Quality Control Technician
Quality control analyst job in Miami Gardens, FL
Overview Day in the Life of a Quality Control Technician Salary: $51,000 - $64,000 Annually 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 •IDOT 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 Benefits Information: At Ozinga, we care about the well-being of our team members both in and out of the workplace.
That's why we're proud to offer a comprehensive benefits package designed to support your health, financial security, and overall quality of life.
Our benefits include: • Medical, Dental, and Vision Insurance - Protecting your health and providing peace of mind.
• Retirement Plan Options - Helping you build a secure future.
• Voluntary Benefits - Helping you to cover unexpected expenses.
• Work-Life Balance - Supporting flexibility so you can thrive in every area of your life.
• Employee Assistance Program - Offering confidential support for personal and professional challenges.
• Wellness Program - Promoting a healthy lifestyle through resources and incentives.
We believe that when our co-workers feel their best, they can do their best.
Join us and experience the difference of working for a company that values you! 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.
Auto-ApplyCompliance & Quality Control Officer
Quality control analyst job in Miami, 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.
Position Overview
We are seeking a Compliance & Quality Control Officer with strong experience in the pharmaceutical industry to
ensure our operations meet all regulatory and quality standards. This role oversees compliance for 305a mail-
order pharmacy, receiving 305b outsourcing medication, retail pharmacy medications, and controlled substances
(Schedules III & IV). In addition, the Compliance Officer will lead the Quality Control Department, supervising a
team of at least four staff members to maintain the highest standards of accuracy, safety, and compliance.
Key Responsibilities
Compliance Oversight
Ensure compliance with 503a mail-order, 503b outsourcing facilities, and retail pharmacy regulations.
Maintain 50-state licensure and handle renewals, audits, and regulatory filings.
Ensure strict adherence to DEA regulations for Schedule III & IV controlled substances.
Oversee OSHA compliance for warehouse operations, including forklift use and high-level storage safety.
Quality Control Leadership
Lead and manage the Quality Control Department, supervising a team of at least four.
Set quality benchmarks and ensure products meet safety, accuracy, and regulatory requirements.
Provide training, guidance, and performance evaluations to QC staff.
Coordinate with pharmacy, warehouse, and operations teams to resolve quality or compliance issues.
Risk Management & Reporting
Conduct internal audits and prepare for external inspections.
Investigate incidents, document findings, and implement corrective actions.
Utilize advanced software and tracking tools for compliance and quality reporting.
Qualifications
Minimum 3-5 years of compliance and quality control experience in the pharmaceutical industry.
Demonstrated ability to lead, supervise, and develop a team.
Strong computer and reporting system skills.
Bilingual (Spanish & English) - required.
Strong knowledge of DEA controlled substance rules (Schedules III & IV) and OSHA warehouse
standards.
Excellent organizational, communication, and problem-solving skills.
Ability to work a flexible schedule as compliance needs require.
Work Schedule
Standard: Monday to Friday, 8:00 a.m. - 4:30 p.m.
Must be flexible to adapt to inspections, audits, or urgent compliance/quality needs.
Salary:
Salary is to be determined and will be negotiable based on experience.
Pay Range$55,000-$75,000 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.
Auto-ApplyQuality Control Microbiologist II
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.
Entry Level R&D and Lab Technician
Quality control analyst job in Pompano Beach, FL
Full-time Description
The R&D and Laboratory Support Technician will support the Research & Development team in the preparation, testing, and documentation of lab batches and experimental formulations. This role will maintain meticulous documentation, and support a variety of formulation and packaging development processes. The position is essential to the success of new product development and product improvements by ensuring consistent execution of lab procedures, accurate data recording, and support during scale-up initiatives.
Primary / Key Essential Functions and Responsibilities
Assist in preparing and modifying lab batches according to standard procedures or under chemist direction.
Maintain accurate lab logs, batch sheets, formulation files, and experimental records.
Conduct basic physical and chemical tests on raw materials, prototypes, and finished products (e.g., pH, viscosity, stability).
Input test results, formulation data, and sample information into the tracking system/database.
Support formulation scale-up trials in collaboration with compounding and manufacturing teams.
Assemble and label packaging components for testing or presentation purposes.
Assist in managing packaging specifications and updating technical documentation.
