Quality assurance specialist jobs in Gainesville, FL - 24 jobs
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Quality Assurance Specialist
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Quality Assurance Monitor
Senior Quality Specialists
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Director of Quality Assurance
Jacobs Management Group
Quality assurance specialist job in Alachua, FL
Ready to make a real impact? This is your chance to lead quality strategy for a global innovator in regenerative medicine. You will shape compliance, risk management, and operational excellence while influencing how life-changing products reach patients safely and effectively.
Why You Should Apply
Drive quality leadership at the center of technical excellence
Influence product development and manufacturing processes worldwide
Collaborate with R&D, Regulatory, and Operations to embed quality into innovation
Play a key role in shaping global quality strategy for life-changing therapies that impact patient outcomes worldwide
What You'll Be Doing
Provide strategic direction for QA and QC teams
Ensure compliance with FDA, ISO, and global regulatory standards
Lead continuous improvement initiatives and risk mitigation strategies
Maintain audit readiness and represent quality systems internally and externally
Partner cross-functionally to integrate quality throughout the product lifecycle
About You
Be able to do the job as described
Skilled in advanced risk management and statistical techniques
Comfortable leading complex quality systems across multiple sites
Adept at fostering a culture of quality and continuous improvement
Strong technical writing and problem-solving expertise
$90k-147k yearly est. 19d ago
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Quality Assurance Lead - Personal Lines Underwriting
Tower Hill Insurance Group, LLC 4.7
Quality assurance specialist job in Gainesville, FL
Candidates must reside within 50 miles of our Alachua/Gainesville office and be willing to work on-site. Tower Hill Insurance Group has an exciting opportunity for a talented Quality Assurance Lead - Personal Lines Underwriting who enjoys intellectual challenges and is seeking a rewarding career with a company that is experiencing growth. Not only is Tower Hill Insurance one of Florida's most trusted names in homeowners insurance, but it offers great opportunities for career advancement and personal growth, along with very competitive benefits and rewards. We are growing at a consistent pace and seek professional individuals with drive, team mentality, who want to make an impact, and are committed to a long-term career in the insurance industry.
The Personal Lines Quality Assurance Lead works closely with Personal Lines Underwriting leadership and staff to provide quality assurance review of Personal Lines Underwriting handling task reviews and phone calls accordance with statutes, filed guidelines, philosophies and set forth by leadership and the company. By analyzing underwriting practices and outcomes, this position identifies areas for improvement and implements effective solutions to enhance operational efficiency and risk management. This role requires a combination of auditing, coaching, negotiation, and presentation skills to create a feedback loop to leadership on training and development opportunities.
ESSENTIAL DUTIES AND RESPONSIBILITIES
* Coordinate and conduct monthly required quality assurance (QA) audits, along with ad hoc requests, to ensure compliance and process consistency.
* Analyze data to identify additional development and/or training opportunities.
* Identify and recommend individualized performance coaching opportunities.
* Present findings and QA trend analyses to Personal Lines Underwriting department through monthly performance review meetings, highlighting results of identified opportunities for improvement.
* Meet with and provide coaching to staff on QA results and agree topics.
* Maintain and report QA audit outcomes in a timely manner to meet SOC 1 compliance requirements.
* Develop and maintain any quality assurance or best practices training aids.
* Update underwriting materials as needed.
* Review level of authority workflows as needed.
* Participate in outside audits of Underwriting processes. (i.e. PWC, Forvis, Reinsurers)
ADDITIONAL DUTIES
This job description reflects the general duties considered necessary to describe the essential functions of the job and should not be considered a complete description of all the work requirements and expectations of the position. Tower Hill reserves the right to assign duties not listed herein as necessary to accomplish the goals of the organization.
Requirements
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
EDUCATION
Bachelor's Degree or higher required.
Equivalent experience may substitute for minimum educational requirements. Equivalent experience may include three (3) years of relevant work experience.
EXPERIENCE
Minimum of three (3) to five (5) years of relevant work experience preferred.
CERTIFICATIONS
N/A
LICENSES
N/A
BENEFITS
* Medical
* Dental
* Vision
* Life & Disability Insurance
* 401(k)
* Health Savings Account
* Accident, Critical Illness and Hospital Indemnity
* Pet insurance
* Paid time off & Holiday pay
We offer competitive pay and benefits, and well-being programs to support you and your family. For more information about our company, careers and Total Compensation visit: Total Compensation - Tower Hill Insurance (thig.com)
Tower Hill Insurance is an equal opportunity employer, and all qualified applicants will receive consideration for employment 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.
Tower Hill Insurance is committed to working with and providing reasonable accommodation for individuals with disabilities. If you need reasonable accommodation because of a disability for any part of the employment process, please send an e-mail to ********************* and let us know the nature of your request and your contact information.
All applicants will receive an acknowledgement that their application has been received. Candidates will not receive status updates regarding their application; however, those candidates selected for further consideration will be contacted by Human Resources.
$92k-110k yearly est. 60d+ ago
We are Looking for Lead QA Tester @ Gainesville, FL.
