533 Production Managers jobs in Singapore

Job Highlights:

We are seeking a motivated Manufacturing Manager to lead and oversee operations in our newly established biotechnology manufacturing plant. You will play a critical role in building a high-performing production team, establishing operational processes, and driving the success of our manufacturing operations.

Job Responsibilities:

• Lead, train, and supervise production technicians and associates to build a high-performing team.
• Plan and monitor daily production to meet targets, KPIs, and quality standards.
• Analyze downtime and production issues, implementing corrective actions to improve efficiency.
• Establish and maintain production processes, ensuring compliance with regulatory and operational standards.
• Maintain inventory accuracy, conduct cycle counts, and resolve discrepancies.
• Drive continuous improvement initiatives in safety, quality, efficiency, and productivity.
• Implement and sustain 6S methodology for a clean, organized, and safe workplace.
• Collaborate with cross-functional teams (Engineering, R&D, Quality) to optimize workflows and resolve operational challenges.

Role Requirement:

• Min. Bachelor's degree in Industrial Engineering, Biotechnology, or related field.
• Min. 6 years of experience in medical devices, biomedical, life sciences, or similar industries with 3 years of team supervision and training in a fast-paced environment.
• Strong understanding of Environmental Health and Safety (EHS) standards, with proven ability to enforce safety protocols.
• Hands-on experience with lean manufacturing principles, waste reduction, and process optimization.
• Strong communication and coaching abilities to motivate teams and provide constructive feedback.

If you are keen to explore this opportunity, kindly send a copy of your updated resume to or simply click the button to APPLY NOW We regret that only shortlisted applicants will be notified.

Tan Sze Ching Shannon - R

EA License No: 16C8261

To plan, schedule, organize, manage and control the production and engineering activities of bulk drug substances in Production Building to achieve targeted production levels cost effectively, efficiently and reliably, within the framework of current Good Manufacturing practices (cGMP), quality, safety, occupational hygiene, responsible environmental protection and in cognizance of the dynamic business environment.

• Focus on the routine manufacture activities to ensure that production of bulk drug substances meets stipulated quality, time and cost specifications and in full compliance with the relevant internal and external requirements, regulations and standards.
• Manage a group of professionals e.g. Manufacturing Engineer/Chemist etc. to trouble shoot all process, manufacturing and customer related issue and implement remedial actions to minimize impact to production.
• Monitor and ensure compliance by section's staff with the various operating procedures, documentation, GMP, safety, occupational hygiene, environmental and regulatory requirements.
• Develop, review and approve all relevant manufacturing documents in accordance to site procedures.
• Support the generation of the capital expenditure (CAPEX) proposal list for budgeting. Work closely with the Technical Operations Team to establish windows for New Production Introduction (NPI) and capital projects implementation.
• Generate operating budget for own section and manage expenditure to ensure achievement of operational targets and drive cost reduction initiatives.
• Ensure information related to routine production activities are actively tracked & captured for consolidation at the departmental level & submitted to management for decision. Perform various tier reviews and ensure visuals for various metrics are updated.
• Manage, develop, and motivate staff to help realize their maximum potential so as to contribute towards achieving the objectives of the department.
• Fulfill the role of Value Stream Embedded GSK Production System (GPS) Practitioner to drive reduction in accidents, defects and waste including continuous improvement within the Value Stream.

• A degree in Chemistry or Chemical Engineering or any relevant field.
• At least 5-8 years of relevant experience in the pharmaceutical, chemical or petrol chemical industry.
• Good commissioning and operational experience in pharmaceuticals plants.
• Very good knowledge of product, production processes and the plant.
• Good engineering maintenance knowledge
• Good statistical knowledge.
• Good troubleshooting skills.
• Good knowledge of GMP, safety, hygiene and environment regulations.
• Good knowledge of NDA registration procedures.
• Good project management skills
• Good presentation skills
• Good communication skills
• Good management skills
• Good interaction skill with other department stakeholders
• Good understanding of the business processes and MERPS
• Good knowledge in LeanSigma principles and application

To learn more about Singapore GSK and our people, please click on this link:

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we're committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

We are seeking a highly motivated and detail-oriented Manufacturing Manager to oversee production operations and drive process improvements within our manufacturing facility. The ideal candidate will have a strong background in engineering and automation, with hands-on experience in production environments such as fragrance, cosmetics, food, or chemical manufacturing. This role requires expertise in GMP standards, process flows, and automation systems, along with strong leadership and problem-solving skills to ensure efficiency, quality, and compliance.

