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Investigator - Lab Operations

Thermo Fisher Scientific

Investigator - Lab Operations

full-timePosted: Jan 12, 2026

Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Cold Room/Freezers -22degreesF/-6degrees C, Fluctuating Temps hot/cold, Laboratory Setting, Loud Noises (Equipment/Machinery), No contact lens allowed; prescriptive glasses will be provided, Office, Rapid flashing lights, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift, Strong Odors (chemical, lubricants, biological products etc.), Various outside weather conditions, Warehouse, Will work with hazardous/toxic materials

Job Description

How will you make an impact?

Initiate and lead quality investigations in the Lab Operations - Analytical Operations (AO) and Development Operations (DO) including OOS and Unexpected results investigations, and Deviations.

 

What will you do:

  • Initiate and lead investigations and authors investigation reports in TrackWise.
  • Provide technical leadership on analytical investigations.
  • Conduct investigations with input from AO/DO supervisor
  • Direct Scientists in the performance of lab investigations.
  • Provide and document adequate training sessions to highlight findings of investigations and their trending to prevent reoccurrence of events.
  • Interact with other departments (e.g., PPT, PM, QA), clients and with Subject Matter Experts (SMEs), as required, to thoroughly investigate incidents, conclusions, and appropriate Corrective Action Preventative Actions (CAPA).
  • Ensure investigations are ready for approval and completed within required timeframe.
  • Provide excellence in data integrity and Good Manufacturing Practice (GMP)/procedural compliance
  • Design and facilitate effective CAPA actions. Own CAPA actions as needed.
  • Challenge the department on quality issues and system improvements.
  • Maintain a safe working environment and report potential hazards.

 

How will you get here:

 

Education:

Bachelor of Science in Chemistry or related science.

 

Experience:

Minimum 5 years analytical chemistry experience within the pharmaceutical industry

Previous experience leading a team is an asset.

Previous experience in providing client service in the contract pharmaceutical industry

Previous method validation and product stability testing/reporting experience in the pharmaceutical industry.

Previous investigation experience in the Good Manufacturing Practices (GMP) analytical laboratory environment.

 

Equivalency:

Equivalent combinations of education, training, and relevant work experience may be considered.

 

Knowledge, Skills and Abilities:

Exceptional Good Manufacturing Practices, Good Laboratory Practices (GLP), International Conference on Harmonization (ICH) and United States Food and Drug Administration (FDA) compliance knowledge. Strong interpersonal and communication skills (both oral and written). Superior problem solving and troubleshooting skills.  Ability to carry out investigations in a non-threatening manner with lab operations staff and effectively interacts with internal and external suppliers and clients.   Excellent organizational skills with proven ability to prioritize when timeline conflicts exist.  Detail oriented.   Ability to work well independently and in a team environment. Experience with Microsoft Office Applications.  Proficiency in the English Language. 

 

Physical Requirements:

Light physical effort and fatigue. Walks, sits or stands for limited periods. May require occasional equipment operation including keyboard equipment. Lifts light items for limited duration. Typically located in a comfortable indoor area. There may be regular exposure to mild physical discomfort from factors such as dust, fumes or odours, temperature extremes, loud noise, strong drafts, or bright lights. Use of Personal Protective equipment may be required and may include any of the following: safety glasses, safety shoes, lab coat, gloves, hair net, beard cover, safety apron, respirator on occasionally.

Benefits

We offer competitive remuneration, annual incentive plan bonus scheme, healthcare, company savings plan, and a range of employee benefits! Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation

Compensation

The salary range estimated for this position based in Canada is $69,400.00–$104,050.00.

Locations

  • Whitby, Ontario, Canada

Salary

Estimated Salary Rangemedium confidence

50,000 - 90,000 USD / yearly

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

Skills Required

  • Exceptional Good Manufacturing Practices (GMP)intermediate
  • Technical leadership on analytical investigationsintermediate
  • Data integrityintermediate
  • Procedural complianceintermediate

Required Qualifications

  • Bachelor of Science in Chemistry or related science (experience)
  • Minimum 5 years analytical chemistry experience within the pharmaceutical industry (experience)
  • Previous experience leading a team (asset) (experience)
  • Previous experience in providing client service in the contract pharmaceutical industry (experience)
  • Previous method validation and product stability testing/reporting experience (experience)
  • Previous investigation experience in GMP analytical laboratory environment (experience)

Responsibilities

  • Initiate and lead quality investigations including OOS and Unexpected results investigations, and Deviations
  • Author investigation reports in TrackWise
  • Conduct investigations with input from AO/DO supervisor
  • Direct Scientists in lab investigations
  • Provide and document training sessions on investigation findings
  • Interact with other departments, clients, and SMEs
  • Ensure investigations are completed within required timeframe
  • Design and facilitate CAPA actions
  • Challenge department on quality issues and system improvements
  • Maintain safe working environment

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Thermo Fisher Scientific logo

Investigator - Lab Operations

Thermo Fisher Scientific

Investigator - Lab Operations

full-timePosted: Jan 12, 2026

Job Description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Cold Room/Freezers -22degreesF/-6degrees C, Fluctuating Temps hot/cold, Laboratory Setting, Loud Noises (Equipment/Machinery), No contact lens allowed; prescriptive glasses will be provided, Office, Rapid flashing lights, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift, Strong Odors (chemical, lubricants, biological products etc.), Various outside weather conditions, Warehouse, Will work with hazardous/toxic materials

Job Description

How will you make an impact?

