Execute technical work packages by generating, reviewing, evaluating, and validating engineering data using established methods and standards to achieve project objectives.
Create a technical selection and specification of instrumentation and automation components based on customer-specific requirements, as well as reviewing related specification and design documents.
Generate technical assessments of customer requests regarding feasibility and advise customers on instrumentation and automation technology issues .
Create standards-compliant circuit diagrams and control cabinet concepts using tools (e.g., SAP, EPLAN Electric P8, and methods and technologies of instrumentation and control engineering) taking into account relevant standards such as UL and CE, and coordinate internal and external partners in the implementation.
Create and maintain GMP-compliant manufacturing and qualification documentation for biopharmaceutical systems and facilities.
Address technical issues through structured problem analysis, implementation of technical solutions within defined project scopes, and support for FAT and SAT activities.
Responsibilities
Execute technical work packages by generating, reviewing, evaluating, and validating engineering data using established methods and standards to achieve project objectives.
Create a technical selection and specification of instrumentation and automation components based on customer-specific requirements, as well as reviewing related specification and design documents.
Generate technical assessments of customer requests regarding feasibility and advise customers on instrumentation and automation technology issues .
Create standards-compliant circuit diagrams and control cabinet concepts using tools (e.g., SAP, EPLAN Electric P8, and methods and technologies of instrumentation and control engineering) taking into account relevant standards such as UL and CE, and coordinate internal and external partners in the implementation.
Create and maintain GMP-compliant manufacturing and qualification documentation for biopharmaceutical systems and facilities.
Address technical issues through structured problem analysis, implementation of technical solutions within defined project scopes, and support for FAT and SAT activities.
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