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Location: San Diego, CA, US, 92121 Business Unit: Energy Conversion Solutions Posting Date: May 21, 2026 Job Description: About Us AMETEK Programmable Power Business Unit (~$160M) is headquartered in San Diego, CA and provides the most advanced Power and Instrumentation solutions for Precision Stimulus, Process Power and Measurement and Switching applications. We also provide a deep expertise in Programmable Power, Data Acquisition and Functional Test applications. Job Summary The Quality Engineer is responsible for ensuring the highest possible reliability and quality of the Manufacturing processes and products. The Quality Engineer will ensure that Ametek’s products and processes meet established quality standards from supply chain to end user by identifying requirements based on customer needs, implementing quality assurance and quality control methods at the points of quality, identifying issues and opportunities, and developing continuous improvement, corrective, and preventive measures. In addition, the Quality Engineer will set up and monitor QMS procedures and processes and support NPD process. Roles & Responsibilities This position has responsibility for: Support implementation of Quality Management System (QMS) procedures and processes per ISO 9001. Perform internal audits of other department functions for compliance with the QMS. Apply strong problem-solving skills including supporting complex issues, CARs. Support new product development, participate on design reviews, evaluate specifications and control limits for product, components and manufacturing. Performs reviews, failure analysis and corrective action reports on reliability and technical issues for both field and internal manufacturing issues. Provide Training and guidance to Quality Technicians and Inspectors. Supports Quality issues in production lines and nonconforming material disposition. Leads quality improvement projects such as reduction or warranty, scrap and yield improvement. Support OpEx Initiatives and expansion projects Act as Quality POC (Point of Contact) to key Customer account when assigned Demonstrate a high level of technical competence related to electronics and electromechanical box build product assembly manufacturing technology, focusing on consistent quality and reliability. Support source inspection process. Provide supplier quality engineering support. Minimum Qualifications (Experience and Skills) Bachelor’s degree in engineering, Manufacturing or Quality. (or equivalent industry experience). 3-5 years of experience in quality or similar industry. Working knowledge of AS9100 and/or ISO 9001:2015. Due to the nature of our programs and products, applicants must have the legal right to work in the U.S. and additionally must be legally authorized to access export-controlled information and source code. Desired Qualifications Developing manufacturing quality standards. Capable of using electrical test equipment such as oscilloscopes, DVM’s Signal Generators etc Use quality tools FMEA, Quality Control Plans, SPC, Metrics and Product/Process Capability that ensures quality attainment via process validation. Ability to generate reports using Excel and Word. IPC 600, IPC 610, and IPC 620 requirements Ability to prepare reports and data for management or customer review. Knowledge of circuits, technical circuits and mechanical designs along with good decision making, judgment and analytical ability. Ability to generate reports using Word and Excel. Power BI proficiency What’s in It for You Competitive compensation, holiday pay, and paid time off Great benefits package that includes health, vision, and dental insurance 401(k), plus matching Flexible spending accounts (FSAs), health savings account (HSA) with AMETEK contribution, life insurance, disability insurance, and family medical leave Employee referral program Tuition reimbursement program Employee assistance program Exciting, fast-paced environment where you could make a true impact Opportunities for career advancement within our business unit and across all other AMETEK business entities Work Environment This job operates in both a professional office and an electronics manufacturing environment. 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. While performing the duties of this job, the employee is regularly required to talk or hear. The employee frequently is required to stand; walk; use hands to finger, handle or feel; and reach with hands and arms. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. This position requires the ability to occasionally lift office products and supplies, up to 30 pounds. Additional Details Location Information: This role is based in San Diego, California, a city renowned for its idyllic blend of sun, sea, and vibrant culture. With a coastal climate and over 70 miles of stunning coastline, it's a haven for beach lovers and outdoor enthusiasts year-round. Explore diverse museums, the historic Gaslamp Quarter, and Balboa Park's gardens and world-famous zoo. Enjoy an active lifestyle with parks, trails, and water sports. Relish international cuisine and experience unique neighborhoods like lively North Park and coastal La Jolla. San Diego offers an irresistible mix of relaxation and adventure. To learn more about our company and our job opportunities, visit us at: https://www.ametek.com/careers #LI-Onsite #LI-LL1 Compensation Employee Type: Salaried Currency: USD Salary Minimum: 85,000 Salary Maximum: 110,000 Incentive: No Disclaimer: Where a specific pay range is noted, it is a good faith estimate at the time of this posting. The actual salary offered will be based on experience, skills, qualifications, market / business considerations, and geographic location. For more information on AMETEK's competitive benefits, please click here. AMETEK, Inc. is a leading global provider of industrial technology solutions serving a diverse set of attractive niche markets with annual sales over $7.5 billion. AMETEK is committed to making a safer, sustainable, and more productive world a reality. We use differentiated technology solutions to solve our customers’ most complex challenges. We employ 22,000 colleagues, in 35 countries, that are grounded by our core values: Ethics and Integrity, Respect for the Individual, Inclusion, Teamwork, and Social Responsibility. AMETEK is a component of the S&P 500. Visit https://www.ametek.com/careers for more information. We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity, status as a veteran, and basis of disability or any other federal, state or local protected class. Individuals who need a reasonable accommodation because of a disability for any part of the employment process should call 1 (866) 263-8359.
