Expoint – all jobs in one place
המקום בו המומחים והחברות הטובות ביותר נפגשים

דרושים Sup Ops Maint Jurong ב-West Pharma ב-Singapore, Singapore

מצאו את ההתאמה המושלמת עבורכם עם אקספוינט! חפשו הזדמנויות עבודה בתור Sup Ops Maint Jurong ב-Singapore, Singapore והצטרפו לרשת החברות המובילות בתעשיית ההייטק, כמו West Pharma. הירשמו עכשיו ומצאו את עבודת החלומות שלך עם אקספוינט!
חברה (1)
אופי המשרה
קטגוריות תפקיד
שם תפקיד (1)
Singapore
Singapore
נמצאו 9 משרות
05.09.2025
WP

West Pharma Production Operator Ops Jurong Singapore, Singapore

Limitless High-tech career opportunities - Expoint
Under the supervision of a trainer or supervisor perform the following duties... process trimmed product through washing and drying process per site SOI’s and work instructions. Ensure that the equipment...
תיאור:
Essential Duties and Responsibilities
  • Under the supervision of a trainer or supervisor perform the following duties...
  • process trimmed product through washing and drying process per site SOI’s and work instructions.
  • Ensure that the equipment is set up accurately.
  • Ensure continual flow of product through the module from the mold press thru the trim press.
  • Operate a mold press to produce molded panels of product following site SOI’s and work instructions.
  • Operate a manual / automatic trim press as needed following site SOI’s and work instructions.
  • Process product through any required special treatments such as sort, silicone, chlorination, etc.
  • As needed, set up pack scales for weighing and packing of finished product and prepare carton labels for boxing and shipping.
  • Alert the Area Supervisor to conditions that may prevent meeting production and quality expectations.
  • Accurately maintain all required documentation and paperwork to ensure product traceability.
  • Inspect molded/trimmed work to ensure quality product is being produced.
  • Move materials into and out of the area as required.
  • Properly clean and prep assigned workstations/equipment during and prior to the next available shift.
  • Promotes and supports a Lean environment.
  • Conforms with and abides by all corporate and site-specific regulations, policies, work procedures, instruction, and all safety rules.
  • Exhibits regular, reliable, punctual and predictable attendance.
  • Performs other duties as assigned based on business needs.
Education
  • High School Diploma or GED preferred
Work Experience
  • No min required
Preferred Knowledge, Skills and Abilities
  • Must possess an acute attention to detail
  • Basic computer skills, i.e. use a mouse/keyboard.
  • Ability to apply Good Manufacturing Practices (GMP)
  • General use of computer work station and ability to use SAP commands is preferred
  • Must be willing and able to work as a team member and make general decisions within authorized job responsibilities
  • Must be able to train and guide others as required.
  • Must be able to read and write in English
Physical Requirements
Medium-Exerting up to 50lb/22kg of force occasionally and/or up to 20lbs/9kg of force frequently, and/or up to 10lbs/4kgs of force constantly to move objects.
Show more
03.09.2025
WP

West Pharma QC Technician Jurong Singapore, Singapore

Limitless High-tech career opportunities - Expoint
Be responsible to support the execution of Mill Control, In-coming, In-process and Final AQL inspection to deem product compliance. Provide technical support, involve in problem-solving and improvement activities to enhance...
תיאור:

Job Summary:

In this role, you will

  • Be responsible to support the execution of Mill Control, In-coming, In-process and Final AQL inspection to deem product compliance.
  • Provide technical support, involve in problem-solving and improvement activities to enhance operational activities.

Essential Duties and Responsibilities:

  • Perform uncured and cured elastomer tests per procedure.
  • Perform auxiliary / component incoming & mold-line in process inspection per procedure.
  • Perform semi-finish / finished goods inspection (visual / dimensional / document review) per procedure.
  • Perform incoming raw materials sampling and retain samples retrieval independently at an external warehouse, per procedure.
  • Ensure all preparations, test assessment, inspection, post activities and retain samples are accurate and adequately documented and controlled (eg SAP system, Ms Office, etc)
  • Ensure all related calibration activities are timely and appropriately performed before use.
  • Highlight daily quality defects & collaborate with production team to trigger early troubleshooting and recovery. Escalate abnormal trends in product quality to team lead to trigger resolution.
  • Coordinate daily operational tasks assignment in QC in the absence of Team Lead.
  • Prepare & actively participate in Tier 1 Shift Start Up and ensure proper handover and takeover for smooth daily operations.
  • Prepare daily reports on time for Tier 2 Department Meeting & Tier 2.5 Production Meeting.

