Sr. Associate, Quality Control Lab - Chemistry
On-site · Fort Worth, Texas, United States
Job Summary
Design, execute, and interpret stability studies for pharmaceutical and sterile products in GMP and regulatory-compliant environments. Prepare, review, and approve stability protocols and reports with a high level of scientific rigor. Provide expert stability guidance to cross-functional teams including Regulatory Affairs, Manufacturing, and R&D. Ensure compliance with SOPs and GxP regulations; investigate out-of-specification results and deviations to drive root-cause analysis and corrective actions. Maintain audit-ready documentation and keep current with evolving regulatory guidelines. Role is second shift Monday–Friday, 2pm–10pm, and supports a safe laboratory environment.
Required Qualifications
- Bachelor’s Degree or Equivalent years of directly related experience (or high school +10 yrs; Assoc.+6yrs; M.S.+0 yrs)
- 2 Years of Relevant Experience
- 1 Years of Demonstrated Leadership
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