Initiate and lead quality investigations in the Lab Operations - Analytical Operations (AO) and Development Operations (DO) including OOS and Unexpected results investigations, and Deviations.

 

What will you do:

  • Initiate and lead investigations and authors investigation reports in TrackWise.
  • Provide technical leadership on analytical investigations.
  • Conduct investigations with input from AO/DO supervisor
  • Direct Scientists in the performance of lab investigations.
  • Provide and document adequate training sessions to highlight findings of investigations and their trending to prevent reoccurrence of events.
  • Interact with other departments (e.g., PPT, PM, QA), clients and with Subject Matter Experts (SMEs), as required, to thoroughly investigate incidents, conclusions, and appropriate Corrective Action Preventative Actions (CAPA).
  • Ensure investigations are ready for approval and completed within required timeframe.
  • Provide excellence in data integrity and Good Manufacturing Practice (GMP)/procedural compliance
  • Design and facilitate effective CAPA actions. Own CAPA actions as needed.
  • Challenge the department on quality issues and system improvements.
  • Maintain a safe working environment and report potential hazards.

 

How will you get here:

 

Education:

Bachelor of Science in Chemistry or related science.

 

Experience:

Minimum 5 years analytical chemistry experience within the pharmaceutical industry

Previous experience leading a team is an asset.

Previous experience in providing client service in the contract pharmaceutical industry

Previous method validation and product stability testing/reporting experience in the pharmaceutical industry.

Previous investigation experience in the Good Manufacturing Practices (GMP) analytical laboratory environment.

 

Equivalency:

Equivalent combinations of education, training, and relevant work experience may be considered.

 

Knowledge, Skills and Abilities:

Exceptional Good Manufacturing Practices, Good Laboratory Practices (GLP), International Conference on Harmonization (ICH) and United States Food and Drug Administration (FDA) compliance knowledge. Strong interpersonal and communication skills (both oral and written). Superior problem solving and troubleshooting skills.  Ability to carry out investigations in a non-threatening manner with lab operations staff and effectively interacts with internal and external suppliers and clients.   Excellent organizational skills with proven ability to prioritize when timeline conflicts exist.  Detail oriented.   Ability to work well independently and in a team environment. Experience with Microsoft Office Applications.  Proficiency in the English Language. 

 

Physical Requirements:

Light physical effort and fatigue. Walks, sits or stands for limited periods. May require occasional equipment operation including keyboard equipment. Lifts light items for limited duration. Typically located in a comfortable indoor area. There may be regular exposure to mild physical discomfort from factors such as dust, fumes or odours, temperature extremes, loud noise, strong drafts, or bright lights. Use of Personal Protective equipment may be required and may include any of the following: safety glasses, safety shoes, lab coat, gloves, hair net, beard cover, safety apron, respirator on occasionally.

Benefits

We offer competitive remuneration, annual incentive plan bonus scheme, healthcare, company savings plan, and a range of employee benefits! Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation

Compensation

The salary range estimated for this position based in Canada is $69,400.00–$104,050.00.

Locations

  • Whitby, Ontario, Canada

Salary

Estimated Salary Rangemedium confidence

50,000 - 90,000 USD / yearly

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

Skills Required

  • Exceptional Good Manufacturing Practices (GMP)intermediate
  • Technical leadership on analytical investigationsintermediate
  • Data integrityintermediate
  • Procedural complianceintermediate

Required Qualifications

  • Bachelor of Science in Chemistry or related science (experience)
  • Minimum 5 years analytical chemistry experience within the pharmaceutical industry (experience)
  • Previous experience leading a team (asset) (experience)
  • Previous experience in providing client service in the contract pharmaceutical industry (experience)
  • Previous method validation and product stability testing/reporting experience (experience)
  • Previous investigation experience in GMP analytical laboratory environment (experience)

Responsibilities

  • Initiate and lead quality investigations including OOS and Unexpected results investigations, and Deviations
  • Author investigation reports in TrackWise
  • Conduct investigations with input from AO/DO supervisor
  • Direct Scientists in lab investigations
  • Provide and document training sessions on investigation findings
  • Interact with other departments, clients, and SMEs
  • Ensure investigations are completed within required timeframe
  • Design and facilitate CAPA actions
  • Challenge department on quality issues and system improvements
  • Maintain safe working environment

Target Your Resume for "Investigator - Lab Operations" , Thermo Fisher Scientific

Get personalized recommendations to optimize your resume specifically for Investigator - Lab Operations. Takes only 15 seconds!

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

Check Your ATS Score for "Investigator - Lab Operations" , 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 Investigator - Lab Operations @ Thermo Fisher Scientific.

10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.