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Location: San Diego, CA, US, 92121 Business Unit: Energy Conversion Solutions Posting Date: Feb 12, 2026 Job Description: About Us: Join AMETEK Programmable Power, a leader in cutting-edge programmable power solutions and systems. We specialize in designing and delivering precision AC and DC programmable power supplies, electronic loads, power subsystems, and compliance test solutions. If you're ready to work at the forefront of differentiated power technologies, this is your opportunity to make an impact in a fast-paced, high-tech environment! Job Summary: Lead a team of Assemblers to perform assembly and sub-assemblies build according to production plan. This position will perform electrical and mechanical assembly operations of complex assemblies and sub-assemblies and be responsible for training and directing daily functions of the assembly group and will support daily production schedules and maintain standard Quality workmanship in the area. In addition, this position will interface with engineering, management and production personnel as needed and will perform electrical and mechanical assembly operations of complex assemblies and sub-assemblies. 1st Shift: Monday through Friday, 5:30 AM to 2:00 PM Overtime: Ability to work overtime Monday through Friday and on weekends as needed/occasionally. Key Responsibilities: Lead team and distributes work daily throughout the shift to meet production schedule. Audits the Quality for compliance to ISO 9001:2015 and AMETEK Workmanship Standards. Coordinate/provide cross training to reduce bottleneck and eliminate Single-Point-Of-Failure. Monitor efficiency to set working standards to achieve daily productivity. Help resolve/escalate issues impacting production. Observes/help enforce all AMETEK Policies/Processes/Procedures and Safety rules/policies. Leads 6S activities (Safety, Sort, Set in Order, Shine, Standardize, Sustain) and Conducts monthly Gemba walks. Hold individuals accountable for tools and equipment preventive maintenance and record keeping. Provide input to annual Performance Appraisal in his/her group. Working lead role/responsibilities - Split 30% leading and 70% working Hold team accountable to perform daily housekeeping at the end of the shift. Run daily Tier 1 meeting with team. Facilitate SQDIP (Tier 2) meeting in the absence of a Supervisor/Manager. Must be available to work a flexible schedule including overtime and weekends. Performs related duties as assigned. Minimum Qualifications: Must require a minimum of 3 - 5 years of related experience. Assembler levels 3 - 5 will vary based on years of experience and scope of responsibility High school diploma or equivalent Must possess good to excellent assembly blueprint reading experience/skills Must be able to use hand tools (i.e. torque wrench, drills and inspection tools) Ability to properly read a variety of measuring devices including rulers, tape measures, and scales Must be able to communicate effectively with others Performs other duties as assigned Due to the nature of Programmable Power 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: Intermediate computer skills IPC-610 and J-STD 001 certification Efficient MS Word and Excel user 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 Additional Details: Location: 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. Salary Range: The annual pay range for this position generally ranges between $20.00 - $25.00. Actual salaries will vary and may be above or below the range based on various factors including but not limited to location, experience, and performance. In addition, AMETEK provides a variety of benefits to employees, including health insurance coverage, an employee assistance program, life and disability insurance, a retirement savings plan, paid holidays and paid time off. To learn more about our company and our job opportunities, visit us at: https://www.ametek.com/careers To learn more about the business unit you’ll be joining, visit us at: Programmable Power: https://www.programmablepower.com/ VTI Instruments: https://www.vtiinstruments.com/ Compensation Employee Type: Hourly Salary Minimum: $40,000 Salary Maximum: $55,000 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.
