Looking to move to Carlsbad and want to connect with local employers? Fill out this form and we’ll help you get recruited.
GROW WITH US: Tandem Diabetes Care creates new possibilities for people living with diabetes, their loved ones, and their healthcare providers through a positively different experience. We’d love for you to team up with us to “innovate every day,” put “people first,” and take the “no-shortcuts” approach that has propelled us to become a leader in the diabetes technology industry. STAY AWESOME: Tandem Diabetes Care is proud to manufacture and sell the Tandem Mobi system and t:slim X2 insulin pump with Control-IQ+ technology — an advanced predictive algorithm that automates insulin delivery. But we’re so much more than that. Our company’s human-centered approach to design, development, and support delivers innovative products and services for people who use insulin. Because many of our own team members live with diabetes, or have a loved one impacted by diabetes, the work is personal, and we are committed to the cause. Learn more at tandemdiabetes.com A DAY IN THE LIFE: The Sr. Supplier Quality Engineer I is responsible for conducting and overseeing supplier audits, qualifying new suppliers, and monitoring the performance of current suppliers. An experienced team member providing quality guidance and support for supplier management activities such as qualifications, change notifications, audits, evaluations and performance to assure conformance to established standards, specifications and risk reduction. Acts as an instrumental member of the team to optimize and continuously improve supplier operations to meet department, business unit and company objectives. Provides suggestions, guidance and feedback to suppliers to ensure quality materials and components are delivered for use in Tandem’s product operations. The Sr. Supplier Quality Engineer I are also responsible for: Manage, lead and/or oversee supplier audits to meet company, quality, and regulatory requirements, including country-specific requirements for the suppliers; responsibilities extend to audits performed by 3rd party contractors. Generate, approve, review and monitor Supplier CAPA plans and activities to investigation and closure, including objective evidence of verification of effectiveness. Partner with Quality, process owners, legal and suppliers to create and revise Quality Agreements, as needed. Qualify, manage, and monitor supplier performance per Tandem supplier management approved processes. Identify gaps in current processes to develop, define, establish, and document new processes, as needed. Demonstrated ability to lead, develop, communicate & implement strategies for continuous improvement and development of existing or new suppliers and contract manufacturer. Ability to build relationships and work with suppliers or contract manufacturer to establish and maintain controlled consistent manufacturing processes and methods suitable to the nature of the components or assembly parts they supply. Independently leads and completes supplier activities such as supplier evaluations, change notifications, and validations. Facilitates quality oversite of Tandem’s 3rd party contract manufacturers. Ability to provide guidance to suppliers or contract manufacturer for quality engineering disciplines and statistics such as but not limited to PFMECA, DMAIC, Lean, Problem-Solving tools, capability analysis, DOE, IQ/OQ/PQ validations. Responsible for reporting quality trends and information to management on the performance of suppliers or contract manufacturers. Follows up with suppliers for component related non-conformances identified during Tandem’s incoming inspection, in-process inspection, final test, quality complaints, and as applicable product returns. WHEN & WHERE YOU’LL WORK: Hybrid: This role will be a mix of in-office work at our Barnes Canyon facility in San Diego, CA and remote work. This position is expected to be in office 2-3 days per week but may vary depending on business demands. WHAT YOU’LL NEED: Direct experience with suppliers and contract manufacturers who produce components or assembly parts in a regulatory environment. Proficient knowledge of Quality Engineering policies, principles and best practices including quality standards: ISO 13485, ISO 14971, ISO 9001 and other appropriate industry standards. Competent in QMS Audit and Process Audit practices with ability to readily recognize non-conformances. Must be able to explain audit results and influence other's understandings of audit observations in a culturally sensitive, tactful, and professional manner. Strong knowledge and application of principles outlined in Good Manufacturing Processes (GMP). Strong knowledge of and demonstrated experience using statistical techniques: sampling theory, probability, capability, and SPC. Strong knowledge of and demonstrated experience using problem solving methodologies: 5-why analysis, fault tree analysis, cause and effect diagram etc. Ability to work independently to identify potential quality issues and implement solutions. Understanding of mechanical drawings & specifications including geometric dimensioning and tolerances (GD&T). Able to assert own ideas and persuade others through effectively consolidating, evaluating, and presenting relevant information. EXTRA AWESOME: Bachelor’s degree in Engineering, preferably Electro-Mechanical Engineering or the equivalent education and applicable work experience. ISO lead auditor, Certified Quality Engineer, or equivalent preferred. Minimum 5 years’ related experience in Supplier Quality or related engineering positions Familiarity in the production of PCB, PCBA, electro-mechanical assemblies and plastic molding is highly desirable. Medical device manufacturing or FDA-regulated industry experience, highly preferred. Supplier or lead quality auditing experience in a regulated company, highly preferred. Experience in managing 3rd party contract manufacturers is a plus. COMPENSATION & BENEFITS: The starting base pay range for this position is $100,000 - $123,000 annually. Base pay will vary based on job-related knowledge, skills, experience and may also fluctuate depending on candidate’s location and the overall job market. In addition to base pay, Tandem offers a competitive compensation package that includes bonus and a robust benefits package. Tandem offers health care benefits such as medical, dental, vision available your first day, as well as health savings accounts and flexible saving accounts. You’ll also receive 11 paid holidays per year, a minimum of 20 days of paid time off (with accrual starting on day 1) and you will have access to a 401k plan with company match as well as an Employee Stock Purchase plan. Learn more about Tandem’s benefits here! YOU SHOULD KNOW: Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable state and local Fair Chance laws and regulations. A conditional offer of employment from Tandem is contingent upon successful completion of a pre-employment screening process comprised of a drug test (excluding marijuana) and background check, which