Job Title: MES Aspentech Engineer for Pharmaceutical Manufacturing
Key Responsibilities:
- Support the deployment configuration and optimization of AspenTech MES in pharmaceutical manufacturing settings.
- Collaborate with clients to translate operational needs and regulatory requirements into AspenTech MES solutions.
- Design configure and test Aspen MES components to align with GxP compliance and manufacturing workflows.
- Provide input on system architecture batch execution models and integration requirements.
- Troubleshoot Aspen MES application and integration issues; support root cause analysis and system improvements.
- Participate in the design and development of electronic batch records (EBRs) within Aspen MES.
- Support validation lifecycle activities (IQ OQ PQ) in compliance with FDA 21 CFR Part 11 and GMP.
- Deliver on-site and remote support during MES deployment commissioning and post-Go Live optimization.
Qualifications and Requirements:
- Bachelors Degree in Computer Science Engineering Information Systems Life Sciences or related disciplines.
- 5 years of experience in MES implementations preferably with AspenTech MES or similar platforms (e.g. Rockwell PharmaSuite Werum PAS-X Siemens Opcenter).
- Experience with Aspen MES configuration and integration
- Familiarity with pharmaceutical batch process automation and data integrity requirements.
- Knowledge of industry regulations and practices: GxP 21 CFR Part 11 Annex 11.
- Strong analytical and problem-solving capabilities.
- Effective communication with both technical and non-technical stakeholders.
- Proactive self-driven and able to work in a fast-paced client-facing environment.
- Team-oriented with a commitment to quality and continuous improvement.
Job Title: MES Aspentech Engineer for Pharmaceutical Manufacturing Key Responsibilities: Support the deployment configuration and optimization of AspenTech MES in pharmaceutical manufacturing settings. Collaborate with clients to translate operational needs and regulatory requirements into AspenTec...
Job Title: MES Aspentech Engineer for Pharmaceutical Manufacturing
Key Responsibilities:
- Support the deployment configuration and optimization of AspenTech MES in pharmaceutical manufacturing settings.
- Collaborate with clients to translate operational needs and regulatory requirements into AspenTech MES solutions.
- Design configure and test Aspen MES components to align with GxP compliance and manufacturing workflows.
- Provide input on system architecture batch execution models and integration requirements.
- Troubleshoot Aspen MES application and integration issues; support root cause analysis and system improvements.
- Participate in the design and development of electronic batch records (EBRs) within Aspen MES.
- Support validation lifecycle activities (IQ OQ PQ) in compliance with FDA 21 CFR Part 11 and GMP.
- Deliver on-site and remote support during MES deployment commissioning and post-Go Live optimization.
Qualifications and Requirements:
- Bachelors Degree in Computer Science Engineering Information Systems Life Sciences or related disciplines.
- 5 years of experience in MES implementations preferably with AspenTech MES or similar platforms (e.g. Rockwell PharmaSuite Werum PAS-X Siemens Opcenter).
- Experience with Aspen MES configuration and integration
- Familiarity with pharmaceutical batch process automation and data integrity requirements.
- Knowledge of industry regulations and practices: GxP 21 CFR Part 11 Annex 11.
- Strong analytical and problem-solving capabilities.
- Effective communication with both technical and non-technical stakeholders.
- Proactive self-driven and able to work in a fast-paced client-facing environment.
- Team-oriented with a commitment to quality and continuous improvement.
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