QC Scientist II Full-time

Job Title

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.

Excellent Benefits Package

Medical, Dental, & Vision benefits-effective Day 1

Paid Time Off & Holidays

401K Company Match up to 6%

Tuition Reimbursement – eligible after 90 days!

Employee Referral Bonus

Employee Discount Program

Recognition Program

Charitable Gift Matching

Company Paid Parental Leave

Career Advancement Opportunities

Location/Division Specific Information

Greenville, NC

Hours: 6pm – 6:30am (2-2-3 schedule with 15% shift differential)

We have industry-leading sterile injectable facilities providing solutions to take crucial products from pre-clinical to the market. Pharmaceutical products come in many different dose forms including inhalations, oral dose, cream/ointment and injectables.

How will you make an impact?

Provides moderately sophisticated analyses in a microbiology environment within defined procedures and practices. Follows standard operation procedures as assigned for monitoring in classified environments. Supports internal development and/or manufacturing operations. Make detailed observations and reviews, documents, and communicate test results. Documenting, reporting and analyzing data in a laboratory setting. Conducts detailed assessments and evaluations, records findings, and shares test outcomes; suggests resolutions. Develops expertise to function as a SME.

What will you do?

• Verifies and processes environmental monitoring data.
• Performs moderately complex validated test methods for routine, special projects and batch related environmental monitoring in clean rooms.
• Leads environmental monitoring in support of validation of test methods for clean rooms.
• Determine which methods will be used.
• Reports or makes determination out-of-specification or unexpected results, due to environmental impacts or other to reach resolution.
• Reading and verification of plates.
• Maintains and troubleshoots instrumentation as needed.
• Verify proper calibration for use.
• Assists in preparing regulatory documents and other communications with outside agencies, clients and/or colleagues from other corporate sites.
• Develops documentation processes.
• Clearly and accurately communicates the results of work by creating documentation of the testing/analysis and obtained results.
• Records and reports results of analysis in accordance with prescribed lab procedures and systems.
• Interacts with clients directly.
• Leads, prepares, and files regulatory documents in support of internal projects.
• Provides communications with outside departments, corporate sites, agencies, and clients.
• Coordinates and assists or leads, prepares and files with writing of SOPs, policy manuals, and other instructional documents.
• Cleans and organizes work area, equipment, and testing materials.
• Performs all duties in strict compliance with Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices, ALCOA, Audits and Safety guidelines.
• Maintains the necessary training, compliance status required by company and facility standards.
• Other duties as assigned.

Education

Bachelor's degree preferred in physical science, preferably in Chemistry or Biology. Associate degree in a science related field required.

Equivalent combinations of education, training, and meaningful work experience may be considered if you at least have an associate degree.

Experience

3-4 years of job-related experience in performing aseptic techniques, clean room activities or related experience.