Assist in creating, revising, and transferring specifications for formulas and packaging.
Maintain up-to-date libraries of raw materials, samples, formulas, and packaging components.
Participate in calibration of lab equipment and ensure instruments are in good working order
Maintain lab cleanliness and organization.
Support regulatory, compliance and qualify initiatives by ensuring documentation accuracy.
Adhere to lab safety protocols, Good Laboratory Practices (GLP), and standard operating (SOP) procedures.
Other duties as assigned
Requirements
Education and/or Experience and Qualifications
Minimum Education: Associate or Bachelor's degree in Chemistry, Chemical Engineering, Cosmetic Science or other related scientific field.
Minimum Experience: Prior laboratory experience preferred; experience in cosmetics or consumer products a plus.
Knowledge, Skills and Abilities
Strong Computer literacy, and data entry accuracy.
Demonstrated ability to work methodically, organize information, and troubleshoot in a lab environment.
High attention to detail , ability to follow instructions and work within SOPs and GMP guidelines.
Critical thinking and adaptability to evolving processes or systems.
Excellent organization and documentation habits.
Strong verbal and written communication skills; strong interpersonal collaboration across departments (Spanish is a plus)
Proficiency in Google Workspace (Sheets, Docs, Drive) and Microsoft Office (Outlook, Word, Excel, and PowerPoint).
Ability to work independently and as part of a collaborative team.
Ability to manage multiple tasks under deadlines in a fast-paced environment.
A collaborative, team-oriented mindset with a proactive and flexible work ethic.
Management / Supervisory Authority
N/A
Physical Requirements
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. While performing the duties of this job, the employee is occasionally required to stand; reach with hands and arms; walk. The employee must frequently sit; use hands to finger, handle, or feel objects, tools or controls; talk or hear. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by the job include close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus. The employee is exposed to inside weather conditions, moderate noise, and vibrations.
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential job functions. External and internal applicants, as well as position incumbents who become disabled, must be able to perform the essential job functions either unaided or with assistance of a reasonable accommodation as determined on a case by case basis.
Quality Control Assistant
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.
Quality Control Technician
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
Associate Scientist/chemist/QC/
Quality control analyst job in Coral Springs, FL
We are seeking a team of Analytical Chemists to join our team, performing routine tests on various samples, including finished products, stability samples, and raw materials. This role involves using techniques such as UV and HPLC in a regulated laboratory environment, evaluating test results, maintaining accurate 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.
* 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.
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.
* Proficiency in HPLC, UPLC, and UV-Vis techniques.
* Familiarity with FDA and GMP regulations.
* Ability to analyze and interpret complex data.
* Working knowledge of instrumentation software used in laboratories.
* Require Bachelors in Chemistry, No Ph.D
Work Environment
This position is based in a lab environment regulated by FDA and GMP standards. The work schedule offers flexibility with a 1st shift from 8am-5pm or a 2nd shift from 2pm-11pm. All training will take place during the first shift.
Job Type & Location
This is a Contract to Hire position based out of Coral Springs, 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 Coral Springs,FL.
Application Deadline
This position is anticipated to close on Dec 6, 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.
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.
QC Technician
Quality control analyst job in Davie, FL
Job Requirements: include the following essential duties and responsibilities:
Develop a thorough knowledge of CHAUVET DJ Product range and a working knowledge of Pro Product including both operation and multiple unit connectivity.
Visually and physically inspect all products to determine they meet specification in regard to Packaging and Presentation, Physical Appearance, Performance and Functionality, using a range of necessary tools for testing.
Safely and responsibly handle / operate hand tool such as calipers, power drills, screw drivers, laser testers, light meters, heat guns, box cutters and others as may be required.
Document and report all issues to QC Supervisor that could lead to customer dissatisfaction, contribute to recurring defects and potential loss of sales. Provide timely feedback to Supervisor regarding product failures or performance concerns.
Make sure Labeling, Barcoding and Silk Screening are accurate and correctly placed.
Participate in department wide training, cross training and mentoring programs for new and existing team members with a view to increasing personal knowledge of Chauvet Products and Control systems specifically DMX protocol and ShowXpress.
Develop skills that aid is successful diagnosis of errors related to product operation or functions.
Partner with Customer Service. Repair Technicians, Sales and Shipping personnel to meet and exceed Chauvet Customer experience.
