Purpose:

To assist Project Manager in the delivery of Project Investment Plan (PIP) objectives in the following areas:

• Delivering site business benefits through implementation of major capital projects (>£10m). This encompass leading a group of multi-disciplinary professionals from inception of the project to the realization of business benefits.
• Safely delivers the engineered, procured, constructed and commissioned Capital Facilities against agreed Scope and Project Plan to meet the business and project objectives and quality expectations.
• Compliance to local government regulatory requirement
• Managing capital project performance management using GSK Production System (GPS) to drive safety, Quality, Cost and Schedule performance and waste elimination through continuous improvements.
• Compliance to applicable industrial standards and ensuring safety & quality compliance in alignment with GSK Global Supply Chain (GSC) requirement
• Communication and escalation of project progress, key risk and support requirements enabling successful delivery of the project and benefits realization.

Key Responsibilities:

• Lead / coordinate a team of multi-disciplinary and multi-functional professionals including engineers, designers, validation engineers, document controller, external contractors, safety & GMP professional and users to ensure capital projects delivery from inception to benefit realization
• Lead the commissioning and qualification execution as per the Project Plan
• Establishes and facilitates the Risk Management strategy including Risk Register, Assessment, Analysis and Contingency Management for the project and documents it in the Project Plan
• Manage and execute projects in compliance with Safety & Quality standards
• Manage and execute capital project implementation in accordance to the Global Capital Project Control Framework throughout the project life cycle and in accordance with local government legislation
• Support the Design Lead to ensure capital facility that meets user requirements in terms of facility’s operability and maintainability in accordance with User Requirement Specification (URS), GSK standard engineering practices and Global Engineering Standards (mandatory).
• Review recommended vendor selection list and submit to Project Manager for endorsement, as well as the approval of technical blueprints for construction works.
• Support Project Manager in coordination, scheduling and reporting of activities related to stakeholder management and, business change management including project communications
• Support Project Manager in the selection of contractors and suppliers and subsequent discharge of their responsibilities in accordance with the contract/purchase order
• Establishes and maintains Project documentation and records and facilitates handover of final project documentation in accordance with customer requirements.
• Support Project Manager to achieve both LEED and Green Mark certification and defined targets

Skills, Knowledge & Experience:

Professional

• Minimum Degree in any engineering discipline
• Minimum 8 years of working experience as Senior Project Engineer position
• Minimum 5 years of relevant experience in the project management field or in chemical/pharmaceutical industry

Technical

• Knowledge of industrial standards
• Knowledge of cost estimation methodology
• Knowledge of project schedule planning and control
• Knowledge of GMP, GEP and EHS requirements
• Appropriate knowledge of Local Standard Operating Procedures (SOP)
• Knowledge of GSK PM standard, Primary Supply Standard Engineering Practices (PMSEPs) relating to project management and Global Engineering Standards (GESs) relating to project management

To learn more about Singapore GSK and our people, please click on this link: https://www.linkedin.com/company/glaxosmithkline/life/gsksingapore

#Li-GSK

Why GSK?

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

GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).

Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.

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:

• Collaborating with Process Engineer & Engineering team to establish QC standards.
• Creating documentation for inspection criteria and quality plans.
• Collaborating with QA, Process, and Product teams to address quality issues through corrective action.
• Conducting in-process audits and final quality control audits with the Process team.

Requirements:

• Diploma in Manufacturing/Quality Engineering or equivalents.
• Minimum 1 year of working experience in Electronics Manufacturing Industry.
• Responsible for controlling Supplier Quality Assurance (SQA).
• Oversight of quality control for incoming, in-process, and outgoing products.
• Knowledgeable in ISO 9001, 14001, 13485, and 45001, and FDA requirements.
• Understanding IPC requirements in PCB assembly and quality standards for various manufacturing processes such as plastic molding, die casting, extrusion, metal stamping, and machining parts.

_______________________________________________________

HOW TO APPLY :

Interested candidates, please submit your resume by clicking on “Quick Apply” or contact [email protected] for more details.

