Process Expert - Pharmaceutical
Hạn nộp hồ sơ: 06/12/2026 (Còn 52 ngày)
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Opella is the purest and third-largest player globally in the Over-The-Counter (OTC) & Vitamins, Minerals & Supplements (VMS) market. We have an unshakable belief in the power of self-care and the role it can play in creating a healthier society and a healthier planet. That's why we want to make self-care as simple as it should be by being consumer-led always, with science at our core.
Through our unique and balanced portfolio of more than 100 loved brands, including 15 global and local high-growth challengers such as : Allegra, Dulcolax and Buscopan, we deliver our mission: helping more than half a billion consumers worldwide take their health in their hands. This mission is brought to life by an 11,000-strong team, 13 best-in-class manufacturing sites, and 4 specialized science and innovation development centers.
We are also proud to be the 1st major fast-moving consumer healthcare company to achieve B Corp certification.
Join us on our mission. Health. In your hands 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 KEY WORK RELATIONSHIP
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.
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. ABOUT YOU
Education: Upstream: Bachelor's degree in Pharmacy, Chemical Engineering, or related field.
Experience: 2-3 years in pharmaceutical manufacturing or process engineering. Knowledge of GMP and regulatory requirements. Familiarity with Lean, Six Sigma, and continuous improvement methodologies. Strong analytical and problem-solving skills.
WHY US? At Opella, you will enjoy doing challenging, purposeful work, empowered to develop consumer brands with passion and creativity. This is your chance to grow new skills and be part of a bold, collaborative, and inclusive culture where people can thrive and be at their best every day.
We Are
Challengers. We are dedicated to making self-care as simple as it should be. That starts with our culture. We are challengers by nature, and this is how we do things: All In Together: We keep each other honest and have each other's backs.
Courageous: We break boundaries and take thoughtful risks with creativity. Outcome-Obsessed: We are personally accountable, driving sustainable impact and results with integrity.
Radically Simple: We strive to make things simple for us and simple for consumers, as it should be.
Through our unique and balanced portfolio of more than 100 loved brands, including 15 global and local high-growth challengers such as : Allegra, Dulcolax and Buscopan, we deliver our mission: helping more than half a billion consumers worldwide take their health in their hands. This mission is brought to life by an 11,000-strong team, 13 best-in-class manufacturing sites, and 4 specialized science and innovation development centers.
We are also proud to be the 1st major fast-moving consumer healthcare company to achieve B Corp certification.
Join us on our mission. Health. In your hands 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 KEY WORK RELATIONSHIP
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.
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. ABOUT YOU
Education: Upstream: Bachelor's degree in Pharmacy, Chemical Engineering, or related field.
Experience: 2-3 years in pharmaceutical manufacturing or process engineering. Knowledge of GMP and regulatory requirements. Familiarity with Lean, Six Sigma, and continuous improvement methodologies. Strong analytical and problem-solving skills.
WHY US? At Opella, you will enjoy doing challenging, purposeful work, empowered to develop consumer brands with passion and creativity. This is your chance to grow new skills and be part of a bold, collaborative, and inclusive culture where people can thrive and be at their best every day.
We Are
Challengers. We are dedicated to making self-care as simple as it should be. That starts with our culture. We are challengers by nature, and this is how we do things: All In Together: We keep each other honest and have each other's backs.
Courageous: We break boundaries and take thoughtful risks with creativity. Outcome-Obsessed: We are personally accountable, driving sustainable impact and results with integrity.
Radically Simple: We strive to make things simple for us and simple for consumers, as it should be.
Thông tin chung
- Thu nhập: Thỏa thuận
Việc làm tương tự khác
Công ty TNHH Tích hợp Hệ thống Quản lý Quốc tế
Hồ Chí Minh
Thỏa thuận
CÔNG TY CỔ PHẦN ĐẦU TƯ XÂY LẮP THÀNH PHÚ
Hồ Chí Minh
Từ 17 - 20 triệu VND
Công ty CP Leo Palace
Hồ Chí Minh
16 triệu - 20 triệu VND
CÔNG TY CỔ PHẦN NGHIÊN CỨU VÀ TƯ VẤN THỊ TRƯỜNG VI NA
Hồ Chí Minh
12,000,000 - 15,000,000 VND
CÔNG TY CỔ PHẦN KIẾN TRÚC VÀ ĐẦU TƯ THƯƠNG MẠI TTT
Hà Nội, Hồ Chí Minh, Cần Thơ, Hải Phòng, Bắc Giang, Bắc Ninh, Bình Dương, Hà Nam, Lào Cai, Nam Định, Ninh Bình, Thái Nguyên, Yên Bái, Khác
22 - 27 triệu
CÔNG TY CỔ PHẦN TẬP ĐOÀN FECON
Hồ Chí Minh, Bắc Giang, Bắc Ninh, Tuyên Quang
20,000,000 - 28,000,000 VND
OPELLA
Xem trang công ty- Địa chỉ công ty: Hi-Tech Park, Lot I8-1-2, D8 Street, City, Long Thạnh Mỹ, Quận 9, Vietnam
- Quy mô: Từ 101 - 500 nhân viên
Thông tin công việc
Vị trí:
Nhân viên
Hình thức làm việc:
Toàn thời gian
Việc làm tương tự
[TP.HCM] Kỹ Thuật Xưởng May - Thu Nhập 25 Triệu++
CÔNG TY TNHH MAY MẶC QTF
Hồ Chí Minh
Từ 25 triệu VND
Nhân Viên QA Dược Phẩm - Yêu Cầu 2 Năm Kinh Nghiệm - Thu Nhập 13 - 15 Triệu
CÔNG TY TNHH TM DƯỢC THUẬN GIA
Hồ Chí Minh
13 - 15 triệu
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