Raw Material Qualification Lead

An established global life sciences manufacturer is expanding operations at its large scale GMP site in Lebanon, Indiana and is seeking a Raw Material Qualification Lead to support ongoing production and new product introduction activities. This is a high‑visibility role within a mature quality organisation, offering strong project continuity and extension potential.

Contract details: W2 Contract | Initial 12 Months with Extension based on Performance

Key Responsibilities:

• Own the end‑to‑end raw material qualification process for GMP manufacturing.
• Lead supplier qualification activities including risk assessments and material approvals.
• Develop and execute raw material qualification strategies for new and existing products.
• Author and review controlled documentation supporting material lifecycle management.
• Support investigations, deviations, and change controls related to raw materials.
• Act as the quality point of contact for material‑related topics across site functions.

Required Experience:

• Background in raw material qualification within pharmaceutical or biologics manufacturing.
• Strong understanding of GMP quality systems and regulatory expectations.
• Experience working with suppliers and cross‑functional site teams.
• Proven ability to lead material qualification activities independently.
• Strong written documentation and stakeholder communication skills.

Mid‑Senior level

Contract

Quality Assurance

Pharmaceutical Manufacturing and Biotechnology Research