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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 The Manufacturing Engineer supports manufacturing operations by assisting with process improvements, troubleshooting production issues, and maintaining stable and efficient manufacturing systems. This entry-level role provides hands-on engineering support on the production floor while developing technical skills in process optimization, data analysis, and equipment systems. The position also supports product trials, testing, and small-scale projects, working closely with Process Engineers, Operations, and R&D to execute improvements and support daily manufacturing needs. 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. Duties: Support analysis and improvement of manufacturing processes to enhance yield, throughput and product quality Assist in troubleshooting production issues on the manufacturing floor and support implementation of corrective actions Collect, organize and analyze process and production data to identify trends and improvement opportunities Support process improvement initiatives using structured problem-solving methods (5 Whys, Fishbone, basic Lean/Six Sigma tools) Assist with process mapping, time studies and documentation of manufacturing processes Work cross-functionally with Operations, Quality, and Maintenance to support implementation of process changes Take ownership of small, well-defined engineering projects with guidance from senior engineers Compile and analyze data using Excel, Minitab or similar tools; provide summaries and recommendations Support development and execution of Design of Experiments (DOE) under guidance Support installation, commissioning and startup of manufacturing equipment Assist in developing and updating standard work instructions (SWIs) and technical documentation Follow all safety, quality and operational standards Additional duties as assigned Skills Strong analytical and problem-solving skills Basic understanding of engineering principles and manufacturing processes Ability to analyze data and identify trends Strong communication skills with ability to explain technical concepts clearly Ability to manage multiple tasks and meet deadlines Proficiency in Microsoft Excel and standard engineering tools Basic technical writing and documentation skills Exposure to mechanical systems, equipment or laboratory environments a plus Abilities Ability to learn quickly and apply engineering concepts in a manufacturing setting Ability to work independently on well-defined tasks and projects with guidance Ability to follow structured problem-solving approaches Strong curiosity and willingness to learn across process, equipment and product domains Ability to work effectively in a fast-paced, hands-on manufacturing environment Strong ownership mindset and attention to detail Minimum Qualifications Bachelor’s degree in Engineering (Mechanical, Chemical, Industrial, or related field) 1+ years experience working in a manufacturing facility Preferred Qualifications Internship or co-op experience in manufacturing, R&D, or engineering environment Exposure to continuous improvement concepts (Lean, Six Sigma) Familiarity with data analysis tools (Excel; JMP, Minitab, or Python a plus) Exposure to CAD tools (AutoCAD, SolidWorks) a plus Experience working with mechanical systems, equipment, or laboratory testing Interest in manufacturing, process engineering, and equipment systems Bilingual preferred (English/Spanish) Physical Requirements Ability to stand and walk for extended periods of time on the manufacturing floor Ability to lift, carry, push, or pull up to 50 pounds occasionally Frequent bending, stooping, kneeling, and reaching to observe processes and troubleshoot equipment Ability to work in a manufacturing environment, including exposure to noise, moving machinery, and varying temperatures Ability to wear required personal protective equipment (PPE), such as safety glasses, gloves, and steel-toe shoes Ability to climb ladders or stairs and access different areas of the production facility as needed Visual acuity to read technical documents, monitor equipment, and inspect product quality Ability to use a computer and standard office equipment for extended periods of time Hearing and speaking to exchange information Dexterity of hands and fingers to demonstrate activities 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. Minimal travel (0-10%) will be required for this position. 50% of the time spent on the production floor and 50% 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. Monday - Friday, 8:00 AM - 4:30 PM
Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions. Manufacturing Technician I Monday – Friday 6:30AM – 3:00PM The Manufacturing Technician I performs fundamental tasks within a GMP environment in support of more complex manufacturing operations. The tasks include, but are not limited to, cleaning and maintaining the work place so that it meets the standards for controlling bioburden levels; cleaning operating equipment per applicable procedures so that it meets the standards established to prevent product contamination and maintaining records/logs neatly and accurately and in accordance with current standard procedures. The technician performs job tasks in a safe manner while following specific department safety rules. PRIMARY RESPONSIBILITIES: Responsible for equipment setup and operation in a biologics processing environment for plasma derived pharmaceuticals. Detailed cleaning of equipment/facilities to MSP/cGMP standards. Complete technical training profile as required. Strict adherence to Dept. Safety Rules. Bulk processing and filtration involving monitoring processing parameters (i.e. pH, weights, separation, assay results). Perform real-time documentation during the production run. ADDITIONAL RESPONSIBILITIES: English fluency both verbal and written. Basic math skills with proficiency in metric system. Accurate documentation skills are a must. Basic computer skills. Mechanical aptitude. Must be available to work any shift, including weekends. Ability to work well with others in a team environment is essential. Self-starter with the ability to work independently and use good judgment. Must be able to handle multiple priorities. Must be proactive, results oriented, and have strong attention to detail EDUCATION: High school diploma or GED required. Associates Degree or Bachelor’s degree preferred. Manufacturing, or experience in pharmaceuticals/biologics processing in a GMP environment is preferred. EXPERIENCE: 1-2 years’ experience in a manufacturing environment preferred. SKILLS & ABILITIES: Accurate documentation and attention to detail oriented. Usage of a 10-key calculator. OCCUPATIONAL DEMANDS: Ability to lift/push 50 lbs. All work is performed in a clean room (sanitized) manufacturing environment and must gown up. Must be able to work in a cold environment, job requires bending or standing for prolonged periods. This job description is accurate at the date of publication. It is intended to provide information essential to understanding the scope and general nature of the work performed by job holders within this position. This job description is not intended to be an exhaustive list of qualifications, skills, duties, responsibilities or working conditions associated with the position. Other duties may be assigned. #BiomatUSA The estimated pay scale for Manufacturing Technician I role based in California, is $18.70-$28.05 per hour. Additionally, the position is eligible to participate in up to 5% of the company bonus pool. We offer a wide variety of benefits including, but not limited to: Medical, Dental, Vision, life insurance, PTO, paid holidays and up to 5% 401(K) match and tuition reimbursement. Final compensation packages will ultimately depend on education, experience, skillset, knowledge, where the role is performed, internal equity and market data. We are committed to offering our employees opportunities for professional growth and career progression. Grifols is a global healthcare organization with employees in 30 countries focused on patient health and providing impactful results. Since our humble beginnings in 1909, Grifols has been a family company that prides itself on its family-like culture. Our company has more than tripled over the last 10 years, and you can grow with us! Third Party Agency and Recruiter Notice: Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate. Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws, including but not limited to, the California Fair Chance Act, the Los Angeles County Fair Chance Ordinance for Employers, and the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance. California Personnel Privacy Policy and Notice at Collection Location: NORTH AMERICA : USA : CA-Vista:USVISTA2 - Vista CA-980 Park Center Drive-AC Learn more about Grifols
*Position Summary* SMSbiotech, Inc is seeking a detail-oriented Quality Assurance Documentation Coordinator to support the day-to-day operations of our Quality Management System (QMS). This role is ideal for an organized, process-driven professional who thrives on keeping systems running smoothly. No prior biology or scientific background is required. The successful candidate will be trained on our cGMP environment and will focus on documentation control, compliance tracking, internal audit coordination, training management, and procurement support. *Key Responsibilities* *QMS Documentation Management* * Maintain, organize, and archive all QMS-controlled documents, including SOPs, work instructions, forms, logbooks, and records. * Ensure documents are reviewed, approved, and distributed according to document control procedures. * Track document revision history and manage version control across the QMS library. * Route documents for electronic or