Looking to move to Carlsbad and want to connect with local employers? Fill out this form and we’ll help you get recruited.
*Folder / Stitcher / Cutter / Inserter / and Inkjet Operators * *1) Paper Cutter Operator* * Experience Required: 1-2 years of experience operating Programable Polar 45” and Saber 36” paper cutters. * Full Time, Part Time, or Temp On-Call positions available * Pay Range: $20 - $27/hr. *2) Bindery Operator* * Working knowledge of bindery or mailing equipment required. * Folders / Stitcher / Cutters / Plow folders / Inserters / Inkjets * Full Time, Part Time, or Temp On-Call positions available * Pay Range: $20 - $27/hr. Full Time, Part Time or Temp On-Call positions available. Comprehensive benefits package including: Medical, dental and life insurance, and a 401(k)-retirement plan Job Types: Full-time, Part-time, Contract, Temporary Pay: $20.00 - $27.00 per hour Benefits: * 401(k) * 401(k) matching * Dental insurance * Health insurance * Life insurance * Paid time off * Vision insurance Work Location: In person
Solatube (A Kingspan Company) is widely recognized as an industry innovator which has earned acclaim around the globe for its unrivaled ability to transform interior spaces with the power of daylight. Based in Vista, California, Solatube (A Kingspan Company) designs and manufactures a full line of daylighting systems and ventilation products. To help us continue to grow our offerings, we’re searching for a Production Operator who will perform any combination of repetitive machine operations and assembly functions to produce quality tubular daylighting devices and accessories safely and efficiently. Responsibilities: Operates work-cell stations (such as but not limited to): assembly, packaging, and soldering Follows written SOP and verbal job specifications and uses knowledge gained by experience May set stops or guides as indicated by prints, diagrams, and instructions Observes machine operation to detect workpiece defects or machine malfunction Positions workpiece against stops, or aligns layout marks Pushes buttons or depresses pedal to activate machine Bolts, clips, screws, cements, tapes, or otherwise fastens parts together using hand tools And/or power tools, riveter, elbow machine and hipot tester Assist with start-up and shut-down procedures Assist with color changeovers Hanging parts on the powder coat line Removing and packaging parts for delivery Ensuring paint booth and powder coating equipment is organized and clean Assist with quarterly maintenance Works in assigned work-cell station and within various rotations as production needs require including other departments Works on line where tasks vary as different model of same article moves along line Responsible for finished good to be shrink-wrapped and staged for delivery to distribution center Meets quality control standards Cleans up work area as required Communicate effectively with peers, supervisors, and management Completes accurately all daily summary, yield cards and scrap reports as required by the Company Performs all duties safely Attends meetings and classes as required Qualifications: High school diploma or equivalent degree and/or experience. Good communication skills. Ability to be a team player. At Solatube (A Kingspan Company), we believe our employees are our greatest resource. We offer a competitive salary, benefits, and vacation package for all full-time permanent positions. Kingspan is proud to be an equal opportunity workplace and is an affirmative-action employer. 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.
Summary At Advanced Accelerator Applications, a Novartis company, we are committed to leading innovation in nuclear medicine and delivering the next generation of targeted radioligand therapy (RLT) to cancer patients. We are looking for dedicated and enthusiastic professionals to join our new manufacturing site in Carlsbad! Production Technicians play an active role in daily production of Radioligand Therapies (RLT) as well as setup and preparation of instruments and equipment. The Production Technician adheres to regulatory requirements while performing job functions, executing production as per batch records and SOPs. Responsibilities are performed within a team and according to an assigned production shift schedule. The Production Technician works closely with the Manager and Lead to ensure production is executed in a safe and timely manner. Shift: Shift schedule will be phased in as the site approaches go-live. We are planning for 12-hour rotating shifts which will include at least one weekend day. About the Role Key Responsibilities: Executes all activities related to the manufacturing of RLT products. Responsibilities include operating and maintaining grade A isolators, focusing on KPI goals as well as ensuring adherence to all state, federal and Novartis radiation safety guidelines. Responsible for successful on-time completion of required training curriculum comprising of the necessary Standard Operating Procedures (SOPs) and Aseptic Techniques, Gowning Qualifications and other relevant training including Health, Safety & Environment (HSE) for the specific role. Supports all technical aspects related to production readiness including manually cleaning the cell and performing sterilization of the isolators. Conducts routine and dynamic environmental monitoring as required. Prepares all materials while maintaining material identity in accordance with the batch monitoring system as defined by procedure. Facilitates a culture of “speaking up” and ensuring all cGMP