Top 53 Qa qc Jobs in Homestead, Fl

Quality Control Specialist
Evolution Research Group —Miami, FL
- $58,000 - $62,000 a year
- Full-time
- HIPAA
- Mid-level
- Neurology
- Health insurance
- Dental insurance
Quick Apply
Pathology Assistant
Medipath, LLC —Coral Gables, FL
- $50 - $60 an hour
- Full-time
- Surgery
- Mid-level
- Office
- Health savings account
- Relocation assistance
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General Construction Project Manager
MCO Construction and Services, Inc. —Miami, FL
- $40 - $45 an hour
- Full-time
- 6 years
- Construction site
- Project management
- Health insurance
- Dental insurance
Quick Apply
Senior/Chief Engineer
Metric Engineering —Florida
- $90 - $120 an hour
- Part-time
- Remote
- Quality control
- Mentoring
- Senior level
Licensed Project Architect
Andvaris Inc —Coral Gables, FL
- $80,000 - $120,000 a year
- Full-time
- Hospitality
- Management
- Office
- Health insurance
- Dental insurance
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1d
Environmental Principal (Assessment & Remediation)
ECS Ltd —Miami, FL
- 11+ years
- Master's degree
- Bachelor's degree
COMPLIANCE MANAGER - HOME IMPROVEMENT LENDING
Lakeview Loan Servicing —Coral Gables, FL
- $100,000 - $120,000 a year
- Full-time
- Remote
- 5 years
- Writing skills
- Research
3d
Vice President, Quality
BioTissue Holdings Inc —Miami, FL
- $219,300 - $275,000 a year
- Full-time
- 11+ years
- Master's degree
- Analysis skills
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Embryologist
Conceptions Florida —Coral Gables, FL
- $47,283 - $178,468 a year
- Weekends as needed
- Blood sampling
- Laboratory experience
- Mid-level
- Disability insurance
- Health insurance
Quick Apply
14d
Medical Technologist 1, Full-Time, Nights, License Required, Jackson South
Jackson Health —Miami, FL
- Full-time
- Hospital
- Mid-level
- Ability to lift 50 pounds
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Head Brewer
Spanish Marie —Miami, FL
- From $25 an hour
- Full-time
- Mid-level
- 3 years
- Contracts
- Employee discount
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8d
Development Manager / Technical Lead for Engineering Consultant
Moffatt & Nichol —Miami, FL
- Full-time
- Background check
- Computer Science
- 5 years
- Wellness program
- Health savings account
Quick Apply
Medical Technologist Lead / Full-Time Day Shift
Coral Gables Hospital —Coral Gables, FL
- Full-time
- Bachelor of Science
- Mid-level
- Bachelor's degree
Quick Apply
9d
Assistant Vice President, Transportation Planning
WSP —Miami, FL
- Master's degree
- Bachelor's degree
- Quality control
- Disability insurance
- Health insurance
Construction Manager
Electronic Environments Co LLC —Doral, FL
- $131,200 - $196,900 a year
- Overtime
- Remote
- Construction site
- 5 years
- Bachelor of Science
- Health savings account
- Paid holidays
Quick Apply
Transportation Senior Project Manager - Aviation
EAC Consulting Inc. —Miami, FL
- $125,000 - $156,000 a year
- Hybrid work
- Marketing
- Analysis skills
- Bachelor's degree
- Tuition reimbursement
- 401(k) matching
Quick Apply
2d
Engineering Director
M2E LLC —Coral Gables, FL
- Full-time
- Construction site
- English
- Master's degree
- Paid holidays
- Health insurance
Power Practice Lead - #2747.35
Wade Trim —Miami, FL
- Full-time
- Hybrid work
- 11+ years
- Office
- Bachelor's degree
- Wellness program
- Disability insurance
Electrical Engineer - Distribution Design
Hanson Professional Services Inc. —Miami, FL
- $147,000 - $175,000 a year
- Full-time
- Bachelor of Science
- Office
- 8 years
- Health insurance
- 401(k) matching
Quick Apply
Licensed Project Architect
WT Group AEC —Coral Gables, FL
- $80,000 - $120,000 a year
- 8 hour shift
- Office
- Master's degree
- Bachelor's degree
- Dental insurance
- 401(k)
Quick Apply

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qa qc jobs near homestead, fl

Quality Control Specialist

Evolution Research Group -
Miami, FL

Quick Apply

Job Details

Full-time
$58,000 - $62,000 a year

Benefits

Health insurance
Dental insurance
Paid time off
401(k) matching

Qualifications

Computer operation
Informed consent
ICH guidelines
Informed consent procedures implementation
Communication with regulatory authorities for clinical trials
Computer skills
Ethical review application preparation
Medical terminology
FDA regulations

Full Job Description

About Company:

Evolution Research Group (ERG) is dedicated to delivering high-quality Phase I–IV clinical trial execution to help sponsors bring lifesaving and life-enhancing therapies to market quickly and safely. Founded in 2014, ERG has grown into a leading neuroscience clinical development company, with affiliate sites across the U.S. and deep expertise in clinical pharmacology, psychiatry, neurology, acute pain, and metabolic disorders. ERG has completed over 5,000 trials and continues to expand into high-need therapeutic areas in the U.S. and globally.

