What Jobs are available for Production Managers in Singapore?

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

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.

Site Name:
Singapore - Jurong

Posted Date:
Oct

Purpose
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.

Responsibilities

• 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.

Knowledge, Skills & Experience

• 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.

Responsibilities:

• Lead and manage the manufacturing operations in Singapore, ensuring safe, efficient, and high-quality production performance on a daily basis.
• Oversee a team of engineers, supervisors, and production staff to meet operational goals and customer delivery commitments.
• Develop and implement production strategies, plans, and schedules to support business objectives and customer demand in a high-mix, low-volume environment.
• Drive continuous improvement initiatives in productivity, quality, cost efficiency, and process optimization.
• Ensure compliance with Singapore export control regulations, company policies, and Country of Origin (COO) requirements.
• Collaborate cross-functionally with R&D, Supply Chain, Quality, and Logistics to ensure seamless operations and successful new product introductions (NPI).
• Monitor key manufacturing metrics and provide regular performance updates and strategic recommendations to senior management.
• Foster a culture of teamwork, accountability, and operational excellence within the manufacturing team.
• Support regional manufacturing activities and serve as a key contact for process standardization and best practice sharing

Your qualifications

• Bachelor's degree in Electronics, Electrical, Mechanical Engineering or related discipline
• Minimum 8 years of experience in manufacturing operations, including at least 3 years in a managerial or supervisory role within a high-mix, low-volume production environment.
• Proven record of improving operational efficiency, implementing lean manufacturing principles, and achieving performance targets.
• Strong understanding of production processes, export control handling, and COO (Country of Origin) requirements.
• Experience working with ERP systems, preferably SAP (PP module).

Interested candidates please apply/forward your resume to

• 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.

• Manage and control activities of our centralized warehouse to ensure proper storage and handling of all materials/products.
• Plan and control 3rd party logistics service quality and efficiencies. Improve on existing network and distribution activities.
• Implement a lean framework and manage warehouse capacity for effective utilization of space and capacity.
• Lead all operational activities and develop effective ordering and stocking strategies to meet customer expectations for product availability.
• Conducts supply chain analyses to optimize distribution operation and footprint for optimal efficiency.
• Establish a training matrix in compliance with procedures and job requirements.
• Deploys and standardized management processes and drives alignment for the organization.
• Manages appropriate KPIs and develops improvement plans (when required) to meet targets
• Assist Senior Management with the development of new service solutions & projects.
• Developing and maintaining appropriate relationships with group and external service providers, developing business relationships and reviewing these regularly, to provide an appropriate distribution network for the business

Job Objective/s

The Manufacturing Manager (ATP) is responsible for overseeing and managing backend manufacturing operations for Indium Phosphide (InP) laser devices, including wafer to die singulation, die handling, assembly, packaging, burn-in, and final testing. The role ensures high-yield, cost-effective, and on-time production while maintaining strict quality and reliability standards. The manager will lead a team of engineers, supervisors, and technicians to achieve operational excellence through continuous improvement, automation, and cross-functional collaboration.

Duties and Responsibilities

1. Operations Management

• Oversee daily backend manufacturing activities, covering wafer to die singulation, die attach, wire bonding, submount assembly, burn-in, and optical/electrical testing.

• Plan and execute production schedules to meet delivery, yield, and cost targets.

• Monitor key operational metrics (throughput, cycle time, yield, equipment uptime).

• Ensure full compliance with EHS, cleanroom, and ISO quality standards.

2. Process & Yield Optimization

• Drive process control and continuous improvement programs to improve yield, reduce rework, and enhance throughput.

• Work with process and equipment engineers to identify and eliminate bottlenecks.

• Implement SPC, DOE, and root cause analysis for performance optimization.

3. People Leadership

• Lead and develop a team of production supervisors, engineers, and technicians.

• Set performance goals, conduct evaluations, and drive skill development.

• Foster a culture of accountability, collaboration, and continuous improvement.

4. Equipment & Automation

• Oversee backend equipment utilization and maintenance programs.

• Work with equipment vendors and engineering teams on upgrades and automation initiatives.

• Support tool qualification, calibration, and preventive maintenance programs.

5. Quality & Reliability

• Collaborate with QA and Reliability Engineering to ensure compliance with product and customer specifications.

• Lead Corrective and Preventive Action (CAPA) programs, utilizing 8D methodology and structured root cause analysis to address non-conformances and implement sustainable solutions.

• Ensure robust traceability, documentation, and statistical process monitoring.

6. Cross-functional Collaboration

• Interface with Front-end Fab, NPD (New Product Development), NPI (New Product Introduction), and PPC (Product Planning Control) teams to ensure smooth technology transfer and production ramp-up.

• Support Engineering Change Notice (ECN), pilot builds, and new product introductions.

• Align with Planning and Procurement to ensure material readiness and capacity planning.

Qualification Guidelines

Minimum Education

Bachelor's or Master's degree in Materials Science, Electrical Engineering, Physics, or related discipline.

Minimum Experience

• Minimum 5 - 8 years of relevant experience in semiconductor or photonics backend manufacturing, with at least 3 years in a leadership role.

• Experience in InP or III-V device assembly/test strongly preferred.

• Proven track record in high-mix, low-to-medium volume environments.

• Familiarity with laser backend assembly processes (Wafer to die singulation, die attach, wire bonding, optical alignment, burn-in).

Specific Knowledge / Skills

• Strong leadership and team development skills.

• Proficiency in Lean Manufacturing, Six Sigma, SPC, and continuous improvement tools will be considered a strong plus.

• Good understanding of yield analysis, failure mechanisms, and reliability testing.

• Strong project management, analytical, and problem-solving abilities.

• Excellent communication and cross-functional collaboration skills.

Responsibilities
Lead and manage the manufacturing operations in Singapore, ensuring safe, efficient, and high-quality production performance on a daily basis.
Oversee a team of engineers, supervisors, and production staff to meet operational goals and customer delivery commitments.
Develop and implement production strategies, plans, and schedules to support business objectives and customer demand in a high-mix, low-volume environment.
Drive continuous improvement initiatives in productivity, quality, cost efficiency, and process optimization.
Ensure compliance with Singapore export control regulations, company policies, and Country of Origin (COO) requirements.
Collaborate cross-functionally with R&D, Supply Chain, Quality, and Logistics to ensure seamless operations and successful new product introductions (NPI).
Monitor key manufacturing metrics and provide regular performance updates and strategic recommendations to senior management.
Foster a culture of teamwork, accountability, and operational excellence within the manufacturing team.
Support regional manufacturing activities and serve as a key contact for process standardization and best practice sharing
Qualifications
Bachelor's degree in Electronics, Electrical, Mechanical Engineering or related discipline
Minimum 8 years of experience in manufacturing operations, including at least 3 years in a managerial or supervisory role within a high-mix, low-volume production environment.
Proven record of improving operational efficiency, implementing lean manufacturing principles, and achieving performance targets.
Strong understanding of production processes, export control handling, and COO (Country of Origin) requirements.
Experience working with ERP systems, preferably SAP (PP module).
Interested candidates please apply/forward your resume to
#J-18808-Ljbffr

• 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.