Krg Technology 4.0
Quality assurance specialist job in Gainesville, FL
Thanks & Regards Kumar.T | Resourcing Executive KRG Technologies, Inc., 25000 Avenue Stanford, Suite #243, Valencia, CA 91355 Direct : ************ Ext : 303 | *************** Job Title : QA Tester
Duration : Full Time
Job Description:
Required Skills:
• Should have 6 years of experience.
• Should have strong testing experience.
• Should have C, SQL and Unix skills.
• Java, Selenium will be added advantage.
Additional Information
.
$84k-106k yearly est. 1d ago
Quality Assurance Monitor
Partnership for Strong Families 4.0
Quality assurance specialist job in Gainesville, FL
The Quality Assurance Monitor is responsible for implementing and supporting continuous quality improvement (CQI) activities related to internal and external services within the child welfare system. This position reports to the Chief of Case Management and Permanency.
ESSENTIAL JOB FUNCTIONS
Quality Assurance & Continuous Improvement:
Conduct comprehensive case file and documentation reviews to assess compliance with performance standards, policies, and procedures.
Lead and support continuous quality improvement activities, including case file reviews, performance scorecard monitoring, incident tracking, exit interviews, complaints and grievances, satisfaction surveys, and departmental performance oversight.
Analyze, interpret, and summarize data to identify trends, assess performance, and develop actionable strategies for improvement.
Develop, revise, and support implementation of policies and procedures related to quality improvement and service delivery.
Assist with tools and systems used to monitor performance and support data-informed decision-making.
Participate in Council on Accreditation (COA) activities, including self-assessments, documentation, and site preparation.
Prepare reports, data summaries, and presentations for the PSF Board of Directors' Quality Assurance Committee.
Collaboration & Stakeholder Engagement:
Represent PSF at internal and external meetings, workgroups, and community forums related to quality assurance.
Coordinate with Information Technology and data teams to ensure alignment of QA processes and reporting systems.
Develop and maintain professional relationships with stakeholders to advance quality and clinical outcomes for children in care.
Qualifications
Required:
Bachelor's degree in Social Work, Psychology, Health Care Administration, Counseling, or a related human services field.
At least 3 years of experience in child welfare, quality assurance, or behavioral health, within the Florida Child Welfare System.
Valid Florida driver's license, reliable transportation, and acceptable driving record.
Preferred:
Master's degree in Social Work, Psychology, or a related discipline.
Experience with psychotropic medication oversight and behavioral health coordination.
Familiarity with FSFN (Florida Safe Families Network) and other child welfare systems.
Knowledge, Skills & Abilities:
Strong analytical and auditing skills with attention to detail.
Understanding of CQI principles, accreditation standards, and performance management.
Excellent interpersonal, communication, and presentation skills.
Ability to coach and consult across departments and disciplines.
Proficiency in Microsoft Office and data management systems.
$46k-79k yearly est. 9d ago
QUALITY ASSURANCE MANAGER
Morrison Healthcare 4.6
Quality assurance specialist job in Gainesville, FL
Quality assurance specialist job in Gainesville, FL
Non-Exempt - This position is responsible for evaluation of the effectiveness of systems and processes in meeting regulatory requirements and protecting the health and safety of the public and PFF employees and reporting on the findings and coordinating and/or assisting in the development of any necessary corrective actions. The EHSQ manager has authorized the QA Specialist to access all work areas and records and the organizational freedom to function effectively without hindrance or reservation, to identify quality problems, stop unsatisfactory work and control further processing of work; initiate, recommend and approve solutions; verify implementation of solutions; and assure that measures of control are applied until proper disposition of a nonconformance, deficiency or unsatisfactory condition has been implemented.
Duties
* Assessments (Vendor Audits, Surveillance)
* Regulatory compliance
* Document Control
* Nonconformance and Corrective Action tracking
* Perform other duties as assigned.
Requirements
* High school graduate or equivalent (college, vocational or job training in a technical field preferred).
* 40-hour OSHA Hazwoper Certification with current 8-hr refresher.
* 16-hour radiation safety training with current 4-hour refresher.
* Auditor
* Annual respirator fit test qualified and ability to function in all levels of personal protective equipment (PPE).
* FORKLIFT OPERATOR SAFETY TRAINING
* General Safety Rules (SOP-001C)
* NNSS Site Requirements Training
* Hazmat Training
* QA Admin Level Training
* ISO 9001: 2015 REQUIREMENTS - QUALITY MANAGEMENT
* PAS LAB ETHICS AND DATA INTEGRITY TRAINING
* Hazmat Training
* RCRA Hazardous Waste Generator Training
* Receipt Inspector
* Attention to detail and organizational skills.
* Personality conducive to teamwork.
* Ability to follow written and oral directives.
* Written and verbal communication skills.
* Displays professionalism.
* Ability to multitask.
* Capacity to apply analytical evaluations to assigned work.
