Description
Validation engineer required for an initial 6 month contract for a global pharmaceutical company located in the South East.The Validation specialist will be responsible for the generation, execution and review of life cycle validation documentation for commissioning of facilities, equipment and processes.
Role and responsibilities:
. To ensure that all documentation is prepared, authorised and completed in a timely manner.
. To ensure that all tasks are carried out in an effective and efficient manner.
. To ensure that appropriate training records are maintained.
. To communicate effectively with others on site and the client associated with the project.
. To supervise work of those undertaking validation activities
. To maintain an understanding of current international regulatory, ISO, corporate and client requirements relevant to the section, to ensure compliance with the sections and site procedures.
. To liaise with the various departments involved in the qualification and validation work to ensure the efficient performance of the related tasks.
. To ensure that adequate training has been received and documented
. To present qualification activities to an auditor
. Comply with GMP requirements and company rules, policies and procedures.
Qualifications/Experience:
. In-depth knowledge and understanding of cGMP.
. Dynamic, self-motivated, pro-active approach to taking on challenging assignments.
. Creativity, judgement and analytical thinking.
If this is you please apply today.