Validation Engineer

South East  ‐ Onsite
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Description

A Validation Engineer is required to join a Pharmaceutical organisation based in the UK. This is a role that will require the successful Validation Engineer to provide on-going technical support to their fill finish facility, ensuring validation activities are in compliance to regulated standards.



Key Responsibilities:



- Generation, execution and review of life cycle validation documentation for commissioning of facilities, equipment and processes

- To ensure that all tasks and appropriate documentation is prepared, authorised and completed in a timely manner.

- To ensure that appropriate training records are maintained and communicate effectively with others on site and the clients associated with the project.

- Overseeing validation activities and maintain an understanding of current international regulatory, ISO, corporate and client requirements relevant to the section. Ensuring compliance with the sections, GMP requirements and company rules, policies and procedures.

- Liaising with the various departments involved in the qualification and validation work to ensure the efficient performance of the related tasks.

- To present qualification activities to an auditor



EH&S:



- Understand emergency procedures and comply with safe systems of work.

- Ensure compliance with environment, health and safety rules, signage and instructions at all times.

- Ensure prompt reporting and investigation of all accidents, near misses and breaches of rules.



Qualifications/Experience:



- Engineering degree in manufacturing, process, mechanical or electrical engineering or related discipline preferred.

- In-depth knowledge and understanding of cGMP.

- Dynamic, self-motivated, pro-active approach to taking on challenging assignments and have the ability to work with critical timelines.

- Outstanding communication skills, both written and oral, and the self-confidence to use these skills to convince others to buy-into proposals and plans.

- The drive and maturity to lead combined with the ability to support and interface effectively with projects and motivate cross-functional teams.



To learn more about this excellent opportunity to join a prestigious Global Pharmaceutical organisation and fulfil a unique and rewarding role, please send in your current CV
Start date
n.a
From
Quanta Consultancy Services
Published at
25.12.2015
Contact person:
Lee Mitchell
Project ID:
1043008
Contract type
Freelance
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