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Niche industrial automation and regulated pharma expertise reduces candidate pool despite metro location.
High due to regulated pharma domain and specialized SCADA and ISA S88 expertise required.
Requires regulated pharma lifecycle experience and specialized SCADA/ISA S88 tool expertise.
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Own end-to-end technical delivery and lead execution of assigned projects ensuring on-time delivery, quality, cost-effectiveness, and customer satisfaction.
Provide technical leadership and act as the single point of contact (SPOC) for projects within Pharma/Life Sciences and CPG domains, ensuring solutions meet customer and regulatory requirements (e.g., GMP, 21 CFR Part 11).
Lead and influence cross-functional teams and manage stakeholder communications and resources throughout the project lifecycle, driving issue, risk, and change management to control scope and cost.
Experience working through complete project lifecycle (Design → Engineering → Commissioning → Validation) in Pharma/Life Sciences industry.
Strong hands-on expertise in automation and control systems including Batch process automation, SCADA/HMI systems, FTBatch / FTView SE / Phase Manager (or equivalents), and compliance with ISA S88 standards and 21 CFR Part 11 requirements.
Proven ability to manage multiple projects simultaneously and work effectively in matrix organizations with demonstrated stakeholder management skills.
Work Experience Required: Not explicitly mentioned in the JD.
Technical expert in Pharma/Life Sciences automation with strong understanding of regulatory environment and technology applications relevant to control systems.
Experienced project leader with demonstrated ability to drive multiple complex projects in parallel while ensuring cost control, quality, and risk mitigation.
Skilled at influencing without authority and managing cross-functional, multi-disciplinary teams and stakeholders in a matrix organization.