Please provide following information in the resume for immediate processing

1) Reasons for leaving current and/or last employment

2) Last drawn and/or current salary

3) Expected salary

4) Date of availability and/or Notice Period

All applications will be treated in strictest confidence and only shortlisted candidates will be notified

Wee Wai Dan

EA License No : 03C5391

EA Reg No : R22109628

Responsibilities:

• Procurement of electronic components, machining, and mechanical parts.
• Engaging in negotiations with suppliers to secure improved pricing, quantities, and delivery fulfilment.
• Generating Purchase Orders in accordance with purchase requisitions.
• Ensuring timely delivery.
• Tracking outstanding backlogs and expediting urgent materials.
• Exploring alternative sourcing methods and facilitating cost reduction initiatives.

Requirements:

• Diploma in Electronic Engineering or equivalents.
• At least 2 years of purchasing experience in electronics manufacturing industry.
• Capable in Microsoft Word and Excel.

____________________________________________________________

HOW TO APPLY :

Interested candidates, please submit your resume by clicking on “Quick Apply” or contact [email protected] for more details.

Please provide following information in the resume for immediate processing

1) Reasons for leaving current and/or last employment

2) Last drawn and/or current salary

3) Expected salary

4) Date of availability and/or Notice Period

All applications will be treated in strictest confidence and only shortlisted candidates will be notified

Wee Wai Dan

EA License No : 03C5391

EA Reg No : R22109628

Responsibilities:

• Manage technical transfer of products/projects in assembly, testing, and customer interactions.
• Offer technical support for manufacturing and testing during product builds.
• Assist QC with technical support in resolving RMA issues.
• Support QA in compliance, regulatory matters, customer interactions, and audits.

Requirements:

• Diploma in Electronics Engineering and above.
• Minimum 2 years of working experience in Electronics Manufacturing Industry.
• Skilled in managing product/project manufacturing, transfers, and troubleshooting.
• Experienced in PCBA manufacturing and testing for products/projects.
• Preferably experienced in a manufacturing environment with ISO13485 and FDA standards.

_______________________________________________________

HOW TO APPLY :

Interested candidates, please submit your resume by clicking on “Quick Apply” or contact [email protected] for more details.

Please provide following information in the resume for immediate processing

1) Reasons for leaving current and/or last employment

2) Last drawn and/or current salary

3) Expected salary

4) Date of availability and/or Notice Period

All applications will be treated in strictest confidence and only shortlisted candidates will be notified

Wee Wai Dan

EA License No : 03C5391

EA Reg No : R22109628

Roles and Responsibilities

• Reports directly to the Production Manager
• Coordinate production workflows in the shopfloor
• Plan and prioritise operations to ensure maximum performance and minimal delay
• Plan a weekly machine loading plan and 3 months forecasted loading plan
• Determine manpower, equipment and raw materials needed to cover production demand
• Recommend to Production Manager on deployment of workers and other staff to meet production and delivery requirements
• Recommend shift schedule to Production Manager accordingly to production needs
• Liaise with Purchasing and Suppliers for material deliveries and outsourcing schedules
• Monitor jobs to ensure they will finish on time
• Address issues whenever they arise with the aim of minimal disruption
• Obtain output information (Number of finished products etc.)
• Prepare and submit status and performance
• Collaborate with Quality, Sales, Store, Engineering and other departments to ensure good production flow and coordination
• Manage and train the assistant planners and subordinates
• Any other duties assigned by the Manager

Requirements

• Diploma or further education/certificates is preferred
• Excellent knowledge of production planning and quality control principle
• Working knowledge of MS Office and ERP Systems
• Strong organisational and problem-solving skills
• Excellent communication abilities
• Able to converse in English and Mandarin
• Willing to learn and be a team player

1. POSITION

Your appointment will be Production Technician. Reporting directly to Production Supervisor, your role and responsibilities are outlined as follows:

a) Carry out production activities under designated role and fulfill the membrane product orders;

b) Able to identify and trouble-shoot onsite and help resolve problems arise during production;

c) Carry out daily and in-process maintenance to ensure system stability and minimize downtime;

d) Support and assist Facilities Maintenance Manager during system breakdown or scheduled preventive maintenance works;

e) Upkeep proper and accurate production logs for production SOP and quality improvement;

f) Perform such duties and tasks as may from time to time be assigned.

