Role : The Validation Engineer II performs qualification / validation activities linked to his / her part of the business (Manufacturing Equipment, Clean utilities)He / She prepares and implements the validation documentation required to assure the proper development of a project.
He / She manages deviations and changes in order to ensure that these are well documented and that corrective actions are taken and followed-
up upon. Main responsibilities : Prepare and implement the validation documentation required to assure the proper development of a project.
Act as a validation representative for projects, with support of his / her Validation Supervisor : 1. Define and implement all validation activities related to the project.
2. Develop the Validation Plans : define validation methodology and approach in line with the Validation Supervisor.- Provide validation expertise for the development of the project.
Analyze, interpret, document and report the testing results.- Ensure the follow-up and tracking of the validation activities.
Update the validation documentation system.- Assure feedback of status and issues to the Validation Supervisor.3. Provide support in all quality-
related issues, including GMP regulations, compliance with internal SOPs, and all aspects of safe, reliable and consistent operation of the system.
4. Manage deviations and changes in order to ensure that these are well documented and that corrective actions are taken and followed-
up upon.5. Support junior validation engineers as well as provide day to day guidance for the execution of Validation activities (Depending on applicant’s expertise)6.
Defend validation topics related to his / her projects during Regulatory Inspection and prepare validation parts of the submission file7.
Assuring the ability to meet the Department goals in respect to Quality, Finances, Fullfilment and EHS Profile : - Minimum Bachelor Degree or equivalent in Engineering, Chemistry, Life Science, or other job related discipline-
2 years' experience in Validation / Quality systems- Project management experience- Excellent communication skills, fluency in english-
Familia with Quality Management and GxP Regulations- Knowledge of Validation Methodologies- Knowledge of Quality Systems, European and FDA regulations, cGMP, GDP-
Knowledge of the manufacturing processes- Excellent analytical skills- Sound industry knowledge, project proficiency, and autonomy expected Work Environment : In Lessines, Takeda is producing drugs for immunological and hematological therapies.
The main activity of the site is the purification of plasma immunoglobulins for the treatment of primary immunodeficiency, as well as the treatment and conditioning of coagulation factors for haemorrhagic disorders (haemophilia A and B).
As a production site, the Lessines factory operates 24 / 7 and employs more than 950 people.
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