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QC Graduate

GE Healthcare

Healthcare Jobs

QC Graduate

full-timePosted: Jan 14, 2026

Job Description

Job Description Summary

To provide Quality Control support during batch manufacture and filling process across the In Process lab.

Job Description

MAIN RESPONSIBILITIES

Graduate role specific:

  • In Process Testing Support e.g. MET, BU etc
  • Running Team DMS Board at Tier 1
  • Supporting EM programme
  • Consumable management
  • 5S support

Roles and Responsibilities:

  • Providing QC support during batch manufacture, ensuring turnaround times are achieved as outlined in QC/Production Service Level Agreement and product release times.
  • This includes In process Chemistry/Microbiological analysis, finished product Chemistry/Microbiological analysis.
  • WFI & Steam sampling and analysis
  • Water collection
  • Actively involved in Investigations e.g. Batch Corrections, EMI, Bioburden etc
  • Performing routine instrument calibrations and calibration checks.
  • Routine maintenance of equipment
  • Ensuring compliance with cGMP, EHS, GxP etc guidelines at all times.
  • Entering and approving results on LIMS/MODA & completion of batch documentation
  • Assisting with audits and ensuring lab is inspection ready as required.
  • Assisting with 5S of In Process Lab.
  • Consumable management – ordering, stock take and following up with vendors on expected delivery times etc.
  • Supporting logbook review and archiving for In Process.
  • Ensure compliance with current pharmacopoeia and all regulatory/company guidelines.
  • Interaction with other departments e.g. Production, Engineering, QA.
  • Assisting in the training and up skilling of colleagues where possible.
  • Liaising with internal and external customers in relation to QC/Production issues
  • Any other duties as required by QC PTL and/or designee.

PRINCIPAL QUALIFICATIONS:

A third level Science Qualification

Skills REQUIRED:

Good communications skills, excellent time management skills, flexibility and agility will be required. Openness to change. Proven ability to work on own initiative and deliver expectations. 

DESIRED WORK EXPERIENCE:

Pharmaceutical experience in a GMP regulated laboratory environment.

Additional Information

Relocation Assistance Provided: No

Locations

  • Cork, Cork, Ireland

Salary

Estimated Salary Rangemedium confidence

40,000 - 75,000 USD / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • In Process Testing (MET, BU)intermediate
  • Chemistry/Microbiological analysisintermediate
  • Instrument calibrations and maintenanceintermediate
  • LIMS/MODA data entryintermediate
  • cGMP and regulatory complianceintermediate
  • Consumable managementintermediate
  • 5S methodologyintermediate
  • Investigation support (Batch Corrections, EMI, Bioburden)intermediate

Required Qualifications

  • Third level Science Qualification (experience)

Responsibilities

  • Providing QC support during batch manufacture and filling process
  • In process and finished product Chemistry/Microbiological analysis
  • WFI & Steam sampling and analysis
  • Performing routine instrument calibrations and maintenance
  • Entering and approving results on LIMS/MODA
  • Ensuring compliance with cGMP, EHS, GxP guidelines
  • Assisting with audits and lab readiness
  • Consumable management and stock control

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GE Healthcare logo

QC Graduate

GE Healthcare

Healthcare Jobs

QC Graduate

full-timePosted: Jan 14, 2026

Job Description

Job Description Summary

To provide Quality Control support during batch manufacture and filling process across the In Process lab.

Job Description

MAIN RESPONSIBILITIES

Graduate role specific:

  • In Process Testing Support e.g. MET, BU etc
  • Running Team DMS Board at Tier 1
  • Supporting EM programme
  • Consumable management
  • 5S support

Roles and Responsibilities:

  • Providing QC support during batch manufacture, ensuring turnaround times are achieved as outlined in QC/Production Service Level Agreement and product release times.
  • This includes In process Chemistry/Microbiological analysis, finished product Chemistry/Microbiological analysis.
  • WFI & Steam sampling and analysis
  • Water collection
  • Actively involved in Investigations e.g. Batch Corrections, EMI, Bioburden etc
  • Performing routine instrument calibrations and calibration checks.
  • Routine maintenance of equipment
  • Ensuring compliance with cGMP, EHS, GxP etc guidelines at all times.
  • Entering and approving results on LIMS/MODA & completion of batch documentation
  • Assisting with audits and ensuring lab is inspection ready as required.
  • Assisting with 5S of In Process Lab.
  • Consumable management – ordering, stock take and following up with vendors on expected delivery times etc.
  • Supporting logbook review and archiving for In Process.
  • Ensure compliance with current pharmacopoeia and all regulatory/company guidelines.
  • Interaction with other departments e.g. Production, Engineering, QA.
  • Assisting in the training and up skilling of colleagues where possible.
  • Liaising with internal and external customers in relation to QC/Production issues
  • Any other duties as required by QC PTL and/or designee.

PRINCIPAL QUALIFICATIONS:

A third level Science Qualification

Skills REQUIRED:

Good communications skills, excellent time management skills, flexibility and agility will be required. Openness to change. Proven ability to work on own initiative and deliver expectations. 

DESIRED WORK EXPERIENCE:

Pharmaceutical experience in a GMP regulated laboratory environment.

Additional Information

Relocation Assistance Provided: No

Locations

  • Cork, Cork, Ireland

Salary

Estimated Salary Rangemedium confidence

40,000 - 75,000 USD / yearly

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • In Process Testing (MET, BU)intermediate
  • Chemistry/Microbiological analysisintermediate
  • Instrument calibrations and maintenanceintermediate
  • LIMS/MODA data entryintermediate
  • cGMP and regulatory complianceintermediate
  • Consumable managementintermediate
  • 5S methodologyintermediate
  • Investigation support (Batch Corrections, EMI, Bioburden)intermediate

Required Qualifications

  • Third level Science Qualification (experience)

Responsibilities

  • Providing QC support during batch manufacture and filling process
  • In process and finished product Chemistry/Microbiological analysis
  • WFI & Steam sampling and analysis
  • Performing routine instrument calibrations and maintenance
  • Entering and approving results on LIMS/MODA
  • Ensuring compliance with cGMP, EHS, GxP guidelines
  • Assisting with audits and lab readiness
  • Consumable management and stock control

Target Your Resume for "QC Graduate" , GE Healthcare

Get personalized recommendations to optimize your resume specifically for QC Graduate. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "QC Graduate" , GE Healthcare

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Answer 10 quick questions to check your fit for QC Graduate @ GE Healthcare.

Quiz Challenge
10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.