MES Engineer

Futran Solutions; New Brunswick (NJ); Hybrid; USD 60,000 - 90,000; Full time

Job summary

An established industry player is seeking a Senior MES Engineer/Validation Lead to oversee computer system validation activities for Manufacturing Execution Systems (MES) in the cell therapy manufacturing sector. This role is tailored for candidates with a robust IT foundation and significant experience in the pharma/biotech industry. The successful candidate will collaborate with QA, Business, and IT teams to ensure compliant deployment of MES solutions. Join a dynamic team that values innovation and compliance in a fast-paced environment, where your expertise will directly impact critical manufacturing processes.

Qualifications

• 4+ years of CSV experience in pharma/biotech environments.
• 3+ years of hands-on MES experience with Emerson Syncade.
• 2+ years of project management experience.

Responsibilities

• Lead validation activities including test preparation and execution.
• Develop validation deliverables like URS and Risk Assessments.
• Collaborate with QA and IT to ensure compliance.

Skills

Computer System Validation (CSV)

Manufacturing Execution Systems (MES)

Project Management

ALM

ServiceNow

SQL Databases

Document Management Systems

Education

Bachelor's degree in Computer Science

Bachelor's degree in Information Systems

Tools

Emerson Syncade

SAP

LIMS

Oracle

Veeva

BMSDocs

Job description

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Direct message the job poster from Futran Solutions

I am Srinivas from Futran Solutions. My client is looking for the below requirement. If you are interested. Please reach me out [e-mail] /(609)-945-2335

Job Title: APP&SYS ENG - MES Engineer- 62352-1

Location: New Brunswick, NJ - Hybrid

Candidates must be onsite 50% of the time at either Summit West, Giralda Farms, Princeton Pike, Lawrenceville, or New Brunswick.

Please indicate on the resume which site they prefer, under the candidate's name.

Must Have List

• 4+ years of Computer System Validation (CSV) experience in regulated pharmaceutical and biotech environments, with strong knowledge of GAMP 5, 21 CFR Part 11, and Computer Software Assurance (CSA) principles.

• 3+ years of hands-on MES experience with Emerson Syncade, including recipe validation, EBR testing, and interface verification with systems such as SAP, LIMS, and Oracle.

• 2+ years of project management experience, demonstrating the ability to prioritize urgent tasks, manage competing deadlines, and adapt effectively within dynamic, cross-functional teams.

• 3+ years of advanced experience with ALM, ServiceNow, SQL databases, and document management systems (e.g., Veeva, BMSDocs), supporting testing, issue tracking, and controlled documentation.

• Holds a Bachelor’s degree in Computer Science or a related technical discipline

o About the Role

We’re seeking a Senior MES Engineer/Validation Lead to take ownership of computer system validation activities for Manufacturing Execution Systems (MES) supporting cell therapy manufacturing. This role is ideal for someone with a strong IT/Computer Science foundation and 3 years of hands-on experience in the pharma/biotech industry. You’ll partner with QA, Business, and IT teams to ensure compliant and efficient deployment of MES & Recipes solutions.

o Key Responsibilities

-Lead end-to-end validation activities including test preparation, authoring of IQ/System/UAT scripts, Dry Run, test data setup, environment readiness, test execution facilitation, and post-execution review.

-Develop and execute validation deliverables including URS, Risk Assessments, IQ/OQ/PQ, and Summary Reports.

-Ensure all activities comply with 21 CFR Part 11, GAMP 5, and internal SOPs.

-Author, Review and Approve validation documentation lifecycle: Validation & Test Plan, requirement , Test Scripts, Assessment documents, and Summary Reports.

-Validate electronic batch records (EBR), MES recipes, interfaces, and integration with systems such as SAP, Oracle, LIMS, CMMS, GPS, and EDMS.

-Collaborate with Business Owners, QA, and IT to align on requirements and ensure CSV deliverables are compliant and audit-ready.

-Coordinate recipe configuration, master data setup, and validation in Syncade MES.

-Ensure validation practices meet GAMP 5, CSA, 21 CFR Part 11, and ALCOA+ data integrity principles.

-Proven ability to manage competing priorities with a flexible workstyle and consistently deliver efficient, compliant results in fast-paced, cross-functional environments.

-Experienced in cross-functional communication, with the ability to interpret and convey business and IT need to Validation; comfortable interacting with QA, business, and technical teams.

-Deep understanding of MES Syncade & Recipes testing phases (IQ, System Testing, Recipe UAT).

-Familiarity with cGMP, GAMP, SDLC, 21 CFR Part 11, and Good Documentation Practices (GDP).

-Demonstrated ability to independently lead system validation efforts across multiple stakeholder groups.

o Basic Qualifications

-Bachelor’s degree in computer science, Information Systems, or a related engineering discipline.

-Minimum 3 years of experience in pharma/biotech, with focus on IT -Validation and Quality Assurance & Compliance

-Experience with MES platforms (Syncade preferred) and electronic batch records (EBR).

-Familiar with tools such as ALM, ServiceNow, SQL databases, and document management systems.

-Knowledge of shop floor operations, process automation, and manufacturing environments are preferable

Thanks & Regards,

Name: Srinivasa Reddy Mallu.

Contact [phone], Ext: 9068

Email Id: [e-mail]

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

• Job function

  Engineering, Science, and Quality Assurance

• Industries

  Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing

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