includes a review of criminal history information. Tandem has good cause to conduct a review of criminal history information of candidates for this position, as this role may involve access to proprietary, sensitive and/or confidential information, including customer protected health information. This review is required to ensure that individuals in such roles uphold high standards of trust and integrity so as to protect the interests of our customers, employees, and stakeholders. SPONSORSHIP: Applicants must be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time. WHY YOU’LL LOVE WORKING HERE: At Tandem, we believe joy fuels excellence. That's why we've built a workplace that celebrates your achievements and supports your well-being. Our team thrives on pushing boundaries and fostering growth, all while maintaining a spirit of fun and camaraderie. This is just one of the ways we stay awesome! Explore the benefits and reasons to love Tandem at https://www.tandemdiabetes.com/careers. BE YOU, WITH US! We embrace the value that every single one of us brings to the table. But sometimes we forget that when we don’t meet 100% of a job description’s criteria – maybe you’re feeling that way right now? We encourage you to apply anyway. Because we want you to be you, with us. Tandem is firmly committed to being an equal opportunity employer and does not discriminate on the basis of age, disability, sex, race, religion or belief, gender identity or expression, marriage/civil partnership, pregnancy/maternity, or sexual orientation. We are an inclusive organization, and we welcome applications from a wide range of candidates. Selection for roles will be based on individual merit alone. REFERRALS: We love a good referral! If you know someone who would be a great fit for this position, please share! APPLICATION DEADLINE: The position will be posted until a final candidate is selected for the requisition or the requisition has a sufficient number of applications. Make a move that matters. Join Tandem Diabetes Care, where we're turning challenges into triumphs every day and where your talents will help shape a healthier, happier tomorrow. #LI-KT1 #LI-Hybrid
Company Overview Solecta is an exciting early-stage, high-tech company focused on solving real customer issues and commercializing polymeric industrial filtration products. Solecta has manufacturing facilities in Oceanside, CA. The company is backed by True North Venture Partners, an investing firm that specializes in commercializing and scaling disruptive innovations. Position Summary To ensure the manufacturing of company products is completed in alignment to prescribed production processes. Provide direction within assigned factory area to production associates. Ensures all operations are safely carried out, tac times are met or exceeded and established quality metrics are achieved. Develop a highly empowered, world-class team to deliver excellent efficiency results. Identify and drive the continuous improvement opportunities within production. Essential Duties and Responsibilities To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills and/or ability required. Other duties as assigned. Supervisory Responsibilities: Hires and trains front-line employees. Organizes, directs, and oversees the schedules and work of front-line employees. Provides constructive and timely performance evaluations. Handles discipline and termination of employees in accordance with company policy. Conducts interviews of potential candidates, tracks / reviews existing staff’s skill set, and issues disciplinary actions as required. Duties: Understands factory objectives and drives team to meet, safety, quality, productivity, and efficiency targets. Determines requirements for standard work instructions and procedures, reviews and provides feedback prior to production release. Has deep understanding of manufacturing processes production line balancing and equipment utilization. Identifies potential safety issues, presents corrective actions, communicates needed changes to Environment Health and Safety (EHS) and safety management team. Establishes process training requirements Uses data from process and develops opportunities for improvement. Tracks capacity utilization and develops plans to make improvements. Driver of 5S in assigned production area. Actively participates in companies change control process. Drives production continuous improvement efforts using lean methodologies. Maintains work area and equipment in a clean and orderly condition. Performs simple equipment maintenance and assists with troubleshooting in resolving machine issues. Skills Excellent verbal and written communication skills. Excellent analytical and technical problem-solving skills. Organizational skills and attention to detail. Time management skills with a proven ability to meet deadlines. Strong supervisory and leadership skills. Understanding of safety and health laws, regulations, and policies. Understanding of raw materials, production processes, quality control, cost management, and other effective manufacturing and distribution techniques. Proficient with Microsoft Office Suite (Microsoft Excel, Word & Email). or related software. Mathematical Skills (add, subtract, multiply, & divide quickly and correctly). Abilities Ability to function well in a high-paced and at times stressful environment. Ability to Communicate information and ideas clearly. This includes the ability to speak, read and write clearly and accurately in English. Ability to work in a team environment. Ability to multi-task. Self-starter with a drive to achieve personal mastery and successfully deliver on commitments Ability to wear protective equipment such as safety glasses, hair net, and hearing protection Ability to work extended hours as needed. Education and Experience Minimum Qualifications High School Diploma or G.E.D. Bachelor’s degree in engineering or science or a related field preferred. 5+ years of manufacturing experience preferred. Experience supervising teams of 10+ associates. Experience with continuous improvement and building a culture of commitment and ownership. Experienced with improving factory organization, throughput, productivity and costs with knowledge of associated incentive systems Knowledge of ERP systems within manufacturing environment NetSuite a plus. Experience working in Production/Manufacturing environment. Experience with assembly/equipment/automated manufacturing. Experience in Membrane Filtration industry. Lean Manufacturing knowledge. Continuous Improvement mindset. Bilingual preferred (English/Spanish). Physical Requirements Prolonged periods of standing and walking through the factory. Prolonged periods of sitting at a desk working on computers. Must be able to lift 50 pounds at times. Visual acuity to inspect products and machinery. Hearing and speaking to exchange information Dexterity of hands and fingers to demonstrate activities Operate a computer and other office productivity machinery Bending at the waist, kneeling or crouching Work Environment The work environment described here is representative of those an employee encounters while performing the essential functions of this job. Fast-paced manufacturing environment. This role routinely involves standard office equipment such as computers, phones, photocopiers, filing cabinets, etc. The role is exposed to a variety of conditions that may be found while walking the production floor. No travel will be required for this position. 80% of the time spent on the production floor and 20% in an office environment. Work extended hours as needed. Solecta, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. 2nd Shift, M-F, 1:30 pm - 10:15 pm
