QC Scientist II

Greenville - USA

Monthly Salary: Not Disclosed

Posted on: 30+ days ago

Vacancies: 1 Vacancy

Job Summary

Work Schedule

12 hr shift/nights

Environmental Conditions

Able to lift 40 lbs. without assistance Adherence to all Good Manufacturing Practices (GMP) Safety Standards Cleanroom: no hair products jewelry makeup nail polish perfume exposed piercings facial hair etc... allowed Cold Room/Freezers -22degreesF/-6degrees C Laboratory Setting Loud Noises (Equipment/Machinery) Rapid flashing lights Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.) Standing for full shift Strong Odors (chemical lubricants biological products etc.) Warehouse Will work with hazardous/toxic materials

Job Description

As part of the Thermo Fisher Scientific team youll 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 worlds toughest challenges like protecting the environment making sure our food is safe or helping find cures for cancer.

Excellent Benefits Package

Review our companys Total Rewards

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 (i.e. classified areas and aseptic processing).
Leads environmental monitoring in support of validation of test methods for clean rooms (i.e. classified areas and aseptic processing).
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

Bachelors 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.

Work Schedule12 hr shift/nightsEnvironmental ConditionsAble to lift 40 lbs. without assistance Adherence to all Good Manufacturing Practices (GMP) Safety Standards Cleanroom: no hair products jewelry makeup nail polish perfume exposed piercings facial hair etc... allowed Cold Room/Freezers -22degree...