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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 Chemist will be a part of the Small Volume Manufacturing team in Carlsbad supporting the small-scale manufacturing process and the experimental products M4Ward™program. The Small Volume team works closely with the R&D, Marketing, Quality Control and Engineering teams. The Small Volume team works to scale up and optimize production of new chemicals transferred from R&D and assist in transitioning production to high volume scale up as needed. Chemical SDS review to conduct and participate in safety reviews Supporting chemical purification by running purification systems and providing technical input on small scale chemical purifications. Perform chemical sampling and packaging and providing technical input on complex container fills and chemical handling Vessel cleaning and break down Maintaining a current chemical inventory Performing equipment setup, maintenance, and troubleshooting Maintaining a clean and efficient lab environment Physical Attributes: Wearing full face air-purifying respirator and other PPE Lifting to 50 pounds Standing, sitting, or walking for up to 8 hours Raising arms up to and possibly above 90-degree angle This is a Day-Shift position: Sunday – Thursday Hours operations 5am-1:30pm Who You Are Minimum Qualifications: Bachelor’s Degree in Chemistry, Biochemistry, Chemical Engineering, or related Life Science discipline. Preferred Qualifications: Knowledge of P&ID’s and basic engineering principles Experience working in gloveboxes Chemical distillation and sublimation knowledge Prior chemistry lab experience handling highly toxic chemicals, acids and bases Strong troubleshooting, documentation, and communication skills A strong focus on quality and safety Experience using Microsoft suite including (Word, Excel, Access, SharePoint) Experience using SAP, Intelex MOC, and LIMS systems Strong data analysis, attention-to-detail and organizational skills Pay Range for this position: $32.00-$50.00 per hour. 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!
Check out our website! GoSolara.com Position Summary: We are Solara Home Energy, and we are growing our Residential Installation team! We are a growing alternative energy company looking to continue building our Residential Installation team to support each other and grow the business, while carefully maintaining our priorities for our customers. We need organized and highly motivated people who are task-oriented team players. We are looking for like-minded business partners that value customer service, respect, and hard work. We value our employee group and strive for a great work environment while offering opportunities for advancement paralleled with company growth. Solara Home Energy is hiring for Installer II. Job sites will be located throughout Escondido, CA; primary job site may change depending on customer project. Installations will be integrated into single family homes, multi-family homes, and apartment homes. This position requires the ability to operate a company vehicle, MUST meet MVR criteria outlined below. Duties & Responsibilities: Execute installation of attachments, racking systems, micro-inverters, optimizers, inverters, rough electrical, finish electrical equipment etc. on 1-3 story new construction buildings. Complete wiring and electrical connections between solar panels, inverters, and electrical panels. Perform layout measurements and ensure panels are properly aligned and secured. Seal and weatherproof roof penetrations to maintain roof integrity. Install conduit, disconnects, and other safety equipment as required by electrical codes. Maintain professional conduct and quality installation. Complete and adhere to all safety training and protocol. Qualifications: High School Diploma or GED required. Minimum of two (2) years of hands-on solar installation experience, including residential new construction and/or retrofit solar installations required. Experience working on residential roofing systems and electrical components preferred. Experience operating company vehicles in a professional capacity preferred. Valid driver's license and ability to meet company MVR requirements Reliable transportation to report to assigned job sites. Ability to pass a criminal background check. Strong work ethic and willingness to learn. Ability to work effectively in a team environment. Strong communication skills and attention to detail. Skills / Knowledge / Abilities: Basic understanding of the entire PV system, how it works, and the ability to install PV systems with minimal foreman oversight. Ability to explain the install process. Ability to follow safety protocol including PPE requirements. Physical Requirements: Ability to work on unlevel surfaces- installation applications will range across all roof types. Ability to perform construction at heights of 1-3 stories. Ability to perform work requiring frequent bending and twisting Ability to lift up to 70 lbs. Ability to climb up and down ladders constantly. Ability to properly secure and wear PPE. Ability to follow safety protocol and direction. Ability to work outdoors in varying degrees of weather. Motor Vehicle Record (MVR) Requirements: Eligibility to operate a company vehicle is contingent upon: Possession of a valid driver's license. Maintenance of an acceptable driving record. Compliance with company fleet safety requirements. Approval under company insurance carrier guidelines. Employment and continued vehicle operation may be subject to periodic MVR reviews. Benefits: 401(k) matching Dental insurance Health insurance Vision insurance Life insurance Paid time off Sick Time Paid Holidays Cell Phone Reimbursement Monday - Friday 5 days a week - 8 hours a day
Company Overview: Nikkiso Clean Energy & Industrial Gases is a leading provider of cryogenic pumps, heat exchangers, process systems, turboexpanders, services, and solutions for the liquefied natural gas (LNG), liquefied hydrogen (LH2), and industrial gases industries. Applications include fueling stations, marine engines, peak shaving, power generation, virtual pipelines, carbon capture, geothermal power and well stimulation. We are a subsidiary of Nikkiso Company Ltd, a leading industrial manufacturer headquartered in Tokyo, Japan, with $1.5 B USD in annual revenue, 8000 + employees worldwide, and publicly traded on the Tokyo Stock Exchange. Job Overview: The Project Manager plans, directs, and coordinates activities of projects to ensure that objectives are accomplished within established specifications, schedules, and budgets. Cryogenic System Projects to include LNG regasification, LNG trailer loading, hydrogen fueling stations, and industrial gas. Annual Salary: $77,070 to $138,765 Responsibilities: Reviews project proposal to determine time frame, funding, limitations, procedures for accomplishing projects, staffing requirements, and allotment of available resources to various phases of projects. Interfaces with project staff to outline work plan and assign duties. Directs activities of staff to ensure project progresses on schedule and within budget. Coordinates