* Professional communications and organizational skills to conduct work independent of direct supervision
* Personality conducive to teamwork
* Detail oriented
Working Conditions
Continuous field/facility work required where there is potential for exposure to hazardous chemicals, radiation, noise, dust, and extreme temperatures. Climbing, walking and lifting will be normal daily requirements. Extensive travelling as required
Quality assurance specialist job in Fleming Island, FL
Baptist Health is hiring a Sr. Quality Specialist to join the Quality team. This position is full-time, in-person opportunity located at Baptist Clay. Responsibilities: Oversees and/or works in tandem with facility-based quality improvement program team and leaders. Establishes facility quality procedures, standards, and specifications; assesses needs and compliance. Advances novice quality team members to proficient quality team leaders through ongoing mentorship, communication, and support. Aligns with the National Association of Healthcare Quality's 8 domains for healthcare quality competency. Actively engages in healthcare quality development through competence and continued learning. Collaborates with Facility Leaders to promote and incorporate healthcare quality objectives into the strategic operating practices through professional communication and relationship building. Interacts and establishes relationships with System Leadership and Boards in partnership with Advanced Quality Team Members. Adopts and utilizes performance improvement frameworks and methodologies to lead projects and change management at the local facility level. Begins leading and/or co-leading projects and/or committees at the healthcare system level. Familiarizes with healthcare processes and initiatives to improve equity in healthcare and the reduction of healthcare disparities. Establishes partnership with Data Intelligence and Quality Improvement Analytics to begin understanding of decision making and future QI initiatives. Promotes a safe healthcare system through detection, mitigation, and reduction of patient harm and participating in the collaborative culture of safety through partnership with System Risk Mgmt.. Integrates compliance and regulatory requirements through preparation and participation in continued readiness activities with System Accreditation Leaders. Fosters a fundamental collaborative environment with System Infection Prevention to improve care and reduce infections within the healthcare system. Establishes an affiliation with the quality improvement and analytics team to support continued quality review and accountability through reporting, analysis, and improvement of contractual requirements.
* Must be a registered nurse.
If interested, apply today
Full/Part Time
Full-Time
Shift Details
Days
Education Required
Bachelor's Degree - Nursing
Education Preferred
Master's Degree
Experience
* 3-5 Years Clinical Nursing Experience Required
* 1-2 years Healthcare Quality Required
Licenses and Certifications
* Basic Life Support (BLS) Required
* Certified Professional in Patient Safety (CPPS) Preferred
* Certified Professional Healthcare Quality (CPHQ) Preferred
* Licensed Registered Nurse Required
Location Overview
Baptist Health, founded in 1955, is North Florida's most comprehensive health care system and the area's only non-profit, mission-driven, locally governed health care provider. Baptist Health has over 200 points of care throughout the Northeast Florida region, including our six award-winning hospitals: Baptist Medical Center Jacksonville, Wolfson Children's Hospital, Baptist Medical Center Beaches, Baptist Medical Center Clay, Baptist Medical Center Nassau and Baptist Medical Center South. The most preferred health care system in the region, Baptist Health also includes 57 primary care offices, as well as home health, behavioral health, pastoral care, rehabilitation services, occupational health and urgent care.
$85k-114k yearly est. 11d ago
QA Supervisor
Niagara Bottling 4.2
Quality assurance specialist job in Middleburg, FL
Quality assurance specialist job in Gainesville, FL
at Ayr Wellness
Ayr Wellness is a leading U.S. multi-state cannabis operator with more than 90 licensed retail locations across Florida, Massachusetts, Pennsylvania, Ohio, New Jersey, Nevada, and soon, Virginia. We cultivate, manufacture, and sell a broad portfolio of high-quality cannabis products, proudly serving both medical patients and adult-use consumers across our markets.
At Ayr, our strength lies in our people. We're re-imagining how we work across every part of our business, and we're looking for builders and doers to roll up their sleeves and help shape what's next.
The cannabis industry is fast-moving, complex, and full of opportunity. Together, we're not only shaping a company, but also building the future of cannabis. At Ayr you'll have the opportunity to make a lasting impact while growing your career alongside a company positioning itself for long-term success.
For more information, please visit ********************
Job Summary
The QA Technician will perform quality assurance/utilization review duties, assist with product testing, and conduct routine inspections to provide data for use in the correction of potential problems and to meet requirements of regulatory agencies.
Duties and Responsibilities
Ensure all cannabis and cannabis containing products produced at the facility are processed and tested in accordance with regulatory agencies
Assist QA team with sample preparation
Create and review transportation manifests/sample submission forms for test samples.
Ensure proper tracking of lab samples using appropriate systems
Communicate to QA Lead or QA Manager when quality issues occur.
Review and document all test results.
Assist in monthly GMP/Sanitation/Security inspections and follow up on corrective actions
Assist in investigating consumer complaints by determining root cause, implementing corrective actions and preventive measures, responding to complaints in the required timeframe, and analysing complaint trends.
Maintain records for GMP training, including QPs, SOPs etc.
Ensure all employees are trained on the procedures for their departments
Follow all Good Manufacturing Practices as outlined in the QA Manual
Qualifications
Must meet the age requirement as outlined by state cannabis agencies
Able to pass all background checks/fingerprinting as required by state cannabis agencies
Able to provide valid badging/credentials as required by state cannabis agencies
Education
High school diploma/GED required
Experience
1-3 years working in the cannabis industry, a laboratory, or in quality assurance preferred.
Competencies (Knowledge, Skills, and Attitude)
Customer Obsessed: Dedicated to creating a remarkable experience for both internal and external customers; builds rapport and maintains meaningful and effective relationships creating trustful, authentic connections; viewed as a good listener and is easy to approach and talk to and is often in the know early in any given situation.
