Location:                                            Singapore

Start Date:                                         ASAP

Contract:                                            12 months contract likely to be extended

The Company

A service provider leading the Pharmaceutical and Medical Device sectors since 1998. A Company that is constantly growing and has over 2000 employees worldwide.

Roles and responsibilities

You will be expected to provide support in site process engineering, installation verification, pre-commissioning, SAT and commissioning of equipment/utilities/ancillaries, used in biotech facilities.

· Follow standard operating procedures and standards in a highly regulated

environment

· Generate and execute procedures/protocols through GMP verification process

· Adhere to safe work practices

· Clearly communicate progress and issues to management and peers and finalize

report writing for test protocols

· Perform all tasks in strict compliance with operating procedures, best practices, and

regulatory requirements

· Accountable for accurately completing GMP documentation

Candidate Requirements

· Chemical Engineering master degree

· At least 3 years related process engineering design experience, with preferred

experience in biotech, with understanding of automated process equipment, systems

architecture and operations, and related components

· Knowledge of cGMPs and main pharmaceutical standards and rules

· Knowledge of process control and P&IDs standard settings and ISA standard symbology

· Knowledge of safety current rules for equipment/ plants design and attention to health

and safety practices within the working environment

· Previous experience in equipment and process and equipment validation is helpful, but

not just focusing on this

· Technical expertise in GMP biotech processes that include upstream & downstream

manufacturing and clean utilities