The Position A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche. The position is located in Oceanside, On-site. The schedule could include a rotating (10-12 hour shift), one weekend day, evening or night hours, or full off-shift hours. In this dynamic role, you will be responsible for producing innovative biotherapeutic medicine by interfacing with highly automated production systems and controls in cGMP manufacturing environment, and maintaining areas in high state of inspection preparedness. Responsibilities include: Training and Compliance: Provide coaching and training on best practices and compliance with Standard Operating Procedures (SOPs). Understand the theory, concepts, and regulations behind biopharma technology and processes. Production and Equipment Operation: Prepare solutions for the production process. Operate systems that clean and sterilize tanks and filtration systems. Operate automated systems for equipment operation and assemble/prepare equipment for production. Continuous Improvement and Troubleshooting: Participate in continuous operational improvement. Troubleshoot equipment and process issues and work with coworkers and supervisors for effective solutions. Documentation and Safety: Review documentation and check all calculations (e.g., tickets, labels, equipment readings). Comply with safety requirements, Good Manufacturing Practices (cGMP), SOP, and manufacturing documentation. Support and Reporting: Provide support to Manufacturing to meet production demands. Provide reports to management summarizing goal unit attainment and anticipate potential problems, taking preventative action as necessary. Supplementary Responsibilities Operate fermenters, centrifuges, other harvest systems and protein purifications units. Operate and clean fixed tank and filtration systems. Operate large scale column chromatography systems. Operate small-scale cell culture areas and systems by operating cleaning, set up, and maintaining 20L batch feed fermenters; inoculating and maintaining spinner seed cultures using aseptic techniques, maintaining cell banks; and performing general seed lab operations. Perform Solution Preparation activities (media and buffer make-up). Clean, assemble, and sterilize equipment using glass washers and autoclaves. Perform automated CIP and SIP of fixed equipment. Who you are: Minimum Qualifications: You have a degree in Life Sciences or Engineering and 1 year related experience, or Associate degree and 3 years experience, or High school and 5 years experience. You have a Biotech certificate from approved program. Physical conditions and PPE requirements: Expected to be on feet for 8 to 11 hours a day. May climb upwards of 6 flights of stairs a day to maneuver within the manufacturing facility Lifting up to 25lbs may be required. Environment requires that gowning in the form of hospital scrubs, bunny suits, gloves and steel toe boots be worn. Also, no make up or jewelry can be worn when working in the clean room environment. May work with hazardous materials and chemicals. All employees with jobs that require access to the Warehouse must be able to pass the Transportation Security Administration (TSA) Security Threat Assessment (STA). Follows established safety and environmental guidelines and procedures for all work performed. Immediately reports safety and environmental incidents including injuries, illnesses, near misses, and safety suggestions. Fosters a positive safety culture in which no one gets hurt. Relocation benefits are not available for this job posting. The expected salary range for this position based on the primary location for this position of Oceanside, CA is $43,300- $65,000. Actual pay will be determined based on experience, level, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below. This position also qualifies for the benefits detailed at the link provided below. Benefits Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants. JOB FACTS Job Sub Category Manufacturing Schedule Full time Job Type Regular Posted Date Jul 10th 2026 Job ID 202607-117708
Corporate Overview Argonaut Manufacturing Services Inc. is a contract manufacturing organization (CMO) headquartered in Carlsbad, CA with over 100,000 square feet of manufacturing space across four locations. The company is dedicated to serving highly innovative companies in the biopharmaceutical and molecular diagnostics industries. Argonaut is a full service, cost-effective partner, providing complete solutions in the areas of formulation, filling and final kitting of reagents and consumables. Argonaut provides quality and regulatory expertise to assure the highest in quality manufacturing and supply chain excellence. Benefits and Pay Range At Argonaut Manufacturing Services we value our employees and are proud to offer a comprehensive benefits package designed to support your well-being and financial future. Eligible employees enjoy: Medical, Dental, and Vision Insurance Company-Paid Life Insurance (1x Annual Salary) Voluntary Life Insurance Options Short-Term and Long-Term Disability Insurance Flexible Spending Account (FSA)Health Savings Account (HSA) 401(k) Retirement Plan with Company Matching 10 Days of Paid Time Off (PTO) 10 Paid Holidays Annually The pay range for this position is $105,000 - $115,000 annually. Actual compensation will be based on factors such as location, skills, education, experience, and other relevant qualifications. Position Overview We are seeking a Technical Writer to join our onsite manufacturing organization in a fast-paced contract manufacturing (CMO/CDMO) environment. This role is responsible for leading high-quality cGMP investigations, driving root cause elimination, and implementing sustainable corrective and preventative actions (CAPAs). The Specialist will play a critical role in advancing continuous improvement initiatives, enhancing process robustness, and improving process reliability. The ideal candidate combines strong technical writing, analytical problem-solving, and cross-functional collaboration to ensure regulatory compliance, reduce recurring quality events, and support inspection readiness. This role is 100% On-Site, Monday - Friday 8 hours/day (excluding lunch break). Overtime, weekends and holidays may be required. Flexible start time between 8:00am and 9:00am with a consistent schedule. Exceptions to the schedule must be approved by the manager in advance. Responsibilities and Duties InvestigationsContinuous Improvement Lead end-to-end cGMP