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Automation Engineer (m/f/d)
Our client is one of the world's top three companies with a leading open access technology platform for the discovery, development and manufacturing of biologics. They are building a brand new team with competent people that can work together to take the company through their exciting growth journey.
Your tasks in detail are:
- You will fill a key position in the global Automation and Integrated Service (AIS) team. Locally you report to the Engineering Head
- You are Subject Matter Expert for automation and instrumentation in support of the Drug Product (DP) automation platform, process control system and PLC -based vendor package units
- You will lead or support the automation project from customer requirement (URS) to commissioning and qualification; you will be responsible for the maintenance program to ensure valid system status
- You will perform activities such as user administration, data backup, system configuration via MBR, troubleshooting and compliance violation investigation
- You will prepare, maintain and update required documentation, SOPs and reports for all phases of GMP activities
- You will prepare and support internal and external audits
- You will perform system health monitoring and continuous improvements
- You will work closely with the production and quality team to support manufacturing on a daily basis, such as retrieving and processing data, reports, and response actions to alarms and escalation of actions
- You will oversee key vendor management to ensure quality service is provided in a timely and efficient manner by vendors
Your Qualifications:
- Bachelor's degree in electrical, computer or chemical engineering with at least 5 years of relevant automation experience
- Prior experience in biologics / chemical process and manufacturing automation support, maintenance, and project management
- Demonstrated experience supporting and operating common automation systems; knowledge of Siemens Control System, IFIX SCADA, Data Histories and Alarm Management. Familiar with GAMP5 and related FDA and EMA cGMP regulations.
- Knowledge of drug product manufacturing process, processing equipment design and automation (CIP / SIP).
Desirable:
- Excellent verbal and written communication skills, leadership abilities, and ethical judgement
- Ability to work collaboratively as part of a team and with other departments
- Ability to work effectively with minimal guidance
Automation Engineer (m/f/d)
- Location Leverkusen
- Salary Negotiable
- Discipline Bioengineering & Medical Engineering
- Reference PR/391528_1668589642
Our client is one of the world's top three companies with a leading open access technology platform for the discovery, development and manufacturing of biologics. They are building a brand new team with competent people that can work together to take the company through their exciting growth journey.
Your tasks in detail are:
- You will fill a key position in the global Automation and Integrated Service (AIS) team. Locally you report to the Engineering Head
- You are Subject Matter Expert for automation and instrumentation in support of the Drug Product (DP) automation platform, process control system and PLC -based vendor package units
- You will lead or support the automation project from customer requirement (URS) to commissioning and qualification; you will be responsible for the maintenance program to ensure valid system status
- You will perform activities such as user administration, data backup, system configuration via MBR, troubleshooting and compliance violation investigation
- You will prepare, maintain and update required documentation, SOPs and reports for all phases of GMP activities
- You will prepare and support internal and external audits
- You will perform system health monitoring and continuous improvements
- You will work closely with the production and quality team to support manufacturing on a daily basis, such as retrieving and processing data, reports, and response actions to alarms and escalation of actions
- You will oversee key vendor management to ensure quality service is provided in a timely and efficient manner by vendors
Your Qualifications:
- Bachelor's degree in electrical, computer or chemical engineering with at least 5 years of relevant automation experience
- Prior experience in biologics / chemical process and manufacturing automation support, maintenance, and project management
- Demonstrated experience supporting and operating common automation systems; knowledge of Siemens Control System, IFIX SCADA, Data Histories and Alarm Management. Familiar with GAMP5 and related FDA and EMA cGMP regulations.
- Knowledge of drug product manufacturing process, processing equipment design and automation (CIP / SIP).
Desirable:
- Excellent verbal and written communication skills, leadership abilities, and ethical judgement
- Ability to work collaboratively as part of a team and with other departments
- Ability to work effectively with minimal guidance