*Looking to fill 1st Shift, position requires availability to start 5:30am, 6:00am, 6:30am or 7:00am Monday to Saturday. Job Summary: The Production Assistant under immediate direction performs a variety of tasks including inspecting, packaging, palletizing, loading, unloading, lifting, and moving production materials. Essential Functions and Responsibilities (not restrictive): Ensures the quality of the product being sliced and packaged meets the company’s production standards and quality. Removes product by hand from conveyor belt to place in packaging. Boxes packaged material according to customers' specifications. Stocks boxes or repackages when needed. Cut and peel casing from salami. Rotates into any line position as needed. Tends production line by watching for equipment malfunctions or product defects. Identify and communicate problems and production issues in a timely manner to Supervisors. Analysis and Critical Control Point (HACCP) training, along with company pre-requisite programs, Standard Operating Procedures (SOP’s), and Standard Sanitation Operating Procedures (SSOP’s). Following set company and OSHA safety rules, regulations, and guidelines at all times. Performs other duties and responsibilities as necessary. Qualification & Experience Requirements: High School Diploma or GED, preferred. 3-6 months’ related manufacturing or food experience, preferred. Knowledge, Skills, Abilities: Ability to work well with others. Ability to multi-task while being detail-oriented. Ability to work in a fast-paced environment. Ability to follow verbal and written instructions accurately. Ability to work with minimal supervision while remaining productive at all times. Ability to use pallet jacks. Ability to use a weight scale. Ability to package 40 pieces per minute. Ability to box 60 packages per minute. Ability to palletize 3 cases per minute. Ability to stand 8+ hours. Ability to work with allergens. Excellent attendance and dependability. Must be able to work flexible hours to include overtime and weekends on short notice. Pay Range : $18.00 per hour. Starting rate of pay may vary based on factors including, but not limited to, position offered, location, education, training, and/or experience.
Somacis Inc., a well-established leader in advanced technology and high-reliability printed circuit board manufacturing with over 50 years of industry expertise, located in Poway, California, is seeking multiple qualified CMM Operators/Programmers for our Quality Assurance department across both shifts. Key Responsibilities: Collaborate with the Quality Assurance team to inspect materials and products to meet internal and external specifications. Document production issues related to materials, processes, and machinery. Test PCBs using a CMM to ensure proper tolerances, measurements, and identify non-conformance. Communicate findings to Quality Engineers. Collect and analyze data for presentation to the management team. Adhere to safety and operational guidelines for handling products, operating machinery, and promoting a safe work environment. Required Knowledge, Skills, and Abilities: Highly motivated, adaptable, innovative, and responsible individuals who produce quality results. 2-3 years of experience in a Quality Assurance role within a manufacturing environment. Ability to read and understand customer specifications, prints, and other related documents to ensure quality standards. Proficiency in working with measuring tools and testing equipment. Experience with GD&T and other quality standards. Strong organizational skills with attention to detail for inspecting products through various stages of the manufacturing process and maintaining documentation. Effective communication skills, both verbal and written. Ability to perform basic mathematical calculations. CMM programming experience is a plus. Applicants must hold U.S. Citizenship, Permanent Resident, Asylee, or Refugee status. Physical Requirements: Frequent use of hands to handle objects, tools, or controls; ability to talk and hear clearly. Occasional standing, walking, and reaching with hands and arms. Ability to move around the facility and production floor. Physical endurance to lift and/or move up to 30 pounds. Specific vision abilities required include close vision, distance vision, depth perception, and the ability to adjust focus. Strong listening skills to gather and process requests, and respond accordingly. Benefits: 401(k) Match Program Medical/Dental/Vision Employer Sponsored LTD Employer Sponsored Life PTO program Tuition reimbursement Qualified applicants must hold U.S. Citizenship, Permanent Resident, Asylee, or Refugee status. Note: Job descriptions are intended to provide an accurate overview of the role but are not exhaustive. They serve as a reference point for fair pay considerations.
