Manufacturing Technician Jobs in Hialeah, FL

Akron Biotech is continuing to transform and further its rapidly growing capabilities and is now seeking highly motivated professionals to join our expanding team. This is an exciting opportunity to play a critical role within our organization that is driving advanced therapy development and commercialization with high quality industrial scale solutions. We manufacture and distribute components and raw materials for cell therapy discovery, development, and commercialization to meet industry needs worldwide. We offer an array of highly competitive benefits and perks to our valued associates. General ResponsibilitiesProvides development and manufacturing operations support including the formulation and aseptic filling of Cryopreservation media, cell culture media, and cell culture supplements. Executes and maintains documentation relating to manufacturing. Supports all technical writing requirements for manufacturing/operations. Author and revise manufacturing batch records, SOPs, work instructions, validation/qualification protocols, forms, logbooks, technical reports, CAPAs, change controls and any other document that may apply. Formulate, fill and finish Akron manufactured products, including cryopreservation media, cell culture media, and supplements. Perform aseptic processes in a controlled or cleanroom environment. Perform in-process testing of products using general laboratory equipment/instrumentation. Utilizes formulas, work instructions or equivalent to monitor the production process. Perform experiments associated with development, improvement and scaling up or optimization of manufacturing and development processes. Troubleshoot problems associated with equipment, process development/production/ including data analysis and internal record keeping. Perform Environmental Monitoring activities as required. Perform the cleanzone cleaning as required. Maintains current knowledge of developments related to product recovery and purification processes. Performs duties in accordance with established laboratory standards. Evaluate, troubleshoot and solve routine problems. Interprets data based on knowledge and experience. Perform process validation and equipment qualification as required. Perform general equipment preventive maintenance. Contribute to maintaining lab and equipment cleanliness. Support and coordinate deviation investigations and implementation of change controls or robust corrective and preventative actions. Support finished product labeling, raw material aliquoting and, re-labeling requirements when necessary. Perform other duties as assigned. RequirementsBS or MS in Biology, Chemistry, Bioengineering or a related field + 2 years minimum experience working in a life science manufacturing role. Detailed oriented with good time management and organizational skills. Ability to work well under pressure and prioritize assignments in a multi-task position. Motivated and able to work independently. Excellent verbal communication skills and people/customer service oriented. Basic knowledge of Outlook, Word, Excel and Software Programs. Requires a strong adherence to cGMPs regulatory compliance and safety requirements, SOPs and other related documents such as SDS and manuals. In addition to competitive compensation, we offer a comprehensive benefits package including: 401K plan with employer match PPO and HMO medical insurance plan availability Company paid dental and vision insurance Company paid short-and long-term disability Company paid life insurance Company paid holidays Generous paid time off allowances Employee referral bonus Employee gym reimbursement program Employee recognition program EOE/DFW

Department: Strategy Title: SR. SEO Specialist GlueIQ is the brainchild of our collective obsession with Creativity, Culture, and Tech. We understand that complex problems are best solved collaboratively, and it was time for a creative consultancy model that could foster those critical connections between people, process, and tools that drive meaningful growth for our clients. KEY RESPONSIBILITIES Collect and analyze data and results, identify trends and insights in order to achieve maximum ROI in search campaigns Track, report, and analyze website and landing environment/Lead Forms and Paid initiatives and campaigns Manage SEO Planning, Recommendations, Cost Estimates, and ROI Estimates Optimize copy and landing pages for search engine marketing Perform ongoing keyword discovery, expansion and optimization Research, recommend, and implement search engine optimization campaigns/plans Maintain updated competitive sets/assessments Develop and implement link building strategy Work with development teams (internal and external) to ensure SEO best practices are being followed in newly developed code Work with editorial and marketing teams to drive SEO in content creation and content programming Recommend changes to website architecture, content, linking and other factors to improve SEO positions for target keywords and audiences KEY REQUIREMENTS Proven SEO experience Have a working knowledge of SEM, PPC campaigns Solid understanding of performance marketing, conversion, and online customer acquisition In-depth experience with website analytics tools (e.g, Google Analytics, Adobe, Etc.) Experience with bid management tools (e.g., Kenshoo) Experience creating A/B and multivariate experiments Working knowledge of HTML, CSS, etc. development and constraints Knowledge of ranking factors and search engine algorithms Up-to-date with the latest trends and best practices in SEO and SEM BENEFITS: Glue-IQ pays 100% of Health plan premium (health, dental, vision) Hybrid working environment (3 days a week of choice in office) 401k Profit-Sharing Plan Client-specific benefits and perks Office is the heart of Coral Gables GlueIQ is strongly committed to hiring a diverse staff, and believes all experiences and perspectives bring value to our clients. GlueIQ does not discriminate on the basis of race, color, gender, disability, age, religion, sexual orientation, national origin, ethnic origin, or any other characteristic protected by state or federal law. The above statements are intended to describe the general nature and level of work being performed. They are not to be construed as an exhaustive list of all responsibilities, duties, and skills required. All employees may be required to perform duties outside of their normal responsibilities from time to time, as needed.