wet-ink signatures and ensure timely completion of approval cycles. *Logs, Forms & Compliance Tracking* * Monitor that all production logs, batch records, equipment logs, cleaning logs, and environmental monitoring forms are completed accurately and submitted on time. * Flag overdue or incomplete records and follow up with responsible personnel to ensure timely closure. * Support deviation, CAPA, and change control documentation by ensuring forms are initiated, routed, and closed within established timelines. *Internal Audit Coordination* * Assist in planning and scheduling the annual internal audit program in accordance with QMS-009 (Internal Quality Audits) or equivalent SOP. * Coordinate audit logistics including scheduling auditors, preparing audit checklists, and distributing audit notifications. * Track audit findings, observations, and corrective actions to closure. * Maintain audit records and compile audit summary reports for management review. *Training Management* * Maintain the training matrix and ensure all personnel complete required training on new and revised SOPs within defined timelines. * Track training completion status, send reminders for upcoming or overdue training, and escalate non-compliance. * Coordinate new-hire onboarding training schedules in collaboration with department leads. * File and organize training records (certificates, sign-off sheets, read-and-understand forms). *Ordering & Procurement Support* * Assist with ordering laboratory and facility supplies, consumables, and QA-related materials. * Track purchase orders, confirm deliveries, and maintain procurement logs. * Coordinate with vendors and suppliers to obtain quotes, certificates of analysis (CoAs), and other required documentation. * Support qualified supplier list maintenance and vendor qualification recordkeeping. *Qualifications* *Required* * High school diploma or equivalent; associate or bachelor’s degree preferred (any field). * Minimum 1–2 years of experience in document control, administrative coordination, quality assurance support, or a similar role (pharmaceutical, manufacturing, or regulated industry preferred). * Strong organizational skills with exceptional attention to detail. * Proficiency in Microsoft Office Suite (Word, Excel, Outlook) and document management systems. * Ability to manage multiple priorities and meet deadlines consistently. * Excellent written and verbal communication skills. *Preferred* * Familiarity with cGMP, FDA regulations, or ISO quality standards (training will be provided). * Experience with electronic quality management systems (eQMS) or document control software. * Prior experience coordinating audits or managing training records. * Basic understanding of procurement and supply chain processes. *Working Conditions* * Office-based role within the SMSbiotech, Inc biomanufacturing facility with occasional access to controlled manufacturing areas (gowning training provided). * Standard business hours with occasional flexibility needed during audits, inspections, or regulatory submissions. * Must be able to work on-site; this is not a remote position. *What We Offer* * Comprehensive on-the-job training in cGMP documentation practices — no science background needed. * Opportunity to grow within a fast-paced biotech startup environment. * Exposure to the full quality system lifecycle in a biomanufacturing setting. * Collaborative team culture with direct mentorship from experienced quality professionals. Pay: $52,000.00 - $68,000.00 per year Benefits: * 401(k) * Dental insurance * Health insurance * Vision insurance Education: * Associate (Required) Language: * English (Required) Location: * San Diego, CA 92121 (Preferred) Ability to Commute: * San Diego, CA 92121 (Required) Work Location: In person
* Assignment Duration: 6 months (extension subject to performance and fit) * Interview Method: Onsite * Work Location: San Diego, CA 92121 * Work Requirement: 100% Onsite * Shift: 1 * Work Days: Mon-Fri * Shift Time: 6:30am - 2:30pm PST * Hours: 8/day, 40/week *Job Description Overview* Performs a variety of operations to assemble mechanical components, sub-assemblies and sheet metal enclosures. Works with assembly prints, wiring diagrams and schematics to assemble drawers, chassis, enclosures and racks. Works on assignments that are complex in nature where judgment and initiative are required in resolving problems and making recommendations. Determines and/or follows methods and sequence of operations in performing hand soldering, wire harnessing and cabling on assembly units. * May be required to perform repair work as necessary. * Performs other duties as needed. * Performs routine go/no-go tests of circuits, components, instruments and mechanical assemblies. * Sets up test devices using hand tools or automatic test methods. * Documents test results. * May maintain logs and records denoting malfunctions.Requires production experience with