interdepartmental functions to minimize delays. Provides technical advice to project staff and meets with them on a regular basis to review program status, resolve problems, and plan future actions. Reviews status reports and modifies schedules or plans as required. Prepares project reports for management and advises status on a regular basis. Interface with customer on all aspects of contract and technical requirements. Anticipates potential schedule delays and initiates plans for alternative actions. Interfaces with customers on schedules, meetings, problems and program status. Performs other duties as assigned. Qualifications: Bachelor’s Degree Business Administration or Mechanical Engineering or related discipline. PMP Certification (Project Management Professional) from the Project Management institute preferred. Five years related manufacturing industry experience. Strong project management, problem solving, and customer service skills. Demonstrated originality and initiative. Considerable flexibility of methods required to meet program goals. Excellent interpersonal relations, customer service, and oral and written communication skills. Excellent MS Office application experience. EEOC Statement: Equal Opportunity Employer/Veterans/Disabled Nikkiso Clean Energy & Industrial Gases Group companies are proud to be equal opportunity employers. 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, or protected veteran status and will not be discriminated against on the basis of disability.
If you’re looking for a special place to build or grow your career, you’ve found it. Whether you’re an experienced professional, a recent college graduate or somewhere in between, IDEX is a place where you can apply your existing skills and learn new ones in an environment where you can make an impact. With interesting opportunities in engineering, marketing, sales, supply chain, operations, HR, finance, and more across more than 40 diverse businesses around the globe, chances are, we have something special for you. Sr. OEM Key Account Manager - Optical Systems Who is IDEX Health & Science (IH&S)? As a business unit of IDEX Corporation, IH&S has a long history of driving growth in life sciences and healthcare by embracing innovation and redefining the supplier-customer relationship. The work we do every day allows us to discover key insights and break new ground to create some of the most meaningful technologies that have a lasting impact on companies, industries, and society. One of business segments is called Life Science Optics and we are looking to add more talent to the team. IDEX HEALTH & SCIENCE, LLC: IDEX Health & Science is the global leader in life science fluidics, microfluidics, and optics, offering a three-fold advantage to customers by bringing optofluidic paths to life with strategic partnerships, solutions, and expertise. As one of the few companies in the world with component, sub-system, and application-level experts, IDEX Health & Science helps instrument developers solve the most demanding fluidic and optical challenges in a wide array of applications. With over 1,200 employees around the world, we believe partnership will change the way the world innovates, leading to new technologies that improve our health, protect our planet, and enrich our lives. For more information visit: www.idex-hs.com Our formula for success is simple. We work hard to maintain a culture where you can own your work; you are encouraged to try new ideas in a collaborative environment; and you can apply your skillset to enable our clients to gain a competitive advantage in their own market. At IDEX Health & Science, you have the opportunity to work with a great group of people, mentor others, and build a great future. SCOPE OF ROLE: As the OEM Key Account Manager - Optical Systems you will develop new business and drive sustained, profitable sales growth for the Life Sciences Optics business across North America. You will identify and qualify prospective customers and applications, build and manage a robust opportunity pipeline, and convert targeted opportunities into long-term customer relationships. You will develop, manage, and guide sales activities; create, review, and update territory and opportunity plans; and adjust strategy as required based on technology, product, geopolitical, market, or competitive forces. A significant part of the role is to build broad and deep relationships with key functional decision makers at prospective and existing customers. You will use Microsoft Dynamics 365 to accurately record critical customer and opportunity information and maintain timely forecasting information. ESSENTIAL DUTIES: Develop New Business and Strengthen Customer Relationships Build and maintain multi-level, cross-functional relationships with key stakeholders at prospective and existing customers, including Executives, RD&E, Procurement, and Supply Chain Create consistent touch points for IDEX and IH&S executives with key stakeholders at target prospects and assigned customers Partner with Market Development, Product Management, and Engineering to identify target applications, gain access to key customer stakeholders, and obtain feedback regarding Optical Systems innovation Develop and Execute North America Territory and Opportunity Plans Develop and execute actions to build the Optical Systems pipeline, win new customers, grow the core business, and capture share Lead and coordinate cross-functional teams across IH&S to support strategic growth plans, new-business pursuits, and updates through Monthly Sales Reviews (MSR) Deliver Profitable, Sustainable New-Business Revenue Growth Develop new Optical Systems business across North America Identify, qualify, and capture new customer and share-gain opportunities Maintain Consistent Operating Rhythms Forecasts - maintain accurate monthly and quarterly opportunity and customer forecasts, and partner with IH&S Finance to analyze and summarize forecast inputs for the Annual Operating Plan (AOP) Key Performance Indicators – measure and communicate KPI performance with key internal and external stakeholders including metrics in areas such as On-time-delivery, Quality and RMA Warranty Returns Pricing – negotiate and implement all price changes including periodic adjustments such as tariffs or other business-related charges EDUCATION AND EXPERIENCE: Required Bachelor’s degree - preferably in Life Sciences or Engineering. Advanced degree is preferred. A minimum of 5 years of sales or business development experience in optical systems, analytical instrumentation, biotechnology, IVD, or related markets Excellent new-business development, customer relationship, and key account management skills, with a proven track record of increasing sales Proven experience negotiating and closing multi-million dollar/multi-year contracts Preferred Optical Systems or analytical instrumentation sales experience is strongly preferred Strong preference for candidates with experience developing new business with instrument OEM companies Solid understanding of IVD/Bio instrumentation techniques such as PCR, proteomics, next-gen sequencing, cytometry & cytology, spatial biology, synthetic biology, immunoassay analysis, clinical diagnostics, and the associated sample preparation methods is useful Knowledge of non-IVD/Bio-specific applications such as chromatography, MS, particle characterization, liquid handling, etc. is useful OTHER SKILLS and ABILITIES: Ability to move strategy to action Ability to collaborate with internal company stakeholders in other functional areas Able to travel approximately 50% as needed throughout North America, with occasional international travel Comfortable working under pressure High-energy, self-starter who brings an owner’s mindset to winning Well-organized including the ability to balance and prioritize short-term activities with long-terms strategic actions Prepare and professionally articulate presentations, legal contracts, and joint strategic planning documents with senior-level executives Proficient in using electronic devices such as mobile phones and computers Outstanding oral and written communication skills in English across many facets of the business. DISCLAIMER: The information in this job description has been designed to indicate the general nature and level of work performed by employees within this remote North America role at IDEX Health & Science. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees assigned to this job. Requirements are subject to possible modification to reasonably accommodate qualified individuals with disabilities. This document does not create an employment contract, implied or otherwise, other than an employment relationship. Are you ready to join a different kind of company where our people, our culture, and our commitments are centered around providing trusted solutions that improve lives around the world? Total Rewards The compensation range for this position is $112,700.00 - $169,100.00, depending on experience. This position may be eligible for performance based bonus plan. Benefits Package Our comprehensive U.S. benefit offerings include: Health benefits, 401(k) retirement savings program with company match, PTO, and more. More information on our benefits and rewards can be found on our career page: https://www.idexcorp.com/careers/our-benefits-and-rewards/ IDEX is an Equal Opportunity Employer. IDEX gives consideration for employment to qualified applicants without regard to race, color, religion, creed, genetic information, sex, sexual orientation, gender identity or expression, marital status, age, national origin, disability, protected veteran status, or any other consideration or protected category made unlawful by federal, state or local laws. Attention Applicants: If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process, please let us know. Likewise, if you are limited in the ability to access or use this online application process and need an alternative method for applying, we will determine an alternate way for you to apply. Please contact our Talent Acquisition Team at [email protected] for assistance with an accommodation. These contact tools may be used only by individuals with a disability for accommodation requests. Do not inquire as to the status of an application. This posting is for an existing vacancy. Artificial intelligence is not used to screen, assess or select applicants.
Payroll Accountant - Remote RQ Construction is seeking a Payroll Accountant to join our Accounting/Finance team. This role owns the accuracy and integrity of our payroll accounting - from posting payroll and reconciling accounts to making sure labor costs land correctly on our projects. You'll work closely with our Accounting, Payroll, & HR teams and play a key role in keeping our financial reporting audit-ready. Since 1996, RQ Construction, LLC has been a leading player in Southern California's robust commercial and governmental Design-Build economy. We now have a national presence with current projects approaching $300M, spanning coast to coast. We are a full-service Design-Build company offering management of projects throughout the United States, with field operations team members who work on location for each of our projects. We specialize in fast-track projects in new commercial construction for both public and private clients, with a primary focus in the Department of Defense market. What RQ Offers Competitive salary: $75,000-$100,000 annually, depending on the candidate's primary home location and applicable geographic pay range. Medical, Dental, and Vision insurance 401(k) with company matching As part of this position, you will: Own the payroll accounting cycle in Oracle - including posting to the general ledger weekly and monthly reconciliations of payroll, benefits, and Workers' Compensation accounts. Maintain a high level of proficiency in the payroll and accounting software (Oracle Human Capital Management and Oracle Fusion ERP) and optimize their use to enhance internal processes and reporting. Prepare documentation for audits (Workers' Comp, OSHA, internal/external) and keep payroll records compliance-ready. Partner with Accounting, Payroll, and Operations departments to identify and resolve discrepancies and support budgeting and forecasting. Take initiative to identify areas of improvement and implement changes Requirements Bachelor's degree in Accounting or related field required. Other education in conjunction with relevant experience may be considered. 2+ years of payroll and accounting experience. Experience working Oracle Human Capital Management and/or Oracle Fusion ERP required. Experience in construction accounting preferred. Proficiency in Microsoft office products. Strong attention to detail and comfort working with compliance-heavy, audit-facing work. Our Mission Our mission is "to provide our customers the best built environment while being the first choice of all stakeholders." RQ offers a variety of services including construction, architectural design, trade services, virtual design and construction, and LEED/sustainable design management for projects ranging from $30M to over $100M. RQ's experience includes projects throughout the nation, including California, Virginia, North Carolina, and internationally at U.S. Naval Base Guantanamo Bay, Cuba. The success of this company has been built on three pillars: Quality, Integrity, and Leadership. Our employees work hard as a team, thrive on innovation, and remain committed to being the first choice of our clients as well as all other stakeholders. Join RQ, apply today! We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, creed, gender (including gender identity and gender expression), religion (all aspects of religious beliefs, observance or practice, including religious dress or grooming practices), marital status, registered domestic partner status, age, national origin or ancestry, physical or mental disability, medical condition (including cancer or a record or history of cancer, and genetic characteristics), sex (including pregnancy, childbirth, breastfeeding or related medical condition), genetic information, sexual orientation, veteran status, or any other basis or status protected by federal, state, or local law or ordinance or regulation.
