Electronic batch records jobs

Operator, Parenteral Operations (Aseptic Filling)

Lilly · Posted Nov 13, 2026

Open

Concord, North Carolina, United States
On-site
Full-time · Associate
$18–$35 per year

Operator, Parenteral Operations (Aseptic Filling)

Lilly · Posted Nov 13, 2026

Open

Concord, North Carolina, United States
On-site
Full-time · Associate
$18–$35 per year

US Industry and Ecosystem Lead

Apple · Posted Nov 12, 2026

Open

Boston, Massachusetts, United States +4 more
On-site
Full-time · Senior
15+ years

Apply with RefersoAI Apply on careers page

Lead Apple’s Life Sciences strategy across pharma and medical device manufacturing, building partner ecosystems and scaling solutions across the Apple platform.

Locations (5)

Boston, Massachusetts, United States
Jersey City, New Jersey, United States
New York City, New York, United States
San Francisco, California, United States
Washington DC, District of Columbia, United States

Responsibilities

US Industry and Ecosystem Lead

Apple · Posted Nov 12, 2026

Open

Boston, Massachusetts, United States +4 more
On-site
Full-time · Senior
15+ years

Apply with RefersoAI Apply on careers page

Lead Apple’s Life Sciences strategy across pharma and medical device manufacturing, building partner ecosystems and scaling solutions across the Apple platform.

Locations (5)

Boston, Massachusetts, United States
Jersey City, New Jersey, United States
New York City, New York, United States
San Francisco, California, United States
Washington DC, District of Columbia, United States

Responsibilities

POMS MES Engineer

NNIT · Posted Nov 12, 2026

Open

United States
2+ years

Apply with RefersoAI Apply on careers page

Support the deployment of standards within POMSnet for EBR, maintain and develop recipes and worksheets for the site, and work closely with manufacturing, quality, IT and automation teams.

Responsibilities

Develop MES solutions in POMSnet
Maintain and develop recipes, worksheets and electronic batch records
Support the deployment of EBR standards within POMSnet
Work with the team to develop workflows within the MES solution
Assist with MES, database and system upgrade activities

Requirements

Third level qualification in computer science, IT, mechatronics, manufacturing engineering or a related discipline
Nice to have: Software validation in the medical devices industry
Nice to have: MES upgrades and database related activities
Nice to have: Validation documentation and GMP compliance
Nice to have: Manufacturing, quality and automation stakeholders experience

Skills

POMSnet GMP manufacturing environment Oracle Manufacturing systems C# coding SQL databases

MES Engineer

Siemens Healthineers · Posted Nov 12, 2026

Open

HGH, KE

Apply with RefersoAI Apply on careers page

Manage daily operation of core SAP modules (PP/MM/SD/QM), master data maintenance, production order execution, inventory control, batch management and customer consignment processes; troubleshoot system errors and ensure consistency between system data and physical inventory. Responsible for MES system configuration, testing, launch and continuous optimization, including electronic batch records, production traceability and equipment data acquisition to support digital workshop operation. Maintain bidirectional data interfaces between SAP and MES, troubleshoot synchronization exceptions, and ensure accurate, real-time and closed-loop cross-system data. Comply with medical device compliance requirements, manage system access control, audit logs and change control, prepare relevant documents to support internal, customer and regulatory audits. Identify business pain points, optimize digital processes, deliver system training, and support factory capacity upgrading and digital transformation.

Responsibilities

Manage daily operation of core SAP modules (PP/MM/SD/QM)
Master data maintenance
Production order execution
Inventory control
Batch management and customer consignment processes

Skills

SAP (PP/MM/SD/QM)MES system configuration Electronic batch records Production traceability Data interface maintenance SAP MES

See full job description

Inspection & Packaging Operator I

RCM Technologies, Inc. · Posted Nov 11, 2026

Open

Manatí, Puerto Rico, Puerto Rico
On-site
Contract · Entry
1–2 years

Apply with RefersoAI Apply on careers page

Support routine parenteral manufacturing and packaging operations at the client's Manatí facility, responsible for visual inspection, line setup, material reconciliation, and GMP documentation.

Responsibilities

Perform manual, semi-automatic, or automatic visual inspection of parenteral products
Execute packaging operations following approved procedures and paper/electronic batch records (eBR)
Conduct line setup, line clearance, in-process verifications, and material/product reconciliation
Complete batch records, logbooks, and electronic system entries accurately in compliance with Good Documentation Practices and data integrity rules
Operate assigned inspection/packaging equipment, computer interfaces, and electronic batch record systems

Requirements

High School Diploma
Associate Degree in Science, Industrial Technology, Mechanics, or related technical field
Nice to have: parenteral product experience
Nice to have: sterile product experience
Nice to have: Spanish fluency

Skills

cGMP compliance Good Documentation Practices (GDP)electronic batch records (eBR)

POMS MES Engineer

NNIT · Posted Nov 11, 2026

Open

Dublin, Leinster, Ireland
2+ years

Apply with RefersoAI Apply on careers page

Support and develop MES solutions using POMSnet at a GMP manufacturing site in Ireland.

