DPS Engineering

What is Validation?

Validation is the key verification process across all technical areas within a Pharmaceutical / Biologics Manufacturing Facility. It defines how the regulations which govern the manufacture of Pharmaceuticals / Biologics are applied and interpreted. A practical understanding of Validation is an essential requirement to assume technical roles in a Pharmaceuticals / Biologics Manufacturing Facility.

Are these programmes recognized in Singapore. (Certification)?

DPS has developed a series of training programmes aligned to the Singapore Workforce Skills Qualifications (WSQ) for Biomedical Manufacturing, validated by the major industry representatives. Candidates will be awarded Statement of Attainment (SOA) for each module successfully completed.

What will my new role / title be in the Pharmaceutical/Biologics Manufacturing Industry?

Your role will be dependant on your skills and experience to date from working within a process driven environment. However, all people coming from another industry may need to adapt and make the necessary adjustments when first entering the Pharmaceutical/Biologics Manufacturing industry. It is important to note that this is a technical programme for those who want to work in the technical areas of a Pharmaceutical/Biologics Manufacturing facility such as in the Production, Engineering, Quality, Technical Services and Validation Department.

Is there an age limit on this programme?

There is no maximum age limit on this programme.

Where is the training held?

The venue is DPS Training Centre / Singapore Polytechnic.

How many people per class?

There are 15-20 students per class.

Who are the lecturers?

The lectures are delivered by industry specialists who have worked in technical roles within the Pharmaceutical/Biologics industry at a senior level for many years and can provide practical examples of what happens in a Pharmaceutical/Biologics Manufacturing Facility.

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