Essential Functions and Responsibilities: Responsible for the supervision of employees in Manufacturing, plans and assigns work, implements policies and procedures, and recommends improvements in Manufacturing methods, equipment, operating procedures and working conditions. Supervises the blending, coating, tablets, bulk, and pharmacy manufacturing operations. Reviews manufacturing batch records and work plans. Performs Visual transactions to assure the timely flow of materials and products. Writes batch records, SOP's, special instructions, discrepancy reports and batch investigations as needed. Enforces Current Good Manufacturing Practices and Standard Operating Procedures. Creates, monitors and maintains safe working environment throughout the operation. For employees on the shift and department, schedules paid time off, participates in annual performance evaluations and administers routine discipline. Performs quality checks to assure product meets quality standards and batch record documentation is complete and accurate. Utilizes staff to efficiently meet daily departmental requirements. Assists in training operators in all phases of the processes Assures the production areas are kept neat and clean. Maintains cost consciousness throughout the operation. Liaison between production and support groups. Enters basic computer data into different databases as needed to support the operation. Plans and directs production activities and establishes production priorities for products in keeping with effective operations and cost factors. Coordinates production activities with procurement, maintenance, and quality control activities to obtain optimum production and utilization of human resources, machines and equipment. Reviews and analyzes production, quality control, maintenance, and operational reports to determine causes of nonconformity with product specifications and operating or production problems. Develops and implements operating methods and procedures designed to eliminate operating problems and improve product quality. Revises production schedules and priorities as result of equipment failure or operating problems. Consults with maintenance personnel in regard to modification of machines and equipment in order to improve production and quality of products. Enforces cross training between different Manufacturing operations Performs other duties as assigned by immediate Supervisor Qualifications: High school diploma plus three to eight years related experience and/or training; or equivalent combination of education and experience. Previous supervisory experience. 3 - 5 years' experience in a manufacturing environment Bilingual (English and Spanish) required Strong knowledge of the GMPs and Safety Knowledge of Word, Excel and Outlook. Ability to handle multiple priorities Basic mathematical skills- with emphasis in division in all units of measure, using whole numbers, common fractions and decimals. Experience with Bosch and Fete machines Other: Must be able to work M- F 10pm to 5:45am Physical Requirements: Handle loads up to 10 lbs., sometimes up to 20 lbs. A lot of walking or standing, bending, squatting or you might stand to use your arms to set up machines, equipment or tools.. Seeing clearly at a distance and up close. Speaking clearly enough to be able to be understood by others. Identifying and understanding the speech of another person. Typical Work Conditions: Person will be subject to food and nutritional bulk ingredients, which may affect the respiratory system or the skin, including an environment subject to odors, dust or airborne allergens. Person will be working in a dry and low moisture environment and exposed to normal work hazards, including a variety of physical conditions such as a proximity to moving mechanical parts. Exposure to noise.

Production Operator Coral Springs, FL 2nd Shift (time range of 12:00 pm to 3:00 am, with 8-hour shifts that may vary daily. Additional hours, including weekends, may be required based on operational needs.) Temporary for 6 months. Pay Range - $20 - $22 Per Hour Depending on the experience Job Summary: As a Production Operator, you will play a vital role in the manufacturing, labeling, and packaging of medical drug products. You will be responsible for ensuring that production processes run smoothly, safely, and efficiently, adhering to the highest standards of quality and compliance. Job Responsibilities: Verify dispensed raw materials for batches and stages components. Assemble production equipment for each batch and perform equipment daily usage checks. Follow and understand all Batch Record and SOP instructions while completing relevant documentation. Document all operational parameters and steps in the batch record for manufacturing and packaging. Perform standard in-process testing procedures daily. Monitor production lines for accuracy, stability, conformity, and product defects. Stage and distribute components for manufacturing and packaging batches. Place product into shipper boxes and attach shipping labels. Document and dispose of all production waste in dedicated waste containers at the end of each batch. Transport finished goods using carts or pallet jacks, including moving in and out of refrigerated coolers. Clean production rooms and equipment, documenting tasks in logbooks. Support Laboratory and QA operations as needed. Work safely as part of a team to achieve all outcomes. Operate in accordance with company values, including Collaboration, Courage, Perseverance, and Passion. Perform major and minor GMP room cleaning tasks. Perform compounding activities, including delicate equipment setup. Troubleshoot minor equipment issues and make in-process adjustments to maintain operating parameters. Assist in coaching and mentoring Level I operators as needed. Execute all Operator I functions. Perform all other relevant duties as assigned. Job Requirements: Computer literacy is required High school diploma or GED equivalent. Minimum of six months of experience and/or training, or equivalent combination of education and experience within a production cGMP environment. Knowledge of FDA cGMP, GDP, and SOPs. Ability to read, interpret, and complete documentation in English. Proficiency in basic math skills, including the ability to use different units of measure and calculate averages. Ability to apply common sense and follow detailed instructions. Physical Requirements and Working Conditions: Must be able to sit, stand, walk, stoop, kneel, crouch, or crawl for at least 8 hours. Ability to frequently lift and/or move up to 50 pounds. Exposure to varying temperatures (2°C to 25°C) and moving mechanical parts. Potential exposure to fumes, airborne particles, toxic, and/or caustic chemicals (PPE Provided). Must be able to wear personal protective equipment (PPE) such as respirators, jumpsuits, eye, and hearing protection. May require additional hours, including weekends, depending on operational needs. ttg Talent Solutions is an Equal Opportunity Employer and recruiting agency. We are committed to creating an inclusive and diverse work environment and welcome applications from all qualified candidates regardless of race, color, religion, gender, sexual orientation, national origin, age, disability, or veteran status. Please note that all offers of employment are contingent upon the successful completion of a drug test and background check. We maintain a drug- and substance-free workplace to ensure the safety and well-being of all employees. At ttg, “We believe in making a difference One Person at a Time,” ttg OPT. IND1

