You are an Industrial Engineer, you are interested in practicing your English skills and you would like to work for a health company ? If so, this opportunity is for you !
As a Validation Engineer, you are expected :
- To be responsible for executing equipment requalification, validation and R&D projects according to Sterigenics procedures on agreed validation protocol.
...
- To plan, organize and coordinate all validation activities related to assigned validation projects (facility and/or EAS projects).
- To identify business process improvement and assist in implementing them.
Your Responsibilities/Duties
1. Review customer or EAS supplied validation or test protocols for executability within the limitation of the facility¿s equipment, Sterigenics operating procedures and compliance with current regulatory standards.
2. Handle periodic customer requalification¿s (protocol and report edition).
3. Organize the execution of validation protocols and technically driven customer and/or EAS projects, which include but are not limited to the following:
- Planning all validation activities, project runs, ancillary resources, lab testing and sample handling, in order to minimize the risk of errors in the execution,
- Cycle programming and preparation of necessary process documents (CSA) and safety assessments,
- Microbiological samples inventory,
- Data collection and analysis (if applicable),
- Assuring proper handling, storage and shipping of bioburden, LAL, biological indicators, sterility, engineering or residual samples to the appropriate laboratory.
4. Ensure validation activities are carried out according to the agreed time-schedule and communicate follow up to relevant persons (validation manager, EAS, sales, etc);
5. Organize work of validation operators for load preparation in collaboration with the validation team leader.
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You are an Industrial Engineer, you are interested in practicing your English skills and you would like to work for a health company ? If so, this opportunity is for you !
As a Validation Engineer, you are expected :
- To be responsible for executing equipment requalification, validation and R&D projects according to Sterigenics procedures on agreed validation protocol.
- To plan, organize and coordinate all validation activities related to assigned validation projects (facility and/or EAS projects).
- To identify business process improvement and assist in implementing them.
Your Responsibilities/Duties
1. Review customer or EAS supplied validation or test protocols for executability within the limitation of the facility¿s equipment, Sterigenics operating procedures and compliance with current regulatory standards.
2. Handle periodic customer requalification¿s (protocol and report edition).
3. Organize the execution of validation protocols and technically driven customer and/or EAS projects, which include but are not limited to the following:
- Planning all validation activities, project runs, ancillary resources, lab testing and sample handling, in order to minimize the risk of errors in the execution,
...
- Cycle programming and preparation of necessary process documents (CSA) and safety assessments,
- Microbiological samples inventory,
- Data collection and analysis (if applicable),
- Assuring proper handling, storage and shipping of bioburden, LAL, biological indicators, sterility, engineering or residual samples to the appropriate laboratory.
4. Ensure validation activities are carried out according to the agreed time-schedule and communicate follow up to relevant persons (validation manager, EAS, sales, etc);
5. Organize work of validation operators for load preparation in collaboration with the validation team leader.
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