Manufacturing Technician Jobs in Hialeah, FL

We are seeking a Commissioning Technician to be a critical piece on the troubleshooting and maintenance of smart thermostats, automated lighting systems, and related low voltage will be centric to the Greater Miami Area. Our Client specializes in designing, installing, and programming occupancy-based HVAC controls and lighting solutions to reduce energy costs in the hospitality, multi-family, military, and higher education markets. We provide exceptional customer experience through our products and services. Our corporate culture focuses on providing customers with excellent service. Key Responsibilities: Install, configure, and integrate smart thermostats, automated lighting systems, and associated low voltage equipment. Performing routine maintenance and troubleshooting issues with lighting controls, dimmers, sensors, and thermostat systems. Read and interpret blueprints, wiring diagrams, and technical documentation to ensure accurate installations. Conduct site assessments to evaluate system requirements and recommend optimal solutions. Program and test systems for functionality and ensure seamless integration with existing infrastructure. Ensure compliance with local codes, safety regulations, and industry standards during installations and repairs. Maintain detailed records of service activities, including installations, repairs, and client interactions. Train clients on using and maintaining installed systems effectively. Collaborate with project managers and team members to deliver projects on time and within budget. Stay informed about advancements in smart thermostat and lighting technologies to provide cutting-edge solutions. Assisting with Support Calls when off the road. Proactive Monitoring of sites and customer-outreach for system optimization. Qualifications: -High School Diploma is required; Associate's or Bachelor's degree in a relevant field is a plus. - Valid driver's license - 3+ years of HVAC experience preferred. - 3+ years of Low Voltage Wiring experience preferred.

Vaco is hiring a QA Technician located in Oakland Park. The ideal candidate should have at least five years of manufacturing or testing facility experience. Primarily performs in-process inspection, evaluation, and testing of products and/or manufacturing processes. Records data, prepares inspection reports, manages non-conformances and corrective action. Assists Quality Assurance engineers with product analysis, Quality Control sampling plans, and the application of statistical techniques for process or product controls. Prepares formal Quality Test reports per company procedures. DELIVERABLES & RESPONSIBILITIES Perform inspection and testing of manufactured products. Perform Quality inspection audits of processes and products using sampling plans, where applicable. Performs First Article Inspection (FAI) of supplied and manufactured products per customer of internal drawings. Operates and maintains testing and inspection equipment and assure proper calibration. Manage Non-Conformance Reports (NCR's) and Corrective Actions Reports (CAR's) Assist with root cause analysis to eliminate and/or prevent non-conforming products Implement and maintain Statistical Process Control (SPC) in manufacturing Assist in development and maintenance of Acceptance Test Procedures (ATPs), and test protocols. Perform other duties according to business needs QUALIFICATIONS (Education, Experience & Skills) Certificate/Diploma from a Technical or Trade school. Minimum of five (5) years of similar experience in a manufacturing or testing facility experience. Certified Quality Inspector (CQI) and/or Certified Quality Technician (CQT) per ASQ guidelines a plus Knowledge of Statistical Process Control (SPC) techniques and application Computer skills; email & general business software (e.g. Ms Office, Outlook, etc.) Demonstrated Communication skills (oral & technical writing) Intermediate Math and Reading Comprehension, and Statistical skills Ability to work effectively alone and within a team environment