*Position Summary* The Quality Assurance (QA) Specialist is responsible for supporting and maintaining compliance with Good Laboratory Practice (GLP) regulations, internal SOPs, and applicable regulatory requirements within a preclinical contract research laboratory. This role performs study-based and process-based audits, manages document control and archiving activities, supports sample accountability oversight, assists with equipment validation activities, and contributes to successful client and regulatory inspections. The QA Specialist works cross-functionally with scientific, operations, and management teams to promote data integrity, quality systems effectiveness, and continuous improvement. *Key Responsibilities* *GLP Study Auditing & Quality Oversight* · Conduct GLP compliance audits including protocols, amendments, raw data, reports, and in-process inspections. · Perform facility, process, and systems audits to verify adherence to SOPs and regulatory requirements (FDA GLP 21 CFR Part 58, OECD GLP). · Document audit findings clearly and objectively; track responses and corrective/preventive actions (CAPAs). · Verify protocol compliance and data integrity (ALCOA+ principles). · Verify proper use of validated systems · Contribute to QA statements and study inspection reports. *Document Control & Archiving* · Maintain controlled documents including SOPs, forms, templates, and policies. · Manage document lifecycle processes (creation, review, approval, revision, distribution, archival). · Ensure proper indexing, retrieval, and retention of study records and raw data. · Oversee secure and compliant GLP archive operations and record transfers. · Conduct periodic archive audits and inventory checks. *Sample Management & Control Oversight* · Audit sample receipt, labeling, storage, tracking, and disposition processes. · Verify chain-of-custody documentation and sample accountability. · Ensure storage conditions and environmental monitoring meet protocol and GLP requirements. · Participate in sample reconciliation and inventory reviews. *Equipment Validation & Quality Systems Support* · Support validation lifecycle activities (IQ/OQ/PQ), equipment qualification, and computerized system validation (CSV). · Review validation protocols, reports, and change control documentation. · Verify calibration and maintenance compliance during audits. · Assist with deviation, CAPA, and change control processes. *Inspection & Client Audit Support* · Assist with preparation and hosting of regulatory inspections and client audits. · Compile documentation packages and support inspection readiness activities. · Participate in mock inspections and internal gap assessments. · Track commitments and responses following inspections. *Quality Systems & Continuous Improvement* · Support training compliance tracking and QA metrics. · Assist in SOP development and quality system improvements. · Participate in risk assessments and process improvement initiatives. *Qualifications* *Education & Experience* Bachelor’s degree in life sciences, quality assurance, or related scientific field required. 2–5 years of QA or laboratory experience in a GLP-regulated environment preferred. Experience in preclinical CRO, pharmaceutical, biotechnology, or regulated research setting highly desirable. *Knowledge & Skills* · Working knowledge of FDA GLP regulations (21 CFR Part 58), OECD GLP, and data integrity principles (ALCOA+). · Familiarity with auditing techniques and quality management systems. · Understanding of document control, archival processes, and equipment validation. · Strong written communication and technical documentation skills. · Ability to interact professionally with clients and regulatory inspectors. · Strong attention to detail and organizational skills. · Quick turn-around on requests, with accuracy and thoroughness being critical. · Ability to handle multiple tasks, respond quickly and efficiently, and keep situations under control in a fast-paced, dynamic work environment · Ability to adapt to changing procedures, policies, and work environments. · Ability to compose clear, concise, and professional written communication. · Ability to meet deadlines and work under pressure. · Flexibility and adaptability with workload, shifting priorities as needed. · Perform tasks for experiments following step-by-step protocols. · Ability to work occasional weekend, early morning, or late-night shifts as required. *Preferred Qualifications* · QA auditing certification or formal GLP training. · Experience with LIMS, electronic data capture systems and Quality Management Systems (e.g., Provantis, Pristima, Xybion). · Experience hosting or supporting FDA, USDA, AAALAC or client inspections. · Experience in FDA (GLP), USDA, AAALAC, OLAW, DEA. · Knowledge of computerized system validation and data integrity assessments. *Work Environment* · Office and laboratory environment within a GLP preclinical research facility. · May involve review of laboratory procedures and study activities in animal research settings. · Occasional extended hours during inspections or audit periods. *Key Competencies* Regulatory compliance focus Critical thinking and risk assessment Professional communication Confidentiality and integrity Collaboration and teamwork Pay: $90,000.00 - $100,000.00 per year Benefits: * 401(k) * Dental insurance * Flexible schedule * Health insurance * Paid time off * Tuition reimbursement * Vision insurance Work Location: In person
