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About the Role
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).
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).
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