Validation Engineer

Vertragsart:
Vor Ort
Start:
keine Angabe
Dauer:
keine Angabe
Von:
Harvey Nash IT Recruitment Switzerland
Ort:
Bern
Eingestellt:
01.08.2015
Land:
flag_no Schweiz
Projekt-ID:
957363

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For 2 different projects in Bern and Oberdorf, Baselland we are looking for 2 Validation Engineers with process validation experience of manufacturing devices.

Position: Validation Engineer (process validations)

Location: Oberdorf, Baselland and Bern

Start date:

End date:

Remediation of Validation Systems:

To provide support for the validation activities associated with equipment, reagents, facilities, cleaning, test methods, and environment ensuring that all compliance issues and requirements of company Validation Policies and Procedures are addressed. Process validations of manufacturing devices.

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 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 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. 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
. Minimum of 2 years working in a regulated environment a minimum 1 of which has been spent carrying out validation and/or testing activities.
. A degree in an appropriate discipline (eg Engineering, Information Systems, or an IT qualification) with a broad technical/educational skills base and substantial related experience
. Minimum of 2 - 5 years working in a regulated industry a minimum 2 of which has been spent carrying out validations.
. Experience in validation of manufacturing process in medical device and pharma environment
. Experience with processes occurring in clean rooms
. German and English spoken and written
. Ideally with a history of previous assignments at specialist Medical Device companies