Priority Setting - Invests their time and others on what's important to deliver business results; quickly and effectively collaborates bringing together the collective intelligence of critical team members and prioritizes what needs to be done to reach the goal; quickly senses opportunities and obstacles in accomplishing a goal; eliminates roadblocks and creates focus that drives success and results.
Results Oriented - Empowered with the knowledge of their potential this person learns quickly when facing new problems; a relentless and versatile learner, open to change, analyzes successes and failures for continuous improvement, experiments and will try anything to find solutions that support an ecosystem of knowledge; enjoys challenge of unfamiliar tasks, quickly grasps the essence and underlying structure of anything.
Functional/Technical Skill - Possesses functional and technical knowledge and skills to perform at a high level of accomplishment; understands how their job function supports being a force for good
Direct reports
No direct reports
Working conditions
This person may be exposed to dust, kief, cleaning chemicals, and fumes. Although systems are in place to remove these byproducts, there is still exposure to some degree. This person will be travelling between dispensaries and manufacturing facilities within AYR Wellness.
Physical requirements
Must be able to stand for extended periods of time, and safely lift up to 25lbs
Must be able to wear required Personal Protective Equipment (PPE) for extended periods of time (i.e. gloves, lab coat, hair net)
Appropriate grooming for work environment (no jewelry, hair must be tied back, no hair outside of PPE)
Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time.
AYR Wellness is an equal opportunity employer. We are committed to building a team that represents a variety of backgrounds, perspectives, and skills. We do not discriminate on the basis of race, color, religion, creed, national origin, ancestry, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, genetic information, marital status, military or veteran status, or any other protected status in accordance with applicable federal, state, and local laws.
$29k-37k yearly est. Auto-Apply 60d+ ago
Training Documentation Specialist
Ncite Partners
Quality assurance specialist job in High Springs, FL
Ncite Partners is currently partnering with a growing plastics manufacturing company in High Springs, Florida that is looking for Training Documentation Specialist for a 4 to 6-month contract assignment.
Highlights:
4 to 6-month contract focused on training documentation for manufacturing processes.
Large stable company with a close-knit family environment
Autonomous role spearheading a critical project
Our Client:
Our client is one of the leading rigid plastics manufacturers in the country. This organization is looking for someone who can update training documentation for the company's fabrication department.
The Role:
Revise and enhance legacy documentation for fabrication processes to align with current best practices and operational standards.
Partner closely with operators and subject matter experts to gather insights and ensure accuracy and relevance in training materials.
Create easy-to-understand training manuals, guides, and process documents tailored for manufacturing personnel.
Standardize documentation to promote consistency in processes and training across the fabrication department.
Take ownership of the 4 to 6-month contract project, working independently to meet deadlines and deliver critical documentation updates efficiently.
Qualifications:
2+ years of training documentation, technical writing, or other applicable experience
Bachelor's degree is preferred
Manufacturing experience is preferred
Comfort in working in a manufacturing environment
$28k-51k yearly est. 38d ago
QUALITY ASSURANCE MANAGER
Compass Group USA Inc. 4.2
Quality assurance specialist job in Gainesville, FL
Quality assurance specialist job in Gainesville, FL
Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
Quality Systems Associate
Summary:
Under the direct supervision of the Quality Systems Manager, perform quality assurance and Training functions to ensure compliance with internal and external regulations and protocol.
Primary responsibilities for role (level-specific responsibilities should be included in the chart below):
* Completes weekly review of equipment QC and maintenance records.
* Documents, investigates, and performs root-cause analysis for deviations and customer complaints, specifically in how they related to product quality and/or donor safety.
* Inspects and releases incoming supplies. Investigates and reports supplies have not met quality specifications and requirements prior to use.
* Performs documentation review for unsuitable test results.
* Assists the Quality Systems Manager to ensure that cGMP regulation, SOPs and regulatory requirements are followed. Duties include:
* Under the direct supervision of the Quality Systems Manager, perform quality assurance and Training functions to ensure compliance with internal and external regulations and protocol.
* Performs all product release activities.
* Reviews lookback information and documentation.
* Reviews waste shipment documentation.
* Reviews unexpected plasmapheresis events including electronic donor chart and related documentation pertaining to exceptions occurring during the donation process.
* Reviews electronic donor chart exceptions impacting donor eligibility/safety and/or product quality.
* Reviews donor deferral notifications from competitor centers.
* Reviews plasma processing documentation to ensure the proper freezing, storage and handling of product.
Quality Systems Associate
* Assist the Quality Systems Manager to ensure center training programs follow procedural requirements as defined in the donor center SOP and/or training programs documents. Duties include:
* Creates, maintains, and audits training records and files to ensure compliance.
* Performs employee training observations to ensure staff competency prior to releasing employees to work independently.
* Conducts required training activities for Center Notifications, Corporate Directives, SOP changes, and initial SOP implementations.
* On an occasional basis, when the Quality Systems Manager is absent, the Quality Systems Associate may be required to perform the following duties:
* Reviews and approves of deferred donor reinstatement activities.
* Assists with completion of the internal donor center audit.
Summary:
* Performs review of monthly trending report.
* Performs review of donor adverse events reports and the applicable related documentation.
* Conducts training to address donor center corrective and preventative measures.
