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About us: One team. Global challenges. Infinite opportunities. At Viasat, we’re on a mission to deliver connections with the capacity to change the world. For more than 35 years, Viasat has helped shape how consumers, businesses, governments and militaries around the globe communicate. We’re looking for people who think big, act fearlessly, and create an inclusive environment that drives positive impact to join our team. What you'll do: Support multiple networking communication products currently in production and future Next Generator products within Viasat Government - Secure Network Systems (SNS). Your responsibilities will include: becoming familiar with the technical design of multiple product lines and working with team members to address a variety of issues, supporting efforts to troubleshoot technical issues from production and the field, supporting qualification efforts for component changes, aiding the transition of prototype units to low rate initial production, lab support and management, setting up and maintaining test and development hardware, and board checkout. The day-to-day: Hands on experience troubleshooting of complex digital systems (Processors, memory, FPGAs, CPLD, microcontrollers) Use of both Windows and Linux operating systems to develop and execute tests Knowledge and use of scripting languages, e.g. PERL, PYTHON a plus Work closely with engineers to devise and monitor tests for troubleshooting problem Identify rework needed to isolate and/or repair problems Integrate and debug design in the laboratory What you'll need: 5+ years hardware troubleshooting or sustaining experience US citizenship and ability to obtain and maintain a SECRET security clearance is required Must be able to prioritize, be detail oriented, and have a history of managing time well to accomplish multiple tasks in parallel Strong written and verbal communication skills, ability to work with a temporally and geographically diverse team Ability to document and report on technical solutions/findings Good working knowledge of MS Office products for documentation creation and modification Familiarity with standard test equipment (i.e., oscilloscopes, spectrum analyzer, power supplies, etc.) Desire to be part of a multidisciplinary team to evaluate and troubleshoot production related issues Ability to travel up to 10% What will help you on the job: Associate’s or Bachelor’s Degree in Electrical Engineering or Computer Engineering Active Security Clearance Familiarity with TCL, Perl, Python or another scripting language Proven experience in debugging, diagnosing, and solving embedded designs issues Familiarity with production-related processes and common failure modes High aptitude for learning Ability to work independently, take initiative, take ownership of tasks and results #LI-BBS Salary range: $28.61 - $45.19 / hourly. For specific work locations within San Jose, the San Francisco Bay area and New York City metropolitan area, the base pay range for this role is $35.58 - $53.37/ hourly : At Viasat, we consider many factors when it comes to compensation, including the scope of the position as well as your background and experience. Base pay may vary depending on job-related knowledge, skills, and experience. Additional cash or stock incentives may be provided as part of the compensation package, in addition to a range of medical, financial, and/or other benefits, dependent on the position offered. Learn more about Viasat’s comprehensive benefit offerings that are focused on your holistic health and wellness at https://careers.viasat.com/benefits. EEO statement: Viasat is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, ancestry, physical or mental disability, medical condition, marital status, genetics, age, or veteran status or any other applicable legally protected status or characteristic. If you would like to request an accommodation on the basis of disability for completing this on-line application, please click here.