SummaryInstall, maintain, and repair internal factory equipment. Supervise employees who perform maintenance and tool making. Accountable for the quality of own work. Subject to direct operations supervision/prescribed work instructions/systems checking. Executes within a well-defined operations framework. There is generally a step by step sequence of standard operational tasks which need to be followed to achieve an end result.Job Description Roles and Responsibilities Ensure that manufacturing premises are fully operational, maintained, and clean. This is manufacturing specific and does not include gardeners, caterers, etc. Developing conceptual knowledge of professional discipline. May include support roles with specialized expertise or technical knowledge in broad area. Applies general knowledge of business developed through education or past experience. Understands how work of own team contributes to the area. Resolves issues using established procedures. Consults supervisor or more senior team members for issues outside of defined instructions/parameters. Collaborates with others to solve issues. For customer facing roles, develops strong customer relationships and serves as the interface between customer and GE. Exchanges technical information, asks questions and checks for understanding. Maintaining site security. Handling global security initiatives. Maintaining employee and visitor badging systems. Required Qualifications Bachelor's degree from an accredited university or college with a minimum of 2 years of relevant experience High school diploma / GED with at least 6 years of relevant experience Desired Characteristics Strong oral and written communication skills. Ability to document, plan, market, and execute programs. This role requires access to U.S. export-controlled information. If applicable, final offers will be contingent on ability to obtain authorization for access to U.S. export-controlled information from the U.S. Government. Additional Information GE Aerospace offers a great work environment, professional development, challenging careers, and competitive compensation. GE Aerospace is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law. GE Aerospace will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable). Relocation Assistance Provided: No

Wondering what's within Beckman Coulter Diagnostics? Take a closer look. At first glance, you'll see that for more than 80 years we've been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, be supported, and always be yourself. We're building a culture that celebrates all our associates' experiences and perspectives. Look again and you'll see we are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful. Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, we're working at the pace of change to improve patient lives with diagnostic tools that address the world's biggest health challenges. The Technician Production-Operations for Beckman Coulter Diagnostics is responsible manufacturing control and calibration products in a Food and Drug Administration (FDA)-regulated environment. In this role, you will perform In-Process testing and calculations of our products to determine acceptance ranges for Beckman Coulter Inc. (BCI) Flow Cytometers (instruments such as FC-500, AQUIOS and NAVIOS). This position is part of the Reagents Manufacturing Department located in Hialeah, FL and will be on-site. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. You will be a part of the Reagents Manufacturing team and report to the Reagents Manufacturing Supervisor. If you thrive in a fast-paced, multifunctional role and want to work to build a world-class Supply Chain a fast-paced, multifunctional role and want to work to build a world-class Supply Chain organization-read on. In this role, you will have the opportunity to: * Compile and analyze test information to determine whether the process or equipment is operating efficiently and to diagnose malfunctions. * Use relevant information and Critical Thinking skills to determine product and process compliance with the Quality System Regulations. * Drives Continuous Process Improvement * Contributes technical expertise and direction for root-cause analysis of product issues as well as implementation and sustainment for product issue remediation. The essential requirements of the job include: * High school degree (or equivalent degree) with 2+ years exp. * Prior experience in manufacturing or assembly line work/machinery * Ability to read and interpret technical documents. Physical/Environment Requirements: * Ability to lift 50 pounds with or without assistance and stand 6 to 7 hours a day. It would be a plus if you also possess previous experience in: * Basic troubleshooting skills to identify minor issues with machinery and ability to read and interpret technical documents. * The position requires concentration for long periods and good hand-eye coordination when working in assembly line process. Stand Up forklift exp. * Ability to perform basic math for keeping accurate levels of inventory and for documenting defects or issues that occur in the operation. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit **************** Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. The EEO posters are available here. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at applyassistance@danaher.com to request accommodation.

Install, maintain, and repair internal factory equipment. Supervise employees who perform maintenance and tool making. Accountable for the quality of own work. Subject to direct operations supervision/prescribed work instructions/systems checking. Executes within a well-defined operations framework. There is generally a step by step sequence of standard operational tasks which need to be followed to achieve an end result. Job Description Roles and Responsibilities * Ensure that manufacturing premises are fully operational, maintained, and clean. This is manufacturing specific and does not include gardeners, caterers, etc. * Developing conceptual knowledge of professional discipline. May include support roles with specialized expertise or technical knowledge in broad area. * Applies general knowledge of business developed through education or past experience. Understands how work of own team contributes to the area. * Resolves issues using established procedures. Consults supervisor or more senior team members for issues outside of defined instructions/parameters. * Collaborates with others to solve issues. * For customer facing roles, develops strong customer relationships and serves as the interface between customer and GE. * Exchanges technical information, asks questions and checks for understanding. * Maintaining site security. * Handling global security initiatives. * Maintaining employee and visitor badging systems. Required Qualifications * Bachelor's degree from an accredited university or college with a minimum of 2 years of relevant experience * High school diploma / GED with at least 6 years of relevant experience Desired Characteristics * Strong oral and written communication skills. * Ability to document, plan, market, and execute programs. This role requires access to U.S. export-controlled information. If applicable, final offers will be contingent on ability to obtain authorization for access to U.S. export-controlled information from the U.S. Government. Additional Information GE Aerospace offers a great work environment, professional development, challenging careers, and competitive compensation. GE Aerospace is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law. GE Aerospace will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable). Relocation Assistance Provided: No

