Job Reference: FRS61838
Job Duration:
Start date: ASAP
Description:
Key Responsibilities:
* Review and approve Site Acceptance Testing (SAT) and Computer System Validation (CSV) documentation.
* Generate and maintain status reports for the automation systems.
* Ensure compliance with cGMP and CSV standards.
* Oversee the resolution of automation system issues impacting C&Q.
* Successfully handover automation systemsto the client team.
Required Skills and Experience:
* Strong knowledge of cGMP and CSV principles.
* Familiarity with Rockwell ControlLogix PLC and Archestra SCADA systems.
* Excellent problem-solving skills and the ability to mitigate system issues effectively.
* Strong communication skills to interact with various teams and stakeholders.
* Ability to generate detailed reports and work plans.
* Experience in reviewing and approving technical documentation.
Preferred Qualifications:* Previous experience in a similar role within Pharma
* Relevant certifications or professional qualifications in automation or related fields
Industry: IT
Salary:
Salary Benefits:
Vacancy Type: Permanent
Job Skills: MES, Automation, Pharma
Contact Name: Fergus Kennedy
Website: -
Direct Application URL: -