Job Id 291935 Carlsbad, California, United States Job Type Full-time Work Your Magic with us! Start your next chapter and join EMD Electronics. Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. Everything we do in EMD Electronics is to help us deliver on our purpose of being the company behind the companies, advancing digital living. We are dedicated to being the trusted supplier of high-tech materials, services and specialty chemicals for the electronics, automotive and cosmetics industries. We foster a global collaborative organization made up of individuals who have the passion to win, obsess about the customer, are relentlessly curious and act with urgency. Together, we push the boundaries of science to make more possible for our customers. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: The Operations Technician will be part of the Chemical Manufacturing team in Carlsbad, CA. The team of Operations Technicians are responsible for receiving, decontaminating, rebuilding, and filling our vessels with ultra-pure chemistries. Specific Responsibilities Include: Conduct manual and automated decontamination of vessels Perform hazardous waste consolidation Perform weekly and monthly regulatory compliance activities Acid-wash stainless steel and quartz vessels Maintain a clean and organized manufacturing environment Support receiving by unloading trucks Assist the Engineering team with troubleshooting system issues Perform data entry task Document and Inspect vessels to ensure quality Physical Attributes: Wear a full-face air-purifying respirator and other PPE Lift up to 50 pounds Location/shift: Onsite position in Carlsbad, CA – day shift Who You Are Minimum Qualifications: High School Diploma or GED 1+ years working in chemical, manufacturing or production. Preferred Qualifications: Experience handling chemicals Background in a fast-paced manufacturing environment Strong skills in troubleshooting, documentation, and communication Ability to read and understand Safety Data Sheets and written work instructions High focus on quality and safety Proficient using Microsoft suite (Word, Excel, Access, SharePoint) Experience with SAP Ability to use hand tools Pay Range for this position: $23.00 - $36.00/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! and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity! US Equal Employment Opportunities The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination. Massachusetts Disclosure It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability. Notice on Fraudulent Job Offers Unfortunately, we are aware of third parties that pretend to represent our company offering unauthorized employment opportunities. If you think a fraudulent source is offering you a job, please have a look at the following information here. WHAT WE OFFER Money makes the world go round. But at our company there’s more than just financial rewards. We offer a range of attractive benefits to help you work your magic. Saving & Finacial Our 401(k) Plan includes a generous company-matching contribution and an additional discretionary contribution each year. We also provide tax-advantaged accounts for you to save for healthcare, commuting expenses, company-provided and buy-up life insurance to help you protect your financial future. Health & Wellness We offer comprehensive medical, dental, & vision coverage-including virtual care through Telehealth & free behavioral health counseling sessions through our Employee Assistance Program. We also offer a wellness incentive program and personalized support to help you navigate and use your benefits. Voluntary Benefits Our voluntary benefits provide additional protection from the high costs of healthcare not covered by health insurance. We also have discount programs that offer exclusive savings on everything from auto, home, and pet insurance to low-interest personal loans. Work/Life Support We have several programs to support your work/life balance, including generous paid time off, back-up day care services, education assistance, and more. OUR RECRUITING PROCESS Depending on the position (level, functional area, country) the process can vary slightly. You apply Complete your online application for your preferred role(s) that match your interests and qualification. If you cannot find a suitable role please join our Talent Zone and stay connected for your next career opportunity. We screen We review your application and if we determine that you are a good fit we will move you to the selection process. We assess You are interviewed by phone, via video and/or face to face. Mutual agreement Ideally you are the perfect match for us! We hope you consider us as your new employer. Work your magic! To guarantee you a smooth start our onboarding preparation begins. Didn't find the right job just yet? No problem at all! We’re always looking to meet new talent and stay in contact with you beyond an application. Join our Talent Zone to stay connected, learn more about our company, career opportunities and events. We’d love to hear from you.
Who are we: Magnaflow is a leading manufacturer and supplier based in Oceanside, CA of premium products to the automotive aftermarket industry such as catalytic convert- ers, performance exhaust and replacement exhaust. Through the Camburg division in Huntington Beach, CA. Magnaflow also supplies race-inspired performance suspension products and vehicle uplifting services, Magnaflow is focused on future growth through both new business development and new product introduction. Our websites are www.magnaflow.com and www.camburg.com. What you will be doing: Welder is responsible for welding metal components and structures in a manufacturing environment. The role involves using various welding techniques to join, fabricate, and repair metal parts. Salary Range: $21.50-27.50/hr. Responsibilities: Perform welding tasks using various methods (MIG, TIG, Stick, or Flux Core) to join metal parts according to blueprints, diagrams, or specifications. Inspect completed welds for quality, ensuring they meet company standards and safety regulations. Maintain and operate welding machines, tools, and safety equipment, ensuring they are in good working order. Perform welding repairs on defective parts or products and rework parts that don't meet quality standards. Follow safety procedures, use