QC Supervisor

4 days ago


West Region, Singapore West Pharmaceutical Services Singapore Pte Ltd Full time $80,000 - $120,000 per year

Location: 15 Joo Koon Circle

Working pattern, rotating shift: 7 to 715, monthly rotating Pitman Shift pattern)

Benefits:

  • Transport provided near MRT (Woodlands, Choa Chu Kang, Jurong East, Boonlay, Pioneer)
  • Transport allowance
  • Shift allowance
  • $1,000 Flexible annual allowance
  • Annual Wage Supplement (AWS) of 1-month basic salary
  • Variable bonus

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 bachelor's degree in engineering or relevant fields

  • Computer literate and good grasp of Microsoft Office

  • Preferably 8 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

  • Preferably minimum 5 years work experience managing a QC team

  • 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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