Process Validation Staff Engineer

at  Thermo Fisher Scientific

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.

EDUCATION:

• Minimum required education: Associate’s degree in a scientific or production related discipline
• Higher level education preferred.

EXPERIENCE:

• 6 years’ experience in the pharmaceutical industry required.
• 2 years validation experience required.

KNOWLEDGE, SKILLS, AND ABILITIES:

• Broad based knowledge of regulatory compliance requirements related to validation and relevant production controls.
• Strong interpersonal and communication skills.
• Ability to efficiently collaborate with others to achieve team goals and expectations.
  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 global 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.
  Apply today! http://jobs.thermofisher.com
  Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

• Lead multiple complex validation activities associated with computers, equipment, and processes.
• Develop and implement validation plans and associated documentation in the NDA drug approval process under the FDA Pre-Approval Inspection programs.
• Coordinate validation associated audit activities; establish rationales and technical defense positions.
• Negotiate with clients the validation requirements for projects. Resolve significant validation, product and regulatory issues. Plan and establish technical communications, document flow, testing requirements, and resources vital to complete the validation of a system.
• Support systems and new product introduction by serving as a technical resource, providing technical expertise, problem solving, and strategies for problem prevention.
• Participate as the validation representative in project team activities and process design to insure CGMP compliance and interdepartmental consistency within the validation program.
• Assure compliance to all applicable regulations by proactively interpreting regulatory and compliance requirements as related to validation.
• Maintain current knowledge and serve as a technical resource for emerging trends and technologies.
• Coordinate and provide training and/or opportunities for career development of others.
• Coordinates the implementation of interdepartmental process validation programs.
• Performs validation functions to ensure accurate and timely completion with frequent decision making, coordination and communications required.
• Builds, reviews, approves, tracks and presents documents and procedures required for compliance with pharmaceutical regulations.
• Identifies areas of non-compliance, review recommendations of others and implement solutions to resolve major quality and productivity issues.