At the Vitrolife Group, we work every day to unlock the full potential of science and technology to reduce the barriers towards building a family. Together we help our customers and their patients to fulfill the dream of having a baby. Schedule: Monday through Friday, 6:30 AM – 3:00 PM Location: Fully onsite cleanroom environment, San Diego, CA Pay Rate: $25 - $28 / hr Employment: Full-Time Position Summary The Production Team Lead coordinates first-shift production activities in a regulated medical device environment, working alongside the team to meet weekly output and quality goals. This is a hands-on working lead role, approximately 50–75% of time is spent in direct production using microscopes and semi-automated equipment, with the remainder dedicated to tracking key metrics (output per hour, yield), ensuring GMP/GDP compliance, supporting training, and managing shift logistics. The ideal candidate brings a strong production background, a quality-first mindset, and the ability to lead by example on the floor. Key Responsibilities • Lead and coordinate day-to-day production activities of the first-shift production team • Participate in manufacturing with the team while monitoring overall production goals • Serve as first point of contact for production flow, issues, and escalation to management • Manage information transfer between 1st and 2nd shift • Ensure compliance with Good Manufacturing Practices (GMP) and related SOPs • Monitor team documentation practices according to Good Documentation Practices (GDP) • Support shift coverage, rotations, and breaks in coordination with management • Lead departmental training activities and maintain compliant training records • Drive continuous improvement in production and product quality with management • Maintain accurate records and documentation per GDP and SOPs • Track and implement corrective action protocols • Troubleshoot robotics and automation equipment; coordinate advanced support as needed • Reinforce workplace standards and company policies through modeling and communication Required Qualifications • 3 to 5 years of related manufacturing experience in a regulated medical device or electronics assembly environment • Previous experience acting as a working lead, senior technician, or informal team lead supporting production teams • Solid understanding of Good Documentation Practices (GDP), Good Manufacturing Practices (GMP), and Good Laboratory Practices (GLP) • Familiarity with FDA regulations and quality processes • Working knowledge of Microsoft Office and large Enterprise Resource Planning (ERP) systems Preferred Qualifications • Experience in production management, assembly, and process improvement • Knowledge of cleanroom operations and medical device assembly • Experience with robotics and automation Work Environment Dress Code: Lab coats, cleanroom shoes, hair nets, and beard covers are required Note: No leggings, face makeup, or perfume permitted in the cleanroom Training: Hands-on training provided by the manufacturing manager and senior technicians Benefits Paid Time Off and 10 Paid Holidays 401(k) with Employer Match Medical, Dental, Vision IVF Coverage to support family building needs GAP Insurance Basic Life and AD&D Coverage Short- and Long-Term Disability Optional AFLAC Supplemental Policies Employee Assistance Program (EAP) Flexible Spending & Health Savings Account An offer of employment is contingent on the successful passing of a background check. 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. Vitrolife Group is a global provider of medical devices and genetic services. Based on science and advanced research capabilities, we develop services and products for personalized genetic information and medical device products. We support our customers by improving their clinical practice for the patient's outcome of fertility treatment. We are currently approximately 1 100 colleagues worldwide, with headquarters in Gothenburg, Sweden. Vitrolife Group's products and services are available in more than 110 countries through our own presence in 30 countries and a network of distributors. Vitrolife Group is a sustainable market leader and aims to be the preferred partner for IVF-clinics by providing superior products and services with the vision of fulfilling the dream of having a baby. The Vitrolife share is listed on Nasdaq Stockholm.