Overtime work may be required and you shall be entitled to overtime pay based on MOM guidelines.

2. SKILLS & Requirements

a) At least completed and passed secondary school.

b) At least one year’s experience as a Production Operator in a manufacturing environment locally.

c) Familiarity with operating and maintaining production tools, machinery and equipment.

d) Excellent attention to detail and ability to follow instructions accurately.

e) Ability to work effectively in a team-oriented environment.

f) Ability to perform repetitive tasks accurately

g) Commitment to maintaining a clean and organized work area.

3. SALARY

Salary and allowances are based on skills and relevant working experience in similar manufacturing environment.

4. HOURS

Working hours of the Company are from Monday to Friday 8:30 am to 6:00 pm.

5. PROBATION

You are required to serve a probation period of three (3) months from the date of commencement.

6. OVERTIME

You shall be entitled to overtime pay and claims based on MOM’s guideline.

Purpose

The Senior QA Validation is responsible for providing quality input and oversight on the following areas during the new product introduction to Singapore Tuas site.

• Design, construction, commissioning and qualification of new facility, equipment technology and system

You are expected to partner with all project members to anticipate, prepare and meet project deliverables on all phases of the project.

As a Senior QA Validation, he/ she represents the project team and point of contact on project quality matters related to equipment and material related activities. He/ she establishes effective working relationship with quality functions of supplier for facility, equipment, systems and material commissioning and qualification, global QA in GSK Vaccines and local site QA in Tuas.

The Senior QA Validation ensures that all commissioning and qualification activities under the project scope is designed in compliance with all applicable GSK Quality policies, regulatory requirement, and GMP practices/ procedures in place and in use within GSK Tuas.

Responsibilities

General Project Quality Management:

• Ensure quality-by-design in all aspects and stages of the project is in alignment with the defined Project Quality System and Quality Plan
• Accountable for quality inputs and ensure compliance to regulatory requirement, QMS, VSOPs and local procedures throughout the project lifecycle with regards to qualification and validation
• Deploys the appropriate project documentation through the project lifecycle.
• Identify and anticipate potential quality issue during the course of the project execution and avoid / minimize disruption to operations and compliance of GMPs.
• Execute quality compliance gap assessment exercises at appropriate stage of the project lifecycle.
• Ensure proper ties-in strategies and solutions between new facility and existing GMP areas to avoid / minimize disruptions to routine GMP operations.

Facility, Equipment, System Design, Development and Qualification :

• Define commissioning and validation approach and ensure deliverables are met per commissioning and validation plan to achieve validation status of the facility, equipment, technology and system.
• As an oversight of the validation activities, ensure all commissioning and validation requirement are met.
• Ensure timely completion of validation activities as per project schedule.

Knowledge, Skills and Experience

We are looking for professionals with these required skills to achieve our goals:

• Min degree in chemistry, science or engineering
• Min 2 years of experience in pharmaceutical industry
• Min 2 years of experience in commissioning & system validation
• Understanding of cGMP and regulatory requirement within pharmaceutical industry.
• Background in Computerized systems
• Background in equipment, facility validation experience
• Good knowledge of safety and environmental regulation
• Hands-on experience in pharmaceutical manufacturing (Preferred)
• Developing Project management skills or had hands-on experience in Project management (Preferred)
• Experience in start-up projects.

Why GSK?

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

GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).

Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves – feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.

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.

Roles and Responsibilities

• Manage daily operations in the Milling/Turning area
• Reports to the Production Manager
• Plan & coordinates to meet the production demand
• Accountable for daily quality and quantity output
• Develop and maintain the working standards reflecting the best practices
• Ensure that machinists carry out according to work instructions
• Implement new methodology for production
• Responds quickly to control the problems highlighted by the visual control systems
• Able to trace product quality conformity and provide appropriate actions
• Take part of the management routines and problems solving workshop
• Daily reporting to Production Manager on production schedules
• Motivates team and sets a good example

Requirements

• Diploma in Mechanical Engineering or equivalent
• Minimum 5 years as a supervisory experience
• Proven leadership skills and strong sense of responsibility
• Good organisation and time management skill
• Experience in Oil & Gas Industry is preferred
• Good in Computer Knowledge (i.e, Excel, MS Words etc)

Perform various activities and tasks requiredin the tablet and capsule final packing equipment.

