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Manager, Validation
full-timeGreenville

Summary

Location

Greenville

Type

full-time

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About this role

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, 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:
As a Validation Manager at Thermo Fisher Scientific, you will manage validation activities that ensure product quality and regulatory compliance. You'll develop validation strategy and oversee a team responsible for qualifying equipment, utilities, facilities, computer systems, and manufacturing processes. Working across functions, you'll ensure validation activities align with cGMP requirements while supporting new product introductions and technology transfers. This role offers the opportunity to make a meaningful impact by maintaining the validated state of systems that help produce therapeutics.
 

EDUCATION/EXPERIENCE:

  • Bachelor's degree in engineering, science, chemistry, biology or related technical discipline. Advanced Degree preferred

  • 6 - 8 years of experience in pharmaceutical/biotech manufacturing industry

  • 2+ years of experience with equipment, process, cleaning, and/or utility validation is required.

  • 3+ years of people management or team leadership experience

  • Demonstrated success managing complex validation projects and programs

  • Experience with validation master planning and change control systems

  • Experience participating in regulatory inspections and customer audits

KNOWLEDGE, SKILLS, ABILITIES:

  • Strong knowledge of cGMP regulations, particularly FDA and EU requirements

  • Expertise in risk assessment methodologies and statistical analysis

  • Proficiency with quality systems and validation documentation

  • Excellent technical writing and documentation skills

  • Strong leadership, communication, and interpersonal abilities

  • Ability to influence and collaborate across functions and levels

  • Knowledge of lean/continuous improvement methodologies

  • Proficient with standard business software applications

NOTE: We are not able to offer relocation assistance or visa sponsorship for this role at this time. We offer competitive salary, an annual incentive bonus plan, 401K with company match up to 6%, tuition reimbursement and a range of other employee benefits! We foster an exciting company culture that encourages innovation, forward-thinking, and an outstanding career and development prospects. Come be a part of the team. We offer competitive salary, an annual incentive bonus plan, 401K with company match up to 6%, tuition reimbursement and a range of other employee benefits! We foster an exciting company culture that encourages innovation, forward-thinking, and an outstanding career and development prospects. Come be a part of the team!

Other facts

Tech stack
Validation,CGMP Regulations,Risk Assessment,Statistical Analysis,Quality Systems,Technical Writing,Leadership,Communication,Interpersonal Skills,Lean Methodologies,Continuous Improvement

About Thermo Fisher Scientific

About Thermo Fisher Scientific
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD.

For more information, please visit www.thermofisher.com.

Team size: 10,001+ employees
LinkedIn: Visit
Industry: Biotechnology Research

What you'll do

  • As a Validation Manager, you will manage validation activities to ensure product quality and regulatory compliance. You will develop validation strategies and oversee a team responsible for qualifying various systems and processes.

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Frequently Asked Questions

What does a Manager, Validation do at Thermo Fisher Scientific?

As a Manager, Validation at Thermo Fisher Scientific, you will: as a Validation Manager, you will manage validation activities to ensure product quality and regulatory compliance. You will develop validation strategies and oversee a team responsible for qualifying various systems and processes..

Why join Thermo Fisher Scientific as a Manager, Validation?

Thermo Fisher Scientific is a leading Biotechnology Research company.

Is the Manager, Validation position at Thermo Fisher Scientific remote?

The Manager, Validation position at Thermo Fisher Scientific is based in Greenville, North Carolina, United States. Contact the company through Clera for specific work arrangement details.

How do I apply for the Manager, Validation position at Thermo Fisher Scientific?

You can apply for the Manager, Validation position at Thermo Fisher Scientific directly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process. You can also learn more about Thermo Fisher Scientific on their website.