Looking to move to Carlsbad and want to connect with local employers? Fill out this form and we’ll help you get recruited.
Why work for PCI Pharma Services? At PCI, we have an uncompromising focus on providing quality and operational excellence and providing the industry leading customer experience. Our people make all of this happen, so providing an industry leading experience for our people is equally as important. By creating an authentic culture of purposeful work, we aspire to be an interesting and fulfilling place for talented individuals to grow careers. We live a philosophy of intentional learning combined with real-life experience supported by a fair and competitive rewards program. We are individuals, teams and a company that believes in our purpose and our approach is simple, the people who work at PCI fuel our business; we don’t say no, we figure out how. Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI. Job Details: The Process Validation Engineer I collaborates with product sponsors to develop process validation programs for each drug product in accordance with the applicable guidance documents. These documents include, but are not limited to, validation master plans, risk assessments, process performance qualification (PPQ) protocols & reports, and continued process verification plans (CPV). Responsibilities: Under the guidance of senior team members, works with clients to develop process validation programs suitable for the applicable drug product(s). Authors and collaborates on product specific validation master plans for each drug product to describe the process validation (PV) philosophy and approach in demonstrating capabilities related to the manufacturing of drug products under the guidance of senior team members. Uses risk assessment tools to evaluate the risks and required mitigation plans associated with the validation of each drug product. Under the guidance of senior team members, may author and collaborate on PPQ protocols and summary reports to describe the procedures, methods, acceptance criteria, and sampling plan required to provide evidence that the drug product processes are reproducible, consistently produce product that meet their quality attributes, and are in a state of control. Responsible for evaluating product and process data to provide on-going assurance that the drug product manufacturing processes remain in a validated state during commercial manufacturing. Writes and reviews Standard Operating Procedures (SOP’s) related to qualification activities. Works closely with cross-functional departments as necessary to resolve issues. Regular and reliable attendance on a full time basis [or in accordance with posted schedule]. Responsible for exhibiting professional behavior with both internal and external business associates that reflects positively on the company and is consistent with the company’s policies and practices. Embodies PCI Pharma Services cultural values and aligns daily actions with department goals and company culture. Requirements: Bachelor’s degree in a Life Sciences discipline or equivalent experience required. Minimum of 0-2 years of relevant experience in validation or process engineering. Strong knowledge of industry guidance documents pertaining to process validation (including, but not limited to FDA guidance for process validation and Annex 15) preferred. Detail oriented and strong written and verbal communication skills. Ability to work independently, within prescribed guidelines, or as a team member. Experience with Microsoft Office applications. The base hourly range for this position is $68,640 to $77,040 plus annual performance bonus eligibility. Final offer amounts are determined by multiple factors including and not limited to specific and relevant experience, credentials, geography and subject matter expertise. Join us and be part of building the bridge between life changing therapies and patients. Let’s talk future For Los Angeles applicants, we abide by the Fair Chance Initiative for Hiring. Learn more about the policy here: FCIHO Equal Employment Opportunity (EEO) Statement: PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. At PCI, Equity and Inclusion are at the core of our company’s purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity – at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture. #LI-KC1 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.
