Aenova Holding GmbH
5 months ago
MES Consultant (m/w/d)
Sign up to save this job, get alerts, and apply with an optimized CV.
Company information
- Company
- Aenova Holding GmbH
- Location
- Prahova Romania
- Posted
- 5 months ago
Job description
Ideal Candidate
Your Profile
•Extensive expertise in the MES environment with deep knowledge of PAS X, particularly in Master Batch Record design, workflow configuration, and confident application of GMP guidelines and CSV requirements.
•Strong understanding of system integration between MES, ERP systems (SAP), and the automation layer, including interfaces to LIMS and SCADA systems, as well as the ability to analytically capture complex pharmaceutical manufacturing processes and translate them into digital workflows.
•Solid understanding of pharmaceutical contract manufacturing, combined with flexibility and resilience to respond to shifting priorities in a dynamic CDMO environment.
•Several years of professional experience (at least 3-5 years) in the pharmaceutical industry, biotechnology, or a similarly regulated environment, complemented by strong communication and presentation skills. ing contract manufacturers and developers for the pharmaceutical industry, with 4,000 employees at 15 locations.
•Extensive expertise in the MES environment with deep knowledge of PAS X, particularly in Master Batch Record design, workflow configuration, and confident application of GMP guidelines and CSV requirements.
•Strong understanding of system integration between MES, ERP systems (SAP), and the automation layer, including interfaces to LIMS and SCADA systems, as well as the ability to analytically capture complex pharmaceutical manufacturing processes and translate them into digital workflows.
•Solid understanding of pharmaceutical contract manufacturing, combined with flexibility and resilience to respond to shifting priorities in a dynamic CDMO environment.
•Several years of professional experience (at least 3-5 years) in the pharmaceutical industry, biotechnology, or a similarly regulated environment, complemented by strong communication and presentation skills. ing contract manufacturers and developers for the pharmaceutical industry, with 4,000 employees at 15 locations.
Job Description
Your Responsibilities
•Analysis and design of production processes including MBR design, covering requirements gathering, fit to standard assessment, modeling of Master Batch Records, and configuration of relevant parameters.
•Ensuring seamless system integration, particularly through connectivity to ERP systems as well as integration of shopfloor machines and equipment.
•Execution of structured release management in a SaaS environment, including evaluation of regular updates and patches and analysis of release notes regarding potential impacts.
•Support and training, especially in 2nd level support with error analysis and troubleshooting, as well as conducting training sessions for key users.
•Further development of the system landscape and production processes by identifying optimization potential and configuring and expanding reports and dashboards for evaluating production KPIs.
Your Motivation
Are you looking for new challenges in a highly competitive environment? And do you want to tackle them creatively and with a high degree of personal responsibility? Do you prefer a "get-it-done" culture and focus on solutions rather than problems? What are you waiting for? We would be happy to explain our corporate benefits in a personal conversation!
•Analysis and design of production processes including MBR design, covering requirements gathering, fit to standard assessment, modeling of Master Batch Records, and configuration of relevant parameters.
•Ensuring seamless system integration, particularly through connectivity to ERP systems as well as integration of shopfloor machines and equipment.
•Execution of structured release management in a SaaS environment, including evaluation of regular updates and patches and analysis of release notes regarding potential impacts.
•Support and training, especially in 2nd level support with error analysis and troubleshooting, as well as conducting training sessions for key users.
•Further development of the system landscape and production processes by identifying optimization potential and configuring and expanding reports and dashboards for evaluating production KPIs.
Your Motivation
Are you looking for new challenges in a highly competitive environment? And do you want to tackle them creatively and with a high degree of personal responsibility? Do you prefer a "get-it-done" culture and focus on solutions rather than problems? What are you waiting for? We would be happy to explain our corporate benefits in a personal conversation!
Required skills
- optimization
- communication
- training
- sap
- troubleshooting
- error analysis
- saas
- presentation
- reports
- gmp
- scada
- pharmaceutical industry
- csv
- biotechnology
- mes
- lims
- release management
- dashboards
- cdmo
- 2nd level support
- pharmaceutical manufacturing
- regulated environment
- pas x
- master batch record
- production kpis
Interested in this position?
Create your free account and tailor your CV to match this job.