Contract: Full Time.
Salary: Competitive (dependent on experience).
Conducting and maintaining of site cGMP validation activities
Supporting of validation activity during designing and commissioning of new equipment
Reviewing and maintaining validation documentation
Supporting production departments in validation activities for processes and equipment
BSC in Life Sciences or related field
Experience working in and managing Validation within a GMP biologics or
Excellent communication and organizational skills
I am looking forward to having a chat with you if you are suitable for this role. For more
information on this exciting opportunity please email a copy of your CV in MS WORD format to
email@example.com using Validation Specialist as the Subject.
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