US_East | Manufacturing & Process Engineer_L4

Expedite Talent Solutions

Albany, NY

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JOB DETAILS

SALARY

$67–$70 Per Hour

SKILLS

Acceptance Testing, Agile Programming Methodologies, Automation, Biology, Biotech and Pharmaceutical, Business Analysis, Computer Science, Computer Systems, Corrective Action, Documentation, Drug Manufacturing, ERP (Enterprise Resource Planning), Error Handling, Gap Analysis, GxP, ISA Standards, Information Technology & Information Systems, Laboratory Information Management System (LIMS), LinkedIn, Manufacturing, Manufacturing Execution Systems (MES), Manufacturing Operations, Manufacturing Process Engineering, Manufacturing Software, Manufacturing/Industrial Processes, Operational Improvement, Performance Management, Problem Solving Skills, Process Validation, Production Support, Quality Management, Regulatory Compliance, Regulatory Requirements, Release Management/Engineering, Requirements Management, Root Cause Analysis, Supervisory Control and Data Acquisition (SCADA), System Integration (SI), System Lifecycle, System Validation, Systems Administration/Management, Technical Delivery, Technical Writing, Testing, Validation Documentation, Writing Skills

LOCATION

Albany, NY

POSTED

4 days ago

"Possible 3 Month CTH | No Fees | Do Not Re-Post| Confidential
TMR ID: 82T1XJ
Role: Digital Engineer - POMS MES
Work location: Albany NY is preferred location
Background and Meet and Greet: MANDATORY
Job Description:
"*** is seeking an experienced POMS MES Techno-Functional SME with deep expertise in Manufacturing Execution Systems (MES) within a GxP-regulated pharmaceutical manufacturing environment. The ideal candidate will serve as a trusted advisor and bridge between business stakeholders, manufacturing operations, quality organizations, validation teams, and technical delivery teams to support, enhance, configure, and implement POMS MES solutions across manufacturing sites.
This role requires a combination of strong functional knowledge of pharmaceutical manufacturing processes, hands-on POMS MES expertise, and familiarity with CSV validation and regulatory compliance requirements.
"

Key Responsibilities:
"Business & Functional Responsibilities
" Collaborate with Manufacturing, Quality, Validation, and IT stakeholders to gather, analyze, and document business requirements.
" Translate business requirements into MES functional specifications, solution designs, and implementation strategies.
" Lead requirements workshops, discovery sessions, fit-gap analyses, design reviews, and user acceptance testing (UAT).
" Partner with manufacturing teams to optimize production workflows and leverage POMS MES capabilities to improve operational performance.
" Drive alignment between MES solutions, manufacturing processes, business objectives, and regulatory requirements.
" Support process harmonization initiatives across manufacturing sites.
MES Technical Responsibilities
" Configure, support, and enhance POMS MES workflows, electronic batch records (EBR), recipes, and manufacturing execution processes.
" Support MES module configuration, troubleshooting, and issue resolution activities.
" Perform root cause analysis and corrective actions for production support issues.
" Support and review MES integrations with enterprise systems such as ERP, LIMS, Historians, Automation/SCADA, and other manufacturing applications.
" Review technical specifications, configuration documentation, and implementation deliverables.
" Assist with system deployments, upgrades, migrations, and release management activities.
" Provide expertise in electronic batch record execution, deviations management, manufacturing investigations, and exception handling.
Validation & Compliance Responsibilities
" Support Computer System Validation (CSV) activities throughout the system lifecycle.
" Author, review, and maintain validation documentation including:
o User Requirements Specifications (URS)
o Functional Requirements Specifications (FRS)
o Design Specifications (DS)
o Installation Qualification (IQ)
o Operational Qualification (OQ)
o Performance Qualification (PQ)
o Traceability Matrices
o Validation Summary Reports (VSR)
" Ensure compliance with:
o FDA 21 CFR Part 11
o GAMP 5 Guidelines
o Good Manufacturing Practices (GMP)
o ALCOA+ and Data Integrity requirements
o Corporate Quality Management System procedures
"

What are the Mandatory skills and skill proficiencies required for this position?
"" Bachelor's degree in Engineering, Computer Science, Information Technology, Life Sciences, or a related field.
" 8 12 years of experience in Life Sciences, Pharmaceutical, or Biotech manufacturing environments.
" 5+ years of hands-on experience supporting or implementing POMS MES solutions.
" Strong understanding of MES concepts, electronic batch records (EBR), batch execution, manufacturing operations, and production workflows.
" Experience working in GxP-regulated environments.
" Solid understanding of pharmaceutical manufacturing processes, validation methodologies, and quality systems.
" Experience supporting MES implementations, enhancements, upgrades, and production support activities.
" Ability to review and interpret functional and technical documentation.
" Strong troubleshooting and analytical problem-solving skills.
"

What are the Optional skills and skill proficiencies for this position?
"" Experience with large-scale MES implementation or site rollout programs.
" Exposure to system integrations involving ERP, LIMS, Historian, SCADA, or automation platforms.
" Knowledge of ISA-95 manufacturing standards and digital manufacturing architectures.
" Experience supporting global manufacturing organizations.
" Familiarity with Agile and hybrid project delivery methodologies
"

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Resumes will be rejected for the following reasons:
- Different format
- Missing details in comments section
- Missing text box in the header
- Photo ID included containing personal information other than legal name and photo
Soemia Pineda - ERM
*** North America
Tel.: +***"

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