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Quality control analyst jobs in Sunny Isles Beach, FL - 93 jobs
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Quality Control Analyst
Quality Control Inspector
Quality Control Technician
Quality Control Microbiologist
Quality Control Chemist
Quality Control Assistant
Quality Control Specialist
Quality Control-Associate Scientist
Quality Control Specialist
The Pharmacy Hub
Quality control analyst job in Miami Gardens, FL
Job DescriptionAbout Us At The Pharmacy Hub, we collaborate with pharmaceutical brands, manufacturers, health brands, telemedicine providers, and healthcare companies to deliver essential products directly to patients. Our expertise allows us to seamlessly distribute pharmaceuticals, medical devices, and other healthcare products to consumers, ensuring greater accessibility and convenience. Core Values The Pharmacy Hub is dedicated to breaking barriers in healthcare by championing access, intervention and affordability. Customer-first mindset - we develop strong partnerships with telehealth platforms and healthcare companies to enhance access and understand their specific needs Innovation for intervention in care - we develop advanced compounding solutions and products to better support patient health outcomes Continuous improvement - we continuously improve our processes and offerings through intelligent, honest and transparent practices to deliver cost-effective solutions that truly benefit our clients and their patients. You will play a pivotal role in maintaining these values and contributing to the company's mission of redefining healthcare delivery through superior pharmacy services. Job Summary We are seeking a detail-oriented Quality Control Technician to support quality assurance and compliance activities within a pharmaceutical and compounding environment. This role supports the Compliance & Quality Control team by assisting with quality monitoring, documentation, and regulatory compliance to ensure the safety, integrity, and accuracy of pharmacy operations. The Quality Control Technician will help monitor quality systems across 503A pharmacy operations, receipt of 503B outsourced medications, non-sterile compounding, controlled substances (Schedules III & IV), retail pharmacy activities, and related warehouse operations. This position works closely with pharmacy, compliance, and warehouse teams to ensure adherence to FDA, DEA, OSHA, and state pharmacy regulations. Key Responsibilities Implement and manage CAPA processes to identify root causes of compliance or quality issues. Document, investigate, and resolve deviations, complaints, or incidents promptly. Recommend and implement corrective/preventive actions, tracking their effectiveness. Collect and analyze data from pharmacy operations, controlled substance handling, warehouse activities, and outsourcing facilities. Prepare regular reports and dashboards to highlight trends, risks, and areas needing improvement. Provide data-driven recommendations to management for operational and compliance improvements. Support Assist with maintaining compliance with DEA regulations (Schedules III & IV), 50-state pharmacy licensure, and OSHA warehouse safety standards. Support internal audits and external inspections by preparing records, reports, and documentation. Ensure policies, SOPs, and training materials are followed consistently. Collaboration & Training Work closely with the Compliance & Quality Control Officer and team members to address quality challenges. Provide training to staff on CAPA, quality assurance procedures, and documentation standards. Promote a culture of continuous improvement and compliance awareness Qualifications Minimum 5 years of quality control, compliance, or regulatory experience in the pharmaceutical, biotech, or healthcare industry. Strong knowledge and hands-on experience with CAPA systems and methodologies. Pharmacy Technician License or willingness to obtain one Ability to analyze data, identify trends, and develop solutions to compliance/quality issues. Proficiency with computer systems, reporting tools, and compliance tracking software. Familiarity with DEA, FDA, OSHA, and state pharmacy regulations. Strong organizational skills with close attention to detail. Excellent written and verbal communication skills; bilingual (Spanish & English) preferred. Ability to work under supervision but also independently when required.f What We Offer Competitive salary. Bonus program based on productivity and efficiency. Flexible scheduling options. Opportunities for growth in a rapidly expanding telepharmacy practice. Collaborative and innovative work environment focused on patient safety and compliance. This is a full-time position, working 44 hours per week, Monday through Friday This is a 100% onsite role; remote or hybrid work is not available. The hourly rate will vary based on experience Pay Range$60,000-$70,000 USD Benefits: 401(k) with up to 4% matching Medical, dental, vision and life insurance Paid time off Paid public holidays At The Pharmacy Hub, we don't just offer jobs-we offer opportunities for career growth and development. We take pride in our fast-paced, team-driven culture and are committed to supporting our employees in achieving success. If you're ready to join a company that values hard work, dedication, and teamwork, apply today! We look forward to welcoming you to The Pharmacy Hub and working together to deliver top-tier pharmacy fulfillment solutions.$60k-70k yearly 6d agoQuality Control Technician
Ozinga
Quality control analyst job in Miami Gardens, FL
Overview Summary: The Quality Control Technician will implement and comply with quality assurance methods and procedures to ensure products and materials are produced in accordance with specifications in a safe and efficient manner. Principal Duties and Responsibilities: Quality Control Analysis: • Conduct tests and inspect concrete to evaluate quality or conformance to specifications • Sample and evaluate quality of materials related to concrete • Monitor equipment operation to ensure that concrete is within tolerance • Record inspection or test data, such as slump, air content, unit weight, temperature, or moisture content • Input test data into company quality control software • Test hardened concrete for compressive strength • Input strength results into company quality control software • Analyze, evaluate, and resolve customer concerns involving specific conditions, situations, quantities, and other influences associated with product • Manage and maintain quality control software for assigned area Production and processing: • Perform aggregates and batch plants tests including aggregate gradation and moisture tests for State and spec projects as required Communication Skills: • Provide information to supervisors, co-workers, and contractors via phone, e-mail or in person • Effectively communicate with dispatch office to successfully ship and test concrete Global Responsibilities: • Regular attendance and physical presence at work is an essential function of this position • This job may require additional duties not listed above and the employee may be asked to perform those duties to meet business needs Qualifications: Education/Specialized Knowledge/Professional Certifications: • High School Diploma or equivalent required • Bachelor's degree in related field preferred • ACI Level 1, NICET Certified or