• Lead and manage daily production operations to ensure safety, quality, efficiency, and on-time delivery.
• Develop, implement, and optimize production processes in alignment with GMP, 5S, and lean manufacturing principles.
• Oversee automation systems, troubleshoot technical issues, and support continuous improvement initiatives.
• Supervise production staff, provide training, and foster a culture of accountability, teamwork, and excellence.
• Monitor and analyze production performance metrics, implement corrective actions, and drive cost reduction initiatives.
• Collaborate with R&D, Quality, Engineering, and Supply Chain teams to support new product introductions and process scale-ups.
• Ensure proper documentation, compliance with industry regulations, and adherence to safety and environmental standards.
• Manage fragrance compounding, blending, and filling processes (where applicable), ensuring consistency and quality.
• Utilize ERP, MES, and other production-related software for planning, scheduling, and reporting.
• Support facility and equipment maintenance to ensure reliable operations.

• Bachelor's Degree in Chemical, Mechanical, Industrial Engineering, or a related field.
• 3–5 years of experience in production operations and automation engineering, preferably in fragrance, cosmetics, food, or chemical manufacturing.
• Strong knowledge of GMP, 5S, and production process flows.
• Hands-on experience with automation systems in a manufacturing environment.
• Solid understanding of fragrance compounding, blending, and filling processes is a strong advantage.
• Proficiency in Microsoft Office and production-related software (ERP, MES).
• CAD design skills and data analysis capabilities are considered a plus.
• Strong leadership, organizational, and communication skills.

Interested applicants for the above advertised position(s), please kindly click the APPLY button below or send in your updated resume.

EA License No.: 13C6305

Registration No.: R LEE JIA HOU)

For candidate who applied for the advertised position is deemed to have consented to us that we may collect, use or disclose your personal information for purpose in connection with the services provided by us.

Job Highlights:

We are seeking a motivated Manufacturing Supervisor to lead and oversee operations in our newly established biotechnology manufacturing plant. You will play a critical role in building a high-performing production team, establishing operational processes, and driving the success of our manufacturing operations.

Job Responsibilities:

• Team Leadership: Recruit, train and supervise a team of production operators to foster a collaborative work environment and meet plant's production objectives. Implement and oversee training plans to enhance employee skills, promote cross-training, and improve workforce flexibility.
• Daily Operations: Plan and monitor daily production activities to meet KPIs such as on-time delivery, production efficiency, failure rates, lead times, manpower allocation and space utilization. Conduct root cause analyses for production delays and downtimes, implementing corrective actions to enhance processes and prevent recurrence.
• Process Setup: Establish and validating production processes, ensuring alignment with regulatory and operational standards.
• Process Optimization: Identify opportunity for continuous improvement in processes, workflows, and resource utilization. Lead data-driven initiatives to improve efficiency, quality, safety, and overall production outcomes.
• Compliance & Safety: Ensure adherence to regulatory standards, safety protocols, and organizational procedures. Champion and sustain the 6S methodology to ensure a clean, organized, and safe production environment.
• Collaboration: Work closely with cross-functional teams, including Quality, R&D, Engineering to resolve operational challenges and optimize workflows.
• Inventory: Ensure inventory accuracy through regular audits, oversee physical counts, and resolve discrepancies to maintain optimal stock levels

Role Requirement:

• Min. Bachelor's degree in Industrial Engineering, Biotechnology, or related field.
• Min. 6 years of experience in medical devices, biomedical, life sciences, or similar industries with 3 years of team supervision and training in a fast-paced environment.
• Strong understanding of Environmental Health and Safety (EHS) standards, with proven ability to enforce safety protocols.
• Hands-on experience with lean manufacturing principles, waste reduction, and process optimization.
• Strong communication and coaching abilities to motivate teams and provide constructive feedback.

