Thermo Fisher Scientific Validation Associate I in Greenville, North Carolina

Job Description

Job Title

Validation Associate I

When you’re part of the team at Thermo Fisher Scientific, you’ll do important work, like helping customers in finding cures for cancer, protecting the environment or making sure our food is safe. Your work will have real-world impact, and you’ll be supported in achieving your career goals.

Location

Greenville, NC

How you will make an impact

Provides direct quality support (e.g. compliance, regulatory assessment, validation) to the business unit, clients

and corporate management. Performs quality functions to ensure accurate and timely completion for activities

and projects of low complexity with routine decision making required.

What you will do

  1. Plans, organizes, executes and tracks multiple tasks of low complexity to ensure timely completion of

deliverables related to key quality functions.

  1. Analyzes data for routine validation and production documentation to determine acceptability, identify

deviations and make appropriate notification.

  1. Prepares documents and reports; gain multidisciplinary consensus with some degree of independence.

  2. Maintains and uses database systems.

  3. Prepares, retrieves and reviews documentation for customer and regulatory audits.

  4. Collaborates with senior personnel to resolve deviations.

  5. Assesses impact of changes of low complexity.

  6. Prepares documents for records archival.

  7. Works in a safe and responsible manner in order to create an injury-free and incident-free workplace.

  8. Complies with all job-related safety and other training requirements.

  9. Performs other duties as assigned.

How you will get here

Education

Bachelor’s degree in physical or biological science or production related discipline is preferred.

Experience

One year of relevant experience in Life Science, Chemistry, Biology, Engineering, Biomedical, or IT is preferred.

Experience

Equivalent combinations of education, training, and relevant work experience may be considered.

Knowledge, Skills, Abilities

Proficient in performing activities within at least one Key Quality Function with minimum direction. Key Quality Functions include: Lab Services, Validation, Batch Disposition, Compliance, Document Management,Customer Relations, and Quality Engineering.

Outstanding attention to detail and organizational skills. Selfstarter, mature, independent and dependable. Ability to work in a fast paced environment under pressure, able to multi-task and is results-oriented. Effective time management and prioritization skills. Requires discretion and independent judgment. Highly effective verbal and written communication skills.

At Thermo Fisher Scientific, each one of our 70,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission—enabling our customers to make the world healthier, cleaner and safer.

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.

If you are an individual with a disability who requires reasonable accommodation to complete any part of our application process, click here at https://jobs.thermofisher.com/page/show/eeo-affirmative-action-statement#accessibility for further assistance.

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.