Validation Engineer Position Available In Miami-Dade, Florida

Validation Engineer 3.8 3.8 out of 5 stars

Coral Gables, FL Commissioning & Qualification Consultant Location:

Coral Springs, FL Type:

On-site Schedule:

Full-time Contract Type:

6-

Month Contract Pay Rate:

20.00/hr – 35.00/hr Job Description We are seeking a knowledgeable and driven Commissioning & Qualification Consultant for a 6-month consulting engagement supporting pharmaceutical operations in Coral Springs, FL. The selected professional will be responsible for the full lifecycle of commissioning and qualification activities, from planning and execution to reporting and regulatory readiness. This role plays a critical part in ensuring systems are validated and compliant, contributing to quality assurance across equipment, facilities, and utilities. Ideal for individuals with validation expertise and a solid understanding of GMP compliance and pharmaceutical regulatory standards. Key Responsibilities Author, review, approve, and execute documentation for Commissioning, Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ). Lead and support cross-functional projects, ensuring on-time execution of qualification activities aligned with project goals. Coordinate efforts and stakeholders involved in commissioning and qualification deliverables. Ensure data integrity by managing all documentation and test results used in GMP decision-making. Maintain system qualification status and support impact assessments for proposed changes. Draft equipment and material specifications; contribute to engineering investigations and resolve technical challenges. Implement best practices in validation and contribute to continuous improvement of qualification systems. Troubleshoot and address deviations affecting equipment or systems to uphold product quality and compliance. Support external regulatory inspections and internal audits by presenting qualification outcomes. Requirements Associate degree in Engineering, Life Sciences, or a technical discipline with a minimum of 1 year of relevant experience. Strong understanding of cGMP and Good Documentation Practices (GDP). Proficiency in 21 CFR 211, 21 CFR 820, Part 11, and ISO standards applicable to pharmaceutical operations. Familiarity with ISPE Baseline Guides and qualification best practices. Strong analytical, communication, and problem-solving skills. Ability to operate with minimal supervision and manage multiple priorities efficiently. ttg Talent Solutions is an Equal Opportunity Employer and recruiting agency. We are committed to creating an inclusive and diverse work environment and welcome applications from all qualified candidates regardless of race, color, religion, gender, sexual orientation, national origin, age, disability, or veteran status. Please note that all offers of employment are contingent upon the successful completion of a drug test and background check. We maintain a drug- and substance-free workplace to ensure the safety and well-being of all employees. At ttg, “We believe in making a difference One Person at a Time,” ttg OPT. IND1