We are partnered with an outstanding Pharmaceutical company located in the Ft-Lauderdale area. They are looking to bring on a Manufacturing Process Technician to their team! With this great opportunity comes a very competitive salary, benefits and more! Your responsibilities will be to conduct laboratory activities including manufacturing process development, manufacturing process scale-up and process transfer activities across equipment, manufacturing scales and sites. Key Responsibilities: Execute laboratory tasks for process development, scale-up, and technology transfer within manufacturing operations. Produce R&D, pilot, pivotal, and commercial-scale batches in accordance with established procedures. Assist in the setup, maintenance, and troubleshooting of manufacturing equipment and coordinate with equipment vendors as needed. Support the formulation and development of orally inhaled and nasal drug products (OINDPs) in line with regulatory guidelines, industry standards, and US FDA cGMP requirements. Contribute to the design and evaluation of new formulation manufacturing technologies when necessary. Assist in drafting and reviewing batch records for R&D, pilot, pivotal, and commercial manufacturing, ensuring adherence to cGMP standards and company SOPs. Accurately complete manufacturing batch records and thoroughly document all related laboratory and manufacturing activities per cGMP guidelines and company SOPs. Collaborate effectively with cross-functional teams and global R&D sites. Foster positive working relationships with team members. Follow all safety procedures and organizational guidelines during laboratory and production tasks. Comply with all corporate policies and operational procedures. Qualifications: High school diploma with a minimum of 5 years of relevant industry experience. A relevant degree, certification, or license is preferred. Demonstrated experience in pharmaceutical manufacturing, especially in solid dosage forms like tablets, capsules, and dry powder inhalation products. Experience with sterile, injectable, and ophthalmic product manufacturing is an advantage.

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 and 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) * Prior experience in manufacturing or assembly line work/machinery, and ability to read and interpret technical documents. * 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; and 2+ years experience working in an FDA-regulated environment/laboratory. * The position requires concentration for long periods and good hand-eye coordination when working in assembly line process. * 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

**Program Objective:** Miami Lakes Educational Center and Technical College is dedicated to developing world-class technicians who can provide the professional customer service necessary to retain loyal Honda customers. **Program Content:** The Honda Professional Automotive Career Training (Honda PACT) Program entered into a cooperative agreement with Robert Morgan Educational Center and Technical College to address the need for highly trained Honda and Acura automotive technicians. The PACT Program was developed as a two-year training program leading to an Advanced Automotive Service Technology Certificate. The curriculum, supported by American Honda Co., Inc. includes academic study, laboratory application, and on the job work experience at Honda and Acura dealerships. **Admission Requirements:** * 16 years of age or older and not currently enrolled in any K-12 program * Occupational interest * High School Diploma/GED from an Accredited High School * Must meet Dealership Employability Standards **Completion Requirements:** The entire program is 2400 hours and students must earn all OCPs, however, students can earn an OCP certificate upon completion of the following OCPs: OCPCOURSEHOURS OCP AAutomotive Maintenance Technician400 Hours OCP BAdvanced Engine Repair Technician200 Hours OCP CAdvanced Automatic Transmission and Transaxle Technician200 Hours OCP DAdvanced Manual Drivetrain and Axle Technician200 Hours OCP EAdvanced Automotive Suspension and Steering Technician200 Hours OCP FAdvanced Automotive Brake System Technician200 Hours OCP GAdvanced Automotive Electrical/Electronic System Technician400 Hours OCP HAdvanced Automotive Heating and Air Conditioning Technician200 Hours OCP IAdvanced Automotive Engine400 Hours Total Hours: 2400 Minimum basic-skills grade levels required for awarding a Full Program Completion Certificate are 10th grade in Math, Reading, and Language on the TABE Test or passing two (2) ASE exams. Additional information can be provided by student services. **Students are expected to complete program competencies.** **Employment Opportunities:** * Honda and Acura Dealerships **Salary:** The salary for automotive technicians at Honda & Acura dealerships will vary from dealership-to-dealership. However, the average wage for this career in Florida is $36.06 hourly or $75,000 annually. **Financial Aid:** Financial aid is available to those who qualify. Applicants must have a high school diploma from an accredited High School or its equivalent. To apply, complete the Free Application for Federal Student Aid, at . Questions pertaining to this matter should be directed to the Financial Aid Office. **Program Cost:** * In-state residents - $2.56 per hour (Subject to change) * Out of state resident - $10.25 per hour (Subject to change) * $20.00 application fee per trimester * Material fee - Varies by program * Identification fee $5.00 per trimester * Liability insurance fee - Varies by program * Students must purchase books/kits and/or uniforms, if applicable **Program Hours:** Monday - Thursday from 8:00 a.m. to 3:15 p.m. **Alternate Location:** Program is also offered at Robert Morgan Educational Center & Technical College: 18180 SW 122nd Ave, Miami, FL 33177. **Find Out More** **Transportation**