We understand that the world we want tomorrow starts with how we do business today, and that’s why we’re inspired to make A Better World for Pets. Antech is comprised of a diverse team of individuals who are committed to each other’s growth and development. Our culture is centered on our guiding philosophy, The Five Principles: Quality, Responsibility, Mutuality, Efficiency and Freedom. Today Antech is driving the future of pet health as part of Mars Science & Diagnostics , a family-owned company focused on veterinary care. Current Associates will need to apply through the internal career site. Please log into Workday and click on Menu or View All Apps, select the Jobs Hub app, then click the magnifying glass to Browse Jobs. The Target Pay Range for this position is $23- $26 hourly. At Antech, pay decisions are determined using factors such as relevant job-related skills, experience, education, training and budget. Job Purpose/Overview The Production Technician will be working in the Production operations area, in a team environment, with other technicians and intra-department personnel to configure, test, manufacture, repair and continuously improve the products that we sell and support. Essential Duties and Responsibilities Assemble, test, and troubleshoot computers and Digital Radiography, Laser, X-Ray, Ultrasound and Network related products. Interpret and apply information from technical manuals; communicate on technical issues with individuals with varying degrees of product familiarity. Troubleshoot hardware and software problems on RMAs and identify, research and resolve technical problems Offer solutions and advice on field problems for customer service staff and peers. Assist, troubleshoot and repair sales department and tradeshow equipment. Develop and follow all administrative procedures as required for manufacturing and repair processes. Process RTV requests for equipment returning to vendor for repair or further evaluation and communicate with vendors on a technical level. Knowledge in system configuration for network communication. Prepare and maintain accurate records of manufactured product (e.g. Production logs, End of Line Certificates). Education and Experience High school diploma required. AA/AS in electronics or 2-5 years experience in manufacturing environment. Minimum 2 years of equivalent experience. Strong teamwork capabilities including the ability to effectively work with leadership, peers and other internal and external individuals through projects, making sure project deadlines are met and projects enhance the goals and strategic direction of the company. Ability to effectively work with executive leaders, team leads, and peers through projects, making sure project deadlines are met. Strong written and oral communication skills. Must work well independently and work in a matrix based organization with minimal direction. Must be able to handle multiple projects and be able to adapt to changes in priority. Technical Experience Experience with installing, maintaining, and repairing hardware and software for business computers and related equipment. Must be familiar with manufacturing pressures and work environments and must be able to communicate effectively, work cross-functionally and assist others as required. Have experience with inputting, accessing, analyzing and integrating data using a computer. Physical requirements Must be able to bend, stoop and lift up to 50lbs. About Antech Antech is a leader in veterinary diagnostics, driven by our passion for innovation that delivers better animal health outcomes. Our products and services span 90+ reference laboratories around the globe; in-house diagnostic laboratory instruments and consumables, including rapid assay diagnostic products and digital cytology services; local and cloud-based data services; practice information management software and related software and support; veterinary imaging and technology; veterinary professional education and training; and board-certified specialist support services. Benefits Antech offers an industry competitive benefits package and continues to invest in and evolve benefits programs that meet the health, wellness and financial needs of our associates. Benefits eligiblity is based on employment status. Paid Time Off & Holidays Medical, Dental, Vision (Multiple Plans Available) Basic Life (Company Paid) & Supplemental Life Short and Long Term Disability (Company Paid) Flexible Spending Accounts/Health Savings Accounts Paid Parental Leave 401(k) with company match Tuition/Continuing Education Reimbursement Life Assistance Program Pet Care Discounts Commitment to Equal Employer Opportunities We are proud to be an Equal Opportunity Employer - Veterans / Disabled. For a complete EEO statement, please see our Career page at Antech Careers . Note to Search Firms/Agencies Antech Diagnostics, Inc. and its subsidiaries and affiliates (Antech) do not compensate search firms for unsolicited assistance unless they have a written search agreement with Antech and the requisition is position-specific. Any resumes, curriculum vitae, and other unsolicited assistance from search firms that do not have a written search agreement or position-specific requisition submitted to any Associate of Antech will be deemed the sole property of Antech and no fee will be paid in the event the candidate is hired by Antech.
