Biopharma Process Engineer / Chemist — Hybrid (CCP)

Merck Gruppe - MSD Sharp & Dohme; Singapore; Hybrid; SGD 20,000 - 29,000; Part time

Benefits offered by this job

Hybrid work arrangement

Job summary

Merck Gruppe - MSD Sharp & Dohme in Singapore is seeking a Process Engineer/Chemist (WDA) to provide technical supply support on the commercialization and manufacture of drug products.

You will participate in investigations, validation, qualification, risk assessments and process safety, while contributing to continuous improvement and a global technical network to share site knowledge. The role also supports new product introductions and transfers between facilities.

Qualifications

• Bachelor’s degree in Chemistry, Biology, Pharmaceutical, or Chemical/Mechanical Engineering.
• Minimum 2 years of relevant experience from oil and gas, semiconductor, or manufacturing industries.
• Good verbal communication and technical writing skills.
• Attention to detail.
• Open to PMETs/Mid-Careerists with no prior biopharma experience.
• Singaporeans/PRs only.
• Two-year contract.

Responsibilities

• Supports all technical or process activities, e.g., investigations, validation and qualification processes, risk and impact assessments and process safety management activities.
• Supports continuous process improvement activities to enhance site performance metrics and contributes to the global company technical network to share site experiences and knowledge and continuously expands on personal expertise.
• Supports the introduction of new products to the site and the transfer of drug products to other facilities.

Skills

Biopharmaceutical Industry

Process Engineering

Chemical Engineering

Quality Assurance

Process Safety

Documentation

Process Validation

Education

Bachelor’s Degree in Chemistry, Biological, Pharmaceutical, and/or Chemical/Mechanical Engineering

Job description

Merck Gruppe - MSD Sharp & Dohme in Singapore is seeking a Process Engineer/Chemist (WDA) to provide technical supply support on the commercialization and manufacture of drug products.

You will participate in investigations, validation, qualification, risk assessments and process safety, while contributing to continuous improvement and a global technical network to share site knowledge. The role also supports new product introductions and transfers between facilities.