If you are keen to explore this career opportunity, kindly send a copy of your resume to  or simply click the button to APPLY NOW We regret that only shortlisted applicants will be notified.

Sharon Yip - R

EA License No: 16C8261

We are partnering with a emerging US-based medical equipment manufacturer focusing on innovations that reduce preventable harm and improve health outcomes for maternal and newborn health issues. As part of their expansion, they are looking to hire the following position for their Singapore team.

Manufacturing Manager / Senior Manufacturing Engineer

Position Overview:

The role is responsible for leading critical initiatives to develop, setup and qualify manufacturing processes, ensure compliance with regulatory standards, and drive innovation in our product development efforts. As a key member of the Technical team, he/she will also be involved in maintaining and enhancing the quality, efficiency and scalability of our manufacturing operations. This role is part of the Engineering team and reports to the VP of Engineering and Manufacturing. This is a pioneering position and the first one in our small team that will be fully dedicated to manufacturing.

Key Responsibilities:

• Lead the collaboration with external vendors and contract manufacturers to define and develop manufacturing equipment and processes for Class I and II products. This includes process characterization, equipment buy-off, validation, and scale-up activities in compliance with ISO 13485 and FDA regulations (21 CFR Part 820).

• Evaluate and enhance existing manufacturing processes to improve efficiency, yield, and cost-effectiveness while maintaining product quality and regulatory compliance for existing products.

• Lead initiatives to implement new technologies, processes and materials to advance manufacturing capabilities and reduce costs.

• Lead root cause analysis and implement corrective/preventive actions (CAPA) to address manufacturing issues or manufacturing related product complaints to prevent recurrence.

• Collaborate with contract manufacturers to develop and review manufacturing procedures, work instructions and other manufacturing documents.

• Close collaboration with cross functional team from Quality Assurance, Supply Chain, Regulatory Affairs and contract manufacturers to ensure product and process integrity throughout the product life cycle.

• Drive continuous improvement initiatives using Lean, Six Sigma, or other methodologies to optimize processes and eliminate waste.

• Collaborate closely with Engineering team, contract manufacturers and external vendors to ensure seamless transfer of new products into manufacturing.

• Support new product introduction through Design for Manufacturability (DFM), process development and production readiness.

• Ensure contract manufacturers and external vendors implement best practices and compliance with international EHS (Environment, Health & Safety) requirements.

Requirements:

• Bachelor's Degree in Engineering (Mechanical, Biomedical or Industrial) with minimum 6-10 years of progressive experience within the medical devices industry (ISO 13485, FDA) with a strong background in manufacturing line setup, process development and optimization, equipment and process validation.

• Lead collaboration with contract manufacturers for at least one manufacturing line setup, process development and optimization, equipment and process validation for Class I or II medical devices.

• Good knowledge and experience with various manufacturing processes eg. automation, semi-automation, assembly, injection molding, extrusion, blow molding, leak tester, packaging sealing, ultrasonic welding, UV adhesive curing etc.

• Develop manufacturing processes for medical devices using methodologies such as Design Thinking, DFM and DFSS techniques.

• Hands-on experience with equipment qualification and buy-off of manufacturing equipment with contract manufacturers.

• Hands-on experience with process validation, test method validation (MSA, GR&R), risk management with responsibility in developing process FMEA, root cause analysis and CAPA.

• Leading and collaborate with cross-functional and international teams from different cultures, locations and time zones.

Skills Requirements:

• Excellent analytical and problem-solving skills, with a strategic mindset and a focus on continuous improvement.

• Strong interpersonal skills with excellent communication skills both orally and in writing.

• Able to travel internationally and outstation at contract manufacturers for period of time.

• Able to influence or drive external vendors or contract manufacturers to meet timeline and deliver positive outcomes.

• Able to prepare protocols and reports for qualifications, validation and testing is essential.

• Certification in statistical analysis, Lean or Design for Six Sigma (Green Belt or Black Belt) with ability to use Minitab (or equivalent system) is desirable.

• Experience in project management is a plus.