*Job Summary* We are seeking a dedicated and detail-oriented Painting & Manufacturing Associate to join our dynamic team. In this role, you will be responsible for supporting various manufacturing processes, assisting with painting, ensuring quality standards are met, and contributing to the overall efficiency of production operations. The ideal candidate will possess a strong work ethic, a commitment to safety, and the ability to work collaboratively in a fast-paced environment. *Responsibilities* * Prepare and paint golf club components * Monitor production processes to ensure compliance with quality standards and specifications. * Complete customer orders from assembly to packaging * Perform routine inspections and troubleshooting of equipment to identify issues promptly. * Assist in the assembly of products, ensuring accuracy and adherence to safety protocols. * Maintain a clean and organized work area, following all safety regulations. * Collaborate with team members to achieve production goals and meet deadlines. * Document production activities accurately as required by company policies. *Experience* * Previous experience in painting & manufacturing or industrial environment is required. * Familiarity with operating machinery or equipment is a plus. * Strong attention to detail and ability to follow instructions carefully. * Excellent communication skills and ability to work effectively in a team setting. * Willingness to learn new skills and adapt to changing processes within the manufacturing environment. Join us as we strive for excellence in manufacturing while fostering a supportive workplace culture! Pay: From $22.00 per hour Benefits: * 401(k) * Employee discount * Flexible schedule * On-the-job training People with a criminal record are encouraged to apply Work Location: In person
The Senior Director of Production is a pivotal leadership role responsible for overseeing all aspects of Upstream or Downstream production operations. This role demands a strategic thinker with extensive experience in production management, operational excellence, lean manufacturing, and cost management. This individual is accountable for the effective utilization of the human and equipment resources involved in the assigned production areas, meeting productivity and cost control targets. This individual supports the VP of Production and site leadership in implementing the long-term strategic roadmap for production, ensuring alignment with overall site strategy, demand, and customer needs. This individual implements initiatives and policies to enhance quality, safety, and operational excellence following GMP manufacturing principles, routinely analyzing production budgets and making necessary adjustments. Additionally, this individual manages the design of the production organization, making appropriate adjustments in size and skillset, and setting and managing performance goals for the production workforce. This individual will directly, and through his direct/indirect team managers, select, hire, and train new team members, routinely evaluate team members to ensure standards of performance are met, and assign responsibilities. What you will do Direct and work with production team of managers, chemists and technicians to manage production workflow, schedule and quality Establish and enforce production and quality standards Motivate team members to deliver exceptional work and exceed expectations Understand customer requirements and prepare production plan accordingly Create, update and implement policies and procedures for manufacturing Develop growth opportunities for employees Maintain professional and technical knowledge by attending educational workshops, reviewing professional publications, benchmarking state of the art industry practices, and participating in professional societies Ensure that reporting employees receive adequate environmental, health and safety training Ensure that any operating or occupational accidents and incidents involving employees reporting to you are properly recorded and investigated to a productive conclusion. This includes ensuring employees are appropriately monitored and managed to address unacceptable levels of performance Ensure a positive safety culture is developed within the area, and is supported by robust safety processes in accordance with industry standards and legislation Ensure safety arrangements are adhered to and protect the health and safety of employees, visitors, contractor, and the public Qualifications PhD in Chemistry /Chemical Engineering or related field with 8-10 years related experience required or Master's Degree in Chemistry/Chemical Engineering with 10-15 years related experience required or Bachelor's Degree in Chemistry / Chemical Engineering with 15 to 20 years’ related experience required 7-9 years Managerial experience in cGMP manufacturing required and 4-6 years Peptide and oligo nucleotide manufacturing experience in upstream and downstream manufacturing preferred Strong knowledge of Chemistry /Chemical Engineering along with cGMP manufacturing focus Proficient with large scale manufacturing and process development Proficient with various in-process analytical methods Excellent written and oral communication skills Basic computer knowledge, including Microsoft Word, Excel and PowerPoint 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 technical and analytical problems Ability to work independently and manage one’s time Communicate effectively and ability to function well in a team environment Base Annual Salary Range: $141,566.40 - $176.958.00 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