Other duties as assigned.
Education and/or Experience:
High school diploma or general education degree (GED); 2-4 years or more experience in repair/service of lighting, small electronics or technical products.
Ability to interpret technical instructions, follows established procedures, and keeps accurate records. Good observation and analytical skills. Attention to detail. Excellent communication and time-management skills with the ability to work independently with little supervision in a fast- paced environment.
Physical Demands:
While performing the duties of this job, the employee is regularly required to use hands to finger, handle, or feel; reach with hands and arms; and talk or hear. The employee frequently is required to stand; walk; and stoop, kneel, crouch or crawl. The employee is occasionally required to sit and climb or balance. The employee must regularly lift and/or move up to ten pounds, frequently lift and/or move up to fifty pounds, and occasionally lift and/or move more than one hundred pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception, and ability to adjust focus. Ability to perform physical work and wear the proper safety equipment at the same time.
Working Conditions:
Work may be performed outside of a climate controlled environment.
Auto-ApplyHeavy Maintenance QC Inspector
Quality control analyst job in Miami, FL
Job Posting Title: QC Inspector, Heavy Maintenance
Reports to: Manager, Quality Control
The QC Inspector - Heavy Maintenance ensures compliance with Global X's Continuous Airworthiness Maintenance Program (CAMP) and FAA regulations. This role is responsible for inspections, surveillance, and audits of heavy maintenance activities to ensure aircraft airworthiness prior to release. The inspector serves as the on-site Quality representative during heavy maintenance events and collaborates closely with vendor personnel, Maintenance Control, and Engineering teams.
ESSENTIAL FUNCTIONS AND RESPONSIBILITIES:
Perform Line Maintenance, Remain Over Night (RON), and Receiving Inspections (RI).
Monitor maintenance work, workmanship, and materials to ensure compliance with Global X procedures and FAA regulations.
Conduct Required Inspection Item (RII) in-process inspections and review related documentation.
Audit completed aircraft records (e.g., logbook pages, work cards, non-routines, engineering documents).
Oversee Heavy Maintenance or Special Maintenance visits.
Perform Borescope inspections when qualified.
Review and approve work documents for accuracy and completeness.
Record discrepancies in logbooks and non-routine forms.
Provide “buy-back” of RII and non-RII maintenance actions.
Approve return-to-service for maintenance, preventive maintenance, and alterations.
Issue airworthiness releases (AWR).
Reject unsatisfactory work and non-conforming parts during inspection.
Prepare and issue audit reports identifying risks, corrective actions, and compliance gaps.
Conduct inspections and audits of contractors, repair vendors, overhaul services, fueling, deicing, and parts suppliers.
Follow all company and safety regulations to maintain a safe work environment.
Perform other duties as assigned by the Director of Quality Control.
SKILLS AND QUALIFICATIONS:
Valid FAA Airframe & Powerplant (A&P) license held for at least 5 years.
Proficiency with TRAX maintenance software.
Documented inspection experience, including RII Authorization.
Preferred: prior experience with NDT methods (Liquid Penetrant, Eddy Current, Borescope).
Strong analytical, problem-solving, and communication skills.
Experience with aircraft parts and materials handling.
WORK LOCATION AND SCHEDULE:
This is a full-time, salaried position based at our Miami base. The QC Heavy Maintenance Inspector will travel regularly to vendor facilities and maintenance sites where heavy checks are performed.
The role requires flexibility in scheduling, including evenings, weekends, and holidays, to support operational needs. Travel may be domestic or international depending on where heavy maintenance events are conducted.
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. While performing the duties of this job, the employee is regularly required to talk or hear. The employee is frequently required to stand; walk; use hands to finger, handle or feel; and reach with hands and arms. The employee is occasionally required to sit, climb, balance, stoop, kneel, crouch or crawl. The employee must frequently lift and move up to 25 pounds and occasionally lift and move up to 70 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus.
OTHER DUTIES:
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time.
Global Crossing Airlines provides equal employment opportunities to all team members and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. 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.
Auto-ApplyQuality Control Inspector Level 1
Quality control analyst job in Doral, FL
Job Details Corporate Headquarters Miami - Doral, FLDescription
For nearly 30 years, DASI has been in the business of providing comprehensive aircraft inventory support for airlines, MROs, OEMs, and distributors. Headquartered in Miami, Florida, with service centers in London and Singapore, DASI is a truly global partner, serving customers' parts and inventory needs in more than 140 countries.
