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Tier-1 employer increases applicant density, but niche pharma MES/GMP skills and seniority moderate competition.
Strong GMP, MES and regulated manufacturing focus reduces cross-industry transferability.
Explicit 8–13 years requirement, mandatory MES/GMP and compliance experience, and certifications create strict filters.
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Lead and develop a team providing 24/7 operational support for manufacturing technology systems ensuring uptime and compliance.
Own key manufacturing systems (e.g., MES, PI Historian), maintaining system reliability, data integrity, and GMP compliance including managing configuration and validation documentation.
Collaborate with global and cross-functional teams to resolve complex system issues, support audits/inspections, drive continuous improvement, and implement technology projects aligned with operational excellence.
8-13 years of experience in Business, Engineering, IT, or related field.
Hands-on experience managing and being a system owner of manufacturing systems like MES or Laboratory systems.
Experience in people management and leading matrixed teams.
Willingness to work later shifts, including evenings or nights, as per business requirements.
Proven leadership in technology-driven manufacturing environments within GMP regulated biopharmaceutical industry.
Strong expertise in technology operations support, system validation, and regulatory compliance (Annex 11 / 21 CFR Part 11).
Experience working with Scaled Agile Framework (SAFe) and demonstrated ability to lead transformation and change management initiatives.