compliance activities are followed. Prepares applicable documents and records such as batch records, shipping documents, and training materials. Given the time sensitive nature of the product, this position will require unplanned overtime to ensure process continuity and completion. Essential Requirements: Bachelor of Science strongly preferred. If the applicant does not have a degree, a minimum of 2 years of experience in a cGMP or aseptic environment is required. External candidates: 2+ years of experience in aseptic pharmaceutical manufacturing. Preferably in drug product filling operations. Current Novartis Associates: Must be a Production Technician for a minimum of 12 months including prior RLT experience and be qualified in at least two critical production isolator tasks Knowledge of cGMP regulations and FDA guidance applicable to aseptic manufacturing. Proficient in MS Office applications. Flexibility to don clean room garments and personal protective equipment (PPE). Near vision performance should be the equivalent of 20/20 with no impairment of color vision. The use of corrective lenses to achieve the desired visual acuity is permitted. Makeup, jewelry, nail polish, perfume/cologne and other potential microbial sources are prohibited in restricted areas. Ability to lift or carry up to 35 pounds. #LI-Onsite Novartis Compensation and Benefit Summary: The salary for this position is expected to range between $27.78 and $51.58 per hour. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards EEO Statement: The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. Accessibility & Reasonable Accommodations The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to [email protected] or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Division Operations Business Unit Innovative Medicines Location USA State California Site Carlsbad Company / Legal Entity U469 (FCRS = US469) AAA USA Inc. Functional Area Technical Operations Job Type Full time Employment Type Regular Shift Work No
Chromalloy is a global engineering & solutions company. We are a leadings provider of aftermarket parts, repairs, and solutions that safely & reliably extend the life of aircraft engines and gas turbines. We develop, manufacture and repair critical turbine components for a range of engine platforms. Our solutions support the engines running the aerospace, energy and defense industries around the world. Video: What We Do Why work at Chromalloy? Chromalloy employees are proud, passionate problem-solvers who strive to live our values every day. A career with Chromalloy is an opportunity to learn from top industry experts, work with important technologies, and unlock a passion for innovation. Join our team of experts, innovators and problem-solvers delivering world-class solutions for our customers. As a global company, we are committed to creating an inclusive environment where all employees feel represented, heard, and able to bring their best selves to work every day. Be part of something bigger with Chromalloy! Our Total Rewards Program is designed to support you today and in the future. • Comprehensive and flexible benefit options starting on day one, including medical, dental, vision, EAP, wellness incentives, and 401(k) with employer matching. • Development & progression opportunities for every employee – regular performance conversations, training and development curriculum, and engineering fellowship programs. • Paid time off, including vacation, sick time, paid holidays, floating holidays, and parental leave—all eligible on your first day of employment! • Competitive pay, including eligibility for quarterly and annual bonuses, depending on role and site. Eligibility for individual benefit plans may vary based on employment status. Job Description - About the Machinist Role: Must be able to set up and operate standard manual machine tools such as Milling Machines (vertical and horizontal), engine lathes, surface grinders and manual machines. Responsibilities Include: • Set up and run various machines in machine shop such as grinders, CNC, VTL, etc. • Set up and operate one or more of the following: CNC Grinders, CNC Milling Machines, CNC Lathe or any other CNC metal-working machine where CNC control knowledge may be directly applied to CSD machine tools operation. • Apply knowledge of mechanics, shop mathematics, metal properties and layout machining procedures. • Read and understand blueprints, sketches and description of parts to be worked on or replaced. • Measure, mark and scribe dimensions and reference points to lay out stock for machining. • Verify dimensions and alignment with measuring instruments such as micrometers, height gauges and gauge blocks. *We are hiring for our second shift (2:30pm-11pm) * Qualifications Education: • High school degree (preferred) • Must be able to read, communicate, and understand English per FAA requirements. Required training: • 3 yrs. experience in a variety of methods and equipment. • Some technical knowledge or experience (preferred) • Aerospace industry (preferred) If this position requires access to export-controlled technology and technical data, as defined in the Export Administration Regulations and or the International Traffic in Arms Regulations, any offer of employment is contingent upon Chromalloy’s determination, in its sole discretion, if any additional authorization for the employee to access such technology is required and obtainable in a manner that meets its immediate business needs prior to beginning work. Chromalloy participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. Any offer of employment will also be conditioned upon the successful completion of a background investigation and drug screen in accordance with company policy and applicable federal and state regulations. Chromalloy is an equal opportunity employer - vets/disabled. In the United States, if you need a reasonable accommodation for the online application process due to a disability, please contact: https://www.chromalloy.com/contact-us/
