Quality Engineer III

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards

Job Description

Location: Marietta, OH. Relocation assistance is NOT provided.

Must be legally authorized to work in the United States without sponsorship now or in the future.

Must be able to pass a comprehensive background check, which includes a drug screening.

When youre part of the team at Thermo Fisher Scientific, youll do important work. And youll have the opportunity for continual growth and learning in a culture that empowers your development. With revenues of more than $40 billion and the largest investment in R&D in the industry, we give our people the resources and opportunities to make significant contributions to the world.
Discover Impactful Work:

As a Quality Engineer III, youll help ensure quality excellence and regulatory compliance across manufacturing operations. Youll help ensure our products meet the highest standards while supporting our mission to enable customers to make the world healthier, cleaner and safer. This role combines technical expertise with quality oversight to maintain robust quality management systems, lead investigations, drive continuous improvement, and ensure GMP/ISO compliance.
A Day in the Life:

Be the SME within the quality group by being hands on in resolving quality issues, conducting risk assessments and managing CAPAs

Support audits

Implement quality initiatives

Interface and influence stakeholders on quality issues/ updates

Interface effectively with internal teams and external customers/regulators

Establish and maintain quality standards

Support a culture of continuous improvement and compliance

How Will You Get Here?

Education:
Minimum Education Required: Bachelors Degree (Preferred Fields of Study: Mechanical or Industrial Engineering or related technical field)

ASQ certifications (CQE, CQA) desired

*Experience: *
Experience Required: 2+ years of experience in quality assurance in regulated industry (pharmaceutical, medical device, or biotech)

Expertise in quality systems including: CAPA and deviation management, change control, risk management, FMEA, document control and internal/ external auditing

Experience with validation and qualification protocols

Knowledge, Skills, Abilities

:
Working knowledge of ISO 13485/9001, and applicable regulatory requirements (FDA, EMA, etc.)

Advanced problem-solving and root cause analysis skills

Excellent project management abilities

Strong verbal and written communication skills

Proficiency with quality management software and MS Office

Knowledge of statistical analysis and quality tools

Ability to work both independently and collaboratively

Strong attention to detail while maintaining broad perspective

Excellent interpersonal skills for cross-functional collaboration

May require up to 10% travel

Additional language skills may be beneficial

Benefits

We offer competitive compensation, annual incentive plan bonus, healthcare, 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!
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 140,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.