Global Pharmaceutical Manufacturer seeks an experienced CSV Validation Specialist.
About the role:
As the Validation Specialist you will be a key member of the team, leading the execution and documentation of validation activities performed during the qualification of computerised systems utilised for sterile product manufacture. Working within the guidelines of cGMP and GAMP, 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:
An enthusiastic approach, coupled with strong organisational and communication
A thorough understanding of pharmaceutical technology and its respective computerised systems validation requirements. Excellent technical authorship skills to develop validation documentation, policies and procedures. Educated to Degree standard (or equivalent) in a Scientific or Engineering
Experience in working for similar aseptic manufacturing pharmaceutical companies. It is essential to have previous experience and an understanding of pharmaceutical equipment and validation requirements, including automated system validation. Sound documentation and numeracy skills are also essential, in addition to an excellent eye for detail