Attend Tier 2.5 Production Meeting as QC representative and follow up actions from the meeting.

  • Train and guide T1 Technicians according to specified coaching methodology and provide constructive feedback to trainee for improvements.
  • Other duties as assigned by superior.

Basic Qualifications:

  • Academic qualification preferably Nitec or Higher Nitec in Engineering or relevant fields, and/or equivalent qualification.
  • Computer literate and good grasp of Microsoft Office.
  • Preferably 3-5 years work experience in QA/QC related activities.
  • Added advantage with SAP, cGMP, Basic Lean and/or ISO working experience.
  • Preferably with exposure to medical device, pharmaceutical or related manufacturing environment.

Preferred Knowledge, Skills and Abilities:

  • Able to be aware of all relevant standard operating procedures as per Company policy as they are related to the position covered by this Job Description
  • Support and contribute to Lean Sigma programs and activities towards delivery of the set target.
  • Able to comply with the company’s safety policy at all times.
    • Proper use of Personal Protective Equipment (PPE) in respective work environments.
    • Report unsafe conditions or acts to responsible persons for corrections and improvements.
    • Always adopt the risk assessment control practice mentioned in HIRA for Mill Control.
    • Attain N3 laser license for the safe use of Lasermike measuring equipment
  • Able to comply with the company’s quality policy at all times.
    • Participate in establishment and maintenance of documented procedure.
    • Participate in monitoring / improvement activities to enhance operational support activities.
  • Good communication & teamwork skills.
  • Self-motivated and positive thinking.
  • Proficiency in workplace English for work applications and interfaces.

Travel Requirements:

  • Not Applicable

Physical and Mental Requirements:

  • 12 hour, 2-2-3 working shift patterns.
  • 20/30 Vision minimum, at near and/or far with at least one eye with or without corrective lenses and no color deficiency.
Show more

משרות נוספות שיכולות לעניין אותך

24.08.2025
WP

West Pharma Production Operator Ops Jurong Singapore, Singapore

Limitless High-tech career opportunities - Expoint
Process trimmed product through washing and drying process per site SOI’s and work instructions. Ensure that the equipment is set up accurately. Ensure continual flow of product through the module...
תיאור:
Essential Duties and Responsibilities

Under the supervision of a trainer or supervisor perform the following duties...

  • Process trimmed product through washing and drying process per site SOI’s and work instructions.
  • Ensure that the equipment is set up accurately.
  • Ensure continual flow of product through the module from the mold press thru the trim press.
  • Operate a mold press to produce molded panels of product following site SOI’s and work instructions.
  • Operate a manual / automatic trim press as needed following site SOI’s and work instructions.
  • Process product through any required special treatments such as sort, silicone, chlorination, etc.
  • As needed, set up pack scales for weighing and packing of finished product and prepare carton labels for boxing and shipping.
  • Alert the Area Supervisor to conditions that may prevent meeting production and quality expectations.
  • Accurately maintain all required documentation and paperwork to ensure product traceability.
  • Inspect molded/trimmed work to ensure quality product is being produced.
  • Move materials into and out of the area as required.
  • Properly clean and prep assigned workstations/equipment during and prior to the next available shift.
  • Promotes and supports a Lean environment.
  • Conforms with and abides by all corporate and site-specific regulations, policies, work procedures, instruction, and all safety rules.
  • Exhibits regular, reliable, punctual and predictable attendance.
  • Performs other duties as assigned based on business needs.
Education
  • High School Diploma or GED preferred
Work Experience
  • No min required
Preferred Knowledge, Skills and Abilities
  • Must possess an acute attention to detail.
  • Basic computer skills, i.e. use a mouse/keyboard.
  • Ability to apply Good Manufacturing Practices (GMP).
  • General use of computer work station and ability to use SAP commands is preferred.
  • Must be willing and able to work as a team member and make general decisions within authorized job responsibilities.
  • Must be able to train and guide others as required.
  • Must be able to read and write in English.
Physical Requirements
Medium-Exerting up to 50lb/22kg of force occasionally and/or up to 20lbs/9kg of force frequently, and/or up to 10lbs/4kgs of force constantly to move objects.
Show more

