Looking to move to Carlsbad and want to connect with local employers? Fill out this form and we’ll help you get recruited.
Introduction THE CITY OF OCEANSIDE IS AN EQUAL OPPORTUNITY EMPLOYER. The City of Oceanside is accepting applications Water Treatment Supervisor. There is currently one vacancy in the Water Utilities Department. Under general direction, to supervise and coordinate water treatment and filtration operations including potable water treatment; to coordinate assigned activities with other divisions, outside agencies and the general public; and to perform a variety of tasks relative to assigned area of responsibility. Examples of Duties The Water Treatment Supervisor coordinates the organization, staffing and operational activities for the performance of water treatment and filtration; operations; participates in the development and implementation of goals, objectives, policies and priorities; recommends and implements resulting policies and procedures; identifies opportunities for improving service delivery methods and procedures; identifies resource needs; reviews with appropriate management staff; implements improvements; directs, coordinates and reviews the work plan for assigned water treatment services and activities; assigns work activities and projects; monitors work flow; monitors and reports amount of water being produced and treated; analyzes and recommends operational procedures and preventive maintenance work; ensures regulatory compliance of water filtration systems; maintains awareness of changes in regulatory requirements and implements changes into operations; inspects water meters, pump stations, reservoirs and pressure control stations; plans and schedules system maintenance; selects, trains, motivates and evaluates water treatment personnel; provides or coordinates staff training; works with employees to correct deficiencies; submits budget recommendations; attends and participates in professional group meetings; stays abreast of new trends and innovations in the field of water treatment system operation; performs related duties and responsibilities as required. Minimum Qualifications Knowledge of: Operational characteristics, services and activities of a comprehensive municipal water treatment and filtration program; Modern and complex principles and practices of water treatment system maintenance; Tools and equipment used in the maintenance, construction and repair of water treatment and filtration systems; Principles of municipal budget preparation and control; Principles of supervision, training and performance evaluation; and Pertinent Federal, State and local laws, codes and regulations. Ability to: Select, supervise, train and evaluate staff; Oversee assigned water treatment plant operations; Ensure compliance with applicable water quality standards, rules and regulations; Coordinate and schedule preventive maintenance programs; Provide technical advice on all operational matters including water treatment and filtration; Read and interpret construction blue prints and schematics; Prepare clear and concise reports; Communicate clearly and concisely, both orally and in writing; and Establish and maintain effective working relationships with those contacted in the course of work. Experience and Training Experience: Four years of responsible water treatment system operation experience including one year of shift operator or supervisory experience. Training: Equivalent to the completion of the twelfth grade supplemented by specialized training in water science, environmental science or a related field. License/Certificate: Possession of an appropriate, valid California driver's license. Possession of a valid Grade IV Water Treatment Plant Operator certificate. Working Conditions and Selection Process Environmental Conditions: Water treatment plant environment; exposure to noise, dust, grease, smoke, fumes, gases, potentially hazardous chemicals; work with water. Physical Conditions: Essential functions may require maintaining physical condition necessary for walking, standing or sitting for prolonged periods of time; moderate or light lifting; operating motorized equipment. Selection Process: All properly completed applications will be reviewed and the most appropriately qualified individuals will be invited to continue in the selection process. Failure to provide all required application materials will result in disqualification from the selection process. The process may include any combination of written exam, oral exam, and/or skills assessment to further evaluate job-related qualifications. Candidates who successfully complete the selection process will be placed on the Eligibility List for a minimum of twelve months. Note: Prospective employees will undergo, and must successfully pass, a background reference check (including fingerprinting) and a medical examination. Drug screening may be required. RESUMES WILL NOT BE ACCEPTED IN LIEU OF COMPLETED APPLICATION FORMS, BUT MAY BE ATTACHED. CANDIDATES WHO REQUIRE A REASONABLE ACCOMMODATION IN THE SELECTION PROCESS SHOULD STATE THEIR NEEDS IN WRITING WHEN SUBMITTING AN APPLICATION PACKAGE. THE PROVISIONS IN THIS BULLETIN DO NOT CONSTITUTE AN EXPRESSED OR IMPLIED CONTRACT. ANY PROVISION CONTAINED IN THIS BULLETIN MAY BE MODIFIED OR REVOKED WITHOUT NOTICE.