This job description is intended to present the general content and requirements for the performance of this job. The description is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Managers and supervisors may assign other duties as needed.
Additional Responsibilities:
Is certified and maintains certification as a Donor Center Technician.
Knowledge, Skills, and Abilities:
Developing command of interpersonal communication, organizational and problem-solving skills. Ability to understand FDA regulations. Strong integrity and commitment to quality and compliance. Good knowledge of mathematics. Legible handwriting. Proficiency with computers. Ability to work flexible scheduling to meet business needs. Performs basic document review and employee observations. Communicates openly with the CQM on issues noted during reviews. Ability to understand and follow SOP's and protocols. Ability to perform primary responsibilities of the Quality Associate role in a proficient manner. Has a basic understanding of cGMP and quality systems. Is able to spend hours sitting and reviewing documentation for accuracy. Demonstrates good organizational skills and attention to detail.
Education:
High school diploma or GED. Obtains state licensures or certifications if applicable.
Experience:
Typically requires no previous related experience.
Occupational Demands Form # 70: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups.
#biomatusa
Third Party Agency and Recruiter Notice:
Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.
Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.
Location: NORTH AMERICA : USA : FL-Gainesville:BTGNS - GainesvilleFL-NW 13th St-BPC
$43k-63k yearly est. 60d+ ago
Supervisor, Quality Control (M-Thurs. 4pm-2:30am)
Fox Factory 4.5
Quality assurance specialist job in Gainesville, FL
What We Do
FOX Factory designs, engineers, manufactures and markets performance-defining products and systems for customers worldwide. Our premium brand, performance-defining products and systems are used primarily on bicycles, side-by-side vehicles, on-road vehicles with and without off-road capabilities, off-road vehicles and trucks, all-terrain vehicles, snowmobiles, specialty vehicles and applications, motorcycles, and commercial trucks. Some of our products are specifically designed for and marketed to a variety of leading cycling and powered vehicle original equipment manufacturers ("OEMs"), while others are distributed to consumers through a global dealer and distribution network. Fox Factory Holding Corp. is the holding company of FOX Factory, Inc. and is publicly traded (FOXF) on Nasdaq.
Why you should join us
Not only do we provide competitive wages, you will also have access to great benefits and employee discounts. But more importantly, it's a fun environment where we truly enjoy working as a team and bringing great products to our customers!
If this sounds like something you would love to do, and a place you want to be a part of, get in touch with us by submitting your application. We look forward to hearing from you!
Position Summary:
Develop, organize, and oversee the quality control system; supervise, train and develop staff; and various other duties as needed to ensure consistent and robust quality control activities on products.
Position Responsibilities:
Set up and maintain all QC related documentation and procedures, including Product Control Plans, Inspection Work Instructions, First Article Inspection Reports, etc.
Set up quality objectives for product, adjust and maintain objectives throughout the life of a part
Maintain reference / sample part library
Maintain any special gauging needed for inspection
Manage all actions related to discovery of non-conforming product
Approve and facilitate required actions related to engineering changes, including documentation
Approve and facilitate required actions related to discontinued product, coordinate between Engineering / Sales / Warehouse
Manage & coordinate rework efforts when required for non-conforming or damaged product, including outsourced processes
Interact with Engineering / Production on potential improvements to product quality control methods
Promote performance improvements in all processes impacting quality
Assist receiving department with quality issues related to incoming product
Supervise and delegate inspection activity throughout the shop
Train quality control employees
Other duties as assigned
Specific Knowledge, Skills or Abilities Required:
Knowledge of the industry and our product is beneficial
Must understand technical drawings, product characteristics, etc.
Thorough knowledge of quality control methods, principles, practices, and equipment
Must be competent with Microsoft Office suite and computers in general
Self-motivated, organized, and detail oriented
Leadership ability
Position Qualifications:
Education:
High School diploma or equivalent
Experience:
3+ years of experience in Quality Control
3+ years of supervisory experience
GD&T; ability to read drawings; be able to train inspectors and technicians
Experience in a manufacturing environment preferred
Work Environment and Physical Requirements:
Manufacturing Environment
May lift up to 50 lbs.
Requires walking, standing, bending and lifting for long periods of time
Vision abilities required to validate and enter data on computer
Disclaimer
: This list does not represent all physical demands. Descriptions are representative of those that must be met by employee to successfully perform the essential functions of the job. Reasonable accommodation may be provided to enable individuals with disabilities to perform the jobs' essential functions.
Note:
FOX provides equal employment opportunities for all employees and applicants for employment without regard to race, color, ancestry, national origin, gender, gender identity, sexual orientation, marital status, religion, age, physical disability (including HIV and AIDS), mental disability, results of genetic testing, or service in the military, or any other characteristic protected by the laws or regulations of any jurisdiction in which we operate. We base all employment decisions -including recruitment, selection, training, compensation, benefits, discipline, promotions, transfers, layoffs, terminations and social/recreational programs - on merit and the principles of equal employment opportunity.
Fox offers an excellent compensation package and wide-ranging opportunities for professional development. Medical, Dental, Vision, Health Spending and Dependent Care Savings Accounts, Disability and Life Insurance benefit programs are available, as is a 401k plan with employer matching. Eligibility for all benefit programs is defined by the applicable plan document or employee handbook.