personal protective equipment (PPE), and ensure the work environment adheres to safety regulations. Work closely with other welders, machinists, and production team members to meet production goals and deadlines. Continuously improve skills and stay updated on new welding techniques and technologies. This position ensures the accuracy or products being welded by placing them into an approved welding fixture and inspecting for fitment to the fixture prior to welding. Welding of stainless-steel products and is familiar with the MIG welding process. This position requires knowledge in proper care, and maintenance of all standard welding equipment, such as changing tips when necessary, and cleaning of the machine. This position requires checking quantities of parts produced for accuracy. Able to adjust to new methods of automation which require nonconventional practices with regards to manufacturing. Inspection parts produced to the company’s quality standards, and fitment to approved measurement devices. Must be able to read drawings, and other manufacturing documents Perform other duties as required What’s in it for you? • Competitive Salary • PTO, Sick Pay, Birthday Holiday, Paid Holidays • Medical, Dental, Vision • 401k Matching (Up to 5%) • Education assistance • Company sponsored events • Growing department and team Requirements: This position requires an individual who is experienced in welding stainless-steel products and is familiar with the MIG welding process. A minimum of 5 years is preferred. This position requires a basic knowledge of OSHA safety regulations. Maintain accurate counts of parts produced daily. Maintain a functional work area that is consistent with Five “S” and Lean Manufacturing principles. Inspect parts produced to the company’s quality standards, and fitment to the fixture. Close and general vision. Good hand eye coordination. This position requires prolonged standing of up to 8 hours at a time. This position requires the lifting of 50 lbs. Any lifting over 50 lbs. is to be lifted with the assistance of other individuals. This position requires reaching above and below the shoulders. Welding helmet. PPE (Steel toe shoes, safety glasses, gloves, earplugs, etc.) Physical Requirements: Must be able to work on feet all day, climb stairs occasionally, and lift 50 pounds with or without accommodations. What’s in it for you? Competitive Salary PTO, Sick Pay, Birthday Holiday, Paid Holidays Medical, Dental, Vision 401k Matching (Up to 5%) Education assistance Company sponsored events Growing department and team
Who are we: MagnaFlow is a leading manufacturer and supplier based in Oceanside, CA of premium products to the automotive aftermarket industry such as catalytic converters, performance exhaust and replacement exhaust. Through the Camburg division in Huntington Beach, CA. Magnaflow also supplies race-inspired performance suspension products and vehicle uplifting services, Magnaflow is focused on future growth through both new business development and new product introduction. Our websites are www.magnaflow.com and www.camburg.com. What you will be doing: A Manufacturing Machine Operator is responsible for setting up, operating, and maintaining machines used in the production process. They ensure that machinery runs smoothly, produces quality products, and operates efficiently while adhering to safety and quality standards. What you need: All employees are required to perform their job with safety as the main priority for themselves and their coworkers. Set up, operate, and tend equipment such as bending, deburring, cutting, packaging, test equipment. Perform minor changeovers, setting adjustments, and troubleshooting. Ensures the accuracy of products being produced by using an approved measurement device prior to releasing to next production steps. Requires ability to properly care, and maintain all the specific machines being operated, such as cleaning of the machine. Product count when applicable, product documentation and properly identifying contents. Maintains a clean, safe work environment and compliance with 5S Double check quantities of parts produced for accuracy. Able to adjust to new methods of automation which require nonconventional practices with regards to manufacturing. Inspect parts produced to the company’s quality standards, and fitment to approved measurement devices. Perform other duties as required Salary Range: $19.50-23.50/hr. What’s in it for you? • Competitive Salary • PTO, Sick Pay, Birthday Holiday, Paid Holidays • Medical, Dental, Vision • 401k Matching (Up to 5%) • Education assistance • Company sponsored events • Growing department and team Requirements: This position requires a basic knowledge of OSHA safety regulations. A minimum of 1 year working in a manufacturing environment preferred Ability to read drawings and other manufacturing documents is desired. Attention to detail Must be able to lift to 50 lbs. Any lifting over 50 lbs. is to be lifted with the assistance of other individuals Requires prolonged standing of up to 8 hours at a time. Close and general vision Good hand eye coordination This position requires reaching above and below the shoulders. Education & Experience: High school diploma or equivalent (some positions may require vocational training or technical certifications in machine operation). Previous experience as a machine operator or in a manufacturing environment is typically preferred but may not be required. On-the-job training may be provided. What you need: Must be able to work on feet all day, climb stairs occasionally, and lift 50 pounds with or without accommodations. What’s in it for you? Competitive Salary PTO, Sick Pay, Birthday Holiday, Paid Holidays Medical, Dental, Vision 401k Matching (Up to 5%) Education assistance Company sponsored events Growing department and team