Provide manufacturing operations support including the formulation and aseptic filling of Cryopreservation media, cell culture media, and cell culture supplements. Execute and maintain documentation relating to manufacturing procedures, ensuring compliance with applicable regulations and industry standards (e.g. FDA 21CFR, cGMP, ISO13485). Support all technical writing requirements for manufacturing/operations, authoring and revising manufacturing batch records, SOPs, work instructions, validation/qualification protocols, forms, logbooks, technical reports, CAPAs, change controls, and other relevant documents. Responsibilities * Formulate, fill, and finish manufactured products, including cryopreservation media, cell culture media, and supplements. * Perform aseptic processes in a controlled or cleanroom environment. * Conduct in-process testing of products using general laboratory equipment/instrumentation. * Utilize formulas and work instructions to monitor the production process. * Perform experiments associated with development, improvement, 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. * Maintain current knowledge of developments related to product recovery and purification processes. * Evaluate, troubleshoot, and solve routine problems, interpreting data based on knowledge and experience. * Perform process validation and equipment qualification as required. * Perform general equipment preventive maintenance and 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. Essential Skills * 2 years minimum relevant experience. * Detail-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 other software programs. * Strong adherence to cGMPs, regulatory compliance, safety requirements, SOPs, and other related documents such as SDS and manuals. Additional Skills & Qualifications * BS or MS in Biology, Chemistry, Bioengineering, or a related field. * 2 years minimum experience working in a life science manufacturing role. Work Environment Will be working in a lab setting as part of a team. Monday to Friday, 9am to 5pm, with a 1-hour lunch break. Pay and Benefits The pay range for this position is $25.00 - $27.00 Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in BOCA RATON,FL. Application Deadline This position will be accepting applications until Jan 17, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: * Hiring diverse talent * Maintaining an inclusive environment through persistent self-reflection * Building a culture of care, engagement, and recognition with clear outcomes * Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

