316 Manufacturing jobs in Woodlands

Join to apply for the Manufacturing Engineer role at Fong’s Engineering and Manufacturing Pte Ltd .

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Direct message the job poster from Fong’s Engineering and Manufacturing Pte Ltd.

The ideal candidate possesses both a high level of technical expertise and an innate passion to build. You will play a critical role in creating and refining processes to improve manufacturing safety, quality, and productivity.

Responsibilities

• Develop manufacturing processes for new products, equipment, and setups.
• Generate and release technical documents (e.g., BOM, work instructions, route card).
• Conduct training for shopfloor personnel.
• Provide support to investigate and resolve process, equipment, and part issues.
• Implement engineering changes for improvements (process, NCR, CAPA, complaints).
• Lead pFMEA activities and perform equipment qualification and process validation.
• Prepare product and process reports by collecting, analyzing, and summarizing data and trends.
• Participate in product transfer activities or new projects.
• Perform other tasks as assigned by supervisors.

Qualifications/Experience

• Diploma/Degree in Engineering.
• Minimum 2 years of relevant experience.
• Experience in manufacturing and assembly of Catheters, Flexible Endoscopes is an advantage.
• Hands-on experience with Process Failure Mode Effects Analysis (PFMEA), Process Validation.
• Manufacturing process know-how and troubleshooting skills.
• Six Sigma training is preferred.

• Executive

• Full-time

• Manufacturing

• Medical Equipment Manufacturing

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Direct message the job poster from Pharmagend Global Medical Services Pte Ltd

KEY DUTIES AND RESPONSIBILITES:

• Support the establishment of new production plants including cream, nasal spray, prefilled syringe and pilot plant.
• Take part in FAT of new machines and equipment.
• Participate in Engineering Batch and Registration Batch for new products.
• Perform all activities in accordance with cGMP.
• Responsible for providing guidance and training for assigned employees.
• To lead production team after the start of new product commercialization.
• Develop and implement operational procedure regarding general practice, machine operation, equipment handling in form of SOP Batch Manufacturing/Packaging Record as well as manufacturing instruction for new plant.
• Troubleshoot and optimize production processes to ensure smooth and efficient operations.
• Be involved in equipment/ process qualification.
• Assist in investigation of process deviation, cGMP and all other compliance related matters, where applicable.
• Ensure compliance to GxP / Safety / Quality policies.
• Undertake any other duties assigned by manager.

REQUIREMENT:

• Strong understanding of safe working practicesand cGMP.
• Possess extensive hands-on experience and knowledge in pharmaceutical manufacturing processes.
• Good mechanical aptitude with the ability to provide technical guidance
• Prior experience in FAT and Engineering Batch is a plus.
• Demonstrate strong analytical and problem-solving abilities to optimize processes and implement effective solutions.
• Excellent attention to detail and ability to multitask.
• Good written and verbal communication
• Willing to work in Tuas area, in cleanroom environment with full gowning.
• Able to commit to rotational shift.

EDUCATION & EXPERIENCE:

• Bachelor’s degree in Science /Mechanical Engineering/Mechatronics Engineering or relevant disciplines
• With 3-5 years of manufacturing experience in Pharmaceutical or relatedindustries.

TO APPLY:

Candidates are encouraged to apply this position via email to with the following information in the resume.

• Work experiences and job responsibilities
• Current and Expected salary
• Reason for leaving
• Date of availability
• Education background

We regret that only shortlisted candidates will be contacted.

• Seniority level Executive

• Employment type Full-time

• Job function Manufacturing, Production, and Engineering
• Industries Medical Equipment Manufacturing, Chemical Manufacturing, and Pharmaceutical Manufacturing

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South West Community Development Council, Singapore 1 day ago

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Join to apply for the Manufacturing Technician role at myGwork - LGBTQ+ Business Community

17 hours ago Be among the first 25 applicants

Join to apply for the Manufacturing Technician role at myGwork - LGBTQ+ Business Community

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This job is with HP, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly.

Manufacturing Technician

Description -

Job Summary

• This role is responsible for analyzing and interpreting schematics, printouts, and specifications to assess the functionality of various functional domains. The role involves the regular maintenance and optimization of equipment, proactive troubleshooting of complex system issues, and participation in debugging and troubleshooting activities for both new and existing products and systems. The role includes providing assistance for the development of new test programs and procedures and ensuring the calibration and validation of testing instruments.
  
