MSD Senior Engineer Pharmaceutical Technical Operations PTO Biotech 

Singapore, Singapore 

208026899

Job Description

• Develop strategies that alignwith business imperatives

• Based in Singapore, the regional hub forAsia Pacific (AP)andtop-ranked biopharmaceutical company on the Straits TimesandStatista’s list of Best Employers in Singapore for two consecutive years (2020, 2021).

• Join thepremier biopharmaceutical companythat has beenin Singapore for more than 25 years and in AP for over 60 years.

Our Engineers support internal and external manufacturing operations remain operational, continuously improve and innovate. With our extensive range of facilities and environments, our Engineers have opportunities across many diverse areas including Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development, Technical Services, Utilities and Validation.

Critical Responsibilities but not limited to:

• Supports or lead with guidance, new product introductions to the site by conducting process and equipment comparisons, new raw materials introduction, development studies, clinical supplies manufacturing, cleaning processes development/ validation and training of technicians as required. Authors protocols, reports and other associated documentation related to a new product introduction. Demonstrates strength in technical writing.

• Is involved in/supports the design and execution of small/ full scale experiments using appropriate methodology and/or simulations for products/ processes to evaluate the impact of proposed changes to validated equipment/ processes. Proactively identify solutions with support from seniors or direct supervisor to address issues that arose duringexperiment/evaluation.

• Provides technical guidance in support of site and divisional capital projects and new facility start-up activities. Ensures that the process design is well thought-out and robust for routine manufacturing.

• Provide technical input independently to the process design to ensure its fit for purpose for routine manufacturing. Responsible to transfer the knowledge of the project and facility to operations colleagues.

• Provides support to product, equipment andmanufacturing/cleaningprocesses in response to deviations/ product complaints/ adverse events to identify point of occurrence, root cause and corrective/ preventative actions.

• Provides support for compliance activities such as audit and regulatory support. Monitors and addresses potential regulatory risks during various phases of the lifecycle process as part of a team.

What you must have:

To be successful in this role, you will have:

Bachelors, Masters or Ph.D. degree in a technical field, including Chemical or Mechanical Engineering, Chemistry, Biological sciences or Pharmaceutical Sciences.

3 to 5 years technical experience in pharmaceutical, oil and gas or semiconductor industries.

WHAT YOU CAN EXPECT

• Limitless opportunities across various areas in Manufacturing; well-structured career path

• A state-of-the-art facility that delivers solution to its customers world-wide

• Highly engaging team that aims to innovate the future

What we look for…

Current Contingent Workers apply

Not Applicable

Accountability, Accountability, Adaptability, Applied Mathematics, Biomedical Sciences, Capital Projects, Cell Culture Process Development, Construction Cost Estimating, Continual Improvement Process, Data Analysis, Engineering Standards, Estimation and Planning, Healthcare Innovation, Maintenance Supervision, Manufacturing Processes, Manufacturing Quality Control, Mechatronics, New Product Development, New Product Introduction Process, Process Improvements, Product Development, Product Formulation, Product Lifecycle, Risk Control Assessment, Safety Management {+ 2 more}

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