See our Medix Biochemica USA (FL) · Weston, FL, USA **Manufacturing Technician** Job Title: Manufacturing Technician Department: Manufacturing Produces biological components and products by setting-up, cleaning, operating, and maintaining equipment; following aseptic procedures; documenting actions. * Prepares for production by reviewing production schedule; studying and clarifying specifications; calculating requirements; assembling and weighing materials and supplies. * Maintains the Washroom and surrounding area in a constant state of cleanliness * Prepares equipment by performing manual cleaning of all equipment/ sanitization of tanks and equipment according to formula; conducting operator inspections; performing preventive maintenance checks * Produces requirements by operating and monitoring equipment; observing varying conditions; adjusting equipment controls; calculating concentrations, dilutions, and yields; adhering to aseptic filtering and filing procedures. * Maintains safe and clean work environment by following current good manufacturing practices (cGMP), and standard operating procedures; complying with legal regulations; monitoring environment. * Ability to comprehend SOP and GMP * Ability to work in ISO certified clean room, fully gowned with mask gloves and goggles * Keeps equipment operating by following operating instructions; troubleshooting breakdowns; calling for repairs; Lifts and moves equipment and supplies. * Documents production by completing forms, reports, and records of equipment and batches. Maintains logs and signs all work completed after each task is performed. * Enhances organization reputation by accepting ownership for accomplishing new and different requests; exploring opportunities to add value to job accomplishments. **QUALIFICATIONS** To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed above are representative of the knowledge, skill, and/or ability required. **EDUCATION and/or EXPERIENCE** Highschool diploma or GED required, bachelor's degree in health science or related discipline is preferred. Knowledge of GMP is preferred **LANGUAGE** **SKILLS** Ability to read, analyze, and interpret common scientific terms. Ability to write reports, documents, standard operating procedures and protocols that conform to prescribed style and format. Ability to effectively present information to top management. Attention to detail, as well as following standard operating procedures is required. **PHISYCAL DEMANDS** While performing the duties of this job, the employee must be able to stand for an extended period. The employee must occasionally lift and/or move up to 50 pounds. **WORK ENVIRONMENT** The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The noise level in the work environment is usually moderate. The manufacturing room is an ISO class 8 clean room which requires a full PAPR gown. The manufacturing work environment is extremely structured and closely monitored by the Manufacturing Supervisor. Medix Biochemica is a rapidly growing *in vitro* diagnostics (IVD) company with Finnish roots and global branches. We've got sites in Espoo, Finland; St. Louis and Miami USA; Shanghai, China; Besancon, France, and Konstanz, Germany with further expansion on the horizon. We develop, produce and supply high-quality IVD raw material products that enable our customers to deliver results to billions of patients. Across disciplines and disease areas, we're always working to shorten our customers' time to market and build quality into every one of their tests. Recently, we've made some bold acquisitions to help us progress with our big ambitions - to be the first-choice raw material partner for the IVD industry. Today, we can provide our customers with the most comprehensive raw material portfolio in the IVD world, and a team made up of the best minds in the business. And we'd love for you to join us. As well as our dedication to the IVD industry, we're dedicated to making Medix Biochemica a great place to work. Our values guide the working practices of over 250 colleagues around the globe. We Care, We Dare, and We Deliver are values we work to uphold, every day! Site Role Manufacturing Locations **We Offer** * **Big enough company to be industry-leading but small enough to have flexibility and the feeling of being part of a community** * **An international and diverse working environment with colleagues passionate about making a difference in the IVD industry** * **A welcoming culture where you can utilise your skills but also grow and develop them alongside our rapidly growing organization** Our heritage provides us with a strong foundation. We are proud of our quality, are explorers at heart, and are all committed team players-it's in our DNA. Our passion, diversity, and values form the foundation of our shared culture. We are passionate about innovation and delivering quality to our customers and people. As part of our We Care value, we strive for a diverse culture of inclusion and belonging. We come from all around the world and have employees in many different countries. This means our team speaks many of different languages. Our employees also have diverse professional backgrounds and education. Some have been with us for only a few months while, others have been here for over 40 years. We also strive for a diverse culture where everyone can be their true selves at work - making a difference in the success of the company and the world around us. Medix Biochemica USA (FL) · Weston, FL, USA **Manufacturing Technician** **Privacy policy for recruitment using Teamtailor** The service for handling recruitments and simplifying the hiring process (the "Service") is powered by Teamtailor on behalf of Medix Biochemica ("Controller" “we” “us” etc.). It is important that the persons using the Service ("Users”) feel safe with, and are informed about, how we handle User's personal data in the recruitment process. We strive to maintain the highest possible standard regarding the protection of personal data. We process, manage, use, and protect User's Personal Data in accordance with this Privacy Policy ("Privacy Policy"). **1. General** We are the controller in accordance with current privacy legislations. The Users' personal data is processed with the purpose of managing and facilitating recruitment of employees to our business. **2. Collection of personal data** We are responsible for the processing of the personal data that the Users contributes to the Service, or for the personal data that we in other ways collects with regards to the Service. *When and how we collect personal data* * make an application through the Service or otherwise, adding personal data about themselves either personally or by using a third-party source such as Facebook or LinkedIn; and * use the Service to connect with our staff, adding personal data about themselves either personally or by using a third-party source such as Facebook or LinkedIn. * provides identifiable data in the chat (provided through the website that uses the Service) and such data is of relevance to the application procedure; We collect data from third parties, such as Facebook, Linkedin and through other public sources. This is referred to as “Sourcing” and be manually performed by our employees or automatically in the Service. In some cases, existing employees can make recommendations about potential applicants. Such employees will add personal data about such potential applicants. In the cases where this is made, the potential applicant is considered a User in the context of this Privacy

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

Job Details Experienced ADMA Biologics FL - Boca Raton, FL N/A Full Time High School Undisclosed Undisclosed Nights 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.