DASI is embracing the potential of online sales and their digital marketplace, which has been growing exponentially and has tremendous potential with the right technology team in place to support and take it to the next level.
Purpose:
At DASI, the role of the QC Inspector is to ensure that all incoming and outgoing material is being checked for compliance to customer and/or DASI standards.
Key accountabilities:
Investigate NCM (Nonconforming Material).
Control the segregation and proper disposition of material designated by the Material Review Board.
Collect data for QA to use in training and performance evaluation of inspection staff.
Coach Inbound and/or Outbound inspection teams to recognize errors and areas for improvement.
Scrap process as required.
Participate in Continuous Improvement Projects (CPAR's).
Perform all other duties as assigned.
Key skills and competences:
Focus on delivering exceptional customer service.
A pro-active team worker with warehouse experience ideally in an aerospace related business
Ability to be flexible, responsive and enthusiastic.
Able to cope well under pressure and resolve issues and problems using their own initiative.
Able to work effectively to tight deadlines and targets.
Looking for a challenging role in which they can develop personally and professionally.
Results driven, taking pride in achieving objectives.
Ability to work in a fast-moving environment where a pro-active, can-do attitude is needed to achieve goals.
Experience and qualifications:
High school diploma or equivalent required.
Minimum 2 years of processing aviation surplus parts is required.
ISO and/or AS Quality Standard knowledge, a plus.
DASI, LLC. and group companies are an Equal Opportunities Employer
QC Inspector - HRL
Quality control analyst job in Miami, FL
TITLE : QC Inspector - HRL
REPORTS TO: Manager, QC.
The QC Inspector is responsible for performing inspection functions in accordance with Global X's Continuous Airworthiness Maintenance Program (CAMP) and FAA regulations. This role ensures that parts, materials, maintenance, and workmanship meet Global X standards, while monitoring performance measures through audits of internal and vendor organizations.
ESSENTIAL FUNCTIONS AND RESPONSIBILITIES:
Perform Line Maintenance, Remain Overnight (RON), and Receiving Inspections (RI).
Monitor maintenance, workmanship, and materials for compliance with Global X procedures and FAA standards.
Perform RII in-process inspections and ensure proper documentation.
Audit completed aircraft records (logbooks, work cards, non-routines, engineering documents, etc.) generated by C-Check, RON, and Line Maintenance.
Provide oversight during Heavy or Special Maintenance visits.
Perform Borescope inspections within qualified method and level.
Ensure accuracy and completeness of all work documents and records.
Initiate discrepancies in maintenance logbooks and non-routine forms.
Provide “buy-back” of RII and non-RII maintenance actions.
Approve return-to-service of maintenance, preventive maintenance, and alterations.
Issue Airworthiness Releases (AWR).
Reject unsatisfactory work or non-conforming parts per procedures.
Prepare and issue audit reports identifying hazards/risks, corrective actions, and track resolution progress.
Conduct inspections and audits of contractors/vendors (e.g., repair/overhaul services, contract maintenance, deicing, fueling, and parts distributors).
Follow all safety rules to maintain a safe working environment.
Perform other duties as assigned by the DOM/DQC.
SKILLS AND QUALIFICATIONS:
Knowledge of the TRAX system.
Valid FAA A&P license, held for at least 5 years.
Previous verifiable inspection experience (OJT, training records, certificates, etc.), including RII Authorization.
Preferred: prior experience with NDT methods such as Liquid Penetrant, Eddy Current, and Borescope inspections.
Strong analytical, problem-solving, and communication skills.
Previous experience with aircraft parts and materials handling.
WORK LOCATION AND SCHEDULE:
This position is based in Harlingen, TX. The standard schedule follows a four-days-on, three-days-off rotation with 10-hour shifts. Work hours and shift assignments may vary, and the schedule is subject to change based on operational needs. Flexibility is required to support the demands of a dynamic aviation maintenance environment.