Join Reva Medical LLC as a Full-Time Extrusion/Assembly Technician and become part of a pioneering team dedicated to revolutionizing medical devices. This onsite role offers a thrilling opportunity to work hands-on with cutting-edge technology, contributing to life-changing innovations in the healthcare industry. You'll play a vital role in the assembly process, collaborating with passionate experts who value problem-solving and integrity. At Reva Medical, our culture fosters high performance and forward-thinking, allowing you to grow professionally while making a tangible impact on patients' lives. Your contributions will directly affect product quality and operational efficiency, enhancing the future of medical care. You will receive great benefits such as Medical, Dental, Vision, 401(k), and Life Insurance. If you are eager to embrace challenges in a traditional yet dynamic environment, this position is your perfect fit! Apply now and help shape the future of medical technology. WHAT IT'S LIKE TO BE A EXTRUSION/ASSEMBLY TECHNICIAN AT EXTRUSION/ASSEMBLY TECHNICIAN As a new Extrusion/Assembly Technician at Reva Medical LLC, you will be responsible for operating extrusion machinery, ensuring precise setup and calibration for optimal performance. Your day-to-day tasks will include inspecting materials and components for quality, following strict assembly protocols, and adhering to established safety standards. You will collaborate closely with team members to troubleshoot any issues that arise during the extrusion and assembly processes. Additionally, you will document production data and maintain accurate records to support continuous improvement efforts. Engaging in routine maintenance and cleaning of equipment will also be essential to ensure operational efficiency. You'll participate in team meetings to share insights and contribute ideas for innovation, helping to foster a culture of high performance. Overall, your role will be pivotal in driving quality and consistency in our medical device manufacturing processes. REQUIREMENTS FOR THIS EXTRUSION/ASSEMBLY TECHNICIAN JOB To be successful as an Extrusion/Assembly Technician at Reva Medical LLC, strong attention to detail is paramount, as you'll be working with intricate components that require precision and accuracy. Excellent problem-solving skills will be essential for identifying and addressing issues during the manufacturing process. A hands-on approach and mechanical aptitude will help you navigate equipment effectively and perform troubleshooting as needed. Additionally, strong communication skills are crucial for collaborating with team members and sharing insights that promote innovation. Time management abilities will enable you to prioritize tasks effectively and meet production deadlines without compromising quality. Adaptability is also key, as you'll be working in a dynamic environment that values forward thinking and continuous improvement. Finally, a commitment to maintaining high standards of integrity and professionalism will ensure you thrive in our high-performance culture, contributing meaningfully to our mission in the medical device industry. MAKE YOUR MOVE Applying for this position is a walk in the park if you feel it's a good fit for you. Best of luck!
Work Your Magic with us! Start your next chapter and join EMD Electronics. Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. Everything we do in EMD Electronics is to help us deliver on our purpose of being the company behind the companies, advancing digital living. We are dedicated to being the trusted supplier of high-tech materials, services and specialty chemicals for the electronics, automotive and cosmetics industries. We foster a global collaborative organization made up of individuals who have the passion to win, obsess about the customer, are relentlessly curious and act with urgency. Together, we push the boundaries of science to make more possible for our customers. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: The Operations Technician 1 – Night Shift will be part of the Chemical Manufacturing team in Carlsbad, CA. The team of Operations Technicians are responsible for filling and completing orders for customers. Hours : Tuesday – Saturday 9:00pm-5:30am, including a 15% shift differential Position will start out on the day shift for 1-3 months and will move to a night shift once fully trained Pull needed vessel(s) for assigned orders Chemical Packaging (Filling with chemical) Conduct safe work practices Ensure quality standards are met Maintain a clean and organized manufacturing environment Comprehend written and verbal instructions Complete assigned day to day tasks other than filling orders Perform data entry Physical Attributes: Use of a full-face air-purifying respirator and other PPE Lift up to 50 pounds Who You Are Minimum Qualifications: High school diploma or GED 6+ months in a role requiring quality and safety 6+ months experience using Microsoft suite including (Word, Excel, Access, SharePoint) Preferred Qualifications: Previous experience handling chemicals Experience with Six Sigma methodologies Previous experience in a fast-paced manufacturing environment Strong troubleshooting, documentation, and communication skills Ability to read and understand Safety Data Sheets and written work instructions Strong focus on quality and safety Experience using SAP and LIMS systems Ability to use hand tools Pay Range for this position - $25/hr - $40/hr The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress! Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!