Boca Raton, FL · Biotech/Pharmaceutical 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 reimbursementprogram * Employee recognition program EOE/DFW

**Job Details** Entry ADMA Biologics FL - Boca Raton, FL Full Time High School Day 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 have an exciting opportunity for a **Manufacturing Technician I, Fractionation in Boca Raton, FL!** The **Manufacturing Technician I, Fractionation** position is under direct supervision of the Group Leader with support and assistance from the Advanced Tech positions. This entry-level position helps with the manufacturing of plasma products by cleaning and sanitizing of equipment and processing areas, preparation of buffer solutions, and other tasks involving plasma receipt, pooling and protein separation. Must be able to be flexible in a 24/7 operation, shifts are 12 hours in duration. **Qualifications** * Cleans and sanitizes equipment before and after use. * Cleans and sanitizes Manufacturing Areas daily. * Operates COP washer. * Receives and de-boxes plasma units. * Operates plasma bottle cutter. * Operates pooling tank lift. * Set up and harvest of centrifuges. * Monitors centrifuge flows and temperatures. * Prepares buffer solutions. * Removes trash (empty plasma bottles, etc.) from the TCP and Fractionation areas. * Maintains stock of gowning supplies. * Make connections on flow panels for product transfers. * Follow manufacturing SOPs and Batch Records. * Additional tasks associated with advancement to the Tech II position. **Education Requirements:** * High School Diploma or GED. Associate degree or equivalent experience preferred. **Experience Requirements:** * GMP experience required. **** Must be able to be flexible in a 24/7 operation, typical shifts are 12 hours in duration from 7a.m. - 7p.m. **** ***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).

Full-time Description Artisan Design Group - or ADG - is a leading supply chain partner to homebuilders throughout the United States. Over 3,000 ADG employees operating out of 135 facilities in 25 states provide a full range of design, procurement, and installation services along with products from the top manufacturers of flooring, cabinets and countertops. Formed in 2016 by the merging of two industry leaders, ADG then acquired over 20 additional companies - each a leader in the geography it serves. We are the premier interior finishings organization in the United States. Our expansive trajectory has been rapid, and we continue to experience explosive growth, thanks to our dedication to high quality work. JOB SUMMARY Distinctive Kitchens and Baths is currently seeking a Production Technician to join the team! Candidate will be responsible for duties such loading cabinet parts, assembling cabinets, and maintaining a clean workspace. Must be able to lift and carry heavy loads. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. Loading cabinet parts to the production lines to assemble Assemble hardware and cabinets as required. Communicate effectively with Coworkers/Supervisor to ensure efficient production and deadlines are met Assist in lifting, carrying, and moving heavy loads as required Inspect finished products for defects to ensure quality standards are met Following health and safety standards. Maintaining a clean workstation and production floor Assisting machining department when needed SUPERVISORY RESPONSIBILITIES This position carries out supervisory responsibilities in accordance with company guidelines, policies and procedures, and applicable laws. Supervisory responsibilities include interviewing, hiring, and training employees; planning, assigning, and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems. None Requirements EDUCATION, EXPERIENCE & 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. Prior experience in a production setting preferred Familiar with production equipment and machinery (Not required but a plus) Sharp attention to detail in favor of identifying defects Self-driven and hard worker Able to work efficiently with minimal supervision Able to work as a team Flexible to work shifts, overtime and weekends as required Able to stand for long hours at a time Able to withstand hot/cold temperatures in the warehouse Physically able to lift, carry and move up to 60lbs PHYSICAL DEMANDS The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Ability to sit at computer monitor for long periods throughout the day. Must possess the ability to stand for long periods of time; to reach with hands and arms; to move among warehouse; to handle documents; to sit, stoop, kneel and crouch; to lift and move up to 60 pounds; to see well enough to discern differences in quality of products. WORK ENVIRONMENT The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. General working conditions Warehouse environment Hot/cold temperatures in the warehouse May have to meet tight deadlines OUR BENEFITS Health Insurance (Medical, Prescription, Dental, and Vision) Life Insurance Disability Insurance Paid Holidays and Time Off 401(k) Plan with company matching Artisan Design Group is committed to a policy of equal employment opportunity for applicants and employees. It is the policy of Artisan Design Group to apply recruiting, hiring, training, promotion, compensation, and professional development practices without regard to actual or perceived race, color, religion, sex (including pregnancy, sexual orientation and gender identity), national origin, age (40 or older), disability or certain classifications based on genetic information, or any other characteristic protected by federal, state or local laws, regulations or ordinances. We are committed to helping individuals with disabilities participate in the workforce and ensuring equal opportunity to apply and compete for jobs. If you need any assistance at any point in the application or hiring process due to a disability and you need an accommodation, please email Accommodations@adgus.net. Please do not use this email address for any other questions. Only inquiries regarding accommodations will be addressed

