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Engineer I, QA

Thermo Fisher Scientific

Engineer I, QA

full-timePosted: Jan 12, 2026

Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

DESCRIPTION:

Position Objective:

This role supports our Cell Culture Media and Oligo Manufacturing processes. Responsible for review and verification of all documentation related to finished good products and independently working to resolve any inconsistencies or problems with quality or compliance issues for these as they arise. Also responsible for supporting where required daily activities of Core QA department.

Essential Functions:

  • Maintain working knowledge of Regulatory and Quality System requirements (ISO13485/FDA CFR).
  • Responsible for reviewing batch records and release of finished product
  • Fully competent in all areas of Finish Goods release process
  • Utilise problem-solving skills related to quality issues ensuring timely resolution for minimal impact.
  • Prepare new documentation and edit/delete revised Standard Operating Procedures, Work instructions, Forms, etc.
  • Utilise Trackwise system – non conformances, deviations, CAPA
  • Provide training and support to other QA staff as required as well as other departments within operations.
  • Participate in customer audits, attend technical visits and fully support and engage in customer calls
  • Embrace site PPI initiatives and ensure all team members adopt this methodology
  • Perform independently without continual direction and exercise considerable latitude in determining technical objectives and solutions to complex problems. Identify and implement opportunities for improvement across the operational function.
  • Participate in personal development to further enhance skills and knowledge relevant to the position.
  • Deputies in Team Supervisor’s absence.
  • Appropriate PPE must be worn and used in accordance with the instructions provided to them.
  • May be required to perform other related duties as required and/or assigned.

Education:

Bachelors/Master’s degree in Chemistry, Microbiology, Engineering or related discipline preferable.

Experience:

Requires a minimum of five year's QA/QC experience in a relevant environment. Knowledge of computer applications and current software (Word/ Excel) is essential.

Strong oral and written communication skills with a demonstrated ability to work in a cross-functional team environment and to effectively interact with all levels in the company. Effective communication skills and the ability to collaborate with internal and external development team members are essential.

Must be a self-starter who can take general concepts and direction and produce desirable results. Also must function effectively and efficiently in a global, multi-site organization.

Contacts:

Will liaise extensively with all other departments on matters relating to quality and service in order to uphold the Company’s commitment to Customer satisfaction. This involves working with people at all levels within the organisation as well as external customers and regulatory bodies. 

Working Conditions:

Works in an office/lab environment but may be required to spend some time in manufacturing and the warehouse. Must be able to work overtime to complete daily tasks if required.

Locations

  • Paisley, Renfrewshire, United Kingdom

Salary

Estimated Salary Rangemedium confidence

75,000 - 130,000 GBP / yearly

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

Skills Required

  • Regulatory knowledge (ISO13485/FDA CFR)intermediate
  • Problem-solvingintermediate
  • Trackwise system (non-conformances, deviations, CAPA)intermediate
  • Strong oral and written communicationintermediate
  • Cross-functional teamworkintermediate
  • Computer applications (Word/Excel)intermediate
  • Training and support provisionintermediate

Required Qualifications

  • Bachelors/Master’s degree in Chemistry, Microbiology, Engineering or related discipline (experience)
  • Minimum of five years QA/QC experience in relevant environment (experience)

Responsibilities

  • Review and verify documentation for finished good products
  • Resolve quality or compliance issues
  • Review batch records and release finished product
  • Prepare/edit SOPs, work instructions, forms
  • Provide training to QA staff and other departments
  • Participate in customer audits and technical visits
  • Embrace PPI initiatives
  • Identify and implement improvements
  • Deputy for Team Supervisor

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Thermo Fisher Scientific logo

Engineer I, QA

Thermo Fisher Scientific

Engineer I, QA

full-timePosted: Jan 12, 2026

Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

DESCRIPTION:

Position Objective:

This role supports our Cell Culture Media and Oligo Manufacturing processes. Responsible for review and verification of all documentation related to finished good products and independently working to resolve any inconsistencies or problems with quality or compliance issues for these as they arise. Also responsible for supporting where required daily activities of Core QA department.

Essential Functions:

  • Maintain working knowledge of Regulatory and Quality System requirements (ISO13485/FDA CFR).
  • Responsible for reviewing batch records and release of finished product
  • Fully competent in all areas of Finish Goods release process
  • Utilise problem-solving skills related to quality issues ensuring timely resolution for minimal impact.
  • Prepare new documentation and edit/delete revised Standard Operating Procedures, Work instructions, Forms, etc.
  • Utilise Trackwise system – non conformances, deviations, CAPA
  • Provide training and support to other QA staff as required as well as other departments within operations.
  • Participate in customer audits, attend technical visits and fully support and engage in customer calls
  • Embrace site PPI initiatives and ensure all team members adopt this methodology
  • Perform independently without continual direction and exercise considerable latitude in determining technical objectives and solutions to complex problems. Identify and implement opportunities for improvement across the operational function.
  • Participate in personal development to further enhance skills and knowledge relevant to the position.
  • Deputies in Team Supervisor’s absence.
  • Appropriate PPE must be worn and used in accordance with the instructions provided to them.
  • May be required to perform other related duties as required and/or assigned.

Education:

Bachelors/Master’s degree in Chemistry, Microbiology, Engineering or related discipline preferable.

Experience:

Requires a minimum of five year's QA/QC experience in a relevant environment. Knowledge of computer applications and current software (Word/ Excel) is essential.

Strong oral and written communication skills with a demonstrated ability to work in a cross-functional team environment and to effectively interact with all levels in the company. Effective communication skills and the ability to collaborate with internal and external development team members are essential.

Must be a self-starter who can take general concepts and direction and produce desirable results. Also must function effectively and efficiently in a global, multi-site organization.

Contacts:

Will liaise extensively with all other departments on matters relating to quality and service in order to uphold the Company’s commitment to Customer satisfaction. This involves working with people at all levels within the organisation as well as external customers and regulatory bodies. 

Working Conditions:

Works in an office/lab environment but may be required to spend some time in manufacturing and the warehouse. Must be able to work overtime to complete daily tasks if required.

Locations

  • Paisley, Renfrewshire, United Kingdom

Salary

Estimated Salary Rangemedium confidence

75,000 - 130,000 GBP / yearly

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

Skills Required

  • Regulatory knowledge (ISO13485/FDA CFR)intermediate
  • Problem-solvingintermediate
  • Trackwise system (non-conformances, deviations, CAPA)intermediate
  • Strong oral and written communicationintermediate
  • Cross-functional teamworkintermediate
  • Computer applications (Word/Excel)intermediate
  • Training and support provisionintermediate

Required Qualifications

  • Bachelors/Master’s degree in Chemistry, Microbiology, Engineering or related discipline (experience)
  • Minimum of five years QA/QC experience in relevant environment (experience)

Responsibilities

  • Review and verify documentation for finished good products
  • Resolve quality or compliance issues
  • Review batch records and release finished product
  • Prepare/edit SOPs, work instructions, forms
  • Provide training to QA staff and other departments
  • Participate in customer audits and technical visits
  • Embrace PPI initiatives
  • Identify and implement improvements
  • Deputy for Team Supervisor

Target Your Resume for "Engineer I, QA" , Thermo Fisher Scientific

Get personalized recommendations to optimize your resume specifically for Engineer I, QA. Takes only 15 seconds!

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

Check Your ATS Score for "Engineer I, QA" , 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 Engineer I, QA @ Thermo Fisher Scientific.

10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.