Associate IS Engineer - MES
Amgen
Associate IS Engineer - MES
Job Description
Role Name: Associate IS Engineer – MES
What you will do
- Collaborate with business and data stakeholders to gather requirements, assess data needs, and ensure data integrity and compliance across ETL pipelines.
- Lead day to day operations and maintenance of Amgen’s MES Platform and hosted applications.
- Stay updated with the latest trends, advancements and standard process for MES Platform ecosystem.
- Analyze and understand the functional & technical requirements of applications, solutions and systems, translate them into software architecture and design specifications.
- Develop and execute unit tests, integration tests, and other testing strategies to ensure the quality of the software following IS change control and GxP Validation process while exhibiting expertise in Risk Based Validation methodology.
- Work on integrating with other systems and platforms to ensure seamless data flow and functionality.
- Stay up to date on MES Features, new releases and best practices around MES Platform Governance.
- End-to-end design, configuration, and implementation of Amgen’s NextGen MES, with a focus on PAS|X platform technical deployments.
- Serve as the technical support for PAS|X MES implementations, including requirements gathering, solution architecture, interface design, and system validation.
- Contribute through all project phases—design, build, test, deployment, and hypercare—ensuring delivery commitments are met.
- Ensure technology strategies for MES system enhancements, scalability, and cloud readiness, supporting Amgen’s digital transformation journey.
- Develop and deliver clear documentation, including functional/technical specifications, validation protocols, and training materials.
- Troubleshoot on MES technical challenges, incident response, and root cause analysis.
What we expect of you
- Master’s or bachelor’s degree and 0 -1 year of Information Systems experience or related field OR Associate’s degree and 2+ years of Information Systems experience or related field
- 2-5 years of experience working in global pharmaceutical Industry
- Experience in building solutions on an MES Platform.
- Experience in managing systems, implementing and validating projects in GxP regulated environments.
- Extensive expertise in SDLC, including requirements, design, testing, data analysis, creating and managing change controls.
- Hands-on experience implementing and supporting PAS|X MES in a GMP-regulated pharmaceutical or biotechnology manufacturing environment.
- Technical expertise in MES solution design, configuration, and integration with SAP (PP, QM, MM modules), and Level 2 automation systems (e.g., PLCs, SCADA, DCS, OPC).
Must-Have Skills
- Experience with IT/OT cybersecurity, data integrity, and cloud-based MES architectures
- Strong skills in technical documentation, stakeholder engagement, and cross-functional communication.
- Experience with PAS|X MES advanced modules (eBR, Equipment Management, Weigh & Dispense, Master Batch Record configuration).
- Experience integrating MES with SAP S/4HANA and/or advanced automation/data platforms.
- Familiarity with ISA-95 standards, data lakes, and supporting digital manufacturing initiatives (e.g., IIoT, AI/ML for manufacturing data).
- Experience working across global, matrixed teams and/or as a technical leader for external vendors/partners.
- Experience with containers / Kubernetes and databases (Oracle / PostgreSQL)
- Outstanding written and verbal communication skills, and ability to translate technical concepts for non-technical audiences.
- Excellent analytical and troubleshooting skills.
- Strong verbal and written communication skills.
- Ability to work effectively with global, virtual teams.
- Team-oriented, with a focus on achieving team goals.
- Strong presentation and public speaking skills.
Compensation
2-5
Locations
- Hyderabad, India
Salary
Salary not disclosed
Estimated Salary Rangehigh confidence
12,000 - 18,000 USD / yearly
Source: xAI estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Experience with IT/OT cybersecurity, data integrity, and cloud-based MES architecturesintermediate
- Strong skills in technical documentation, stakeholder engagement, and cross-functional communication.intermediate
- Experience with PAS|X MES advanced modules (eBR, Equipment Management, Weigh & Dispense, Master Batch Record configuration).intermediate
- Experience integrating MES with SAP S/4HANA and/or advanced automation/data platforms.intermediate
- Familiarity with ISA-95 standards, data lakes, and supporting digital manufacturing initiatives (e.g., IIoT, AI/ML for manufacturing data).intermediate
- Experience working across global, matrixed teams and/or as a technical leader for external vendors/partners.intermediate
- Experience with containers / Kubernetes and databases (Oracle / PostgreSQL)intermediate
- Outstanding written and verbal communication skills, and ability to translate technical concepts for non-technical audiences.intermediate
- Excellent analytical and troubleshooting skills.intermediate
- Strong verbal and written communication skills.intermediate
- Ability to work effectively with global, virtual teams.intermediate
- Team-oriented, with a focus on achieving team goals.intermediate
- Strong presentation and public speaking skills.intermediate
Required Qualifications
- Master’s or bachelor’s degree and 0 -1 year of Information Systems experience or related field OR Associate’s degree and 2+ years of Information Systems experience or related field (experience)
- 2-5 years of experience working in global pharmaceutical Industry (experience)
- Experience in building solutions on an MES Platform. (experience)
- Experience in managing systems, implementing and validating projects in GxP regulated environments. (experience)
- Extensive expertise in SDLC, including requirements, design, testing, data analysis, creating and managing change controls. (experience)
- Hands-on experience implementing and supporting PAS|X MES in a GMP-regulated pharmaceutical or biotechnology manufacturing environment. (experience)
- Technical expertise in MES solution design, configuration, and integration with SAP (PP, QM, MM modules), and Level 2 automation systems (e.g., PLCs, SCADA, DCS, OPC). (experience)
Responsibilities
- Collaborate with business and data stakeholders to gather requirements, assess data needs, and ensure data integrity and compliance across ETL pipelines.
