Job Title: CQV Lead

Duration: 9+ Months

Location: Davie, FL



Job Description:

Shift Schedule: Monday - Friday 8.00AM to 5.00PM

Temp to perm: Possible based on openings and performance



Core essential skill sets:

1. Minimum Master’s or PhD in Engineering (Chemical, Mechanical, Electrical, Industrial, Automation, or related) with 3+ years of experience

2. Hands-on CQV experience in a GMP Oral Solid Dose (OSD) facility supporting manufacturing and/or packaging operations.

3. Proven experience developing and executing IQ/OQ/PQ protocols and final reports in regulated environments.

4. Experience with Computerized System Validation (CSV), data integrity, and 21 CFR Part 11 compliance.

5. Strong understanding of OSD unit operations and equipment (e.g., blending, granulation, compression, coating, encapsulation and relevant automation including historian).