משרות נוספות שיכולות לעניין אותך

28.06.2025
WP

West Pharma Production Senior Operator Ops Jurong Singapore, Singapore

Limitless High-tech career opportunities - Expoint
Under the supervision of a trainer or supervisor perform the following duties... process trimmed product through washing and drying process per site SOI’s and work instructions. Ensure that the equipment...
תיאור:
Essential Duties and Responsibilities
  • Under the supervision of a trainer or supervisor perform the following duties...
  • process trimmed product through washing and drying process per site SOI’s and work instructions.
  • Ensure that the equipment is set up accurately.
  • Ensure continual flow of product through the module from the mold press thru the trim press.
  • Operate a mold press to produce molded panels of product following site SOI’s and work instructions.
  • Operate a manual / automatic trim press as needed following site SOI’s and work instructions.
  • Process product through any required special treatments such as sort, silicone, chlorination, etc.
  • As needed, set up pack scales for weighing and packing of finished product and prepare carton labels for boxing and shipping.
  • Alert the Area Supervisor to conditions that may prevent meeting production and quality expectations.
  • Accurately maintain all required documentation and paperwork to ensure product traceability.
  • Inspect molded/trimmed work to ensure quality product is being produced.
  • Move materials into and out of the area as required.
  • Properly clean and prep assigned workstations/equipment during and prior to the next available shift.
  • Promotes and supports a Lean environment.
  • Conforms with and abides by all corporate and site-specific regulations, policies, work procedures, instruction, and all safety rules.
  • Exhibits regular, reliable, punctual and predictable attendance.
  • Performs other duties as assigned based on business needs.
Education
  • High School Diploma or GED preferred
Work Experience
  • No min required
Preferred Knowledge, Skills and Abilities
  • Must possess an acute attention to detail
  • Basic computer skills, i.e. use a mouse/keyboard.
  • Ability to apply Good Manufacturing Practices (GMP)
  • General use of computer work station and ability to use SAP commands is preferred
  • Must be willing and able to work as a team member and make general decisions within authorized job responsibilities
  • Must be able to train and guide others as required.
  • Must be able to read and write in English
Physical Requirements
Medium-Exerting up to 50lb/22kg of force occasionally and/or up to 20lbs/9kg of force frequently, and/or up to 10lbs/4kgs of force constantly to move objects.
Show more

משרות נוספות שיכולות לעניין אותך

28.06.2025
WP

West Pharma Sup Ops Maint Jurong Singapore, Singapore

Limitless High-tech career opportunities - Expoint
People Leadership: Supervise a team of Technicians across 3 levels:T1 (entry level) – provide hands-on guidance and close supervision.T2 (intermediate level) – support development of autonomy and technical judgment.T3 (Team...
תיאור:
Job Summary

The Maintenance Supervisor is a people manager responsible for leading and developing a multi-tier team of Technicians (T1–T3) across electrical, mechanical, pneumatic, hydraulic, and PLC-based systems. The Supervisor ensures reliable operation and compliance of all production and utility equipment supporting the manufacturing of pharmaceutical-grade rubber stoppers. This position requires both strong leadership and sound technical expertise to drive team performance, ensure safe practices, and maintain production uptime.