The Sr. Quality Assurance Specialist fulfills a critical role in Quality Assurance. This individual will contribute an advanced level of understanding of GMP system improvements, technical documents, and review of GMP documentation and reports. This individual must also provide GMP and related guidance, data analysis, and technical review of QC data. in some instances, this role may act as the deputy for the Manager, Quality Assurance. What you will do Perform all duties pertaining to a QA specialist I, II, III, in addition to those listed below. Support real time batch record review in a timely manner and with high accuracy, performing usage decisions in electronic batch release systems. Suggest and implement improvements in quality systems and SOPs taking into account LEAN GMP approaches. Reviewing and approval of all GMP documentation, which includes BPRs, validation protocols, data, reports, etc. Reviewing, analyzing, and trending data to extract relevant information. Work closely with other functions and sites to close out quality records, investigations e.g., OOS, and approval of documents and changes e.g., MBPRs, analytical procedures, protocols, reports, and specifications/global specifications. Suggests/recommends and implements new policies and procedures to improve existing processes and products. Problem resolutions with GMP systems as well as guiding on GMP topics. Be an active part in increasing the quality culture in the organization e.g., by guidance and training of other departments and sites. Perform GMP audits for internal operations, GMP compliance improvements and provide GMP compliance guidance to other departments and BAM Sites as needed. Support actively and able to take the lead in customer/authority audits. Writing new and revising current standard operating procedures (SOPs), specifications, etc. In addition, provide technical assistance on production and quality systems documents. Qualifications Bachelor's Degree in organic chemistry or related field required or Master's Degree in organic chemistry or related field preferred Bachelor's Degree in a science related field and a minimum of 5 years' experience in a GMP manufacturing setting required or Associate's Degree in a science related field and a minimum of 7 years' experience in a GMP manufacturing setting required 4-6 years experience in Quality Assurance required 4-6 years experience with GMP document control, validation, qualification and calibration preferred 4-6 years Ability to work in ISO7 and ISO8 control environment and support real time batch record review required 4-6 years experience in internal auditing as well as working with regulatory agencies preferred Excellent written and oral communication skills Basic computer knowledge, including Microsoft Word, Excel and PowerPoint Ability to effectively organize, multitask and work in fast-paced, deadline driven work environment. Ability to communicate in a proactive and solution-focused manner, including keeping management aware of potential issues. Detail oriented with the ability to troubleshoot and resolve problems. Ability to work independently and manage one's time. Communicate effectively and ability to function well in a team environment. Certified Quality Process Analyst - ASQ preferred or CQA preferred or CQE certification desired preferred Annual Salary Range: $97,174.20 - $133,614.80 Placement of new hires in these wage ranges is based on several factors including education, skill sets, experience, and training. Total Rewards We offer all Team Members a total rewards package including competitive pay, annual performance bonus, a generous benefit package with comprehensive Medical/Dental/Vision coverage, 401(k) plan with employer contribution, and paid vacation, personal and sick days. Corporate Social Responsibility Bachem takes responsibility for future generations by a careful handling of resources and avoiding environmental risks. We continually improve our ecological performance and develop and implement new approaches for enhancing employees’ environmental awareness. EcoVadis has awarded Bachem Gold Medal status in their assessment of Bachem. Bachem Americas is an Equal Opportunity Employer As an equal opportunity employer, we celebrate the diversity of our team and are committed to building an inclusive workplace where individuals are hired and advanced based on merit, skills, and qualifications. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status, or other legally protected status. At Bachem, you’ll find a diverse, multicultural team. The (a) in the job title stands for all. We welcome applications from all candidates. What matters are your skills and motivation—regardless of age, gender, background, religion, or sexual orientation. Please note: unsolicited resumes from recruitment agencies will not be considered. Nearest Major Market: San Diego
To ensure Bachem can meet the demands of its evolving business and diverse customer base, the Senior Director, Technical Operations leads the local Technical Operations organization and ensures that site manufacturing technology, technical capabilities, and operational readiness are aligned with site strategy, customer needs, global standards, and regulatory expectations. The role provides senior leadership for technical operations across manufacturing science, technology transfers, product stewardship, process optimization, validation support, automation and digitalization initiatives, technical documentation, and lifecycle management. The Senior Director, Technical Operations leads scientists, chemists, engineers, technical writers, process specialists, and other technical experts supporting clinical and commercial manufacturing, major capital investments, new product introductions, and transfers within the Bachem network or from client sites to BAM. The role partners closely with Manufacturing, Quality, Engineering, Supply Chain, R&D, Project Management, and global TechOps to strengthen process robustness, inspection readiness, operational excellence, and future site capabilities. This position reports to the Vice President of Global Technical Operations. What you will do Ensure adequate technical support for clinical and commercial products through Process Performance Qualification (PPQ), technology transfer, process monitoring, troubleshooting, product stewardship, validation support, manufacturing readiness, lifecycle management, complex troubleshooting, and process optimization activities requiring expertise beyond the capabilities of the Commercial Manufacturing Team (CMT), ensuring robust, compliant, and reliable manufacturing operations. Lead technology transfer activities including internal site transfers and transfers from client sites to BAM, ensuring robust transfer governance, technical risk assessment, process