PHYSICAL DEMANDS:
The QC Inspector role is performed in a safety-sensitive aviation environment that includes both office settings and aircraft maintenance areas, such as hangars, line stations, and ramp operations. The position requires frequent exposure to varying weather conditions, noise levels, and physical activities associated with aircraft inspections. QC Inspectors must be able to stand, walk, bend, climb, and climb into confined spaces as needed to access aircraft structures and components. The role also involves extended periods of reviewing technical documents and records. Strict adherence to safety protocols and regulatory requirements is essential to maintain a safe and compliant work environment.
OTHER DUTIES:
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time.
Global Crossing Airlines provides equal employment opportunities to all team members and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. 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.
Auto-Apply*Quality Control Inspector
Quality control analyst job in Miami, FL
Quality Control Inspector Immediate need for a Quality Control Inspector for a manufacturing and construction company in Miami, FL to join our team. The ideal candidate will play a crucial role in ensuring that our products meet or exceed industry standards and customer expectations.
RESPONSIBILITIES:
* Ensure all products and processes comply with AISC, company, and industry quality standards.
* Inspect raw materials, in-process components, and finished steel products through visual checks, measurements, and NDT methods to verify conformance to specifications.
* Perform inspections on fabricated and erected steel structures to confirm compliance with design and detailing requirements.
* Document and report inspection findings, nonconformities, and root cause analyses; collaborate with production and engineering teams to implement corrective and preventive actions.
* Participate in design and scope reviews, validation, and final product approval processes.
* Maintain quality documentation, inspection records, and provide data for management review meetings.
* Support continuous improvement initiatives to enhance product quality, process efficiency, and safety compliance.
* Ensure adherence to all AISC quality assurance procedures, regulatory requirements, and company safety policies.
* Contribute to training, audits, and professional development activities as needed.
QUALIFICATIONS:
* 2+ years' experience with Structural Steel required.
* Knowledge of AISC Process.
* Detail oriented with ability to multi-task in a fast-moving environment with shifting priorities and changing requirements.
* Fluent in the English language, in both oral and written form, required, bilingual in the Spanish language preferred.
* Leadership abilities and able to identify and resolve problems.
* Strong proficiency with Microsoft Office tools required.
* Proficient in the ability to read and interpret drawings and technical documentation; and
* Ability to work well under pressure and be able to assist in expediting shipments when necessary, working in conjunction with Production and Shipping schedules.
* Ability to foster and promote a positive work environment.
EDUCATION/TRAINING/EXPERIENCE:
* 3+ years of responsibility in quality management required; within a manufacturing environment preferred.
* Experience working in a manufacturing environment preferred.
* Must have experience using various mechanical inspection tools, such as computers, micrometers, height gauge, radius gauge, pin gauges, protractors, and calipers.
* Experience working with machined parts, assemblies, and/or sub-assemblies preferred.
* Civil or Industrial Engineer preferred.
BENEFITS:
* 401(k) with matching contributions
* Health insurance (medical, dental & vision)
* Paid time off
QC Inspector
Quality control analyst job in Miami, FL
Quality Control Inspector
Miami International Airport
Quality Control Inspectors report to the Quality Manager. This position requires certification under FAR Part 65, subparts D, E and acceptable training and experience. A minimum of three years documented verifiable experience or acceptable training on Transport Category Aircraft (including military types) is preferred. [FAR: 65. Subpt-D, 65. Subpt-E].
Duties and responsibilities include:
Ensuring that aircraft maintenance work, materials and practices conform to the regulations and company policies and procedures.
Reviewing paperwork, including maintenance forms, parts tags, work cards, maintenance orders and log sheets, etc. for proper completion per company requirements.
Perform facility audits, work in progress audits and ramp and stockroom checks for cleanliness and organization.
Coordinating RII inspection requirements for scheduled work.
Accomplishing RIIs in accordance with the company procedures.
Performing receiving inspection of parts, materials and components to ensure conformity with company requirements.
Perform routine inspections of company tooling for condition, security and calibration.
Making recommendations to overcome deficiencies in procedures, manuals or with aircraft or equipment.
Performs additional duties and responsibilities as directed in other company manuals such as the Fueling and CASS Manuals.
Perform any additional duties and responsibilities as directed by the Quality Manager or Director of Quality.
Requirements
Qualifications and Requirements
Must hold a current Airframe & Powerplant license.
Must be flexible to work any shift as necessary including weekends and holidays.
Must be legally authorized to work in the United State and able to acquire airport security clearance.
