Perform risk-based commissioning, qualification and validation of pharmaceutical and biopharmaceutical equipment, utilities and process.
Executed / develop validation protocols using a risk-based approach that meets regulatory requirements and industry best practices.
Develop risk assessment, system impact assessments, protocols and reports that support the qualification and validation of process and utility systems.
Be part of the team that review, analyse, interpret, and summarize system and process performance data of executed activities for report and presentation to management.
Be part of the team that investigate deviations, write investigation reports and create summary reports.
Exercise good judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions.Professional Skills and Experience:
At least Bachelor's degree in technical discipline such as Engineering or Science or with experience relevant to the . Graduates of related discipline may also apply.
1 - 3 years of relevant experience in Pharmaceutical industry.
Fresh graduate applicant is welcome but preferably with internship experience in pharmaceutical industry.
Preferably with familiarity to the best practice / standards / regulations in the pharmaceutical industry.
Preferably with good knowledge of Validation Lifecycle approach (URS, FAT/SAT, commissioning, I/O/PQ Protocols, etc), guidelines, international regulatory requirements and other industry best practices.Offering:
Consulting roles for international healthcare clients in strategically relevant projects.
Work in a professional consultancy environment within a highly motivated team.
Opportunity to take on responsibility and to help shape our organization.
Excellent career development and growth opportunities in a growing premier consulting organization.
Structured training program and peer mentoring system to support competence and personal growth.
Not Specified
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