vocational experience in mechanical assembly. * Reading, writing and basic arithmetic skills. * The ability to work from established drawings and experience in soldering, wire-wrapping and cable harnessing. * Ability to use hand tools and testing equipment. *Top 3 Required Skills* 1. Component polarity knowledge 3. Ability to read schematic/drawings 4. Good communication (written and verbal) and soft skills *Technologies* - MS Teams, IPC-610 *Keywords* - IPC-610, SMT machine experience, Polarity, ESD *Education Requirement* - HS Diploma or equivalent *Required Years of Experience* * Must have experience in the IPC-610 standard and circuit board assembly experience with SMT machine. Must have knowledge with electronic components placement and polarity * Preferred to have experience in the Siemens machine or ASM, Ekra pastes print, AOI *Physical Requirements* * Pushing Weight Limit = 25 * Pulling Weight Limit = 25 * Lifting Weight Limit = 25 Pay: $20.00 - $24.00 per hour Benefits: * 401(k) * Dental insurance * Health insurance * Paid time off * Vision insurance Work Location: In person
AleSmith Brewing Company is dedicated to creating the world’s highest quality beer while promoting an understanding and appreciation of craft beer and its styles and traditions to those we faithfully call our customers. We operate at the highest level of integrity and display excellence in all we do, from brewing to collaborating with each other and the organizations of our craft, and most of all, to the way we treat our customers. Job purpose The *Packaging Assistant- Late Shift (2:00pm-10:30pm)* will assist in all packaging operations, including cleaning, maintaining all Packaging equipment, and keeping warehouses and supplies organized. Also, to assist with regular brewery and packaging equipment maintenance while following safety procedures and Company SOP’s (Standard Operating Procedures). Duties and responsibilities Include the following. Other duties may be assigned. * Assists with setup, cleaning, and operation of packaging machinery * Places packages in boxes, applies carriers, and stacks finished product * Operates forklift to move pallets around warehouse * Assists with conducting inventory and related documentation * Operates keg washing machine to wash and sanitize kegs * Assists in the troubleshooting, repair and preventative maintenance of brewery equipment * Performs general cleaning duties, such as cleaning floors, drains, packaging equipment, and all packaging areas * Assist in the transition of duties and communication between shifts * Participate in continuing education related to brewery and packaging operations, and safety and regulatory requirements * Assist in resolving customer issues and ensure customer satisfaction while maintaining the integrity of the Company * Follows all safety procedures and SOP’s and wear safety, personal protective equipment (PPE) Qualifications 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, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. * Must be at least 21 years of age * Ability to work some evenings, nights, weekends, and holidays * Proficiency in communication, including verbal and written skills * Ability to work with hazardous cleaning chemicals * Ability to routinely lift, push and pull 55 lbs * Ability to stand and walk for up to 10 hours a day * Be motivated, hard-working, safety-minded and innovative with a commitment to representing and enjoying the culture and success of AleSmith * Be an exceptional team player with the ability to work independently as well * Ability to stay organized and follow checklists, departmental guidelines and SOP’s AleSmith Brewing Company provides equal employment opportunities to all employees and applicants for employment regardless of race, color, religion, gender, sexual orientation, gender identity or expression, national origin, ancestry, age, genetic information, marital status, pregnancy, medical condition, physical disability, mental disability, veteran status or any other characteristic protected by state or federal law. Job Type: Full-time Pay: $20.00 per hour Benefits: * 401(k) * 401(k) matching * Dental insurance * Employee assistance program * Employee discount * Health insurance * Life insurance * Paid time off * Referral program * Retirement plan * 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. Under close supervision, this position is responsible for developing, analyzing and reporting on quality plans, programs and discrepancies related to assembly, process, mechanical, electrical and electro-mechanical systems. Investigates problems and develops dispositions and corrective actions to non-routine discrepancies. Ensures that quality performance and products conform to established company and regulatory standards. Interfaces with manufacturing, engineering, customers, vendors and subcontractor representatives to ensure requirements are met. DUTIES AND