  

• Analyzes and comprehends schematics, printouts, and specifications when necessary to conduct assessments aimed at ascertaining the operational status of functional domains.
• Maintains and optimizes a wide range of equipment on a daily basis, proactively enhancing functionality and preventing potential issues.
• Assists in troubleshooting complex system operational issues, identifying root causes, and implementing effective solutions.
• Participates alongside engineers in the debugging and troubleshooting of new and existing products and systems.
• Assists in developing fresh test programs and procedures as required to accommodate emerging technologies.
• Maintains the regular calibration and validation of testing instruments.
• Ensures customer satisfaction by regularly meeting their needs and delivering assignments on time, actively engaging in project meetings.
• Acquires job skills and completes routine assignments/tasks, adhering to guidelines, and ensuring confidentiality in all dealings with company data.
• Assists in implementing new processes, supports department-level operational plans, and shares technical information with colleagues and clients.
• Solves defined problems using established procedures, and delivers basic technical, administrative, or operative tasks under direct instruction and close supervision.
  
  

• High School Diploma/General Education Diploma (GED)/Higher Secondary education or commensurate work experience or demonstrated competence.
• Typically has 0-2 years of work experience, preferably in equipment operation and troubleshooting , or a related field.
  
  

• Agile Methodology
• Automation
• Business Process
• Chemistry
• Data Analysis
• Fabrication
• Inventory Management
• Key Performance Indicators (KPIs)
• Merchandising
• New Product Development
• Process Improvement
• Project Management
• Purchasing
• SAP Applications
• Selling Techniques
• SQL (Programming Language)
• Supply Chain
• Technical Support
• Warehousing
• Workflow Management
  
  

• Effective Communication
• Results Orientation
• Learning Agility
• Digital Fluency
• Customer Centricity
  
  

• Impacts own work and acts as a team member by providing information in support of team efforts.
  
  

• Works on assignments that are routine in nature where limited judgment and/or minimal problem resolution is required.
  
  

• This job description describes the general nature and level of work performed in this role. It is not intended to be an exhaustive list of all duties, skills, responsibilities, knowledge, etc. These may be subject to change and additional functions may be assigned as needed by management.
  
  

• Seniority level Entry level

• Employment type Full-time

• Job function Management and Manufacturing

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Join to apply for the Manufacturing Engineer role at Agilent Technologies

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Join to apply for the Manufacturing Engineer role at Agilent Technologies

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• Improves products, processes and components to meet agreed-upon objectives.
• May redesign products or components to meet cost objectives, component technology obsolescence and customer requirements.
• Participates actively in new product introduction, including influencing the design of the product to ensure manufacturability and conformance with the global supply chain, enabling prototyping while in the R&D lab, testing the reliability of prototypes and managing the transition into production.
• Supports and implements the transition of products and manufacturing processes from prototype to full production and through the entire life cycle of the product.
• Partners with procurement and technical services to improve/sustain products and processes.
• May direct the work of third-party vendors and/or partners to meet contract specified deliverables, performance or business objectives.
• Will identify and manage ERP data such as bill of material and routing.
• Solves a broad range of problems varying in scope and complexity
• Experience in Optics & Lasers will be an added advantage
• Knowledge of basic programming, Excel macro skills will be an added advantage.
  
  

• Improves products, processes and components to meet agreed-upon objectives.
• May redesign products or components to meet cost objectives, component technology obsolescence and customer requirements.
• Participates actively in new product introduction, including influencing the design of the product to ensure manufacturability and conformance with the global supply chain, enabling prototyping while in the R&D lab, testing the reliability of prototypes and managing the transition into production.
• Supports and implements the transition of products and manufacturing processes from prototype to full production and through the entire life cycle of the product.
• Partners with procurement and technical services to improve/sustain products and processes.
• May direct the work of third-party vendors and/or partners to meet contract specified deliverables, performance or business objectives.
• Will identify and manage ERP data such as bill of material and routing.
• Solves a broad range of problems varying in scope and complexity
• Experience in Optics & Lasers will be an added advantage
• Knowledge of basic programming, Excel macro skills will be an added advantage.
  
  

• Bachelors or Masters Degree in Electrical & Electronic Engineering, Mechanical Engineering or equivalent.
• Able to read/write & converse Mandarin
• Typically, 4+ years relevant experience for entry to this level.
• Requires in-depth knowledge and experience in job and ability to work independently.
  
  

• Seniority level Associate

• Employment type Full-time

• Job function Manufacturing

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Seletar, North East Community Development Council, Singapore 2 months ago

Johor Baharu, Johore, Malaysia 3 days ago

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Direct message the job poster from ESCO ASTER PTE LTD

Esco Lifesciences Group is Singapore’s most globalized life sciences company, with annual revenues close to SGD 200M and global operations in over 42 locations and 26 direct countries across North America, Europe, Asia, Oceania.