investigations (deviations, non-conformances, complaints) with a focus on root cause identification, risk mitigation, and prevention of recurrence Apply structured root cause methodologies (e.g., 5 Whys, Fishbone, FMEA) to identify systemic issues and drive continuous improvement Develop, implement, and track CAPAs, ensuring effectiveness, sustainability, and measurable outcomes Analyze and trend data to identify recurring issues and improvement opportunities DocumentationQuality Systems Evaluate and collaborate on cGMP-compliant documentation, including SOPs, production records, studies, validation protocols, and reports Initiate and manage change controls in support of process, equipment, and continuous improvement initiatives Ensure documentation meets cGMP and FDA regulatory expectations, with a focus on clarity, accuracy, and compliance Cross-Functional Collaboration Partner with Manufacturing, Engineering, Facilities, Finance and Quality to implement process improvements Contribute to inspection readiness by maintaining high-quality investigation and documentation standards Lead interdepartmental continuous improvement initiatives Requirements and Qualifications Bachelor's degree in biology, Chemistry, Engineering, or related scientific discipline 5+ years of experience in investigations in a cGMP manufacturing, quality, or continuous improvement role (CMO/CDMO experience preferred) Demonstrated experience leading GMP investigations and authoring deviations, non-conformances, complaints, CAPAs, and change controls Strong technical writing skills with the ability to translate complex technical information into clear, compliant documentation Hands-on experience with root cause analysis tools (5 Whys, Fishbone, FMEA) and data trending/metrics analysis Working knowledge of cGMP regulations, FDA expectations, and Quality Systems Proven ability to collaborate effectively in a cross-functional, onsite manufacturing environment Proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook) Experience with eQMS/document management systems (MasterControl preferred) Preferred Qualifications Experience in a contract manufacturing (CDMO/CMO) environment supporting multiple clients Experience supporting regulatory inspections and client audits Experience using Enterprise resource planning (ERP) data in investigations Knowledge, SkillsAbilities Strong analytical thinking and problem-solving skills Excellent written and verbal communication Ability to manage multiple priorities and concurrent investigations Strong attention to detail and organizational skills Sound judgment balancing compliance, quality, and business needs Ability to work independently with minimal supervision Argonaut Manufacturing Services, Inc. is proud to be an equal opportunity employer committed to providing employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age or disability, or any other class protected by Federal, State or local laws. Argonaut complies will all employment eligibility verification requirements of the Immigration and Nationality Act and all must have the authorization to work in the US.
The Position A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche. The position is located in Oceanside, On-site. The schedule could include a rotating (10-12 hour shift), one weekend day, evening or night hours, or full off-shift hours. In this dynamic role, you will be responsible for producing innovative biotherapeutic medicine by interfacing with highly automated production systems and controls in cGMP manufacturing environment, and maintaining areas in high state of inspection preparedness. Responsibilities include: Training and Compliance: Provide coaching and training on best practices and compliance with Standard Operating Procedures (SOPs). Understand the theory, concepts, and regulations behind biopharma technology and processes. Production and Equipment Operation: Prepare solutions for the production process. Operate systems that clean and sterilize tanks and filtration systems. Operate automated systems for equipment operation and assemble/prepare equipment for production. Continuous Improvement and Troubleshooting: Participate in continuous operational improvement. Troubleshoot equipment and process issues and work with coworkers and supervisors for effective solutions. Documentation and Safety: Review documentation and check all calculations (e.g., tickets, labels, equipment readings). Comply with safety requirements, Good Manufacturing Practices (cGMP), SOP, and manufacturing documentation. Support and Reporting: Provide support to Manufacturing to meet production demands. Provide reports to management summarizing goal unit attainment and anticipate potential problems, taking preventative action as necessary. Supplementary Responsibilities Operate fermenters, centrifuges, other harvest systems and protein purifications units. Operate and clean fixed tank and filtration systems. Operate large scale column chromatography systems. Operate small-scale cell culture areas and systems by operating cleaning, set up, and maintaining 20L batch feed fermenters; inoculating and maintaining spinner seed cultures using aseptic techniques, maintaining cell banks; and performing general seed lab operations. Perform Solution Preparation activities (media and buffer make-up). Clean, assemble, and sterilize equipment using glass washers and autoclaves. Perform automated CIP and SIP of fixed equipment. Who you are: Minimum Qualifications: You have a degree in Life Sciences or Engineering and 1 year related experience, or Associate degree and 3 years experience, or High school and 5 years experience. You have a Biotech certificate from approved program. Physical conditions and PPE requirements: Expected to be on feet for 8 to 11 hours a day. May climb upwards of 6 flights of stairs a day to maneuver within the manufacturing facility Lifting up to 25lbs may be required. Environment requires that gowning in the form of hospital scrubs, bunny suits, gloves and steel toe boots be worn. Also, no make up or jewelry can be worn when working in the clean room environment. May work with hazardous materials and chemicals. All employees with jobs that require access to the Warehouse must be able to pass the Transportation Security Administration (TSA) Security Threat Assessment (STA). Follows established safety and environmental guidelines and procedures for all work performed. Immediately reports safety and environmental incidents including injuries, illnesses, near misses, and safety suggestions. Fosters a positive safety culture in which no one gets hurt. Relocation benefits are not available for this job posting. The expected salary range for this position based on the primary location for this position of Oceanside, CA is $43,300- $65,000. Actual pay will be determined based on experience, level, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below. This position also qualifies for the benefits detailed at the link provided below. Benefits Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws. If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.
