Remote POMS MES Techno-Functional SME — Pharma

Capgemini; New York (NY); Hybrid; USD 73,000 - 174,000; Full time

Benefits offered by this job

Vacation & holidays

Healthcare

Retirement plans

Life & disability insurance

Employee assistance programs

Job summary

Capgemini Engineering seeks an experienced POMS MES Techno-Functional SME for a GxP-regulated pharmaceutical manufacturing environment. You will serve as a trusted advisor linking business, manufacturing, quality, and IT to support and implement POMS MES across sites.

Your role includes requirements gathering, design reviews, UAT, and validating CSV activities, with emphasis on regulatory compliance and MES configurations across ERP/LIMS/SCADA integrations.

Qualifications

• Bachelor's degree in Engineering, Computer Science, Information Technology, Life Sciences, or a related field.
• 8-12 years in Life Sciences, Pharmaceutical, or Biotech manufacturing environments.
• 5+ years hands-on experience supporting or implementing POMS MES solutions.
• Strong understanding of MES concepts, EBR, batch execution, and production workflows.
• Experience in GxP-regulated environments.
• Ability to review functional and technical documentation.

Responsibilities

• Collaborate with Manufacturing, Quality, Validation, and IT stakeholders to gather and document business requirements.
• Translate requirements into MES functional specs, designs, and implementation strategies.
• Lead requirements workshops, discovery sessions, fit-gap analyses, design reviews, and UAT.
• Partner with manufacturing teams to optimize production workflows using POMS MES.

Skills

POMS MES

Regulatory compliance

CSV validation

Business analysis

GxP experience

Education

Bachelor's degree in Engineering/CS/IT/Life Sciences

Tools

ERP

LIMS

Historians

SCADA

ISA-95

Job description

Capgemini Engineering seeks an experienced POMS MES Techno-Functional SME for a GxP-regulated pharmaceutical manufacturing environment. You will serve as a trusted advisor linking business, manufacturing, quality, and IT to support and implement POMS MES across sites.

Your role includes requirements gathering, design reviews, UAT, and validating CSV activities, with emphasis on regulatory compliance and MES configurations across ERP/LIMS/SCADA integrations.