The Director of Production oversees all production operations within their department to ensure deadlines are met and projects are completed within the operational budget. The Director of Production oversees all assigned personnel. The incumbent will select, hire and train new employees and contribute in appointing managers and supervisors; routinely evaluate team members to ensure standards of performance are met and assign responsibilities for each project. The Director of Production implements quality-control programs and policies, routinely analyzes production budgets, and make changes as necessary. Throughout the production process, the Director oversees the process to ensure safety procedures are followed and performance goals are met. The Director of Production also creates production reports for review by top executives. What you will do Supervise and manage a team of Production Managers, Chemists and Technicians Direct and work with production team of managers, chemists and technicians to manage production workflow, schedule and quality Monitor production activities and adjust schedule to ensure on-time delivery Develop process improvements to optimize production speed and quality Establish and enforce production and quality standards Motivate team members to deliver exceptional work and exceed expectations Organize job trainings for team members to achieve business objectives Maintain all production related documentations for future reference purposes Ensure that final product meets quality standards and customer specifications Understand customer requirements and prepare production plan accordingly Create, update and implement policies and procedures for manufacturing Evaluate new equipment and technologies Enforce cGMP guidelines Maintain a clean and safe work environment by educating and directing personnel on the use of control points, equipment and resources Maintain compliance with established safety policies and written procedures Develop growth opportunities for employees Maintain professional and technical knowledge by attending educational workshops, reviewing professional publications, benchmarking state of the art industry practices, and participating in professional societies Ensure that reporting employees receive adequate environmental, health and safety training Ensure that any operating or occupational accidents and incidents involving employees reporting to you are properly recorded and investigated to a productive conclusion. This includes ensuring employees are appropriately monitored and managed to address unacceptable levels of performance Ensure a positive safety culture is developed within the area, and is supported by robust safety processes in accordance with industry standards and legislation Ensure safety arrangements are adhered to and protect the health and safety of employees, visitors, contractor, and the public Qualifications PhD in Chemistry / Biological Chemistry / Chemical Engineering or related field with 5+ years relevant experience required or Master's Degree in Chemistry / Biological Chemistry / Chemical Engineering with 10+ years relevant experience required or Bachelor's Degree in Chemistry / Biological Chemistry / Chemical Engineering with 15+ years relevant experience required Managerial experience in cGMP manufacturing and Peptide and oligo nucleotide manufacturing experience in upstream and downstream manufacturing Strong knowledge of chemistry / / Biological chemistry/ chemical engineering along with cGMP manufacturing focus Proficient with large scale manufacturing and process development Proficient with various in-process analytical methods Excellent written and oral communication skills Basic computer knowledge, including Microsoft Word, Excel and PowerPoint 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 technical and analytical problems Ability to work independently and manage one’s time Communicate effectively and ability to function well in a team environment Base Annual Salary Range: $129,992.80 - $162,491.00 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
Performs the set-up, calibration, testing, and troubleshooting of circuits, components, instruments, and mechanical assemblies. Determines and may develop test specifications, methods, and procedures from blueprints, drawings, and diagrams. May complete rework on assemblies and/or systems as a result of testing. Work in production environment to perform testing and troubleshooting of various components Some manual assembly operations are required as part of the test function Carefully follow production documentation and processes, including keeping detailed records of testing and rework performed Work closely with engineering to solve production problems, including setting up and performing complex manual testing. Work on NPI and existing product qualifications. Works from a variety of documents including test specifications, wiring diagrams, schematics, etc. where complete information is frequently lacking or from general oral engineering instructions requiring technical judgment, initiative and experience Complies with standard test procedures and specifications to perform tests on highly complex electronic developmental and production components, subassemblies and systems Verifies and analyzes test results; troubleshoots, repairs and adjusts equipment so that their performance complies with test requirements and that the quality of the product is assured, and determines when rework is necessary to ensure product compliance Proactively influence plans to establish and maintain necessary test infrastructure to ensure testing is performed in a sustainable and reliable manner Communicate daily production status, testing progress, and issues to supervisors, engineering, and team members. Provide accurate daily reports and maintain clear documentation of completed work and outstanding issues. Experience: No experience is required in area of responsibility. Basic