- Lead day to day operations and maintenance of Amgen’s MES Platform and hosted applications.
- Stay updated with the latest trends, advancements and standard process for MES Platform ecosystem.
- Analyze and understand the functional & technical requirements of applications, solutions and systems, translate them into software architecture and design specifications.
- Develop and execute unit tests, integration tests, and other testing strategies to ensure the quality of the software following IS change control and GxP Validation process while exhibiting expertise in Risk Based Validation methodology.
- Work on integrating with other systems and platforms to ensure seamless data flow and functionality.
- Stay up to date on MES Features, new releases and best practices around MES Platform Governance.
- End-to-end design, configuration, and implementation of Amgen’s NextGen MES, with a focus on PAS|X platform technical deployments.
- Serve as the technical support for PAS|X MES implementations, including requirements gathering, solution architecture, interface design, and system validation.
- Contribute through all project phases—design, build, test, deployment, and hypercare—ensuring delivery commitments are met.
- Ensure technology strategies for MES system enhancements, scalability, and cloud readiness, supporting Amgen’s digital transformation journey.
- Develop and deliver clear documentation, including functional/technical specifications, validation protocols, and training materials.
- Troubleshoot on MES technical challenges, incident response, and root cause analysis.
Tags & Categories
Associate IS Engineer - MES
Amgen
Associate IS Engineer - MES
Job Description
Role Name: Associate IS Engineer – MES
What you will do
- Collaborate with business and data stakeholders to gather requirements, assess data needs, and ensure data integrity and compliance across ETL pipelines.
- Lead day to day operations and maintenance of Amgen’s MES Platform and hosted applications.
- Stay updated with the latest trends, advancements and standard process for MES Platform ecosystem.
- Analyze and understand the functional & technical requirements of applications, solutions and systems, translate them into software architecture and design specifications.
- Develop and execute unit tests, integration tests, and other testing strategies to ensure the quality of the software following IS change control and GxP Validation process while exhibiting expertise in Risk Based Validation methodology.
- Work on integrating with other systems and platforms to ensure seamless data flow and functionality.
- Stay up to date on MES Features, new releases and best practices around MES Platform Governance.
- End-to-end design, configuration, and implementation of Amgen’s NextGen MES, with a focus on PAS|X platform technical deployments.
- Serve as the technical support for PAS|X MES implementations, including requirements gathering, solution architecture, interface design, and system validation.
- Contribute through all project phases—design, build, test, deployment, and hypercare—ensuring delivery commitments are met.
- Ensure technology strategies for MES system enhancements, scalability, and cloud readiness, supporting Amgen’s digital transformation journey.
- Develop and deliver clear documentation, including functional/technical specifications, validation protocols, and training materials.
- Troubleshoot on MES technical challenges, incident response, and root cause analysis.
What we expect of you
- Master’s or bachelor’s degree and 0 -1 year of Information Systems experience or related field OR Associate’s degree and 2+ years of Information Systems experience or related field
- 2-5 years of experience working in global pharmaceutical Industry
- Experience in building solutions on an MES Platform.
- Experience in managing systems, implementing and validating projects in GxP regulated environments.
- Extensive expertise in SDLC, including requirements, design, testing, data analysis, creating and managing change controls.
- Hands-on experience implementing and supporting PAS|X MES in a GMP-regulated pharmaceutical or biotechnology manufacturing environment.
- Technical expertise in MES solution design, configuration, and integration with SAP (PP, QM, MM modules), and Level 2 automation systems (e.g., PLCs, SCADA, DCS, OPC).
