Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Cold Room/Freezers -22degreesF/-6degrees C, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs 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, facilities and utilities
• 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