Role at a glance
- Job function
-
Manufacturing & Skilled Trades Quality Assurance & Quality Control
- Salary
- Not Disclosed
- Location
- Ferentino, Italy
- Work arrangement
- On-site
- Employment
- Full-time
- Education
- Bachelor's Degree required, prior experience preferred.
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Role Summary
This fixed-term Investigation & Client Quality Specialist role sits within a quality assurance team focused on consistent execution of quality standards and regulatory compliance. The role centers on ensuring product quality and driving continuous improvement in a GMP environment.
What You'll Do
- Ensure product quality
- Drive continuous improvement initiatives
- Collaborate with cross-functional teams to maintain quality and compliance standards in a GMP environment
Generated from the employer's posting. Verify important details before applying.
View full postingQualifications
Bachelor's degree with knowledge of cGMP and quality systems, plus analytical, documentation, and communication skills in a GMP environment.
Required
- Bachelor's Degree
- 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 in both Italian and English
- Ability to work independently and collaborate effectively with cross-functional teams
Preferred
- Prior experience
- Experience in pharmaceutical sterile, medical device or regulated industry
- Preferred fields of study: Chemistry, Biology, Biotechnology, Engineering, or related scientific/technical field
- Additional certifications in Quality Systems or GMP
- Experience with continuous improvement methodologies (Lean, Six Sigma)
Original job description
Content provided by the employer
Original job description
Content provided by the employer
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob 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
About the company
Thermo Fisher Scientific
Large Enterprise
Thermo Fisher Scientific is a global leader in serving science, providing a wide range of analytical instruments, reagents, and software solutions for healthcare, pharmaceuticals, and life sciences research. With a commitment to innovation and quality, the company enables customers to make significant advancements in scientific discovery and healthcare diagnostics. Thermo Fisher operates in more than 50 countries and employs over 80,000 people, fostering a collaborative environment aimed at enhancing global health and safety. Through its broad portfolio of brands and technologies, the company plays a vital role in accelerating life-changing research and improving patient outcomes worldwide.