Top 154 validation engineer Jobs in miami lakes fl

Quality Engineer
Clinical Diagnostic Solutions, Inc. —Plantation, FL
- $70,000 - $80,000 a year
- Full-time
- Mid-level
- Bachelor's degree
- In-person
- Health insurance
- Dental insurance
Quick Apply
10d
Principal Technical Project Manager, Technology & Digital, FT,8:30A-5P
Baptist Health South Florida —Coral Gables, FL
- $122,475.25 - $159,217.83 a year
- Full-time
- 11+ years
- Master's degree
- In-person
- Wellness program
- Health insurance
6d
Data Scientist
Brooksource —Miami, FL
- $50 - $55 an hour
- Contract
- Hybrid work
- Computer Science
- Mid-level
- SQL
- Health savings account
- Paid holidays
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VDI Infrastructure Engineer
Compucom Staffing —Miami, FL
- $36.95 - $49.25 an hour
- Contract
- US work authorization
- Fair chance
- In-person
- Paid parental leave
- Health savings account
Quick Apply
AI Sr. Developer (Secret Clearance Required)
Deloitte —Miami, FL
- $107,600 - $198,400 a year
- Full-time
- Computer Science
- 5 years
- Travel
6d
Data Scientist
Subway —Miami, FL
- $102,700 - $128,400 a year
- Azure
- Computer Science
- Mid-level
- 401(k)
- Tuition reimbursement
Quick Apply
Sr Data Engineer
Pediatric Associates —Plantation, FL
- Full-time
- Remote
- DevOps
- Master's degree
- Bachelor's degree
Data Scientist
Agile Defense —Doral, FL
- Azure
- Mid-level
- Office
Quick Apply
Staff Engineer Research and Development (Onsite)
Cordis —Miami Lakes, FL
- Full-time
- 6 years
- Engineering
- Master's degree
Quality Assurance Engineer
Aveva Drug Delivery Systems —Miramar, FL
- $75,000 - $85,000 a year
- Bachelor of Science
- Engineering
- English
- Paid holidays
- Health insurance
Data Engineer
Contact Government Services, LLC —Miami, FL
- $112,597.33 - $152,810.66 a year
- Full-time
- Hybrid work
- 7 years
- SQL
- IT
- Health insurance
- Dental insurance
Quick Apply
Junior Operational Excellence Engineer
AVEVA DRUG DELIVERY SYSTEMS INC —Miramar, FL
- $50,000 - $60,000 a year
- Nights as needed
- Entry level
- Under 1 year
Manual QA
Stellar IT Solutions LLC —Miami, FL
- $40 - $45 an hour
- 5 years
- DevOps
- SQL
Quick Apply
Principal Technical Project Manager, Technology & Digital
Baptist Health South Florida —Coral Gables, FL
- $122,475.25 - $159,217.83 a year
- 11+ years
- Master's degree
- In-person
- Wellness program
- Health insurance
6d
Agentic Software Engineer I
Deloitte —Miami, FL
- $61,700 - $121,500 a year
- Full-time
- Azure
- Computer Science
- Up to 50% travel
3d
Machine Learning & Operations Engineer
OptiTrack —Miami, FL
- Full-time
- Remote
- Azure
- System design
- Mid-level
- Paid holidays
- Disability insurance
Quick Apply
Software Engineer (Backend), Content Foundations
Scribd, Inc. —Miami, FL
- $126,000 - $196,000 a year
- Full-time
- System design
- Mid-level
- Residential
- Paid parental leave
- Disability insurance
10d
Lead Quality Technician
SIMTEC Silicone Parts —Miramar, FL
- $25 - $31 an hour
- Full-time
- Background check
- Team management
- Mentoring
- Health insurance
- Dental insurance
Quick Apply
Network Engineer
WPLG, Inc —Pembroke Park, FL
- Full-time
- Hybrid work
- Background check
- Mid-level
- 3 years
Quick Apply
Associate Director, Data Science
Chewy —Plantation, FL
- $186,500 - $265,000 a year
- Full-time
- Computer Science
- 8 years
- SQL
- Paid holidays
- Health insurance

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Quality Engineer

Clinical Diagnostic Solutions, Inc.
Plantation, FL

Quick Apply

Job Details

Full-time
$70,000 - $80,000 a year
10 days ago

Benefits

Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance
Life insurance

Qualifications

Teamwork
Interpersonal skills
ISO standards
Bachelor's degree
Attention to detail
Regulatory/legal compliance standards in production
Biomedical regulatory compliance
Productivity software
Quality audits
Quality systems
Cross-functional communication
FDA regulations

Full Job Description

Description

The Quality Engineer supports and executes design control, risk management, and validation activities for Class II hematology reagents and controls. This role in ensuring products and processes meet regulatory, quality, and performance requirements. The position works cross-functionally with R&D, Manufacturing, and Quality teams to support compliant product development, process validation, and lifecycle maintenance. Quality measurement trending, procedure/document review, and auditing. The position is expected to take ownership of defined design control documentation and reviews, supporting accelerated project timelines while maintaining regulatory compliance.