ESSENTIAL DUTIES AND RESPONSIBILITIES Adhere to the Company’s Quality Management System to ensure compliance with applicable regulatory requirements. Establish, document, conduct, and maintain the company document control system, including but not limited to document approval, distribution, changes, and storage/retrieval Ensure all controlled documentation is reviewed and completed per established procedures and requirements Manage the Change Control Board (CCB) and any tasks associated with the processing of controlled documentation Manage the preparation, processing, and distribution of quality manufacturing documentation Manage and maintain the storage system for all hardcopy and electronic records, including the organization and numbering of quality system documentation Inspect device components and finished devices per established inspection procedures Maintain and create new inspection plans as required Review and maintain completed device history records Support the nonconforming materials system, including material review board (MRB) efforts Coordinate activities with engineering and other departments to ensure production schedules are met by ensuring appropriate documentation is complete and ready Manage the company training program, ensuring that applicable requirements are met in a timely manner Identify and drive continuous improvement opportunities related to document control processes Maintain the integrity of all applicable quality documents and records Provide ongoing communication and regular status updates to senior management team Interface and collaborate with other departments, outside vendors, stakeholders, etc. Perform other duties as required SUPERVISORY RESPONSIBILITIES Direct Reports: Yes N/A QUALIFICATIONS The requirements listed below are representative of the knowledge, skill, and/or ability required for this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Proficient knowledge of ISO13485 and 21 CFR Part 820, Part 11 Proficient knowledge of Quality System Regulations ISO 14971 Basic blueprint reading (GD&T) Basic skill with precision measuring instruments (e.g. micrometers, calipers, gauges, optical comparators, etc.) Must be flexible and able to adapt to change Strong written and verbal communication skills Highly detail-oriented Must be able to exercise independent judgment and discretion Communicates and works well with employees of all positions Project collaboration experience involving external stakeholders Computer literacy with standard software applications EDUCATION AND/OR EXPERIENCE Bachelor’s degree required 3+ years of experience in a medical device manufacturing environment CERTIFICATES, LICENSES, REGISTRATIONS N/A WORK ENVIRONMENT The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. The work environment is an industrial setting dedicated to the production and assembly of medical devices that utilize machinery, equipment, and specialized processes to transform raw materials into finished products. The work environment also includes a typical office setting. PHYSICAL DEMANDS Analysis of Physical Demands N = Never R = Rarely Less than 1 hour per week O = Occasional 1% to 33% of time F = Frequent 34% to 66% of time C = Constant over 66% of time Activity Frequency Activity Frequency Lifting/Carrying N R O F C Twisting/Turning N R O F C Under 10 lbs Reach over shoulder 11-20 lbs Reach over head 21-50 lb Reach outward 51-100 lbs Climb Over 100 lbs Crawl Pushing/Pulling N R O F C Kneel Under 10 lbs Squat 11-20 lbs Sit 21-50 lbs Walk-Normal Surfaces 51-100 lbs Walk-Uneven Surfaces Over 100 lbs Walk-Slippery Surfaces Other N R O F C Stand Keyboard/Ten Key Bend Fingering (fine dexterity) Driving N R O F C Handling (grasping, holding) Automatic Trans Repetitive Motion - Hands Standard Trans Repetitive Motion - Feet Monday - Thursday 5:30 am - 3:30 pm
Requisition Number: 210872 Job Description Cintas is seeking a Warehouse Associate - Wastewater Technician. Responsibilities include the overall operation and upkeep of the facility's wastewater system based on applicable local or national pollution ordinances; mixing the chemical amounts required to wash uniforms and other ancillary products, such as floor mats, shop towels and dust mops. The position is physical and requires standing for 7 hours of an 8 hour shift, as well as repeated lifting, bending, stretching and twisting. Daily accuracy and productivity of work is necessary for inventory control and accountability. Additional responsibilities include housekeeping and adherence to health and safety standards. Skills/Qualifications Required Ability to stand for 7 hours of an 8 hour shift Preferred Appropriate certification and/or licensing (including state specific), where applicable Knowledge of local and national wastewater regulation and ordinance Benefits Cintas offers comprehensive and competitive medical, dental and vision benefits, with premiums below the national average. We offer flexibility with four different medical plan options; one plan is offered at zero cost. Additionally, our employee-partners enjoy: • Competitive Pay • 401(k) with Company Match/Profit Sharing/Employee Stock Ownership Plan (ESOP) • Disability, Life and AD&D Insurance, 100% Company Paid • Paid Time Off and Holidays • Skills Development, Training and Career Advancement Opportunities Compensation A reasonable estimate of base salary for this role ranges between $19.25 - $24.08/Hour. The range takes into account factors that are considered in making compensation decisions including, but not limited to, skill sets, experience and training, and other business and organization needs. Please note, it is not typical for an individual to be hired at or near the top of the range for their role and compensation decision are dependent on the facts