Oral Formulation Scientist: From Lab to GMP

MSD Malaysia; Rahway (NJ); Presencial; USD 87 000 - 137 000; Tempo integral

Resumo da oferta

Merck & Co., Inc. in Rahway, New Jersey is seeking a pharmaceutical scientist to support formulation development from first-in-human stages through final market definitions.

You will work in a matrix team to design, develop, and scale drug product formulations, contributing to manufacturing process robustness. Qualifications include a BS/MS in Chemical/Biomedical/Pharmaceutical sciences and 2+ years in industry, with strong data analysis, MS Office, and software like JMP/Minitab/MATLAB.

Qualificações

• Bachelor's or Master's degree in Chemical Engineering, Biomedical Engineering, Pharmaceutical Sciences or related discipline with a minimum of 2 years relevant industrial experience.
• Experience applying scientific principles in lab or pilot plant environments.
• Strong data analysis and proficiency in MS Office and statistical software.

Responsabilidades

• Develops and applies basic principles to execute work in a lab or pilot plant to develop solid oral drug products.
• Lead manufacturing operations in non-GMP and GMP environments.
• Executes routine experiments and interprets data independently.
• Operate and troubleshoot equipment and processes.
• Collaborate within a matrix team from first-in-human formulations to final market formulation and process robustness.

Conhecimentos

Pharmaceutical industry experience

Independent data analysis

Strong verbal and writtencommunication

Microsoft Office

JMP

Minitab

MATLAB

Formação académica

Bachelor's or Master's in Chemical/Biomedical/Pharmaceutical sciences

Ferramentas

gSOLIDS

SolidWorks

ANSYS Polyflow

Descrição da oferta de emprego

Merck & Co., Inc. in Rahway, New Jersey is seeking a pharmaceutical scientist to support formulation development from first-in-human stages through final market definitions.

You will work in a matrix team to design, develop, and scale drug product formulations, contributing to manufacturing process robustness. Qualifications include a BS/MS in Chemical/Biomedical/Pharmaceutical sciences and 2+ years in industry, with strong data analysis, MS Office, and software like JMP/Minitab/MATLAB.