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Process Engineer (Biologics Manufacturing)

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Amaris Consulting

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Location:
Singapore , Singapore

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Category:

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Contract Type:
Not provided

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Salary:

Not provided

Job Description:

Your missions: Support end-to-end manufacturing processes for biologics production (drug substance); Monitor and optimize process performance to ensure efficiency, quality, and compliance; Troubleshoot process deviations and implement corrective and preventive actions (CAPA); Collaborate with cross-functional teams including Production, Quality, Validation, and Engineering; Contribute to process validation activities and continuous improvement initiatives; Ensure adherence to GMP, safety, and regulatory requirements; Support documentation including SOPs, batch records, and technical reports. Your profile: Bachelor’s degree in Chemical Engineering, Biotechnology, Bioprocess Engineering, or related field; 2–5+ years of experience in biopharmaceutical or biologics manufacturing (); Strong understanding of GMP and regulatory standards; Experience in drug substance processes such as fermentation, purification, or filtration; Familiarity with process validation and troubleshooting in a manufacturing environment; English fluent; You demonstrate strong analytical and problem-solving skills; You demonstrate the ability to work in a fast-paced, cross-functional environment. What we offer: An international community, bringing together 110+ different nationalities; An environment where trust has a central place: 70% of our key leaders started their careers at the first level of responsibilities; A robust training system with our internal Academy and 250+ available modules; A vibrant workplace that frequently gathers for internal events (afterworks, team buildings, etc.); At Mantu, sustainability is part of everything we do. You’ll have the opportunity to turn your ideas into action and make a tangible impact. Every day, our teams bring our ESG commitments to life, from reducing our footprint to driving positive change within our communities. Through our WeCare Together program, you’ll be empowered to design and lead projects that create real social or environmental impact, with the company’s full support. Amaris Consulting is proud to be an equal-opportunity workplace. We are committed to promoting diversity within the workforce and creating an inclusive working environment. For this purpose, we welcome applications from all qualified candidates regardless of gender, sexual orientation, race, ethnicity, beliefs, age, marital status, disability, or other characteristics.

Job Responsibility:

  • Support end-to-end manufacturing processes for biologics production (drug substance)
  • Monitor and optimize process performance to ensure efficiency, quality, and compliance
  • Troubleshoot process deviations and implement corrective and preventive actions (CAPA)
  • Collaborate with cross-functional teams including Production, Quality, Validation, and Engineering
  • Contribute to process validation activities and continuous improvement initiatives
  • Ensure adherence to GMP, safety, and regulatory requirements
  • Support documentation including SOPs, batch records, and technical reports

Requirements:

  • Bachelor’s degree in Chemical Engineering, Biotechnology, Bioprocess Engineering, or related field
  • 2–5+ years of experience in biopharmaceutical or biologics manufacturing
  • Strong understanding of GMP and regulatory standards
  • Experience in drug substance processes such as fermentation, purification, or filtration
  • Familiarity with process validation and troubleshooting in a manufacturing environment
  • English fluent
  • You demonstrate strong analytical and problem-solving skills
  • You demonstrate the ability to work in a fast-paced, cross-functional environment
What we offer:
  • An international community, bringing together 110+ different nationalities
  • An environment where trust has a central place: 70% of our key leaders started their careers at the first level of responsibilities
  • A robust training system with our internal Academy and 250+ available modules
  • A vibrant workplace that frequently gathers for internal events (afterworks, team buildings, etc.)

Additional Information:

Job Posted:
April 23, 2026

Employment Type:
Fulltime
Work Type:
On-site work
Job Link Share:

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