· Operate all relevant equipment, clean, assemble and maintain the cleanliness of the equipment.

· Perform and maintain the documentation of operations in accordance with cGMP requirement.

· Operate the equipment appropriately in accordance with Standard Operating Procedure / batch document.

· Perform online monitoring of in process parameters / checks throughout the batch.

· Complete all relevant records and other documentation required for packing and related equipment in the work area.

· Perform all activities in accordance with cGMP.

· Maintain the cleanliness of work area to ensure cGMP compliance.

· Perform all other relevant duties required to meet the schedule.

· Check relevant material and product details against batch document

· Co-ordination with Engineering for break down rectification of both primary and secondary packing lines

· Involve in equipment / process qualification.

· Participate in investigation of process deviation, cGMP and all other compliance related matters, where applicable.

· Ensure compliance to GxP / Safety / Quality policies.

REQUIREMENT

· Good understanding of safe working practices and cGMP.

· Experience in bottle or blister oral solid dosage packing is preferred.

· A good team player with positive learning attitude.

· Willing to work in Tuas area, in cleanroom environment with full gowning.

EDUCATION & EXPERIENCE

· Minimum GCE 'O' level or NITEC or Higher NITEC or Diploma in Biotechnology / Biomedical / Mechanical / Mechatronics Engineering or relevant disciplines

· With 2-5 years of manufacturing experience in Pharmaceutical or related industries.

· Entry level NITEC / Higher NITEC / Diploma candidates are welcome to apply.

To assist in loading ,unloading ,shipping and receiving warehouse item.

Transporting materials to different locations within the facility.

Picking & Packing orders by DO.

Quality assurance (QA) duties ,including reporting product damage and shortages.

Ensuring that forklift driving areas are free from spills or obstructions.

Upkeep & Daily checks to ensure forklift is in good working condition.

Keeping up to date on health and safety requirements and forklift operating procedures

Perform other job-related functions as and when required by Supervisor.

Requirements:

1-3 years related experience in warehouse.

Prior forklift experience is preferred.

Possess valid certification to operate forklift (5 ton and above)

Must be comfortable working in the hot environment.

Must be able to work in a fast paced, warehouse environment.

Ability to work independently with strong attention to detail.

Proactive attitude and willingness to learn.

World No.1 player in industry is hiring Associate Engineers

Company Introduction

Angel Group owns the world’s largest share for the manufacture of casino playing cards and related equipment. Angel has 70 years of history; started from Japan and now has offices in USA, Singapore, Australia, Macau, Philippines, Mexico and France with a total of over 500 employees in the world. We are the first company in the Jurong Innovative District and this four-storey building is our next regional Headquarters, with an R&D Centre and factory.

Job Description

• Execute production as per production schedule and meet targeted output as set by management.
• Perform initial level of troubleshooting of equipment-related problems to minimise downtime.
• Interact with staff support to ensure smooth and optimum level of machine operational efficiency.
• Establish effective preventive maintenance.
• To control the quality of outputs using advanced technologies.
• To control the flow of various goods and materials through digital quantity monitoring system.
• Mange multiple priorities.
• Other related tasks.

Other information

• Location : West
• Company coach available from Jurong East MRT
• Working Hrs : 8:30AM – 5:30PM Off on Sat & Sun
• Lunch and uniform including safety gear are provided.

Job Description

Responsibilities

• Loading and uploading of goods onto vehicle according to delivery order
• Perform pickups and collection for the company covering specific areas
• Ensuring safe receipt, retrieval and dispatching of goods
• Delivering goods to our customers in a safe, courteous, and timely manner
• Establishing and maintaining excellent customer service during delivery
• To perform duties as tasked
• Class 3/4 Driving licence
• Able to work night shift and split shift
• Able to work ot on weekend and public holiday

JOB DETAILS

Vacancies available for Singaporeans and Residents only

Salary

$3,000- $6,000

JOB TYPE

Full-time

Permanent

Qualifications

All races are welcome

Candiates are required to load and unload of goods of at least 10kg

Candidates are required to handle heavy equipment

REQUIREMENTS

Must be able to work as ateam

Able to speak and understand simple English

Must be able to work 10hours shifts

T & C Manufacturing is looking for candidates with the following pre-requisites:

• Min. GCE "O" Level (chemistry and biology).
• Some Knowledge and experience in laboratory work.