Since 1980, NAI has been a leader in nutritional health, bringing whole food-based supplements to a global population. NAI is a leading expert and manufacturer of dietary supplements, and we are involved in every facet of the industry, including research, development, manufacturing, marketing, and advocacy. As a company, we continue to grow with manufacturing locations in Vista and Carlsbad, CA. We are looking for seasoned and entry level candidates that are interested in working for global company with opportunities for growth, development, competitive pay, and benefits. Summary: The Quality Assurance Specialist supports the Quality Systems department by helping maintain and improve the quality of products, services, and processes within the organization. This role ensures regulatory compliance, leads quality improvement initiatives, analyzes data to identify areas for enhancement, and collaborates with cross-functional teams to investigate root causes and implement effective improvements. Experience in the dietary supplement, food, pharmaceutical, or medical device industries is required. Responsibilities also include conducting internal audits, coordinating CAPA and nonconformance investigations from start to finish, and performing document control functions. Essential Duties & Responsibilities: Prepare and implement quality systems policies and procedures. Document quality activities and create audit reports. Maintain complaint and nonconformance records and tracking systems, including conducting root cause analyses and implementing corrective actions. Identify training needs and make recommendations for improvement to ensure company-wide compliance. Develop and maintain the Foreign Supplier Verification Program (FSVP) and Supplier Qualification Program, including associated policies and procedures. Ensure that program performance and quality conform to applicable standards such as the Therapeutic Goods Act 1989, the PIC/S Guide to Good Manufacturing Practice for Medicinal Products, FDA 21 CFR Part 111 (GMP for Dietary Supplements), and FSMA. Manage supplier selection, qualification, audits, improvement initiatives, and ongoing monitoring to support both new and existing materials and services. Review and approve supplier documentation (e.g., desktop audits, self-surveys, certifications, third-party audit reports). Prepare clear, accurate, and evidence-based supplier audit reports for management while maintaining comprehensive documentation. Evaluate supplier performance through product performance reviews, supplier questionnaires, and audits to identify improvement opportunities and verify corrective and preventive actions. Perform risk assessments as required. Recommend actions for supplier qualification and de-qualification by establishing and managing processes and criteria for qualification, monitoring, and issue resolution (including co-manufacturers). Manage supplier nonconformances and corrective/preventive actions (CAPAs), ensuring suppliers develop and implement effective plans in accordance with NCR and CAPA processes. Trend and track supplier audit findings and perform follow-ups to ensure CAPA completion. Conduct audits and post-audit meetings using industry-accepted auditing techniques and team-based approaches, leveraging interpersonal communication skills. Generate Product Quality Review (PQR) reports on an annual basis. Perform document control activities, including processing change orders from initiation to closure, data entry, and filing. Enter relevant data into the MRP system (e.g., BaaN), as required. Act as an administrator for the electronic Quality Management System (QMS) and perform the following functions: Onboard new employees in the system. Assign or modify employee profiles and job roles. Inactivate or terminate employee profiles. Perform change control activities. Generate various QMS reports as needed. Create training curriculums and job roles. Assist with troubleshooting and password resets. Track and trend Quality Systems metrics. Perform other duties as assigned by the supervisor or manager. Any required clarification or interpretation of responsibilities will be addressed by the supervisor or manager. Qualifications: Knowledge of US FDA cGMP Title 21 CFR 111 &117. Knowledge of Standardize Information of Dietary Ingredients (SIDI). Knowledge of Food Safety Modernization Act (FSMA). Knowledge of Foreign Supplier Verification Programs (FSVP). Minimum of 3-5 years auditing experience; CQA preferred. Minimum of a Bachelor’s degree in a related technical field or a minimum of 5 years Quality Assurance Specialist experience in food, supplement, pharmaceutical, or medical device industry required. Required Skills/Work Experience: In-depth knowledge of quality assurance principles, terminology, methods, and tools. Strong computer skills, including proficiency with word processing, spreadsheets, databases, and electronic document change control systems. Demonstrates accuracy and thoroughness in day-to-day activities; continuously seeks ways to improve quality and applies feedback to enhance