We are hiring a Senior Manager of Product Compliance to join our Product team! DISCOVER Watkins Wellness, a leader in the Wellness industry, is seeking a strategic and experienced Senior Manager of Product Compliance to lead global product compliance initiatives across all product lines. This role is critical in ensuring our products meet regulatory and safety standards in every market where we operate. You will oversee compliance systems, manage audits, and coordinate with internal and external partners to maintain certifications and regulatory listings. In addition, you will modernize compliance infrastructure to support scalability and efficiency, while monitoring regulatory trends and engaging with industry bodies to influence future standards. This position requires strong leadership, cross-functional collaboration, and the ability to lead complex compliance programs that protect our brand and customers worldwide. YOUR RIPPLE EFFECT Are you a strategic compliance leader? Lead the development and execution of global product compliance strategies for all product lines, ensuring adherence to regulatory and safety standards across multiple markets. Do you excel at modernization? Drive enhancements to compliance systems and infrastructure, implementing scalable solutions and maintaining accurate compliance metrics for reporting and audits. Are you passionate about risk management? Conduct regular audits and risk assessments, identify compliance gaps, and coordinate remediation efforts with Masco Internal Audit and Legal teams. Do you enjoy collaboration? Partner with Engineering, Product, and external certifiers to maintain regulatory listings, oversee third-party testing, and engage with industry bodies to influence future standards. Are you committed to education and leadership? Develop and update training materials for compliance champions, ensure annual reviews are completed, and prepare executive-level summaries for quarterly certifications and annual audits. WHAT YOU BRING Bachelor’s degree in Engineering, Regulatory Affairs, or a related field. 10+ years of experience in product compliance or regulatory affairs, preferably in a manufacturing or consumer products environment. Strong understanding of global regulatory frameworks, including safety and environmental standards. Experience leading cross-functional teams and managing complex projects. Excellent communication and analytical skills. Willingness to travel up to 15%. Experience working in a test laboratory and familiarity with Oracle Fusion; knowledge of Smartsheet or Workfront is a plus. Certified Regulatory Compliance Professional (RCP) or similar certification preferred. WHAT YOU’LL GET Watkins Wellness, we believe that everyone should ‘Feel good. Live well’. We offer employees the opportunity to join a dynamic, growing industry leader with an outstanding and well-deserved reputation for leadership and commitment to our employees, customers and community. Our employees are eligible to receive exceptional health and wellness benefits, paid time off, company bonus, profit sharing, 401k match, education assistance, and much more. We are proud of the people we are and the products we make — products that make a difference to the health and well-being of others. We look for candidates that exhibit The Watkins Way (always Ethical, endeavors to be Transparent, embraces Inclusion, welcomes Diverse backgrounds and perspectives, Accommodating, believes in Work-Life Balance, puts Safety First, Accountable, values Relationships, Passionate, Team Player, and Goal Driven). The employee must frequently lift and move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, color vision, peripheral vision and depth perception. The noise level in the work environment is usually quiet. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire. Hiring Range: $111,500.00-$175,000.00 Many factors affect actual compensation including but not limited to experience, education, skills, and geographic location Company: Watkins Manufacturing Shift 1 (United States of America) Full time Hiring Range: $111,300.00 - $174,900.00 Actual compensation may vary based on various factors including experience, education, geographic location, and/or skills. Watkins (the “Company”) is an equal opportunity employer and we strive to employ the most qualified individuals for every position. The Company makes employment decisions only based on merit. It is the Company’s policy to prohibit discrimination in any employment opportunity (including but not limited to recruitment, employment, promotion, salary increases, benefits, termination and all other terms and conditions of employment) based on race, color, sex, sexual orientation, gender, gender identity, gender expression, genetic information, pregnancy, religious creed, national origin, ancestry, age, physical/mental disability, medical condition, marital/domestic partner status, military and veteran status, height, weight or any other such characteristic protected by federal, state or local law. The Company is committed to complying with all applicable laws providing equal employment opportunities. This commitment applies to all people involved in the operations of the Company regardless of where the employee is located and prohibits unlawful discrimination by any employee of the Company. Watkins is an E-Verify employer. E-Verify is an Internet based system operated by the Department of Homeland Security (DHS) in partnership with the Social Security Administration (SSA) that allows participating employers to electronically verify the employment eligibility of their newly hired employees in the United States. Please click on the following links for more information. E-Verify Participation Poster: English & Spanish E-Verify Right to Work Poster: English & Spanish
Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Leica Biosystems, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. At Leica Biosystems, we’re not just shaping the future of cancer diagnostics — we’re transforming lives. Our mission of “Advancing Cancer Diagnostics, Improving Lives” is the driving force behind everything we do. As a global leader with the most comprehensive portfolio spanning from biopsy to diagnosis, we empower clinicians with innovative, reliable solutions so they can give patients timely, accurate answers when they need them most. When you join Leica Biosystems, you’re not just taking a job; you’re becoming part of a passionate team that knows every moment matters when it comes to cancer. You’ll help develop diagnostic solutions that turn anxiety into answers, and aid the acceleration of next-generation, life-changing therapies. Surrounded by a diverse and collaborative global community, you’ll be inspired each day to stretch, grow, and make an impact. Learn about the Danaher Business System which makes everything possible. The Senior Engineer, Quality Assurance for Leica Biosystems is responsible for providing Quality Engineering support for end-to-end design, software, and hardware development projects. This position reports to the Manager, Quality Assurance and is part of the Quality Assurance team located in Vista, California and will be an on-site role. In this role, you will have the opportunity to: Work independently and with cross-functional project team members to develop process and design deliverables including quality plans, design, software development, manufacturing and auditing documentation, test methods, and Device History Records and assist with the development of project verification and validation activities Own the development and maintenance of the product risk management process, hazard analysis, and assist with cybersecurity, FMEAs for multiple projects in accordance with ISO 14971 and ISO 62304 Assist in troubleshooting and root cause analysis for issues faced during execution of process verifications, validations, and Design Transfer to manufacturing in accordance with established procedures and transfer schedules Work closely with Research and Development and Regulatory Affairs on deliverables for global regulatory submissions, including FDA pre-submissions, 510k, and IVDR CE certifications Participate in the performance and documentation of internal and external audits and respond to audit findings by proposing and implementing necessary corrective actions The essential requirements of the job include: BS/BA in Engineering or a technical field Minimum of five years of experience in quality field in a medical device, IVD, or similarly regulated industry with emphasis on software development Experience with design controls within a regulated industry including strong working knowledge of ISO 13485, ISO 14971 and 21 CFR 820 Demonstrated experience in problem solving, root cause analysis, and implementing corrective and preventive actions to prevent recurrence Ability to effectively communicate (verbal and written) information in English (Ability to communicate in Spanish is a plus) Travel, Motor Vehicle Record & Physical/Environment Requirements: Ability to travel up to 10% of the time (domestic) Ability to lift, move, or carry equipment up to 20 lbs It would be a plus if you also possess previous experience in: Effective presentation/communication skills and project/resource management skills Ability to work independently and in a team environment, including with management and technical staff Experience with Agile software development, Cybersecurity, and AI knowledge The salary range for this role is $130,000 - $142,000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future. This job is also eligible for bonus/incentive pay. We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees. Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law. #LI-LCS Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit www.danaher.com.
*NOTE:* *No free parking available at the location and parking is not reimbursed. Not downtown in La Jolla - need to be able to get there. Location - 4365 Executive Drive, San Diego, CA 92121 * *Job Summary:* This is a hands-on position; candidate will be assisting with *office services *related tasks such as *printing/copying/scanning; sending out overnight packages and regular mail; *may need to assist with *conference room setups (food/beverage); coordinate incoming requests with onsite staff. * *Duties:* * Works with *copiers*, need to be able to worker on *PRINTERS/Copiers!!! *Look up the printers used. * Personnel that have experience in the industry, previously worked at a law firm and *customer service oriented. * Job Type: Temp-to-hire Pay: $30.00 per hour Work Location: In person
*Company Overview* Pro Spot International, Inc. is a leading manufacturer of resistance spot welding equipment, specializing in the collision repair industry. Since 1986, we have been committed to innovation and quality, managing our own machine shop and R&D department to develop cutting-edge solutions. *Summary* We are seeking a dedicated Quality Manager to join our team in California. In this role, you will be pivotal in ensuring our products meet the highest quality standards, contributing significantly to our mission of delivering exceptional welding solutions globally. The Quality Manager plans, organizes, directs and participates in the day to day quality assurance and control activities in accordance with ISO9001 and the Pro Spot quality management system. *Responsibilities* * Support the implementation of effective, efficient, and documented Quality Systems throughout the company compliant with ISO 9001. Develop/update and implement Quality procedures and forms, including training. * Drive data collection, analysis, and reporting for established Quality reports including Discrepant Material, Cost of Quality, Supplier Report Cards, production line First Pass Yield, Quality System/Control Plan Audits, and customer quality report cards. * Develops and implements standards and methods for inspection, testing, and evaluation, utilizing knowledge from various engineering fields, including chemical, computer, electrical, or mechanical. * Maintain an