and circumstances of each decision. Company Information Cintas Corporation helps more than one million businesses of all types and sizes get Ready™ to open their doors with confidence every day by providing products and services that help keep their customers’ facilities and employees clean, safe, and looking their best. With offerings including uniforms, mats, mops, towels, restroom supplies, workplace water services, first aid and safety products, eye-wash stations, safety training, fire extinguishers, sprinkler systems and alarm service, Cintas helps customers get Ready for the Workday®. Headquartered in the U.S., Cincinnati, OH, Cintas is a publicly held Fortune 500 company traded over the Nasdaq Global Select Market under the symbol CTAS and is a component of both the Standard & Poor’s 500 Index and Nasdaq-100 Index. Cintas Corporation is proud to be an Equal Opportunity Employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy), national origin, age, genetic information, disability, protected veteran status, or any other characteristic or category protected by local, state, or federal law. This job posting will remain open for at least five (5) days. Job Category: Production Hourly Organization: Rental Employee Status: Regular Schedule: Full Time Shift: 1st Shift
Direct hire for full time/part time positions. * Follow ECO changing Fine Pitch SMT components including capacitors, resistors, ICs * Rework PCAs that do not pass QA * Populate CCA for prototypes * Screw/unscrew CCA into enclosures * Cable Assembly * Package finished goods for shipping Requirements: * Previous work experience soldering fine pitch components * Basic hand tools knowledge * Comfortable with repetitive work in fast paced environment * High School Diploma preferred * Cable Crimp and Inspection a plus * Can solder 0402, 0603, QFP, TSOP, Through-Hole * Job Types: Full-time, Part-time, Contract Pay: $26.00 - $32.00 per hour Expected hours: 22 – 40 per week Benefits: * Dental insurance * Flexible schedule * Health insurance * Paid time off * Vision insurance Work Location: In person
*Job description* We are a growing cookie manufacturer company in San Marcos looking for an office admin/customer service assistant to join our team! This is a *FULL-TIME / IN-OFFICE* position with room for growth for the right person. *Your job will include a variety of duties and responsibilities, including, but not limited to:* - Being the liaison between the Office/Production/Fulfillment/Logistics/Retail Stores/Sales Team/HQ. - Answer customer service phone line and emails. - Responding to daily customer emails, complaints & needs. - Printing and organizing orders for production and fulfillment. - Filing & organizing as needed. - Company’s website coordination with marketing team on website transition for promotions and new products. - Inventory Management & budgeting for office supplies & retail needs. - Company & team meetings- including taking meeting notes & compiling department task lists - Company Calendar Management - updating company board & calendar each month with current events, holidays & coordinating calendars with the COO & directors of each department including production and shipping departments. *Requirements:* - Experience with Microsoft Office - excel, word, etc. – mandatory. - Experience with Shipstation and Shopify desired not mandatory. - Fluent: English (Required) / Spanish knowledge – desired not mandatory. - Experience with customer service in a retail or office environment is mandatory. - Higher education degree desired but not mandatory. - Some experience with QuickBooks desired. - Flexibility during our peak seasons. **Being a cookie company, Valentines Day, Mother's Day, Thanksgiving, and Christmas Day will require more attention to detail along with more hours. Overtime will be required during peak seasons. *Looking for these qualities in an employee:* - Responsible & Self-Motivated - Friendly and outgoing - Committed to being a team member, must work well with others - Able to multitask (this is extremely important!) - Comfortable answering customer calls/emails and complaints - Must be organized - Have great prioritizing & time management skills - Excellent English: verbal and written communication skills. Spanish is a plus. - Flexibility with schedule - Reliable, integrity is a non-negotiable in our office This is a *FULL-TIME / IN-OFFICE* position. The pay range to start is $18-$21 an hour, DOE. . **PLEASE BRING IN YOUR RESUME FOR THE INTERVIEW Job Type: Full-time Pay: $18.00 - $20.00 per hour Benefits: * 401(k) * 401(k) matching * Employee discount * Health insurance * Vision insurance Experience: * Customer service: 1 year (Required) Language: * Spanish (Preferred) Shift availability: * Day Shift (Required) Ability to Commute: * San Marcos, CA 92078 (Required) Ability to Relocate: * San Marcos, CA 92078: Relocate before starting work (Required) Work Location: In person
