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mRNA Quality Operations specialist

Thermo Fisher Scientific

Healthcare Jobs

mRNA Quality Operations specialist

full-timePosted: Jan 12, 2026

Job Description

Work Schedule

Other

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift

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:
Join Thermo Fisher Scientific mRNA Business Unit as Quality Operations specialist and contribute to ensuring product quality and regulatory compliance. As a member of our Quality team, you'll help enable our mission of making the world healthier, cleaner and safer through quality oversight of pharmaceutical manufacturing operations. Your expertise will help maintain high standards of quality while supporting production of life-changing medicines.

REQUIREMENTS:
• At least 1 years of experience in pharmaceutical quality assurance or related GMP environment
• Preferred Fields of Study: Chemistry, Pharmacy, Biology, Biotechnology or related scientific field
• Comprehensive knowledge of GMP regulations, FDA guidelines and quality systems
• Expertise in batch record review, deviation investigations and CAPA management
• Strong understanding of aseptic manufacturing processes and controls
• Preferred proficiency in quality documentation systems (e.g. TrackWise, Documentum) and Microsoft Office applications
• Professional communication skills both written and spoken
• Ability to manage multiple priorities in a dynamic environment
• Strong attention to detail and analytical problem-solving skills
• Effective interpersonal and communication abilities
• Experience supporting regulatory inspections and customer audits
• Ability to work effectively with cross-functional teams
• Ability to work various shifts as required (Monday to Friday)
• Knowledge of root cause analysis and quality improvement tools
• Experience with clean room operations and gowning procedures preferred

• Proficiency in written ad spoken Italian and English

Join us at Thermo Fisher Scientific to contribute to world-changing work and build a fulfilling career. Apply today at http://jobs.thermofisher.com.

Thermo Fisher Scientific is an equal opportunity employer and is committed to providing resources and opportunities for the success of our diverse workforce. We value integrity, intensity, innovation, and involvement in our pursuit of enabling our customers to make the world healthier, cleaner, and safer.

Locations

  • Monza, Monza e Brianza, Italy

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

  • Comprehensive knowledge of GMP regulations, FDA guidelines and quality systemsintermediate
  • Expertise in batch record review, deviation investigations and CAPA managementintermediate
  • Strong understanding of aseptic manufacturing processes and controlsintermediate
  • Preferred proficiency in quality documentation systems (e.g. TrackWise, Documentum) and Microsoft Office applicationsintermediate
  • Professional communication skills both written and spokenintermediate
  • Strong attention to detail and analytical problem-solving skillsintermediate
  • Knowledge of root cause analysis and quality improvement toolsintermediate
  • Experience with clean room operations and gowning procedures preferredintermediate
  • Proficiency in written and spoken Italian and Englishintermediate

Required Qualifications

  • At least 1 years of experience in pharmaceutical quality assurance or related GMP environment (experience)
  • Preferred Fields of Study: Chemistry, Pharmacy, Biology, Biotechnology or related scientific field (experience)

Responsibilities

  • Contribute to ensuring product quality and regulatory compliance
  • Provide quality oversight of pharmaceutical manufacturing operations
  • Support regulatory inspections and customer audits
  • Work effectively with cross-functional teams
  • Manage multiple priorities in a dynamic environment

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Thermo Fisher Scientific logo

mRNA Quality Operations specialist

Thermo Fisher Scientific

Healthcare Jobs

mRNA Quality Operations specialist

full-timePosted: Jan 12, 2026

Job Description

Work Schedule

Other

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift

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:
Join Thermo Fisher Scientific mRNA Business Unit as Quality Operations specialist and contribute to ensuring product quality and regulatory compliance. As a member of our Quality team, you'll help enable our mission of making the world healthier, cleaner and safer through quality oversight of pharmaceutical manufacturing operations. Your expertise will help maintain high standards of quality while supporting production of life-changing medicines.

REQUIREMENTS:
• At least 1 years of experience in pharmaceutical quality assurance or related GMP environment
• Preferred Fields of Study: Chemistry, Pharmacy, Biology, Biotechnology or related scientific field
• Comprehensive knowledge of GMP regulations, FDA guidelines and quality systems
• Expertise in batch record review, deviation investigations and CAPA management
• Strong understanding of aseptic manufacturing processes and controls
• Preferred proficiency in quality documentation systems (e.g. TrackWise, Documentum) and Microsoft Office applications
• Professional communication skills both written and spoken
• Ability to manage multiple priorities in a dynamic environment
• Strong attention to detail and analytical problem-solving skills
• Effective interpersonal and communication abilities
• Experience supporting regulatory inspections and customer audits
• Ability to work effectively with cross-functional teams
• Ability to work various shifts as required (Monday to Friday)
• Knowledge of root cause analysis and quality improvement tools
• Experience with clean room operations and gowning procedures preferred

• Proficiency in written ad spoken Italian and English

Join us at Thermo Fisher Scientific to contribute to world-changing work and build a fulfilling career. Apply today at http://jobs.thermofisher.com.

Thermo Fisher Scientific is an equal opportunity employer and is committed to providing resources and opportunities for the success of our diverse workforce. We value integrity, intensity, innovation, and involvement in our pursuit of enabling our customers to make the world healthier, cleaner, and safer.

Locations

  • Monza, Monza e Brianza, Italy

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

  • Comprehensive knowledge of GMP regulations, FDA guidelines and quality systemsintermediate
  • Expertise in batch record review, deviation investigations and CAPA managementintermediate
  • Strong understanding of aseptic manufacturing processes and controlsintermediate
  • Preferred proficiency in quality documentation systems (e.g. TrackWise, Documentum) and Microsoft Office applicationsintermediate
  • Professional communication skills both written and spokenintermediate
  • Strong attention to detail and analytical problem-solving skillsintermediate
  • Knowledge of root cause analysis and quality improvement toolsintermediate
  • Experience with clean room operations and gowning procedures preferredintermediate
  • Proficiency in written and spoken Italian and Englishintermediate

Required Qualifications

  • At least 1 years of experience in pharmaceutical quality assurance or related GMP environment (experience)
  • Preferred Fields of Study: Chemistry, Pharmacy, Biology, Biotechnology or related scientific field (experience)

Responsibilities

  • Contribute to ensuring product quality and regulatory compliance
  • Provide quality oversight of pharmaceutical manufacturing operations
  • Support regulatory inspections and customer audits
  • Work effectively with cross-functional teams
  • Manage multiple priorities in a dynamic environment

Target Your Resume for "mRNA Quality Operations specialist" , Thermo Fisher Scientific

Get personalized recommendations to optimize your resume specifically for mRNA Quality Operations specialist. Takes only 15 seconds!

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

Check Your ATS Score for "mRNA Quality Operations specialist" , 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

Answer 10 quick questions to check your fit for mRNA Quality Operations specialist @ Thermo Fisher Scientific.

Quiz Challenge
10 Questions
~2 Minutes
Instant Score

Related Books and Jobs

No related jobs found at the moment.