Essential Duties and Responsibilities
  • People Leadership: Supervise a team of Technicians across 3 levels:
    • T1 (entry level) – provide hands-on guidance and close supervision.
    • T2 (intermediate level) – support development of autonomy and technical judgment.
    • T3 (Team Leads) – mentor and coordinate execution through delegation
  • Conduct performance reviews, coaching, and development planning for all direct reports.
  • Facilitate daily Tier meetings, assign tasks, and manage shift rosters.
  • Technical Responsibilities:
    • Troubleshoot and resolve complex equipment issues involving electrical, mechanical, pneumatic, and hydraulic systems, including PLC-controlled machinery.
    • Ensure completion and accuracy of preventive and corrective maintenance using the site’s CMMS (SAP or equivalent).
    • Participate in root cause analysis (RCA), failure mode analysis, and implement countermeasures for chronic issues.
  • Compliance and Documentation:
    • Ensure all maintenance activities are compliant with cGMP, safety, and cleanroom standards.
    • Maintain accurate maintenance records, risk assessments, and job safety analyses (JSAs).
    • Support audits and inspections by regulatory bodies and internal QA.
  • Continuous Improvement:
    • Drive 5S, TPM, and reliability-centered maintenance (RCM) initiatives.
    • Collaborate with Engineering to support equipment upgrades and utility modifications.
  • Collaboration and Communication:
    • Serve as the primary communication bridge between maintenance personnel, production, engineering, and QA.
    • Coordinate with external contractors or vendors during maintenance shutdowns or installations.
Education
  • Diploma or Degree in Mechanical, Electrical, or Mechatronics Engineering (or equivalent technical discipline).
  • Minimum 8 years of experience in plant maintenance, including at least 3 years in a people management role, preferably within a pharmaceutical manufacturing or processing environment.
Preferred Knowledge, Skills and Abilities
  • Excellent leadership and interpersonal skills with a passion for mentoring.
  • Hands-on troubleshooting and analytical skills.
  • Proficiency in SAP or other CMMS platforms.
  • Ability to read technical schematics, wiring diagrams, and mechanical drawings.
  • Good written and verbal communication skills in English.
  • Resilient under pressure and able to make decisions in fast-paced environments.
Physical Requirements
Sedentary-Exerting up to 10lbs/4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time.
Additional Requirements
  • Ability to work in challenging environments, including areas characterized by heat and dust, as well as in cleanroom settings.
  • Physical endurance, flexibility, visual and hearing ability are required to perform tasks effectively.
  • Willing to support execution of critical tasks beyond normal working hours should the need arise.
  • Committed to lifelong learning to remain abreast of industry trends and new technologies.
  • A team player and ability to work collaboratively with all levels.
  • Conduct training with confidence, patience, empathy, and motivation.
Show more

משרות נוספות שיכולות לעניין אותך

02.05.2025
WP

West Pharma Sr QC Technician Jurong Singapore, Singapore

Limitless High-tech career opportunities - Expoint
Be responsible to support the execution of Mill Control, In-coming, In-process and Final AQL inspection to deem product compliance. Provide technical support, involve in problem-solving and improvement activities to enhance...
תיאור:

Job Summary:

In this role, you will

  • Be responsible to support the execution of Mill Control, In-coming, In-process and Final AQL inspection to deem product compliance.
  • Provide technical support, involve in problem-solving and improvement activities to enhance operational activities.

Essential Duties and Responsibilities:

  • Perform uncured and cured elastomer tests per procedure.
  • Perform auxiliary / component incoming & mold-line in process inspection per procedure.
  • Perform semi-finish / finished goods inspection (visual / dimensional / document review) per procedure.
  • Perform incoming raw materials sampling and retain samples retrieval independently at an external warehouse, per procedure.
  • Ensure all preparations, test assessment, inspection, post activities and retain samples are accurate and adequately documented and controlled (eg SAP system, Ms Office, etc)
  • Ensure all related calibration activities are timely and appropriately performed before use.
  • Highlight daily quality defects & collaborate with production team to trigger early troubleshooting and recovery. Escalate abnormal trends in product quality to team lead to trigger resolution.
  • Coordinate daily operational tasks assignment in QC in the absence of Team Lead.
  • Prepare & actively participate in Tier 1 Shift Start Up and ensure proper handover and takeover for smooth daily operations.
  • Prepare daily reports on time for Tier 2 Department Meeting & Tier 2.5 Production Meeting.

