QC Scientist I

1 month ago

High Point, North Carolina, United States Thermo Fisher Scientific Full time

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materials

Job Description

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

Review our company's at this link: 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

Provides analyses in a chemistry or microbiological environment within defined procedures and practices. Performs analytical methods for testing on raw materials, samples, stability, production intermediates, environmental monitoring, sterility tests, growth promotion, microbial limits tests, and/or and antimicrobial efficiency tests. Supports internal development and/or manufacturing operations. Makes detailed observations and reviews, documents, and communicates test results; recommends solutions.

Essential Functions:

  • Conducts chemical and physical testing of pharmaceutical raw materials, packaging components, finished products, microbiological, and stability samples by internally developed and compendial test methods.
  • Implements validated test methods for pharmaceutical raw materials and finished products for strength, impurities, identity, and dissolution by HPLC, GC, dissolution, spectroscopy, and traditional quantitative analysis, using HPLC, GC, LC/MS, dissolution, spectroscopy, and/or traditional wet chemical testing.
  • Recognizes and reports out-of-specification or unexpected results and non-routine analytical and product problems; recommends solutions.
  • Maintains and troubleshoots analytical instrumentation as needed.
  • Clearly and accurately communicates the results of work by documenting of the testing/analysis and obtained results.
  • Records and reports results of analysis in accordance with prescribed lab procedures and systems.
  • Provides communications with outside departments.
  • Cleans and organizes work area, instrumentation, and testing materials.
  • Cleans HPLC and dissolution systems after use.
  • Performs all duties in strict compliance with Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices, and Safety guidelines.
  • Maintains the necessary compliance status required by company and facility standards.

Education/Experience:

Bachelor's Degree in Chemistry, Microbiology, Biology, Biochemistry, or related field requred. Typically requires no experience performing tests or analyses for pharmaceutical raw materials, finished products, or microbiological samples. Experience with common office software and chromatographic data acquisition systems.

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