating closely with team members. We evaluate these factors thoughtfully to establish a secure and trusted workplace for all. Applications will be accepted until the position is filled or the posting is removed, unless otherwise set forth on the following webpage. Please visit this link for information about anticipated application deadlines: https://pwc.to/us-application-deadlines The salary range for this position is: $124,000 - $280,000, plus individuals may be eligible for an annual discretionary bonus. For roles that are based in Maryland, this is the listed salary range for this position. Actual compensation within the range will be dependent upon the individual's skills, experience, qualifications and location, and applicable employment laws. PwC offers a wide range of benefits, including medical, dental, vision, 401k, holiday pay, vacation, personal and family sick leave, and more. To view our benefits at a glance, please visit the following link: https://pwc.to/benefits-at-a-glance #LI-Hybrid