performance. Maintains a “right first time” mindset by actively monitoring own work to ensure quality. Proven experience in supplier management, including qualification, auditing, and performance evaluation. Effective leadership and interpersonal skills with the ability to influence and collaborate across plant and corporate teams. Solid technical knowledge of quality systems and familiarity with relevant government regulations and certification standards. Excellent verbal and written communication skills. Proficient in statistical analysis and quality-related software tools. Experience working with third-party auditors and certifying bodies such as SGS, NSF, ASI, USP, and TGA. Subject matter expertise in GMP, HACCP, Allergen Control, ISO, GFSI, and FSMA requirements. Strong problem-solving abilities with a track record of identifying and resolving issues efficiently. Decisive and confident in making timely and sound decisions. Demonstrates sound judgment and provides clear rationale for decisions. Actively involves appropriate stakeholders in the decision-making process. Excellent organizational skills with the ability to multi-task and work independently with minimal supervision. Works effectively both independently and in a collaborative team environment. Physical/Mental Requirements: Must be able to work in an office or production environment. Specific vision abilities required by this job include close vision, color vision, peripheral vision, depth perception, and the ability to adjust focus. While performing the duties of this job, the employee is regularly required to walk; use hands to finger, handle, or feel; reach with hands and arms; stoop and kneel; talk and hear. The employee is frequently required to sit and stand. Travel Requirements: Must be able and willing to travel regularly between the company's three facilities located in Vista and Carlsbad, CA, as needed to support quality operations and cross-site collaboration. Occasional travel may be required to perform on-site audits and inspections of supplier facilities, both domestic and/or international. This is not a primary function of the role and is typically limited to up to 1–2 times per year. NAI is an Affirmative Action/Equal Opportunity Employer and will consider all applications without regards to race, sex, age, color, religion, national origin, intersectionality, veteran status, physical or mental disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. Upon this conditional offer of employment, a satisfactory completion of a background check (including criminal records check) with submission and passing a pre-employment post offer drug test is required prior to beginning employment. Any offer of employment may be rescinded if the background check reveals disqualifying information, and/or it is discovered that the candidate knowingly withheld or falsified information. Failure to satisfactorily complete the background check may affect the continued employment of a current NAI employee who was conditionally offered the position. Upon successful completion of the background check process, we will determine the date when your employment begins. NAI utilizes E-Verify to electronically verify employment eligibility. Benefits: Medical plan options – Two HMO and one PPO Dental, vision, life insurance and other voluntary benefit options. 3 weeks’ vacation and 11 paid holidays 401K including company matching and profit sharing $1,000 Employee Referral Bonus Quarterly employee lunches, Employee of Month and other recognition programs Opportunities for advancement Comprehensive training Tuition Reimbursement and more! Ability to Commute: Carlsbad, CA 92008 (Required) Work Location: In person Monday through Friday, 8:00 AM to 5:00 PM
*Job Title:* Woodshop Fabricator Assistant *Location:* Poway, CA *Pay Range:* $22 – $28/hour *About the Role:* We are seeking a skilled Woodshop Fabricator Assistant to join our team in Poway. This is not an entry-level position – we are looking for candidates with hands-on experience and a strong understanding of wood fabrication techniques. The ideal candidate is detail-oriented, safety-conscious, and ready to support our production team in creating high-quality custom wood products. *Responsibilities:* · Assist lead fabricators in measuring, cutting, assembling, and finishing wood products. · Operate and maintain woodshop machinery and hand tools safely and efficiently. · Read and interpret drawings, blueprints, and project specifications. · Perform quality checks to ensure products meet company standards. · Maintain a clean, organized, and safe work environment. · Assist with inventory management and material handling as needed. · Collaborate with team members to meet project deadlines. *Qualifications:* · Prior experience in a woodshop or fabrication environment required. · Proficiency with hand tools, power tools, and woodworking machinery. · Ability to read and interpret technical drawings and measurements. · Strong attention to detail and commitment to quality. · Good physical stamina and ability to lift moderate weights. · Team-oriented with good communication skills. *Compensation & Benefits:* · Competitive pay based on experience · Health and dental insurance · Simple IRA (eligibility for full-time employees) · Paid sick leave: 40 hours annually, in compliance with California law *Schedule:* · Alternative work schedule: Monday through Thursday, 10-hour shifts · Fridays may be required for overtime depending on project needs · Some overtime is mandatory based on job deadlines and workload · No weekend work If you’re a skilled woodshop professional looking for a supportive team and the opportunity to grow your craft, we’d love to hear from you! Job Type: Full-time Pay: $22.00 - $28.00 per hour Benefits: * Dental insurance * Health insurance * Retirement plan * Vision insurance Work Location: In person