Work Your Magic with us! Start your next chapter and join EMD Electronics. Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us. Everything we do in EMD Electronics is to help us deliver on our purpose of being the company behind the companies, advancing digital living. We are dedicated to being the trusted supplier of high-tech materials, services and specialty chemicals for the electronics, automotive and cosmetics industries. We foster a global collaborative organization made up of individuals who have the passion to win, obsess about the customer, are relentlessly curious and act with urgency. Together, we push the boundaries of science to make more possible for our customers. This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. Your Role: The Operations Technician will be part of the Chemical Manufacturing team in Carlsbad, CA. The team of Operations Technicians are responsible for receiving, decontaminating, rebuilding, and filling our vessels with ultra-pure chemistries. Specific Responsibilities Include: Conduct manual and automated decontamination of vessels Perform hazardous waste consolidation Perform weekly and monthly regulatory compliance activities Acid-wash stainless steel and quartz vessels Maintain a clean and organized manufacturing environment Support receiving by unloading trucks Assist the Engineering team with troubleshooting system issues Perform data entry task Document and Inspect vessels to ensure quality Physical Attributes: Wear a full-face air-purifying respirator and other PPE Lift up to 50 pounds Location/shift: Onsite position in Carlsbad, CA – day shift Who You Are Minimum Qualifications: High School Diploma or GED 1+ years working in chemical, manufacturing or production. Preferred Qualifications: Experience handling chemicals Background in a fast-paced manufacturing environment Strong skills in troubleshooting, documentation, and communication Ability to read and understand Safety Data Sheets and written work instructions High focus on quality and safety Proficient using Microsoft suite (Word, Excel, Access, SharePoint) Experience with SAP Ability to use hand tools Pay Range for this position: $23.00 - $36.00/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!
By joining Bio-Techne, you’ll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide. Pay Range: $81,900.00 - $134,550.00 Cliniqa, a Bio-Techne brand, is seeking an outstanding Scientist with a PhD or equivalent professional experience to join our Manufacturing group charged with developing or optimizing procedures for both small- and large-scale processes. This role will lead product initiatives to enable novel products through integration of reagents, instrumentation, analysis algorithms and software. This position will support all stages of manufacturing, including activities such as prototype optimization, guard-banding, design lock, verification, validation, and design transfer. This position will lead key project deliverables (e.g. verification/validation plans, technical reports, design control documents, protocol guides), contribute to design control and technical risk analysis, and independently design, execute, and analyze complex experiments and large data sets to inform design decisions and risk mitigation. Independently design and carry out experiments leading to the development/ optimization of key biological intermediates and purifications. Gain understanding of various types of purification methods and support design and characterization of novel methods. Apply/ learn new characterization methods for the sensitive detection or quantification of multimodal biomarkers from clinical specimens or in process reagent qualification. Lead the creation of protocols, presentations, standard operating procedures, design verification and validation procedures, quality control procedures, and technical reports to support lab infrastructure, new product initiatives, and on-market product investigations. Contribute to design control and associated documentation for new product initiatives, including drafting of user needs, design inputs/outputs, risk analysis and mitigation, and design transfer. Train and mentor co-workers on equipment and procedures and lead data analysis and interpretation. Provide substantial, high-quality contributions to projects by working independently, communicating effectively within team and cross-functionally, and leveraging the active support of others. Organize, analyze, and/or visualize complex datasets using analytical software (JMP, R, or Python) and statistical comparisons and clearly communicate results or complex scientific topics to technical and non-technical audiences. Lead and contribute to design and execution of experimental plans or processes to support objectives within the organization. Apply scientific methods and process design principles to improve product development and manufacturing processes. Who You Are & What You Bring Required: A PhD in Chemistry, biomedical engineering, or related field or a Master’s degree plus 6-8 years of relevant industry experience. Bachelor’s degree is acceptable with 10+ years of related experience. Strong Chromatography knowledge. Prior demonstrated experience developing and validating/verifying purification procedures under design control using a requirements-driven, risk-based approach within the biotech industry or clinical laboratory. A strong track record of independence, productivity and creative problem-solving. Expertise in one or more technical areas and considered a resource by colleagues to develop similar skills. Demonstrated ability to independently design and implement experimental plans or processes to support objectives within the organization, including optimization and guard banding of product prototypes. Excellent written and verbal communication skills and attention to detail. A passion for improving patient care through diagnostic technologies. Preferred: Proficiency with Excel, JMP, Python and/or R. Experience with establishing DOE protocols and interpretation of the data Familiarity with standards and guidelines for validating critical procedures Ability to contribute to early-stage product prototype development where needed is a plus. Ability to apply statistical analysis to large data sets, especially with code, is a plus. Why Join Bio-Techne: We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield. We invest in our employees’ financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA. We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more. We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging. We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave. We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table. Bio-Techne is an E-Verify Employer in the United States. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.
