Thermo Fisher
Investigation & Client Quality Specialist
Ferentino, Italy
Get past the screening software and onto a recruiter's desk
hirly rewrites your resume for this job — matching the keywords and skills in the posting, moving your most relevant experience to the top, and writing a cover letter to fit. About 30 seconds.
- Keywords matched to this posting
- Fit score before you apply
- Cover letter included
Matched against 2.3M live jobs from 200,000+ employers in 200+ countries.
Tailor my resume for this job →hirly's read of this role
- Seniority
- Mid level
- Country
- IT
- Work mode
- On-site / unstated
- First seen by hirly
- 27 Sept 2026
Derived automatically from the posting. Upload your resume above to see how the role scores against it.
the posting
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:
- At Thermo Fisher Scientific, you'll join a quality assurance team focused on ensuring consistent execution of quality standards and regulatory compliance. You'll play a vital role in enabling our customers to make breakthrough discoveries and innovations that make the world healthier, cleaner and safer. You'll ensure product quality, drive continuous improvement initiatives, and collaborate with cross-functional teams to maintain the highest standards of quality and compliance in a GMP environment.
- REQUIREMENTS:
- Bachelor's Degree required, prior experience preferred. Experience in pharmaceutical sterile, medical device or regulated industry preferred
- Preferred Fields of Study: Chemistry, Biology, Biotechnology, Engineering, or related scientific/technical field
- Additional certifications in Quality Systems or GMP preferred
- Strong knowledge of cGMP, ISO standards (13485/9001), and international regulatory requirements
- Experience with quality systems and documentation including batch records, SOPs, deviations, CAPA
- Proficiency in quality management software systems (TrackWise, SAP, etc.)
- Demonstrated ability to perform detailed documentation review and quality assessments
- Strong analytical and problem-solving skills for quality investigations and root cause analysis
- Excellent written and verbal communication skills both Italian and English
- Ability to work independently and collaborate effectively with cross-functional teams
- Experience conducting internal quality audits and supporting external regulatory audits
- Proficient computer skills including Microsoft Office applications
- Strong attention to detail and commitment to accuracy
- Ability to prioritize and adapt in a changing environment
- Experience with continuous improvement methodologies (Lean, Six Sigma) preferred
- May require up to 10% travel
- Must be able to work in controlled environments wearing required PPE
Similar jobs
- Quality Specialist - Quality Management (M/F/D)Bakerhughes · IT-FI-FLORENCE-VIA FELICE MATTEUCCI 2First seen yesterday
- Customer Quality SpecialistIrcagroup · VergiateFirst seen 9d ago
- Customer Quality SpecialistAbb · Frosinone, Frosinone, ItalyFirst seen 12d ago
- Project Quality Specialist INTERNSHIPHitachi · Milan, Lombardy, ItalyFirst seen 2d ago
- Quality Specialist ICrawford Job Listings Global · Iloilo, PhilippinesFirst seen today
Want this one?
Upload your resume and hirly rewrites it for this job and writes the cover letter — in about thirty seconds, before you sign up.
Tailor my resume for this job