Process Engineer (6 Month)

Job Type
Emp Type
Full Time
Construction and Engineering
Functional Expertise
Countries, Positions, Regions
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Job Description

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Process Engineer Singapore 6 months contract with extension

Location:               Singapore

Start Date:                  ASAP

Contract:               6 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