NRMCA Short Course completion on aggregates or concrete are required • Valid driver's license required •I DOT PCC Level I or WDOT PCCTEC I certification(s) or higher are preferred(IL South, IL North, and WI region only) • Knowledge of raw materials, production processes and quality control are preferred Experience: • Experience in related field preferred Skills/Abilities: • Able to read, write, and speak English preferred • Able to operate a smart phone/device • Proficient in Microsoft Office Suite Working Conditions: • Operation within a fast-paced environment • Exposed to moving mechanical parts, vehicles, heavy construction equipment, toxic or caustic chemicals, and outside weather conditions • Noise level is usually moderate, but can be high and requires personal hearing protection on occasion at job sites, plants and laboratories • Must be able to work through stressful situations while maintaining professionalism and composure • Local travel required Physical Requirements: • Regularly required to talk or hear; frequently is required to stand; walk; use hands to finger, handle or feel; and reach with hands and arms • Occasionally required to sit; climb or balance; and stoop, kneel, crouch or crawl • Must be able to stand and move about job sites with uneven and unpaved ground while managing concrete delivery onsite • Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus • Must be able to frequently bend in order to obtain samples from stockpiles or ground, climb ladders with buckets of admixtures, and push wheelbarrows of concrete • Must be able to operate buttons, levers, and other controls located on various equipment • Must be able to work long and flexible hours as necessary • Must be able to maneuver in and around our plants, yards and jobsites as necessary • Lift/Carry up to 55pounds frequently • Lift up to 100 pounds occasionally Ozinga is an Equal Opportunity Employer. We consider applications for all positions without regard to race, color, religion, creed, gender, national origin, age, disability, sexual orientation, citizenship status, genetic information, or any other legally protected status.$33k-48k yearly est. Auto-Apply 1d agoQuality Control Assistant
Quality Aircraft Parts
Quality control analyst job in Miami Gardens, FL
Quality Aircraft Parts has an immediate opening for an Quality Control Assistant. This is a full-time position, reporting to the Director of Quality Control. A & P Licenses are required. We are conveniently located near the Opa-Locka Executive Airport and less than 10 miles from Miami International Airport, our facility meets and exceeds the highest industry standards. Responsibilities include but are not limited to: Incoming inspection In process inspections Manual maintenance Testing inspection Final inspections Requirements: Ability to adapt in a fast-paced environment Must have strong attention to detail and communication skills, both oral and written Ability to multitask and meet deadlines This is a FULL-TIME POSITION, Tuesday - Friday 7:30am to 6:00pm We are an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.$27k-37k yearly est. 60d+ agoQuality Control Microbiologist II
Vivex Biologics Inc.
Quality control analyst job in Miami, FL
Description: The Quality Control Microbiologist II is responsible for performing microbiological testing and managing results of incoming raw materials, in-process samples, and final product samples. Review and analyze testing data to ensure internal specifications are in accordance with standard operating procedures requirements. Ensure testing results are accurate, and results are available in a timely manner. Must write and review procedures, reports, and investigations. Performs all functions in accordance with standard operating procedures, all applicable federal and state regulatory and accrediting standards requirements. Requirements: Perform microbiology testing including, but not limited to reading of cultures, gram staining, microbial limit test, cell count and cell viability testing, growth promotion testing, and biochemical testing. Support the environmental monitoring program (EM), Stability Program, and the Dose Audit Program. Perform microbial characterization including subcultures of samples, gram stain, biochemical testing, and final identification using VITEK 2. Conduct testing of clean utilities of the facility, including but not limited to performing TOC, pH, and conductivity testing. Review and analyze test results according to internal standard procedures to ensure proper management, tracking, and disposition of materials and products. Performs reviews and approval of routine testing documents. Responsible for reporting and analyzing all variances, errors, and deviations to Quality Management. Maintain proper documentation and trend analysis of QC test results. Perform laboratory cleaning and maintenance of equipment. Maintains the laboratory stock of media, reagents and laboratory supplies. Lead QC validations and supports interdepartmental validations and qualifications that require microbiological testing. Support Write investigations, deviations, and change controls. Manages the implementation of controlled changes and corrective actions. Participate in the on-call weekend schedule. Perform other duties as assigned by QC Management Qualifications Education/Experience: Bachelor's degree in science with at least 3-4 years of experience in a regulated environment (e.g., Biologics, Medical Device, Pharmaceutical, etc.). Associate's degree in science with at least 4 years of experience in a regulated environment (e.g., Biologics, Medical Device, Pharmaceutical, etc.). Skills: Excellent interpersonal, verbal, and written communication skills required. Must demonstrate excellent organizational and record-keeping skills. Must be detail oriented with the ability to multi-task in a high-pressure environment. Proficient in Microsoft Office. Working conditions Fast paced, lab-oriented work environment. Evening and weekend work may be required. Physical requirements While performing the duties of this job, the employee is regularly required to sit or stand for prolonged periods of time. The employee may occasionally be required to pull, lift and/or move up to 20 pounds. Direct Reports No direct reports. Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job any time. VIVEX Biologics is an equal opportunity employer (EEO) and expressly prohibits any form of workplace discrimination and/or harassment based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.$37k-52k yearly est. 15d agoScientist/chemist/QC/Associate Scientist
Actalent
Quality control analyst job in Fort Lauderdale, FL