Corporate Overview Argonaut Manufacturing Services Inc. is a contract manufacturing organization (CMO) headquartered in Carlsbad, CA. The company is dedicated to serving highly innovative companies in the biopharmaceutical, life sciences and molecular diagnostics industries. Argonaut is a full service, cost-effective partner, providing complete solutions in the areas of formulation, filling and final kitting of reagents and consumables. Argonaut provides quality and regulatory expertise to assure the highest in quality manufacturing and supply chain excellence. Benefits and Pay Range At Argonaut Manufacturing Services we value our employees and are proud to offer a comprehensive benefits package designed to support your well-being and financial future. Eligible employees enjoy: Medical, Dental, and Vision Insurance Company-Paid Life Insurance (1x Annual Salary) Voluntary Life Insurance Options Short-Term and Long-Term Disability Insurance Flexible Spending Account (FSA)Health Savings Account (HSA) 401(k) Retirement Plan with Company Matching 10 Days of Paid Time Off (PTO) 10 Paid Holidays Annually The pay range for this position is $110,000 - $149,000 annually. Actual compensation will be based on factors such as location, skills, education, experience, and other relevant qualifications. Position Overview Argonaut Program Managers (PMs) are responsible for managing cross-functional activities for a portfolio of clients in domestic and international markets, overseeing all aspects and management of development and/or cGMP manufacturing projects. PMs are accountable for project scope development, creating comprehensive schedules, monitoring deliverables and milestones, contributing to feasibility studies, and marshalling internal colleagues and subject matter experts to deliver on-time and on-budget for Argonaut clientele. This role is 100% on-site position Monday - Friday 8 hours/day (excluding lunch break). Overtime, weekends and holidays may be required. Flexible start time between 7:00 am - 9:00 with a consistent schedule. Exceptions to the schedule must be approved by the manager in advance. Responsibilities and Duties Lead, build and oversee multiple cross-functional project teams of representatives from relevant functions; chair internal and customer project teams Develop full-scale project plans / schedules with work breakdown structure; define, track, and maintain accountability for milestones, schedules, and timelines Responsible for overall project knowledge and execution according to agreed upon deliverables and timelines Identify and manage project dependencies and critical path and go / no-go decisions Perform risk assessments and propose risk mitigation strategies for projects Prepare weekly / monthly reports, agendas, meeting minutes, and presentations Communicate all project issues / needs to both internal and external stakeholders, and provide frequent presentations on project status to Executive Management Customer contact on all project related issues and communication; ensure appropriate and timely communication is maintained Evaluate, highlight, and escalate unresolved issues, potential obstacles, and resource constraints to supervisor and / or key stakeholders Represent the "Voice of the Client" while maintaining primary allegiance to Argonaut and colleagues Assist and contribute as needed to the quoting process for Change Orders and new business opportunities Communicate any changes in project scope with internal teams and Business Development; communicate clearly to the clients and ensure changes are fully documented Assist Business Development in maintaining and nurturing client relationships Strategic portfolio overview within Commercial/Program Management Organization Identify, contribute to, and lead internal initiatives for continuous improvement of business processes, project delivery and profitability Change management and training of colleagues within and outside the department aimed at improving performance on projects Requirements and Qualifications The successful candidate will work out of our offices based in Carlsbad CA - this is not a remote position Bachelor's degree in a scientific related discipline (BSc / MSc / B Eng / MEng Chemistry / Molecular Biology / Engineering or relevant discipline; project Management accreditation (PMP preferred). Minimum of 3 years of project management experience (life science CMO / CDMO preferred); Strong working knowledge of laboratory techniques and manufacturing. Experience with ERP software (Netsuite preferred), MS Office (MS Excel a must), MS Project (or similar Project Management platforms such as Jira) and MasterControl (or similar QMS) Deadline-driven with a high level of organizational and planning skills; results oriented Strong analytical, problem-solving / solutions orientation; intellectual curiosity Thrives on collaboration, openness, and a shared sense of purpose - able to influence without authority; capable of working independently as required Proven multi-tasking skills with ability to handle multiple projects simultaneously, motivate teams, work within aggressive timelines collaboratively with cross-functional departments; capable of effectively managing competing priorities; presenting ideas clearly and concisely Exceptional client service/focus and interpersonal skills; work effectively under pressure to meet deadlines; exceptional oral and written communication skills Argonaut Manufacturing Services, Inc. is proud to be an equal opportunity employer committed to providing employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age or disability, or any other class protected by Federal, State or local laws. Argonaut complies with all employment eligibility verification requirements of the Immigration and Nationality Act and all must have the authorization to work in the US.
Corporate Overview Argonaut Manufacturing Services Inc. is a contract manufacturing organization (CMO) headquartered in Carlsbad, CA with over 100,000 square feet of manufacturing space across four locations. The company is dedicated to serving highly innovative companies in the biopharmaceutical and molecular diagnostics industries. Argonaut is a full service, cost-effective partner, providing complete solutions in the areas of formulation, filling and final kitting of reagents and consumables. Argonaut provides quality and regulatory expertise to assure the highest in quality manufacturing and supply chain excellence. Benefits and Pay Range At Argonaut Manufacturing Services we value our employees and are proud to offer a comprehensive benefits package designed to support your well-being and financial future. Eligible employees enjoy: Medical, Dental, and Vision Insurance Company-Paid Life Insurance (1x Annual Salary) Voluntary Life Insurance Options Short-Term and Long-Term Disability Insurance Flexible Spending Account (FSA)Health Savings Account (HSA) 401(k) Retirement Plan with Company Matching 10 Days of Paid Time Off (PTO) 10 Paid Holidays Annually The pay range for this position is $130,000 - $140,000 annually. Actual compensation will be based on factors such as location, skills, education, experience, and other relevant qualifications. Position Overview The purpose of this position is to provide support services by means of executing the analysis of in-process, finished product and stability test samples. Further support services includes processing and testing of environmental monitoring and raw material samples. QC personnel are responsible for