825 Manufacturing jobs in Woodlands

Job Description

Job Description

• Preparation of coconut water and coconut meat.
• Check the quality and quality control of all the foods items to meet the food safety standards.
• Maintaining cleanliness of workplace.
• Assist in other ad hoc duties when required

Job Requirements

Job Requirements

• Able to carry load of at least 15kg.
• Able to cope with the food production environment (work in clean and cool environment)

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

• Works with general workers, assisting the Operations manager in running production line
• Manages and oversees daily food production
• Supervising and training employees
• Implementing processes to reduce costs
• Analyzing and reporting on performance
• Oversee efficiency of operational processes
• Analyze business requirements and customer needs
• Research methods to improve operations and reduce costs
• Monitor and report on department performance
• Provide administrative support (e.g. updating inventory)
• Ensure compliance with company policies and regulations
• Previous experience as an operations supervisor or similar role
• Excellent project management skills
• Team leadership

Requirements

At least 2 years of work experience in related field

Able to work on weekends & Public Holidays

Physically fit and able to carry heavy goods when required

Purpose: Responsible for the complete end-to-end planning, direction, and coordination of all the manufacturing processes related to system integration for a specific project. Together with the program team, the Manufacturing Engineer is to ensure that assembly can meet costs, quality, and delivery requirements.

Key Areas of Responsibilities:

• Design of production layout to enable production to fulfill build plan forecast or pre-defined production run rate.
• Define requirements for assembly tools and equipment to support product realization and build plan.
• Participate actively in PQP to ensure that risks are identified, and preventive actions defined and implemented.
• Implement a certification program for assembly to ensure that assembly module leads are trained and certified to carry out specific assembly tasks.
• Collaborate with the Process Engineer in the design of the assembly Kit Kart for issue of materials into the clean room and effective handling of materials inside the production area.
• Lead in resolving technical problems faced by Assembly, and resolve internal and customer quality complaints.
• Monitor assembly capacity of the program, and perform ramp assessment when required, to fulfill build plan system delivery.
• Contribute to the system build progress meetings together with the program team to meet on-time delivery targets.
• Evaluate assembly efficiency and implement improvements to achieve the calculated standard time.
• Monitor all customer's consigned equipment to ensure all are inventoried, calibrated, and maintained regularly.
• Identify and implement improvements to shorten production cycle time, improve overall production efficiency, improve quality performance, enhance safety or to boost sustainability.
• Support and participate in company continuous improvement program.

• Diploma/Bachelor in Engineering (Mechanical, Mechatronics, Electrical, Precision or Industrial Engineering) or related field.
• At least 3 years of experience as an engineer in the manufacturing assembly environment.
• Lean Six Sigma Green certified is preferred.
• Strategic, creative, and systemic thinking.
• Excellent leadership and effective communication with all levels of associates and management.

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Job Description:

• Night shift production supervisory & manpower planning / deployment to support overall production output commitment.
• Responsible for fulfillment of daily production target, conducting manpower training and assessment.
• Daily production data compiling reports to identify lapses and plan recovery.
• Supervising, coordinating, and scheduling the activities of workers who process, package, test, and grade food and beverage products.
• Establishing methods to meet work schedules and coordinating work activities with other departments.
• Resolving work problems and recommending measures to improve productivity and product quality.
• Requisitioning materials and supplies.
• Ensuring food quality, sanitation, and safety policies are followed.
• Managing inventory control and shipping activities.
• Implementing new procedures to lower inventory losses.
• Developing menu items and recipes for a variety of food products.

Job Requirements:

• Min NITEC / Diploma / Degree in any courses
• Min 5 years of supervisory experience in manufacturing industry

Job Description:

• 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.
• Leads/participates in safety risks assessments or participates in process hazard analysis as an operations representative (PHA)
• Actively resolve batch related document errors in a timely manner
• Communicates all events/issues effectively with relevant stakeholders
• Provide inputs for investigation – impact assessment and appropriate CAPA
• Ensures overall plant upkeep during the shift and ensuring plant is always in audit ready mode
• Oversees deliverables ahead, anticipates complexities and prevents potential
• Ensures processes are running as per planned schedule with minimal delays. Highlights 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
• Adheres to safe work environment in accordance with regulatory and global/local EHS policies
• Candidate must be highly motivated, be 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

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift

Job Description

Responsibilities

• Assemble Single-Use Bio-Processing Containers for critical sterile liquid-handling applications in the biopharmaceutical industry.
• Follow standard work instructions and interpret technical drawings to ensure consistent product quality.
• Maintain strict adherence to ISO 13485:2016, ISO 22301:2019, and current Good Manufacturing Practices (cGMP) documentation standards to ensure regulatory compliance and quality assurance.
• Complete all relevant training before performing any task.
• Timely completion of relevant batch records with adherence to Good Documentation Practice (GDP).
• Participate in Practical Process Improvements (PPI) to improve production efficiency and product quality.
• Adhere to all safety protocols and guidelines to maintain a safe working environment.
• Work collaboratively with team members, including engineers, quality assurance, and maintenance personnel.
• Communicate effectively with supervisors and colleagues to ensure smooth production operations.
• Ensure accurate storage and handling of materials to prevent contamination or damage.
• Perform any other duties as assigned by the Manager.

Requirements

• Minimum 2 years of relevant experience in pharmaceutical manufacturing.
• Minimum GCE 'O' Level/Nitec.
• Physically fit to lift objects up to 20kg when required.

Responsibilities:

• Lead and execute multiple Change Records (Planned events) for the assigned area for creation of new Batch Records and Standard Operation Procedures for Production,
• Support Change Records Assessment and GMP documentation Review.
• Responsible for providing support to the assigned manufacturing operations by developing, coordinating and facilitating small to medium projects to ensure planned, predictable production operations in compliance with GMP regulations.
• Lead and execute Continuous Process Improvements, CAPAs and Change Records in assigned area.
• Provide routine and ad hoc support for planning, coordinating, execution, and performance improvement of key manufacturing processes such as product change over.
• Lead project teams to trouble shoot medium to complex problems and support continuous process improvement. Facilitate root cause analysis (RCA) with input from SMEs, develop and implement change to improve performance.
• Collaborate with multidisciplinary teams to achieve project objectives.
• Assist in experimental design and troubleshooting as needed.

About You:

• Bachelor's degree in a relevant life science field (e.g., biology, biotechnology, biochemistry).
• Candidates with Batch Record Creation experience in a GMP environment in biologics or pharmaceutical industry are preferred.
• Strong attention to detail, organizational skills, and the ability to work independently or in a team.
• Excellent communication skills, both written and verbal, in English.
• Adherence to safety protocols and regulatory compliance.

Duration: 9-months contract role