Conducts manufacturing process development, manufacturing process scale-up and process transfer activities across equipment, manufacturing scales and sites. Conducts manufacture of lab scale R&D, pilot scale, pivotal scale and commercial scale batches. Contribute towards installation, maintenance and troubleshooting of manufacturing equipment and interface with equipment vendors. Contribute towards development of orally inhaled and nasal drug products (OINDPs) by following regulatory guidelines, industry best practices, US FDA cGMPs, and other relevant guidelines. Contribute towards the development and evaluation of new formulation manufacturing technologies where required. **Essential Duties and Responsibilities** Conducts standard and advanced laboratory activities including formulation and manufacturing process development, manufacturing process scale-up and process transfer activities across equipment, manufacturing scales and sites. Conducts manufacture of lab scale R&D, pilot scale, pivotal scale and commercial scale batches by following written documentation. Contribute towards installation, maintenance and troubleshooting of manufacturing equipment and interface with equipment vendors. Contribute towards development of orally inhaled and nasal drug products (OINDPs) by following regulatory guidelines, industry best practices, US FDA cGMPs, and other relevant guidelines. Document and report all laboratory and manufacturing activities according to cGMPs and Transpire Bio's SOPs. Work and communicate effectively with other functional groups and across global respiratory R&D sites. Establish and maintain effective relationships with team members. Conduct lab work in accordance with SOPs; follow Transpire Bio safety rules and procedures. Comply with all Transpire Bio Corporate guidelines and policies. **Qualification Requirements** **THIS ROLE REQUIRES PREVIOUS EXPERIENCE IN A MANUFACTURING TECHNICIAN OR MACHINE/PRODUCTION OPERATOR ROLE IN PHARMACEUTICAL MANUFACTURING**. High school diploma with 5 years of work experience. A relevant degree, certification, or license may be required. Experience as a technician in the manufacture of pharmaceutical products. Experience in the manufacture of tablets, capsules, injectables, ophthalmics, other sterile products is preferred. A driver's license. Ability to multitask and liaise with professionals in different fields. Ability to explain problems simply and clearly. Proficiency in MS Office. Exercise independent judgement and discretion. Ability to understand verbal and written instructions. Ability to follow health and safety regulations. Excellent mathematical and problem-solving skills.

CAREER in BEER? WE WANT TO SPEAK TO YOU! * Nights and weekends off? Check! * Learning from the very best in the beer industry? Check! * Visiting great bars and breweries each day? Check! * Great launching point to grow within the beer industry? Check! The AHFP company motto is "TRUST us for the Perfect Pint." Our mission is to provide great-tasting draft beer to the consumer, the way the brewmaster intended and to grow draft beer sales. Job Summary: As a Draft Beer Quality Technician (DQT), you are responsible for cleaning and servicing draft beer lines to ensure local bars and restaurants serve the highest quality pints of draft beer. A typical day will involve visiting customer locations to keep their draft beer systems clean and building relationships with managers, owners, and bartenders on their route. Candidates must demonstrate reliability, attention to detail, mechanical skills, self-motivation, and a willingness to provide excellent quality of work and customer service. No previous experience is required as we provide training on draft beer system operations, maintenance, and troubleshooting. Qualifications: * High School Diploma or GED * Must be at least 18 years of age * Have a valid drivers license * Able to lift 50+ lbs * Hands-on quick learner Benefits: * A benefits package valued at more than $10k*. This includes a 401(k) plan with company matching, medical coverage plans customized to suit your needs, and a commitment to work/life balance through our paid time off (PTO) programs, paid company holidays * Enrollment into our "Stop the Slip" safety program where you receive non-slip shoes. * Eligibility for health, dental, and vision coverage subject to a 60-day waiting period. * AHFP pays a portion of the employee's monthly medical insurance premium to offset the cost of their plan * Free telemedicine through First Stop Health is provided to employees and their immediate family members who enroll in health benefits * Use of an AHFP-owned cell phone with minutes and data paid. * Bi-annual performance reviews with pay increases Salary: * $18.00+ growth opportunities and overtime hours * Performance incentive of $4 per additional beer tap cleaned outside of assigned lines Transportation: * Personal and reliable vehicle required. * Mileage & vehicle reimbursement- AHFP provides TAX-FREE monthly reimbursement for mileage and the cost of increasing your current insurance coverage to our required minimums. Employees are automatically enrolled in our vehicle reimbursement program, where reimbursements are calculated based on position level, zip code, and driving responsibilities. Schedule: * Full-time position with work scheduled Monday-Friday from 7:00 am-4:30 pm. (no nights, early mornings, or weekends but regular overtime opportunities are available)

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.