General Atomics (GA), and its affiliated companies, is one of the world’s leading resources for high-technology systems development ranging from the nuclear fuel cycle to remotely piloted aircraft, airborne sensors, and advanced electric, electronic, wireless and laser technologies. We have an exciting opportunity for a Machinist to join our Inertial Fusion Technology (IFT) division within the Energy group. The components to be machined are normally high-precision and in small quantities. Production schedules are reasonable but due dates are often inflexible. Salary potential commensurate with willingness/ability to grow professionally. DUTIES AND RESPONSIBILITIES: With minimal oversight and direction, performs complex functions related to machine tools. Ensures project development schedules and goals are met. Plans the layout, fabrication and testing of mechanical devices. Performs setup and operates any type of precision machine tool, including numerically controlled (CNC), to make original parts, tools, mechanisms and devices. Solves extremely complex problems relative to work arrangement, unusual materials, machine settings, tools, product specification, and fabrication methods for production process. Provides direction and/or training to other machinists in a lead role. Programs, performs setup and runs difficult prototype and first run production jobs. Programs, performs setup and operates conventional and CNC mills and lathes. Plans sequence of machine operation using drawings, sketches or other written or verbal instructions. Assists with the development of concepts, ideas, and methods for solving milling/machining problems. Performs precision work to exacting tolerances for R&D and/or production engineers. Acts as a lead and advisor including training for knowledge transfer. Reviews and interprets job requests including drawings and service requests. Supports the preparation of the schedule and cost estimate as needed for each project. Orders and expedites materials needed. Utilizes and interprets engineering drawings from sketches, graphic illustrations or verbal/written correspondence to plan sequence of operations. Responsible for machining licensing and renewal. Determines cutting or grinding tools to be used, method of holding, and machine speeds and feeds. Assists others with job layout. Performs such operations as turning, facing, boring, chamfering, turning tapers, drilling, grooving, reaming, machine compound angles, multiple angles, radii, splines and keyways. Performs all types of helical and spiral milling, drilling, reaming, boring, tapping, slotting, and dovetailing on ferrous and non-ferrous metals and their alloys. Designs and fabricates tools and tooling aids to assist in machine setups utilizing various shop equipment. Ensures that preventive maintenance is being performed including coordination with maintenance vendors and working the procurement process to order and schedule. Responsible for observing all laws, regulations, and other applicable obligations wherever and whenever business is conducted on behalf of the Company. Expected to work in a safe manner in accordance with established operating procedures and practices. Other duties as assigned or required. We recognize and appreciate the value and contributions of individuals with diverse backgrounds and experiences and welcome all qualified individuals to apply. 50931 Job Qualifications: Typically requires an associate's degree, technical/trade school training or equivalent and fifteen or more years related experience. Additional experience may be substituted for formal education. Must be customer focused and possess: ability to perform complex set-up and fabrication of machined parts with no direction; ability to lead, instruct and train machinist staff on operations, practices and techniques used in the machine shop; a high degree of initiative and extensive knowledge of machining equipment including ability to use judgment and safe practices; ability to read, interpret and explain complex or unusual engineering drawings, sketches and verbal and written instructions; skills to maintain the flow of work within the unit using independent judgment in solving unusual problems of diverse scope; strong interpersonal skills and written communication skills to interface with employees, management and customers/outside representatives; and basic computer skills. The ability to work both independently and lead in a team environment is essential as is the ability to work extended hours as required. Salary:$87,070 - $132,963Travel Percentage Required 0 - 25Relocation Assistance Provided Not Provided US Citizenship Required? YesClearance Required? No Clearance LevelSenior (8+ years) WorkstyleOnsite
Camp Pendleton - Night Meat Room Custodian Cleans and keeps in an orderly condition commissary’s meat cutting room. Will be pressure washing floors and cleaning equipment between uses to incude countertops, cutting tools, grinders, working in cold environment and other meat processing equipment. Requirements: Physical ability to move large, bulky and/or heavy objects up to 50 pounds. Physical ability to perform tasks that may require prolonged standing, repetitive bending, and other activities necessary to perform job duties.
