Validation Engineer Senior 35383J


Category: Pharmaceutical / Science
Job Type: Contract

Posted on:
Last Updated:

JobTitle Validation Engineer Senior 35383J

About Company  Our client based in Limerick is seeking a Validation Engineer Senior to join its expanding team.

Duration of Role 12 months

Summary Objective 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 Johnson & Johnson Validation Policies and Procedures are addressed.

Job Duties 

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 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 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.

Requirements
no visa processing

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 years working in a regulated environment a minimum 1 of which has been spent carrying out validation and/or testing activities.

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.

Benefits
Benefits of working with Independent Solutions

> Excellent Team of Colleagues

> Access to high-value projects

> Excellent Technical Project Managers

> Excellent pay & conditions

 

Independent Solutions are Approved Suppliers for Multinational Pharma Biotech, Medical Device, clients with locations based here in Ireland.

At Independent Solutions, we will not require you to become an employee of Independent Solutions, we will facilitate and support you to become an independent contractor, thereby reaping the maximum rewards from your contract role.

We work in the area, we know the business, we are not a recruitment agency!

We continue to partner and grow our client base and thereby ensure that we have continuous supply of excellent roles

Yes, of course we benefit from having YOU with US, but we can assure YOU that YOU too will benefit …

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