Validation Engineer

Lewisville, TX, US • Posted 30+ days ago • Updated 11 hours ago

Full Time

On-site

Fitment

Dice Job Match Score™

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Job Details

Skills

Quality Management
Regulatory Compliance
IT Management
Microbiology
Chemistry
Integrity Engineering
Regulatory Affairs
Packaging Engineering
Product Packaging
QA Management
SAP BASIS
Scheduling
Management
Reporting
Interfaces
Quality Assurance
Process Improvement
Quality Improvement
Design Of Experiments
Statistical Process Control
Process Engineering
Consumer Goods
FOCUS
Science
Six Sigma
Manufacturing
Communication
Decision-making
Leadership
Project Management
Presentations
Training

Summary

Responsibilities:

Designs, engineers, and implements quality systems to ensure regulatory compliance and quality improvements.
This includes designing, planning, and executing validation activities for Over the Counter (O.T.C.) Drugs in accordance with Food & Drug Administration (FDA) regulatory guidelines.
Supports quality engineering initiatives (i.e., conducting process capability studies and process improvement investigations), to improve quality, capacity, and efficiency while reducing costs.
Independently plan, perform and/or coordinate validation projects to ensure timely completion.
Draft and coordinate execution of validation documents for Equipment Qualification (IQOQPQ), Process Validation and Cleaning Validation/Verification.
Draft/or provide technical guidance for SOPs/Work Instructions and other master documents. Remain current with industry and regulatory agency trends.
Provide technical leadership for deviation investigations. Analyze data and provide recommendations for improvements in manufacturing process, and equipment.
Prepare protocols and other technical documents, and participate in the interpretation of data, collaborating with other departments. Other responsibilities as directed.
Interfaces with personnel in Quality Assurance Laboratories (Microbiology (QCM) and Chemistry (QCA)), Process Development, Product Integrity, Engineering, Contract Services, Regulatory Affairs, Package Engineering, Scheduling, Packaging, Processing and Central Weigh to design, plan, write protocols, execute, document results, and gain the required approvals for all validation activities. Validation activities include, but are not limited to product processing, product packaging, and utilities.
Collaborates with Site/Corporate Engineering or Process Development and directs all Qualification activities for newly purchased equipment.
Develops validation master plan, qualification, and validation schedule. Ensures that validation/qualification projects and timelines are structured in accordance with FDA regulatory guidelines. Informs Quality Assurance management of status of validation projects on a regular basis.
Plans and organizes all validation execution activities, including scheduling validation runs, collecting and analyzing data, and documenting results. Coordinates with management, the allocation of all resources towards validation efforts.
Compiles validation and other technical work in report format for future use, including building a technology base of pertinent continuous quality improvement related issues and solutions. Implements re-validation process improvements as required.
Interfaces with personnel in Quality Assurance, Packaging, Processing, etc. to identify potential areas for product quality and process improvement.
Identifies the source of variation in all manufacturing processes and seeks to reduce unnecessary variation, through the use of various statistical and quality improvement tools (i.e. experimental design, statistical process control).
Interacts With Engineering, Process Development, Commercialization, Quality, Stability.

Requirements:

Experience: 3+ years.
Field of Experience: food, drug or cosmetic consumer products manufacturing.
Education: Bachelor/University Degree, Education Focus: Engineering, Science.
Certs: CQIA, quality engineer, 6 sigma would be a plus.
Must possess strong technical skills. Experience with Good Manufacturing Practices and certification by ASQ, as a CQE, or CRE is strongly preferred.
Must possess excellent written and oral communication skills and the ability to facilitate communications between various groups to achieve quality objectives.
Must be detail driven and results-oriented to support independent decision making, and able to prioritize work per business needs in a fast-paced environment.
Must have excellent interpersonal and leadership skills to effectively lead teams to meet objectives.
Must possess excellent project management skills to coordinate multiple projects and adhere to tight timelines.
Must have good presentation skills to provide training to various groups within the Company.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: 91116760
Position Id: 3a17374882ddeb9778836d03ffef10ca
Posted 30+ days ago

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Validation Engineer

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Job Details

Skills

Summary

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