Csv & Quality Consultant (junior Consultant)

3 weeks ago


Singapur, Singapore Nityo Infotech Full time
At least Bachelor’s degree in technical discipline such as Engineering or Science or with experience relevant to the Job Description. Graduates of related discipline may also apply. · Fresh graduate with internship experience in pharmaceutical industry will be given preference. · Preferably with familiarity to the best practice / standards / regulations in the pharmaceutical industry. · Preferably with basic technical knowledge of at least one (1) software solution (PCS / DCS / SCADA / MES / LIMS) · Preferably with basic knowledge of at least one (1) industrially used programming language (Visual Basic / C++ / C# / Javascript) · 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.

Experience Required

2 - 3 Years

Industry Type

IT

Employment Type

Permanent

Location

Malaysia

Roles & Responsibilities

Perform risk-based commissioning, qualification and validation of computer / computerized systems and processes. · Executed / develop validation protocols using a risk-based approach that meets customer quality, regulatory requirements, and industry best practices. · Develop design review, risk assessment, system impact assessments, traceability matrix, protocols and reports that support the qualification and validation of computer / computerized systems and software solutions. · Perform quality review of all system lifecycle specifications and documents against customer global / local quality processes, regulatory requirements, and industry best practices. · Control and manage all project and system lifecycle specifications and documentation according to quality processes. · Be part of the team that designs, executes, and optimizes qualification / validation strategies for a variety of platforms and software solutions, 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.

Expertise & Qualification

At least Bachelor’s degree in technical discipline such as Engineering or Science or with experience relevant to the Job Description. Graduates of related discipline may also apply. · Fresh graduate with internship experience in pharmaceutical industry will be given preference. · Preferably with familiarity to the best practice / standards / regulations in the pharmaceutical industry. · Preferably with basic technical knowledge of at least one (1) software solution (PCS / DCS / SCADA / MES / LIMS) · Preferably with basic knowledge of at least one (1) industrially used programming language (Visual Basic / C++ / C# / Javascript) · 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.


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