*CNC Mill Set Up Machinist Needed (POWAY)* Employment type: *full-time* Job title: *CNC Mill Setup Machinist* Premier CNC machine shop in San Diego County. We are looking for 1st shift CNC Mill setup machinists with a minimum of 5 years of experience. Shift is 7AM-3:30PM M-F Job requirements: * Experience setting up CNC mills (either 3, 4, or 5 axis are acceptable) * Ability to check your own work with various types of basic inspection equipment * Able to read blueprints and have an understanding of dimensioning and tolerancing * Ability to follow instructions and provide consistent quality * Must work well with others in a team environment What this position offers: * Steady paycheck as we have long-term customers and a stable workload * 401K/profit sharing * Health/Dental insurance * We pay top dollar for the right candidate Recruiters please do not reply CNC, Setup, Set-up, S/U, mill, haas, fanuc, mori, matsuura, doosan Job Type: Full-time Pay: $26.00 - $35.00 per hour Benefits: * 401(k) * 401(k) matching * Dental insurance * Health insurance * Life insurance * Paid time off * Parental leave * Retirement plan * Vision insurance Education: * High school or equivalent (Required) Experience: * CNC machining: 2 years (Required) Shift availability: * Day Shift (Preferred) Work Location: In person
*Job Summary* The Production Planner will be responsible for planning and coordinating production activities to ensure timely delivery of products. This role involves scheduling, material sourcing, and close collaboration with engineering, procurement, and production teams. This position works under the guidance of Project Managers and the Director of Engineering and Operations to align planning activities with overall project and organizational goals. This role requires an understanding of manufacturing processes, ERP systems, and continuous improvement methodologies to enhance overall production efficiency and product quality. *Work Environment:* This role operates in both an office setting and a production warehouse. The Production Planner is expected to communicate with production personnel and front office staff to ensure successful completion of work. A typical day may include, but is not limited to: working with Epicor to plan jobs, updating or editing router (job traveler) documents, walking the shop floor to check job status, verifying material or part availability, checking condition of parts to determine usability or need for rework, and communicating with procurement, engineering, sales, and production departments to stay updated on current status. *Key Responsibilities:* * Create and update Methods of Manufacturing in Epicor ERP * Print and distribute travelers (routers) for production jobs * Communicate with sales, engineering, and production teams regarding job priorities and details * Develop and maintain production schedules to meet customer demand * Source and identify materials required for production * Coordinate with procurement and production to ensure material availability and workflow efficiency * Monitor job progress and adjust schedules as needed to meet deadlines * Qualifications: * Education: High School Diploma required; some college preferred * Experience: 1–3 years in production planning or related field * Technical Skills: Experience using an ERP system (Epicor experience preferred), Microsoft Office Suite (Excel, Word, Outlook), Project management tools or Task management tools. * Warehouse awareness and safety * Understanding of engineering drawings. *Preferred Skills:* * Exposure to Lean Manufacturing Principals * Comfort identifying different types of material types and their various alloy types. * Open to learning and continuous improvement * Sense of urgency and ability to handle multiple projects at same while maintaining high quality work. *Company Culture:* We foster an environment of accountability, high-quality work, ownership, empowerment, and collaboration. Team members are encouraged to take initiative and contribute to process improvements. *Performance Metrics:* * Schedule Adherence: % of jobs completed on time * Accuracy of Travelers/Routers: Error rate in documentation * Material Availability: % of jobs started without material delays * Communication Effectiveness: Timeliness and clarity of updates to engineering and production * ERP Data Accuracy: Completeness and correctness of manufacturing methods and job details * Continuous Improvement Contributions: Number of process improvement suggestions implemented *Benefits: Full Time* * Competitive pay * 401K with match * Medical, Dental & Vision Insurance benefits * Overtime opportunities * Collaborative work environment * Growth and learning opportunities *Equal Employment Opportunity Statement:* Flotron Inc. is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, or veteran status. Job Type: Full-time Pay: $30.00 - $37.00 per hour Expected hours: No less than 40 per week Benefits: * 401(k) * Dental insurance * Flexible spending account * Health insurance * Health savings account * Paid time off * Vision insurance Work Location: In person
