Urgent Role || Lead GxP Validation Engineer @Fort Worth, TX || Contract (All Visa)
Why This Role Stands Out
Step into a pivotal role where you'll lead critical GxP validation efforts and drive quality improvements within a reputable organization. This position is ideal for experienced validation engineers seeking to expand their expertise and make a significant impact. Apply today to leverage your skills and contribute to groundbreaking projects in Fort Worth!
Quick Overview
Job Description
Position: Lead GxP Validation Engineer
Location: Fort Worth, TX (5 days onsite)
Employment: Contract
Job Description:
The Quality Control Analyst II is responsible for maintaining high standards of laboratory operations and ensuring compliance with regulatory requirements.
Key responsibilities include:
- Performs microbiological validations for raw materials and finished products, including Bioburden, Endotoxin, Sterility, and PET.
- Provides support to QC Microbiology laboratories.
- Conducts equipment qualifications. -Organizes and assists with Media Fill and Reads.
- Identifies ongoing quality issues, prevents potential problems, and suggests improvements.
- Interprets and evaluates analyses for accuracy and precision against established specifications, recommending and implementing corrective actions when necessary.
- May be responsible for analytical and protocol report writing, as well as standard operating procedures.
- Strictly adheres to Good Documentation Practices (GDP).
- Collaborates with and supports coworkers to enhance the organization's overall capabilities.
- Communicates effectively with production, maintenance, warehouse, and other relevant functions.
- Participates in problem-solving and troubleshooting.
- Supports training needs of team members and works cohesively with the team.
- Coordinates with and supports other departments to ensure smooth workflow execution.
- Ensures the availability of supplies and equipment to meet schedules and carries out tasks as defined by the schedule.
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