understanding, validation readiness, clear documentation of transfer requirements and lessons learned. Establish and maintain structured checklists, standards, governance processes, and sustainable knowledge-transfer practices for intra-site and inter-site technology transfers. Lead and implement efforts to improve manufacturing efficiency, process robustness, and operational excellence for clinical and commercial products, including troubleshooting manufacturing deviations, root cause investigations, process change controls, implementation and effectiveness reviews of CAPAs, data analytics, data mining, trending, process simulations, and digital process-intelligence approaches that strengthen process understanding and monitor commercial process health. Lead technical support for manufacturing activities, special events, site ramp-up activities, and new product introductions, ensuring effective coordination with Manufacturing, Quality, Engineering, Supply Chain, R&D, and Project Management to support successful execution and operational readiness. Establish and ensure alignment of technology requirements, technical capabilities, automation and digitalization priorities, and platform technologies with site strategy, future product needs, global standards, and long-term operational excellence objectives while identifying opportunities to leverage emerging technologies and industry best practices. Serve as a member of the site leadership team and the extended science and technology network, representing Technical Operations in site strategy, global TechOPS alignment, operational readiness, cross-site harmonization of technical standards, risk-management practices, and long-term technical strategy development across the network. Coach, develop, and retain internal technical talent by building future-ready capabilities, conducting after-action reviews, strengthening knowledge management, establishing best-practice guidelines, fostering accountability, innovation, and continuous improvement, and building a high-performing Technical Operations organization. Partner with cross-functional and global stakeholders across Supply Chain, Quality Control, Quality Assurance, Procurement, Production, Facilities, Engineering, Project Management, R&D, and Global TechOPS to drive COGS improvement, strengthen risk portfolio management, support regulatory inspections and inspection readiness, participate in GEMBA walks, oversee process-validation and PPQ activities, support pre-approval inspection preparation, and ensure appropriate technical documentation and CMC-related technical content. Promote process safety, equipment stewardship, and a state-of-the-art technical work environment. Qualifications Master's Degree in chemical, biochemical engineering, pharmaceuticals sciences or any other chemistry or engineering related fields or PhD in chemical, biochemical engineering, pharmaceuticals sciences or any other chemistry or engineering related fields 10+ years of GMP experience in pharmaceutical, biotech, CDMO, process development, manufacturing science, technical operations, or manufacturing operations, with strong exposure to clinical and commercial manufacturing environments. 5+ years of senior leadership experience in Technical Operations, manufacturing science, process development, or related technical functions, including leadership of cross-functional or matrix teams, technology transfers, process optimization, validation support, technical documentation, lifecycle management, and digital or data-driven improvement initiatives. Strong knowledge of GMP, quality systems, regulatory frameworks, validation expectations, process safety principles, and inspection-readiness requirements for pharmaceutical manufacturing. Demonstrated decision-making, analytical, troubleshooting, and problem-solving skills; familiar with Lean Six Sigma, operational excellence, data analytics, trending, and proactive process-monitoring approaches in manufacturing environments. Proven ability to lead and develop managers, technical experts, and cross-functional teams with diverse scientific, engineering, manufacturing, quality, and documentation backgrounds. Strong project and stakeholder management skills with the ability to communicate effectively with site leadership, global functions, customers, regulatory interfaces, and external stakeholders. Good understanding of business financial management, budget planning, CAPEX support, COGS improvement opportunities, and business-case development for technical operations and manufacturing technology investments. Proven ability to collaborate across multiple sites and functions, influence without direct authority, align stakeholders through matrix leadership, and implement global technical standards in local operations. Proven ability to build a high-performing Technical Operations organization, develop future-ready talent, drive change, and integrate new technologies, automation, digital tools, and innovation for operational excellence. Strong technical understanding of manufacturing processes, equipment, technology transfer, product stewardship, lifecycle management, CMC-related technical documentation, FMEA, SOPs, qualification protocols, ERP/MES systems, and process-intelligence tools. Annual Salary Range: $141,566.40 - $194,653.80 Placement of new hires in these wage ranges is based on several factors including education, skill sets, experience, and training. Total Rewards We offer all Team Members a total rewards package including competitive pay, annual performance bonus, a generous benefit package with comprehensive Medical/Dental/Vision coverage, 401(k) plan with employer contribution, and paid vacation, personal and sick days. Corporate Social Responsibility Bachem takes responsibility for future generations by a careful handling of resources and avoiding environmental risks. We continually improve our ecological performance and develop and implement new approaches for enhancing employees’ environmental awareness. EcoVadis has awarded Bachem Gold Medal status in their assessment of Bachem. Bachem Americas is an Equal Opportunity Employer As an equal opportunity employer, we celebrate the diversity of our team and are committed to building an inclusive workplace where individuals are hired and advanced based on merit, skills, and qualifications. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status, or other legally protected status. At Bachem, you’ll find a diverse, multicultural team. The (a) in the job title stands for all. We welcome applications from all candidates. What matters are your skills and motivation—regardless of age, gender, background, religion, or sexual orientation. Please note: unsolicited resumes from recruitment agencies will not be considered. Nearest Major Market: San Diego