Job Purpose The Operations Processing Technician I support the processing and documentation requirements of tissue during the cleaning, cutting, shaping, inspecting, and packaging operations for transplantation purposes. The Operations Processing Technician I is also responsible for ensuring that all equipment and supplies used for processing are maintained and ready for use, and that all Processing Room maintenance is completed daily while complying with Quality Assurance requirements as mandated by federal, state, and trade regulations. Duties and Responsibilities Promotes Lean behaviors across the organization (includes leading and participating in Try storming, Brainstorming and other Lean related initiatives) Preparation of aseptic processing, environmental set-up including all equipment supplies and monitoring of sterile rooms as per SOP requirements. Processing of all allografts for clinical use such as bone, soft tissues, skin, autografts and other tissues as instructed by Processing Supervisor, Team Lead or designee. Daily activities include: Preparation and preservation of all types of bone, soft tissue, and birth tissue for cutting and shaping into allografts. Lyophilization Treatment of tissue with liquid nitrogen when applicable Tissue allograft Culture sampling and packaging as specified by SOPs. Decalcification of bone as applicable per SOPs. 5. Familiarity and knowledge of information contained in the Tissue Bank Manuals. 6. Applies Problem Solving Techniques and 5 WHY's analysis to address Non-Conformities, Correction reports, and Customer Complaints as well as Technical Challenges by means of applying the root cause analysis process. 7. Ensures that Processing Operations comply to State and Federal Regulations and AATB Standards. 8. Driven by a challenging sense of urgency for customer delivery and Quality Standards during Processing. 9. Coordinates with Supporting Teams During the Process of Product Transfer for Execution of pilot runs at the Processing Stage. 10. Uses Judgment to Identify, Troubleshoot and resolve Day-to-Day Technical Operations Flow interrupters. Requirements Qualifications Bachelor's Degree in science or related with a minimum of 0-1-year relevant experience or Associate degree with 1 or more years of relevant experience. Tissue Banking experience Preferred. Strong analytical, planning critical thinking, and troubleshooting skills. Ability to effectively communicate with multidisciplinary teams. Qualifications include: Computer Processing Lean Behaviors Problem Solving Strong Interpersonal and organizational skills Good documentation skills Written, Verbal and strong communication skills Attention to detail Working Conditions Majority of the work is performed indoors and in a cleanroom environment. Must be willing to work weekends and evening hours as necessary. Must be willing to accommodate travel if necessary. Physical Requirements The ability to stand for extended periods of time. Occasional lifting/pushing heavy objects up to 50 pounds. Direct Reports No Direct Reports.

Vitamin Manufacturing Employment Type: Large Projects Industry: Vitamin, Supplements Manufacturing Pay Rate: $18 per hour Schedule: Monday to Friday, 7 AM to 3:30 PM Job Description: Production Workers Various stations available Blending: Opening boxes of raw material, loading products into a blender with a vacuum feeder, weighing containers, and replacing when empty. Granulator: Load products into the machine, weigh, and replace containers when empty. Sieving: Load product into the machine with a vacuum feeder, weigh containers and replace when full of the empty container. Miller: Manually load products into machines, weigh containers, and replace them when empty. Packaging: Load products into a metal detector with a vacuum feeder, seal bags, and seal boxes with the final product, and place them onto pallets. Benefits: Excellent Benefits

About us Neocis is an established start-up revolutionizing dentistry with Yomi, the first, and only FDA cleared robot for assisted dental surgery. The company collaborates closely with leading clinicians to develop innovative technologies that help advance patient care and improve quality of life. Based in Miami, Florida. Neocis is venture-backed with funding from several prominent investors. What's in it for you? * You'll thrive in our innovative and collaborative environment * Make an immediate impact on life-changing technology. Avoid silos and "not my job" mentality in our smaller, fast paced, startup environment * We offer sabbatical, parental leave and unlimited PTO policies * Generous 401K plan with 4% company match * Comprehensive benefits package that includes medical, dental and vision. The role: Manufacturing Technician The Manufacturing Technician is responsible for performing a variety of duties in the electronic, mechanical, electromechanical, and/or optical areas. The role constructs, troubleshoots, calibrates, adjusts, tests, diagnoses, and maintains equipment, components, devices, or systems, working from schematics, engineering drawings and written or verbal instructions. What you'll do * Builds, tests and integrates subassemblies, independently or in partnership, in order to manufacture "Yomi". * Performs calibration and alignment checks using CMM arm; performs adjustments, modifications and replacements as directed; prepares prescribed compounds and solutions. * Builds Field Replaceable Units (FRU) and Consumables in order to fulfill customer sales orders. * Occasionally provides troubleshooting, testing and or assembly aid in the field. * Constructs, troubleshoots, calibrates, adjusts, tests, diagnoses, and maintains test equipment, components, devices and/or systems. * Interprets schematics, engineering drawings and written or verbal instructions and procedures. * Operates related equipment, conducts tests and reports data in prescribed format. * Supports and participates in planned and unplanned internal, regulatory and/or notified body audits. Provides information that is timely, accurate and substantiated by objective evidence. * Conducts manufacturing, quality control and R&D tasks per approved operational procedures or as defined by the requestor of the tasks. * Maintains company working areas and local environment in accordance with applicable general operating procedures. * Assures that all measuring instruments in use are within calibration limits. * Responsible for ensuring compliance with all local, national, international and company regulations, policies and procedures for Health, Safety and Environmental compliance. * Completes training as applicable for Good Manufacturing Practices (GMP) related tasks. * Follows all applicable Quality and Safety procedures. * Follows Good Documentation Practices (GDP). What you'll bring * High school diploma and on-the-job training or postsecondary certificate or associate's degree * Advanced problem-solving and debugging experience in mechanical and electrical assemblies. * Ability to review Engineering drawings and accompanying specifications. * 5S and Lean Manufacturing experience. * Proficient in Microsoft Excel, Powerpoint and Word. * Good verbal and written communication skills. * Ability to use bench top test equipment and custom manufacturing test stations. * Ability to escalate equipment downtime as needed. * Knowledge of the English and Metric measuring systems with the ability to perform mathematical conversions to each. * Ability to work overtime as required. * Experience with GMP requirements and medical industry requirements * Able to define Preventative Maintenance procedures and review/maintain spare parts for the equipment. * Experience in process and tooling development, test method development, data acquisition and analysis. * General metrology skills (e.g., experience with machinist microscopes, calipers, ROI and weight scales). * Experience with all requirements of electrical LOTO, chemical handling and hazardous waste guidelines. * Clear understanding of EHS requirements. * Progressive technical certifications preferred. What else? * This is not a supervisory role * The position will require up to 5% travel in and out of state * Reasonable accommodation may be made to enable candidates with disabilities to perform this role * The main location of this role is in a medical devices manufacturing facility and requires: * This position requires the regular use of office and role specific equipment such as * This position requires the regular use of, at a minimum: torque wrenches, calipers, multimeters, hex keys, CMM arm, CNC engraver * Prolonged periods working on a computer * Ability to lift/push/carry items up to 30 pounds Position Type and Work Schedule This is a full-time position. This position occasionally requires long hours and weekend work. Other Duties Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities and activities may change at any time with or without notice. #LI-Onsite

