Abbott

Quality Engineer (Validation)

Abbott
HealthcareSingaporeFull-time1 months ago

About the role

AI summarised

Quality Engineer (Validation) role at a healthcare/pharmaceutical company, responsible for ensuring timely execution of change control and validation activities, including developing and reviewing validation protocols, leading FMEA, managing validation review processes, and supporting audits. Requires a degree in Science or Engineering, knowledge of GMP/GDP, and experience in manufacturing.

HealthcareFull-timeGeneral

Key Responsibilities

  • Comply to all policies and standards.
  • Develop, execute and review validation protocols and related documentation in accordance with Abbott procedures and policies.
  • Lead Failure Mode Effects Analysis (FMEA) for new equipment installations or changes.
  • Manages site Validation Review processes (VRB), review and approve site change controls (plant and laboratories related) and validation change requests.
  • Perform root cause analysis and identify corrective and preventive actions in addressing quality events
  • Support resolution of validation events and escalate concerns in a timely manner.
  • Support in equipment and process walkdowns
  • Weekly, Monthly and Quarterly reporting as required for own business area
  • Support Monthly and Quarterly Quality Management Review (QMR) and Business Management Review (BMR)
  • Coordinate and support periodic plant stoppage activities related to validation and change control functions
  • Develop and execute business area improvement projects
  • Participate in internal and external audits

Requirements

  • Degree in a Science or Engineering discipline.
  • Diploma in a Science or Engineering discipline with minimum 3 years working experience.
  • Knowledge of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP) in a food or pharmaceutical manufacturing industry.
  • Familiarity in developing SOPs and work flows
  • Knowledge of problem-solving tools (e.g. 6M Analysis, Fishbone, 5 Whys, etc.).
  • Familiarity with international and technical standards is a plus (ISO, FSSC etc)
  • Proficient in Microsoft applications (Powerpoint, Word, Excel)
  • Team player with initiative, drive, good communication skills and a strong command of written English
  • Ability to do data analysis using Minitab, JMP is a plus.
  • Experience in manufacturing process design and equipment design or application is a plus.
  • Proven problem-solving capability, customer focus and commitment to continuous improvement.