A Big Opportunity for ...
• Prepare cost estimates and manage capital expenditure within the budget.
• Ensure initiation of procurement of capital machinery through URS, conduct technical analysis of offers, and after successful FAT (Factory Acceptance Test), ensure smooth handover of machines followed by commissioning and qualification (both for process and utility areas) with the support of consultants and foreign technical experts or specialized teams.
In short, the incumbent will accomplish the job from conception to completion with necessary support from other departments.
• Coordinate with vendors and cross-functional teams such as QA, Production, and Commercial to meet project timelines and budgets.
• Work extensively and professionally with consultants (as applicable).
• Develop technical documentation, including CAD drawings, project plans, and specifications.
• Understand local government regulatory requirements for infrastructure and environment and obtain required approvals accordingly.
• Coordinate with consultants and technical experts to ensure that the facility complies with pharmaceutical cGMP, health & safety, and regulatory standards (e.g. WHO, Local Drug Authority, etc.).
• Arrange regular follow-up meetings, provide regular progress feedback to management, and escalate issues whenever required.
• Prepare cost estimates and manage capital expenditure within the budget.
• Ensure initiation of procurement of capital machinery through URS, conduct technical analysis of offers, and after successful FAT (Factory Acceptance Test), ensure smooth handover of machines followed by commissioning and qualification (both for process and utility areas) with the support of consultants and foreign technical experts or specialized teams.
In short, the incumbent will accomplish the job from conception to completion with necessary support from other departments.
• Coordinate with vendors and cross-functional teams such as QA, Production, and Commercial to meet project timelines and budgets.
• Work extensively and professionally with consultants (as applicable).
• Develop technical documentation, including CAD drawings, project plans, and specifications.
• Understand local government regulatory requirements for infrastructure and environment and obtain required approvals accordingly.
• Coordinate with consultants and technical experts to ensure that the facility complies with pharmaceutical cGMP, health & safety, and regulatory standards (e.g. WHO, Local Drug Authority, etc.).
• Arrange regular follow-up meetings, provide regular progress feedback to management, and escalate issues whenever required.