Wondering what's within Beckman Coulter Diagnostics? Take a closer look. At first glance, you'll see that for more than 80 years we've been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, be supported, and always be yourself. We're building a culture that celebrates all our associates' experiences and perspectives. Look again and you'll see we are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful. Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, we're working at the pace of change to improve patient lives with diagnostic tools that address the world's biggest health challenges. The Technician Production-Operations for Beckman Coulter Diagnostics is responsible manufacturing control and calibration products in a Food and Drug Administration (FDA)-regulated environment. In this role, you will perform In-Process testing and calculations of our products to determine acceptance ranges for Beckman Coulter Inc. (BCI) Flow Cytometers (instruments such as FC-500, AQUIOS and NAVIOS). This position is part of the Reagents Manufacturing Department located in Hialeah, FL and will be on-site. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time. You will be a part of the Reagents Manufacturing team and report to the Reagents Manufacturing Supervisor. If you thrive in a fast-paced, multifunctional role and want to work to build a world-class Supply Chain a fast-paced, multifunctional role and want to work to build a world-class Supply Chain organization-read on. In this role, you will have the opportunity to: Compile and analyze test information to determine whether the process or equipment is operating efficiently and to diagnose malfunctions. Use relevant information and Critical Thinking skills to determine product and process compliance with the Quality System Regulations. Drives Continuous Process Improvement Contributes technical expertise and direction for root-cause analysis of product issues as well as implementation and sustainment for product issue remediation. The essential requirements of the job include: High school degree (or equivalent degree) with 2+ years exp. Prior experience in manufacturing or assembly line work/machinery Ability to read and interpret technical documents. Physical/Environment Requirements: Ability to lift 50 pounds with or without assistance and stand 6 to 7 hours a day. It would be a plus if you also possess previous experience in: Basic troubleshooting skills to identify minor issues with machinery and ability to read and interpret technical documents. The position requires concentration for long periods and good hand-eye coordination when working in assembly line process. Stand Up forklift exp. Ability to perform basic math for keeping accurate levels of inventory and for documenting defects or issues that occur in the operation. Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. For more information, visit **************** Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes. The EEO posters are available here. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at applyassistance@danaher.com to request accommodation.

At Truemont Materials, we engage our team members to take what nature gives us and mold it into concrete products that are usable, lasting, and have the look of natural stone. Our concrete products are wet cast in molds made from real weathered stone. We are an experienced, results-oriented, collaborative group catering to a growing industry of concrete products. We thrive around developing new ideas, products, systems, and technologies, along with analyzing and improving on existing ones. We are currently looking for team players to join our production, performing tasks in a manufacturing setting in order to safely craft concrete products in a timely and efficient manner. We produce a variety of retaining wall blocks, and light pole bases. Ideal candidates are dependable individuals who perform all tasks with a safety-mindset and who understand the importance of delivering a high-quality, finished product. We offer full-time, year-round, steady work. Regular wage reviews and skill enhancement training are provided to grow your knowledge and increase wages. Overtime and occasional weekends may be required. Additionally, we offer a progressive benefits package, including excellent health insurance, paid time off, profit sharing, paid holidays, 401k employer match, partial paid family leave, adoption/foster care and educational reimbursement options, product discounts and more! The work environment is fast-paced, rewarding and over time a high level of expertise can be developed along with the ability to spot and correct errors. Requirements include being on your feet for long periods and being able to lift objects in excess of 50 lbs. A Valid driver's license, and previous experience in a manufacturing or construction setting is a bonus. Some of the specific duties performed are: Clean and prep empty molds for filling Operate controls on concrete pouring machinery to fill molds Remove excess concrete from molds for a clean finish Ensure products are being filled to the proper heights and cleaned thoroughly Operate machinery and equipment, such as forklifts, to sort, stack, transport, and load/unload product Package and label finished products for inventory Inspect for quality related issues as it relates the molds and forms Maintain machinery and equipment through daily inspections and cleanliness Work in a safe and responsible manner that abides by all company procedures and OSHA standards. Learn and perform other production related duties as needed If you have the drive to succeed, and also love working with your hands, go for it and apply today! To learn more about who we are, visit ************************** Truemont Materials is an equal opportunity employer; everyone is encouraged to apply.

Job Details Experienced ADMA Biologics FL - Boca Raton, FL Full Time High School Day ManufacturingDescription ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a Manufacturing Technician I, Purification in Boca Raton, FL! The Manufacturing Technician I, Purification is under direct supervision of the Group Leader. It is mainly responsible for the manufacturing of plasma products through protein precipitation/separation and other tasks involving plasma receipt, plasma pooling, and protein separation. The Protein Purification Manufacturing Technician will also clean and sanitize equipment before and after use, make and verify connections on flow panels, perform pH and conductivity measurements, performs chemical and buffer additions and may assist Group Leader in training other tech positions. Qualifications Cleans and sanitizes equipment before and after use. Responsible for production operations. Make and verify connections on flow panels. Perform pH and conductivity measurements. Performs chemical and buffer additions. Operation of Ultrafiltration system. Initiate product processes on the Process Automated System (PAS). Column chromatography using up to 80cm columns. Take and prepare product samples. Order and maintain raw material inventories. Complete Batch records. Assist Group Leader in training of other tech positions. Education Requirements: High School Diploma or GED. Associate degree or equivalent experience preferred Experience Requirements: 4 years of experience is required. GMP experience required. Protein purification experience preferred. ** Must be able to be flexible in a 24/7 operation, typical shifts are 12 hours in duration. ** In addition to competitive compensation, we offer a comprehensive benefits package including: 401K plan with employer match and immediate vesting Medical, Vision, Life and Dental Insurance Pet Insurance Company paid STD and LTD Company Paid Holidays 3 Weeks' Paid Time Off (within the first year) Tuition Assistance (after the first year) Easily accessible to Tri-Rail Free shuttle to the Boca Tri-Rail station ADMA Biologics uses E-Verify to confirm the employment eligibility of all newly hired employees. To learn more about E-Verify, including your rights and responsibilities, please visit ********************* ADMA Biologics is an Equal Opportunity Employer.