*Job Summary* We are seeking a *Production Manager* with a strong understanding of engineering exhibits – both indoor and outdoor to join our team. In this role, you will oversee the planning, fabrication, and execution of high-quality exhibit solutions, ensuring seamless integration of design, engineering, and production. *Duties* * Supervise daily production activities to ensure operational efficiency and adherence to safety protocols. * Manage the end-to-end production process for exhibits, ensuring quality, efficiency, and adherence to project timelines. * Collaborate with designers, engineers, and fabricators to translate creative concepts into structurally sound and visually impactful exhibits. * Oversee material selection, fabrication techniques, and assembly processes to ensure durability and functionality. * Coordinate with internal teams and external vendors to maintain budget, scheduling, and quality standards. * Identify and resolve production challenges, optimizing workflows and problem-solving technical issues. * Ensure all exhibits comply with safety regulations, engineering best practices, and client specifications. * Maintain clear communication with stakeholders to align expectations and deliver outstanding exhibit experiences. * Oversee the maintenance and operation of machinery, including forklifts and power tools, ensuring all equipment is functioning properly. * Train and mentor production staff on best practices for assembly, use of hand tools, and safety procedures. * Collaborate with other departments to coordinate production schedules and meet delivery deadlines. * Conduct regular inspections of the manufacturing facility to ensure compliance with quality standards. * Analyze production data to identify areas for improvement and implement corrective actions as needed. *Qualifications* * Proven experience in exhibit production, fabrication, and engineering. * Must have 3-5 years of Production Manager experience. * Strong understanding of materials, structural integrity, and production techniques for exhibits. * Ability to manage multiple projects simultaneously in a fast-paced environment. * Proven experience in a manufacturing facility or factory setting, with a strong understanding of production processes. * Mechanical knowledge is essential, with the ability to troubleshoot equipment issues effectively. * Engineering knowledge as it relates to fabrication and production of large scale exhibits preferred * Proficient in using hand tools and power tools safely and efficiently. * Must have experience using a table saw. * Strong leadership skills with the ability to motivate and manage a diverse team. * Excellent problem-solving abilities, organizational skills, great communicator and attention to detail. * Must have the ability to travel 25% of time. * Ability to work in a fast-paced environment while maintaining high-quality standards. We look forward to welcoming a skilled Production Manager who can contribute positively to our team and help drive our manufacturing success! Job Type: Full-time Pay: $120,000.00 - $150,000.00 per year Benefits: * Paid time off Work Location: In person
PEP Creative is now hiring crew members for a special event production company. We are a full service production company that sets up events for corporate, social and local businesses in hotels, clubs, parks, concert halls and other venues around San Diego and Southern California. Looking to hire crew members for in-house and on-site work setting up events at hotels and other venues. Experience in the Special Events Industry is preferred, but not required. We will train, as needed. Experience in event lighting (moving lights, lighting technician, etc) is a plus. *Responsibilities to include:* Loading and unloading trucks Event production set up and strike (split shifts and evening work) on job site Maintaining and organizing inventory in warehouse and on job site Upkeep of inventory (cleaning and painting, when needed) Physical ability to lift up to 75 pounds Operate Forklifts, Boom lifts, Scissor lifts, etc (we will train) Operate and run small to large mobile Generators (we will train) *Benefits* Competitive pay with overtime Health insurance and 401k available when Full Time Status is reached Work Remotely * No Job Type: Full-time Pay: $18.00 - $26.00 per hour Benefits: * 401(k) * Dental insurance * Flexible schedule * Health insurance * Life insurance * Paid time off * Retirement plan * Vision insurance Education: * High school or equivalent (Required) License/Certification: * Driver's License (Required) Shift availability: * Day Shift (Preferred) * Night Shift (Preferred) * Overnight Shift (Preferred) Ability to Relocate: * San Diego, CA 92121: Relocate before starting work (Required) Work Location: In person
