Process Development Engineer

ArrowBiome Pte. Ltd.

Singapore

On-site

SGD 70,000 - 110,000

Full time

6 days ago
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Job summary

ArrowBiome Pte. Ltd. in Singapore seeks a Process Development Engineer to support in-house manufacturing and development of biologically active ingredient processes and particle-based formulations.

You will run bench-scale operations, document batches, and contribute to scale-up and transfer readiness, with a focus on reliability and reproducibility. Candidates should hold a relevant science degree and have up to 5 years of lab experience, with strong emphasis on experimental discipline and data

Qualifications

  • Bachelor-level degree in chemistry, polymers, materials science, chemical engineering, pharma or biology.
  • Up to 5 years' relevant lab experience is desirable.
  • Internship or final-year project work is considered.

Responsibilities

  • Run bench-scale formulation and particle-processing activities per procedures.
  • Deliver batches safely and reproducibly, including multi-day experiments.
  • Characterise samples and perform in-process testing (moisture, particle size, microscopy).
  • Maintain lab equipment, calibration, consumables and safety practices.
  • Troubleshoot routine issues and raise deviations when needed.
  • Maintain accurate batch records and support change-control activity.

Skills

Lab formulation
Batch execution
Characterisation
Lab safety
Troubleshooting

Education

Bachelor's degree in Chemistry/Polymer/Materials Science or related

Tools

Electronic lab notebooks

Job description

The bench work that turns validated science into a product you can make the same way, batch after batch, at growing volume.

Careers / Open positions · Process Development Engineer

Biopolis, Singapore Operations · Process Development Full-time · Permanent · On-site

ArrowBiome is a Singapore biotechnology company developing science-based solutions for microbiome management. We combine biotechnology, formulation science and disciplined process development to translate laboratory research into reproducible, scalable products. This role sits at the exact point where that translation happens.

The role, in one sentence

You support in-house laboratory manufacturing and process development across a biologically active ingredient process and a particle-based formulation process — and you make the batches reliable, reproducible and well documented.

Why this seat exists, and why now

Our platforms are validated and our first products are in market. Demand is growing, and with it the volume of in-house laboratory manufacturing we run — across a biologically active ingredient process and a particle-based formulation process. This role adds dedicated engineering capacity to that bench.

The immediate priority is reliable, reproducible and well-documented in-house batches. As the process matures, the role extends into optimisation, scale-up and manufacturing-transfer support — so the work you do in the first months becomes part of the foundation for how we manufacture at volume.

Now — in-house manufacturing & process development
  • Run the bench. Execute laboratory-scale formulation and particle-processing activities per approved procedures and safety requirements.
  • Deliver batches, safely and repeatably. Run routine batches safely and reproducibly, including multi-day experiments, with increasing independence.
  • Characterise and test. Perform physicochemical characterisation and in-process testing — moisture, particle size and distribution, microscopy, viscosity.
  • Own the lab and its safety. Maintain lab equipment, calibration schedules and consumables; own EHS practice including solvent and powder handling, and risk assessments.
  • Troubleshoot, and elevate honestly. Resolve routine issues within authorised limits, and raise deviations promptly rather than absorbing them.
As we scale — optimisation & transfer readiness
  • Keep the record straight. Maintain accurate batch records, equipment logs and deviation documentation; support batch-record and change-control practice.
  • Make batches comparable. Produce structured, traceable process records that can be compared across batches, with quantitative acceptance criteria.
  • Prepare the handover. Support approved optimisation and reproducibility studies, and contribute to specifications for future scale-up and transfer.

Required

The foundation

A bachelor's degree in Chemistry, Polymer or Materials Science, Chemical Engineering, Pharmaceutical or Biological Sciences, or a related field — and up to 5 years' relevant lab experience. Strong internship or final-year project work is genuinely considered.

Required

The technical core

Experience in protein production (expression and purification), or a strong foundation in it. Sound fundamentals in particles, colloids, dispersions or formulation.

Required

The habits

Careful experimental technique, disciplined record-keeping, and safe solvent and chemical handling. Familiarity with particle or physicochemical characterisation methods, including an understanding of their resolution limits.

A strong advantage

None of these are gates. Each one shortens your runway, and we would rather tell you which than leave you guessing.

  • Industrial protein production. Expression and purification in an industrial, pilot or scale-up setting.
  • Unit operations. Filtration, purification, concentration or drying.
  • Repeat-batch discipline. Repeat-batch operations or pilot-scale manufacturing, and ISO- or GMP-style documentation.
  • Structured data. Electronic lab notebooks, structured data tools, or basic statistics and DOE.

What good looks like in this role

Someone outside the company can pick up your batch records and understand exactly what was made, how, and whether it met specification — without asking you. That is the standard we work to, and it is why we hire for judgement and discipline as much as for technique.

At a glance

Detail

Employment Full-time, permanent

Location On-site, Biopolis, Singapore

Level Up to 5 years' experience

Reports into R&D and operations, working closely with the CTO

Employment is subject to valid authorisation to work in Singapore and satisfactory reference checks. Remuneration, leave, benefits and other terms are governed by the final employment contract, company policy and applicable Singapore law. This advertisement is not an employment contract; duties may be reasonably adjusted to meet operational requirements. Applicant privacy: personal data submitted is collected, used and disclosed only as necessary to assess your application and meet legal obligations — please do not include NRIC number, date of birth, marital or family status, photographs or medical information at this stage.

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