Biopharma Validation Analyst I - Impact & Growth

PCI TRGR Penn Pharmaceutical Services Ltd; Rockford (IL); On-site; USD 27,000 - 31,000; Full time

Benefits offered by this job

Paid time off

Health insurance (dental & vision)

Flexible spending account

401(k) plan

Job summary

PCI TRGR Penn Pharmaceutical Services Ltd is seeking a Validation Analyst I located in Rockford, IL. The role involves ownership of limited risk validation projects under supervision, developing and executing validation protocols, and supporting audits.

You will coordinate with internal teams and customers to ensure timely approvals and closure of validation activities. The ideal candidate has 1–3 years of related experience, strong analytical skills, and familiarity with cGMP/GXP and 21 CFR

Qualifications

• High School Diploma or GED and/or 1-3 years related experience
• Basic Mathematical Skills
• Basic Computer Skills: ability to perform basic computer tasks and operate common programs
• Professional Proficiency: ability to read and participate effectively in conversations

Responsibilities

• Perform validation activities to ensure compliance to government and customer requirements.
• Prepare validation protocols, validation statements, reports, summaries, and master validation plans for new customer / product / system project launch and maintain existing validated processes at multiple sites.
• Ensure validation documentation completion, accuracy, and closure, including coordinating approvals.
• Investigate validation deviations, documenting in formal reports, and ensure corrective action to complete project.

Skills

Basic Math

Basic Computer Skills

Professional Communication

Logical Reasoning

Education

High School Diploma or GED

Tools

Common computer programs

Job description

PCI TRGR Penn Pharmaceutical Services Ltd is seeking a Validation Analyst I located in Rockford, IL. The role involves ownership of limited risk validation projects under supervision, developing and executing validation protocols, and supporting audits.

You will coordinate with internal teams and customers to ensure timely approvals and closure of validation activities. The ideal candidate has 1–3 years of related experience, strong analytical skills, and familiarity with cGMP/GXP and 21 CFR