Work Schedule Standard (Mon-Fri) Environmental Conditions Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Loud Noises (Equipment/Machinery), Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift, Will work with hazardous/toxic materials Job Description Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our distributed team offers an outstanding blend of innovative technologies, convenient purchasing, and pharmaceutical products. Shift Information 1st Shift – Monday through Friday 4:30 am –2:30 pm PST Discover Impactful Work: As a Technician II at Thermo Fisher Scientific's Carlsbad, California location, you will play a crucial role in the manufacturing department, responsible for producing Protein Gels. By following documentation and procedures, you will ensure the highest quality standards are met. With responsibilities tasks such as operating equipment, staging, visual inspection for gel defects, material handling and inventory control and basic troubleshooting of equipment. Join our a team that is molding the future of biosciences and genetic sciences. A day in the Life: Operate an assortment of semi-automated and manual filling and packaging equipment, including basic troubleshooting equipment. Maintain a disciplined environment and enforce departmental and company policies. Operate a variety of industrial equipment including auto loaders, filling pumps, auto-labelers, automated pick and place and packaging machines. Accurate completion of required manufacturing documentation under ISO9001 guidelines. Assist department by staging raw materials; cleaning laboratory equipment and off-loading automated filling lines. Meets production targets, quality, EHS and PPI goals and objectives. Perform all work activities in a safe manner. Maintain a safe and clutter free work area and report property damage and /or safety hazards to the Supervisor, Human Resources, Safety Specialist or Senior Management immediately. Keys to Success: Education High school diploma or equivalent required. Experience 2+ years of experience in a manufacturing environment and/or experience in biotech or chemical manufacturing required. Knowledge, Skills, Abilities Good verbal and written communication skills. Ability to follow standard operating procedures and cGMP’s. Strong social skills; ability to prioritize and lead through sophisticated processes/projects. Ability to define problems, collect data, establish facts, and draw valid conclusions. Familiarity with data entry tools, such as Microsoft Word & Excel. Previous experience with SAP and other business software a plus. Physical Requirements / Work Environment Ability to regularly lift and/or move up to 10 to 50 pounds. Ability to wear personal protective equipment when required (PAPR). Benefits We offer a competitive annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation! Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Watch as our colleagues explain five reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation, and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation, and support patients in need. StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued. Apply today! http://jobs.thermofisher.com Thermo Fisher Scientific upholds equal employment opportunity and affirmative action principles, ensuring fairness in hiring practices regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other legally protected status. Compensation and Benefits The hourly pay range estimated for this position based in California is $16.78–$25.17. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes: A choice of national medical and dental plans, and a national vision plan, including health incentive programs Employee assistance and family support programs, including commuter benefits and tuition reimbursement At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards
Overview: About Pacira Pacira BioSciences, Inc. is a leading provider of non-opioid pain management and regenerative health solutions dedicated to improving outcomes for health care practitioners and their patients. Our in-depth knowledge of non-opioid pain management, coupled with our passion for advancing patient care, drives our commitment to providing solutions that address unmet medical needs and improve clinical results. Why work with us? Rarely do you have an opportunity to do work that really matters. What drives us is our mission. What makes us successful are our people. At Pacira, you are part of an inclusive culture that fosters collaboration, growth, and innovative thinking - a place where you can make an impact and help change the standard of care in non-opioid pain management. Be part of our movement, let’s pursue excellence together. Summary: The Senior Quality Engineer will support and ensure the implementation of robust and compliant design control practices across both new product development and sustaining engineering activities for the iovera product line. This role serves as a quality representative within cross-functional teams, driving compliance with regulatory requirements (e.g., 21 CFR 820, ISO 13485) and internal quality standards. The Senior QE will play a key role in evaluating design changes, risk management activities, and quality documentation throughout the product lifecycle, while also supporting complaint investigations and continuous improvement initiatives. Responsibilities: Essential Duties & Responsibilities: The following statements are intended to describe the general nature and level of work being performed