Job Descriptions as follows:

1. To perform sensory evaluation, chemical and microbiological analysis on products and raw materials.
2. Understand sampling plan and methods of sampling and carry out raw materials and products sampling according to sampling plan if necessary.
3. Preparation of laboratory culture media and reagents when necessary
4. Prepare product sample upon request by customers or for internal and external lab testing
5. To record all information required into the provided inspection form and master list.
6. Maintain good housekeeping of the lab and equipments.
7. To inform QC HOD on lab inventory status to purchase necessary items and equipments for analysis.
8. Report to HOD if any non-conformances found on raw materials and products.
9. Keeping retained raw material product sample according to production date for future reference in case any quality dispute from customers.
10. To participate in company level activity task and duty from time to time.

• Ensure that all quality check procedures that put in place by the company are followed during every production phase.
• Educate production team on quality control issues and work with production supervisor to improve overall company safety and product quality.
• Create process checklists and coordinate quality inspections with production supervisor.
• Checklists and documents are to be filed properly.
• Maintains safe and healthy work environment by following standards and procedures, and complying with legal regulations.

• Plan and Develop the Project Idea. Every project starts as an idea. ...
• Create and Lead Your Dream Team. ...
• Monitor Project Progress and Set Deadlines. ...
• Solve Issues That Arise. ...
• Manage the Money. ...
• Ensure Stakeholder Satisfaction. ...
• Evaluate Project Performance.
• A Project Manager manages strategic and essential client projects. They complete their various projects within schedule and budget. Besides giving progress reports, their ability to identify project risks and opportunities are crucial in their daily roles.

Job Description

• Coordinate and supervise the daily production activities of assigned staff.

• Ensure that production goals and objectives are met in a timely and efficient manner.

• Monitor production performance, identify areas of improvement, and take corrective action as needed.

• Ensure that production processes are carried out in accordance with established safety and quality standards.

• Maintain a safe, clean, and organized work environment.

• Train and mentor production staff in the use of equipment and processes.

• Monitor and document employee attendance and performance.

• Able to develop basic training materials & conduct training.

• Develop and implement production schedules and workflows.

• Enforce company policies and procedures in a consistent and fair manner.

• Monitor consumable inventory levels, forecast & raise PR.

• Troubleshoot production issues and resolve them in a timely manner.

• Collaborate with project team, quality control, warehouse and other staff.

• Able to go on-site for meetings, survey & lead on-site job (e.g. shipyard).

Qualifications

• Min. diploma in related field.

• Holds forklift licence.

• Holds class 3 or above driving licence.

• Holds SSSC (Shipyard Supervisors Safety Course).

Skills / Knowledge / Experience

• Min. 2 years of experience in a production or manufacturing environment.

• Knowledge of production processes and equipment.

• Able to prioritize and manage multiple tasks.

• Able to work in a fast-paced & dynamic environment.

• Preferably experience in Quality Management System (QMS) related to ISO9001 and/or API is advantage.

• Proficient in Microsoft Excel (Intermediate), Word and ERP systems.

• Hands-on & willing to learn new skills.

• Good organizational, problem-solving, and communication skills.

• Able to work independently and as part of a team.

• Strong attention to detail and accuracy.

• Good problem-solving skills.

• Good communication abilities.

• Experience in Semi-con, Electronics Contract Manufacturing and/or Oil & Gas Industry are welcome.

