Automation Validation Engineer

Full Time Permanent

Global Pharmaceutical Manufacturer seeks an experienced Automation Validation Engineer.

About the role:

As an Automation Validation Engineer, you will be a key member of the team, leading the execution and documentation of validation activities performed during the qualification of equipment and automated Inspection systems utilised for sterile product manufacture.

Working within the guidelines of cGMP, you will be responsible for the generation of accurate protocols and reports and ensuring that all work is performed within production time constraints.

Skills and experience:

You will have an enthusiastic approach, coupled with strong organisational and communication skills. You will have a sound understanding of pharmaceutical technology and its respective validation requirements.
You will also have excellent technical authorship skills to develop validation documentation, policies and procedures.
Experience with automated manufacturing systems and visual inspection systems would be advantageous (Brevetti, Marchesini, Bosch)
We would like you to be educated to Degree standard (or equivalent) in a Scientific or Engineering discipline. You may have worked for similar aseptic manufacturing pharmaceutical companies. It is essential to have previous experience and an understanding of pharmaceutical equipment and validation requirements. Sound documentation and numeracy skills are also essential, in addition to an excellent eye for detail and a continuous improvement mind set


Looking for more jobs listings visit our website Bird Online Jobs  Search over 200,000 live job vacancies updated daily. Get noticed by over 10,000+ potential employers upload your CV to our partner site here