We are seeking a dedicated Associate Scientist to perform routine tests on various samples including finished products, stability samples, and raw materials using techniques such as UV and HPLC in a regulated laboratory environment. This role involves evaluating test results, maintaining accurate lab documentation, and ensuring compliance with SOPs and cGMP standards. Responsibilities * Conduct routine tests of finished products, stability samples, raw materials, and CV samples using techniques such as assays, chromatographic purity, and particle size distribution. * Evaluate test results and determine the acceptability of samples based on the results. * Maintain accurate lab notebooks and complete all related analytical reports and documentation in compliance with SOPs. * Ensure laboratories are maintained with good housekeeping practices and in compliance with cGMP standards. * Review notebooks promptly and ensure compliance with SOPs. * Analyze and interpret results in both written and oral formats. * Assist in training new analysts. * Conduct laboratory investigations and initiate Quality Events, CAPA, and Change Controls as needed. * Follow all SOPs and safety guidelines to ensure compliance with a cGMP environment. Essential Skills * Proficiency in HPLC, UPLC, and UV-Vis techniques. * Strong analytical chemistry. * Familiarity with FDA and GMP regulations. * Ability to analyze and interpret complex data. Additional Skills & Qualifications * Bachelor's degree in Chemistry or related scientific field with 1-2 years of related experience in pharmaceutical analysis, or a Master's degree with 1 year of experience. * Problem-solving skills involving several concrete variables in standardized situations. * Ability to perform necessary computations and interpret graphs. * Working knowledge of instrumentation software used in laboratories. Work Environment This position is based in a lab environment regulated by FDA and GMP standards. The work schedule is 2nd shift from 2pm-11pm, with all training taking place during the 1st shift. Job Type & Location This is a Contract to Hire position based out of Fort Lauderdale, FL. Pay and Benefits The pay range for this position is $29.00 - $35.00/hr. 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 Fort Lauderdale,FL. Application Deadline This position is anticipated to close on Jan 17, 2026. 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. 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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.$29-35 hourly 6d agoQuality Control Technician
Supermix
Quality control analyst job in Miami, FL
Entry Level Technician Responsibilities Sample and test materials used to produce concrete (sand, rock, etc.) Sample and test concrete in the laboratory; to include temperature, slump, air content, unit weight, and casting test cylinders Maintain accurate quality control records Troubleshoot quality control issues and report priority concerns to the QC Manager Accurate Sample labeling Maintain company vehicles and property in accordance with company policy. Education, Licenses, and Skills: High School Diploma or Equivalent Experience Valid Driver License with driving record that meets company standards Detail Oriented Work well with others **Company will provide training and certification** Full Benefits offered: Medical Dental Vision 401K Vacation$34k-48k yearly est. 60d+ agoQuality Control Technician
Shasta
Quality control analyst job in Miami, FL
The Quality Control Technician will be responsible for all aspects of the quality programs and functions. These include maintaining all HACCP, food safety records, plant audits, mock recall programs and training the plant on these issues and procedures. Performs testing to validate the microbiological quality of current and new ingredients, suppliers, and packages. Provides test data to assure the production of high quality products. Tests current and new concentrate ingredients in process and finished concentrates, and beverages products in development and finished products. The QC Technician will also work with the R&D Team on new product launches. ESSENTIAL DUTIES AND RESPONSIBILITIES: • Knowledge of all cleaning agents and applications, external, internal, cleaners, and sanitizers. • Properly document and follow all procedures set forth in the frequency guide and standards. • Ability to properly fill out batch reports, calculate variations in batch sizes, proper attributes, standards, and other data required on batch report documented per formula.• Ability to properly measure and follow proper mixing procedures.• Ability to evaluate and troubleshoot batch and make corrections.• Ability to perform all testing, evaluations, and documentation of results while following procedures.• Ability to troubleshoot and take corrective action on the line.• Ability to properly prepare batch tanks for batching, tank rinsing, tank sanitation, odor, and tasting.• Full knowledge and capabilities to perform internal pest control program, location of stations, checking and cleaning of stations, and proper documentation on hand of pest control program.• Assist supervisors in resolving Quality Control issues, tracking quality trends, recommending and implementing plans to improve quality and production efficiency.• Responsible for compliance with Federal and State legislation by establishing and enforcing quality standards; testing materials and product. • Ability to collect, analyze and summarize process quality information and trends. • Computer literacy required with proficiency in Microsoft Office products including Excel and Word. • Typically faces situations that have a variety of interpretations and require careful evaluation. LANGUAGE SKILLS:Ability to read, analyze, and interpret common information, reports and other documents. Ability to respond to common inquiries or complaints from customers, regulatory agencies, or company representatives. Ability to effectively present information to management. 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. While performing the duties of this job, the employee is regularly required to walk, stand for long periods of time, sit and talk or hear. The employee frequently is required to use hands and fingers, to handle, or feel, sit for long periods of time, stand frequently, bend, squat, reach and turn to access files and office equipment. Must be able to lift 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. Field positions will be exposed to various unfamiliar conditions where Personal Protective Equipment (PPE) must be worn and which may include, but are not limited to manufacturing and warehouse plants, and other locations as directed by supervisor. The noise level in the work environment is usually moderate, but increases significantly in warehouse and manufacturing plants. MINIMUM 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. • High School Diploma or GED preferred or equivalent experience. • 2-3 years hands-on work experience in the carbonated soft drink industry preferred.• Experience in quality control testing procedures and internal and external sanitation of beverage equipment with a clear understanding of all aspects of blending, product attributes recordkeeping, yields, etc.• Strong computer skills, including Microsoft business applications and various reporting software.• Exceptional interpersonal and verbal communication skills• Understands and can follow all OSHA required training.• Must be 18 years or older• Favorable background and drug exam. • Ability and willingness to work a flexible Full Time schedule that may include weekends and holidays.• Must be able to provide own transportation to various locations in organizational service areas, as required by duties. Shasta Beverages, Inc. provides equal employment opportunities to all applicants for employment without regard to race, color, religion, sex, national origin, age, disability, gender, genetics, gender identity, disabled veterans or sexual orientation.$29k-39k yearly est. 4d agoQC Chemist
Prime Matter Labs
Quality control analyst job in Miami Gardens, FL
