Quality Control Analyst II — Microbiology & GMP

Techtrueup; Fort Worth (TX); On-site; USD 52,000 - 56,000; Full time

Job summary

Techtrueup is seeking a Clinical and Scientific - Quality Control Analyst II for a 12-month contract at our Fort Worth, TX location. The role focuses on maintaining high laboratory standards and regulatory compliance.

The incumbent will perform microbiological validations (Bioburden, Endotoxin, Sterility, PET), support QC Microbiology labs, conduct equipment qualifications, and ensure GDP compliance while collaborating across departments to sustain quality and efficiency.

Qualifications

• Bachelor’s Degree or equivalent years of related experience (or high school + 8 yrs; Assoc. + 4 yrs)
• The ability to fluently read, write, understand and communicate English.

Responsibilities

• 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).
• 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.

Skills

Pharma regulations

Quality control

Documentation

Team collaboration

Education

Bachelor’s Degree or equivalent

Job description

Techtrueup is seeking a Clinical and Scientific - Quality Control Analyst II for a 12-month contract at our Fort Worth, TX location. The role focuses on maintaining high laboratory standards and regulatory compliance.

The incumbent will perform microbiological validations (Bioburden, Endotoxin, Sterility, PET), support QC Microbiology labs, conduct equipment qualifications, and ensure GDP compliance while collaborating across departments to sustain quality and efficiency.