Why join us? We offer a supportive culture, meaningful work, and the opportunity to contribute to cutting-edge research alongside industry leaders. Plus, we offer competitive benefits include medical and dental coverage, a matching 401(k), and paid time off to recharge.

Job Description:

The Quality Control Specialist is responsible for oversight on clinical research operations by way of inspecting and evaluating processes, procedures, and adherence to applicable regulations and guidelines. The QC Specialist reviews data, identifies trends, and communicates all incidents as they relate to clinical research to Site Leadership and where necessary, the Quality Assurance department. Additionally, assists in education and training teams to reduce quality related problems and increase understanding of our culture of quality. The QC Specialist is guided by Good Clinical Practices (GCP), International Conference on Harmonization (ICH) guidelines, Health Insurance Portability and Accountability Act (HIPAA) and company standard operating procedures and policies.

Responsibilities:

Working knowledge of FDA regulations, GCP/ICH guidelines, clinic SOPs and individual protocols.
Perform Quality Control sampling to maintain audit and inspection readiness of studies.
Work with Site Leadership and the Quality Assurance department to identify training needs and organize training interventions to meet quality standards.
Coordinate with site staff, vendors, and contract employees to obtain quality data.
Review things such as but not limited to: Source Documents, eCRF’s, Essential Documents, Logs, and procedure required documentation with coordinators and staff to ensure quality, completeness, and accuracy.
Issue queries as applicable for all reviewed documentation and trends queries for systemic issues. Report feedback to Site Leadership and Quality Assurance department.
Review essential documents and other regulatory files to ensure any outstanding issues or commitments are being managed to completion.
Support Site leadership by assisting or facilitating onsite sponsor visits and documenting any minutes or actions where applicable.
Oversee that implementation of action items and effectiveness checks of those items are being completed and report delays or concerns to Site Leadership or QA department as applicable.
Perform QC functions as directed by the Site Leadership in consult with the QA department and Director of Training and Development.
May assist with developing or reviewing site processes such as Work Instructions.
Comply with the confidentiality of research data.
Study, learn and comply with ERG site standard operating procedures, and other policies, practices, and regulations where applicable.
Maintain current training with SOP, WPs, CITI GCP, & HIPAA
Possess a sound and in-depth understanding of each protocol that has been assigned as a primary responsibility and a general understanding of all active study protocols.
Attend meetings, study initiation visits, and all other study-related visits as applicable to the role.
Always represent research site in a professional manner when interacting with sponsors, volunteers, outside venders and fellow employees.
Additionally, this role may encompass responsibilities beyond those outlined above, as required by the evolving needs of the organization. This job description is intended as a foundation and may be subject to expansion or modification to best suit ERG’s objectives.

Skills and Qualifications:

Education and experience
- Minimum of two years of experience conducting or managing clinical pharmaceutical/device research studies or experience in the clinical research industry.
Requirements
- Able to communicate with providers, co-workers, sponsors, and others in a collaborative and courteous manner.
- Must be able to identify and communicate about research problems and processes across various levels of the organization.
- Good organizational and interpersonal skills
- Attention to detail.
- Must be self-motivated and able to perform tasks independently.
- Knowledgeable in medical terminology, source documentation, informed consent, IRB submissions and reporting, and electronic data capture to communicate effectively with physicians and staff.
- Able to initiate or modify behavior to achieve desired outcomes in spite of environmental factors, priorities, or problems that might not be well defined or that are subject to change.
- Understand regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference of Harmonization (ICH) guidelines.
- Excellent communication skills (interpersonal, written, verbal)
- Basic computer skills to include Word, Excel, as well as proprietary applications unique to the clinical research industry (such as RealTime CTMS)

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Refine Your Search

qa qc jobs in homestead, fl

Quality Control Specialist

Pathology Assistant

General Construction Project Manager

Senior/Chief Engineer

Licensed Project Architect

Environmental Principal (Assessment & Remediation)

COMPLIANCE MANAGER - HOME IMPROVEMENT LENDING

Vice President, Quality

Embryologist

Medical Technologist 1, Full-Time, Nights, License Required, Jackson South

Head Brewer

Development Manager / Technical Lead for Engineering Consultant

Medical Technologist Lead / Full-Time Day Shift

Assistant Vice President, Transportation Planning

Construction Manager

Transportation Senior Project Manager - Aviation

Engineering Director

Power Practice Lead - #2747.35

Electrical Engineer - Distribution Design

Licensed Project Architect

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