Analyzes Products and Materials and the composition of their ingredients. Includes the following. Other duties may be assigned. Following approved procedures and under general direction: Develops formulas, processes, and methods for solution of technical problems. - Provides input to the development of procedures. - Follows established procedures and documents all findings and results timely, concisely, clearly and accurately. - Analyzes compounds to determine chemical and physical properties. - Conducts research on manufactured products to develop and improve products. - Conducts research into composition, structure, properties, relationships, and reactions of matter. - Prepares standards and specifications for processes, facilities, products, and tests. - Measures products for compliance to standards and specifications and reports same. - Contributes to a continuous improvement process to lower product costing and/or add product value. - Follow Prime Enterprises, Inc. SOPs, STPs and cGMP. - Keeps records updated, distributed, and filed. Job Performance Standards: Neither suffers nor contributes to any injury or accident. Maintains an exemplary attendance and punctuality performance record. Adheres to all Prime Personnel Policies as established by the company. Performs all tasks and assignments in a safe and timely manner. Strives toward continuous self-improvement in personal productivity. Skills: requires a combination of technical skills, analytical capabilities, and attention to detail. Candidate should have a solid working knowledge of laboratory instrumentation such as FTIR, HPLC. Candidate must have a demonstrated proficiency in laboratory instrument troubleshooting and knowledge of statistical techniques. Education: Minimum of a BS in Chemistry, Chemical Engineering or Biochemistry. Degrees in other scientific disciplines will be considered.$43k-55k yearly est. 60d+ agoQuality Control Inspector - 2nd Shift
Tuuci
Quality control analyst job in Hialeah, FL
Description Job Title Quality Control Inspector Company Snapshot: Born in Miami more than a quarter of a century ago, Tuuci is the global leader in premium shade and placemaking products for hospitality, commercial, and residential outdoor settings. From locations in North America, Europe and Asia, our teams strive to meet and exceed the Tuuci vision: to help people live their best life outdoors through inspiring design, enduring performance, and convivial service. We work in a fun, fast-paced, and diverse environment in which close collaboration and the spirited exchange of ideas are encouraged. Our culture supports our vision by encouraging creativity, driving excellence, and supporting personal growth and development. Tuuci is searching for a team member who embodies passion and performance in the Quality Control department. The Quality Control Inspector position inspects raw materials, finished products and the procedures of the entire production cycle to ensure efficiency and consistency. Other responsibilities include but not limited to: Essential Duties and Responsibilities: Conduct audit inspection on the in-process, process procedure and finished goods products by confirming specifications using drawings and procedures. Approve or reject raw materials with respect to quality standards. Document inspection results by completing reports and logs. Assist in determining the root cause and the implementation of a corrective action. Organize the disposition of rejected materials and log all rejected materials. Measure products with rulers, calipers, gauges, or micrometers. Monitor operations to ensure that they meet production standards; recommend adjustments to the production process. Document the QC results by preparing reports of the findings; ensure materials are checked in with the required paperwork and is in proper condition. Maintain safe and healthy work environment by following standards and procedures. Assist in the development of SOPs. Other tasks as assigned. Education and Qualifications: We prefer candidates with 2 years of quality control, receiving and inspection experience. Experience working in warehouse or manufacturing environment. Experience with reading engineering drawings, measuring tools and proficiency in MS Word and Excel. Lift up to 45lbs. Must be Fluent in English and Spanish. This is a full-time, day shift position hours are Monday through Friday from 7:00am to 3:30pm and occasionally require overtime up to 5:30pm and Saturdays. Tuuci is an equal opportunity employer. All applicants and employees are to be treated equally with the same rights and privileges with respect to recruiting, hiring, promotions, demotions, transfers, separations, compensation, and benefits regardless of their age, race, color, creed, religion, or ethnic origin, sex, sexual orientation, pregnancy-related status, marital status, veteran status, physical or mental disability, where the individual is otherwise qualified, or any other category protected by applicable law. This employer participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. If E-Verify cannot confirm that you are authorized to work, this employer is required to give you written instructions and an opportunity to contact Department of Homeland Security (DHS) or Social Security Administration (SSA) so you can begin to resolve the issue before the employer can take any action against you, including terminating your employment. Employers can only use E-Verify once you have accepted a job offer and completed the Form I-9. *************$30k-41k yearly est. Auto-Apply 3d agoQuality Control Inspector
Miami Air International
Quality control analyst job in Miami, FL
Miami Air International, with its modern fleet of Boeing 737 aircraft, is the premier provider of private group air transportation, commonly called chartered flights. It's not just a flight. This is a travel experience that is tailored to delight your group. We understand that each group is unique and personalizing the right services and flight amenities is critical, and at the heart of why you are considering a charter. All we do is charter. And we do a lot! Our business is built to only serve groups like yours, and you are our number one priority. In addition to concentrating our efforts on being the best in those things you want from any airline - like industry leading safety-programs and over 25 years of proven reliability and financial stability - we provide a suite of services unparalleled by any other airline. Sound like a match? You're in luck. Miami Air is currently seeking a highly motivated and personable individual to join the company as a Quality Control Inspector responsible for the efficient and economic determination of the airworthiness of aircraft, engine, appliance and component maintenance actions as assigned, and conduct inspections in accordance with the Maintenance Program, AD, SB or other requirement to ensure aircraft, engines, appliances and components are maintained to a prescribed standard in order to continue their airworthiness. Functions & Responsibilities Perform preliminary, in progress, hidden damage, and final inspections. Performs special inspections as detailed by the requesting or requiring document. Performs Required Inspection Item (RII) and Buy Back inspections. Perform receiving inspections to ensure the use of legal, conforming and applicable parts and materials. Ensure that inspections and surveillance are performed as required on necessary maintenance actions in order to assure