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Timestamp
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1786505971
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Fetch Consultant ID
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51
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Unique ID
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c189a
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Running No
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10137
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Method
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Solo
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Edit
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No
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Frontend
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True
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Role
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Consultant
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Requestor View
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No
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Status
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Accepted
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| Who's Hiring? |
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Consultant In Charge
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Kimberly Wong
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Company Profile
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Astrazeneca Singapore Pte Ltd
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UEN
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199002462M
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Client Manager
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Mohamed Osman – C – Valid
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Designation
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Global CAPEX Procurement
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Type of Placement
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Contract (KF)
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Urgency
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High
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Mode of Communication
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Email
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Visibility
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Publish
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Job Posting Date
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12/08/2026
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Posting Validity (Days)
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90
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| Job Posting Details |
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Enable AI
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No
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| Basic Details |
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Job Title
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DL SME
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Job Type
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Contract
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SSOC
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Other engineering professional n.e.c.
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Number of Headcount Required
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1
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Expected Date to Join
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01/10/2026
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Work Hours Per Week
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40
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Period
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Months
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No.
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12
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Salary Type
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Range
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Hide Salary
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No
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Negotiable
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Yes
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Currency
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SGD
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Min
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8,000
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Max
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10,000
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Period
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Monthly
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Add Allowance
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No
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| Entitlements |
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Work from home
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No
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Primary Work Location
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Singapore 339510
Singapore
Map It
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Classifications of Location
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Tuas
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Country
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Afghanistan
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| Job-Specific Details |
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Level of Competency
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Mid-senior Position
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Years of Relevant Experience
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8
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Classification
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Technical
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Sector
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Manufacturing
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Project Experience
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- Pharmaceutical Manufacturing
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Specialization
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- API / Drug Substance Engineering
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Professional Characteristics
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- Strong technical
- analytical
- problem-solving
- leadership
- stakeholder management skills
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Primary Responsibilities
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- Provide engineering design support for API production, including chemical warehouse, material transfers and logistics, purification, chromatography, evaporation, freeze dryers, reactors, filter dryers and solvent break tanks.
- Engage with key stakeholders to ensure their needs are understood and reflected in the Basic Design (BD).
- Prepare Project Technical Requirements Specifications for systems, specifying performance requirements and applicable standards.
- Ensure relevant specifications are provided to the Design Contractor.
- Define and agree with the Design Contractor the required design deliverables for BD and Detailed Design (DD).
- Review Contractor responses to Project Technical Requirements to ensure requirements are correctly incorporated.
- Attend project meetings as required.
- Ensure User Requirement Specifications (URS) are complete, technically correct and appropriate for C&Q execution, including CPP/CQA/CMA GMP, GEP and SHE requirements.
- Participate in procurement strategy for technical work packages, including contractor pre-qualification, selection and technical scope.
- Produce regular Design Assurance Reports to ensure ongoing technical alignment.
- Identify value engineering opportunities.
- Ensure key SHE and GMP requirements are reflected in design deliverables.
- Participate in SHE risk assessment activities and ensure appropriate mitigations are incorporated into the design.
- Provide technical guidance to Work Package Owner teams.
- Ensure technical solutions are aligned with customer, cost and schedule requirements.
- Provide input to project planning.
- Review and provide input on mechanical packages.
- Support development of redundancy strategy and maintenance philosophy.
- Review and provide input to the Sustainability Checklist.
- Respond to construction queries where the Design Contractor is unable to provide answers.
- Answer Design Contractor queries as required.
- Review Design Contractor enquiry specifications and participate in bid review/selection for relevant systems.
- Review sample drawings and calculations to ensure correct interpretation of project requirements.
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| Competencies |
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Minimum Qualifications
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Bachelor's Degree or equivalent
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Specify the Field of Study
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Yes
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Field of Study
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- Chemical Engineering
- Mechanical Engineering
- Pharmaceutical Engineering
- Process Engineering
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Language Spoken
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Language Written
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Key Skills
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Are the Key Skills selections good enough?
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Yes
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| Summary of Key Requirements |
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Summary of Key Requirements
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- Strong engineering experience in API / Drug Substance production and pharmaceutical manufacturing.
- Experience with relevant API production systems such as reactors, chromatography, evaporation, freeze dryers, filter dryers, solvent systems, chemical warehouses and material transfer/logistics.
- Experience supporting engineering design for pharmaceutical/API production facilities.
- Strong understanding of GMP, GEP and SHE requirements and their application in engineering design.
- Experience reviewing technical requirements, URS, design deliverables, drawings and calculations.
- Able to provide technical guidance to project/work package teams and design contractors.
- Experience with mechanical/process equipment packages and technical procurement activities is preferred.
- Strong communication, stakeholder management and technical review skills.
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Featured
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No
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On Hold
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No
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