Must be fluent in the English language (written and spoken).
Must be willing to travel on short notice.
Have Boeing 767 aircraft maintenance experience, or equivalent experience working on wide body aircraft.
Have at least two years of Quality control experience (preferred).
Have strong analytical skills.
Able to read and understand technical documents (AMM, IPC's SRM's, EO's, AD's, etc.)
Able to identify problems, collect data, and develop corrective actions.
Able to interact with Federal Aviation representatives.
Physical Requirements.
Must be able to lift 25 pounds.
Quality Control Inspector
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.
Auto-ApplyGL QC Technician Level 2 (Nutrition)
Quality control analyst job in Deerfield Beach, FL
Job Details Entry Oxygen Development, LLC Deerfield Beach - Deerfield Beach, FL Full Time High School $16.00 - $20.00 Hourly Not Applicable Any NutritionDescription
Missions
Comply with Good Manufacturing Practices (GMP) and relevant laws and regulations for cosmetics and OTC products.
Guarantee quality at each Bill of Material level (RAW, PKG, BULK, WIP, FG).
Scope
Packaging, Pressed Pans, Hot Pours and Finished Products.
Functions
GMP: Follow GMP training. Report and coach where necessary.
Issue the batch code and expiration date according to customers' requirements.
Set up work orders to ensure that all specifications are met by validating the first ten pieces (TBOM, Spectrum, Standard) - Correct items received, Torque test, Jacomex, Fill Weight, Appearance, Bulk Temperature, Bulk Color, Pan/Compact Compatibility, Date Code - Expiration Date Printing…
Support production in the assessment of quality aspects necessary to complete the production in accordance with the specifications established.
Create sample number in Oracle for any products requiring micro testing.
Provide retains, micro, pre-shipment and OTC samples (if applicable) to Quality Assurance.
Incoming components: inspect to supplier drawing, artwork, and color standards. Report any deviations to the QC Manager and reject or raise nonconformance as appropriate. Work with Customer Service Representative and Purchasing by reporting all issues regarding CSCs and Direct Buy / Turnkey, Respectively.
Outgoing Inspection: Inspect Finished Goods and WIP's (Part finished items / work in progress) to ISO-2859. Record results on the inspection sheet.
Reworks: When reworks resulting from quarantine inspection or customer complaint are required, support production by checking that reworks are done in accordance with the instructions from Quality.
Perform a gazebo with all involved departments for any non-conformances or red zone issues. Document each non-conformance by following the Non-Conforming SOP (Issuance of a Non-Conformance number, description of the non-conformance, and corrective action / reworks instruction if applicable).
Send pre-ship samples and OFA submissions to the customer in timely manner (24 hours) as required. Edit logs and submission forms accordingly.
Update the status in Oracle for Packaging, PPOs, and Finished Goods as required.
Ensure all issues are communicated to QC Manager and that any deviations are documented.
Key Performance Indicators
% FG RFT.
% WIP RFT.
% Rej PKG lots.
Qualifications
Education
High School Diploma or equivalent.
Some education in mathematics and English. A formal qualification in mechanical engineering would be advantageous.
Experience in Cosmetics Manufacturing and assembly or similar FMCG.
Work Experience
Knowledge of Quality Assurance.
Experience in related industries: Cosmetics, Personal Care, Consumer Goods, Pharmaceutical, Food & Beverage.
Skills
Analytical skills.
Employee management skills.
Business and functional expertise.
Strategic thinking.
High performer under pressure.
Excellent written and verbal communication skills (Spanish a plus).
Proven problem solving and analytical skills.
Demonstrate creativity, flexibility, and use of innovative approaches.
Abilities
Positive & Communicative.
Questioning & Challenging.
Accountable & Transparent.
Team Oriented.
“Can do” problem solving attitude.
Process Focused.
Results oriented.
Quality focused.
Lack of blame attitude.
Working Conditions
Perform repetitive tasks.
Regularly working in a noisy environment.
Sitting for long periods of time.
Frequently working in normal office environment.
Physical Demands
Light physical activity as necessary.
Climbing stairs.
May require prolonged sitting at desk.
Vertical and Horizontal Footbridges
VERTICAL - QC Manager.
HORIZONTAL - Purchasing, NPD, Production.