the use of approved data, material, tools, test equipment and that high standards of workmanship are present. Provide guidance and assistance to maintenance personnel in order to train, maintain and enhance compliance to programs, policies and procedures. Conduct daily audits of aircraft work packages including checks/inspections forms, log pages, routines and non-routines, modification orders, etc. to ensure completion, correctness, use of appropriate references to approved data in all entries and forms. Review the aircraft and engine logbooks, using the same criteria as described in item f above, at checks and during accomplishment of any maintenance. At the appropriate checks, transcribes all pilot reports and deferred maintenance items to the appropriate work forms. Conduct records analysis of audits and reviews of data/information for continuing analysis and surveillance reports as identified by the Manager, QC/QA & Training. Lead and maintain the current the Structural Defect Log as assigned. Review and address the calibrated tools and equipment status and shelf-life status and ensure correction of any discovered discrepancies during the first 10 days of each month. Perform as a “Designated Instructor” in areas and/or on subjects as qualified and approved by the Manager, Maintenance Training and QA. Perform the inspections of S.O.S. Tag items and documents results per the S.O.S. program. Complete safety and housekeeping checks of hangar and line work areas on a routine basis as designed and assigned by the Manager, QC/QA & Training. Perform other duties as necessary within the scope of quality. Qualifications & Requirements Associate degree A&P Mechanic License Airman's Certificate with A&P ratings for a minimum of 3 years. 3 years of experience as licensed A&P mechanic with 2 years of maintenance experience on large aircrafts. Boeing 737 experience, Classic and NG preferred. ETOPS and RVSM operations experience. Knowledgeable of the FARs, GMM, Maintenance Programs. Excellent written and oral communication skills. Proficient with Microsoft applications. Knowledge of TRAX systems, a plus. Knowledgeable of manuals and publications skills, a plus. Miami Air International provides equal employment opportunities to all legally eligible and authorized to work applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.$21k-32k yearly est. Auto-Apply 60d+ agoQuality Control Inspector - 2nd shift
Complete Turbine Services
Quality control analyst job in Coral Springs, FL
QUALITY CONTROL BENCH INSPECTOR Responsibilities include but are not limited to: Reading and adhering to the published Workscope, as revised. Performing Receiving Inspection of incoming engines to identify visual non-conformances on the engines as-received. Documenting discrepancies (Damage Report) and generating Non-Routines, Manila Tags or 227's as required to initiate the repair of the noted discrepancies per SOP 14-006 R1. Performing Incoming & Outgoing Inventory Inspection of LRUs. Perform EMU and/or piece part inspection of disassembled engines, identifying and documenting non-conformances. Recording the status of all inspected parts on the QC 227C (Unserviceable and Serviceable parts alike), and proper routing of parts to restore them to serviceable condition in a timely and accurate manner. Routing parts to Outside Vendors and accurately documenting identification data and work required in Quantum. Also responsible for overseeing maintenance actions in progress and documenting required data on maintenance forms as maintenance actions are accomplished. Minimum Job requirements: Minimum FAA “P” Certificated; 2 years Minimum CF6 engine experience; Ability to navigate the OEM Manuals and to read and understand technical data; must have working knowledge of the Quantum Operating System. Requirements MINIMUM REQUIREMENTS: Must possess a valid FAA A&P or Powerplant Certificate Read & Write English Able to Read and Comprehend OEM Engine Manuals, IPC's, SPM's, AMM's and other Approved Data 2 Years' Experience on CF6 Engines (is a plus) Computer Skills Able to use MS Outlook (Email), Word & Excel Must be COACHABLE (Able to Listen, Learn and Follow Instructions) / Have a Good Attitude / 2 Years with CTS Engines ** Applicants must be U.S. Citizens or Permanent Residents to be considered, we don't have sponsor plans at the moment**$27k-40k yearly est. 3d agoDock QC Inspector
Pero Family Farms Careers
Quality control analyst job in Delray Beach, FL
Title: Dock QC Inspector Reports to: QC Manager Type: Full-Time | Onsite | Non-Exempt Pero Family Farms is a market share leader with over a century of dedication, commitment and integrity. Operating since 1908, Pero is the farm trusted by retailers and consumers alike. We are a fully integrated farming operation, with departments that specialize in organic farming, logistics, global supply chain management, national sales operations, food processing operations, and strategic marketing functions. Our operation includes over 35,000 acres spanning across the East Coast of the United States from Florida to New York, with distribution and production facilities in several different states. We pride ourselves in maintaining a strong family heritage and tradition that has been dedicated to quality, innovation, and excellent customer service that has been feeding America's families for over a century. Our family's passion for farming remains unwavering, with a vision to continue the tradition for many generations to come, whilst maintaining the reverence and trust it has established with the American consumer. As we expand our offering to include an assortment of organic vegetable options; we have become one of the largest organic vegetable growers in the country and we are looking to grow our workforce family. Join us in continuing and strengthening our position as a market share leader dedicated and trusted by retailers and consumers alike. JOB SUMMARY Assure consistent product Safety and Quality by testing, measuring and verifying raw materials. Performance of procedures that comply with stated corporate mission and strategic plan, corporate policies, and customer product specifications. Requirements RESPONSIBILITIES AND DUTIES Color, Sizing and grade evaluation of fresh perishable produce Calibrations on weight scales, thermometers and all applicable testing tools or detectors G.M.P. monitoring of operation to assure food safe environment Color code enforcement; sanitation, organics handling, allergen control Hold and release program Rework Program Shelf-life evaluation and sensory testing as required Paperwork, filing, notifications and data entry for Team site/Quality System Other duties as required SKILLS Good communication skills, including basic written and spoken English, to ensure understanding of safety procedures and documentation Basic computer skills Microsoft Office: Excel, Word A working knowledge of English and basic math Ability to collaborate with management PHYSICAL & ENVIRONMENTAL CONDITIONS Required to stand, sit, walk for long periods of time Frequent use of hands for simple, firm grasping and writing Frequent bending, stopping, reaching, climbing Frequent lifting, carrying 5 pounds to 50 pounds Frequent use of cutting utensils (i.e. knives, peeler) Exposure to product fumes such as onions, peppers, etc. Exposure to varying temperatures of 45 degrees or less Exposure to chemicals such as chlorine, etc. Works overtime as required EDUCATION & EXPERIENCE Minimum High School education / G.E.D. preferred or applicable certification Understanding of Produce Standards, and or basic produce experience preferred Must be able to drive to outside locations for inspections; required for dock staff COMPANY BENEFITS/PERKS 401(k) Health, Dental, Vision Insurance and more Paid Time Off (PTO) The company (Pero) reserves the right to alter, amend, expand or contract these duties and responsibilities as the companies needs evolve.$27k-40k yearly est. 60d+ agoQUALITY CONTROL INSPECTOR