About Us At *Silflex Shielding (a division of American Ceramic Technology, Inc.)*, we are optimistic about the future and committed to providing high-quality products and services that outperform the competition. Our work environment emphasizes safety, quality, and teamwork. The success of our company depends on the dedication and attitude of our employees, and we look forward to building strong, productive working relationships. We manufacture specialized *radiation shielding products* that require precision, attention to detail, and hands-on mechanical skill. This is a physically demanding role where you will work with heavy materials, complex molds, and production equipment. You will get your hands dirty—mixing, pouring, assembling, and inspecting parts—and your contribution will directly support the safety and reliability of products delivered to our customers. Duties and Responsibilities * Interpret *work travelers, SOPs, and mechanical drawings* to determine material formulas, tooling, and production steps. * Accurately weigh, measure, and mix heavy powders, liquids, and compounds; adjust formulas as required to meet specifications. * Assemble, adjust, and disassemble molds (aluminum, flat, molded, and 3D-printed) using hand tools; troubleshoot basic mold and equipment issues. * Pour and level materials into molds with precision, ensuring correct tolerances, dimensions, and surface quality. * Safely demold parts (up to 100 lbs.), inspect for defects, and clean molds for reuse. * Perform final inspections including weight, dimensions, surface cleanliness, and documentation with logs, forms, and photographs. * Operate equipment such as hydraulic presses and laser machines according to established procedures. * Maintain strict attention to safety, cleanliness, and proper use of solvent-based cleaning agents. * Package, label, and prepare products for shipment. * Participate in problem-solving and root cause analysis with team members. * Work long shifts (10–12 hours starting at 7:00 AM) with regular overtime and Saturday work required. * Accept that this position is *physically demanding and hands-on*—you will be lifting, cleaning, and working with heavy and sometimes messy materials daily. Qualifications * High school diploma or equivalent required; trade school or technical training preferred. * *3–5 years of experience* in a manufacturing, fabrication, or production environment. * Ability to read and interpret *mechanical drawings and design prints*. * Strong mechanical aptitude and troubleshooting skills. * Proficiency with measurement tools (tape measures, calipers, squares). * Experience working with powders, liquids, or composite materials preferred. * Must safely lift up to 100 lbs. on a regular basis. * Comfortable working in a *dirty, hands-on environment* involving heavy lifting and use of solvents. * Excellent attention to detail and commitment to product quality. * Strong organizational skills with ability to handle multiple tasks in a fast-paced environment. * Ability to read, write, and speak English clearly for safety and production instructions. * Capable of working independently with minimal supervision and as part of a team. * Willingness and ability to work long hours, overtime, and weekends. Benefits * Competitive starting pay of *$25/hour* with overtime opportunities. * Health insurance eligibility after 90 days of full-time employment. * Paid holidays and vacation time after one year of employment. * 24 hours of annual Paid Time Off (PTO) for personal needs. * A strong safety culture and supportive team environment. How to Apply Interested candidates should submit their resume by email to: *[email protected]* Please include *“Manufacturing Technician Application”* in the subject line. Job Type: Full-time Pay: $25.00 - $30.00 per hour Expected hours: No less than 40 per week Work Location: In person
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 the quality and regulatory expertise to assure the highest in quality manufacturing and supply chain excellence. Pay Range The pay range for this position is $21.00 - $24.00 per hour. Actual compensation will be based on factors such as location, skills, education, experience, and other relevant qualifications. Position Overview We are seeking a Material Handler II for a temporary-to-hire opportunity. This role offers the chance to contribute immediately while demonstrating the skills and qualities needed for potential conversion to a regular, long-term position with Argonaut Manufacturing Services, Inc. As a Material Handler II, you will transport materials, supplies, and finished products to designated locations. You will also maintain inventory by identifying, labeling, and keeping materials and supplies in stock, recording inventory locations, and reporting shortages. In addition, you will locate materials and supplies by pulling and verifying items listed on production orders. 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 6:00 am - 8:00 am with a consistent schedule. Duties and Responsibilities Perform various routine physical tasks involved in one or more of the following: receiving, storing, packaging, shipping or distributing of materials, parts, supplies, and/or equipment. Set up racking nomenclature. Kit manufacturing production runs. Prepare and maintain prescribed records, reports and documentation accurately and neatly. Perform all material stocking, assembly, customer service, data entry and clerical functions as needed. Adhere to prescribed safety and quality standards and all written procedures and work instructions. Maintain a neat and orderly work area. Conduct complete inventory checks of all stock types as needed. Education and Experience Requirements High School Diploma or equivalent, plus one-year minimum experience in warehouse, receiving and shipping along with some experience in manufacturing. International shipping experience is a plus. Demonstrated computer proficiency using an ERP system, spreadsheet and word processing software. Ability to work independently under general guidelines and supervision and in a team-based environment effectively Experience working both independently and in a team-based environment. Skills and Abilities Effective interpersonal skills, ability to interface well with team and cross-functional teammates Strong organizational skills, must be detailed oriented Must be able to work in a fast-paced environment Must be able to read, write and verbally communicate in English. Ability to communicate effectively with people in other disciplines Perform other duties as requested 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.
