Occupli is partnering with a leading multinational pharmaceutical manufacturing organisation to source an experienced Validation Engineer for a 12-month contract assignment.
This role will play a critical part in delivering validation activities across key projects with a strong focus on equipment performance qualification including cleaning and sterilisation processes.
Key Responsibilities:
Lead planning and execution of Equipment/Engineering Performance Qualification (EMPQ) activities
Develop Validation Master Plans and associated validation lifecycle documentation
Author and execute validation protocols and comprehensive summary reports
Analyse validation data and provide clear technical conclusions
Update and improve SOPs and validation documentation as required
Troubleshoot and resolve technical challenges during study execution
Collaborate effectively within cross-functional project teams while also operating independently
Requirements
Proven experience in EMPQ planning and execution within a regulated pharmaceutical manufacturing environment
Strong technical writing skills with a high level of documentation accuracy
Ability to work with minimal supervision and drive deliverables to completion
Confident communicator with strong problem-solving capability
Benefits
This is an excellent opportunity for a validation professional who thrives in a dynamic compliance-driven manufacturing environment and can deliver high-quality results with limited oversight.
Required Skills:
5 years experience in EHS within pharmaceutical biotech medical device chemical or other manufacturing environments. Developing knowledge of Construction Safety Process Safety and regulatory compliance. Ability to conduct basic risk assessments and support EHS documentation and reporting. Strong communication teamwork and problem-solving abilities.
Required Education:
Degree in Environmental Chemical Safety Engineering or a related technical field
Occupli is partnering with a leading multinational pharmaceutical manufacturing organisation to source an experienced Validation Engineer for a 12-month contract assignment.This role will play a critical part in delivering validation activities across key projects with a strong focus on equipment pe...
Occupli is partnering with a leading multinational pharmaceutical manufacturing organisation to source an experienced Validation Engineer for a 12-month contract assignment.
This role will play a critical part in delivering validation activities across key projects with a strong focus on equipment performance qualification including cleaning and sterilisation processes.
Key Responsibilities:
Lead planning and execution of Equipment/Engineering Performance Qualification (EMPQ) activities
Develop Validation Master Plans and associated validation lifecycle documentation
Author and execute validation protocols and comprehensive summary reports
Analyse validation data and provide clear technical conclusions
Update and improve SOPs and validation documentation as required
Troubleshoot and resolve technical challenges during study execution
Collaborate effectively within cross-functional project teams while also operating independently
Requirements
Proven experience in EMPQ planning and execution within a regulated pharmaceutical manufacturing environment
Strong technical writing skills with a high level of documentation accuracy
Ability to work with minimal supervision and drive deliverables to completion
Confident communicator with strong problem-solving capability
Benefits
This is an excellent opportunity for a validation professional who thrives in a dynamic compliance-driven manufacturing environment and can deliver high-quality results with limited oversight.
Required Skills:
5 years experience in EHS within pharmaceutical biotech medical device chemical or other manufacturing environments. Developing knowledge of Construction Safety Process Safety and regulatory compliance. Ability to conduct basic risk assessments and support EHS documentation and reporting. Strong communication teamwork and problem-solving abilities.
Required Education:
Degree in Environmental Chemical Safety Engineering or a related technical field
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