Dieses Jobangebot ist archiviert und steht nicht mehr zur Verfügung.
Vakante Jobangebote finden Sie unter Projekte.
Vakante Jobangebote finden Sie unter Projekte.
Validation Engineer - Cleaning Validation
Eingestellt von Randstad (Schweiz) AG
Gesuchte Skills: Engineer, Client
Projektbeschreibung
Validation Engineer
Randstad Professionals are one of the leading recruitment companies in Switzerland and with a dedicated IT contracting team in Zurich. We are excited to help you in your search. We focus on finding the best contracts for the best contractors.
We are looking for a Validation Engineer for our client based in Bern, who will lead the validation activities for equipment cleaning validation, clean room qualification (IQ/OQ/PQ) and disinfection validation according to the client's internal requirements, Validation Policies and Procedures. This position is related to USP, DSP and Fill Finish processes.
Primary Tasks and Responsibilities
- Managing Complexity/Technical Accountability
- Serves as technical expert for the Validation process and responsibilities to ensure compliance
- Responsible for the validation approach
- Responsible for writing risk assessments, validation plans and reports
- Resolves & manages technical operational problems in area of expertise
- Suggest and sometimes may implement innovation and continuous improvement within the Validation process
- Facilitates successful team behavior within Quality Systems and across functional areas
- Manages relationships externally and internally.
- Builds cross-functional and cross-departmental support
- Influences and persuades so as to bring about technical and process improvements.
- 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 client's Policies and Procedures.
Technical Profile Requirements
- Deep knowledge and at least 3-5 years experience in equipment cleaning validation, clean room qualification and disinfection validation in the pharmaceutical industry
- High understanding of GMP, Compliance, Validation Practices including the system development life cycle and Regulatory expectations
If this role is the right fit, our dedicated and expert team is looking forward to hearing from you.
Good to know you!
Randstad Professionals are one of the leading recruitment companies in Switzerland and with a dedicated IT contracting team in Zurich. We are excited to help you in your search. We focus on finding the best contracts for the best contractors.
We are looking for a Validation Engineer for our client based in Bern, who will lead the validation activities for equipment cleaning validation, clean room qualification (IQ/OQ/PQ) and disinfection validation according to the client's internal requirements, Validation Policies and Procedures. This position is related to USP, DSP and Fill Finish processes.
Primary Tasks and Responsibilities
- Managing Complexity/Technical Accountability
- Serves as technical expert for the Validation process and responsibilities to ensure compliance
- Responsible for the validation approach
- Responsible for writing risk assessments, validation plans and reports
- Resolves & manages technical operational problems in area of expertise
- Suggest and sometimes may implement innovation and continuous improvement within the Validation process
- Facilitates successful team behavior within Quality Systems and across functional areas
- Manages relationships externally and internally.
- Builds cross-functional and cross-departmental support
- Influences and persuades so as to bring about technical and process improvements.
- 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 client's Policies and Procedures.
Technical Profile Requirements
- Deep knowledge and at least 3-5 years experience in equipment cleaning validation, clean room qualification and disinfection validation in the pharmaceutical industry
- High understanding of GMP, Compliance, Validation Practices including the system development life cycle and Regulatory expectations
If this role is the right fit, our dedicated and expert team is looking forward to hearing from you.
Good to know you!
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
IT Entwicklung, Ingenieurwesen/Technik