Full-Time

Manager – Digitalization & Manufacturing Apps

Posted on 5/9/2026

Evonik

Evonik

No salary listed

Birmingham, AL, USA + 1 more

More locations: West Lafayette, IN, USA

Hybrid

Hybrid role; occasional travel to sites as needed.

Category
Engineering Management (1)
Requirements
  • Bachelor’s degree in Computer Science (or equivalent) with 10+ years of relevant professional experience.
  • Strong background in application development or system administration, with broad knowledge of software and hardware systems.
  • Proven experience leading complex projects and cross-functional teams across multiple stakeholders.
  • Advanced knowledge of GxP and GAMP Computer System Validation (CSV) in regulated environments.
  • Strong critical thinking, problem-solving, and decision-making skills in technical and business scenarios.
  • Experience with risk assessment, business impact analysis, and continuity planning, including identifying vulnerabilities and controls.
  • Excellent communication and documentation skills, with the ability to prioritize work, collaborate across cultures, and travel as needed.
Responsibilities
  • Lead, coach, and develop a team of application analysts responsible for supporting and administering healthcare applications, ensuring high performance, accountability, and alignment with GMP compliance requirements.
  • Oversee the full lifecycle support of GMP applications, including Computerized System Validation (CSV), system maintenance, troubleshooting, and ensuring systems remain compliant with regulatory standards.
  • Serve as a global project manager for GMP-related IT initiatives, leading complex, cross-site projects that impact multiple healthcare locations and ensuring successful execution from planning through completion.
  • Manage project scope, timelines, budgets, and risks, proactively identifying potential barriers, resolving issues, and ensuring projects are delivered on time and within cost expectations.
  • Partner with cross-functional business teams to assess operational needs, gather requirements, and identify opportunities to improve or implement IT solutions that enhance efficiency and performance.
  • Ensure all IT solutions align with GMP regulations and internal standards, maintaining compliance while supporting business objectives and long-term strategic goals.
  • Act as a key liaison between stakeholders, including QA, IT, business users, and external partners, balancing priorities and ensuring clear, effective communication across all groups.
  • Collaborate with internal IT teams and external vendors to troubleshoot technical issues, implement system enhancements, and ensure reliable performance of GMP applications.
  • Contribute to leadership activities, including setting departmental goals, supporting personnel decisions, and helping define and execute the organization’s digitalization and IT strategy.
  • Maintain strict adherence to cGMP, quality, and ESHS standards, ensuring proper documentation, safety practices, training compliance, and immediate reporting of any risks impacting product quality or workplace safety.

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