QC Validation Engineer IIIThermo Fisher Scientific • Detroit, Michigan, United States of America

QC Validation Engineer III

Thermo Fisher Scientific • Detroit, Michigan, United States of America

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Location : Detroit, MI. Relocation assistance is NOT provided.

Must be legally authorized to work in the United States without sponsorship.
Must be able to pass a comprehensive background check, which includes a drug screening.

At Thermo Fisher Scientific team, you’ll discover impactful work, innovative thinking and a culture dedicated to working the right way, for the right reasons - with the customer always top of mind. The work we do matters, like helping customers find cures for cancer, protecting the environment, making sure our food is safe and delivering COVID-19 solutions. As the world leader in serving science, with the largest investment in R&D in the industry, our colleagues are empowered to realize their full potential as part of a fast-growing, global organization that values passion and unique contributions.

A Day in the Life :

Ensure product quality and regulatory compliance across pharmaceutical manufacturing operations.

Lead complex validation projects for laboratory equipment, analytical test methods, equipment, processes, utilities, and computer systems

Collaborate with cross-functional teams to maintain cGMP standards.

Contribute to continuous improvement initiatives, support team members providing technical expertise.

This role offers professional growth opportunities as you help enable life-changing therapies through robust validation strategies and execution.

Minimum Requirements :

Education

Minimum Required Education : Bachelor of Science (BS) degree in Science or Technical field.

Experience

3+ years of validation experience in a lab environment

Manufacturing validation experience is a plus

Experience leading complex validation projects and coordinating cross-functional teams

Experience with regulatory inspections and client audits preferred

Knowledge, Skills, Abilities

Strong knowledge of cGMP regulations, including FDA, EMA and ISO requirement

Experience writing and executing validation protocols, including IQ / OQ / PQ documentation

Expertise in risk assessment methodologies and statistical analysis

Proficiency with validation of manufacturing equipment, utilities, cleaning processes and computer systems

Strong technical writing and documentation skills

Advanced problem-solving abilities and root cause analysis experience

Excellent verbal / written communication and interpersonal skills

Proficiency with relevant software tools (MS Office, statistical packages, validation systems)

Knowledge of lean manufacturing and continuous improvement methodologies

Ability to work in cleanroom environments when required

Flexibility to work extended hours or alternate shifts based on project needs

May require travel on as needed basis

Physical Requirements / Work Environment

Work requires standing for long durations, managing materials, and operating quality inspection instruments in a manufacturing setting.

Benefits

We offer competitive remuneration, 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 100,000+ 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.

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