Provide manufacturing operations support including the formulation and aseptic filling of Cryopreservation media, cell culture media, and cell culture supplements. Execute and maintain documentation relating to manufacturing procedures, ensuring compliance with applicable regulations and industry standards (e.g. FDA 21CFR, cGMP, ISO13485). Support all technical writing requirements for manufacturing/operations, authoring and revising manufacturing batch records, SOPs, work instructions, validation/qualification protocols, forms, logbooks, technical reports, CAPAs, change controls, and other relevant documents. Responsibilities * Formulate, fill, and finish manufactured products, including cryopreservation media, cell culture media, and supplements. * Perform aseptic processes in a controlled or cleanroom environment. * Conduct in-process testing of products using general laboratory equipment/instrumentation. * Utilize formulas and work instructions to monitor the production process. * Perform experiments associated with development, improvement, 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. * Maintain current knowledge of developments related to product recovery and purification processes. * Evaluate, troubleshoot, and solve routine problems, interpreting data based on knowledge and experience. * Perform process validation and equipment qualification as required. * Perform general equipment preventive maintenance and 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. Essential Skills * 2 years minimum relevant experience. * Detail-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 other software programs. * Strong adherence to cGMPs, regulatory compliance, safety requirements, SOPs, and other related documents such as SDS and manuals. Additional Skills & Qualifications * BS or MS in Biology, Chemistry, Bioengineering, or a related field. * 2 years minimum experience working in a life science manufacturing role. Work Environment Will be working in a lab setting as part of a team. Monday to Friday, 9am to 5pm, with a 1-hour lunch break. Pay and Benefits The pay range for this position is $25.00 - $27.00 Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: * Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available * Life Insurance (Voluntary Life & AD&D for the employee and dependents) * Short and long-term disability * Health Spending Account (HSA) * Transportation benefits * Employee Assistance Program * Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Boca Raton,FL. Application Deadline This position will be accepting applications until Jan 17, 2025. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. Diversity, Equity & Inclusion At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through: * Hiring diverse talent * Maintaining an inclusive environment through persistent self-reflection * Building a culture of care, engagement, and recognition with clear outcomes * Ensuring growth opportunities for our people The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Job Details Entry 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 have an exciting opportunity for a Manufacturing Technician I, Fractionation in Boca Raton, FL! The Manufacturing Technician I, Fractionation position is under direct supervision of the Group Leader with support and assistance from the Advanced Tech positions. This entry-level position helps with the manufacturing of plasma products by cleaning and sanitizing of equipment and processing areas, preparation of buffer solutions, and other tasks involving plasma receipt, pooling and protein separation. Must be able to be flexible in a 24/7 operation, shifts are 12 hours in duration. Qualifications Cleans and sanitizes equipment before and after use. Cleans and sanitizes Manufacturing Areas daily. Operates COP washer. Receives and de-boxes plasma units. Operates plasma bottle cutter. Operates pooling tank lift. Set up and harvest of centrifuges. Monitors centrifuge flows and temperatures. Prepares buffer solutions. Removes trash (empty plasma bottles, etc.) from the TCP and Fractionation areas. Maintains stock of gowning supplies. Make connections on flow panels for product transfers. Follow manufacturing SOPs and Batch Records. Additional tasks associated with advancement to the Tech II position. Education Requirements: High School Diploma or GED. Associate degree or equivalent experience preferred. Experience Requirements: GMP experience required. ** Must be able to be flexible in a 24/7 operation, typical shifts are 12 hours in duration from 7a.m. - 7p.m. ** 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.