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Timestamp
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1786505169
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Fetch Consultant ID
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51
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Unique ID
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e344a
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Running No
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10136
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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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DS SME
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Job Type
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Contract
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SSOC
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Process engineer
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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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- Drug Substance
- Process Engineering / Biopharmaceutical Engineering / mAb Process Engineering
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Professional Characteristics
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- Strong technical expertise in Drug Substance / mAb biopharmaceutical processes
- Experienced in translating technical requirements into engineering design deliverables
- Strong stakeholder management and communication skills
- Strong understanding of GMP/GEP/SHE and engineering requirements
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Primary Responsibilities
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- Provide engineering design support for mAb Drug Substance processes, including process equipment, buffer/media preparation, CIP, central dispensing/logistics and DS process utilities.
- Work closely with the design teams to develop designs and translate technical requirements into engineering deliverables.
- Work with site Operations and global technical teams to align technical requirements and provide technical direction to the design team.
- Attend design discussions and drive a risk-based design-to-cost approach.
- Support and review User Requirement Specifications (URSs) to ensure they are technically complete, correct and appropriate for C&Q execution.
- Review and approve URSs within the relevant technical area.
- Review and comment on engineering deliverables from design consultants and equipment suppliers.
- Attend supplier visits for critical equipment packages as required.
- Carry out periodic Design Assurance reviews (30%, 60%, 90%) and identify value engineering opportunities.
- Provide technical support for HAZOP, SWIFT and LOPA studies and ensure appropriate risk mitigation is incorporated into the design.
- Work with Work Package Owners and C&Q partners to ensure technically compliant delivery of equipment packages.
- Support procurement strategy for technical work packages, including contractor selection and technical scope.
- Review and approve DQ protocols for critical equipment packages.
- Ensure SHE, sustainability targets, SME engagement and company standards are incorporated into proposed solutions.
- Take on increasing responsibilities as the mAbs SME as global technical support is reduced.
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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
- Biochemical Engineering
- Bioprocess Engineering
- Pharmaceutical Engineering
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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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- Degree in Chemical Engineering, Biochemical Engineering, Bioprocess Engineering, Pharmaceutical Engineering or related discipline
- Relevant experience in pharmaceutical / biopharmaceutical engineering or process design
- Experience in Drug Substance / mAb processes is highly preferred
- Knowledge of process equipment including single-use bioreactors, chromatography, TFF, buffer/media preparation, CIP systems and DS utilities
- Experience with URS, engineering design reviews and DQ
- Experience supporting HAZOP, SWIFT, LOPA or similar risk assessments
- Experience working with design consultants, equipment suppliers and C&Q teams
- Good understanding of GMP, GEP and SHE requirements
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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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