Job Purpose: Our Testing Lab Technician will perform a variety of laboratory procedures of technical nature ensuring compliance with company, customer, industry and regulatory requirements. This position supports the business and our customers by performing standardized tests, producing and documenting reliable results, preparing technical reports and maintaining safe laboratory environment. Job Responsibilities: Conduct testing such as ISTA distribution and cold chain tests. Document test data and test reports using Good Documentation Practices. Interpret and execute industry test standards from organizations such as ISTA, ASTM, and customer protocols. Safely operate test lab equipment. Work on multiple projects simultaneously. Maintain responsive communication with sales reps and customers regarding test status, updates, and results. Work collaboratively with internal departments. Perform other duties as assigned. Additional Responsibilities & Qualifications: Minimum 1 year industry or testing lab experience or packaging related degree. Have a basic understanding of packaging principles and types of corrugated boxes. ISTA Packaging Dynamics Professional certification preferred. Ability to work independently, successfully manage accounts, work under pressure, and adapt to changes in the work environment is essential. CAD software experience (ArtiosCAD, Solidworks) preferred. Work Experience: 1-3 years of related job experience. Ability to work in a team environment. Ability to work quickly and efficiently. Excellent verbal, written, people, and diplomacy skills are required. Must be highly motivated, flexible and deadline driven. Proficient with Microsoft Office Suite. Strong customer service skills (friendly, courteous and helpful). Strong planning and organization skills are required. Strong problem-solving and attention to detail skills are required. Education: Bachelor's Degree Preferred Working Conditions and Physical Requirements: Ability to lift and move up to 50 pounds. Frequent standing, walking, bending, and reaching. Ability to handle packaging samples and testing equipment safely. Ability to work in both laboratory and warehouse environments. What We Offer Engaging and inclusive culture with employee-led Employee Resource Groups, Veritiv Cultural Alliance, recognition platform, etc. Extensive training opportunities, professional development programs, career pathing, and mentorship opportunities. Collaborative atmosphere with our customers and suppliers to create healthier, safer and more sustainable communities through our responsible operations and innovative solutions. Healthcare benefits (including medical, dental, vision, and health savings account), life, AD&D, and disability insurance, 401k, paid time off, tuition reimbursement, employee assistance program, and other fringe benefits. About Veritiv Together with its subsidiaries, Veritiv is the leading full-service provider of packaging solutions. Veritiv also provides JanSan, hygiene, print and publishing products and services. Veritiv serves customers in a wide range of industries, through team members around the world helping shape the success of its customers. For more information, visit www.veritiv.com and connect with the Company on LinkedIn. Veritiv is an Equal Opportunity/Affirmative Action employer. EEO Policy US | EEO Policy Mexico This description does not attempt to define the job's essential functions as defined by applicable disabilities law.
General Atomics Aeronautical Systems, Inc. (GA-ASI), an affiliate of General Atomics, is a world leader in proven, reliable remotely piloted aircraft and tactical reconnaissance radars, as well as advanced high-resolution surveillance systems. Under supervision, the Composite Technician Assembler is responsible for fabricating, assembling, and repairing advanced composite structures using materials such as carbon fiber, Kevlar, and fiberglass. This role involves reading and interpreting blueprints, preparing molds, and performing material lay-up, curing, and finishing processes. The technician assembles components by trimming, drilling, bonding, and fastening parts to meet precise engineering specifications. They ensure quality through detailed inspections and collaborate with other teams to resolve assembly challenges. Maintaining a safe and organized work environment is essential, as is adherence to safety procedures and documentation requirements. This position requires strong attention to detail, manual dexterity, and experience with composite materials or aerospace components. DUTIES & RESPONSIBILITIES: Part Alignment & Fit-Up: Precisely align and fit composite parts and subassemblies according to engineering drawings and specifications, ensuring proper orientation and fit between components. Bonding & Joining: Apply structural adhesives, sealants, and bonding agents to join composite components. Use proper techniques to ensure strong, durable bonds and prevent contamination. Mechanical Fastening: Install fasteners such as rivets, bolts, and screws using hand and power tools. Verify torque values and fastener placement according to specifications. Component Integration: Assemble complex structures by integrating hardware (inserts, bushings, brackets) and mating composite parts with metallic or non-metallic elements. Surface Preparation: Prepare bonding surfaces by sanding, cleaning, and treating as required to ensure optimal adhesion and structural integrity. Tooling & Fixtures: Set up and use assembly jigs, fixtures, and templates to maintain dimensional accuracy and repeatability during assembly processes. Functional Testing: Perform basic functional checks (fit, movement, alignment) and preliminary inspections to verify assembly quality before final inspection. Documentation: Record assembly steps, process parameters, and any deviations from standard procedures. Communicate findings and issues to supervisors or engineering teams. Collaboration: Work closely with engineering, quality, and fabrication teams to resolve assembly challenges and improve processes. Assist in the preparation of molds and forms. Mark and cut tape, woven material, honeycomb, adhesive and similar materials following templates, guides or specific dimensions and sequences following specific instruction. Route, drill, trim and sand to blueprint dimensions and tolerances. Maintain records as required. Support quality process by maintaining work area in an orderly condition by returning tools, equipment and material to storage areas. 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. Additional Functions: 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. Job Qualifications Typically requires High School diploma or equivalent. Must be customer focused and desirable knowledge of safety practices, OSHA, tool, equipment and materials used in the field. Knowledge of surface preparation, material and techniques for surface finishing. Must possess ability to read and interpret drawings to understand customer requirements. Physical ability to lift to 50 lbs. and ability to work from ladders. Interpersonal skills and written communication skills to work as a team. Be able to interface with employees and upper management from other departments and effectively communicate status of job and estimated completion dates. Ability to obtain and maintain a DoD secret clearance is required. Job Category Manufacturing Experience Level Entry-Level (0-2 years) Workstyle Onsite Full-Time/Part-Time Full-Time Hourly Pay Range Low 38,230 Pay Range High 56,838 Travel Percentage Required 0% - 25% Relocation Assistance Provided? No US Citizenship Required? Yes Clearance Required? Desired Clearance Level Secret Search Jobs at | General Atomics and Affiliated Companies