Esco Aster Pte Ltd is an affiliate of Esco Lifesciences Group and was first incorporated in 2017.

Esco Aster is a contract research development and manufacturing organization founded and deeply rooted by scientists enabling fellow scientists to translate their bench work into commercially available products at affordable prices.

Our scientific work is in emerging and frontier biology utilizing cells as a final product or deriving products from cells which often we use cells as the factory to derive our target product.

Our first commercial breakthrough success is Esco Aster is commercially first in class being first in the world to be certified for cultivated/cell-based meat to FSSC 22000 and by a competent food regulatory body.

We are first in the region to operate an end-to-end integrated full cell line creation/immortalization or engineered cell line, cell culture process development, analytical development for stem cells and exosomes with full cGMP Capabilities from Drug Substance and small-scale fill & finish for final Cell Therapy Product.

The work we do creates a remarkable and lasting impact on our world. We offer you an opportunity to be part of this exciting journey to own your career and firsthand exposure to new emerging modalities supporting translational sciences.

Join us as we redefine BioSolutions for One World and One Health for the current and future generations to come.

One World Biosolutions for One Health.

Who we’re looking for

Physical / Mental Requirements / Work Environment:

• Strong leadership and communication skills.
• Ability to stay focused under pressure and adapt proactively.
• Critical thinker with a systematic and meticulous approach.
• Curious and self-motivated to stay updated on cell/gene therapy and emerging technologies.
• Committed to safety, quality, compliance, and timely delivery.
• Cleanroom and GMP manufacturing settings.
• Requires standing for long periods, working with sterile systems, and wearing full gowning/PPE.
• May engage in overtime during campaign activities or urgent troubleshooting.

The Scope

To lead and manage the successful technology transfer, manufacturing execution, and commercial readiness of cell and gene therapy products in a cGMP environment, ensuring compliance, efficiency, and delivery excellence throughout the product lifecycle.

Primary work location: Ayer Rajah Crescent, Singapore

Job Responsibilities

• Lead cross-functional biotechnicians and act as the bridge between process development and manufacturing.
• Collaborate with internal/external stakeholders including QA, QC, MSAT, and commercial teams.
• Serve as Manufacturing Subject Matter Expert (SME) during audits, inspections, and due diligence.
• Manage end-to-end technology transfers (internal and external).
• Oversee execution of Process Performance Qualification (PPQ), Aseptic Process Simulations (APS), and engineering/pilot runs.
• Oversee cell culture, purification, and fill-finish operations in a single-use, aseptic, cGMP facility.
• Ensure readiness of raw materials, equipment, and team for autologous/allogeneic campaigns.
• Monitor, document, and troubleshoot manufacturing activities, ensuring compliance with SOPs and regulatory requirements.
• Author, review, and manage cGMP documentation: SOPs, batch records, risk assessments, protocols, etc.
• Lead manufacturing change control, deviation investigations and implement CAPAs.
• Lead the implementation of electronic batch records.
• Potentially leading a small team.
• Undertake other tasks as assigned by the management based on project needs.

Requirements

• Minimum Bachelor’s Degree in Biotechnology related disciplines, Chemical Engineering, Pharmaceutical Science or relevant discipline with 2 years or more experience in a cGMP/aseptic environment in biologics or cell and gene therapy.
• Minimum of 4-6 years in cGMP Biologics or cell and gene therapy manufacturing with relevant industry knowledge, hands on equipment experience and technical expertise.
• Strong knowledge of cGMP practices and global regulatory requirements such as USFDA GMP, EU GMP, HSA GMP and PIC/S GMP.
• In-depth knowledge of the drug development process and commercialization pathways.
• Proficient in MS Office Suite (Microsoft Word, PowerPoint, Excel).
• Able to work independently and task oriented in a dynamic environment.
• Strong team player with a strong set of interpersonal skills.
• Excellent written and verbal communication skills.
• Experience in bringing cell and gene therapy products through clinical development to market is an added advantage.
• Proven track record in regulatory strategy and interactions is an added advantage.
• Proficient in MS Office Suite (Microsoft Word, PowerPoint, Excel).
• Able to work independently and task oriented in a dynamic environment.
• Strong team player with a strong set of interpersonal skills.
• Excellent written and verbal communication skills.

Apply now by submitting a Cover Letter and CV to .

• Seniority level Mid-Senior level

• Employment type Full-time

• Job function Management and Manufacturing

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South West Community Development Council, Singapore 1 day ago

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Company Overview:

Are you ready to see your career take flight? At GE Aerospace, we believe the world works better when it flies. We are a world-leading provider of jet engines, components, and integrated systems for commercial and military aircraft. We have a relentless dedication to the future of safe and more sustainable flight and believe in our talented people to make it happen.