RESPONSIBILITIES: Develops corrective action plans, nonconformance and summary reports, travelers, and other quality records; identifies and analyzes root cause, adequate disposition, corrective action, trends, incomplete operations and errors. Coordinates and may provide training to responsible personnel and supervisors to get records corrected, prevent recurrence, and improve processes. Develops and maintains corrective action and inspection databases, analyze data for trends, creates charts and reports, reviews results with management; prepares statistical analysis reports, specifications and other documents or reports as required. Reviews records and data for various elements of the company's quality system to ensure compliance and summarizes results (ex: ESD inspections, training records, oven charts, material out time cards, etc.) Coordinates with responsible personnel and supervisors to obtain corrective action. Plans, coordinates and prepares reports for internal audits of the company Quality Management System; conducts audits of manufacturing records on shop floor. 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. Have a detailed knowledge of QA processes, SAP, Windchill, Inspection Criteria, and Manufacturing Standards. Ability to effectively perform cross-functional interface between the Quality, the Production Floor, Design Engineering if needed, and Management to achieve the goals assigned to this position. Additional Functions Other duties as assigned or required. We recognize and appreciate the value and contributions of individuals with diverse backgrounds and experiences and welcome all qualified individuals to apply. Job Qualifications Typically requires a Bachelors degree in Manufacturing Technology, Mathematics or related field. May substitute additional experience as a quality analyst in lieu of education. Requires a basic understanding of quality procedures and system requirements in a manufacturing environment as well as basic knowledge of quality concepts and principles including the ability to read and understand engineering drawings and specifications; the ability to identify and interpret data; the ability to prepare detailed statistical reports and documents; interpersonal, verbal and written communication skills to explain general information effectively with all levels of employees; organization skills to maintain flow of work within the unit; the ability to establish priorities; and general knowledge of computer operations and applications and word processing and spreadsheets. Ability to work both independently and in a team environment is essential as is the ability to work extended hours as required. Job Category Quality Experience Level Entry-Level (0-2 years) Workstyle Onsite Full-Time/Part-Time Full-Time Salary Pay Range Low 51,650 Pay Range High 87,290 Travel Percentage Required 0% - 25% Relocation Assistance Provided? No US Citizenship Required? Yes Clearance Required? No Search Jobs at | General Atomics and Affiliated Companies
Company Overview: Charles Koll jewelry works is a leader in the fine custom jewelry design & manufacturing. Our team is made up of skilled craftsman, technicians and designers who work onsite in a dynamic, creative, and challenging environment that enables our clients to experience the joy of fine jewelry making. Job Description: We are seeking skilled and detail-oriented Goldsmiths to join our team. The ideal candidate will have experience in jewelry manufacturing and repair. As a Goldsmith at Charles Koll jewelry works, you will work closely with our design team and operations to bring unique jewelry to life, ensuring each item meets our standards of excellence. If you have an open mind, are team oriented, have a desire to grow with our company and a willingness to learn Responsibilities: * Minimum Mandatory Skills * Read and interpret design drawings and technical specifications. * Strong Communication Skills * Conduct quality assurance checks to ensure all your work meets the company’s quality standards. * Committed to deadlines * Maintain tools and equipment * Ensure a clean and safe working environment. * Jewelry Repair in gold, silver and Platinum * Ring resizing * Chain repair * Polish and refurbishing * Plating * Stone Tightening * Custom Jewelry Manufacturing * Clean castings for setting * Additional Skills * Stone setting: Prong, bezel, channel, pave ect * Hand engraving * Laser Repair Qualifications: * Strong attention to detail and a commitment to craftsmanship with a desire to improve. * Good communication skills for effective collaboration with team members and clients. * Physical dexterity and vision necessary to work with small, detailed items. * Professional certification or training in Jewelry Design or Metal Arts but not necessary. Compensation & Benefits: * Competitive salary $25-$50 per hour depending on skill * Overtime * Health, dental and vision benefits package. * 2 weeks paid vacation * Opportunities for professional development and training. * A creative and supportive work environment. * Relocation Bonus Job Type: Full-time Pay: $25.00 - $50.00 per hour Benefits: * Employee discount * Health insurance * On-the-job training * Opportunities for advancement * Paid time off * Professional development assistance * Relocation assistance Work Location: In person
