Overview
In this role you ensure batch documentation and release decisions meet GMP, food and feed safety standards, while supporting shop floor QA, audits, and continuous improvement. You act as the quality gate for batch disposition and drive CAPA and corrective actions across cross-functional teams. You will adapt QA processes to maintain product quality, patient safety, and regulatory compliance in a fast-paced manufacturing environment. This position offers a chance to impact quality culture and strengthen compliance in ADM’s production operations.
Responsibilities
- Batch review and release: verify batch records, ensure conformity to procedures, approve CofA, and disposition batches
- Line audits and shop floor QA support: conduct inspections, escalate issues, and guide production teams
- Internal audit support: assist audits, document review, and implement following actions
- Product Quality Reviews (PQRs): collect data, write reports, analyze trends and deviations, support cross-functional improvements
- Non-Conformance and Deviation Management: assist investigations and implement CAPAs
- Documentation and Quality Systems: maintain QA records, update SOPs and quality procedures, communicate across departments
- Continuous Improvement: identify process improvements and participate in quality initiatives
Key requirements
- Degree in a STEM related subject (preferable but not essential)
- At least 2 years’ experience in a quality role within a Pharmaceutical or Food Manufacturing environment
- Strong attention to detail
- Good communication and interpersonal abilities
- Ability to work effectively in a fast-paced manufacturing environment
- GMP
- food safety standards
- documentation and records management
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