Validation Technologist
- Recruiter
- Confidential
- Location
- Salisbury
- Salary
- Competitive
- Posted
- 14 Sep 2020
- Closes
- 22 Sep 2020
- Sectors
- Health, Nursing & Social Care
- Contract Type
- Permanent
- Hours
- Full Time
GxP Recruitment invites applications on behalf of our biopharmaceutical client in Wiltshire where an excellent opportunity has arisen for a Validation Technologist to join their team on a permanent basis.
Job Purpose:
The post holder will be required to write, review and where appropriate approve validation reports prior to execution, followed by report generation. The core activities will include
• Autoclaves (BSEN 285)
• Depyrogenation ovens
• Extraction Tanks
• Centrifuges
• Vessels
And Facilities and utilities.
Key duties include:
* Generate, review (technical) and execute process validation protocols
* Create validation reports
* Using the Electronic Quality Management System (master control) to manage appropriate corrective action plans and report through the non-conformance system, for failures/performance issues.
* Write and review Risk assessments
* Manage work schedule as planned by the validation schedule co-ordinator
* Coordinate Contractor or permanent resources to deliver timely documentation in support of Validation activities
* Ensure Validation procedures are aligned with regulatory requirements
* Meet all internal regulatory training requirements (internal training provided)
The ideal candidate:
* Degree qualified in relevant field
* Previous biopharma-based experience ideally
* BSEN-285 Sterilisation. Steam sterilisers. Large Sterilisers would be beneficial
* Equipment validation
* Understanding of the validation life cycle
* PC literate
Job Purpose:
The post holder will be required to write, review and where appropriate approve validation reports prior to execution, followed by report generation. The core activities will include
• Autoclaves (BSEN 285)
• Depyrogenation ovens
• Extraction Tanks
• Centrifuges
• Vessels
And Facilities and utilities.
Key duties include:
* Generate, review (technical) and execute process validation protocols
* Create validation reports
* Using the Electronic Quality Management System (master control) to manage appropriate corrective action plans and report through the non-conformance system, for failures/performance issues.
* Write and review Risk assessments
* Manage work schedule as planned by the validation schedule co-ordinator
* Coordinate Contractor or permanent resources to deliver timely documentation in support of Validation activities
* Ensure Validation procedures are aligned with regulatory requirements
* Meet all internal regulatory training requirements (internal training provided)
The ideal candidate:
* Degree qualified in relevant field
* Previous biopharma-based experience ideally
* BSEN-285 Sterilisation. Steam sterilisers. Large Sterilisers would be beneficial
* Equipment validation
* Understanding of the validation life cycle
* PC literate