by an individual assigned to this job. Other duties may be assigned. Collaborate with R&D and cross-functional teams to ensure design control requirements are met throughout all phases of product development and lifecycle management. Support design verification and validation activities, risk management, and design review processes to ensure products meet applicable safety, performance, and regulatory requirements. Evaluate and provide quality input on engineering design changes, ensuring appropriate documentation, traceability, and risk assessment are conducted. Contribute to the continuous improvement of design control processes, templates, and procedures to align with current regulatory expectations and business needs. Participate in sustaining engineering projects, providing quality oversight to maintain compliance and support product improvements. Support the complaint handling process by reviewing and analyzing complaint data, participating in root cause analysis, and identifying design-related trends or failure modes. Assist in the preparation of quality deliverables for regulatory submissions, including 510(k)s, technical files, and IDE-related documentation. Support internal and external audits by preparing and presenting relevant design history and risk documentation. Collaborate with cross-functional teams including Regulatory Affairs, Operations, Manufacturing, and Quality Assurance to ensure consistent and aligned approaches to design quality. Contribute to management review inputs and quality metric tracking related to design control and product quality performance. Perform other quality-related duties assigned by management, including but not limited to supporting CAPA investigations, nonconformance (NC) evaluations, data analysis, and continuous improvement initiatives. Occasional travel may be required to support product development activities, supplier visits, or audits. Supervisory Responsibilities: This role does not have supervisory responsibilities. Interaction: The incumbent works closely with various departments (e.g., QC, QA, Operations, Regulatory and within R&D). Qualifications: Education and Experience: BS Degree or higher in engineering field required (e.g., Electrical, System, Mechanical engineering) Experience with design or sustaining engineering required Minimum 7 years’ experience in design or sustaining engineering required Knowledge, Skills, and Abilities: A practical and working knowledge of ISO 13485, 21 CFR 820 Experience with Design Controls Statistical knowledge and understanding of measurement uncertainty Detail oriented, well organized and have excellent communication skills Able to accomplish objectives with minimal supervision 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 accommodation may be made to enable individuals with disabilities to perform the essential functions. Duties of this job may involve standing and/or walking, but for most part sitting for extended periods of time. Duties also involve daily keyboard data entry. Close vision and the need to focus on computer screen, use of hands, fingers and wrist to type on keyboard and manipulate mouse. Will need to lift and move boxes of paper and binders weighing up to 20 pounds. Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. Typical office setting with a laboratory, offices, warehouse, and cubicles. Noise level is moderate with consistent printer, telephone ringing and conversation. Benefits: Medical, Prescription, Dental, Vision Coverage Flexible Spending Account & Health Savings Account with Company match Employee Assistance Program Mental Health Resources Disability Coverage Life insurance Critical Illness and Accident Insurance Legal and Identity Theft Protection Pet Insurance Fertility and Maternity Assistance 401(k) with company match Flexible Time Off (FTO) and 11 paid holidays Paid Parental Leave Pay Transparency: The base pay range for this role is $120,000 annually to $165,000 annually. The range is what we reasonably expect to pay for this role. The range considers a wide range of factors that are considered in making compensation decisions, including but not limited to: geographic markets, business or organizational needs, skill sets, experience, training, licensure, and certifications. EEO Statement: EEO Statement: Pacira is proud to be an Equal Opportunity Employer and does not discriminate against applicants because of race, color, religion, sex (including gender identity, sexual orientation, and pregnancy), national origin, age (40 or older), veteran status, disability or genetic information, or any other characteristic protected under applicable federal, state, or local law. At Pacira we are committed to intentionally cultivating a culture of inclusion where all feel welcomed and valued for their background, perspectives, and experiences. We hold one another accountable to promote trust and transparency in support of our communities and collective purpose. Agency Disclaimer: Pacira Biosciences, Inc. (Hereafter, Pacira) does not accept unsolicited resumes from recruiters or employment agencies in response to the Pacira Careers page or a Pacira social media post. Pacira will not consider or agree to payment of any referral compensation or recruiter fee relating to unsolicited resumes. Pacira explicitly reserves the right to hire said candidate(s) without any financial obligation to the recruiter or agency. Any unsolicited resumes, including those submitted to hiring managers, are deemed to be the property of Pacira.