inventory, and coordinate calibration, of all measurement instruments and gauges. * Directs workers engaged in measuring, testing, and tabulating data concerning quality and reliability. * Formulates and maintains the quality management system objectives. * Duties also may include driving improvement “Kaizen” events with a team and the development of processes to ensure that quality, cost, and efficiency requirements are met. * Interfaces with all engineering components within the organization as well as customers and suppliers on quality related issues. * Be the representative of the Quality System for the plant facing internal and external customers. This includes developing reports and presenting the performance and direction of the manufacturing Quality System to senior management. * Support DFMEA/PFMEA activity with Design and Manufacturing Engineering. * Decide whether to accept a product or continue business with a supplier based on a review by the procurement team. * Reviews all data obtained during all quality control activities to ensure consistency with company policies and procedures. * Develops new approaches to solve problems identified during quality control activities. * Maintains prompt and thorough RCA (Root Cause Analysis) of internal Quality deviations with a strong emphasis on corrective and preventative actions. * Keeps the management team abreast of significant issues or developments identified during quality control activities and actions being taken to improve the situation. * Designs and implements quality assurance training programs for key personnel in conjunction with managers. * *Qualifications* * Bachelor's degree in Engineering, Quality or related field. * 5 years of experience in quality management within a manufacturing environment. * Strong knowledge of ISO 9001 standards and quality assurance methodologies. * Experience with quality audits and inspection processes. * Excellent analytical skills with attention to detail. * Ability to manage multiple projects effectively. * Strong communication and leadership skills. * ASQ certification * Experience with MRP/ERP, GD&T, Lean, Kaizen and Six Sigma If you are passionate about maintaining high-quality standards and want to make an impact in the manufacturing industry, we invite you to apply today and join our innovative team at Pro Spot International! Job Type: Full-time Pay: Up to $120,000.00 per year Benefits: * 401(k) * 401(k) matching * Dental insurance * Flexible spending account * Health insurance * Life insurance * Paid time off * Vision insurance Application Question(s): * Do you have experience with ISO9001? Education: * Bachelor's (Required) Experience: * Quality Management: 5 years (Required) License/Certification: * ASQC Certification (Required) Ability to Commute: * Carlsbad, CA 92010 (Required) Work Location: In person
Quality Assurance Inspector I Monday – Friday, 8:30am - 5:00pm The Quality Assurance Inspector I plays a pivotal role in ensuring the quality and integrity of Argen products. This position is responsible for inspecting in-process and finished goods within manufacturing areas to ensure compliance with ISO 13485:2016, FDA regulations, customer specifications, Argen requirements, and applicable procedures. Essential Duties and Responsibilities Conduct in-process and final inspections and testing as required. Perform visual inspections of finished products. Participate in internal assessments and audits. Maintain accurate inspection and test records. Identify and properly label non-conforming materials. Communicate product/material acceptability to production personnel. Assist with technical problem-solving and special projects. Maintain lot traceability, log sheets, and housekeeping standards. Follow safety policies and regulations to ensure safe work practices. Ensure lab cleanliness and safety standards are upheld. Perform thorough inspections during and after production to ensure quality and compliance. Verify product labeling for accuracy and regulatory compliance. Clear and prepare production lines for subsequent runs. Review and validate Device History Records (DHRs) for completeness and compliance. Perform other duties as assigned. Experience & Qualifications High school diploma or equivalent required. Experience in a GMP-regulated facility is a plus. Completion of 8 hours of Quality Training (PTC) required. Strong attention to detail. Proficiency in basic arithmetic and problem-solving. Understanding of raw materials, production processes, and quality control. Familiarity with administrative procedures and computer systems. Effective written and verbal communication skills. Ability to interpret technical drawings, artwork, and procedures. Commitment to safety and quality standards. Ability to follow site protocols, policies, and procedures. Flexible, motivated, and capable of working independently. Strong organizational and time-management skills. Problem-solving abilities. Ability to learn technical concepts through documentation and training. Preferred knowledge of regulatory standards including: cGMP ISO 13485 21 CFR Part 820 CMDR SOR/98-282 93/42/EEC RDC 16/2013 MHLW MO 169 TG(MD)R Sch3 Mon- Fri 8:30am - 5:00pm