Compliance & Quality Control Officer
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.
Position Overview
We are seeking a Compliance & Quality Control Officer with strong experience in the pharmaceutical industry to
ensure our operations meet all regulatory and quality standards. This role oversees compliance for 305a mail-
order pharmacy, receiving 305b outsourcing medication, retail pharmacy medications, and controlled substances
(Schedules III & IV). In addition, the Compliance Officer will lead the Quality Control Department, supervising a
team of at least four staff members to maintain the highest standards of accuracy, safety, and compliance.
Key Responsibilities
Compliance Oversight
Ensure compliance with 503a mail-order, 503b outsourcing facilities, and retail pharmacy regulations.
Maintain 50-state licensure and handle renewals, audits, and regulatory filings.
Ensure strict adherence to DEA regulations for Schedule III & IV controlled substances.
Oversee OSHA compliance for warehouse operations, including forklift use and high-level storage safety.
Quality Control Leadership
Lead and manage the Quality Control Department, supervising a team of at least four.
Set quality benchmarks and ensure products meet safety, accuracy, and regulatory requirements.
Provide training, guidance, and performance evaluations to QC staff.
Coordinate with pharmacy, warehouse, and operations teams to resolve quality or compliance issues.
Risk Management & Reporting
Conduct internal audits and prepare for external inspections.
Investigate incidents, document findings, and implement corrective actions.
Utilize advanced software and tracking tools for compliance and quality reporting.
Qualifications
Minimum 3-5 years of compliance and quality control experience in the pharmaceutical industry.
Demonstrated ability to lead, supervise, and develop a team.
Strong computer and reporting system skills.
Bilingual (Spanish & English) - required.
Strong knowledge of DEA controlled substance rules (Schedules III & IV) and OSHA warehouse
standards.
Excellent organizational, communication, and problem-solving skills.
Ability to work a flexible schedule as compliance needs require.
Work Schedule
Standard: Monday to Friday, 8:00 a.m. - 4:30 p.m.
Must be flexible to adapt to inspections, audits, or urgent compliance/quality needs.
Salary:
Salary is to be determined and will be negotiable based on experience.
Pay Range$55,000-$75,000 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.
Quality Control Labeling Inspector
Quality control analyst job in Miami, FL
Job Purpose
The QC Labeling Inspector is responsible for maintaining a high level of inventory accuracy and integrity within the Tissue Bank. Performs final product labeling and inspections, manages transport and storage of quarantine tissue, and maintains labeling supplies. Promotes Lean Behaviors across the organization (This includes Participating in Try storming, Brainstorming and Lean Related Initiatives). Promotes Usage of Problem Solving. Ensure that Labeling Operations are in Compliance with the State and Federal Regulations and AATB Standards.
Duties and Responsibilities
Preparation of the QC Labeling areas as specifically described in SOPs.
Performs final inspection of products for proper specifications, label accuracy, and compliance with applicable regulations, standards and Vivex Biologics, Inc. quality requirements.
Combines components for final products.
Applies labels to final product and adds package inserts, boxes, etc.
Maintains accurate inventory of post-processing, quarantine products (frozen and room temperature).
Performs disposition of nonconforming products as directed.
Coordinates and stages products for sterilization.
Monitors freezers and responds to alarms.
Supports nonconformance investigations, when applicable.
Maintains knowledge of applicable regulations and standards related to storage, handling, labeling and inspections of tissue.
Maintains effective communication with management when issues arise to obtain appropriate instructions to address the issues.
Performs other duties as assigned by management.
Requirements
Qualifications
High School/Minimum of 4 Years of Relevant Experience.
Associate/Minimum of 1 Years of Relevant experience.
Bachelors/Minimum of 0-1 Years of Relevant experience
Working Conditions
Work is indoors in environmentally controlled conditions. Overtime may be required to meet production deadlines. Some on-call and weekends may be required.
Physical Requirements
Able to stand for extended period. Able to lift 25 lbs. without assistance.
Must be able to infrequently lift, push, pull and carry boxes weighing up to 25 pounds.
Walk, squat and bend over for intervals of 15-30 minutes, with or without reasonable accommodation.
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, Inc. 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, transfers, leaves of absence, compensation and training.
Vivex Biologics, Inc. 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.
Quality Control Assistant
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.