*Charles Koll Jewelry Works* — a San Diego leader in fine custom jewelry — is seeking a *highly skilled Stone Setter / Goldsmith* with a passion for craftsmanship, design, and detail. Our ideal candidate thrives on collaboration, bringing unique one-of-a-kind pieces to life through expert bench work and setting precision. *About the Role* This position focuses on *custom jewelry creation*, not mass production. You’ll be part of a small, experienced team that delivers heirloom-quality work every time. *Responsibilities* * Execute complex stone setting across all setting styles (prong, bezel, pavé, channel, flush, tension, etc.) for custom and one-of-a-kind designs * Collaborate closely with CAD designers, goldsmiths and operations to refine setting style before production * Perform precision assembly, soldering, laser welding and finishing on platinum and gold custom pieces * Evaluate designs for durability and make recommendations when needed * Work creatively and efficiently to meet project timelines while maintaining Charles Koll’s uncompromising quality standards * Maintain organized workspace, tools, and shared resources *Qualifications* * Minimum *5+ years of fine jewelry bench experience* with a focus on *custom, one-of-a-kind work and setting* * Mastery in *stone setting under microscope* — including micro pavé and intricate layouts * Expert-level understanding of *metal behavior, stone fragility, and jewelry engineering* * Familiarity with *CAD and casting workflows* for collaborative project planning * Strong communication skills and pride in craftsmanship * Laser welding experience *Why Work With Us* * Join a legacy San Diego custom jewelry house known for innovation, integrity, and artistry. In business since 1991 with a new state of the art facility. * Work alongside master jewelers and designers on meaningful, creative projects * Full time hourly $40-$60 per hour * Flexible schedule * Benefits package: health, dental, vision, and paid time off * Supportive, growth-oriented environment focused on long-term employee retention * Overtime * Relocation bonus Job Type: Full-time Pay: $40.00 - $60.00 per year Benefits: * Employee discount * Health insurance * Opportunities for advancement * Paid time off * Professional development assistance Work Location: In person
Summary: Responsible for part assembly, building and testing of optical, electrical and mechanical instrumentation. Performs work according to written instructions and training provided by the Manufacturing and Production Managers and Process Engineers. Performs in-process and final testing on product. Provides general support within the manufacturing team, including handling, preparation and packaging of incoming and outgoing products. All work performed within ISO9001 environment. Duties and Responsibilities include the following. Other duties may be assigned. Assemble, manufacture, and deliver instruments per established work instructions, travelers, and processes. Design, build and maintain product assembly jigs and test equipment, if needed Develop and maintain the instrument manufacturing Work Instructions for product assembly and sub-assemblies, as required Evaluate and solve production problems. Cross-train fellow assemblers or conduct training to introduce new processes as needed Effectively document manufacturing, assembly, and quality processes on provided process documents. Responsible for the effective time management of tasked instrument line deliveries and manufacturing run completions to meet expected dates and deadlines. Take, and store data from processes effectively. Attend project kick off meetings and ensure project materials are available. Ability to effectively interface with development engineers and program managers. Ability to work with minimal supervision. Strong knowledge of hand tools, machinery and electrical test equipment. Ability to interpret engineering drawings, manufacturing instructions and test specifications. Perform assembly level quality assurance and calibration functions. Works with quality managers and quality technicians to ensure equipment meets required calibration and expectations. Evaluates, and improves manufacturing methods, utilizing knowledge of product design, materials and parts, fabrication processes, tooling and production equipment capabilities, assembly methods, and quality control standards. Participate in sustaining engineering design reviews. Attend weekly manufacturing meetings. Mandatory attendance for all-hands SOC safety, security and HR meetings.