Why work for PCI Pharma Services? At PCI, we have an uncompromising focus on providing quality and operational excellence and providing the industry leading customer experience. Our people make all of this happen, so providing an industry leading experience for our people is equally as important. By creating an authentic culture of purposeful work, we aspire to be an interesting and fulfilling place for talented individuals to grow careers. We live a philosophy of intentional learning combined with real-life experience supported by a fair and competitive rewards program. We are individuals, teams and a company that believes in our purpose and our approach is simple, the people who work at PCI fuel our business; we don’t say no, we figure out how. Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. Job Details: We are looking for a Drug Product Manufacturing Associate II who is responsible for executing GMP production of injectable pharmaceuticals by following all applicable SOP's. Manufacturing associates are responsible for preparing equipment and materials for GMP aseptic production and operating equipment such from glasswashers, autoclaves, depyrogenation ovens and automated filling machines. Responsibilities: Participate in one or more areas of the aseptic manufacturing injectable pharmaceuticals using GMP's in FDA regulated facility. Assists technical personnel with troubleshooting mechanical issues that arise with manufacturing equipment. Performs various semi-routine manufacturing tasks under the guidelines of established SOP’s and cGMP regulations. Troubleshoots manufacturing processes that are semi-complex in level under cGMP guidelines and under the supervision of management. Assists in the research and implementation of new methods and technologies to enhance operations. Prepares components, media, buffers, and other solutions as needed. Accurately documents data and writes/reviews batch records under cGMP guidelines. Prepares material components for production. Regular and reliable attendance on a full time basis [or in accordance with posted schedule]. Responsible for exhibiting professional behavior with both internal and external business associates that reflects positively on the company and is consistent with the company’s policies and practices. Embodies PCI Pharma Service’s cultural values and aligns daily actions with department goals and company culture. Requirements: High school diploma required. Bachelors in a science or engineering discipline preferred. Minimum of two (2) years of relevant experience in manufacturing, laboratory, mechanical or engineering positions. Ability to work with cross functional teams. Detail oriented with strong written and verbal communication skills. Ability to work independently, within prescribed guidelines, or as a team member. Demonstrated ability to follow detailed directions in a manufacturing GMP environment. Familiarity with cGMP, manufacturing, machine operations, and data entry. Must be familiar with Microsoft Office applications. The base hourly range for this position is $24.08 to $27.09 plus annual performance bonus eligibility. Final offer amounts are determined by multiple factors including and not limited to specific and relevant experience, credentials, geography and subject matter expertise. Join us and be part of building the bridge between life changing therapies and patients. Let’s talk future Equal Employment Opportunity (EEO) Statement: PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. At PCI, Equity and Inclusion are at the core of our company’s purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity – at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture. #LI-KC1 #HP Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
By joining Bio-Techne, you’ll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide. Pay Range: $23.20 - $31.90 Position Summary: A Manufacturing Production Coordinator organizes and oversees the manufacturing production process to ensure efficient operation and on-time delivery of goods Duties and Responsibilities: Assess and coordinate the readiness of the production process, ensuring all materials are available Create and manage production schedules, allocate resources efficiently, and monitor progress to meet delivery deadlines Order labels and production materials, and manage inventory levels Act as a liaison between production, materials, accounting, quality, and other teams, ensuring smooth workflow and timely project updates Track material requirements, reconcile material usage, resolve discrepancies, and perform inventory control functions Assemble and review batch records to ensure accuracy and completeness Record, track, and report on production activities and key metrics, often using specific manufacturing and inventory management systems Ensure products meet quality standards and assist in troubleshooting issues during the production process Collaborate with other departments to coordinate production schedules and resolve issues with regards to readiness Maintain project documentation, including timelines, status reports, and post-mortem analyses Communicate with external vendors, monitor invoices, and provide information to management and other departments regarding production status Present at tier meetings to provide updates on production status, challenges, and opportunities that are readiness-related Knowledge, Skills and Abilities Required: Organizational & Time Management Skills: Ability to handle multiple tasks, prioritize effectively, and work in a fast-paced environment Communication Skills: Excellent verbal and written communication for effective collaboration with various teams and stakeholders Attention to Detail: A keen eye for detail to prevent errors and ensure accuracy Problem-Solving Skills: The ability to identify and resolve issues that arise during the production process Technical Proficiency: Experience with production scheduling, data entry, and familiarity with manufacturing systems and quality control standards Experience: Often requires experience in a manufacturing environment, material handling, or inventory control Minimum Job Requirements: 2-5 years’ experience in similar role preferably with a Manufacturing company. Excellent problem-solving skills, strong communication and interpersonal skills. Ability to work under pressure and meet deadlines. Why Join Bio-Techne: We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield. We invest in our employees’ financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA. We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more. We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging. We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave. We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table. Bio-Techne is an E-Verify Employer in the United States. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.