Job Scope

• Handle general worker administration: work pass application / renewals, insurance & security bond applications, medical checkups, flight and dormitory arrangements
• Receive delivery of goods and issuance of tax invoice and delivery orders
• Other general administration activities

Requirements

• Minimum GCE O Levels qualification or equivalent
• Minimum 2 years experience in Construction or Manufacturing Industry
• Proficient in computer and internet use

Responsibilities:

• Oversee inventory to meet production demands and avoid shortages.
• Collaborate with internal teams and suppliers to ensure timely material delivery.
• Adjust production schedules as necessary to meet deadlines.
• Ensure product quality by working closely with the testing team.
• Schedule production staff according to workload requirements.
• Utilize ERP/MRP systems for streamlined planning and scheduling.
• Supervise production staff for effective task completion as required.

Requirements :

• Diploma in Manufacturing Engineering or equivalent.
• At least 1 year of working experience in electronics manufacturing.
• Experienced in material planning, inventory management, and proficient in ERP and MRP systems.
• Possess leadership and supervisory skills.

_________________________________________________________

HOW TO APPLY :

Interested candidates, please submit your resume by clicking on “Quick Apply” or contact [email protected] for more details.

Please provide following information in the resume for immediate processing

1) Reasons for leaving current and/or last employment

2) Last drawn and/or current salary

3) Expected salary

4) Date of availability and/or Notice Period

All applications will be treated in strictest confidence and only shortlisted candidates will be notified

Wee Wai Dan

EA License No : 03C5391

EA Reg No : R22109628

RESPONSIBILITIES

•To operate, assemble and monitor machinery and production equipment according to production specifications

•Assist with packing and shipment preparation of raw materials

•To ensure production floor align with 5S Policy in terms of hygiene, health and safety standards

•Execute basic testing, quality checks, detection of production/machinery technical errors and storage of raw materials

•Ability to perform lifting and transfer of heavy loads and high awareness of safety precautions

•Perform ad hoc duties when necessary

REQUIREMENTS

•Minimum 1 – 3 years of work experience in similar roles

•Understands basic flow of production process

•Independent and able to work under minimal supervision

•Physical Dexterity

He has to served as a technician, technical management section chief, deputy factory director, and factory director. He is also responsible for the production and operation management of the entire factory, rationally dispatching all factors such as raw oil entering the factory, intermediate production, and product delivery, so that production can be continuous for 24/7 hours, and on this basis, reducing operating costs and improving economic benefits; he is also responsible for the design, optimization and improvement of the biodiesel production process to make the biodiesel production process more reasonable and the equipment selection more appropriate, which is finally reflected in higher reaction efficiency, faster rate, more energy-saving, and lower production cost.

Requirements:

Bachelor Degree of Chemical Engineering

At least 8-10 years of relevant work experience in the related field

Must have indepth understanding of Biodiesel Products.

Excellent communication and interpersonal skills, capable of effective communication at all levels;

Strong analytical and problem-solving abilities, capable of independently completing tasks;

Proficient in office software with good writing and report preparation skills;

Strong sense of responsibility, detail-oriented, and able to handle high work pressure.

Responsibilities:

• Perform cable and high-power unit assembly tasks with provided training.
• Air leak testing.
• Production maintenance.

Requirements:

• Soldering and testing skills with provided training.
• Experience in manufacturing experience.

_________________________________________________________

HOW TO APPLY :

Interested candidates, please submit your resume by clicking on “Quick Apply” or contact [email protected] for more details.

Please provide following information in the resume for immediate processing

1) Reasons for leaving current and/or last employment

2) Last drawn and/or current salary

3) Expected salary

4) Date of availability and/or Notice Period

All applications will be treated in strictest confidence and only shortlisted candidates will be notified

Wee Wai Dan

EA License No : 03C5391

EA Reg No : R22109628

Job Description :

Responsible for overall coordination with MS internal teams, MS contractors, etc. meeting deliverable milestone/timelines

1. Gather hardware requirements BOM (model, delivery dates etc.) from various IT teams.

2. Build up rack matrix / elevations and manage the same, based on the requirement from different silos.

3. Co-ordinate with the Datacenter vendors for the buildout of the DC space with respect to the Racks, Cabling installation.

4. Centralize all installation requests for different IT Teams. Co-ordinate with the teams for Raising Change Management request.

5. Work closely with different IT third party vendors for equipment delivery. Co-ordinate with the teams for Raise access request to service providers.