*Hiring Full TimeWarehouse Associate for: Cleaning, Testing, and FBA Packaging. * *Primary Function is: Cleaning, Quality Control of Electronics, and Packaging for Shipment.* Join a winning team that continues to grow in this market with ample room for growth opportunities. We have been in business for 20 years, and continue to dominate our space. *Full-Time Position for someone who is extremely hard working, fast with hands, and loves to get things done without being micromanaged. This is a starting position with lots of room for upside in a fast growing company. * *WHO WE ARE:* Best in Industry Electronics Refurbishing Company. 20 YEAR ESTABLISHED AND GROWING E-COMMERCE BUSINESS IN THE RENEWED ELECTRONICS SPACE. *WHO YOU ARE:* Hard working, punctual, willing to learn and get their hands dirty. Appreciates a casual work environment where everyone gets along and handles their roles and responsibilities to make a winning team. Please note: this is not a standard "pick and pack" warehouse role. *ROLES & RESPONSIBILITIES* * Cleaning Small Electronic Plastics for Refurbishing Purposes (Removing stains, stickers, etc.. and cleaning out battery compartments for contact points) * Replacing Cosmetic Parts with Basic Tools * Able to test electronics for basic functionality * Accurately tagging items with defects and faults for returns with reason codes * Ability to Clean and Refurbish Electronics using tools and parts provided (no toxic chemicals are used) * Attention to Detail while also maintaining speed and accuracy * Being able to manage multiple projects and staying organized * Kitting / Packing up items for shipments across various Platform * Ability to support in grading quality of units (1-5) *EXPERIENCE Required* * 1+ years of experience in a fast paced office/warehouse environment * Extremely Organized with Meticulously Detail Oriented * Ability to Juggle Changing Schedule and Tasks Daily * Working with Cleaning of Products / Spaces and Willing to get hands dirty * You enjoy making things more efficient and solving problems on your own *What We Do Best and Offer* * *Laid Back / Casual Work Environment with Focus on the Job and Performance (not politics)* * *New Warehouse Space with Top of the Line Organization and Tools* * *High Level Small Team that Works Well Together* * *Work / Life Balance* * *We are growing as a company giving continual opportunities* Please include WHC72825 in your title and also a *short paragraph* as to why we would love to have you in this roll. Please note all applications without this will ignored. *We look forward to hearing from you.* _If you are a fit, next steps/process looks like:_ 2-Hour Paid Trial Interview/Test Day Contract to Employee Hire Full Time Employment Only. Job Type: Full-time Pay: From $19.50 per hour Benefits: * Flexible schedule * Opportunities for advancement * Paid time off Work Location: In person
*Hiring Full Time Warehouse Production Associate for: Cleaning, Testing, and FBA Packaging. * *Primary Function is: Refurbishing/Cleaning, Quality Control of Electronics, and Packaging for Shipment.* Join a winning team that continues to grow in this market with ample room for growth opportunities. We have been in business for 20 years, and continue to dominate our space. *Full-Time Position for someone who is extremely hard working, fast with hands, and loves to get things done without being micromanaged. This is a starting position with lots of room for upside in a fast growing company. * *WHO WE ARE:* Best in Industry Electronics Refurbishing Company. 20 YEAR ESTABLISHED AND GROWING E-COMMERCE BUSINESS IN THE RENEWED ELECTRONICS SPACE. *WHO YOU ARE:* Hard working, punctual, willing to learn and get their hands dirty. Appreciates a casual work environment where everyone gets along and handles their roles and responsibilities to make a winning team. Please note: this is not a standard "pick and pack" warehouse role. *ROLES & RESPONSIBILITIES* * Cleaning Small Electronic Plastics for Refurbishing Purposes (Removing stains, stickers, etc.. and cleaning out battery compartments for contact points) * Replacing Cosmetic Parts with Basic Tools * Able to test electronics for basic functionality * Accurately tagging items with defects and faults for returns with reason codes * Ability to Clean and Refurbish Electronics using tools and parts provided (no toxic chemicals are used) * Attention to Detail while also maintaining speed and accuracy * Being able to manage multiple projects and staying organized * Kitting / Packing up items for shipments across various Platform * Ability to support in grading quality of units (1-5) *EXPERIENCE Required* * 1+ years of experience in a fast paced office/warehouse environment * Extremely Organized with Meticulously