Attend Tier 2.5 Production Meeting as QC representative and follow up actions from the meeting.

  • Train and guide T1 Technicians according to specified coaching methodology and provide constructive feedback to trainee for improvements.
  • Other duties as assigned by superior.

Basic Qualifications:

  • Academic qualification preferably Nitec or Higher Nitec in Engineering or relevant fields, and/or equivalent qualification.
  • Computer literate and good grasp of Microsoft Office.
  • Preferably 3-5 years work experience in QA/QC related activities.
  • Added advantage with SAP, cGMP, Basic Lean and/or ISO working experience.
  • Preferably with exposure to medical device, pharmaceutical or related manufacturing environment.

Preferred Knowledge, Skills and Abilities:

  • Able to be aware of all relevant standard operating procedures as per Company policy as they are related to the position covered by this Job Description
  • Support and contribute to Lean Sigma programs and activities towards delivery of the set target.
  • Able to comply with the company’s safety policy at all times.
    • Proper use of Personal Protective Equipment (PPE) in respective work environments.
    • Report unsafe conditions or acts to responsible persons for corrections and improvements.
    • Always adopt the risk assessment control practice mentioned in HIRA for Mill Control.
    • Attain N3 laser license for the safe use of Lasermike measuring equipment
  • Able to comply with the company’s quality policy at all times.
    • Participate in establishment and maintenance of documented procedure.
    • Participate in monitoring / improvement activities to enhance operational support activities.
  • Good communication & teamwork skills.
  • Self-motivated and positive thinking.
  • Proficiency in workplace English for work applications and interfaces.

Travel Requirements:

  • Not Applicable

Physical and Mental Requirements:

  • 12 hour, 2-2-3 working shift patterns.
  • 20/30 Vision minimum, at near and/or far with at least one eye with or without corrective lenses and no color deficiency.
Show more

משרות נוספות שיכולות לעניין אותך

17.04.2025
WP

West Pharma Sr QC Technician Jurong Singapore, Singapore

Limitless High-tech career opportunities - Expoint
Perform cGMP Data Review on the analytical data generated in Lab Operations which may include raw materials and finished goods, product performance, container closure integrity, particle analysis, and/or microscopy/investigation. Review...
תיאור:
Job Summary
In this role you will be responsible to independently provide analytical review of the data generated for internal and external customers as well as supporting post-production related Quality activities such as finished batch release, including sterilization, packaging specifics, work order approval and support additional quality department activities. This position also requires maintaining knowledge of the current local and/or International regulations/guidelines/policies applicable to West's products and services.
Essential Duties and Responsibilities
  • Perform cGMP Data Review on the analytical data generated in Lab Operations which may include raw materials and finished goods, product performance, container closure integrity, particle analysis, and/or microscopy/investigation
  • Review the analytical raw data generated by laboratory operations according to established methods, protocols, Compendia and Work Instructions for cGMP compliance
  • Review Electronic Data and Audit Trails for data integrity compliance
  • Review Lab Operations Methods, Protocols, and Work Instructions for cGMP Compliance
  • Responsible to review and approve of samples and / or batch release including review and approval of the finished Device History File documentation and Certificate of Compliance issuing.
  • Responsible to review and approve of relevant packaging and respective graphics artwork
  • Maintain working knowledge of computer software packages including MS Office suite, Adobe, MasterControl, LIMS, and LMS
  • Collaborate as needed on proposed path forward regarding documentation questions
  • Support preparations for periodical management reviews
  • Initiate processes in SAP as needed related to finished batch release and sterilization processes
Additional Responsibilities
  • Provide a “Customer Service” attitude when interacting with internal and external customers while accomplishing work, production, and achieving quality standards.
  • Maintain a clean, orderly, and safe workstation and environment at all times.
  • Conform with and abide by all regulations, policies, work procedures, instruction, and safety rules.
  • Exhibit regular, reliable, and punctual attendance.
  • Perform other duties as assigned based on business needs.
  • Keep current with new GMP compliance guidance and internal QA procedures
  • Support new GMP compliance guidance and Data Integrity initiatives
Education
  • Bachelor's Degree Technical Studies or Science or equivalent experience preferred
Work Experience
  • 0-3 years of experience required and
  • Minimum 2 years of cGMP experience preferred
Preferred Knowledge, Skills and Abilities
  • Able to be aware of all relevant standard operating procedures as per Company policy
  • Support and contribute to Lean Sigma programs and activities towards delivery of the set target
  • Possess ability to work independently and as part of a team with self-motivation, adaptability, and a positive attitude
  • Willingness to learn new and review new analytical techniques
  • Meet individual and departmental goals as required
Physical Requirements
Sedentary-Exerting up to 10lbs/4kgs of force occasionally, and/or negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects, including the human body. Sedentary work involves sitting most of the time.
Additional Requirements
  • Ability to learn, understand, and remember normal tasks.
  • Ability to hear, speak, and understand conversation in English.
  • Must maintain the ability to work well with others in a variety of situations.
  • Must be able to multi-task, work under time constraints, problem solve, and prioritize.
  • Read and interpret data, information and documents
  • Work under deadlines with constant interruptions
Show more