compliance to QC policies and procedures within the QC laboratory, company policies, and cGMP guidelines. This position will report to the Director, Quality Control. This role is an on-site position Monday - Friday 8 hours/day (excluding lunch break). Overtime, weekends and holidays may be required. Flexible start time between 7:00 am - 9:00 am with a consistent schedule. Responsibilities and Duties Management of incoming samples utilizing a laboratory information system (LIMS) or other means. Perform detailed chemical analysis of samples from production, routine monitoring, stability and validation or qualification studies using compendial and non-compendial methods Utilize advanced instruments such as HPLC/UHPLC, SoloVPE, Maurice (cIEF and SDS Page), FTIR and UV/Vis Spectrophotometers Author protocols and reports including but not limited to, method qualification, method verification, method validation and method suitability. Apply and adhere to data integrity principals to sample handling and analysis Manage deviation/OOS investigations and implement CAPAs and change controls per GMP requirements Author and revise QC related SOPs as required Interface with product Sponsors on QC related inquiries. Participate in the review and approval of Manufacturing Batch Records for QC related activities Execute analytical method transfer activities, including product-specific test methods Train junior personnel in appropriate laboratory and safety procedures Execute Installation and Operational Qualification of analytical instrumentation where applicable Directly contributes to daily laboratory operations for QC Chemistry in full compliance with applicable SOPs and safety guidelines Requirements and Qualifications Undergraduate degree (B.A. or B.S.) in a Life Science discipline A minimum of 7 years' experience in a GMP-compliant Quality Control function within the medical device and/or biopharmaceutical fields A high level of personal and professional integrity and trustworthiness with strong work ethic and the ability to work independently with minimal direction Analytical experience in the following methodologies: Buffer Characterization (pH, conductivity, osmolality), Concentration (UV/Vis and/or Fluorescence), Chromatography (HPLC, Electrophoresis) The ability to work effectively within cross functional teams comprised of Manufacturing, Tech Transfer, Quality Assurance, and Senior Management An affinity for precise and detailed documentation skills. The ability to effectively influence and contribute to a dynamic and fast-paced work environment A strong work ethic and a high level of accountability Strong oral and written communication and listening skills Excellent Problem-solving skills Argonaut Manufacturing Services, Inc. is proud to be an equal opportunity employer committed to providing employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age or disability, or any other class protected by Federal, State or local laws. Argonaut complies will all employment eligibility verification requirements of the Immigration and Nationality Act and all must have the authorization to work in the US.
Sr. Automation Engineer .buttontext2321358db7e7bf1e a{ border: 1px solid transparent; } .buttontext2321358db7e7bf1e a: focus{ border: 1px dashed #004080 !important; outline: none !important; } Bachem is a leading, innovation-driven company specializing in the development and manufacture of peptides and oligonucleotides. With over 50 years of experience and expertise Bachem provides products for research, clinical development and commercial application to pharmaceutical and biotechnology companies worldwide and offers a comprehensive range of services. Bachem operates internationally with headquarters in Switzerland and locations in Europe, the US and Asia. The company is listed on the SIX Swiss Exchange. For further information, see www.bachem.com. A brief overview The Sr. Automation Engineer manages automation systems and projects within a regulated pharmaceutical manufacturing environment, conducting design evaluations and recommending improvements to enhance product quality and operational efficiency. The role defines required hardware, software, and network architecture, and drives project milestones to design, develop, and optimize process automation while supporting cross‑functional project teams. What you will do Responsible for Installation and qualification of automation systems for batch processing tanks, solvent recovery system, filter dryers, HPLCs, filtration system, Lyophilizers, ultra-low freezers, HVAC, solvent distribution and recovery system, compressed air, purified water, and wastewater system. Collaborate with production and controls team to develop and streamline production process in automating the new and existing system by harmonizing and leveraging technology developed by Center of Excellence (Bachem Headquarters). Develop and train cross-functional team members on utilization and maintaining new automation systems for equipment and system – by creating roadmap, improving existing process, creating new procedures, job aids, SOPs and protocols as well as training of staff for these expectations. Troubleshoot and monitor automation systems and trends to ensure that equipment works to its specifications and appropriate capacities Support engineering team and coordinates engineering activities to design, develop, and execute the automation part of strategic investment projects. Ensures compliance of company policies, procedures and objectives regarding processes, initiatives, and projects Qualifications Bachelor's degree in engineering or related field, or 8+ years of qualified work experience in lieu of degree Minimum of 5 years’ qualified work experience Experience with SCADA/HMI platforms, such as Ignition, FactoryTalk View ME/SE, and WinCC. Experience with industrial fieldbus communication protocols such as Ethernet/IP, and ProfNet, and the ability to implement system network topology for Ethernet and serial communications. Experience with Copadata Zenon, Ignition, and PlantPAX SCADA platforms Experience with Omron PLC/IO, iFIX. Experience with BACnet/IP and MSTP protocols and BMS systems. Experience with OSI PI, Zenon, and MSSQL Working Knowledge of ISA and IEE Standards and Industry Codes as they relate to Chemical, Pharmaceutical facilities, or related facilities. Knowledge of NEC, UL 508A. Working Knowledge of ISA and IEE Standards and Industry Code as it relates to Chemical, Pharmaceutical facilities or related facilities Knowledge of NEC, UL, and FDA title 21 standards and requirements Technical knowledge of automation, controls, instrumentation, batch programming, Programmable Logic Controllers, Distributed Control Systems, Supervisory Control and Data Acquisition systems, Building Automation Systems, IT and OT networks and technologies Knowledge of batch processing and recipe management Direct complete project life cycle from design, planning, and implementation to validation. Act as project manager across multiple projects Experience with electrical and program troubleshooting Ability to safely work with electrical circuits up to 480VAC Excellent written and oral communication skills Ability to effectively organize, multitask, and work in a fast-paced, deadline driven work environment Detail oriented with the ability to troubleshoot and resolve problems. Ability to work independently, manage one’s time, and function well in a team environment Base salary range: $118,004 - $162,256 Placement of new hires in this wage range 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. .buttontext71be19411ba8c841 a{ border: 1px solid transparent; } .buttontext71be19411ba8c841 a: focus{ border: 1px dashed #004080 !important; outline: none !important; } 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. .right-align { text-align: right; } Nearest Major Market: San Diego