We Are Bosch. At Bosch, we shape the future by inventing high-quality technologies and services that spark enthusiasm and enrich people's lives. Our areas of activity are every bit as diverse as our outstanding Bosch teams around the world. Their creativity is the key to innovation through connected living, mobility, or industry. Let's grow together, enjoy more, and inspire each other. Work #LikeABosch Reinvent yourself: At Bosch, you will evolve. Discover new directions: At Bosch, you will find your place. Balance your life: At Bosch, your job matches your lifestyle. Celebrate success: At Bosch, we celebrate you. Be yourself: At Bosch, we value values. Shape tomorrow: At Bosch, you change lives. Florida Heat Pump Manufacturing , located in Fort Lauderdale, Florida, is a joint venture between Robert Bosch (BOSCH Group) and Carrier Corporation. FHP Manufacturing is a leader in the production of geothermal and water source heat pumps, providing some of the most efficient heating and cooling comfort solutions in the industry. Job Description The Lean Manufacturing Specialist (BPS Implementer) is an essential role that will lead initiatives to improve safety, quality, delivery cycle times, operational costs, and customer satisfaction. You will assure that the manufacturing plant adheres to the Bosch Production System guidelines. You will also work within a team environment focused on problem-solving, buy-in, and support the introduction of new work standards in the manufacturing sector as well as its support functions in the pursuit of operational excellence. Your responsibilities may include, but is not limited to: Will steer optimizations in safety, quality, delivery, costs, and support new product introductions. Lead or participate in GEMBA walks and drive Continuous Improvements (CI) Provide improvement project leadership and/or support Cross-Functional initiatives Facilitate small group meetings to brainstorm, gather information or solidify action plans Collect data, analyze, and formulate improvements to existing standards or to introduce new work standards Will collect data from shop floor observations, time studies, or ERP (SAP) data extracts that may include, but are not limited to inventory calculations, lot size calculations, changeover requirements, customer pull patterns, material delivery loops, storage capacities, etc. Spearhead work instruction changes and train staff to new standardized work conditions Steer classroom training, shop floor training, or hands-on simulations Conduct post-implementation effectiveness process confirmations or audits Embrace different ideas or perspectives and practice consensus leadership Develop close working relationship with all manufacturing and logistic associates Evaluate BPS maturity and drive maturity improvement for various Value Stream areas Qualifications Minimum Qualifications: Bachelor's Engineering required -Industrial, Ergonomics, or Logistics preferred 3+ year of Lean Manufacturing experience Proficient with Microsoft products (i.e. TEAMS, Excel, Outlook, Word, Visio, Power Point, etc.) Preferred Qualifications: Previous Manufacturing experience with demonstrated process improvement know-how Ability to work independently as well as in a team setting, technical and non-technical Strong interpersonal skills and able to communicate effectively across all levels Strong analytical skills, and solid problem-solving abilities (i.e. 8Ds and/or PSS projects) Prior Value stream mapping knowledge -ideally using MS Visio Willing to manage multiple improvement projects Familiarity of PFMEA, DFMEA and Control Plans Additional Information Indefinite U.S. work authorized individuals only. Future sponsorship for work authorization unavailable. Salary Range: The U.S. base salary range for this full-time position is $77,000 - $97,000 . Within the range, individual pay is determined based on several factors, including, but not limited to, work experience and job knowledge, complexity of the role, job location, etc. In addition to your base salary, Bosch offers a comprehensive benefits package that includes health, dental, and vision plans; health savings accounts (HSA); flexible spending accounts; 401(K) retirement plans with an employer match; wellness programs; life insurance; short- and long-term disability insurance; paid time off; parental leave, adoption assistance; and reimbursement of education expenses. Learn more about our full benefits offerings by visiting: ************************ Pay ranges included in the postings generally reflect base salary; certain positions may include bonus, commission, or additional benefits. EEO/OFCCP : Bosch is an equal opportunity employer and makes all employment decisions on the basis of merit. Bosch is fully committed to compliance with all applicable laws providing equal employment opportunities and to providing equal employment opportunity to all associates and applicants for employment without regard to race, gender, sex, pregnancy, childbirth (or related medical conditions, including but not limited to, lactation), national origin or ancestry, religion, gender identity, sexual orientation, age, disability, veteran status, genetic information or any other characteristic protected by law. This equal employment opportunity policy applies to all terms and conditions and aspects of employment including, but not limited to, recruitment, hiring, retention, training, placement, promotion, advancement, transfers, job assignments, layoffs, leaves of absence, termination, and compensation. Our management team is dedicated to this policy with respect to all aspects of employment. Bosch is dedicated to maintaining compliance with all federal, state, and local law, including but not limited to, affirmative action plan requirements, EEO-1 and VETS-4212 reporting, and I9 / work authorization guidance.