EA Personnel Registration No: R

EA License No: 12C6254

We are seeking a driven and experienced Manufacturing Manager to lead production operations for our fragrance manufacturing facility . This role is responsible for ensuring efficient, high-quality, and compliant production processes, while driving automation, continuous improvement, and team development .

• Oversee daily manufacturing activities to ensure timely and efficient production.
• Develop and execute production plans in coordination with supply chain and planning teams.
• Optimize workflow, resource utilization, and inventory management.

• Implement and maintain automation systems to improve productivity and consistency.
• Collaborate with engineering teams on process design, layout, and continuous improvement initiatives.
• Troubleshoot equipment issues and recommend technical upgrades or solutions.

• Ensure compliance with GMP , ISO standards , and company quality procedures.
• Monitor quality control processes and lead root cause analysis for quality issues.
• Work closely with QA/QC teams to maintain product standards and reduce waste.

• Lead, train, and motivate production staff to meet performance and safety standards.
• Conduct performance evaluations and ensure continuous skill development.
• Promote a culture of accountability and continuous improvement on the shop floor.

• Enforce workplace safety policies and ensure compliance with health and environmental regulations.
• Lead risk assessments and implement preventive measures for operational hazards.
• Promote a clean, organized, and safe working environment in line with 5S principles .

• Degree/Diploma in Chemical, Mechanical, Industrial Engineering , or related discipline.
• Min 3 years of experience in production operations and automation , preferably in fragrance, cosmetics, food, or chemical manufacturing .
• Strong knowledge of GMP , 5S , production flow optimization, and lean manufacturing practices.
• Proficient in Microsoft Office , and familiar with ERP , MES , or production planning systems.
• Experience with CAD software and data analysis tools is an advantage.
  Strong leadership, communication, and problem-solving skills.

If interested, please submit your application to with your expected salary and resume.

We regret that only short-listed candidates will be contacted shortly. By submitting your application or resume, you agree to the collection, use, retention, and sharing of your personal information with potential employers for their assessment.

JDA WMS Pte Ltd | EA Personnel: Pham Thi Tuyet Mai

EA License No: 23S1595 | EA Registration No: R

• Plan, organize, and direct manufacturing operations to meet production targets and quality standards.
• Lead and supervise production teams, including supervisors, technicians, and operators.
• Monitor key performance indicators (KPIs) such as output, efficiency, waste, and downtime.
• Implement and ensure compliance with health, safety, and environmental regulations.
• Drive process improvements and cost reductions through Lean Manufacturing and Six Sigma principles.
• Coordinate with planning, procurement, engineering, and maintenance teams for seamless production flow.
• Ensure proper maintenance of equipment and minimize unplanned downtime.
• Maintain accurate production records and reporting systems.
• Manage inventory levels of raw materials, WIP, and finished goods to avoid stockouts or overstocking.
• Recruit, train, and develop manufacturing staff to maintain a high-performing team.
• Ensure compliance with company policies, industry standards, and regulatory requirements.

• Bachelor's degree in Manufacturing, Engineering, Industrial Management, or a related field.
• Minimum 5 years of experience in manufacturing leadership roles.
• Strong knowledge of manufacturing processes, production planning, and quality control systems.
• Excellent leadership, communication, and problem-solving skills.
• Proficient in Microsoft Office and manufacturing software
• Strong organizational and analytical skills.

We are partnering with a emerging US-based medical equipment manufacturer focusing on innovations that reduce preventable harm and improve health outcomes for maternal and newborn health issues. As part of their expansion, they are looking to hire the following position for their Singapore team.

Manufacturing Manager / Senior Manufacturing Engineer

Position Overview:

The role is responsible for leading critical initiatives to develop, setup and qualify manufacturing processes, ensure compliance with regulatory standards, and drive innovation in our product development efforts. As a key member of the Technical team, he/she will also be involved in maintaining and enhancing the quality, efficiency and scalability of our manufacturing operations. This role is part of the Engineering team and reports to the VP of Engineering and Manufacturing. This is a pioneering position and the first one in our small team that will be fully dedicated to manufacturing.

Key Responsibilities:

· Lead the collaboration with external vendors and contract manufacturers to define and develop manufacturing equipment and processes for Class I and II products. This includes process characterization, equipment buy-off, validation, and scale-up activities in compliance with ISO 13485 and FDA regulations (21 CFR Part 820).

