Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Laboratory Setting, Loud Noises (Equipment/Machinery), Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products etc.), Will work with hazardous/toxic materials
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:
We are seeking a Validation Analyst to provide basic business/system support of software systems and/or laboratory instrumentation. You will work with staff of various departments and the client to initiate and complete performance qualification (PQ) validation. You will facilitate the validation process and implementation of system upgrades, including guiding, testing, supporting the introduction and ongoing support of software systems. This position offers excellent opportunities for professional growth while contributing to meaningful scientific advancement through technology.
REQUIREMENTS:
* Bachelor's degree required, 1-2 year GMP experience preferrable
* Preferred Fields of Study: Computer Science, Information Technology, or related field
Client-focused approach with strong interpersonal skills, and strong oral and written communication skills and ability to teach others
* Strong attention to details and problem-solving skills
* Demonstrated competency with Microsoft Office Suite (Word, Excel, PowerPoint, and Project). Proven ability to learn new computer software with minimum of instruction
* Positive attitude, enthusiasm toward work, and the ability to work well with others
* Effective organization and time management skills with the ability to adapt and adjust to changing priorities and manage multiple assignments with challenging/conflicting deadlines
* Solid understanding of clinical trials operational processes and terminology and solid understanding of the software development life cycle (SDLC)
* Strong troubleshooting skills and ability to analyze software defects, assess the cause of test failures, and explain how errors are produced
* Ability to attain, maintain, and apply a working knowledge of GCPs, applicable SOPs/WPDs, and process maps
* Ability to review and critique SDLC documentation including requirements, functional design, system design, and test plans. Ability to assess the cause of test failures
* Demonstrated ability to coordinate project activities and work and communicate effectively on a multi-disciplinary team
Travel may be required