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Process Engineer

Salary undisclosed

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Process Engineer – Singapore – 12 months contract with extension

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 expected to provide support in site process engineering, installation verificiation,

pre-commissioning, SAT and commissioning of equipment/utilities/ancillaries, used in

biotech facilities.

You will also be required to:

 Be responsible for documentation development, SOP drafting, sequence of operation

optimization and documentation

 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

 Provide feedback to leadership regarding potential issues and concerns with

documentation

 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

 Ability to manage priorities, deliverables, and scheduled milestones

 Requires strong interpersonal, verbal communication, and technical writing skills

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