6. Physical rack and stacking of IT equipment (e.g. power connections, patching, iLO configuration) handover to different IT silos.

7. Knowledge on cabling, Panduit products

8. Update equipment inventory management system and rack elevations.

9. Coordinate and escort Telco carrier vendors for circuit installations. Witness testing.

10. Coordinate and supervise installation of MS cabling contractor, witness any cabling testing onsite testing

11. Prepare defect lists for different MS contractors and Service providers installation.

12. Centralize all decommission requests for different IT silos. Raising change management request.

13. Work with disposal vendors on equipment disposal, HDD degaussing and update store room inventory records

14. Provide weekly reporting on project construction status to regional team.

15. Document management

16. Data Centre Power-down management: coordination with different vendors and all IT silos for DC power down events

17. Equipment Disposal : obtain all hardware equipment to be decommissioned from all teams, and work with IT Finance, IT Business Management, IT Security, and approved

Job Level Specific Duties :

• Able to work in Shifts when there is any shortage of resources

• Monitor the Service Now Queue and accept the tickets, assign the tasks to the team

• Audit regular Audit to check if the Inventory management systems is updated regularly by the team

• Update respective tools to support the operations

• Perform user acceptance testing of any new tools

• Create ad-hoc reports

• Update Sharepoint sites

• Proactively identify potential issues and drive resolution to avoid customer impact and facilitate continuous improvement.

• Identify opportunities for growth within the customer environment.

Education / Qualification :

· Typically requires 6-8 years relevant experience.

· Undergraduate degree or equivalent combination of education and work experience.

Skills :

· Language: Fluent in English and Mandarin would be an additional advantage

· Experience/Knowledge: Data center related work experience

· Good understanding of server installation procedure

· Good understanding of data center infrastructure and its resiliency design (UPS, Generator, CRAC, cabling, containment routes, etc). CDCP is a plus

· IT Hardware: (not limited to)

· Cable (UTP/fiber) patching and testing technique

· Working in a fast paced, dynamic environment and can work under pressure

· Project Management is a plus, such as PMP

· Excellent Communication skills

· Solid analytical, problem solving, negotiation and communication skills

· Solid organizing and planning skills, with ability to support multiple projects and multiple end-user communities simultaneously

· Solid experience with Excel, Microsoft Project

. Would be a good team player

Job description

Responsibilities:
• Manage and oversee all aspects of production operations.
• Develop and implement strategies to improve production efficiency and meet production targets.
• Lead and motivate a team of production supervisors and operators.
• Ensure compliance with safety standards and regulations.
• Monitor production outputs and quality to meet customer requirements.
• Work closely with cross-functional teams to coordinate production schedules and resolve any production issues.
• Implement and maintain standard operating procedures for production processes.
• Analyze production data and metrics to identify areas for improvement.
• Manage inventory levels and coordinate with procurement to ensure adequate supply of materials.
• Participate in budgeting and cost control initiatives.

Responsibilities:

• Lead and manage fragrance production operations to meet production target and customer’s specifications

• Provide leadership and work directions to the production team in consistent with business objectives and company policies.

• Responsible for the production manpower planning, hiring, allocation and cost control.

• Ensure finished products that comply with customer specifications and company regulatory requirements and standards

• Investigate and find out the root cause with regards to customer complaints and internal rejects

• Work closely with Planning, Purchasing and Research & Development Departments to ensure efficient stocks level of raw materials to meet timely delivery of finished products

• Ensure that the Standard Operating Procedures (SOP's) are current, accurate and team are trained in the relevant job according SOPs.

• Initiate reviews of production budget, processes, policies and procedures to improve efficiency, reduce cost and increase productivity whilst maintaining industry standards of quality and safety

• Monitor, study and improve on machine utilization, work & material, production cost performance and initiates cost reduction program

• Identify, plan and coordinate developmental training needs for staff to maintain standards of competencies.

Qualifications:

• Degree in Chemical Engineering, Manufacturing, or related field
• 5 years of experience in a Chemical manufacturing operation
• 3 or more years of experience in a Managerial or leadership role
• Demonstrated good organizational and interpersonal skills and able to communicate well with all levels of staff in the organization.