Validation Engineer III

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products etc.)

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:

Join our validation engineering team, where you'll ensure product quality and regulatory compliance across pharmaceutical manufacturing operations. As a Validation Engineer III, you'll lead complex validation projects for equipment, processes, utilities, and computer systems while collaborating with cross-functional teams to maintain GMP standards. You'll contribute to continuous improvement initiatives, support team members, and provide technical expertise during client and regulatory audits. This role offers professional growth opportunities as you help enable life-changing therapies through robust validation strategies and execution.

REQUIREMENTS:

Advanced Degree plus 3 years of experience, or Bachelor's Degree plus 5 years of experience in validation in pharmaceutical/biotech manufacturing or comparable regulated industry

Preferred Fields of Study: Engineering, Life Sciences, Chemistry or related technical field

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

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

Experience leading complex validation projects and coordinating cross-functional teams

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)

Experience With Regulatory Inspections And Client Audits Preferred

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 up to 25% travel
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