Gotworx Staffing
Quality control analyst job in Tamarac, FL
GotWorX, Inc. Is currently seeking a Quality Control Inspector for our client based in the Tamarac area. This is a temp-hire opportunity for the right candidate. Client is currently offering a salary of $ 18 pay rate, plus a benefits package once perm employee! Overview: The Quality Control Inspector ensures that incoming, in process, and finished parts are within all required specifications per drawings and work instructions. It is the Quality Control Inspector s responsibility to implement good documentation practices (GDP) and proper material identification, preventing nonconforming material from continuing through the process without proper approval, to ensure that the customer gets parts that function properly every time. Responsibilities: Performs area specific internal quality audits Performs area specific 5S audits Performs random in-process audits in designated areas Performs first piece inspection audits for team members as required Maintains and stores inspection equipment appropriately Verifies presence of calibration sticker before using measurement device Notifies manager of equipment with past due calibration Notifies manager of calibrated items that need attention Reviews and provides feedback on procedures, policies, and processes Applies proper sampling methods (AQL) managing risk and cycle time Interprets and inspects mechanical drawings (GD&T literate) Maintains all inspections records or other required documentation Coordinates, implements, and documents containment actions Actively supports conducting root cause investigations In order to be considered, we require: High School Diploma or GED required Prior experience in quality control field preferred Prior inspection experience preferred Prior forklift experience preferred Prior machining / CNC experience preferred Prior SAP experience preferred Candidates will be required to complete a background check and drug screen before beginning work.$18 hourly 60d+ agoQuality Control Chemist
Verdant Specialty Solutions
Quality control analyst job in University Park, FL
Verdant Specialty Solutions is a dynamic, innovation-driven specialty chemicals company with a global footprint. Born from the McIntyre Group of the 1970s and relaunched in 2021, Verdant combines the agility of a small business with the safety, reliability, and scale of a larger organization, offering personal attention backed by industry-leading manufacturing and technical capabilities. With over 375 product offerings, nine strategic sites across the U.S. and Europe, and a steadfast commitment to sustainability, compliance, and customer-centric solutions, Verdant brings functional chemistry to life safely, reliably, and responsively. Are you a hands-on chemist who loves ensuring quality, safety, and operational excellence? Verdant Specialty Solutions, a global specialty chemical company serving world-leading consumer, industrial, and energy brands, is looking for a Quality Control Chemist to join our University Park team. Why this role is exciting: * Play a key role in a fast-growing, start-up-like environment with global impact * Work with cutting-edge specialty surfactant chemistries for top-tier clients * Contribute directly to safety, quality, and operational excellence across multiple sites * Opportunities to grow professionally in a collaborative, innovative culture What you will do: * Perform in-process, final product, and raw material analyses * Certify products for shipment and maintain accurate lab records * Collaborate with operators, engineers, and QC colleagues to optimize processes * Participate in process improvements, investigations, and quality initiatives * Maintain compliance with ISO 9001, EFfCI, GMP, RSPO, and HSSE standards * Operate lab systems (SAP) to track data, generate certificates, and manage inventories$43k-55k yearly est. 22d agoQuality Control Technician
The Pharmacy Hub
Quality control analyst job in Miami Gardens, FL
Job DescriptionAbout Us At The Pharmacy Hub, we collaborate with pharmaceutical brands, manufacturers, health brands, telemedicine providers, and healthcare companies to deliver essential products directly to patients. Our expertise allows us to seamlessly distribute pharmaceuticals, medical devices, and other healthcare products to consumers, ensuring greater accessibility and convenience. Core Values The Pharmacy Hub is dedicated to breaking barriers in healthcare by championing access, intervention and affordability. Customer-first mindset - we develop strong partnerships with telehealth platforms and healthcare companies to enhance access and understand their specific needs Innovation for intervention in care - we develop advanced compounding solutions and products to better support patient health outcomes Continuous improvement - we continuously improve our processes and offerings through intelligent, honest and transparent practices to deliver cost-effective solutions that truly benefit our clients and their patients. You will play a pivotal role in maintaining these values and contributing to the company's mission of redefining healthcare delivery through superior pharmacy services. Job Summary We are seeking a detail-oriented Quality Control Technician to support quality assurance and compliance activities within a non-sterile compounding pharmacy environment. This role supports day-to-day quality control functions, documentation accuracy, and regulatory compliance related to compounded preparations, controlled substances, and pharmacy operations. Key Responsibilities Perform routine quality control checks in a non-sterile compounding environment Verify compounding documentation, batch records, logs, and labels for accuracy and completeness. Assist with tracking deviations, errors, or quality issues related to compounded preparations. Assit with CAPA activities by collecting data, maintaining logs, and confirming that corrective actions are completed Maintain accurate and organized quality and compliance records. Assist with internal audits, inspections, and preparation of supporting documentation. Work closely with pharmacists, compounding technicians, and compliance staff. Follow and reinforce quality assurance and documentation standards. Participate in quality, safety, and compounding-related training. Collect and document quality data related to compounding operations and pharmacy workflows. Assist in identifying trends or recurring issues and escalate concerns to the Quality team. Support basic reporting and tracking of quality metrics. Qualifications High School Diploma or GED. 1-2 years of experience in a compounding pharmacy, pharmaceutical lab, healthcare, or regulated production environment Strong attention to detail and ability to follow written procedures Basic understanding of quality control principles and regulated