Responsibilities

Develop MES solutions in POMSnet
Maintain and develop recipes, worksheets and electronic batch records
Support the deployment of EBR standards within POMSnet
Work with the team to develop workflows within the MES solution
Assist with MES, database and system upgrade activities

Requirements

Third level qualification in computer science, IT, mechatronics, manufacturing engineering or a related discipline
Nice to have: software validation in the medical devices industry
Nice to have: MES upgrades
Nice to have: database related activities
Nice to have: validation documentation

Skills

POMSnet MES GMP Oracle Manufacturing OMD C#SQL

Parenteral Manufacturing Technician

Inteldot · Posted Nov 11, 2026

Open

Manati, Puerto Rico, Puerto Rico
On-site
Full-time · Associate
2–3 years

Apply with RefersoAI Apply on careers page

Support pharmaceutical and biologics manufacturing operations within a regulated sterile manufacturing environment, executing routine and critical manufacturing activities associated with pharmaceutical formulation, preparation, filling, and lyophilization processes.

Responsibilities

Execute pharmaceutical manufacturing activities associated with formulation, preparation, filling, and lyophilization processes
Perform equipment setup, changeover, cleaning, sanitization, sterilization, and line clearance according to approved procedures
Operate manufacturing equipment, including formulation tanks, filling systems, autoclaves, isolators, and associated processing equipment
Perform Cleaning-in-Place (CIP) and Sterilization-in-Place (SIP) operations
Execute sterilization cycles and pre- and post-use filter integrity testing

Requirements

High school diploma or equivalent
Nice to have: Sterile parenteral manufacturing
Nice to have: Biologics manufacturing
Nice to have: Lyophilization processes
Nice to have: Isolator operation

Skills

cGMP Aseptic techniques Sterile manufacturing Formulation

MES Specialist – (eBR) Developer

Inteldot · Posted Nov 11, 2026

Open

Manati, Manatí, Puerto Rico
5+ years

Apply with RefersoAI Apply on careers page

Provide technical and operational support for Electronic Batch Record (eBR) applications within a regulated pharmaceutical manufacturing environment.

Responsibilities

Develop, configure, maintain, and troubleshoot MES Electronic Batch Records (eBRs)
Provide technical expertise in MES/eBR design, programming, configuration, and implementation
Troubleshoot, debug, and resolve MES application issues
Evaluate existing eBR workflows and recommend improvements
Review proposed MES/eBR design changes for compliance

Requirements

Bachelor’s degree in engineering, Computer Science, Information Systems, or a related technical discipline
Nice to have: Emerson Syncade Enterprise MES (EMES)
Nice to have: Integration between MES, ERP, LIMS, automation platforms
Nice to have: FDA 21 CFR Part 11
Nice to have: Electronic records and signatures

Skills

Manufacturing Execution Systems (MES)Emerson Syncade Electronic Batch Records (eBR)Microsoft SQL Server

CSV Specialist – MES/EBR Validation

Inteldot · Posted Nov 11, 2026

Open

Manati, United States

Apply with RefersoAI Apply on careers page

Provide validation and documentation support for Manufacturing Execution Systems (MES) and Electronic Batch Records (eBRs) in a regulated pharmaceutical manufacturing environment.

Responsibilities

Develop, review, update, execute, and maintain computerized system validation documentation in accordance with GMP regulations and data integrity principles.
Support validation lifecycle documentation including URS, Functional Specifications, Design Specifications, Configuration Specifications, Risk Assessments, and Traceability Matrices.
Develop and execute IQ/OQ testing protocols and document validation results.
Coordinate activities with cross‑functional technical and business teams.
Prepare and review validation reports and summary reports.

Requirements

Bachelor’s degree in engineering, Computer Science, Information Technology, Life Sciences, Chemistry, or a related technical discipline
Nice to have: Syncade Enterprise MES (EMES)
Nice to have: Electronic batch record implementation
Nice to have: CSV risk assessments
Nice to have: Data Integrity Assessments

Skills

Computerized System Validation (CSV)Manufacturing Execution Systems (MES)Electronic Batch Records (eBRs)FDA cGMP regulations Good Documentation Practices (GDP)Data Integrity principles URS Functional Specifications Design Specifications Configuration Specifications Risk Assessments Traceability Matrices IQ/OQ testing protocols Application Lifecycle Management (ALM) tools

See full job description

Electronic batch records jobs

Compensation

Responsibilities

Requirements

Skills

Benefits

Locations (5)

Responsibilities

Locations (5)

Responsibilities

Responsibilities

Requirements

Skills

Responsibilities

Skills

Responsibilities

Requirements

Skills

Responsibilities

Requirements

Skills

Responsibilities

Requirements

Skills

Responsibilities

Requirements

Skills

Responsibilities

Requirements

Skills

Requirements

Skills

Requirements

Skills

Benefits