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Validation Engineer
Eingestellt von Berry Technical
Gesuchte Skills: Engineer, Support, Engineering
Projektbeschreibung
Validation Engineer/3 Month Contract/Switzerland/up to 760CHF per day
My client a global pharmaceutical giant requires a Validation Engineer to provide support for the validation activities associated with software equipment, ensuring that all compliance issues and requirements of my clients Validation Policies and Procedures are addressed.
Primary Tasks and Responsibilities:
*Managing Complexity/Technical Accountability
*Serves as technical expert for the Validation process and responsibilities to ensure compliance
*Continuous Learning/Managing Risk.
*Resolves & manages technical operational problems in area of expertise.
*Suggest and sometimes may implement innovation and continuous improvement within the Validation process.
*Implements initiatives in the Validation Process that will deliver customer value at lowest cost.
*Facilitates successful team behavior within Quality Systems and across functional areas.
*Manages relationships externally and internally.
*Builds cross-functional and cross-departmental support, fostering overall effectiveness.
*Fosters harmony within Quality Systems.
*Influences and persuades so as to bring about technical and process improvements.
*Ensure accuracy and maintenance of the Johnson & Johnson Validation Master List.
*Review and approve Validation Master Plans, Protocols, Summary Reports and other documentation associated with validations, as appropriate for each validation exercise.
*Ensure all validation activities and documents are authorized and appropriate compliance approval is gained.
*Ensure that all validation activities are carried out and reported in a timely manner.
*Ensure compliance through assisting in audits.
*Through effective communication and training initiatives develop staff in projects and validation teams to ensure that validation projects are carried out in accordance with Johnson & Johnson Policies and Procedures.
*Facilitates, encourage and coordinate continuous improvement with respect to validation activities.
*Keep management informed of significant quality issues in a manner commensurate with the potential impact of the issue on public health, employee health & safety, company operations, and/or the environment.
*Lead by example, inculcating the Credo values in all actions within the workplace.
Technical Profile Requirements:
*Knowledge of bespoke validation.
*Process knowledge and documentation.
Desirable:
*In depth knowledge of 21 CFR 820, 21 CFR 11 and European regulations associated with the medical device industry.
*High understanding of GMP, Compliance, Validation Practices including the system development life cycle and Regulatory expectations.
*Working experience of validation computer systems for use in a FDA regulated environment.
Justification for Request: To support the CSV activities in the project "Purified Water System"
Non-Technical Profile Requirements:
*Must be able to lead and give direction to Validation Projects and Teams.
*Individual must also be an active team member in Validation activities
Methodology/Certification Requirements:
*Qualification in an appropriate discipline (eg Engineering, Information Systems, or Life Science with additional IT qualification) with a broad technical/educational skills base.
*Working experience in a regulated environment and carrying out validation and/or testing activities.
Non-Technical profile requirements:
*Some flexibility in working hours is required.
*Must be able to work on multiple simultaneous tasks with limited supervision.
*Quick learner, motivated self-starter.
*Excellent customer service, interpersonal, communication and team collaboration skills.
*Able to follow change management for internal guidelines.
Language proficiencies:
*Due to the nature of the role English and Italian spoken and written is required.
My client a global pharmaceutical giant requires a Validation Engineer to provide support for the validation activities associated with software equipment, ensuring that all compliance issues and requirements of my clients Validation Policies and Procedures are addressed.
Primary Tasks and Responsibilities:
*Managing Complexity/Technical Accountability
*Serves as technical expert for the Validation process and responsibilities to ensure compliance
*Continuous Learning/Managing Risk.
*Resolves & manages technical operational problems in area of expertise.
*Suggest and sometimes may implement innovation and continuous improvement within the Validation process.
*Implements initiatives in the Validation Process that will deliver customer value at lowest cost.
*Facilitates successful team behavior within Quality Systems and across functional areas.
*Manages relationships externally and internally.
*Builds cross-functional and cross-departmental support, fostering overall effectiveness.
*Fosters harmony within Quality Systems.
*Influences and persuades so as to bring about technical and process improvements.
*Ensure accuracy and maintenance of the Johnson & Johnson Validation Master List.
*Review and approve Validation Master Plans, Protocols, Summary Reports and other documentation associated with validations, as appropriate for each validation exercise.
*Ensure all validation activities and documents are authorized and appropriate compliance approval is gained.
*Ensure that all validation activities are carried out and reported in a timely manner.
*Ensure compliance through assisting in audits.
*Through effective communication and training initiatives develop staff in projects and validation teams to ensure that validation projects are carried out in accordance with Johnson & Johnson Policies and Procedures.
*Facilitates, encourage and coordinate continuous improvement with respect to validation activities.
*Keep management informed of significant quality issues in a manner commensurate with the potential impact of the issue on public health, employee health & safety, company operations, and/or the environment.
*Lead by example, inculcating the Credo values in all actions within the workplace.
Technical Profile Requirements:
*Knowledge of bespoke validation.
*Process knowledge and documentation.
Desirable:
*In depth knowledge of 21 CFR 820, 21 CFR 11 and European regulations associated with the medical device industry.
*High understanding of GMP, Compliance, Validation Practices including the system development life cycle and Regulatory expectations.
*Working experience of validation computer systems for use in a FDA regulated environment.
Justification for Request: To support the CSV activities in the project "Purified Water System"
Non-Technical Profile Requirements:
*Must be able to lead and give direction to Validation Projects and Teams.
*Individual must also be an active team member in Validation activities
Methodology/Certification Requirements:
*Qualification in an appropriate discipline (eg Engineering, Information Systems, or Life Science with additional IT qualification) with a broad technical/educational skills base.
*Working experience in a regulated environment and carrying out validation and/or testing activities.
Non-Technical profile requirements:
*Some flexibility in working hours is required.
*Must be able to work on multiple simultaneous tasks with limited supervision.
*Quick learner, motivated self-starter.
*Excellent customer service, interpersonal, communication and team collaboration skills.
*Able to follow change management for internal guidelines.
Language proficiencies:
*Due to the nature of the role English and Italian spoken and written is required.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Ingenieurwesen/Technik, Sonstiges