workflows. Hands-on experience with non-sterile compounding. Familiarity with USP , FDA guidance, and state pharmacy regulations. Experience supporting quality assurance or compliance functions What We Offer Competitive salary. Bonus program based on productivity and efficiency. Flexible scheduling options. Opportunities for growth in a rapidly expanding telepharmacy practice. Collaborative and innovative work environment focused on patient safety and compliance. Work Schedule Evening: 3:00 p.m. - 12:00 a.m Overnight: 9:00 p.m. - 6:00 a.m This is a full-time position, working 40 hours per week, Monday through Friday This is a 100% onsite role; remote or hybrid work is not available. The hourly rate will vary based on experience Pay Range$20-$25 USD Benefits: 401(k) with up to 4% matching Medical, dental, vision and life insurance Paid time off Paid public holidays At The Pharmacy Hub, we don't just offer jobs-we offer opportunities for career growth and development. We take pride in our fast-paced, team-driven culture and are committed to supporting our employees in achieving success. If you're ready to join a company that values hard work, dedication, and teamwork, apply today! We look forward to welcoming you to The Pharmacy Hub and working together to deliver top-tier pharmacy fulfillment solutions.$20-25 hourly 3d agoQuality Control Assistant
Quality Aircraft Parts
Quality control analyst job in Miami Gardens, FL
Job Description Quality Aircraft Parts has an immediate opening for an Quality Control Assistant. This is a full-time position, reporting to the Director of Quality Control. A & P Licenses are required. We are conveniently located near the Opa-Locka Executive Airport and less than 10 miles from Miami International Airport, our facility meets and exceeds the highest industry standards. Responsibilities include but are not limited to: Incoming inspection In process inspections Manual maintenance Testing inspection Final inspections Requirements: Ability to adapt in a fast-paced environment Must have strong attention to detail and communication skills, both oral and written Ability to multitask and meet deadlines This is a FULL-TIME POSITION, Tuesday - Friday 7:30am to 6:00pm We are an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.$27k-37k yearly est. 23d agoQuality Control Microbiologist I
Vivex Biologics
Quality control analyst job in Miami, FL
The Quality Control Microbiologist I is responsible for performing microbiological testing and managing results of incoming raw materials, in-process samples, and final product samples. Review and analyze testing data to ensure internal specifications are met in accordance with standard operating procedures requirements. Ensure testing results are accurate, and results are available in a timely manner. Performs all functions in accordance with standard operating procedures, all applicable federal and state regulatory and accrediting standards requirements. Requirements Perform microbiology testing including, but not limited to reading of cultures, gram staining, microbial limit test, cell count and cell viability testing, growth promotion testing, and biochemical testing. Support the environmental monitoring program (EM), Stability Program, and the Dose Audit Program. Perform microbial characterization including subcultures of samples, gram stain, biochemical testing, and final identification using VITEK 2. Conduct testing of clean utilities of the facility, including but not limited to performing TOC, pH, and conductivity testing. Review and analyze test results according to internal standard procedures to ensure proper management, tracking, and disposition of materials and products Responsible for reporting all variances, errors, and deviations to Quality Management. Maintain proper documentation and trend analysis of QC test results. Perform laboratory cleaning and maintenance of equipment. Maintains the laboratory stock of media, reagents and laboratory supplies. Support validations and qualifications that require microbiological testing. Participate in audits and inspections, accreditation, and licensing activities as needed. Supports investigations, complaints, and deviations contributing to the formulation and implementation of corrective actions. Participate in the on-call weekend schedule. Perform other duties as assigned by QC Management. Qualifications Education/Experience: Bachelor's degree in science with at least 0-2 years of experience in a regulated environment (e.g., Biologics, Medical Device, Pharmaceutical, etc.). Associate's degree in science with at least 2 years of experience in a regulated environment (e.g., Biologics, Medical Device, Pharmaceutical, etc.). Required/Preferred Experience: Hands on Environmental Monitoring experience in a regulated GMP environment (cleanroom EM, viable/non-viable monitoring, trend analysis, excursions). Skills: Excellent interpersonal, verbal, and written communication skills required. Must demonstrate excellent organizational and record-keeping skills. Must be detail oriented with the ability to multi-task in a high-pressure environment. Proficient in Microsoft Office. Working conditions Fast pace, lab-oriented work environment. Evening and weekend work may be required. Physical requirements While performing the duties of this job, the employee is regularly required to sit or stand for prolonged periods of time. The employee may occasionally be required to pull, lift and/or move up to 20 pounds. Direct Reports No direct reports. Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job any time. VIVEX Biologics is an equal opportunity employer (EEO) and expressly prohibits any form of workplace discrimination and/or harassment based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. VIVEX Biologics complies with the Americans with Disability Act (ADA) which prohibits discrimination against qualified individuals with disabilities who, with or without reasonable accommodation, can perform the essential functions of a job.$37k-52k yearly est. 5d agoQuality Control Inspector
Miami Air International
Quality control analyst job in Miami, FL
Miami Air International, with its modern fleet of Boeing 737 aircraft, is the premier provider of private group air transportation, commonly called chartered flights. It's not just a flight. This is a travel experience that is tailored to delight your group. We understand that each group is unique and personalizing the right services and flight amenities is critical, and at the heart of why you are considering a charter.$21k-32k yearly est. Auto-Apply 60d+ agoQuality Control Technician
The Pharmacy Hub
Quality control analyst job in Miami Gardens, FL
