Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
Scoutfield Logo

See all jobs on Scoutfield

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
Thermo Fisher Scientific

Visual Inspector II – 12 Hour Rotating Shift

Thermo Fisher Scientific

. Perform manual and/or automated visual inspection of finished or in-process pharmaceutical products, including vials, syringes, and bottles .

Posted 9/15/2026full-timeSingapore • SingaporeMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in visual inspection of pharmaceutical products, adhering to Good Manufacturing Practices (GMP) and data integrity principles. Capable of maintaining cleanliness and organization in manufacturing environments while ensuring compliance with safety and quality standards.

Highest-signal resume keywords
Visual InspectionGood Manufacturing Practices (GMP)Data IntegrityAttention to DetailSafety Compliance

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Visual InspectionBasic Understanding of GMPData Integrity PrinciplesAseptic TechniquesInspection Equipment ChecksStock ChecksRepetitive Visual TasksCold Room OperationsPackaging and Transferring ProductsCleaning and Maintaining Equipment
Soft Skills
Good Communication SkillsAbility to Work IndependentlyTeam CollaborationWillingness to Perform Repetitive TasksStrong Commitment to Quality
Industry Keywords
Pharmaceutical ManufacturingVisual InspectionCGMPEHS ComplianceBatch RecordsCleanroom EnvironmentCold RoomQuality ConcernsEnvironmental IssuesOperational Excellence

About the role

Key responsibilities & impact
  • Perform manual and/or automated visual inspection of finished or in-process pharmaceutical products, including vials, syringes, and bottles
  • Identify and reject units with visual defects, including particulates, cracks, leaks, cosmetic defects, fill-volume abnormalities, labeling issues, and container-closure or integrity defects
  • Record inspection results accurately in batch records, logbooks, or electronic systems
  • Maintain data integrity by completing records legibly, contemporaneously, accurately, and according to GDP requirements
  • Support investigations by providing inspection data, observations, and relevant information
  • Perform basic inspection equipment checks and line clearance before use
  • Maintain cleanliness and organization of inspection areas
  • Report equipment malfunctions, environmental issues, quality concerns, and abnormalities promptly
  • Package and transfer final products to the cold room
  • Complete required training before performing assigned tasks
  • Follow aseptic techniques and practices during aseptic operations
  • Clean and maintain production equipment and classified manufacturing areas
  • Transfer materials required for manufacturing batches
  • Load and unload materials, equipment, or batches during production activities
  • Perform stock checks of consumables and report material needs
  • Follow safety, quality, EHS, business compliance, cGMP, and other compliance requirements
  • Conduct in-process inspections and checks
  • Load and unload vials at the tray loader station
  • Perform assigned facility cleaning duties
  • Carry out other duties assigned by the Manager

Requirements

What you’ll need
  • Minimum “O” Level, NITEC, ITE, or equivalent qualification
  • Prior experience in pharmaceutical manufacturing, visual inspection, or a GMP-regulated environment is an advantage
  • Good visual acuity and color vision; must be able to pass periodic eye tests
  • Basic understanding of GMP and data integrity principles
  • Ability to work independently and as part of a team
  • Willingness to perform repetitive tasks for extended periods
  • Ability to sit or stand for prolonged periods
  • Ability to perform repetitive visual tasks with sustained focus and attention to detail
  • Willingness to work shifts, if required
  • Good communication skills and ability to report issues promptly
  • Strong commitment to safety, quality, compliance, and operational excellence
  • Able to lift 40 lbs. without assistance
  • Adherence to all Good Manufacturing Practices (GMP) safety standards
  • Ability to work in cleanroom, cold room/freezer, office, and warehouse environments
  • Ability to use required PPE and comply with gowning and cleanroom restrictions

Benefits

Comp & perks
  • Competitive remuneration
  • Annual incentive plans
  • Healthcare benefits
  • Employee development opportunities
  • Opportunities for growth and development
  • Collaborative environment