HME has been creating innovative products for the drive-thru and pro-audio industries since 1971. From the very beginning, we've known these solutions would never have happened without the customer-focused people who make up our company. HME has a team environment with a culture of collaboration, learning, and growth. With subsidiaries located in California, Missouri, Canada, UK, India, and China, companies around the world depend on HME for clear, reliable communication solutions. From setting the standard for drive-thru headsets and timer systems in the quick service restaurant (QSR) industry to developing professional audio equipment used in the Olympic Games, HME strives to create the newest, most innovative products on the market while providing quality care and attention to its customers. At HME you will have the opportunity to learn and grow while developing our future products. Come join our team! We are currently recruiting for a QA Inspection Lead, 2nd shift (2:30 pm - 11:00 pm). What you will do in the position: Interprets inspection requirements/standards as required by inspection team. Mentors/trains inspection personnel as required. Prioritizes and manages daily/tactical material inspection tasks and resources to optimize flow. Continually fosters 5S. Lean disciplines and methodology deployment within inspection team and their work areas. Ensures standard operating procedures are followed. Substitutes in supervisor's absence. Recommends to supervisor, adjustments to, operating standard and inspection methods via skip lot, inspection by pass etc. to optimize flow. May be directed to support MRB, FAI, Metric development, and special projects. Substitutes in supervisor's absence. As directed by Inspection Supervisor, may also support MRB, First Article, Metric development, special projects and other related tasks. What you will need to succeed: Qualifications Possess all senior inspector qualifications. Ability to train others in inspection skills and techniques both electrical and mechanical. Excellent verbal, reading and writing skills to interpret complex instructions and/or requirements. Ability to lead and motivate departmental personnel. Ability to work well with others in a team fashion, both inside and outside the company, in the supervisor’s absence. Expert in the interpretation and application of IPC solder requirements and complex mechanical measurement techniques. Experience 6+ years related experience Education High School Diploma - Required BA or BS (college graduate) - Preferred Travel: 0% The posted pay range, $30-$40/hour plus a 10% shift differential, is what we reasonably expect to pay for the role. This may vary depending on experience and other factors. Our benefits package includes tuition reimbursement; 3 weeks paid vacation your first year, paid holidays, medical, vision, and dental coverage, pet insurance, life insurance, and 401K contributions. The physical demands and work environment described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The employee will occasionally lift and move up to 10 pounds.
HME has been creating innovative products for the drive-thru and pro-audio industries since 1971. From the very beginning, we've known these solutions would never have happened without the customer-focused people who make up our company. With subsidiaries located in California, Missouri, Canada, UK, India, and China, companies around the world depend on HME for clear, reliable communication solutions. Come join our team! We are currently recruiting for a Receiving Inspector I. In this role, you will perform visual, close-tolerance mechanical, and electronic inspection of parts, materials and assemblies at incoming, in process, final production, first article and Product Development to ensure compliance to requirements and standards. This is a 1st shift position working Monday - Friday from 5:30 am - 2:00 pm. Key Responsibilities QA Inspection Support Performs basic to intermediate electro-mechanical inspections for conformance to HME requirements. Identifies, reports, and quarantines non-conforming material. Performs First Article Inspections to determine conformance to HME requirements. Performs and records results of a variety of test procedures with precision and accuracy with supervision. Applied Quality Support Applies sampling principles to material inspections per HME requirements. Applies external standards to material inspection when required; including IPC-A-600 and IPC-A-610. Administrative Quality Support Accurately performs material transactions appropriate to inspection findings using HME enterprise resource planning system. Reliably and accurately records inspection results to appropriate quality documents. Performs process and quality record audits to identify, correct, and prevent process deficiencies. Qualifications: Ability to interpret basic electro-mechanical part and assembly drawings and perform basic mechanical measurements with minimal supervision. Basic knowledge in the use and application of measurement tools including CMM, calipers, micrometers, height, pin, thread, and radius gauges, etc. Basic working knowledge of X, Y, Z coordinate system and GD&T dimensioning. Proficient in basic application of test methodologies, procedures and techniques. Ability to apply basic math in the course of inspections including addition, subtraction, multiplication, division and numeric conversions. Understanding of ERP (Enterprise Resource Planning) systems for transacting/moving materials. Demonstrate an understanding of basic quality terms, definitions and concepts. Demonstrate understanding of basic statistical terms and techniques. Demonstrate a working knowledge of ANSI/ASQ Z1.4, Sampling Procedures and Tables for Inspection by Attributes. Demonstrate the ability to apply ASQ 7 quality tools (Pareto, Fishbone, Flowchart, Control Chart, Check Sheet, Scatter diagrams, and Histograms). Demonstrate the ability to plot data and recognize out-of-control conditions. Understanding of MS Office applications required. IPC 610 Certification preferred. 1+ years of related experience. High School Diploma - Required Technical School or Certificate - Preferred The posted pay range is $18 - $21.58 per hour. This may vary depending on experience and other factors. Our benefits package includes tuition reimbursement; 3 weeks paid vacation your first year, paid holidays, medical, vision, and dental coverage, pet insurance, life insurance, and 401K contributions. The physical demands and work environment described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The employee will occasionally lift and move up to 10 pounds, 50 pounds with assistance.
