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Quality Control Analyst II

Techtrueup


Job Location:

Fort Worth, TX - USA

Monthly Salary: Not provided by the employer
Posted: 27 August 2026 (15 hours ago)
Application Deadline: 24 November 2026
Vacancies: 1 Vacancy

Job Summary

Job Title: Clinical and Scientific - Quality Control Analyst II
Work Location: 6201 South Fwy Fort Worth TX 76134
Duration: 12 Months 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 organizations 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.

Qualifications: 

  • Bachelors 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.

Desired Competencies:

  • Strong knowledge of pharmaceutical regulatory requirements
  • Excellent Communication skills in both verbal and written form
  • Highly attentive to details and comfortable speaking up 
  • Self-Starter with the ability to follow up on and complete multiple projects simultaneously with little direction
  • Able to work overtime and flexible work hours to meet department goals.

Additional Information :

All your information will be kept confidential according to EEO guidelines.


Remote Work :

No


Employment Type :

Contract


About Company

At Fusion Plus Solutions Inc, we believe that it’s an exceptional company - a company of people proud of the work they do and the solutions they provide. By understanding what drives our specialty industries, becoming involved in our communities on a professional and personal basis, f ... View more

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