Tuyển dụng Process Engineer tại Hồ Chí Minh

A. Job Purpose

• This role reports directly to the HCMC Operational Excellence Manager of Opella.

• The Process Expert is accountable for qualifying and stabilizing production processes, developing standards, and driving continuous improvement initiatives. Ensure compliance with regulation, GMP and HSE through process optimization and data-driven decision-making.

• This is key position for problem solving of process/production deviation.

• This role is to manage upstream processes at Solid workshop

B. Key working relationships:

Internal:

• Operational Excellence Manager – Direct reporting and alignment on improvement priorities.

• APU Manager – Coordinate on process implementation and troubleshooting.

• QA/QC – Ensure process compliance and resolve quality issues.

• Engineering & Maintenance – Collaborate on equipment-related process improvements.

• Digital/Data Team – Align on KPI tracking and digitalization projects.

• TTI – key contact for launching projects

• KSOL – key contact for MSEP initiatives

• ME – key contact for process improvement

External:

• Regulatory Auditors – Provide process documentation and support during audits.

• Technology Vendors – Assist in implementing process automation and digital tools.

C. Key Accountabilities

Focus: Process optimization, cost efficiency, compliance, data and technology.

Process Stabilization & Standardization

• Develop and maintain SOPs and process standards in compliance with GMP/ HSE.

• Monitor process performance and implement corrective actions.

Continuous Improvement

• Identify opportunities, propose initiatives for efficiency gains and cost reduction.

• Support Lean, Six Sigma, and OPS programs at the workshop level.

Data Analysis & KPI Monitoring

• Collect and analyze production data to identify trends and deviations.

• Provide insights to improve productivity and reduce variability.

Project Support

• Participate in new product launches, compliance upgrades, and improvement projects on behalf of production and transfer to APU.

• Coordinate with EM and QA team to implement the qualifications and lead the training, documentation, standardization at production to meet the user requirement and transfer to APU.

Compliance & Audit

• Prepare process-related documentation and support internal/external audits.

Yêu cầu công việc

• Upstream: Bachelor’s degree in Pharmacy, Chemical Engineering, or related field.

Experience:

• 2–3 years in pharmaceutical manufacturing from research & development or quality validation function.

• Knowledge of GMP and regulatory requirements.

• Familiarity with Lean, Six Sigma, and continuous improvement methodologies.

• Strong analytical and problem-solving skills.

Quyền lợi

• Thưởng: Thưởng doanh số theo quý
• Chăm sóc sức khoẻ: Bảo hiểm chăm sóc sức khỏe cho nhân viên và người thân
• Nghỉ phép có lương: 21 ngày phép năm và chế độ nghỉ thai sản dành cho nhân viên nam lên đến 14 tuần