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 Chemist will be a part of the Small Volume Manufacturing team in Carlsbad supporting the small-scale manufacturing process and the experimental products M4Ward™program. The Small Volume team works closely with the R&D, Marketing, Quality Control and Engineering teams. The Small Volume team works to scale up and optimize production of new chemicals transferred from R&D and assist in transitioning production to high volume scale up as needed. Chemical SDS review to conduct and participate in safety reviews Supporting chemical purification by running purification systems and providing technical input on small scale chemical purifications. Perform chemical sampling and packaging and providing technical input on complex container fills and chemical handling Vessel cleaning and break down Maintaining a current chemical inventory Performing equipment setup, maintenance, and troubleshooting Maintaining a clean and efficient lab environment Physical Attributes: Wearing full face air-purifying respirator and other PPE Lifting to 50 pounds Standing, sitting, or walking for up to 8 hours Raising arms up to and possibly above 90-degree angle This is a Day-Shift position: Sunday – Thursday Hours operations 5am-1:30pm Who You Are Minimum Qualifications: Bachelor’s Degree in Chemistry, Biochemistry, Chemical Engineering, or related Life Science discipline. Preferred Qualifications: Knowledge of P&ID’s and basic engineering principles Experience working in gloveboxes Chemical distillation and sublimation knowledge Prior chemistry lab experience handling highly toxic chemicals, acids and bases Strong troubleshooting, documentation, and communication skills A strong focus on quality and safety Experience using Microsoft suite including (Word, Excel, Access, SharePoint) Experience using SAP, Intelex MOC, and LIMS systems Strong data analysis, attention-to-detail and organizational skills Pay Range for this position: $32.00-$50.00 per hour. 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!
At ACON labs, we are making a difference in medical care by offering medical devices for diagnosing a variety of conditions. In addition, we are able to streamline and reduce costs for the physician and/or patient directly. Come join us in developing the latest technologies that enhance human life and be a part of our growing, dynamic company. We are looking for a Production Equipment Maintenance Technician onsite at our San Diego location. The Production Equipment Maintenance Technician is responsible for the maintenance of production equipment and equipment verification in an ISO 13485 compliant manufacturing facility. Assigned tasks will be conducted in both routine and non-routine conditions. *Some Essential Duties and Responsibilities:* · Perform routine preventive maintenance and repairs on automated pneumatic and electromechanical medical device manufacturing equipment. · Troubleshoot equipment issues and implement solutions to minimize downtime. · Ensure the acceptance, daily maintenance, and timely repair of production equipment. · Collaborate with other departments to identify and implement process improvements. · Maintain equipment accounts, maintenance records, and malfunction maintenance records of production equipment. · Perform validation of equipment in production and other departments as needed. · Assist in training operators on standard equipment operation, adjusting and optimizing equipment operation procedures. · Adhere to all safety protocols and guidelines. *Education and /or Experience:* * High school diploma or equivalent required; technical certification or degree preferred, or an equivalency using a combination of education and experience. * Minimum of 3 years' experience in automated equipment maintenance in an FDA-regulated manufacturing environment. *Required Knowledge, Skills and Abilities:* * Experience with operating manual and semi-automated manufacturing equipment using gross and particularly fine motor skills are required. * Expected to display Good Manufacturing Practice (GMP) documentation habits and workmanship in a manufacturing environment according to SOPs or directed work instructions. * Must be able to communicate effectively across multiple audiences in a professional demeanor. * Ability to adapt and handle multiple and simultaneous assigned tasks. * Knowledge of quality systems for medical devices (ISO 13485 and FDA QSR) is preferred. * English fluency required. Bilingual in English/Spanish a plus. The salary range for this position takes into account a wide range of factors including education, experience, knowledge, skills, geography, and abilities of the candidate, in addition to internal equity and alignment with market data. At ACON it is not typical for an individual to be hired at or near the top range for their role and compensation decisions are dependent on the facts and circumstances of each case. The salary range for this position is $30.00 -$40.00 per hour. ACON offers a comprehensive benefits package including medical, dental, vision, life, and disability insurance, along with a 401(k) plan, employee assistance program, paid time off (including sick time), and paid Holidays. All benefits are non-contractual, and ACON may amend, terminate, or enhance the benefits provided, as it deems appropriate. Job Type: Full-time Pay: $30.00 - $40.00 per hour Benefits: * 401(k) * 401(k) matching * Dental insurance * Employee assistance program * Employee discount * Flexible spending account * Health insurance * Life insurance * Vision insurance Application Question(s): * How many years of experience do you have in automated equipment maintenance in an FDA regulated manufacturing environment? * How much experience do you have troubleshooting PLC or HMI systems? Experience: * Electrical troubleshooting: 3 years (Preferred) Work Location: In person