The Opportunity We're experiencing exceptional growth with demand for our precision instruments. We're seeking an experienced Manufacturing Manager to lead our production operations, dramatically scale our output, and build the manufacturing infrastructure needed to meet this exciting market demand. This is a unique opportunity to make an immediate, measurable impact on a growing company. Key Responsibilities · Lead and optimize manufacturing operations for complex optical instruments and systems · Scale production capacity from current levels to double, triple, etc.. · Manage and mentor technical manufacturing staff · Identify and eliminate production bottlenecks through process analysis and improvement · Develop and implement production schedules that balance quality, efficiency, and delivery commitments · Establish and maintain quality standards for precision optical and mechanical assemblies · Coordinate with engineering, quality assurance, and supply chain teams to ensure seamless production flow · Implement manufacturing best practices, lean principles, and continuous improvement initiatives · Troubleshoot technical manufacturing challenges involving optics, mechanics, electronics, and software integration · Manage equipment, tooling, and facility requirements for scaled production · Develop SOPs, work instructions, and training programs for manufacturing personnel
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: $73,100.00 - $120,200.00 Responsible for supporting Quality Engineering requirements for change control, continuous improvement, and customer complaints handling and satisfaction. Will serve as a subject matter expert and liaison between company and customers with the goal of resolving quality and manufacturing issues and ensuring positive channels of communication to ensure customer satisfaction. Duties and Responsibilities: Key member of complaint and MRB investigation teams. Analyze, identify, develop and implement manufacturing, production, and other process improvements which will improve capability, and/or performance. Meet with appropriate teams and/or individuals to offer recommendations and share results. Responsible for change control process, perform risk assessment and facilitate the change control plan writing and execution. Monitor change implementation process and close change plan in a timely manner. Responsible for implementation and validation of a new electronic Quality Management System. Prepare quality information and trending data to be shared in the management review meeting. Enable positive communication channels internally and externally to ensure the highest level of customer satisfaction. Actively participate in internal, customer, and third-party audits. Other duties as assigned. Minimum Job Requirements : Bachelor of Science degree in Quality, Biology, Chemistry or similar. Minimum 2 years’ experience as a Quality professional in a manufacturing environment. Diagnostics, pharmaceutical or Biological products manufacturing environment is preferred. Proficient in understanding and application of ISO13485. Auditing, Six Sigma and Lean Manufacturing experience a plus. Knowledge, Skills and Abilities Required: Manage time wisely and effectively prioritize multiple competing tasks. Ability to identify and solve problems, develop innovate solutions, act decisively and apply good judgement. Readily able to offer opinions and take action when the position may be unpopular. Skilled at handling situations diplomatically. Proven team player who has demonstrated capabilities in the following areas: excellent communication, interpersonal skills, well developed problem-solving skills; solid organizational skills and the demonstrated ability to be self-directed and effectively relate to all levels of the organization. Strong computer skills a must, to include Word, Excel, PowerPoint; experience with Access Database 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.
Description: The Production Associate is an entry level position responsible for operating and monitoring the mushroom processing equipment per M2 Ingredients policies, procedures, and applicable laws. This position processes raw materials into a finished product. Primary job responsibilities are to operate production equipment, clean appropriate equipment, and pack off finished products. Essential Duties and Responsibilities: Responsible for reporting on food safety and/or quality problems to personnel with the authority to initiate corrective actions. Operate and monitor mushroom processing equipment per internal specifications. Accurately document activities through HACCP forms, sanitation checklists, and daily production reports. Fill out production paperwork accurately and legibly. Understand and follow the Company's HACCP and GMP guidelines for processing and production. Operate all equipment and machinery per company SOP guidelines. Report any machinery issues to management. Break-down, clean and set up machinery and equipment after production. Participate in product and equipment change overs. Perform pre and pos operation sanitation process and inspections of equipment to ensure product safety. Read and interpret documents such as safety rules, operating and maintenance instructions, and procedures. Observe all safety guidelines and report safety concerns to management. Maintain a clean and safe work area. Ensure that production requirements and standards are met consistently. Make every effort to increase productivity and efficiency without compromising quality. Relay information to co-workers on shift as well as other departments. Demonstrate a positive and professional attitude. Able to work overtime as required, including weekends. Requirements: Qualifications: High school diploma or general education degree (GED); or one to three months related experience and/or training; or equivalent combination of education and experience. Previous GMP training desired but not required. Experience in dietary supplement or Food industry (21 CFR 111) preferred.