Indianapolis $90,000-$115,000 Permanent
Job Responsibilities:
Execute validation plans for manufacturing equipment and processes.
Prepare IQ/OQ/PQ protocols and reports for GMP compliance.
Identify and mitigate risks in process validation.
Support audits and regulatory inspections.
Job Qualifications:
Bachelor’s in Engineering (Mechanical, Chemical, or Biomedical).
2+ years in validation within pharmaceuticals or biotech.
Familiarity with GAMP 5 and 21 CFR Part 11.
Strong technical writing and analytical skills.
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