משרות נוספות שיכולות לעניין אותך

Limitless High-tech career opportunities - Expoint
Under the supervision of a trainer or supervisor perform the following duties... process trimmed product through washing and drying process per site SOI’s and work instructions. Ensure that the equipment...
תיאור:
Essential Duties and Responsibilities
  • Under the supervision of a trainer or supervisor perform the following duties...
  • process trimmed product through washing and drying process per site SOI’s and work instructions.
  • Ensure that the equipment is set up accurately.
  • Ensure continual flow of product through the module from the mold press thru the trim press.
  • Operate a mold press to produce molded panels of product following site SOI’s and work instructions.
  • Operate a manual / automatic trim press as needed following site SOI’s and work instructions.
  • Process product through any required special treatments such as sort, silicone, chlorination, etc.
  • As needed, set up pack scales for weighing and packing of finished product and prepare carton labels for boxing and shipping.
  • Alert the Area Supervisor to conditions that may prevent meeting production and quality expectations.
  • Accurately maintain all required documentation and paperwork to ensure product traceability.
  • Inspect molded/trimmed work to ensure quality product is being produced.
  • Move materials into and out of the area as required.
  • Properly clean and prep assigned workstations/equipment during and prior to the next available shift.
  • Promotes and supports a Lean environment.
  • Conforms with and abides by all corporate and site-specific regulations, policies, work procedures, instruction, and all safety rules.
  • Exhibits regular, reliable, punctual and predictable attendance.
  • Performs other duties as assigned based on business needs.
Education
  • High School Diploma or GED preferred
Work Experience
  • No min required
Preferred Knowledge, Skills and Abilities
  • Must possess an acute attention to detail
  • Basic computer skills, i.e. use a mouse/keyboard.
  • Ability to apply Good Manufacturing Practices (GMP)
  • General use of computer work station and ability to use SAP commands is preferred
  • Must be willing and able to work as a team member and make general decisions within authorized job responsibilities
  • Must be able to train and guide others as required.
  • Must be able to read and write in English
Physical Requirements
Medium-Exerting up to 50lb/22kg of force occasionally and/or up to 20lbs/9kg of force frequently, and/or up to 10lbs/4kgs of force constantly to move objects.
Show more
בואו למצוא את עבודת החלומות שלכם בהייטק עם אקספוינט. באמצעות הפלטפורמה שלנו תוכל לחפש בקלות הזדמנויות Sup Ops Maint Jurong בחברת West Pharma ב-Singapore, Singapore. בין אם אתם מחפשים אתגר חדש ובין אם אתם רוצים לעבוד עם ארגון ספציפי בתפקיד מסוים, Expoint מקלה על מציאת התאמת העבודה המושלמת עבורכם. התחברו לחברות מובילות באזור שלכם עוד היום וקדמו את קריירת ההייטק שלכם! הירשמו היום ועשו את הצעד הבא במסע הקריירה שלכם בעזרת אקספוינט.