electronics knowledge or related hands-on experience is a plus. Ability to obtain and/or maintain a Security Clearance. About Frontgrade At Frontgrade, we build mission-critical electronics that perform without compromise in the world’s most demanding environments, from deep space to national defense. With decades of proven heritage, we deliver high-reliability components, subsystems, and integrated solutions trusted when failure is not an option. But our strength is not just in what we build. It is in the people who make it possible. From engineers and product managers to sales teams, marketers, and skilled manufacturing professionals, every role plays a direct part in enabling missions that protect, explore, and connect our world. We move with purpose, collaborate across disciplines, and take pride in delivering solutions our customers rely on in the highest-stakes environments. If you want your work, whatever your specialty, to contribute to something bigger, you will find your place at Frontgrade. Why Work for Us We believe mission success starts with taking care of our people. That’s why we offer competitive health, wealth, and wellbeing benefits from day one. You’ll also find real opportunities to learn, grow, and advance, whether you’re building technical expertise, leading teams, or expanding into new areas. Here, your growth is part of the mission. Additional Information This position may require access to technology, materials, software or hardware that is controlled by either ITAR or EAR U.S. export laws. As a condition of any job offer, in order to be employed in this position, you may need to obtain a U.S. Government export license(s), as required by law. Other benefits include: Immediate Medical (FSA and HSA), Dental, and Vision 401K Match with 100% immediate vesting 9X80 compressed work schedule for qualifying roles Career Opportunity and Growth Tuition Reimbursement/Student Loan Repayment Generous PTO and 11 paid Holidays per year (9 designated holidays and 2 floating holidays) 8 weeks of 100% Paid Family Leave
*Responsibilities include:* · Operates a tablet press and heavy machinery according to policy and procedures · Cleans and maintains a tablet press according to policy and procedure · Troubleshoots mechanical problems as they arise · Measures, weighs, counts, and compounds medications · Mixes pharmaceutical preparations according to formulation logs · Establishes and maintains accurate patient records by entering correct lot numbers and expiration dates of compounded medications. · Maintains proper storage and security conditions for drugs · Receives and stores incoming supplies, verifies quantities against invoices, and informs supervisors of stock needs and shortages · Packages medications · Cleans and maintains additional compounding equipment and work areas as needed · Performs other duties as assigned 职位类型全职 薪资 $18.00至$24.00每小时 工作经验: * Tablet press in Supplements: 3 年 (首选) Work Location: 现场办公
*Overview* Join our dynamic manufacturing team as a Capsule Filler Operator and become a vital part of producing high-quality, life-enhancing health products. In this energetic role, you will operate capsule filling machinery with precision, ensuring each capsule is filled accurately and efficiently. Your attention to detail and commitment to quality will help us maintain the highest standards in a cleanroom environment, supporting our mission to deliver safe and effective products to customers worldwide. This paid position offers an exciting opportunity to develop your skills in manufacturing, materials handling, and quality control within a fast-paced, collaborative setting. *Duties* * Set up and operate capsule filling machinery according to standard operating procedures (SOPs) and CGMP (Current Good Manufacturing Practice) guidelines. * Monitor the filling process for accuracy, consistency, and adherence to quality standards. * Conduct routine inspections of equipment, performing basic mechanical troubleshooting and maintenance as needed. * Ensure the cleanliness and sanitation of the cleanroom environment by following strict sanitation protocols. * Handle materials safely using warehouse equipment such as pallet jacks and forklifts; assist with materials handling and inventory management. * Perform quality control checks throughout the production process, including verifying capsule weight, fill volume, and integrity. * Assist with packaging finished capsules securely for shipment while maintaining compliance with FDA regulations. * Document production activities accurately in logs and reports, maintaining detailed records for traceability. * Support sanitation efforts by cleaning equipment and work areas regularly to uphold cleanliness standards. * Collaborate with team members in a manufacturing environment to meet production goals efficiently while adhering to safety protocols. *Requirements* * Previous experience in manufacturing, warehouse work, or packaging environments is preferred but not mandatory; training will be provided. * Basic math skills for measurements, weight checks, and inventory counts. * Familiarity with forklift operation, pallet jacks, or other warehouse equipment is a plus; certification is advantageous but not required. * Knowledge of CGMP practices, FDA regulations, and cleanroom procedures is highly desirable. * Mechanical aptitude with the ability to troubleshoot machinery issues confidently. * Strong attention to detail to ensure product quality and safety standards are met consistently. * Ability to follow detailed instructions precisely while working efficiently in a fast-paced setting. * Commitment to maintaining a sanitized environment through proper sanitation procedures. * Excellent teamwork skills with the ability to communicate effectively within a collaborative manufacturing team. Join us in producing top-tier capsules that make a difference! We’re dedicated to fostering an inclusive environment where your skills grow alongside our mission of delivering safe, effective health solutions worldwide. This is more than just a job — it’s an opportunity to contribute meaningfully while advancing your career in manufacturing and quality assurance. Pay: $18.50 - $24.00 per hour Work Location: In person