$49k-73k yearly est. Auto-Apply 60d+ ago
Medication Adherence Quality Coordinator
Innovacare 3.7
Quality assurance specialist job in Lake City, FL
This position is responsible to serve as primary liaison between Pharmacies and Innovacare Partners for the purposes of achieving and enhancing overall quality performance and metrics for InnovaCare Partner practices. The Medication Adherence Quality coordinator needs to have the ability to manage multiple tasks at once, prioritize information to be shared with the practice and collaborate across all staff in the practice.
RESPONSIBILITIES
The Medication Adherence Coordinator is responsible for navigation of specialty and comprehensive pharmacy therapies. Responsibilities include, but are not limited to, the following: knowledge of pharmacy prescription processing, strong communication, customer service, and motivational interview skills, with the ability to problem solve independently while working within a team structure.
Ensure overall medication procurement and patient adherence management through proactive touch points telephonically include patients and pharmacies.
Review and collate multiple sources of medical and pharmacy related information in assessing therapy appropriateness, effectiveness and patient adherence.
Independence in performance of daily functions with the ability to effectively solicit collaboration with extended team members as appropriate.
Participate in quality improvement initiatives and meetings as requested by management.
Performs other duties and responsibilities as assigned.
Continually educate self on latest information related to Stars Rating Program, Quality Measures, and thresholds as established by payers and other contracting entities.
Supports special projects as assigned.
Represents the company in special activities for providers and patients relations.
EDUCATION AND EXPERIENCE
High School Diploma or equivalent
Pharmacy Technician, Medical Assistant, and/or LPN experience preferred
Two years' experience in a health-care related field
GENERAL KNOWLEDGE/SKILLS
Ability to effectively communicate with patients regarding their medication therapies, adherence and overall drug management
Excellent communication skills including proper phone etiquette
Computer skills: proficient in Word, Excel, Power Point and Outlook.
Ability to respond to a high volume of work and always maintain a polite and professional attitude.
Able to function with frequent interruptions.
Ability to prioritize workloads for maximum efficiency.
Customer Service Skills: practicing, valuing and supporting service to both internal and external customers
Time Management Skills: establishing priorities and accomplishing tasks in a timely manner
Team Work: ability to work in a team environment to create solutions to problems
Ability to work independently
Strong analytical and problem-solving skills; ability analyze and interpret data
Ability to effectively present and explain infomriaton and respond to questions
Project management skills
$55k-82k yearly est. Auto-Apply 60d+ ago
Quality Assurance Lead - Personal Lines Underwriting
Tower Hill Insurance Group 4.7
Quality assurance specialist job in Gainesville, FL
Full-time Description
Candidates must reside within 50 miles of our Alachua/Gainesville office and be willing to work on-site.
Tower Hill Insurance Group has an exciting opportunity for a talented Quality Assurance Lead - Personal Lines Underwriting who enjoys intellectual challenges and is seeking a rewarding career with a company that is experiencing growth. Not only is Tower Hill Insurance one of Florida's most trusted names in homeowners insurance, but it offers great opportunities for career advancement and personal growth, along with very competitive benefits and rewards. We are growing at a consistent pace and seek professional individuals with drive, team mentality, who want to make an impact, and are committed to a long-term career in the insurance industry.
The Personal Lines Quality Assurance Lead works closely with Personal Lines Underwriting leadership and staff to provide quality assurance review of Personal Lines Underwriting handling task reviews and phone calls accordance with statutes, filed guidelines, philosophies and set forth by leadership and the company. By analyzing underwriting practices and outcomes, this position identifies areas for improvement and implements effective solutions to enhance operational efficiency and risk management. This role requires a combination of auditing, coaching, negotiation, and presentation skills to create a feedback loop to leadership on training and development opportunities.
ESSENTIAL DUTIES AND RESPONSIBILITIES
· Coordinate and conduct monthly required quality assurance (QA) audits, along with ad hoc requests, to ensure compliance and process consistency.
· Analyze data to identify additional development and/or training opportunities.
· Identify and recommend individualized performance coaching opportunities.
· Present findings and QA trend analyses to Personal Lines Underwriting department through monthly performance review meetings, highlighting results of identified opportunities for improvement.
· Meet with and provide coaching to staff on QA results and agree topics.
· Maintain and report QA audit outcomes in a timely manner to meet SOC 1 compliance requirements.
· Develop and maintain any quality assurance or best practices training aids.
· Update underwriting materials as needed.
· Review level of authority workflows as needed.
· Participate in outside audits of Underwriting processes. (i.e. PWC, Forvis, Reinsurers)
ADDITIONAL DUTIES
This job description reflects the general duties considered necessary to describe the essential functions of the job and should not be considered a complete description of all the work requirements and expectations of the position. Tower Hill reserves the right to assign duties not listed herein as necessary to accomplish the goals of the organization.
Requirements
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
EDUCATION
Bachelor's Degree or higher required.
Equivalent experience may substitute for minimum educational requirements. Equivalent experience may include three (3) years of relevant work experience.
EXPERIENCE
Minimum of three (3) to five (5) years of relevant work experience preferred.
