Formulation Chemist — Flexible Hours & Growth

Nomion Medicines

Yaur

On-site

IDR 1,070,399,000 - 1,482,091,000

Full time

5 days ago
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Benefits offered by this job

Flexible working hours
Attractive salary based on experience
30 days/year holiday
Full travel compensation
Young and energizing team

Job summary

Nomion Medicines, a dynamic startup, seeks a Formulation Chemist to design, develop, and optimize pharmaceutical formulations across multiple dosage forms. You will perform hands-on lab work—blending, granulation, and tableting—while designing experiments, interpreting data, and documenting all work per GMP standards.

Join a collaborative team, contributing to diverse projects with technical and scientific challenges.

Qualifications

  • Hands-on scientist with strong background in formulation development.
  • Experience designing, developing, and optimizing pharmaceutical formulations.
  • Experience in GMP or regulated settings preferred.
  • Ability to design and perform experiments independently.
  • Detail-oriented with emphasis on manufacturability and stability.

Responsibilities

  • Design, develop, and optimize pharmaceutical formulations across various dosage forms.
  • Hands-on lab work such as blending, granulation, and tableting.
  • Design experiments, interpret data, and document work according to GMP standards.
  • Collaborate with analytical chemists, QA, and project managers to ensure robust formulations.
  • Ensure formulations are robust, stable, and fit for purpose.

Skills

Hands‑on mindset
Formulation development
Experimental design
Data interpretation
Documentation accuracy

Education

BSc/MSc/PhD in Pharmaceutical Sciences or related field

Tools

GMP environment
Laboratory techniques

Job description

Nomion Medicines, a dynamic startup, seeks a Formulation Chemist to design, develop, and optimize pharmaceutical formulations across multiple dosage forms. You will perform hands-on lab work—blending, granulation, and tableting—while designing experiments, interpreting data, and documenting all work per GMP standards.

Join a collaborative team, contributing to diverse projects with technical and scientific challenges.

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