Under supervision, this position will perform battery pack assembly work. Perform all job requirements in accordance with applicable Standard Operating Procedures and Safety Procedures. *Duties and responsibilities* * Assemble battery cells, modules, and packs using hand tools, automated equipment, and assembly fixtures. * Perform welding (spot, ultrasonic, or laser) and soldering of electrical connections as required. * Conduct visual and functional inspections on subassemblies and completed products. * Operate equipment such as cell stackers, formation machines, test chambers, and thermal cycling equipment. * Follow strict safety procedures for handling high-voltage systems, hazardous materials, and chemical processes. * Accurately document assembly processes, test results, and material usage in manufacturing records. * Maintain a clean, organized, and safe work environment * Adhere to all company policies, regulatory guidelines, and ISO or other applicable quality standards. * Other duties such as project management as assigned *Qualification* * high school graduate or equivalent, AA degree preferred * Very good attention to details * Handy, resourceful, and alert * Ability to communicate effectively * Works well with electronically devices and semi auto machines * At least 1 years manufacturer working experiences *Working conditions* * Wear assigned PPE while handling electrode and battery * Wear a mask all the time inside the building *Physical requirements* * Capable of standing and walking for extended periods. * Must be able to bend, squat, reach, and climb on a frequent basis. * Must be able to lift, push and pull up to 35 pounds. Job Type: Full-time Pay: From $21.00 per hour Benefits: * 401(k) * 401(k) matching * Dental insurance * Health insurance * Life insurance * Paid time off * Vision insurance Work Location: In person
Date Posted: 2025-10-09 Country: United States of America Location: PW192: Carlsbad 5940 Darwin Court , Carlsbad, CA, 92008 USA Position Role Type: Onsite U.S. Citizen, U.S. Person, or Immigration Status Requirements: U.S. citizenship is required, as only U.S. citizens are authorized to access information under this program/contract. Security Clearance: None/Not Required Pratt & Whitney is working to once again transform the future of flight—designing, building and servicing engines unlike any the world has ever seen. And because transformation begins from within, we’re seeking the people to drive it. So, calling all curious. Come ready to explore and you’ll find a place where your talent takes flight—beyond the borders of title, a country or your comfort zone. Bring your passion and commitment and we’ll welcome you into a tight-knit team that takes our mission personally. Channel your drive to make a difference into shaping an organization and an industry that’s evolving fast to the future. At Pratt & Whitney, the difference you make is on display every day. Just look up. Are you ready to go beyond? What You Will Do: We are seeking a skilled and detail-oriented Composites Lab Technician to join our advanced manufacturing team. In this role, you will operate sophisticated equipment in our preforming laboratory to fabricate high-quality preforms for ceramic matrix composite turbine engine parts. You will play a critical role in supporting the development of components for aerospace applications while maintaining strict quality and safety standards. Operate and maintain all equipment in the preforming (composites) lab, including ply cutters, and ovens to fabricate preforms for ceramic matrix composite turbine engine parts Perform layup operations on tools and debulk parts according to established work instructions and technical specifications Maintain and organize tooling used in preforming processes; provide input and recommendations for tool design improvements Monitor raw material supplies, track inventory levels, and ensure adequate stock of materials required for ongoing operations Load equipment with parts according to documented configurations and process conditions; verify accuracy and completeness of setup Program equipment and adjust settings to accommodate new processes, materials, or production requirements Conduct regular preventive and corrective maintenance on preforming equipment; troubleshoot mechanical and operational issues Monitor preforming processes during operations, respond promptly to alarms, diagnose problems, and take appropriate action or escalate as needed Support facility and equipment upgrade projects, including testing, validation, and implementation activities Assist in the development and execution of experimental designs aimed at process improvements and optimization Maintain comprehensive documentation of all processes, including electronic and paper records, in compliance with quality system requirements Adhere to all AS9100 quality management system requirements, including standard operating procedures (SOPs), internal policies, manufacturer specifications, and safety protocols Perform additional duties as assigned to support operational needs Qualifications You Must Have: HS diploma (or equivalent, e.g. G.E.D in the US) with a minimum of 2 years of relevant experience Must have proficient computer experience with MS Office Qualifications We Prefer: AA/AS degree or other 2-year post high school training with a minimum of 4 years of relevant experience Manufacturing background Previous aerospace or chemical industry experience is preferred Experience working within a formal quality system like ISO 9001 AS9100 Demonstrated mechanical