Deviation Manager

Deviation Manager – Hybrid (Indiana)

12-Month Contract (W2) | Flexible Hourly Rate

We are currently supporting a major pharmaceutical manufacturing site in Indiana in the search for an experienced Deviation Manager. This is a 12-month initial contract with strong potential for extension. The position offers a hybrid working arrangement: three weeks per month on-site, with one week remote.

Key Responsibilities:

• Lead and manage deviation investigations from initiation through to closure.
• Drive effective root cause analysis and implement corrective and preventive actions (CAPAs).
• Collaborate with cross-functional teams including QA, Manufacturing, and Engineering.
• Ensure all investigations are compliant with internal procedures and regulatory standards.
• Support audit readiness and contribute to continuous quality improvement efforts.

Requirements:

• Experience managing deviations within a GMP-regulated pharmaceutical or biotech environment.
• Solid understanding of FDA and ICH guidelines.
• Proven ability to lead investigations and communicate effectively across departments.
• Strong documentation and analytical skills.
• Previous experience working in a large-scale manufacturing setting is preferred.

Details:

• Location: Indiana (3 weeks on-site, 1 week remote)
• Contract Length: 12 months (initial)
• Engagement: W2
• Rate: Flexible based on experience
• Start: ASAP or negotiable

If you’re interested in learning more, please get in touch or apply directly. Confidential discussions are welcomed.