EHS & GMP Compliance Manager - Biotech R&D

Morimatsu LifeSciences

Singapore

On-site

SGD 80,000 - 110,000

Full time

14 days+
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Job summary

Morimatsu Group is expanding internationally and seeks an R&D Engineer to lead or support the design of processes and equipment for biotech and pharmaceutical products. The role involves creating design documentation, defining standards, and collaborating with suppliers and project teams.

The candidate should have 5+ years in bio-pharma, strong English, and travel flexibility to support global initiatives and regulatory compliance.

Qualifications

  • MSc/BSc in chemical/biochemical/pharmaceutical/biotech engineering or similar.
  • 5+ years in bio-pharmaceutical/pharma; biotech experience preferred; R&D in bio USP/DSP, fill & finish, pharma production management, GMP.
  • Experience with international teams or customers.
  • Fluent English; Chinese a plus.
  • Willingness to travel domestically and internationally.
  • Familiar with engineering software such as AutoCAD, COMOS, ASPEN, NavisWorks.

Responsibilities

  • Lead or support R&D or construction projects in biotech/pharma.
  • Develop and review design docs: layouts, P&IDs, process descriptions, production capacity calculations.
  • Define equipment standards and specs.
  • Perform risk analysis and post-evaluation.
  • Develop product documentation and support patents.
  • Promote standardization; contribute to SOPs.
  • Interact with suppliers and conduct functional tests.
  • Attend trainings and seminars to learn new technologies.

Skills

Fluent English
Communication
Team collaboration
Independent work
Willing to travel

Education

MSc/BSc in chemical/biochemical/pharmaceutical/biotech engineering

Tools

AutoCAD
COMOS
ASPEN
NavisWorks

Job description

Morimatsu Group is expanding internationally and seeks an R&D Engineer to lead or support the design of processes and equipment for biotech and pharmaceutical products. The role involves creating design documentation, defining standards, and collaborating with suppliers and project teams.

The candidate should have 5+ years in bio-pharma, strong English, and travel flexibility to support global initiatives and regulatory compliance.

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