Detail Oriented * Ability to Juggle Changing Schedule and Tasks Daily * Working with Cleaning of Products / Spaces and Willing to get hands dirty * You enjoy making things more efficient and solving problems on your own *What We Do Best and Offer* * *Laid Back / Casual Work Environment with Focus on the Job and Performance (not politics)* * *New Warehouse Space with Top of the Line Organization and Tools* * *High Level Small Team that Works Well Together* * *Work / Life Balance* * *We are growing as a company giving continual opportunities* Please include WHC72825 in your title and also a *short paragraph* as to why we would love to have you in this roll. Please note all applications without this will ignored. *We look forward to hearing from you.* _If you are a fit, next steps/process looks like:_ 2-Hour Paid Trial Interview/Test Day Contract to Employee Hire Full Time Employment Only. Job Type: Full-time Pay: From $19.50 per hour Benefits: * Flexible schedule * Opportunities for advancement * Paid time off Work Location: In person
_Quality Assurance Associate_ *Qualifications:* * Bachelor’s degree, biology or related field preferred but not required * Familiarity with cGMP, ISO 13485 requirements, FDA, and international quality * Computer skills *Duties and Responsibilities* * Assist in ISO 13485 audit, customer audit and US FDA audit * Stay current with all regulatory procedures and documentation in order to maintain compliance with GMP, QSRs, FDA, ISO, CE and customer requirements. * Develop procedures and practices to optimize product quality, safety, and reliability. * Work with Production and R&D to review and optimize or develop validation protocols. * Ensure compliance of product labeling and advertising. * Accomplish medical device quality assurance objectives. * Develops and updates quality assurance plans * Validates quality processes. * Maintains and improves product quality. * Prepares quality documentation and reports. It is the policy of Epitope Diagnostics to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Epitope Diagnostics will provide reasonable accommodations for qualified individuals with disabilities. Job Type: Full-time Pay: $52,000.00 - $72,000.00 per year Benefits: * 401(k) matching * Dental insurance * Health insurance * Paid time off Work Location: In person
About Us: For more than six decades, the skilled thinkers, makers, and doers at Frontgrade have embraced our mission to solve complex technology challenges across the U.S. and around the globe. We’re the leading provider of high reliability and radiation assured solutions for defense, space, intelligence, commercial, and civil applications, and our products are designed to perform in the harshest of environments. From human spaceflight and space exploration to missile defense, electronic warfare, and healthcare tech advancements, our talented team stays in lockstep with our customers to ensure the success of their missions. Do you want to help shape the future? In an environment where innovation and ideas go hand-in-hand? Then come join the Frontgrade Team! Why Work For Us We take care of our people and provide competitive health, wealth and wellbeing benefits – from day one. You’ll also discover learning and development opportunities so you can take your career to the next level – and beyond. Other benefits include: Competitive Benefits: Medical (FSA + HSA), Dental, and Vision Immediate 401K Vesting/Matching Career Opportunity and Growth Tuition Reimbursement Student Loan Repayment Generous PTO and 11 paid Holidays per year (8 regular and 3 floating) 8 weeks of 100% Paid Family Leave *Profit Sharing Plan applies to all non-Annual Incentive Plan and non-Sales Incentive Plan employees. Summary: We are seeking a results-driven and strategic Continuous Improvement Manager to lead and drive lean initiatives across our aerospace manufacturing operations. This role is critical in identifying opportunities, implementing improvements, and sustaining gains to optimize quality, efficiency, and cost-effectiveness. The ideal candidate will have a strong background in lean manufacturing, Six Sigma methodologies, and change management within a regulated aerospace environment. Responsibilities: KEY RESPONSIBILITIES Lead the development and execution of lean manufacturing strategies across all production areas. Drive the deployment of Continuous Improvement (CI) tools such as 5S, Kaizen, Value Stream Mapping (VSM), Root Cause Analysis, and Standard Work. Analyze production processes and data to identify areas for improvement in quality, delivery, and cost. Partner with cross-functional teams including Engineering, Quality, Supply Chain, and Production to drive CI initiatives. Mentor and train employees at all levels on