jobs in WEST PHARMACEUTICAL SERVICES SINGAPORE PTE. LTD.

全职 QC Supervisor 工作, 薪水 up to SGD 6,800, WEST PHARMACEUTICAL SERVICES SINGAPORE PTE. LTD. West Region (Singapore) 公司招聘中 - Ricebowl

QC Supervisor

WEST PHARMACEUTICAL SERVICES SINGAPORE PTE. LTD.

West Region (Singapore)

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工作地点

  • 15 JOO KOON CIRCLE West Region (Singapore) Singapore

职位描述

岗位职责

Location: 15 Joo Koon Circle 

Working pattern, rotating shift: 7 to 715, monthly rotating Pitman Shift (2-2-3 pattern)

MRT Pick up points: Woodlands, Choa Chu Kang, Jurong East, Boon Lay, Pioneer

Job Summary:  

In this role, you will 

  • Be accountable for day-to-day performance of team/s safety, quality, delivery, cost and productivity 

  • Manage teams of QC Technicians & Team Leads in execution of QC processes, schedule and personnel to ensure smooth operational activities work-flow and work compliance 

  • Promote better quality mindset through inter-department collaborations  

Essential Duties and Responsibilities: 

  • Oversee resource management and team schedules for smooth execution of daily operational tasks in QC while meeting daily inspection targets and support Work In Progress (WIP) controls within team/s 

  • Ensure proper product release and rework activities per procedures to support delivery requirements 

  • Lead product characteristics trend monitoring with effective escalation and follow-ups 

  • Demonstrate leadership, teamwork, and problem-solving support to resolve escalated operational issues collaboratively and ensure proper batch segregation 

  • Define goals, clearly communicate these objectives and monitor/correct/recognize work performance respectively. Coach and counsel QC employees 

  • Manage and resolve QC employee's relation issues and disputes 

  • Manage onboarding activities for new QC employees for training and qualification 

  • Manage ongoing activities for existing QC employees for training and requalification 

  • Identify future training needs and enhance QC employees career opportunities 

  • Responsible to review SOI revisions to enhance improvements for better workflow 

  • Manage Deviation/Out-of-Spec report closures, batch dispositions while ensuring proper root cause analysis and CAPA identification 

  • Accountable for on time operational updates for Tier 1, Tier 2, Tier 2.5 & Tier 3 of the LDMS system 

  • Attend Tier 2, Tier 2.5 as QC representative, and facilitate Tier 1 (Shift Start Up) within QC 

  • Promote and support site initiatives including safety programs, lean initiatives, training programs and consistently interpret and apply policies, procedures among employees 

  • Manage non-routine requests from departments (eg validations, investigations, improvements, projects, product transfers, non-routine testings, non-conformance reports, etc) 

  • Other duties as assigned by superior

Basic Qualifications:  

  • Academic qualification of Diploma in engineering or relevant fields 

  • Computer literate and good grasp of Microsoft Office

  • Added advantage with SAP, cGMP, Basic Lean and/or ISO working experience

  • Preferably with exposure to medical device, pharmaceutical or related manufacturing environment 

  • Preferably 8 years work experience in QA/QC related activities

  • Able to work independently with minimum supervision 

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

    • Minimize waste, always ensure efficient work execution by continuous improvements

  • Able to comply with the company’s safety policy at all times

    • Ensure use of Personal Protective Equipment (PPE) in respective work environments for all members within the shift/s 

    • Report unsafe conditions or acts to responsible persons for corrections and improvements

    • Ensure risk assessment control practices are adopted per HIRA for all members within the shift/s 

    • Ensure all legal licenses required for the proper usage of QC equipment are effective for all members within the shift/s 

  • Able to comply with the company’s quality policy at all times  

    • Lead monitoring / improvement activities to enhance operational support activities 

    • Participate in establishment and maintenance of documented procedure

  • Excellent communication & teamwork skills

  • Self-motivated and positive thinking

  • Ability to remain calm and professional under pressure

  • Proficiency in workplace English for work applications and interfaces

  • Time management skills

Physical and Mental Requirements:  

  • Manufacturing environment with rotating working shift patterns 

  • Overtime and being on-call are required. Occasionally required to work on different 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 


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