About Us At The Pharmacy Hub, we collaborate with pharmaceutical brands, manufacturers, health brands, telemedicine providers, and healthcare companies to deliver essential products directly to patients. Our expertise allows us to seamlessly distribute pharmaceuticals, medical devices, and other healthcare products to consumers, ensuring greater accessibility and convenience. Core Values The Pharmacy Hub is dedicated to breaking barriers in healthcare by championing access, intervention and affordability. Customer-first mindset - we develop strong partnerships with telehealth platforms and healthcare companies to enhance access and understand their specific needs Innovation for intervention in care - we develop advanced compounding solutions and products to better support patient health outcomes Continuous improvement - we continuously improve our processes and offerings through intelligent, honest and transparent practices to deliver cost-effective solutions that truly benefit our clients and their patients. You will play a pivotal role in maintaining these values and contributing to the company's mission of redefining healthcare delivery through superior pharmacy services. Job Summary We are seeking a detail-oriented Quality Control Technician to support quality assurance and compliance activities within a non-sterile compounding pharmacy environment. This role supports day-to-day quality control functions, documentation accuracy, and regulatory compliance related to compounded preparations, controlled substances, and pharmacy operations. Key Responsibilities Perform routine quality control checks in a non-sterile compounding environment Verify compounding documentation, batch records, logs, and labels for accuracy and completeness. Assist with tracking deviations, errors, or quality issues related to compounded preparations. Assit with CAPA activities by collecting data, maintaining logs, and confirming that corrective actions are completed Maintain accurate and organized quality and compliance records. Assist with internal audits, inspections, and preparation of supporting documentation. Work closely with pharmacists, compounding technicians, and compliance staff. Follow and reinforce quality assurance and documentation standards. Participate in quality, safety, and compounding-related training. Collect and document quality data related to compounding operations and pharmacy workflows. Assist in identifying trends or recurring issues and escalate concerns to the Quality team. Support basic reporting and tracking of quality metrics. Qualifications High School Diploma or GED. 1-2 years of experience in a compounding pharmacy, pharmaceutical lab, healthcare, or regulated production environment Strong attention to detail and ability to follow written procedures Basic understanding of quality control principles and regulated workflows. Hands-on experience with non-sterile compounding. Familiarity with USP , FDA guidance, and state pharmacy regulations. Experience supporting quality assurance or compliance functions What We Offer Competitive salary. Bonus program based on productivity and efficiency. Flexible scheduling options. Opportunities for growth in a rapidly expanding telepharmacy practice. Collaborative and innovative work environment focused on patient safety and compliance. Work Schedule Evening: 3:00 p.m. - 12:00 a.m Overnight: 9:00 p.m. - 6:00 a.m This is a full-time position, working 40 hours per week, Monday through Friday This is a 100% onsite role; remote or hybrid work is not available. The hourly rate will vary based on experience Pay Range$20-$25 USD Benefits: 401(k) with up to 4% matching Medical, dental, vision and life insurance Paid time off Paid public holidays At The Pharmacy Hub, we don't just offer jobs-we offer opportunities for career growth and development. We take pride in our fast-paced, team-driven culture and are committed to supporting our employees in achieving success. If you're ready to join a company that values hard work, dedication, and teamwork, apply today! We look forward to welcoming you to The Pharmacy Hub and working together to deliver top-tier pharmacy fulfillment solutions.$20-25 hourly Auto-Apply 3d agoQuality Control Microbiologist II
Vivex Biologics
Quality control analyst job in Miami, FL
The Quality Control Microbiologist II is responsible for performing microbiological testing and managing results of incoming raw materials, in-process samples, and final product samples. Review and analyze testing data to ensure internal specifications are in accordance with standard operating procedures requirements. Ensure testing results are accurate, and results are available in a timely manner. Must write and review procedures, reports, and investigations. Performs all functions in accordance with standard operating procedures, all applicable federal and state regulatory and accrediting standards requirements. Requirements Perform microbiology testing including, but not limited to reading of cultures, gram staining, microbial limit test, cell count and cell viability testing, growth promotion testing, and biochemical testing. Support the environmental monitoring program (EM), Stability Program, and the Dose Audit Program. Perform microbial characterization including subcultures of samples, gram stain, biochemical testing, and final identification using VITEK 2. Conduct testing of clean utilities of the facility, including but not limited to performing TOC, pH, and conductivity testing. Review and analyze test results according to internal standard procedures to ensure proper management, tracking, and disposition of materials and products. Performs reviews and approval of routine testing documents. Responsible for reporting and analyzing all variances, errors, and deviations to Quality Management. Maintain proper documentation and trend analysis of QC test results. Perform laboratory cleaning and maintenance of equipment. Maintains the laboratory stock of media, reagents and laboratory supplies. Lead QC validations and supports interdepartmental validations and qualifications that require microbiological testing. Support Write investigations, deviations, and change controls. Manages the implementation of controlled changes and corrective actions. Participate in the on-call weekend schedule. Perform other duties as assigned by QC Management Qualifications Education/Experience: Bachelor's degree in science with at least 3-4 years of experience in a regulated environment (e.g., Biologics, Medical Device, Pharmaceutical, etc.). Associate's degree in science with at least 4 years of experience in a regulated environment (e.g., Biologics, Medical Device, Pharmaceutical, etc.). Skills: Excellent interpersonal, verbal, and written communication skills required. Must demonstrate excellent organizational and record-keeping skills. Must be detail oriented with the ability to multi-task in a high-pressure environment. Proficient in Microsoft Office. Working conditions Fast paced, lab-oriented work environment. Evening and weekend work may be required. Physical requirements While performing the duties of this job, the employee is regularly required to sit or stand for prolonged periods of time. The employee may occasionally be required to pull, lift and/or move up to 20 pounds. Direct Reports No direct reports. Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job any time. VIVEX Biologics is an equal opportunity employer (EEO) and expressly prohibits any form of workplace discrimination and/or harassment based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin, age, genetic information, disability, or veteran status. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.$37k-52k yearly est. 60d+ ago
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How much does a quality control analyst earn in Sunny Isles Beach, FL?
The average quality control analyst in Sunny Isles Beach, FL earns between $32,000 and $78,000 annually. This compares to the national average quality control analyst range of $40,000 to $86,000.
Average quality control analyst salary in Sunny Isles Beach, FL
$50,000
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