Additional Location(s): N/A Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions. About the role: Primary focus is to build product by following processes and instructions to meet validation and build goals. Work Mode At Boston Scientific, we value collaboration and synergy. This role follows a onsite work model, requiring employees to be in our local office five days per week. Relocation Relocation assistance is not available for this position at this time. VISA Boston Scientific will not offer sponsorship or take over sponsorship of an employment VISA for this position at this time. Your responsibilities will include: Assemble, repair, inspect and/or test products following instructions. Ability to read and comprehend basic instructions and other work-related documents, written in English. Work with engineers on process modifications and suggest process improvement opportunities. Set up and operate a variety of manufacturing machines or equipment following written instructions in English. Clean tools and equipment per instructions. Record information on approved documents. Dispose hazardous waste material on corresponding hazardous waste areas. Resolve problems and make routine recommendations. Train other employees when necessary. Maintain all certifications required to remain in compliance. Work overtime as required. Sit and/or stand for extended periods of time as needed. Required qualifications: High School Diploma or equivalent 2 years to less than 5 years of work experience in manufacturing and/or assembly Ability to use and adjust a microscope Ability to work with small parts for an extended period of time This position requires proficiency in communication and understanding of English, including reading work instructions to consistently build defect free medical products. Preferred qualifications: Previous medical device experience preferred, but not required. Experience with soldering, hand tools and power tools/drills. Experience working with catheters and in a cleanroom environment. Experience with Lean Manufacturing and related principles and working directly with the engineers to make continuous improvement changes. Experience with maintaining accurate records including training files and shop floor paperwork. Experience training others. Experience working in a pre-production environment. Requisition ID: 624745 Among other requirements, Boston Scientific maintains specific prohibited substance testing requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a drug test as a pre-employment requirement. The goal of the drug testing is to increase workplace safety in compliance with the applicable law. As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most – united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do – as a global business and as a global corporate citizen. So, choosing a career with Boston Scientific (NYSE: BSX) isn’t just business, it’s personal. And if you’re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you! At Boston Scientific, we recognize that nurturing a diverse and inclusive workplace helps us be more innovative and it is important in our work of advancing science for life and improving patient health. That is why we stand for inclusion, equality, and opportunity for all. By embracing the richness of our unique backgrounds and perspectives, we create a better, more rewarding place for our employees to work and reflect the patients, customers, and communities we serve. Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identify, gender expression, veteran’s status, age, mental or physical disability, genetic information or any other protected class. Boston Scientific maintains a prohibited substance free workplace. Pursuant to Va. Code § 2.2-4312 (2000), Boston Scientific is providing notification that the unlawful manufacture, sale, distribution, dispensation, possession, or use of a controlled substance or marijuana is prohibited in the workplace and that violations will result in disciplinary action up to and including termination. Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination.