and technical aptitude and experience Forklift, cranes and other material handling equipment. What We Offer: Medical, dental, vision benefits Life, short term disability, long term disability benefits Paid time off including vacation, sick leave, holidays 401-K with company match Other innovative benefits including deals and discounts Learn More & Apply Now! In addition to transforming the future of flight, we are also transforming how and where we work. We’ve introduced role types to help you understand how you will operate in our blended work environment. This role is: Onsite: Employees who are working in Onsite roles will work primarily onsite. This includes all production and maintenance workers, as they are essential to the development of our engines. Candidates will learn more about role type and current site status throughout the recruiting process. For onsite and hybrid roles, commuting to and from the assigned site is the employee’s personal responsibility. The salary range for this role is $22.40 - $42.01 per hour; however, Raytheon Technologies considers several factors when extending an offer, including but not limited to, the role and associated responsibilities, a candidate’s work experience, location, education/training, and key skills. As part of our commitment to maintaining a secure hiring process, candidates may be asked to attend select steps of the interview process in-person at one of our office locations, regardless of whether the role is designated as on-site, hybrid or remote. Hired applicants may be eligible for benefits, including but not limited to, medical, dental, vision, life insurance, short-term disability, long-term disability, 401(k) match, flexible spending accounts, flexible work schedules, employee assistance program, Employee Scholar Program, parental leave, paid time off, and holidays. Specific benefits are dependent upon the specific business unit as well as whether or not the position is covered by a collective-bargaining agreement. Hired applicants may be eligible for annual short-term and/or long-term incentive compensation programs depending on the level of the position and whether or not it is covered by a collective-bargaining agreement. Payments under these annual programs are not guaranteed and are dependent upon a variety of factors including, but not limited to, individual performance, business unit performance, and/or the company’s performance. This role is a U.S.-based role. If the successful candidate resides in a U.S. territory, the appropriate pay structure and benefits will apply. RTX anticipates the application window closing approximately 40 days from the date the notice was posted. However, factors such as candidate flow and business necessity may require RTX to shorten or extend the application window. RTX is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability or veteran status, or any other applicable state or federal protected class. RTX provides affirmative action in employment for qualified Individuals with a Disability and Protected Veterans in compliance with Section 503 of the Rehabilitation Act and the Vietnam Era Veterans’ Readjustment Assistance Act. Privacy Policy and Terms: Click on this link to read the Policy and Terms
Knitting Operator FutureStitch, Inc. Location: Oceanside, CA Schedule: Monday–Friday | 8:00 AM – 5:00 PM About the Role As a Knitting Operator at FutureStitch, you’ll play an essential role in producing our high-quality socks and knitted products. You’ll ensure our knitting machines run efficiently, maintain yarn consistency, and uphold strict quality standards. This position requires attention to detail, teamwork, and a commitment to maintaining a clean and organized work environment. Key Responsibilities Ensure knitting machines are running efficiently throughout the shift. Attend to red lights and any machine issues immediately to minimize downtime. Maintain yarns on creels at all times to ensure uninterrupted production. Ensure that no more than six socks are left unchecked in the basket at any given time. Check each sock’s toe seam from the outside for quality and consistency. Perform a full inspection of the last sock; if it meets quality standards, place it in the box for packaging. Remain on the knitting room floor during the shift to monitor operations. Keep the knitting department clean and organized at all times. Sweep the main passage twice per shift using a wide broom to maintain a clean environment. Monitor trimming filters and empty them as needed to prevent machine issues. Maintain a clean, safe, and organized work area. Perform other duties as needed. Qualifications & Skills Previous experience operating knitting or textile machinery preferred. Strong attention to detail and commitment to product quality. Ability to work efficiently in a fast-paced manufacturing environment. Good communication skills and a positive team attitude. Willingness to learn and adapt to new equipment and production methods. Must be reliable and punctual. Physical Requirements Ability to stand for long periods and walk between machines throughout the shift. Ability to lift and carry up to 25 lbs. regularly. Manual dexterity for handling yarns, needles, and fine materials. Ability to bend, reach, and move comfortably around machinery. Tolerance for moderate to high noise levels in a factory setting. Why Join FutureStitch At FutureStitch, we take pride in craftsmanship, creativity, and community. You’ll be part of a diverse and innovative team that values growth, inclusion, and purpose in everything we make.
