Associate Engineer
About this opportunity
Position: Associate Engineer
Location: Tuas, Singapore
About the Job
The Manufacturing team is expanding and seeking an Associate Engineer, Manufacturing – Downstream (Process) to support routine downstream biopharmaceutical manufacturing operations, with a focus on process robustness.
The Associate Engineer, Manufacturing – Downstream (Process) supports day‑to‑day downstream manufacturing operations by ensuring that downstream processes (e.g, seed train, cell culture, bioreactor operations, multi-column chromatography, viral inactivation) are executed consistently, within defined process parameters, and in compliance with GMP requirements.
The role operates within a defined process scope and supports Manufacturing Operations by monitoring process performance, analyzing trends, supporting investigations, and contributing to continuous improvement of downstream process robustness.
As required, the role may support New Product Introduction (NPI), process startup, and validation activities, primarily from an execution, monitoring, and documentation standpoint.
This position reports to the Senior Manager, Manufacturing and works closely with cross‑functional teams.
Key Responsibilities:
1. Routine Manufacturing & Asset Care Support (Primary Focus)
Support routine downstream manufacturing operations within assigned scope.
Monitor critical process parameters, trends, and process performance indicators to ensure operations remain within defined control limits.
Identify process deviations, abnormalities, or drift; document observations and escalate issues in a timely manner.
Provide day‑to‑day technical support to Manufacturing Operations related to downstream process execution.
Act as operational process SME for assigned downstream unit operations, supporting safe, compliant, and consistent process performance.
Support updates to downstream SOPs, batch records, and process documentation related to new or modified processes.
2. Downstream Process Robustness & Performance
Support routine review and trending of downstream process data to identify variability, recurring issues, or opportunities for improvement.
Support implementation of process improvements aimed at enhancing robustness, yield, consistency, or operational reliability.
Collaborate with MSAT and Automation teams to support effective use of digital tools and process data
3. Support to New Product Introduction (NPI) & Startup (Limited Scope)
Support NPI and process startup activities as assigned, such as:
Execution support during engineering runs, PPQ, or startup manufacturing
Process data collection, verification, and documentation
Support of process readiness and operational handover activities
Participate in downstream process risk assessments (e.g. FMEA) by gathering information and supporting action tracking.
Support updates to downstream SOPs, batch records, and process documentation related to new or modified processes.
4. Deviation, Investigation & CAPA Support
Participate in process related deviations and investigations
Escalate complex issues to Senior Engineers in a timely manner.
5. GMP, Safety & Compliance
Perform assigned activities in compliance with GMP, EHS, and site requirements.
Support audit and inspection readiness through accurate and timely documentation.
6. Continuous Improvement
Identify and propose improvement opportunities related to downstream process robustness, control, or execution.
Participate in OE / Lean / continuous improvement initiatives focused on downstream manufacturing processes.
About You
Knowledge, Skills & Competencies
Basic understanding of downstream biopharmaceutical processes (e.g. seed train, cell culture, bioreactor operations, multi-column chromatography, viral inactivation).
Working knowledge of GMP requirements and process data integrity principles.
Basic data analysis and trending capability to support process performance monitoring.
Able to work effectively within cross‑functional teams with appropriate guidance.
Demonstrates structured problem‑solving and analytical thinking.
Good technical writing and communication skills.
Strong team player with a continuous learning mindset.
Qualifications / Requirement
Diploma or Bachelor’s degree in Biotechnology, Biochemical Engineering, Chemical Engineering, Life Sciences, or related discipline.
3–4 years of experience in downstream biopharmaceutical manufacturing, process support, or manufacturing operations in a regulated environment.
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Job details
How this role compares
Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.
We currently track 801 comparable Associate Manufacturing & CMC roles across 95 biopharma companies.
Salary context
174 of 801 peers report a salary range (USD, annualized)
Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.
Where these roles are based
Top locations among the 801 comparable roles
+ 34 more countries
Seniority mix
801 of 801 peers have a known seniority level
Therapeutic area mix
13 of 801 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
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How we calculate "similar"
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Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.