Site Overview:

For more than 40 years, our advanced facilities in Singapore have led aerospace innovation across Asia Pacific. From automating processes to leveraging smart factory technologies, robotics, and additive manufacturing, GE Aerospace is shaping the future of aviation at GE Aerospace Engine Services Singapore (GEAESS).

GEAESS is our largest site for engine component Maintenance, Repair, and Overhaul (MRO), responsible for more than 60% of our global repair volume.

Role Overview:

• Manufacturing engineering tasks that do not require 4 year degree. Primarily tactical responsibilities. This does not include general administrative work.

• Broadening knowledge of own technical discipline to execute policy/strategy. May include support roles with specialized technical field of knowledge; still acquiring higher level knowledge and skills.

• Basic understanding of key business drivers; uses this understanding to accomplish own work. Good understanding of how work of own team integrates with other teams and contributes to the area.

• May have some autonomy to make decisions within a defined framework. Resolves issues in situations that require good technical knowledge and judgment within established procedures. Consults more senior team members for issues outside of defined instructions/parameters.

• A job at this level requires good interpersonal skills and may be required to lead a junior team. For customer facing roles, develops strong customer relationships and serves as the interface between customer and GE. Explains technical information to others.

Ideal Candidate

The ideal candidate should combine strong technical knowledge with hands-on experience and has a deep understanding of maintenance processes, lean manufacturing, and regulatory compliance. He possesses strong communication skills, the ability to document and plan programs effectively, and a collaborative mindset to integrate their work with broader team efforts while fostering strong customer relationships when required.

Required Qualifications

• For roles outside of the USA- This role requires basic experience in the Manufacturing & Manufacturing Engineering Specialist. Knowledge level is comparable to a Bachelor's degree from an accredited university or college ( or a high school diploma with relevant experience).

• For roles in USA - Bachelor's degree from an accredited university or college (or a high school diploma / GED with at least 6 years of experience in Job Family Group(s)/Function(s)).

Preferred Qualifications

• Strong oral and written communication skills.

• Ability to document, plan, market, and execute programs.

At GE Aerospace, we have a relentless dedication to the future of safe and more sustainable flight and believe in our talented people to make it happen. Here, you will have the opportunity to work on really cool things with really smart and collaborative people. Together, we will mobilize a new era of growth in aerospace and defense. Where others stop, we accelerate.

Relocation Assistance Provided: No

Forevermark is the diamond brand from De Beers Group. Every Forevermark inscribed diamond is natural, hand-selected, and comes with a promise that it is beautiful, rare, and responsibly sourced. Only the most beautiful diamonds are chosen from carefully selected mines around the world, including South Africa, Botswana, Namibia, and Canada; less than 1% of the world's natural diamonds are eligible to become Forevermark. Each diamond is expertly cut and polished by Forevermark Diamantaires before it can receive the inscription using proprietary technology.

The Forevermark Design & Innovation Centre, located in Milan, creates iconic jewellery designs that celebrate the natural beauty of Forevermark diamonds. These designs are showcased on the red carpet and available in authorized Forevermark Jewellers worldwide. Each diamond embodies our values of integrity, support for the advancement of women, inclusion and diversity, and protection of the natural world.

1. Monitoring Production for Quality Control / Standards:
   • Visit production sites to conduct thorough inspections of jewelry, utilizing expertise in gems, diamonds, metals, and jewelry manufacturing, adhering to company quality standards.
   • Issue orders to factories for production lines as per the planned pipeline.
   • Support the design team in developing and reviewing sample lines; address quality issues promptly.
   • Execute quality control best practices to ensure inventory and finished products meet standards.
   • Manage inspection processes to ensure product conformity.
   • Identify and institutionalize new techniques in production; monitor industry and competition for best practices.
2. Vendor/Supplier Management:
   • Scout and select vendors based on capabilities, performance, and quality standards.
   • Onboard new vendors and familiarize them with company norms and SOPs.
   • Seek continuous improvement, cost reduction, and process efficiencies in collaboration with product development, design, and category management.
   • Leverage jewelry manufacturing knowledge to challenge suppliers and optimize timelines and costs.
   • Collaborate with suppliers to maintain sourcing standards.
   • Manage supplier development timelines and conduct routine cost and risk analyses.
3. Administrative and Strategic Responsibilities:
   • Maintain seasonal production calendars to meet deadlines.
   • Coordinate with cross-functional teams for sourcing operations.
   • Conduct market research on trends, new suppliers, and cost-saving opportunities.
   • Lead supplier audits to ensure compliance with ethical, legal, and industry standards.
4. Skills and Qualifications:
   • Bachelor’s degree in supply chain management, business administration, or related field; master’s preferred.
   • 12-15+ years of experience in diamond sourcing or jewelry industry.
   • Strong background in production or sourcing within reputed organizations.
   • Knowledge of jewelry manufacturing, trends, and category specifics.
   • Understanding of contract laws, regulations, and compliance.
   • Excellent negotiation, analytical, problem-solving, and communication skills.
   • Proficiency in sourcing software and industry tools.