Job Details Level: Experienced Position Type: Full Time Education Level: High School Salary Range: Undisclosed Job Shift: Day Job Category: Manufacturing Description ADMA Biologics is a biopharmaceutical company relentlessly committed to creating superior products for immunodeficient patients at risk for infection. It is our devotion to this underserved population that fuels us and our hands-on approach to production and development that sets us apart. If you are looking for a dynamic, innovative, growing company in the biopharmaceutical industry that is committed to excellence and integrity, then consider ADMA Biologics. We currently have an exciting opportunity available for a Manufacturing Technician I, Purification in Boca Raton, FL! The Manufacturing Technician I, Purification is under direct supervision of the Group Leader. It is mainly responsible for the manufacturing of plasma products through protein precipitation/separation and other tasks involving plasma receipt, plasma pooling, and protein separation. The Protein Purification Manufacturing Technician will also clean and sanitize equipment before and after use, make and verify connections on flow panels, perform pH and conductivity measurements, performs chemical and buffer additions and may assist Group Leader in training other tech positions. Qualifications * Cleans and sanitizes equipment before and after use. * Responsible for production operations. * Make and verify connections on flow panels. * Perform pH and conductivity measurements. * Performs chemical and buffer additions. * Operation of Ultrafiltration system. * Initiate product processes on the Process Automated System (PAS). * Column chromatography using up to 80cm columns. * Take and prepare product samples. * Order and maintain raw material inventories. * Complete Batch records. * Assist Group Leader in training of other tech positions. Education Requirements: * High School Diploma or GED. Associate degree or equivalent experience preferred Experience Requirements: * 4 years of experience is required. GMP experience required. Protein purification experience preferred. Must be able to be flexible in a 24/7 operation, typical shifts are 12 hours in duration. In addition to competitive compensation, we offer a comprehensive benefits package including: * 401K plan with employer match and immediate vesting * Medical, Vision, Life and Dental Insurance * Pet Insurance * Company paid STD and LTD * Company Paid Holidays * 3 Weeks' Paid Time Off (within the first year) * Tuition Assistance (after the first year) * Easily accessible to Tri-Rail * Free shuttle to the Boca Tri-Rail station ADMA Biologics uses E-Verify to confirm the employment eligibility of all newly hired employees. To learn more about E-Verify, including your rights and responsibilities, please visit ********************* ADMA Biologics is an Equal Opportunity Employer.

Job Details Undisclosed Miami - Hialeah, FL N/A Undisclosed Undisclosed Undisclosed Undisclosed Undisclosed UndisclosedDescription Job Purpose: Monitor job and sample quality to ensure adherence to the required specifications while actively working with the facility to improve processes and enhance Client satisfaction. Scope: Work with the employees, Client and management team to ensure products are produced to the Company and the Client's specifications and expectations. Essential Job Responsibilities: Know all safety features and safety rules. Safety & quality conscious at all times Demonstrate good housekeeping skills Responsible for monitoring plant adherence to company quality procedures and notifying management of deviation Ensure Client samples are of the highest quality through selection and inspection Aide in the management and training of Quality Procedures Aide in root cause investigation and corrective action implementation Manage the Nonconforming Product Procedure Manage Nonconformance Report data by logging the information and tracking the NCR through closure Ensure proper maintenance and completion of quality records for specified shift. Perform product inspection audits at set intervals at each machine to ensure product being produced meets or exceeds the specified standards. Drive the improvement of our quality metrics (Client complaints, internal nonconformance's, PPM defect rate, ect.) to meet the goals set forth by management Computer literate Sufficient organizational and mathematical skills Good verbal and written communication skills Able to work with employees at all levels of the organization Able read and understand a variety of instructions furnished in written, oral, diagram, or schedule form Competencies for Achieving Essential Job Responsibilities Focusing on Client Needs Exhibiting Interpersonal Skills Quality/Attention to Detail Problem Solving Communication Skills Initiative Self-directed Planning and Organizing Dependability Accountability Professional Decorum Job Knowledge Safety Awareness Qualifications Experience In: > 3 years' experience in commercial print and bindery operations Knowledge Knowledge and understanding of commercial print terminology Knowledge and understanding of basic print and bindery defects Overall understanding of commercial print process Technical Skills Direct experience using a PC computer as it relates to word processing and spreadsheets Excellent telephone and email etiquette Proficient in basic math applications Strong verbal and written communication skills Culture and Motivational Fit The mission for all Southeastern associates is to protect and enhance our clients' brand. Every decision we make, every action we take with the products and services we offer needs to reflect the sole purpose of serving that mission. Our associates are expected to work collaboratively, communicate honestly and respectably, embrace change, and focus on processes that contribute to a positive client experience. We value associates that embrace new learnings and are adaptable to an ever-changing work environment. Physical Requirements: Must be able to sit, stand, climb or kneel as required. Must have visual acuity necessary to read materials required to complete job tasks. This may include but is not limited to: video display terminals, product labels and production schedules. Must be able to complete repetitive motion of hands and arms to input/retrieve information from computer. Must be able to bend/reach to get materials from floor, high and low shelves as required. Complexity: (Refers to complexity of analyzing data or complex issues regarding direction, problems solution and decision making) Due the nature of print and print Client needs, problem solving and decision making during the sales and print process is necessary on a regular basis. Independent Thinking: (Refers to innovations or creative approaches used and indicate the frequency with which they are performed. Indicate the degree to which this position is governed by procedures and standards). People in this position must be able to find balanced solutions that adhere to policies/procedures and yet satisfy Client needs on a regular basis. They must be able to bridge the gap between company and Client needs. This is not necessarily an exhaustive list of all responsibilities, skills, duties, requirements, efforts or working conditions associated with the job. While this is intended to be an accurate reflection of the current job, management reserves the right to revise the job or to require that other or different tasks be performed when circumstances change (i.e., emergencies, changes in personnel, workload, rush jobs, or technological developments).

