West Pharma Sr QC Technician Jurong 

Singapore, Singapore 

312316496

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.