Benefits: 401(k) Dental insurance Employee discounts Health insurance Paid time off Training & development Vision insurance Belching Beaver Brewery is a thriving craft beer brewery dedicated to producing high-quality and innovative products for our community. We take pride in our commitment to excellence and our vibrant team-oriented culture. We are seeking a bottling/canning line operator to join our production teams. The ideal candidate will have a strong work ethic, positive attitude and is comfortable working in a fast-paced brewery production facility. Position responsibilities include but are not limited to packaging cans into boxes, palletizing finished cases and storing/organizing pallets in finished goods inventory. Flexibility and the ability to work effectively as part of a team is essential for success in this position. Cross-training into other brewery departments available based on good performance. Hours: Monday-Friday 6:30am-03:00pm Pay: $19/hour Forklift certification and production experience are preferred but not required. To apply for this bottling/canning line operator position at Belching Beaver Brewery, please submit your resume and cover letter detailing your relevant experience and why you are interested in joining our team. Responsibilities: Operate and maintain the bottling/canning line equipment efficiently and safely. Set up and adjust machinery for bottling/canning operations, ensuring proper speed, pressure, and quality control. Monitor the bottling/canning line during operation, making adjustments as necessary to maintain smooth production. Perform routine maintenance and cleaning of the equipment, ensuring optimal performance. Collaborate with the brewing team to ensure that the correct beer is being packaged and labeled accurately. Troubleshoot and resolve any equipment malfunctions or production issues promptly. Ensure compliance with all safety protocols and quality standards. Maintain accurate production records and reports. Qualifications: Must be 21 years old Strong organizational skills and attention to detail Ability to work effectively in a fast-paced, dynamic environment Forklift Certification is a plus, but we will re-train Benefits: 401(k) retirement plan Health, dental, and vision insurance Paid time off (PTO) Paid Holidays Employee discounts on brewery products Hourly compensation based on experience Belching Beaver Brewery is an equal opportunity employer committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment based on protected characteristics outlined by federal, state, or local laws.
With extensive experience in developing biologics and bioconjugates, we offer a seamless service delivered by fully integrated teams, from early discovery to commercial manufacturing. Forward-thinking and committed, we find the best solution and use the right technologies to design, develop and manufacture your products to ensure we get vital medicines to patients quickly and safely. We are dedicated to quality excellence. We are driven to get better treatments to market, efficiently and responsibly by reducing timelines and delivering the highest quality products and services. We are Abzena. More than a CDMO, we are a responsible and dedicated partner that takes care of your products from concept to patient. The Production Scheduler is responsible for creating, maintaining, and optimizing detailed, finite production schedules in a strictly regulated Current Good Manufacturing Practice (cGMP) environment. This role acts as the key bridge between Manufacturing, Supply Chain, Quality Assurance, and Materials Management to ensure on-time production and optimal resource utilization. The ideal candidate will manage complex production sequences including commercial/clinical manufacturing, Tech Transfer, and Validation while ensuring compliance with all regulatory standards and safety protocols. Responsibilities Production Scheduling: Develop, publish, and maintain daily and weekly detailed manufacturing schedules based on the Master Production Schedule and balance customer demand with available resources. Utilize Access Orchestrate and IFS for planning, scheduling and execution. You'll need to be proficient in these systems, generating reports, analyzing data, and making informed decisions. Capacity Planning: Analyze plant capacity, labor, and machine availability to optimize throughput, minimize changeover times, and avoid bottlenecks. Work closely with production managers to ensure the Master Production Schedule is achieved. Material Readiness: Collaborate with MSAT, Supply Chain/Procurement to ensure raw materials, components, and APIs are available in accordance with the production schedule. Quality Compliance: Coordinate with Quality Assurance (QA) and QC labs to ensure batch records, testing, and releases are aligned with production timelines. Deviation Management: Proactively manage schedule changes, unexpected downtime, or material shortages, providing, and implementing, "what-if" scenario analysis. Data Integrity: Maintain accurate data within the ERP system, including work orders, lead times, and routing, to support accurate planning. Documentation: Ensure all scheduling activities comply with SOPs and cGMP requirements for audit readiness. Management: Monitor and report on key performance indicators (KPIs) such as production attainment, schedule adherence, and inventory accuracy (return to stock). Use this data to identify areas for continuous improvement for point of use materials which may be attributed as pass through costs for clients. Planning: Apply standard principles and best practices in all aspects of master scheduling for daily activities. A strong understanding of planning, scheduling, and inventory management concepts is essential. Qualifications BA/BS or MA/MS degree that included laboratory work in biology, microbiology, chemical engineering or related field, or degree in operations with minimum 5 years’ experience scheduling for laboratory work. Minimum 5 years of experience in manufacturing operations, preferably in a GMP environment. Experience with MRP and scheduling systems. Experience in IFS (MRP) and Access Orchestrate (Scheduling) preferred. Analytical Thinking: Ability to interpret complex data and make decisions based on capacity constraints. Communication: Excellent verbal and written skills to coordinate with multiple departments. Attention to Detail: High precision in documentation and scheduling to avoid compliance risks. Problem-Solving: Ability to act with urgency to resolve scheduling deviations. Curiosity: A desire to learn the details of the work you plan for, the ability to ask and answer ‘what-if’ questions, and a continuous improvement mentality to drive process improvements. FLSA: Exempt Abzena is an equal opportunity employer that is committed to diversity and inclusion in the workplace. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws. This policy applies to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, and training.