*Job Summary* We are seeking an experienced Validation Specialist to join our team. This position requires a highly skilled and experienced professional who is familiar with a variety of validation & engineering concepts, practices, and procedures. This role is critical in ensuring that our products meet the highest standards of quality and compliance with FDA regulations, ISO 13485, ISO 9001, and CGMP. *Responsibilities* * Performs IQ/OQ/PQ of the ISO aseptic facility, warehouse, product design, and manufacturing processes (Includes building management system, manufacturing/QC equipment). * Responsible for establishing and executing URS specifications, validation protocols, and final reports. * Participate in Design Control meetings and maintain Design Control files/Master Validation Plan. * Communicate project updates, risks, and outcomes to stakeholders and leadership. * Maintains a clean and safe work environment and follows all safety policies and procedures. * Performs all work as per GMP/CFR/ISO/Internal standards. *Experience* * Minimum Bachelor's Degree in Engineering or Science; and 3-5+ years of hands-on validation experience in the biotechnology industry is desired; or an equivalent combination of education and experience. * Previous experience with USP Purified Water Systems preferred. * Familiar with Design Control for Class III Medical Devices. * GMP/CFR/ISO experience required. * Familiarity with aseptic processing and clean room environments * Computer literate, proficient in Microsoft Word and Excel. * Previous experience with an electronic QMS system preferred. * Experience writing Change Controls, SOPs, protocols, reports, and validation documents under a Quality Management System. *Further Details* This will be a contract-to-hire position. This position will begin as a temporary contract but has the potential for conversion to a permanent full-time position. Successful performance and a good cultural fit will be evaluated for permanent conversion. Compensation based on experience. The candidate will be regularly required to sit and stand for extended periods, be able to lift up to 25 pounds, and may be exposed to caustic chemicals. Job Types: Contract, Temp-to-hire Pay: From $30.00 per hour Education: * High school or equivalent (Preferred) Experience: * validation: 2 years (Preferred) Work Location: In person
*Job Summary* We are seeking a dedicated and skilled Manufacturing Technician to join our team. In this role, you will be responsible for ensuring the efficient operation of manufacturing equipment and processes. The candidate must follow cGMP policies and regulatory guidelines to perform critical tasks in the manufacture of our Class III Medical Devices and other pharmaceutical products. *Duties* * Maintain records to comply with cGMP requirements. * Write, review, revise, and follow detailed Work Instructions, Standard Operating Procedures, and Manufacturing Batch Records to perform critical tasks related to formulation, filtration, fill and packaging of drug products and/or medical devices. * Setup of production equipment, including filling machines, ovens, washers and, balances. * Qualify to perform various aseptic operations in ISO 5 clean rooms, including manual and automated aseptic fills. * Perform visual inspection of components and in-process packaging materials. * Operate various packaging machinery. * Clean and sanitize production facilities. * Comply with all regulatory and company policies and procedures * Document production data and maintain accurate records of operations. * Follow all safety guidelines and procedures to maintain a safe working environment. *Requirements* * High school diploma or equivalent; technical certification or degree in a related field is a plus. * 1-3 years of experience in a cGMP environment for pharmaceutical manufacturing, and specific experience in aseptic manufacturing. * GMP/CFR/ISO experience required. * Previous experience with an electronic QMS system preferred. * Ability to gown and work in a classified area as required. * Excellent attention to detail and commitment to quality assurance. * Ability to work effectively in a team-oriented environment. * Strong communication skills, both verbal and written. * Willingness to work flexible hours, including overtime as needed. *Further Details* This will be a contract-to-hire position. This position will begin as a temporary contract but has the potential for conversion to a permanent full-time position. Successful performance and a good cultural fit will be evaluated for permanent conversion. Compensation based on experience. The candidate will be regularly required to sit and stand for extended periods, be able to lift up to 25 pounds, and may be exposed to caustic chemicals. Job Types: Contract, Temp-to-hire Pay: From $25.00 per hour Benefits: * Flexible schedule * On-the-job training Experience: * aseptic manufacturing: 1 year (Preferred) Work Location: In person