CERTIFICATIONS
N/A
LICENSES
N/A
BENEFITS
Medical
Dental
Vision
Life & Disability Insurance
401(k)
Health Savings Account
Accident, Critical Illness and Hospital Indemnity
Pet insurance
Paid time off & Holiday pay
We offer competitive pay and benefits, and well-being programs to support you and your family. For more information about our company, careers and Total Compensation visit: Total Compensation - Tower Hill Insurance (thig.com)
Tower Hill Insurance is an equal opportunity employer, and all qualified applicants will receive consideration for employment 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.
Tower Hill Insurance is committed to working with and providing reasonable accommodation for individuals with disabilities. If you need reasonable accommodation because of a disability for any part of the employment process, please send an e-mail to ********************* and let us know the nature of your request and your contact information.
All applicants will receive an acknowledgement that their application has been received. Candidates will not receive status updates regarding their application; however, those candidates selected for further consideration will be contacted by Human Resources.
$92k-110k yearly est. 60d+ ago
QA Supervisor (Nights)
Niagara Bottling 4.2
Quality assurance specialist job in Middleburg, FL
Supervisor, Quality Control - Friday-Sunday - 6am-630pm
Fox Factory 4.5
Quality assurance specialist job in Gainesville, FL
What We Do
FOX Factory designs, engineers, manufactures and markets performance-defining products and systems for customers worldwide. Our premium brand, performance-defining products and systems are used primarily on bicycles, side-by-side vehicles, on-road vehicles with and without off-road capabilities, off-road vehicles and trucks, all-terrain vehicles, snowmobiles, specialty vehicles and applications, motorcycles, and commercial trucks. Some of our products are specifically designed for and marketed to a variety of leading cycling and powered vehicle original equipment manufacturers ("OEMs"), while others are distributed to consumers through a global dealer and distribution network. Fox Factory Holding Corp. is the holding company of FOX Factory, Inc. and is publicly traded (FOXF) on Nasdaq.
Why you should join us
Not only do we provide competitive wages, you will also have access to great benefits and employee discounts. But more importantly, it's a fun environment where we truly enjoy working as a team and bringing great products to our customers!
If this sounds like something you would love to do, and a place you want to be a part of, get in touch with us by submitting your application. We look forward to hearing from you!
Position Summary:
Develop, organize, and oversee the quality control system; supervise, train and develop staff; and various other duties as needed to ensure consistent and robust quality control activities on products.
Position Responsibilities:
Set up and maintain all QC related documentation and procedures, including Product Control Plans, Inspection Work Instructions, First Article Inspection Reports, etc.
Set up quality objectives for product, adjust and maintain objectives throughout the life of a part
Maintain reference / sample part library
Maintain any special gauging needed for inspection
Manage all actions related to discovery of non-conforming product
Approve and facilitate required actions related to engineering changes, including documentation
Approve and facilitate required actions related to discontinued product, coordinate between Engineering / Sales / Warehouse
Manage & coordinate rework efforts when required for non-conforming or damaged product, including outsourced processes
Interact with Engineering / Production on potential improvements to product quality control methods
Promote performance improvements in all processes impacting quality
Assist receiving department with quality issues related to incoming product
Supervise and delegate inspection activity throughout the shop
Train quality control employees
Other duties as assigned
Specific Knowledge, Skills or Abilities Required:
Knowledge of the industry and our product is beneficial
Must understand technical drawings, product characteristics, etc.
Thorough knowledge of quality control methods, principles, practices, and equipment
Must be competent with Microsoft Office suite and computers in general
Self-motivated, organized, and detail oriented
Leadership ability
Position Qualifications:
Education:
High School diploma or equivalent
Experience:
3+ years of experience in Quality Control
Experience in a manufacturing environment preferred
Work Environment and Physical Requirements:
Manufacturing Environment
May lift up to 50 lbs.
Requires walking, standing, bending and lifting for long periods of time
Vision abilities required to validate and enter data on computer
Disclaimer
: This list does not represent all physical demands. Descriptions are representative of those that must be met by employee to successfully perform the essential functions of the job. Reasonable accommodation may be provided to enable individuals with disabilities to perform the jobs' essential functions.
Note:
FOX provides equal employment opportunities for all employees and applicants for employment without regard to race, color, ancestry, national origin, gender, gender identity, sexual orientation, marital status, religion, age, physical disability (including HIV and AIDS), mental disability, results of genetic testing, or service in the military, or any other characteristic protected by the laws or regulations of any jurisdiction in which we operate. We base all employment decisions -including recruitment, selection, training, compensation, benefits, discipline, promotions, transfers, layoffs, terminations and social/recreational programs - on merit and the principles of equal employment opportunity.
Fox offers an excellent compensation package and wide-ranging opportunities for professional development. Medical, Dental, Vision, Health Spending and Dependent Care Savings Accounts, Disability and Life Insurance benefit programs are available, as is a 401k plan with employer matching. Eligibility for all benefit programs is defined by the applicable plan document or employee handbook.
$49k-73k yearly est. Auto-Apply 4d ago
Quality Systems Associate
Grifols Sa 4.2
Quality assurance specialist job in Ocala, FL
Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
Quality Systems Associate
Summary:
Under the direct supervision of the Quality Systems Manager, perform quality assurance and Training functions to ensure compliance with internal and external regulations and protocol.
