Pharmaceutical Validator
3 days ago
Parkville Location Job
Job Summary:
- Duration: One year (possibly extended)
- Number of roles: Two
- Team size: Ten
- Work arrangement: All onsite
- Working hours: Monday to Friday standard hours
- Reports to: Validation Manager
Key Responsibilities:
- Conduct validation activities associated with changes to existing plant, equipment, and processes and project validation activities as determined by the Validation Project Facilitation department to deliver successful validation outcomes for the business.
- Conduct validation activities in accordance with Quality Management System, Site Validation Master Plan, Business Improvement, and Validation procedures to meet requirements of all codes, regulations, and policies.
- Temperature mapping
- Media fills
- SOP updates
- Drafting protocols and reports.
Essential Qualifications:
- A relevant science or engineering tertiary qualification is required.
Preferred Qualifications:
- Experience in pharmaceutical manufacturing industry is highly desirable.
Required Skills:
- Sound knowledge of cGMP and validation principles.
- Good verbal and written communication skills.
- Good presentation, interpersonal, and time management skills.
- Strong customer focus.
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