Corporate Overview Argonaut Manufacturing Services Inc. is a contract manufacturing organization (CMO) headquartered in Carlsbad, CA. The company is dedicated to serving highly innovative companies in the biopharmaceutical and molecular diagnostics industries. Argonaut is a full service, cost-effective partner, providing complete solutions in the areas of formulation, filling and final kitting of reagents and consumables. Argonaut provides quality and regulatory expertise to assure the highest in quality manufacturing and supply chain excellence. Benefits and Pay Range Benefits for this position are available, subject to applicable eligibility requirements. These include: Medical, Dental, and Vision Insurance Company-Paid Life Insurance (equal to 1X annual salary) Voluntary Life Insurance Options Long-Term and Short-Term Disability Insurance Flexible Spending Account (FSA) and Health Savings Account (HSA) 401(K) Retirement Plan 10 Days of Paid Time Off (PTO) 10 Paid Holidays Annually The pay range for this position is between $33.00 - $45.00 per hour. Factors which may affect starting pay within this range may include geography/market, skills, education, experience, and other qualifications of the successful candidate. Position Overview The purpose of this position is to provide support services to QC and manufacturing, primarily by receiving and testing raw materials, and managing shipping of materials and products to customers and 3rd party testing labs. The QC Associate may also support the QC department by means of executing the analysis of in-process, finished product, and stability test samples. QC personnel are responsible for compliance with QC policies and procedures within the QC laboratory, company policies, and cGMP guidelines. This position will report to the Director, Quality Control. This role is an on-site position Monday - Friday 8 hours/day (excluding lunch break). Overtime, weekends and holidays may be required. Flexible start time between 7:00 am - 9:00 am with a consistent schedule. Exceptions to the schedule must be approved by the manager in advance. Responsibilities and Duties Execute incoming inspection of raw materials in accordance with company policy and procedures Oversee sample receipt and disposition for testing within the QC lab Assist in the expedition of test sample shipment to sponsors and 3rd party laboratories Execute deviation/OOS investigations and implement CAPAs and change controls per GMP requirements, as needed Directly contributes to daily laboratory operations for QC Chemistry in full compliance with applicable SOPs and safety guidelines Occasionally analyzes in-process, release, and stability test samples in accordance with established QC test methods and specifications May assist in the execution of analytical method transfer activities, including product-specific test methods Assists QA in calibration/preventive maintenance activities associated with lab instrumentation Requirements and Qualifications Undergraduate degree (B.A. or B.S.) in a Life Science discipline Applicable academic or industrial laboratory experience High-level of personal and professional integrity and trustworthiness with strong work ethic and the ability to work independently with minimal direction 5-10 years' GMP experience in a Quality Control function within the biopharmaceutical field Experience with raw materials and sample management in a GMP environment The ability to perform daily tasks with a keen attention to detail An affinity for precise and detailed documentation skills The ability to work effectively and contribute to a dynamic and fast-paced work environment Well-developed oral communication and listening skills Argonaut Manufacturing Services, Inc. is proud to be an equal opportunity employer committed to providing employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age or disability, or any other class protected by Federal, State or local laws. Argonaut complies will all employment eligibility verification requirements of the Immigration and Nationality Act and all must have the authorization to work in the US.
Advanced Test Equipment Corporation (ATEC) is seeking a detail-oriented *Quality Test Technician* to support quality assurance and order fulfillment activities for rental and sale equipment. This role plays a critical part in ensuring equipment is fully functional, complete, and customer-ready prior to shipment while supporting ATEC’s Quality Management System (QMS) and operational excellence. *Key Responsibilities* *Quality Inspection & Functional Verification* * Perform functional checks on returned rental equipment using approved QA checklists * Verify equipment configuration, accessories, and overall condition to ensure completeness and readiness for shipment * Ensure equipment is clean, presentable, and meets company quality standards prior to release *Documentation & Systems* * Accurately record inspection and function check results in *Fluke Met/Team Asset Management Software* * Document findings to support traceability, audit readiness, and compliance with the Quality Management System (QMS) * Maintain organized and accurate records in accordance with company procedures *Issue Identification & Escalation* * Identify out-of-tolerance conditions, discrepancies, or failures * Escalate technical or quality issues to the Laboratory or Quality team as appropriate * Confirm and validate “Failed in Field” issues reported through Technical Support cases *Cross-Functional Collaboration* * Coordinate with Quality, Laboratory, Order Processing, Shipping, and Technical Support teams * Support resolution of order-related issues, shipment holds, and quality concerns * Assist in ensuring on-time, accurate order fulfillment and shipment readiness *Operational Support* * Support shipment readiness by re-verifying equipment following corrective actions * Assist with troubleshooting and basic issue reproduction for escalation to technical team. * Contribute to continuous improvement by identifying recurring quality issues *What You Bring* * Familiarity with quality systems, inspection processes, or ISO-based environments (ISO 9001 / ISO 17025 preferred) * Strong attention to detail and documentation accuracy * Ability to follow SOPs, checklists, and work instructions Pay: $28.00 - $31.00 per hour Benefits: * 401(k) * 401(k) matching * Dental insurance * Employee assistance program * Employee discount * Flexible spending account * Health insurance * Life insurance * On-the-job training * Professional development assistance * Referral program * Tuition reimbursement * Vision insurance Work Location: In person