Overview: At Pacira, innovation meets purpose. Pacira BioSciences, Inc. is a pioneer in non-opioid pain management and regenerative health solutions. Today, we’re building on that legacy with next-generation innovations for chronic, postsurgical, and musculoskeletal pain. Our culture is built on collaboration, innovation, and a shared commitment to helping patients recover faster. We are redefining what’s possible in pain management—and we can’t do it without talented people like you. Why Join Us? At Pacira, every career is more than a job. Our mission drives us, and every day, we challenge ourselves to achieve the extraordinary. Integrity is at the core of who we are. We value diverse perspectives and the collective strength of a unified team. Join the team in making better possible for patients everywhere. Summary: This role leads daily activities and performs manufacturing tasks and operations at an advanced level for bulking and weigh and dispense operations required in the preparation and sterile production of liquid injectable, sustained-release pharmaceutical products under cGMP regulations and aseptic cleanroom conditions. 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: Work directly with supervisor to coordinate daily activities for process and personnel. Maintain scheduling timeline while adhering to GMP and SOP guidelines. Identify and implement process improvements. Transact materials in ESI to maintain accurate inventory levels Perform routine inventory cycle counts Maintain production areas and records - OEE spreadsheets, Manufacturing Tracker Spreadsheets and Shift Pass downs. The required tasks and areas of assignment include: CIP, SIP, and solution prep, set-up and preparation of the area for bulk manufacturing, perform GMP area cleaning, utilize the automated control systems, and other routine tasks Perform Weigh and Dispense Operations utilizing protocols and SOPs by weighing the required quantity for each material according to the Manufacturing Batch Record (MBR). Use computer system and weighing balance equipment. Understand critical process parameters and steps of activities sufficiently to act as a trainer for new employees. Complete GMP documentation (Batch Records, Forms, Charts, Data Entry). Read, comprehend, and adhere to standard operating procedures (SOPs). Participate in the development and production of pipeline products. Author or assist in drafting and revising departmental procedures and practices. Identify and communicate floor observations to supervisory staff. Maintaine a high level of proficiency with process equipment and automated control systems with the ability to troubleshoot, escalate issues, and determine corrections. Provide guidance to less experienced operators on gowning, interventions, and aseptic manipulations, and maintain aseptic gown qualifications and APS participation. Assist in maintaining the production areas and records in a cGMP state. Adhere to all EH&S policies, procedures, and guidelines. Supervisory Responsibilities / Interactions: This role has no direct supervisor responsibilities. Qualifications: Qualifications, Education, and Experience: 5 years of industry experience in the pharmaceutical or closely related industry required A high school diploma/GED is required Knowledge, Skills, and Abilities: Organizational skills and an ability to perform assignments with a high degree of independence The ability and willingness to work as a member of a team, good interpersonal skills Ability to work with minimal direct supervision and be self-driven to meet the schedule Must have good attention to detail, documentation skills, and the ability to follow written procedures in a GMP environment Must possess strong written and verbal English communication skills Must have strong organizational skills and the ability to multi-task Must understand and be proficient with basic arithmetic calculations, including calculating elapsed time and ratio calculations Computer proficiency, including knowledge of Microsoft Word, Outlook, and Excel applications, is required Ability to accommodate production requirements that may occasionally require 50+ hour workweeks, including extended day hours and weekends Ability to work a 12-hour shift (includes overtime eligibility) Ability to work weekends 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. While performing the duties of this job, the employee is regularly required to sit, talk, move between spaces, and reach with hands and arms. Close vision and the need to focus on the computer screen, use of hands, fingers, and wrist to type on the keyboard, and manipulate the mouse. Will need to lift and move items weighing up to 50 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. Employee is required to work in a cleanroom environment, which requires gowning consisting of coverall, foot and head coverings, facemask, and gloves. Noise level is moderate with consistent equipment operation. Benefits: 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 $32.88 per hour. to $45.22 per hour. This role is classified as non-exempt and eligible for over-time. 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.