We prioritize safety, diversity, and sustainability in our operations. Successful candidates will undergo background screening, including criminal checks and qualification validation.

Role and Responsibilities:

• Able to start and stop the production line according to protocol and set the required parameters.
• Keeps accurate records and notes on production sheets.
• Follow test procedures on finished goods and record results that this may include: melt flow, specific gravity, hardness (test stand and handheld), etc.
• Operate forklift and hand trucks.
• Communicate with shift supervisor about processing problems and be able to troubleshoot and make necessary/permitted adjustments to fix them.
• Document and communicate adjustments according to protocol.
• Disassemble, clean, and reassemble equipment.
• Assist Debagging and Packing operators when needed.
• Assist to conduct QC/QA tests including sample preparation.
• Follow up to put-away/release the finished goods and change the status (downgrade/update) in the system
• Complete any other assignment given by the Supervisor.
• Continuous improvement and lean initiatives:
• Be able to put forward with good ideas and effective suggestion on continuous improvement.
• Be a member of the continuous team and, actively participate in departmental or cross-functional improvement projects, to drive process improvements, cost reduction, and operational excellence.
• Be competent to implement effective corrective and preventive actions to address issues.

Job Requirement:

• Minimum SPM passed English or 3 years’ experience in Polymer Extrusion
• Minimum N level or 3 years’ experience in Polymer Extrusion
• Possess Forklift License
• Trained with 6-Sigma Yellow Belt
• Have a good understanding on Lean Basics, RCA and LSW
• Strong Communication Skills
• Possess Forklift License
• Must be able to lift and carry up to 25kg
• Ability to perform duties under specific time requirements
• Ability to adapt to changing duties and responsibilities
• Able to listen and speak clearly
• No color blindness, skin allergy
• Able to work rotating shift, overtime as assigned
• Able to work on weekend as assigned
• Ability to work in a dusty, hot and humid environment

• Contribute to Life Science projects for Antaes Asia clients
• Drive initiatives to enhance operational processes and equipment performance, aiming to achieve the highest standards of manufacturing excellence.
• Lead thorough investigations into non-conformance incidents, developing comprehensive reports on issues related to quality and Environment, Health, and Safety (EHS) observed during manufacturing or batch reviews.
• Proactively monitor existing processes and equipment to identify opportunities for improvement and implement effective solutions.
• Provide strategic input and recommendations on operational improvements that align with business targets and contribute to overall manufacturing success.
• Review and contribute to the development of batch-related recipes (such as those in POMS and DeltaV), manual operations procedures, and additional manufacturing documentation to ensure accuracy and efficiency.
• Offer expert input or review the design of batch and cleaning manufacturing recipes within the Distributed Control System (DCS).
• Lead and manage digitalization projects that align with and support the company's strategic business objectives, enhancing automation and efficiency.
• Conduct training sessions for operators on processes and procedures, ensuring compliance and proficiency in operational practices.
• Lead/participate in safety risk assessments or participate in process hazard analysis as an operations representative (PHA).
• Actively resolve batch-related document errors in a timely manner.
• Communicate all events/issues effectively with relevant stakeholders.
• Provide inputs for investigation – impact assessment and appropriate CAPA.
• Ensure overall plant upkeep during the shift and ensure the plant is always in audit-ready mode.
• Oversee deliverables ahead, anticipate complexities, and prevent potential issues.
• Ensure processes are running as per planned schedule with minimal delays. Highlight effectively to shift supervisor if delays are expected.
• Contribute to the promotion of Antaes services on top of assistance provided to clients.

Job Requirements:

• Diploma/ Degree in Chemistry, Chemical Engineering, Science or equivalent
• Minimum 3 years of pharmaceutical, biopharmaceutical experience in Quality and/or Compliance (GMP) environment.
• Adhere to a safe work environment in accordance with regulatory and global/local EHS policies.
• Candidate must be highly motivated, able to work independently as well as in a team, and have good organizational and oral and written communication skills.
• Excellent communication skills, both written and verbal, in English.