General Atomics Electromagnetic Systems (GA-EMS) designs and manufactures first-of-a-kind electromagnetic and electric power generation systems. GA-EMS’ expanding portfolio of specialized products and integrated system solutions support critical fleet, space systems and satellites, missile defense, power and energy, and process and monitoring applications for defense, industrial, and commercial customers worldwide. With consultative direction, this position is responsible for supporting the manufacturing production process, with focus on the design, development, and implementation of new or revised production processes for the efficient and economical fabrication of parts, components, sub-assemblies, and final assemblies. DUTIES AND RESPONSIBILITIES: Develops, implements, and maintains methods, operation sequence and processes in the manufacture or fabrication of parts, components, sub-assemblies, and final assemblies. Applies technical knowledge to analyze, investigate and resolve manufacturing and engineering related problems. Designs the sequence of production operations, specifying procedures for the fabrication of applicable tools and equipment, and adapting machinery. Collaborates with product design engineering on technical specifications that will best utilize equipment and manufacturing techniques. Investigates, dispositions and justifies product, drawing, and specification non conformances. Estimates manufacturing costs and determines time standards. Ensures that production processes and procedures are in compliance with regulations. Maintains records and reporting systems for coordination of manufacturing operations. Performs supplier audit and oversight as necessary to ensure conforming product being delivered. Communicates technical responses to supply base questions during proposal efforts, manufacturing efforts and post manufacturing efforts. Supports on-site supplier kick off meetings to discuss manufacturing plan, schedule and supplier deliverables. Assist with development, status and needs of the project plan to the Control Account Manager. Maintains the strict confidentiality of sensitive information. Performs other duties as assigned. 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. 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 a bachelors in engineering or a related technical field as well as fourteen or more years of manufacturing engineering experience. May substitute equivalent experience in lieu of education. Experience in LEADING teams to up-scale production lines across the entire manufacturing process using lean principles (Define Value, Value Stream Mapping, Creating Flow, Establish Pull, ect). Extensive knowledge in both Operations and Manufacturing Engineering disciplines related to complex welded and machined parts preferred Must possess the ability to understand new concepts quickly and apply them accurately throughout an evolving environment and organize work assignments to meet established timetables. Good communication, computer, documentation, presentation, and interpersonal skills are required, as well as the ability to work both independently and as part of a team. Ability to obtain and maintain DoD Secret Clearance. Job Category Engineering Experience Level Senior (8+ years) Workstyle Onsite Full-Time/Part-Time Full-Time Salary Pay Range Low 116,480 Pay Range High 208,505 Travel Percentage Required 0% - 25% Relocation Assistance Provided? Yes US Citizenship Required? Yes Clearance Required? No Search Jobs at | General Atomics and Affiliated Companies
Technician Putter Engineering performs custom golf club assembly assignments of a non-routing nature and with significant complexity and variety. This position is responsible for in-house custom building of primarily putters, but may extend to other clubs when necessary Essential Functions and Key Responsibilities: Perform putter and golf club assembly to a high degree of technical specifications with quality and accuracy Modify standard components and finished product to meet special technical requirements Provide and assist golf professionals with company products and service by adjusting, repairing or replacing component parts Service and repair finished products when necessary. May troubleshoot finished product and make simple repairs as specified or deemed necessary. May make simple adjustments to correct minor deficiencies or meet individual requirements Perform routine analysis to check accuracy, applicability and reasonableness of specifications to finished product Inspect component parts for flaws, scratches or other cosmetic defects to ensure quality workmanship of product Follow prescribed work methods or explicit instruction Maintain equipment and tools necessary for use in area of assignment Perform work in accordance with sound safety practices Assist RDE in prototyping products on an adhoc basis Performs other related duties and assignments as required Knowledge and Skills Requirements: Ability to communicate fluently in English both verbally and in writing and demonstrated skills in reading and following written directions in English Strong interpersonal and public relations skills to deal courteously and professionally with tour professionals and cross-functional co-workers Strong knowledge of golf terminology and design, including club assembly process and related standards Advanced custom club assembly skills, including loft, lie, and face angles Considerable knowledge of the methods, materials, tools and practices used in the building and design of product Proficient in simple arithmetic skills and ability to read measurement tools Strong attention to detail and ability to detect defects and make proper recommendations or repairs Demonstrated skill in the use of standard equipment and hand tools specific to area of assignment Grinding, cutting and sandblasting abilities with different metal types preferred Preferred ability to use CNC milling machine in order to engrave lines, initials, names and logos to golf club heads Proficient in Microsoft Suite (Word, Excel, Outlook, PowerPoint, Access, Project Education, Work Experience, and Professional Certifications: High School graduate or equivalent GED required 1 year additional technical or trade school education above high school level preferred 5+ years of experience regarding modification of existing putter parts in order to create non-standard clubs strongly preferred Experience with CNC milling machines preferred Passion/interest/knowledge for competitive golf preferred Experience with modern tools (AI) preferred Work Environment / Physical Requirements: Normal office conditions Primarily lab/warehouse environment, exposure to irritant fumes, solvent, dirt, dust and noise and varying temperature conditions Ability to stand for prolonged periods of time Ability to work extended hours as necessary Able to work efficiently and accurately in an atmosphere of frequent interruption Light physical effort equal to frequent lifting or moving of lightweight materials TaylorMade is a performance driven organization and our total rewards approach to compensation is designed to support this. We consider many factors in determining base compensation, including position scope, job related knowledge, education, skills, experience, and work location. The expected hourly rate for this position is $25 - $30 per hour. Additional benefits, such as health & wellness, performance bonuses, product discounts, holidays, paid time off, etc. may also be offered in accordance with our plans. #LI-onsite #LI-ZH1 TaylorMade Golf Company is an equal opportunity employer. All qualified applicants receive consideration for employment without regard to race, religious creed, color, national origin or ancestry, physical or mental disability, medical condition, genetic information, marital status, sex, pregnancy, gender, gender identity, gender expression, age, sexual orientation, military and veteran status or any other basis protected by federal, state or local law, ordinance, or regulation.