Primary responsibilities for role (level-specific responsibilities should be included in the chart below):
* Completes weekly review of equipment QC and maintenance records.
* Documents, investigates, and performs root-cause analysis for deviations and customer complaints, specifically in how they related to product quality and/or donor safety.
* Inspects and releases incoming supplies. Investigates and reports supplies have not met quality specifications and requirements prior to use.
* Performs documentation review for unsuitable test results.
* Assists the Quality Systems Manager to ensure that cGMP regulation, SOPs and regulatory requirements are followed. Duties include:
* Under the direct supervision of the Quality Systems Manager, perform quality assurance and Training functions to ensure compliance with internal and external regulations and protocol.
* Performs all product release activities.
* Reviews lookback information and documentation.
* Reviews waste shipment documentation.
* Reviews unexpected plasmapheresis events including electronic donor chart and related documentation pertaining to exceptions occurring during the donation process.
* Reviews electronic donor chart exceptions impacting donor eligibility/safety and/or product quality.
* Reviews donor deferral notifications from competitor centers.
* Reviews plasma processing documentation to ensure the proper freezing, storage and handling of product.
Quality Systems Associate
* Assist the Quality Systems Manager to ensure center training programs follow procedural requirements as defined in the donor center SOP and/or training programs documents. Duties include:
* Creates, maintains, and audits training records and files to ensure compliance.
* Performs employee training observations to ensure staff competency prior to releasing employees to work independently.
* Conducts required training activities for Center Notifications, Corporate Directives, SOP changes, and initial SOP implementations.
* On an occasional basis, when the Quality Systems Manager is absent, the Quality Systems Associate may be required to perform the following duties:
* Reviews and approves of deferred donor reinstatement activities.
* Assists with completion of the internal donor center audit.
Summary:
* Performs review of monthly trending report.
* Performs review of donor adverse events reports and the applicable related documentation.
* Conducts training to address donor center corrective and preventative measures.
This job description is intended to present the general content and requirements for the performance of this job. The description is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Managers and supervisors may assign other duties as needed.
Additional Responsibilities:
Is certified and maintains certification as a Donor Center Technician.
Knowledge, Skills, and Abilities:
Developing command of interpersonal communication, organizational and problem-solving skills. Ability to understand FDA regulations. Strong integrity and commitment to quality and compliance. Good knowledge of mathematics. Legible handwriting. Proficiency with computers. Ability to work flexible scheduling to meet business needs. Performs basic document review and employee observations. Communicates openly with the CQM on issues noted during reviews. Ability to understand and follow SOP's and protocols. Ability to perform primary responsibilities of the Quality Associate role in a proficient manner. Has a basic understanding of cGMP and quality systems. Is able to spend hours sitting and reviewing documentation for accuracy. Demonstrates good organizational skills and attention to detail.
Education:
High school diploma or GED. Obtains state licensures or certifications if applicable.
Experience:
Typically requires no previous related experience.
Occupational Demands Form # 70: Work is performed in a plasma center. Exposure to biological fluids with potential exposure to infectious organisms. Exposure to electrical office and laboratory equipment. Exposure to extreme cold below 32 degrees F while performing reviews in plasma freezers. Personal protective equipment required such as protective eyewear, garments, gloves and cold-gear. Work is performed mostly while sitting for up to 4 to 6 hours per day and standing from 2 to 4 hours per day. The position does require bending and twisting of neck up from 2 to 4 hours per day. Frequent hand movement of both hands with the ability to make fast, simple, movements of the fingers, hands, and wrists. Ability to make precise coordinated movements, of the fingers to grasp and manipulate objects. Frequent foot movement; may squat, crouch or sit on one's heels on rare occasion. Occasionally walks, bends and twists at waist. Light lifting of 15lbs. with a maximum lift of 50lbs. May reach below shoulder height. Hearing acuity essential. Color perception/discrimination, near vision and far vision correctable in one eye to 20/30 and to 20/100 in the other eye. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences. Works independently with little guidance or reliance on oral or written instructions. Performs a wide range of tasks as dictated by variable demands and changing conditions. Relates sensitive information to diverse groups.
#biomatusa
Third Party Agency and Recruiter Notice:
Agencies that present a candidate to Grifols must have an active, nonexpired, Grifols Agency Master Services Agreement with the Grifols Talent Acquisition Department. Additionally, agencies may only submit candidates to positions that they have been engaged to work on by a Grifols Recruiter. All resumes must be sent to a Grifols Recruiter under these terms or they will be considered a Grifols candidate.
Grifols provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability. We will consider for employment all qualified applicants in a manner consistent with the requirements of all applicable laws.
Location: NORTH AMERICA : USA : FL-Ocala:USOCA - Ocala FL-NE 14th St-GBPC
$43k-63k yearly est. 20d ago
Learn more about quality assurance specialist jobs
How much does a quality assurance specialist earn in Gainesville, FL?
The average quality assurance specialist in Gainesville, FL earns between $32,000 and $87,000 annually. This compares to the national average quality assurance specialist range of $41,000 to $97,000.
Average quality assurance specialist salary in Gainesville, FL
$53,000
What are the biggest employers of Quality Assurance Specialists in Gainesville, FL?
The biggest employers of Quality Assurance Specialists in Gainesville, FL are: