Cache of job #13900055

Job Title

Validation Engineer (Limerick)

Employer

Careerwise Recruitment

Location

Munster, Limerick

Description

VALIDATION ENGINEER required by CareerWise Recruitment for our multinational contact lens manufacturer in the Mid-West. Initial 12 month contract on offer. The VALIDATION ENGINEER will provide support for the validation activities associated with equipment, reagents, facilities, cleaning, test methods and environment. THE ROLE: * Serves as technical expert for the Validation process and responsibilities to ensure compliance. * 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 behaviour 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 authorised 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. REQUIREMENTS: * 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. * Must be able to lead and give direction to Validation Projects and Teams. * Individual must also be an active team member in Validation activities. * Qualification in an appropriate discipline (e.g. Engineering, Information Systems, or Life Science with additional IT qualification) with a broad technical/educational skills base. * Minimum of 2 - 5 years working in a regulated industry a minimum 2 of which has been spent carrying out validations. Please call JP O'Connor today for further information on 021 201 9097 or email: jpoconnor@careerwise.ie. CareerWise Recruitment (In Search of Excellence. CareerWise Recruitment specialises in the multinational sector in Ireland which predominantly encompasses the Medical Device, Sciences/Pharma and ICT industries. We also work into the Indigenous Engineering and Food Processing/Agri sectors. Established in 1999, CareerWise Recruitment is recognised by many of the major indigenous and multinationals companies to be one of Irelands leading specialist Technical and Executive Recruitment firms. We operate out of multiple locations in Ireland and have offices in Cork, Shannon, Galway and Dublin. Supporting Business Demands & Growth since 1999. CareerWise Recruitment accepts that you do not wish your CV to be forwarded to any client company without your prior consent and gives an absolute assurance that this wish will be respected at all times. This job originally appeared on RecruitIreland.com.

Date Added

2134 days ago

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