General Summary: Operates critical food packaging machines at maximum efficiency for food production. Benefits and Culture We offer a competitive compensation and benefits package designed to help employees live a healthier life, build rewarding careers and save for the future. Reser's offers choices whenever possible, because we recognize the diverse and ever changing needs of our employees. Benefits include medical, dental, vision, AD&D, life, 401(k) with discretionary match, wellness programs, paid holidays and vacation time to name few! We strive to be your Employer of Choice. As one of our five cornerstones, this means that we go all-out to create an environment where people choose a lasting career because Reser’s care about their personal development & safety, and delivers a rewarding work experience. Visit our website to learn more about our competitive benefit programs - https://www.resers.com/careers/#benefits Principal Duties and Responsibilities 1. Operates a machine and ensures quality and conformity of packaged products. 2. Assembles and configures machine according to current specifications. 3. Ensures the machine operates within established guidelines and specifications. 4. Loads and stores correct consumables before and after each product run. 5. Washes and resets equipment during product changes according to company guidelines. 6. Maintains machine equipment and supplies and a clean orderly work area. 7. Reports machine problems according to company procedures and guidelines as needed. 8. Completes required paperwork as needed. 9. Displays mechanical aptitude for trouble shooting and preventive maintenance. 10. Displays strong leadership ability with caring attitude towards people and equipment 11. Follows company safety guidelines, HACCP requirements and Good Manufacturing Practices. 12. Regular attendance and punctuality are required due to working with people, items and equipment that are at the facility. Job Specifications 1. 1+ years’ experience as a Machine Operator 2 is required. 2. Must be certified to operate critical food packaging machines. 3. Must be able to read, write, and speak English and be understood. 4. English/Spanish bilingual a plus. Working Conditions 1. Refrigerated food manufacturing plant. 2. The environment may be wet or dry and temperatures may range from 25°F to 110°F. 3. Requires walking and standing for long periods of time. 4. Repetitive lifting, kneeling, and bending with packages in excess of 50 lbs. is required. 5. Production demands may require overtime and/or evening or weekend scheduling. Compensation: $24.75 per hour/ Non-exempt Recipe for Success Reser’s is the leading provider of fresh refrigerated deli salads, side dishes, and prepared foods for the supermarket, club store, and food service industries. Family owned and operated, Reser’s has been a proud sponsor of good times at racetracks, picnics, BBQs, music festivals, and affordable family meals since 1950. Reser’s family of brands include Reser’s American Classics, Main St Bistro, Stonemill Kitchens, and more. With more than 4,500 employees, Reser’s operates 14 facilities in the US, Mexico, and Canada and actively supports the communities it serves. 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.
*Hiring Full Time Warehouse Production Associate for: Cleaning, Testing, and FBA Packaging. * *Primary Function is: Refurbishing/Cleaning, Quality Control of Electronics, and Packaging for Shipment.* Join a winning team that continues to grow in this market with ample room for growth opportunities. We have been in business for 20 years, and continue to dominate our space. *Full-Time Position for someone who is extremely hard working, fast with hands, and loves to get things done without being micromanaged. This is a starting position with lots of room for upside in a fast growing company. * *WHO WE ARE:* Best in Industry Electronics Refurbishing Company. 20 YEAR ESTABLISHED AND GROWING E-COMMERCE BUSINESS IN THE RENEWED ELECTRONICS SPACE. *WHO YOU ARE:* Hard working, punctual, willing to learn and get their hands dirty. Appreciates a casual work environment where everyone gets along and handles their roles and responsibilities to make a winning team. Please note: this is not a standard "pick and pack" warehouse role. *ROLES & RESPONSIBILITIES* * Cleaning Small Electronic Plastics for Refurbishing Purposes (Removing stains, stickers, etc.. and cleaning out battery compartments for contact points) * Replacing Cosmetic Parts with Basic Tools * Able to test electronics for basic functionality * Accurately tagging items with defects and faults for returns with reason codes * Ability to Clean and Refurbish Electronics using tools and parts provided (no toxic chemicals are used) * Attention to Detail while also maintaining speed and accuracy * Being able to manage multiple projects and staying organized * Kitting / Packing up items for shipments across various Platform * Ability to support in grading quality of units (1-5) *EXPERIENCE Required* * 1+ years of experience in a fast paced office/warehouse environment * Extremely Organized with Meticulously Detail Oriented * Ability to Juggle Changing Schedule and Tasks Daily * Working with Cleaning of Products / Spaces and Willing to get hands dirty * You enjoy making things more efficient and solving problems on your own *What We Do Best and Offer* * *Laid Back / Casual Work Environment with Focus on the Job and Performance (not politics)* * *New Warehouse Space with Top of the Line Organization and Tools* * *High Level Small Team that Works Well Together* * *Work / Life Balance* * *We are growing as a company giving continual opportunities* Please include WHC72825 in your title and also a *short paragraph* as to why we would love to have you in this roll. Please note all applications without this will ignored. *We look forward to hearing from you.* _If you are a fit, next steps/process looks like:_ 2-Hour Paid Trial Interview/Test Day Contract to Employee Hire Full Time Employment Only. Job Type: Full-time Pay: From $19.00 per hour Benefits: * Flexible schedule * Opportunities for advancement * Paid time off Work Location: In person