CI principles and tools to build a continuous improvement culture. Facilitate kaizen events and workshops to address key operational challenges and drive measurable improvements. Implement and sustain key performance indicators (KPIs) to track progress and impact of improvement initiatives. Develop business cases for improvement projects, including ROI and cost-benefit analysis. Ensure all improvement efforts comply with AS9100 and other regulatory requirements. Report out CI initiatives and progress to senior leadership on a regular basis. Qualifications: QUALIFICATIONS & EXPERIENCE Bachelor’s Degree in business or a technical field Minimum 6 years of experience leading continuous improvement initiatives in an manufacturing environment Experience with LEAN, Six Sigma and expertise in Lean Six Sigma methodologies as described under the responsibilities Fluency in CI methodologies, especially strong practical Lean deployment experience Ability to produce evidence of successful results from prior CI work experience US Citizenship required for eligibility to obtain/maintain a security clearance Applicable experience in lieu of a Degree may be considered. ADDITIONAL INFORMATION This position requires access to technology, materials, software or hardware that is controlled by either ITAR or EAR U.S. export laws. As a condition to this job offer, in order to be employed in this position, you must be able to obtain an U.S. Government export license(s), as required by law. Pay Range: $121,915.80 - $152,394.74 annually. Applicable pay within the posted range may vary based on factors including, but not limited to, geographical location, job function of the position, education, and experience of the successful candidate. Employment Transparency: WE ARE AN EQUAL OPPORTUNITY EMPLOYER We welcome differences and celebrate new ideas. We believe the diversity of our people inspires our creativity and drives our innovation. Everyone is welcome here, regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, protected veteran status, or genetic information. We are committed to working with and providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation due to a disability for any part of the employment process, please email [email protected]. If you have relevant skills that are not reflected in your resume, we welcome your application and encourage you to share more in an optional cover letter or to join our Talent Community Connect Portal - Connect (icims.com).
Overview: This position will support the Manufacturing Engineering group typically working as an assignee on smaller scale Manufacturing Engineering projects or tasks related to larger scale Manufacturing Engineering projects. The tasks/projects performed by this individual will typically be monitored or managed by a Manufacturing Engineer. Responsibilities: Undertakes and successfully completes simple or basic project/process development tasks. Measure products using standard metrology practices. Compile and analyze data using statistical analysis techniques. Designs, procures, and fabricates simple tooling and fixtures. Generate and modify manufacturing process documentation and assure that manufacturing processes and related documentation follow established policies and procedures per Resonetics established Quality Management System. Support execution of process and equipment validations IQ/OQ/PQ/MVP/TMV). Create process documentation and training where applicable (Manufacturing Process, Manufacturing, Setup, Preventive Maintenance etc.). Identifies areas for improvement, suggests solutions, and submits idea records. Additional duties/projects as assigned. Required Qualifications: Currently enrolled and actively pursuing a (BS or MS) in Physics or relevant Engineering discipline. Good communication skills, comfortable with leading and providing project status updates to functional management and process teams. Tireless work ethic and understanding of deadline management. Good writing skills, able to write reports, manufacturing procedures and assist with validation activities. Familiar with formal problem-solving techniques (Cause & effect analysis, 5 Why’s, etc.) Effective interpersonal skills and adeptness in working with culturally diverse employee population. Ability to navigate ambiguity and negotiate alignment with stakeholders. Preferred Qualifications: Experience with statistical analysis skills (process capability, equivalence studies, regression, ANOVA, DOE). Familiar with SolidWorks (or equivalent) for tooling/fixture design. Well versed in GD&T and print generation. Experience with industrial lasers, interventional device design and manufacturing, device assembly. Exposure to medical device manufacturing or regulated environment.