Job Responsibilities

· Maintain Design History Files (DHF) for reagent and control products

· Actively support development and review of: Design inputs and outputs

· Verification and validation protocols/reports

· Ensure traceability: User needs → design inputs → outputs → V&V

· Participate and host in design reviews and document meeting outputs and risk reviews.

· Support risk management activities in accordance with ISO 14971

· Review and approve (within defined scope) Validation and Qualification protocols, reports and activities

· Support validation of: Mixing tanks, filling equipment, and storage systems and Laboratory test methods (e.g., stability, bioburden, performance)

· Review document validation data in accordance with approved protocols

· Support investigations related to: Nonconformances and Out-of-specification (OOS) results

· Lead in root cause analysis and corrective actions (CAPA)

· Work with Manufacturing to ensure:

Proper implementation of SOPs
Process consistency for reagent production

· Review of Quality Documentation including Change Orders and production records. Labeling accuracy (including lot-specific data) and Material specifications

· Ensure compliance with applicable regulatory expectations for in vitro diagnostics (IVDs)

· Ensure documentation aligns with: FDA 21 CFR Part 820 and ISO 13485 Support internal and external audits by preparing documentation and responding to requests

· Identify opportunities to improve: Validation processes, Documentation clarity and compliance

· Support implementation with Quality projects and Objectives

· Support Change Order process, review and approvals.

· Participate in quality system improvements and standardization efforts

· Support internal and external audit programs

· Reviews, analyzes, and reports on quality discrepancies related to process and manufacturing

· Performs quality and regulatory tasks assigned and ensure cross training

· Participates on project teams as assigned by management.

· Performs other related duties required or as directed that are related to position

Preferred Qualifications

GMP or regulated environments

Understands and interprets regulatory, FDA, ISO and other industry standards.

Develop team culture to provide an optimum environment for employees’ growth and contribution.

Operates with appreciable latitude for actions and/or decisions on day-to-day activities. However, is expected to seek guidance on novel or controversial problems that may impact the business significantly. Demonstrated mindset of Quality as a partner and enabler to R&D and Operations

Pre-requisites/Job Experience

· Bachelors Degree in life sciences, enginerring field, or an alternative Bachelors degree program with certificate

· 2-5 years of experience in: Medical devices, diagnostics, biotech, or pharmaceutical environment. An equivalent combination of education/training and experience will be considered.

· Project experience in: Validation, lab testing, or quality systems preferred

· Self-starter with ability to manage workload with minimal direction/supervision.

· Proficient in Microsoft Office Suite

· Understanding and working knowledge of QSR/ISO regulations.

· Able to communicate both orally and in written form clearly and concisely throughout all levels within the company.

· Strong interpersonal skills.

· Ability to work within a team environment, utilize collaborative techniques, and build relationships outside of the department as well as outside the company (suppliers, regulatory agencies, etc.).

· Ability to deliver, meet deadlines, and is result orientated.

· Strong critical thinking/reasoning and problem-solving skills required to address issues in the most efficient and effective manner.

· Able to multi-task and support/prioritize projects, adapt to shifting priorities, and able to resolve problems / conflicts.

· Strong attention to detail

· Good written and verbal communication

· Ability to follow procedures while applying quality requirements pragmatically to support business needs and learn quickly

· Team-oriented with willingness to ask questions, challenge constructively and seek guidance

Physical Requirements

Must be able to lift a minimum of 25 pounds.

· Work may occasionally involve processes that require following safety precautions and use of personal protective equipment

Job Type: Full-time

Pay: $70,000.00 - $80,000.00 per year

Benefits:

401(k)
Dental insurance
Health insurance
Life insurance
Paid time off
Vision insurance

Application Question(s):

How many years of project experience in validation?

Education:

Bachelor's (Preferred)

Experience:

Medical Device: 2 years (Preferred)

Work Location: In person

Quick Apply

Refine Your Search

validation engineer jobs in miami lakes fl

Quality Engineer

Principal Technical Project Manager, Technology & Digital, FT,8:30A-5P

Data Scientist

VDI Infrastructure Engineer

AI Sr. Developer (Secret Clearance Required)

Data Scientist

Sr Data Engineer

Data Scientist

Staff Engineer Research and Development (Onsite)

Quality Assurance Engineer

Data Engineer

Junior Operational Excellence Engineer

Manual QA

Principal Technical Project Manager, Technology & Digital

Agentic Software Engineer I

Machine Learning & Operations Engineer

Software Engineer (Backend), Content Foundations

Lead Quality Technician

Network Engineer

Associate Director, Data Science

I want to receive the latest job alert for validation engineer in miami lakes fl

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