Work Schedule

First Shift (Days)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office

Job Description

How you will make an impact:

 

You enjoy working with people. You are collaborative, upbeat and optimistic. You are passionate about science, eager to learn and develop your career in the pharmaceutical industry.  As part of the Pharma services team group, our Cincinnati site develops and manufactures oral drug products for a wide range of small and large pharma companies, including tablets, capsules, and other complex dosage forms employing an array of manufacturing processes.

 

As a member of the QC Team, you will review work in laboratory notebooks for completeness, correctness, and adherence to all SOP’s regarding laboratory notebook procedures and good documentation practices.

 

Responsibilities Include:

Perform manual calculation of data, sampling and sample preparation procedures, solution preparations, and work done using both validated and unvalidated test methods.Review chromatographic data (using Empower V3.2) for correctness of integration, identification, and calculation.Ensure the correct HPLC/GC conditions were used, including but not limited to sample/column temperature, wavelength, flow rate, scale of peaks, and gradient conditions.Review data collected and results derived from other laboratory instrumentation such as Karl Fischer titrators and IR and UV spectrometers as well as data recorded by observation or other physical testing.Work closely with analyst when errors are suspected to identify cause and resolution.Review results entered into LIMS system, ensuring they match the data contained in the analysis performed and that they fall within established trends and specifications.Approves’ or ‘Not Approves’ these data based on Patheon SOPs regarding stability, finished product, ad-hoc or investigation samples.Notifies Data Review supervisor, or other appropriate supervisor, when unusual or out-of-the-ordinary data results are observed.

 

Minimum Qualifications:

Bachelors Degree (Chemistry or Biology, preferred)Minimum 3 years prior laboratory experience

 

Desired Qualifications:

Pharmaceutical industry experience

 

Experience:

An equivalent combination of education, training, and relevant work experience will be considered.

 

Knowledge, Skills, Abilities:

Proven understanding of analytical chemistry (HPLC, GC, Dissolution) and documentation requirementsAbility to work independently and meet client timelinesOrganizational and interpersonal skills, including strong oral and written communication skills, and the ability to multi-task and adjust to changing prioritiesComfortable working with Microsoft Office

 

At Thermo Fisher Scientific, each one of our 75,000 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