Associate Validation Analyst II
Associate Validation Analyst II
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Salary Not Disclosed
1 Vacancy
Job Description
Work Schedule
Standard (Mon-Fri)Environmental Conditions
Able to lift 40 lbs. without assistance Adherence to all Good Manufacturing Practices (GMP) Safety Standards Laboratory Setting OfficeJob Description
At Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research development and delivery of life-changing therapies. With clinical trials conducted in 100 countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio our work spans laboratory digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on now and in the future.
Essential Functions and Other Job Information:
Participates as a member of project teams contributing to direction on future enhancements to the system reviewing change requests and ensuring effective communication and accuracy in testing.
Provides validation support for new releases and modifications to applications throughout the software development life cycle. Prepares validation plans test cases and validation summary reports and executes test cases.
Reviews and approves change controls associated with validated systems per SOP and ensures test scripts challenge the functional requirements and adequately demonstrate the application meets the expectations of the business customer. Reviews PQ and change control documentation with leadership per SOP.
Executes test scripts accurately to produce evidence that the computer system consistently performs its intended functions accurately and reliably. Creates updates and manages data within the testing environment sufficient to accurately test software functionality.
Provides ongoing business support to users during the implementation and continued use of validated platforms ensuring that appropriate training support and maintenance is provided.
- Bachelors degree or equivalent and relevant formal academic / vocational qualification
- Previous experience that provides the knowledge skills and abilities to perform the job (comparable to 2 years).
- 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
Required Experience:
IC
Employment Type
Full-Time
