Process Engineer, PTO at MSD
Singapore, , Singapore -
Full Time


Start Date

Immediate

Expiry Date

08 Dec, 25

Salary

0.0

Posted On

09 Sep, 25

Experience

1 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Lean Manufacturing, Manufacturing, Equipment Qualification, Process Engineering, Process Optimization, Raw Materials, Process Control, Process Safety, Product Introduction, Regulatory Compliance, Capital Projects, Continuous Improvement

Industry

Pharmaceuticals

Description

Job Description

REQUIRED SKILLS:

Applied Engineering, Applied Engineering, Capital Projects, Contractor Oversight, Driving Continuous Improvement, Engineering Standards, Equipment Qualification, Estimation and Planning, GMP Compliance, GMP Validation, Lean Manufacturing, Manufacturing, Manufacturing Quality Control, Manufacturing Scale-Up, New Product Development, New Product Introduction (NPI), Process Control, Process Engineering, Process Optimization, Process Safety, Process Scale Up, Product Development, Product Portfolio Management, Raw Materials, Regulatory Compliance {+ 5 more}

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Responsibilities

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 transfer, key supporting documentation and associated regulatory requirements. Demonstrates ability in technical writing for investigations, change request, PPQ reports and CMC sections.
  • 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 during experiment/evaluation.
  • Support site and divisional capital projects and new facility start-up activities if applicable. Provide technical input to the process design to ensure it is fit for purpose for routine manufacturing in collaboration/support from colleagues. Responsible to transfer the knowledge of the project and facility to Integrated Process Team (IPT) colleagues.
  • Provides technical support related to the product, equipment and manufacturing/cleaning processes in response to deviations/product complaints/adverse events to identify point of occurrence, root cause and corrective/preventative actions.
  • Provide technical support for compliance activities such as audit and regulatory support. Collects data and documents to be presented to regulators during site inspections and for regulatory submissions. Demonstrates an understanding of the manufacturing lifecycle of a product including technical requirements, analytical regulatory guidelines/expectations associated with global regulatory submissions.
  • Supports product portfolio activities. Examples (but not limited to) include managing documentation updates, SOPs, batch sheets, recipes), quality risk assessments, change control management/filing support (if applicable) and validation activities such as equipment qualification, simple process validation and cleaning validation/monitoring activities. Expected to have a basic knowledge of respective compliance topics related to the above-mentioned activities and Quality by Design (QbD) and executes the requirements in support of a QbD filing where applicable.
  • Support routine supply manufacture by providing ongoing technical support to the IPT, participates in Tier processes and implement opportunities for improvement utilizing Production Systems tools. Support the activities and Quality by Design and executes the requirements in support of a QbD filing where applicable.
  • Supports routine supply manufacture by providing ongoing technical support to the IPT, participates in Tier processes and implement opportunities utilizing Production System tools. Support the activities to ensure optimum production runs, constraints and non-conformance identification and troubleshoots to resolve basic issues in production system.
  • Proactively monitors the performance of process parameters, critical quality attributes and equipment/module/unit operations performance during manufacturing and cleaning. Participates in Prospective Process Analysis (PPA), statistical analysis and response to shifts and trends in process performance. In addition, participates in Continued Process Verification and Annual Product Review activities as part of product lifecycle management. Demonstrates basic knowledge of statistical and risk analysis tools to identify action required to ensure product robustness across various types of manufacturing equipment and processes. Demonstrates understanding of product CPP, CQA, CpK and where applicable, sterile boundary of the current validated processes. Familiar with raw materials and PCC (product contact components) used for the products under his/her responsibility.
  • Participates in the collaboration and sharing of best practices across global company network.
  • Complies with all divisional and site-specific policies, guidelines and procedures. Demonstrates and promotes Environmental, Health and Safety (EHS) leadership behaviours, ensuring that all activities are carried out in accordance with EHS requirements. Actively participates in GEMBA safety walks. participates in process hazard analysis (PHA), and applicable process safety management (PSM) activities related to the new/inline products.
  • Where applicable, develops SOPs, gap analyses and procedures for Quality/EHS subsystems/topics in compliance with regulatory requirements, divisional and corporate policies and guidelines.
  • Demonstrate leadership behaviours in alignment with Company Leadership standards (Individual Contributor). Practices Inclusion as the How. Engages in personal career development with manager assistance through annual Performance Management Process (PMP), Employee Development Plan (EDP) and career mapping.
  • Any other duties as assigned by the Supervisor.
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