· Evaluate and enhance existing manufacturing processes to improve efficiency, yield, and cost-effectiveness while maintaining product quality and regulatory compliance for existing products.

· Lead initiatives to implement new technologies, processes and materials to advance manufacturing capabilities and reduce costs.

· Lead root cause analysis and implement corrective/preventive actions (CAPA) to address manufacturing issues or manufacturing related product complaints to prevent recurrence.

· Collaborate with contract manufacturers to develop and review manufacturing procedures, work instructions and other manufacturing documents.

· Close collaboration with cross functional team from Quality Assurance, Supply Chain, Regulatory Affairs and contract manufacturers to ensure product and process integrity throughout the product life cycle.

· Drive continuous improvement initiatives using Lean, Six Sigma, or other methodologies to optimize processes and eliminate waste.

· Collaborate closely with Engineering team, contract manufacturers and external vendors to ensure seamless transfer of new products into manufacturing.

· Support new product introduction through Design for Manufacturability (DFM), process development and production readiness.

· Ensure contract manufacturers and external vendors implement best practices and compliance with international EHS (Environment, Health & Safety) requirements.

Requirements:

· Bachelor's Degree in Engineering (Mechanical, Biomedical or Industrial) with minimum 6-10 years of progressive experience within the medical devices industry (ISO 13485, FDA) with a strong background in manufacturing line setup, process development and optimization, equipment and process validation.

· Lead collaboration with contract manufacturers for at least one manufacturing line setup, process development and optimization, equipment and process validation for Class I or II medical devices.

· Good knowledge and experience with various manufacturing processes eg. automation, semi-automation, assembly, injection molding, extrusion, blow molding, leak tester, packaging sealing, ultrasonic welding, UV adhesive curing etc.

· Develop manufacturing processes for medical devices using methodologies such as Design Thinking, DFM and DFSS techniques.

· Hands-on experience with equipment qualification and buy-off of manufacturing equipment with contract manufacturers.

· Hands-on experience with process validation, test method validation (MSA, GR&R), risk management with responsibility in developing process FMEA, root cause analysis and CAPA.

· Leading and collaborate with cross-functional and international teams from different cultures, locations and time zones.

Skills Requirements:

· Excellent analytical and problem-solving skills, with a strategic mindset and a focus on continuous improvement.

· Strong interpersonal skills with excellent communication skills both orally and in writing.

· Able to travel internationally and outstation at contract manufacturers for period of time.

· Able to influence or drive external vendors or contract manufacturers to meet timeline and deliver positive outcomes.

· Able to prepare protocols and reports for qualifications, validation and testing is essential.

· Certification in statistical analysis, Lean or Design for Six Sigma (Green Belt or Black Belt) with ability to use Minitab (or equivalent system) is desirable.

· Experience in project management is a plus.

EA Personnel Registration No: R

EA License No: 12C6254

• Plan, organize, and direct manufacturing operations to meet production targets and quality standards.
• Lead and supervise production teams, including supervisors, technicians, and operators.
• Monitor key performance indicators (KPIs) such as output, efficiency, waste, and downtime.
• Implement and ensure compliance with health, safety, and environmental regulations.
• Drive process improvements and cost reductions through Lean Manufacturing and Six Sigma principles.
• Coordinate with planning, procurement, engineering, and maintenance teams for seamless production flow.
• Ensure proper maintenance of equipment and minimize unplanned downtime.
• Maintain accurate production records and reporting systems.
• Manage inventory levels of raw materials, WIP, and finished goods to avoid stockouts or overstocking.
• Recruit, train, and develop manufacturing staff to maintain a high-performing team.
• Ensure compliance with company policies, industry standards, and regulatory requirements.

• Bachelor's degree in Manufacturing, Engineering, Industrial Management, or a related field.
• Minimum 5 years of experience in manufacturing leadership roles.
• Strong knowledge of manufacturing processes, production planning, and quality control systems.
• Excellent leadership, communication, and problem-solving skills.
• Proficient in Microsoft Office and manufacturing software
• Strong organizational and analytical skills.