Part-Time Bench Jeweler (Repairs Focused) *Julez Bryant Fine Jewelry* Encinitas, CA (Off-Site / Remote Position) *Position Type:* Part-Time *Schedule:* Flexible *Requirement:* Must have personal jeweler’s bench and repair equipment About Us At Julez Bryant Fine Jewelry, we create meaningful fine jewelry rooted in craftsmanship, artistry, and timeless design. Every piece is thoughtfully designed to celebrate individuality while honoring heirloom-quality techniques and materials. As our brand continues to grow, we are seeking a highly skilled and detail-oriented Bench Jeweler to support our repair and restoration needs. Position Overview We are looking for an experienced Part-Time Bench Jeweler with a strong focus on fine jewelry repairs and restoration. This off-site role will work closely with the Julez Bryant team to ensure all client pieces are serviced with exceptional craftsmanship, precision, and care. The ideal candidate takes pride in quality workmanship, understands the importance of client heirloom pieces, and can independently manage repair projects while maintaining luxury-level standards. Responsibilities * Perform fine jewelry repairs including: * Ring sizing * Soldering and laser work * Chain repairs * Prong retipping and rebuilding * Stone tightening * Polishing and refinishing * Rhodium plating prep and finishing * Restore and refurbish client heirloom and sentimental jewelry pieces * Assist with occasional custom jewelry production and assembly projects * Work with precious metals including gold, platinum, and silver * Maintain high standards of craftsmanship and attention to detail * Communicate timelines, repair updates, and project needs with the Julez Bryant team * Ensure all completed repairs meet brand quality standards before return to clients * Maintain organized handling and care of all jewelry pieces and materials Qualifications * Previous bench jeweler experience required * Strong repair background in fine jewelry * Proficiency in soldering, polishing, assembly, and restoration work * Experience working with delicate and high-value jewelry pieces * Ability to work independently and efficiently manage deadlines * Excellent attention to detail and pride in craftsmanship * Strong communication and organizational skills * Stone setting experience is a plus * Experience with laser welding preferred but not required * Must have personal jeweler’s bench and necessary repair tools/equipment Ideal Candidate * Passionate about craftsmanship and fine jewelry restoration * Reliable, self-motivated, and highly detail-oriented * Understands the sentimental value behind client jewelry pieces * Excited to contribute to a growing luxury jewelry brand * Values artistry, quality, and collaboration Compensation * Competitive hourly pay based on experience * Flexible part-time schedule * Opportunity to grow alongside a creative and expanding fine jewelry brand Pay: $20.00 - $25.00 per hour Work Location: Hybrid remote in Encinitas, CA 92024
Join a Leading Medical Device Manufacturing Team We are hiring a *Machine Operator I* to support a fast-paced medical device manufacturing environment in San Diego, CA. This is an excellent opportunity for candidates who are: ✔ reliable ✔ detail-oriented ✔ eager to learn ✔ comfortable working in manufacturing environments Entry-level and trainable candidates are encouraged to apply. Responsibilities * Operate manufacturing equipment following SOPs and work instructions * Monitor machine performance and maintain operational logbooks * Support material handling and production operations * Maintain accurate documentation and production records * Follow GMP, GDP, safety, and quality procedures * Assist technicians with equipment troubleshooting when needed * Support preventative maintenance activities * Maintain clean and organized work areas * Verify raw materials and finished goods during production * Ensure product quality and process accuracy at all times Qualifications * High School Diploma or GED required * Ability to: * read * write * speak English * perform basic math * Comfortable working in fast-paced manufacturing environments * Strong communication and teamwork skills * Good attendance and reliability required * Willingness to learn and follow procedures Preferred Experience * Machine operation * Manufacturing or production work * Assembly or warehouse experience * GMP or regulated environments * Production documentation * Troubleshooting experience What Makes Someone Successful Here ✔ Good attitude ✔ Team player ✔ Attention to detail ✔ Fast learner ✔ Reliable attendance ✔ Able to follow instructions ✔ Comfortable with repetitive work Work Environment * Medical device manufacturing environment * PPE required * Safety shoes required * Clean and organized production floor * Team-oriented environment Shift Schedule 1st Shift 6:00 AM – 2:30 PM ✔ Occasional overtime available ✔ Weekend overtime occasionally offered What May Disqualify Candidates * Multiple short-term jobs * Poor attendance history * Inability to use basic computers * Poor communication skills Apply Today This is a great opportunity for dependable candidates looking to grow within manufacturing and medical device production environments. Pay: $18.00 - $19.00 per hour Benefits: * Employee assistance program * Professional development assistance * Referral program Work Location: In person