Process Engineer, PTO

4 hours ago

Singapore MSD Full time

Overview
Be part of the team that ensures sustainable products meet standard quality and are committed to deliver to customers worldwide. Based in Singapore, the regional hub for Asia Pacific (AP) and a top-ranked biopharmaceutical company on the Straits Times and Statista’s list of Best Employers in Singapore for three consecutive years (2020, 2021, 2023). Join the premier biopharmaceutical company that has been in Singapore for more than 25 years and in AP for over 60 years.
Job Title
Process Engineer
The Opportunity
Be part of the team that ensures sustainable products meets standard quality and committed to deliver to customers worldwide
Based in Singapore, the regional hub for Asia Pacific (AP) and top-ranked biopharmaceutical company on the Straits Times and Statista’s list of Best Employers in Singapore for three consecutive years (2020, 2021, 2023).
Join the premier biopharmaceutical company that has been in Singapore for more than 25 years and in AP for over 60 years.
Our Manufacturing Operations teams are the people that make our products. We work in the manufacturing plants with a “Safety First, Quality Always” mindset striving for continuous improvement. We work in the local plant connected to our global manufacturing network to ensure the highest quality of raw materials, intermediates and finished products.
Job Purpose
The PTO Process Engineer/Chemist provides technical supply support on the commercialization and manufacture of all drug products with minimal support from seniors or direct supervisor (seeking support/ escalating efficiently where needed). He/ she supports all technical/ process activities (for example) investigations, validation and qualification processes, risk assessments and process safety management activities under his/ her responsibilities.
What Will You Do
Supports new product introductions to the site by supporting and/or conducting process and equipment comparisons, new raw material introduction, development studies, clinical supplies manufacturing, cleaning processes development/validation and training of technicians as required. Authors PPQ protocols, reports and other associated documentation related to a new product introduction. Expected to have a basic knowledge of product development, scale-up and technical

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