Mô tả công việc
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
D. About you
Education:
• 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
Thông tin khác
NGÀY ĐĂNG
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CẤP BẬC
Nhân viên
NGÀNH NGHỀ
Sản Xuất > Nghiên Cứu & Phát Triển
KỸ NĂNG
R&D, Validation, Quality, Process Engineering
LĨNH VỰC
Dược phẩm
NGÔN NGỮ TRÌNH BÀY HỒ SƠ
Tiếng Anh
SỐ NĂM KINH NGHIỆM TỐI THIỂU
Không hiển thị
QUỐC TỊCH
Không hiển thị
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Thông tin chung
Nơi làm việc
- Hi-Tech Park, Lot I8-1-2, D8 Street, City, Long Thạnh Mỹ, Quận 9, Vietnam