i-Pharm GxP
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.
Seniority level Mid‑Senior level
Employment type Contract
Job function Quality Assurance
Industry Pharmaceutical Manufacturing and Biotechnology Research
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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.
Seniority level Mid‑Senior level
Employment type Contract
Job function Quality Assurance
Industry Pharmaceutical Manufacturing and Biotechnology Research
#J-18808-Ljbffr