EBR Designer
GSK
July 02, 2026
On-site
Marietta, PA
Operations
Position Summary
The role is primarily responsible for the development, creation, update, and testing of electronic batch records (eBR) in the Siemens OpCenter platform within the agreed timeline. The role gathers user requirements from production teams, converts them into executable eBRs, and supports testing, training, and documentation.
Responsibilities
- Engage process owners/stakeholders to acquire process information for eBR design.
- Design and create/update business process documentation for eBR to support MES implementations and eBR lifecycle.
- Convert business process documentation into eBR in MES.
- Create testing and validation documentation to meet functional/user requirements.
- Test and validate eBR and associated protocols against existing manufacturing processes.
- Connect eBR to external systems (e.g., OSI-PI, SAP) to pull data into eBR.
- Support and train end-users; troubleshoot eBR issues; support exception management (e.g., data correction in eBR).
- Drive continuous improvement using MES data and Gemba Walks; share best practices.
- Create documentation to support LSOP creation and training materials.
- Compile and maintain relevant SAP and MES master data.
Qualifications / Requirements
- Bachelor’s degree in engineering, computer science, information systems, or related field (or equivalent experience).
- 3+ years’ experience in a manufacturing environment.
- 2+ years’ experience with MES design, eBR development, or similar digital manufacturing tools.
- Experience creating process documentation (flowcharts, Visio).
- Experience with testing/validation in a regulated environment.
- Hands-on experience with Siemens OpCenter (or another MES platform).
Preferred
- Experience in pharmaceutical or biotech manufacturing.
- Integration tech familiarity (OSI-PI, SAP, APIs) and basic scripting/coding.
- GMP documentation/validation protocol and compliance experience.
- Customer-focused, organized; able to work independently in a matrix.
- Strong written/verbal communication and cross-functional teamwork.
Application instructions
If you require an accommodation or assistance to apply, contact us at usrecruitment.adjustments@gsk.com.
The role is primarily responsible for the development, creation, update, and testing of electronic batch records (eBR) in the Siemens OpCenter platform within the agreed timeline. The role gathers user requirements from production teams, converts them into executable eBRs, and supports testing, training, and documentation.
Responsibilities
- Engage process owners/stakeholders to acquire process information for eBR design.
- Design and create/update business process documentation for eBR to support MES implementations and eBR lifecycle.
- Convert business process documentation into eBR in MES.
- Create testing and validation documentation to meet functional/user requirements.
- Test and validate eBR and associated protocols against existing manufacturing processes.
- Connect eBR to external systems (e.g., OSI-PI, SAP) to pull data into eBR.
- Support and train end-users; troubleshoot eBR issues; support exception management (e.g., data correction in eBR).
- Drive continuous improvement using MES data and Gemba Walks; share best practices.
- Create documentation to support LSOP creation and training materials.
- Compile and maintain relevant SAP and MES master data.
Qualifications / Requirements
- Bachelor’s degree in engineering, computer science, information systems, or related field (or equivalent experience).
- 3+ years’ experience in a manufacturing environment.
- 2+ years’ experience with MES design, eBR development, or similar digital manufacturing tools.
- Experience creating process documentation (flowcharts, Visio).
- Experience with testing/validation in a regulated environment.
- Hands-on experience with Siemens OpCenter (or another MES platform).
Preferred
- Experience in pharmaceutical or biotech manufacturing.
- Integration tech familiarity (OSI-PI, SAP, APIs) and basic scripting/coding.
- GMP documentation/validation protocol and compliance experience.
- Customer-focused, organized; able to work independently in a matrix.
- Strong written/verbal communication and cross-functional teamwork.
Application instructions
If you require an accommodation or assistance to apply, contact us at usrecruitment.adjustments@gsk.com.