Equipment Technician About the Company: RelaDyne, Inc. is the established leader in lubricant sales, distribution, equipment reliability services, and value-added services. Our location is currently looking for a motivated Equipment Technician with a strong work ethic. Please apply or share with your friends today! Benefits * Free Health Insurance option * Competitive Benefits Package * 401(k) with Company Match * Paid Time Off * Day shift Job Objective: Provide equipment technician services to customers in a safe, cost effective, timely, and professional manner. Responsibilities: * Strong mechanical knowledge and aptitude. * Able to understand and apply company policies and procedures in the areas of safety, health, and environmental. * Effectively maintain up to date and accurate repair logs. * Responsible for installing, maintaining, and repairing of all RelaDyne equipment. * Repair equipment in the most cost-effective manner. * Diagnose equipment problems and communicate issues with department manager. * Properly fill out all requests for parts form and document all parts and time on job sheets. * Strong aptitude to use a variety of different tools needed to effectively complete the equipment set up. Additional Responsibilities: * Follow SOP's (Standard Operating Procedures) for Fuel and Lube Equipment. * Effectively update the customer repair spread sheet in a timely manner. * Effectively set up proper Fuel, Lube, or DEF equipment at new customer site. Competencies: * Collaboration Skills * Decision Making * Results Driven Measurements: * Customer Satisfaction * Accurate and current equipment records * Productivity (Day's work in a day) * Safety (number of days without violation or injury) Work Environment: * While performing the duties of this job, the employee is regularly exposed to outdoor weather conditions. The noise level in the work environment is usually moderate. Know Your Rights: Workplace Discrimination is Illegal - (click for more information) Equal Opportunity Employer/Disability/Veterans RelaDyne, and its affiliates, is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ethnicity, sex, age, gender identity, sexual orientation or identity, genetic information, status as a protected veteran, status as a qualified individual with disability, or any other protected class status. We endeavor to make this site accessible to any and all users. If you would like to contact us regarding the accessibility of our website, need assistance completing the application process, or would like to request alternative methods of applying, please contact us.

Install, maintain, and repair internal factory equipment. Supervise employees who perform maintenance and tool making. Accountable for the quality of own work. Subject to direct operations supervision/prescribed work instructions/systems checking. Executes within a well-defined operations framework. There is generally a step by step sequence of standard operational tasks which need to be followed to achieve an end result. **Job Description** **Roles and Responsibilities** + Ensure that manufacturing premises are fully operational, maintained, and clean. This is manufacturing specific and does not include gardeners, caterers, etc. + Developing conceptual knowledge of professional discipline. May include support roles with specialized expertise or technical knowledge in broad area. + Applies general knowledge of business developed through education or past experience. Understands how work of own team contributes to the area. + Resolves issues using established procedures. Consults supervisor or more senior team members for issues outside of defined instructions/parameters. + Collaborates with others to solve issues. + For customer facing roles, develops strong customer relationships and serves as the interface between customer and GE. + Exchanges technical information, asks questions and checks for understanding. + Maintaining site security. + Handling global security initiatives. + Maintaining employee and visitor badging systems. **Required Qualifications** + Bachelor's degree from an accredited university or college with a minimum of 2 years of relevant experience + High school diploma / GED with at least 6 years of relevant experience **Desired Characteristics** + Strong oral and written communication skills. + Ability to document, plan, market, and execute programs. _This role requires access to U.S. export-controlled information. If applicable, final offers will be contingent on ability to obtain authorization for access to U.S. export-controlled information from the U.S. Government._ **Additional Information** GE Aerospace offers a great work environment, professional development, challenging careers, and competitive compensation. GE Aerospace is an Equal Opportunity Employer (****************************************************************************************** . Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law. GE Aerospace will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable). **Relocation Assistance Provided:** No GE Aerospace is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.

Akron Biotech is continuing to transform and further its rapidly growing capabilities and is now seeking highly motivated professionals to join our expanding team. This is an exciting opportunity to play a critical role within our organization that is driving advanced therapy development and commercialization with high quality industrial scale solutions. We manufacture and distribute components and raw materials for cell therapy discovery, development, and commercialization to meet industry needs worldwide. We offer an array of highly competitive benefits and perks to our valued associates. General Responsibilities Provides development and manufacturing operations support including the formulation and aseptic filling of Cryopreservation media, cell culture media, and cell culture supplements. Executes and maintains documentation relating to manufacturing. Supports all technical writing requirements for manufacturing/operations. Author and revise manufacturing batch records, SOPs, work instructions, validation/qualification protocols, forms, logbooks, technical reports, CAPAs, change controls and any other document that may apply. Formulate, fill and finish Akron manufactured products, including cryopreservation media, cell culture media, and supplements. Perform aseptic processes in a controlled or cleanroom environment. Perform in-process testing of products using general laboratory equipment/instrumentation. Utilizes formulas, work instructions or equivalent to monitor the production process. Perform experiments associated with development, improvement and scaling up or optimization of manufacturing and development processes. Troubleshoot problems associated with equipment, process development/production/ including data analysis and internal record keeping. Perform Environmental Monitoring activities as required. Perform the cleanzone cleaning as required. Maintains current knowledge of developments related to product recovery and purification processes. Performs duties in accordance with established laboratory standards. Evaluate, troubleshoot and solve routine problems. Interprets data based on knowledge and experience. Perform process validation and equipment qualification as required. Perform general equipment preventive maintenance. Contribute to maintaining lab and equipment cleanliness. Support and coordinate deviation investigations and implementation of change controls or robust corrective and preventative actions. Support finished product labeling, raw material aliquoting and, re-labeling requirements when necessary. Perform other duties as assigned. Requirements BS or MS in Biology, Chemistry, Bioengineering or a related field + 2 years minimum experience working in a life science manufacturing role. Detailed oriented with good time management and organizational skills. Ability to work well under pressure and prioritize assignments in a multi-task position. Motivated and able to work independently. Excellent verbal communication skills and people/customer service oriented. Basic knowledge of Outlook, Word, Excel and Software Programs. Requires a strong adherence to cGMPs regulatory compliance and safety requirements, SOPs and other related documents such as SDS and manuals. In addition to competitive compensation, we offer a comprehensive benefits package including: 401K plan with employer match PPO and HMO medical insurance plan availability Company paid dental and vision insurance Company paid short-and long-term disability Company paid life insurance Company paid holidays Generous paid time off allowances Employee referral bonus Employee gym reimbursement program Employee recognition program EOE/DFW