General Summary Monitors key process control points during production operations. Documents and reports any food safety or quality issues so that corrective actions can be taken. Benefits and Culture We offer a competitive compensation and benefits package designed to help employees live a healthier life, build rewarding careers and save for the future. Reser's offers choices whenever possible, because we recognize the diverse and ever changing needs of our employees. Full-time employee benefits include medical, dental, vision, AD&D, life, 401(k) with discretionary match, wellness programs, paid time off, company paid holidays and a variety of voluntary benefit options. We strive to be your Employer of Choice. As one of our five cornerstones, this means that we go all-out to create an environment that shows we are committed to investing in employee growth and creating a culture of belonging where employees want to build a lasting career. Visit our website to learn more about our competitive benefit programs - https://www.resers.com/careers/#benefits Principal Duties and Responsibilities • Documents and reports any food safety or quality issues and participates in determination of corrective actions to be taken • May assist with pre-operational inspection of production plant and equipment and completion or related documentation • Performs process verification checks at critical food safety and quality points according to the facility’s Food Safety Plan and Quality Plan. • Participates in determination of corrective actions when verification checks do not meet the limits defined in the facility’s Food Safety Plan and Quality Plan. • Verifies the facility’s environment including items such as temperature throughout the production facility, sanitizer concentrations and other food safety related conditions. • Completes Hold Tags and Cooling Tags, if appropriate, to isolate non-conforming ingredients or products. • Conducts and documents the daily product review; participates in evaluation of key sensory attributes of finished products. • Responsible for maintaining records, completing documentation, following proper documentation protocols as assigned • Adherence and monitor of programs including HACCP Program, good manufacturing practices, foreign material control, plant sanitation, product quality assurance and other programs as assigned • As part of monitoring CCPs (Critical Control Points), must be trained in HACCP (Hazard Analysis Critical Control Point) and adhere to approved HACCP plan(s). Job Specifications • Associate degree in a science related field or 1+ years in a Quality Assurance position or equivalent experience. • Basic knowledge of GMP's, Food Safety, and Safety requirements • Ability to read, write and speak in English at a level of proficiency to clearly understand items such as food safety documentation, ingredient labels, etc. is required. • Basic computer skills; e-mail, Word, Excel. • Regular attendance and punctuality are required. Working Conditions • Food processing, warehouse and food laboratory environment. • The environment may be wet or dry and temperatures may range from 25oF to 110oF. • Regularly required to stand and walk, ability to climb ladders, bend, reach and occasionally lift up to 40 lbs. • Production demands may require overtime and/or evening or weekend scheduling. Compensation $20.60 + $1.00 shift differential per hour/ non-exempt Recipe for Success Reser’s is the leading provider of fresh refrigerated deli salads, side dishes, and prepared foods for the supermarket, club store, and food service industries. Family owned and operated, Reser’s has been a proud sponsor of good times at racetracks, picnics, BBQs, music festivals, and affordable family meals since 1950. Reser’s family of brands include Reser’s American Classics, Main St Bistro, Stonemill Kitchens, and more. With more than 4,500 employees, Reser’s operates 14 facilities in the US, Mexico, and Canada and actively supports the communities it serves. Equal Opportunity Employer This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
*Job Summary* We are seeking a skilled Fabricator/Welder to join our team. The ideal candidate will have experience in TIG welding Aluminum, Stainless Steel and Titanium as well as MIG welding. The candidate must be able to interpret drawings, tolerancing and weld call-outs and must be able to hold +/- .030" tolerance on weldments. Fabrication experience (forming, etc.) and creating fixtures for repeatability when fabrication a plus. Job Type: Full-time Pay: $23.73 - $28.00 per hour Benefits: * 401(k) * 401(k) matching * Dental insurance * Health insurance * Paid time off * Vision insurance Work Location: In person