
Senior Validation Specialist
2 weeks ago
Job Overview
We are seeking a Validation Professional to provide support for projects and maintain schedules for initiatives involving validation.
Key Responsibilities:
- Plan, coordinate and execute validation activities according to quality management systems and site validation master plans.
- Perform validation tasks for project work.
- Deliver CSV computer systems validation results including reports, plans and specifications.
- Coordinate all computer systems validation activities including drafting and reviewing key validation documentation.
- Review various regulatory risk assessments and protocols related to computer system validation practices.
- Effectively collaborate with local and global stakeholders.
Requirements:
- Relevant tertiary qualifications in Science, Engineering or Computer Science.
- Specific experience in validation within the pharmaceutical/medical device industry within a GMP environment.
- Strong understanding of computerised systems validation or process validation in the pharmaceutical industry.
- Excellent verbal and written communication skills.
- Good presentation, interpersonal and time management skills.
Opportunities:
This is an excellent opportunity for a skilled professional to develop their skills and experience in CSV and be involved in diverse local and global projects.
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