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Quality Engineer III - 1 year contract

Thermo Fisher Scientific

Quality Engineer III - 1 year contract

full-timePosted: Jan 12, 2026

Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards

Job Description

Purpose of the Job

The Quality Engineer ensures that biopharmaceutical manufacturing at Thermo Fisher Scientific Groningen aligns with international quality standards (FDA, EMEA, ICH).
This involves developing, implementing, maintaining, and auditing Quality Systems across manufacturing on daily basis.


Job and Position Context

The Groningen site manufactures Bulk Drug Substances (BDS) via mammalian cell culture.
This facility follows all rules and regulations of current Good Manufacturing Practice (cGMP) set by individual jurisdiction health and welfare ministries.


Key Responsibilities

The Quality Engineer ensures cGMP manufacturing activities are completed according to requirements, adhering to SOPs and regulatory guidelines.
Responsibilities include:

  • Engaging directly with manufacturing operations to ensure compliance, document review, and deviation handling.
  • Supporting all phases of batch documentation, including initiation, authoring, approval, and mastering.
  • Reviewing and approving cGMP documentation.
  • Ensuring alignment of Standard Operating Procedures and documentation practices for efficient quality release of materials.
  • Conducting incident investigations to understand root causes and prevent recurrence.
  • Using electronic databases (e.g., Trackwise) to document quality-related events.
  • Operating under various quality oversight models based on manufacturing modes.
  • Communicating effectively in electronic, written, and verbal forms with shareholder dpeartments (QC, ENG, MSAT, OPS)
  • Performing internal audits.
  • Performing quality controls before line clearance controls and driving change-over activities.


Skills and Networking

  • Ensure product compliance with cGMP and customer requirements.
  • Continuously develop expertise in quality assurance.
  • Collaborate closely with QA Officers and other departments.
  • Engage with internal and external QA professionals and specialists.


Quality and SHE

Work according to Safety, Health, and Environmental (SHE) guidelines and GMP standards.

Locations

  • Groningen, Netherlands

Salary

Estimated Salary Rangemedium confidence

75,000 - 130,000 USD / yearly

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

Skills Required

  • cGMP complianceintermediate
  • Document review and approvalintermediate
  • Deviation handling and incident investigationintermediate
  • Root cause analysisintermediate
  • Internal auditingintermediate
  • Trackwise (electronic databases)intermediate
  • SOP alignmentintermediate
  • Communication with QC, ENG, MSAT, OPSintermediate
  • Quality controls and line clearanceintermediate

Required Qualifications

  • Expertise in quality assurance (experience)
  • Knowledge of FDA, EMEA, ICH standards (experience)

Responsibilities

  • Ensure cGMP manufacturing compliance
  • Support batch documentation (initiation, authoring, approval, mastering)
  • Review and approve cGMP documentation
  • Conduct incident investigations
  • Perform internal audits
  • Engage with manufacturing operations
  • Drive change-over activities

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Thermo Fisher Scientific logo

Quality Engineer III - 1 year contract

Thermo Fisher Scientific

Quality Engineer III - 1 year contract

full-timePosted: Jan 12, 2026

Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards

Job Description

Purpose of the Job

The Quality Engineer ensures that biopharmaceutical manufacturing at Thermo Fisher Scientific Groningen aligns with international quality standards (FDA, EMEA, ICH).
This involves developing, implementing, maintaining, and auditing Quality Systems across manufacturing on daily basis.


Job and Position Context

The Groningen site manufactures Bulk Drug Substances (BDS) via mammalian cell culture.
This facility follows all rules and regulations of current Good Manufacturing Practice (cGMP) set by individual jurisdiction health and welfare ministries.


Key Responsibilities

The Quality Engineer ensures cGMP manufacturing activities are completed according to requirements, adhering to SOPs and regulatory guidelines.
Responsibilities include:

  • Engaging directly with manufacturing operations to ensure compliance, document review, and deviation handling.
  • Supporting all phases of batch documentation, including initiation, authoring, approval, and mastering.
  • Reviewing and approving cGMP documentation.
  • Ensuring alignment of Standard Operating Procedures and documentation practices for efficient quality release of materials.
  • Conducting incident investigations to understand root causes and prevent recurrence.
  • Using electronic databases (e.g., Trackwise) to document quality-related events.
  • Operating under various quality oversight models based on manufacturing modes.
  • Communicating effectively in electronic, written, and verbal forms with shareholder dpeartments (QC, ENG, MSAT, OPS)
  • Performing internal audits.
  • Performing quality controls before line clearance controls and driving change-over activities.


Skills and Networking

  • Ensure product compliance with cGMP and customer requirements.
  • Continuously develop expertise in quality assurance.
  • Collaborate closely with QA Officers and other departments.
  • Engage with internal and external QA professionals and specialists.


Quality and SHE

Work according to Safety, Health, and Environmental (SHE) guidelines and GMP standards.

Locations

  • Groningen, Netherlands

Salary

Estimated Salary Rangemedium confidence

75,000 - 130,000 USD / yearly

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

Skills Required

  • cGMP complianceintermediate
  • Document review and approvalintermediate
  • Deviation handling and incident investigationintermediate
  • Root cause analysisintermediate
  • Internal auditingintermediate
  • Trackwise (electronic databases)intermediate
  • SOP alignmentintermediate
  • Communication with QC, ENG, MSAT, OPSintermediate
  • Quality controls and line clearanceintermediate

Required Qualifications

  • Expertise in quality assurance (experience)
  • Knowledge of FDA, EMEA, ICH standards (experience)

Responsibilities

  • Ensure cGMP manufacturing compliance
  • Support batch documentation (initiation, authoring, approval, mastering)
  • Review and approve cGMP documentation
  • Conduct incident investigations
  • Perform internal audits
  • Engage with manufacturing operations
  • Drive change-over activities

Target Your Resume for "Quality Engineer III - 1 year contract" , Thermo Fisher Scientific

Get personalized recommendations to optimize your resume specifically for Quality Engineer III - 1 year contract. Takes only 15 seconds!

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

Check Your ATS Score for "Quality Engineer III - 1 year contract" , Thermo Fisher Scientific

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
Quiz Challenge

Answer 10 quick questions to check your fit for Quality Engineer III - 1 year contract @ Thermo Fisher Scientific.

10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.