Become part of a team that champions wellness worldwide. CAPTEK® Softgel International is a global leader in the development and production of high-quality nutraceutical supplements. As a contract manufacturer organization (CMO), we collaborate with innovators from some of the world’s most successful brands. Summary: Responsible for the safe operation of the washroom area. Ensure all equipment, tanks, utensils and parts are properly cleaned and sanitized. Ensure that the washroom is clean and organize throughout the shift. Essential Duties and Responsibilities: • Follow cGMP (current Good Manufacturing Practices). • Adhere to SOPs (Standard Operating Procedures) and batch records to ensure process and specifications are done correctly. • Follow GDP (Good Documenting Practices) by documenting activities in the batch records, logbooks, equipment and all controlled forms in a timely manner. • Adhere to all safety policy and operate all equipment in a safe manner. • Adhere to gowning procedure and must always wear the required PPE (personal protective equipment). • Communicate effectively with the team, Lead, Supervisors and Manager to identify washroom needs and any issues that will affect production quality and throughput. • Good housekeeping practices. Maintain, clean and organize the washroom including wall sinks and floors. • Provide hands-on training for new production employees. • Foster a team environment by working closely and efficiently with all other departments. • Support continuous improvements by suggesting ideas and changes that will benefit daily processes and procedures. • Make sure all incoming and going equipment and tanks are labeled appropriately. • Clean and sanitize all tanks, utensils, machine parts, etc. Sanitize with 70% alcohol solution. • Clean all tanks, equipment, utensils, parts, trays to accommodate production and minimize downtime. • Remove leftover compounding and gelatin with supervisor's approval. • Support general cleaning outside the washroom area. Qualifications: Minimum high school diploma or G.E.D preferred. Education/Experience: • Previous experience working with production equipment preferred. • To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. 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 occasionally exposed to work near moving mechanical parts, fumes, or airborne particles and risk of electrical shock. The noise level in the work environment is usually moderate. 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. Physical demands require sitting for extended periods of time, walking, bending, reaching, carrying, and occasionally lifting and/or moving objects up to 25 pounds. Specific vision abilities required by this job include Close vision, Peripheral vision, and the ability to adjust focus. While performing the duties of this job, the employee is occasionally required to use hands to finger, handle, or feel; reach with hands and arms; climb or balance; stoop, kneel, crouch, or crawl and talk or hear. CAPTEK is an equal employment opportunity employer. In order to provide equal opportunities to all individuals, employment decisions will be based on merit, qualifications, and abilities, not on any mental or physical disability. We comply with the law regarding reasonable accommodation for disabled employees and applicants. We do not discriminate on the basis of actual or perceived race, color, national origin, ancestry, sex (which includes pregnancy, childbirth, breastfeeding and medical conditions related to pregnancy, childbirth or breastfeeding), reproductive health decisions, gender, gender identity, gender expression, religious creed, disability (mental and physical) including HIV and AIDS, medical condition (cancer and genetic characteristics ), genetic information, age, marital status, sexual orientation, military and veteran status, or any other characteristic protected by federal, state or local law. Our management team is dedicated to this policy with respect to recruitment, hiring, placement, promotion, transfer, training, compensation, benefits, employee activities and general treatment during employment. Thank you for your interest in joining the CAPTEK team. You will be contacted shortly if your application is selected.