Must-Have Skills
- Experience with IT/OT cybersecurity, data integrity, and cloud-based MES architectures
- Strong skills in technical documentation, stakeholder engagement, and cross-functional communication.
- Experience with PAS|X MES advanced modules (eBR, Equipment Management, Weigh & Dispense, Master Batch Record configuration).
- Experience integrating MES with SAP S/4HANA and/or advanced automation/data platforms.
- Familiarity with ISA-95 standards, data lakes, and supporting digital manufacturing initiatives (e.g., IIoT, AI/ML for manufacturing data).
- Experience working across global, matrixed teams and/or as a technical leader for external vendors/partners.
- Experience with containers / Kubernetes and databases (Oracle / PostgreSQL)
- Outstanding written and verbal communication skills, and ability to translate technical concepts for non-technical audiences.
- Excellent analytical and troubleshooting skills.
- Strong verbal and written communication skills.
- Ability to work effectively with global, virtual teams.
- Team-oriented, with a focus on achieving team goals.
- Strong presentation and public speaking skills.
Compensation
2-5
Locations
- Hyderabad, India
Salary
Salary not disclosed
Estimated Salary Rangehigh confidence
12,000 - 18,000 USD / yearly
Source: xAI estimated
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Experience with IT/OT cybersecurity, data integrity, and cloud-based MES architecturesintermediate
- Strong skills in technical documentation, stakeholder engagement, and cross-functional communication.intermediate
- Experience with PAS|X MES advanced modules (eBR, Equipment Management, Weigh & Dispense, Master Batch Record configuration).intermediate
- Experience integrating MES with SAP S/4HANA and/or advanced automation/data platforms.intermediate
- Familiarity with ISA-95 standards, data lakes, and supporting digital manufacturing initiatives (e.g., IIoT, AI/ML for manufacturing data).intermediate
- Experience working across global, matrixed teams and/or as a technical leader for external vendors/partners.intermediate
- Experience with containers / Kubernetes and databases (Oracle / PostgreSQL)intermediate
- Outstanding written and verbal communication skills, and ability to translate technical concepts for non-technical audiences.intermediate
- Excellent analytical and troubleshooting skills.intermediate
- Strong verbal and written communication skills.intermediate
- Ability to work effectively with global, virtual teams.intermediate
- Team-oriented, with a focus on achieving team goals.intermediate
- Strong presentation and public speaking skills.intermediate
Required Qualifications
- Master’s or bachelor’s degree and 0 -1 year of Information Systems experience or related field OR Associate’s degree and 2+ years of Information Systems experience or related field (experience)
- 2-5 years of experience working in global pharmaceutical Industry (experience)
- Experience in building solutions on an MES Platform. (experience)
- Experience in managing systems, implementing and validating projects in GxP regulated environments. (experience)
- Extensive expertise in SDLC, including requirements, design, testing, data analysis, creating and managing change controls. (experience)
- Hands-on experience implementing and supporting PAS|X MES in a GMP-regulated pharmaceutical or biotechnology manufacturing environment. (experience)
- Technical expertise in MES solution design, configuration, and integration with SAP (PP, QM, MM modules), and Level 2 automation systems (e.g., PLCs, SCADA, DCS, OPC). (experience)
Responsibilities
- Collaborate with business and data stakeholders to gather requirements, assess data needs, and ensure data integrity and compliance across ETL pipelines.
- Lead day to day operations and maintenance of Amgen’s MES Platform and hosted applications.
- Stay updated with the latest trends, advancements and standard process for MES Platform ecosystem.
- Analyze and understand the functional & technical requirements of applications, solutions and systems, translate them into software architecture and design specifications.
- Develop and execute unit tests, integration tests, and other testing strategies to ensure the quality of the software following IS change control and GxP Validation process while exhibiting expertise in Risk Based Validation methodology.
- Work on integrating with other systems and platforms to ensure seamless data flow and functionality.
- Stay up to date on MES Features, new releases and best practices around MES Platform Governance.
- End-to-end design, configuration, and implementation of Amgen’s NextGen MES, with a focus on PAS|X platform technical deployments.
- Serve as the technical support for PAS|X MES implementations, including requirements gathering, solution architecture, interface design, and system validation.
- Contribute through all project phases—design, build, test, deployment, and hypercare—ensuring delivery commitments are met.
- Ensure technology strategies for MES system enhancements, scalability, and cloud readiness, supporting Amgen’s digital transformation journey.
- Develop and deliver clear documentation, including functional/technical specifications, validation protocols, and training materials.
- Troubleshoot on MES technical challenges, incident response, and root cause analysis.
Tags & Categories