Associate Scientist/chemist/QC/
Quality control analyst job in Coconut Creek, FL
Actalent is Hiring a Team of ChemistJob Description We are seeking a team of Analytical Chemists to join our team, performing routine tests on various samples, including finished products, stability samples, and raw materials. This role involves using techniques such as UV and HPLC in a regulated laboratory environment, evaluating test results, maintaining accurate 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.
+ 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.
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.
+ Proficiency in HPLC, UPLC, and UV-Vis techniques.
+ Familiarity with FDA and GMP regulations.
+ Ability to analyze and interpret complex data.
+ Working knowledge of instrumentation software used in laboratories.
+ Require Bachelors in Chemistry, No Ph.D
Work Environment
This position is based in a lab environment regulated by FDA and GMP standards. The work schedule offers flexibility with a 1st shift from 8am-5pm or a 2nd shift from 2pm-11pm. All training will take place during the first shift.
Job Type & Location
This is a Contract to Hire position based out of Coconut Creek, 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 Coconut Creek,FL.
Application Deadline
This position is anticipated to close on Dec 3, 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.
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 (%20actalentaccommodation@actalentservices.com) for other accommodation options.
QC Inspector - HRL
Quality control analyst job in Miami, FL
TITLE: QC Inspector - HRL
REPORTS TO: Manager, QC.
The QC Inspector is responsible for performing inspection functions in accordance with Global X's Continuous Airworthiness Maintenance Program (CAMP) and FAA regulations. This role ensures that parts, materials, maintenance, and workmanship meet Global X standards, while monitoring performance measures through audits of internal and vendor organizations.
ESSENTIAL FUNCTIONS AND RESPONSIBILITIES:
Perform Line Maintenance, Remain Overnight (RON), and Receiving Inspections (RI).
Monitor maintenance, workmanship, and materials for compliance with Global X procedures and FAA standards.
Perform RII in-process inspections and ensure proper documentation.
Audit completed aircraft records (logbooks, work cards, non-routines, engineering documents, etc.) generated by C-Check, RON, and Line Maintenance.
Provide oversight during Heavy or Special Maintenance visits.
Perform Borescope inspections within qualified method and level.
Ensure accuracy and completeness of all work documents and records.
Initiate discrepancies in maintenance logbooks and non-routine forms.
Provide “buy-back” of RII and non-RII maintenance actions.
Approve return-to-service of maintenance, preventive maintenance, and alterations.
Issue Airworthiness Releases (AWR).
Reject unsatisfactory work or non-conforming parts per procedures.
Prepare and issue audit reports identifying hazards/risks, corrective actions, and track resolution progress.
Conduct inspections and audits of contractors/vendors (e.g., repair/overhaul services, contract maintenance, deicing, fueling, and parts distributors).
Follow all safety rules to maintain a safe working environment.
Perform other duties as assigned by the DOM/DQC.
SKILLS AND QUALIFICATIONS:
Knowledge of the TRAX system.
Valid FAA A&P license, held for at least 5 years.
Previous verifiable inspection experience (OJT, training records, certificates, etc.), including RII Authorization.
Preferred: prior experience with NDT methods such as Liquid Penetrant, Eddy Current, and Borescope inspections.
Strong analytical, problem-solving, and communication skills.
Previous experience with aircraft parts and materials handling.
WORK LOCATION AND SCHEDULE:
This position is based in Harlingen, TX. The standard schedule follows a four-days-on, three-days-off rotation with 10-hour shifts. Work hours and shift assignments may vary, and the schedule is subject to change based on operational needs. Flexibility is required to support the demands of a dynamic aviation maintenance environment.
PHYSICAL DEMANDS:
The QC Inspector role is performed in a safety-sensitive aviation environment that includes both office settings and aircraft maintenance areas, such as hangars, line stations, and ramp operations. The position requires frequent exposure to varying weather conditions, noise levels, and physical activities associated with aircraft inspections. QC Inspectors must be able to stand, walk, bend, climb, and climb into confined spaces as needed to access aircraft structures and components. The role also involves extended periods of reviewing technical documents and records. Strict adherence to safety protocols and regulatory requirements is essential to maintain a safe and compliant work environment.
OTHER DUTIES:
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time.
Global Crossing Airlines provides equal employment opportunities to all team members and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. 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.
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