Lead automation and data projects across the DSD manufacturing sites, from concept and design through commissioning, validation, and user adoption.
Own technical delivery of SCADAs(Ignition, Wonderware etc ), DCSs (Emerson DeltaV), MESs ( PharmaSuite, OpCenter, MasterControl etc), and data capture/historization systems (OPC, Aveva PI, Kepware, Litmus etc).
Design and deploy data collection architectures that enable secure, reliable data flow from shop-floor automation systems to enterprise analytics platforms.
Champion change management and adoption, ensuring stakeholders and site users fully embrace new digital solutions.
Define and enforce standards for system design, configuration, and data management consistent with GMP, GAMP 5, Annex 11 and 22, 21 CFR Part 11, and cybersecurity best practices.
Collaborate cross-functionally with process engineering, IT/OT, validation, and operations to deliver integrated, business-ready solutions.
Manage vendors and system integrators, ensuring adherence to technical specifications, schedule, and cost.
Drive the Connected Plant and digital enablement strategy, increasing plant maturity and improving data visibility across the Drug Substance network.
Travel frequently (>50%) to provide on-site leadership, support project execution, and facilitate system handover and training.

Requirements

BS or higher in Engineering (Electrical, Chemical, Mechanical, or Software Engineering) or related technical field required
Advanced degree and/or certifications (PMP, ISA, GAMP) preferred
8+ years of progressive experience in automation, process control, or digital manufacturing within a regulated (GMP) environment.
Proven record of leading automation and/or data infrastructure projects across multiple facilities or business units.
Strong experience with at least one of the following systems: Emerson DeltaV, Rockwell/Allen-Bradley, Siemens, Ignition, (Other level 2/3 systems would also be considered)
Expertise in data integration, capture, and historization systems (OPC, Kepware, Litmus, Aveva PI).
Familiarity with IT/OT infrastructure including Virtualization, VLANs, network segregation, and cybersecurity.
Demonstrated leadership in change management, stakeholder alignment, and user adoption of new technologies
Biopharmaceutical or chemical manufacturing experience strongly preferred.
Demonstrated involvement in digital transformation or connected manufacturing programs
Working in a FDA/EMA regulated industry, particularly one adhering to GAMP 5, Annex 11 and 21 CFR Part 11 requirements.

Benefits

A choice of national medical and dental plans, and a national vision plan, including health incentive programs
Employee assistance and family support programs, including commuter benefits and tuition reimbursement
At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard skills

automationdata integrationprocess controldigital manufacturingdata capturedata historizationsystem designconfigurationdata managementchange management

Soft skills

leadershipstakeholder alignmentuser adoptioncollaborationproject execution

Certifications

PMPISAGAMP