QC Scientist I
QC Scientist I
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Salary Not Disclosed
1 Vacancy
Job Description
Work Schedule
First Shift (Days)Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards Laboratory Setting OfficeJob 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 SOPs 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 adhoc or investigation samples.
- Notifies Data Review supervisor or other appropriate supervisor when unusual or outoftheordinary 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 requirements
- Ability to work independently and meet client timelines
- Organizational and interpersonal skills including strong oral and written communication skills and the ability to multitask and adjust to changing priorities
- Comfortable working with Microsoft Office
At Thermo Fisher Scientific each one of our 75000 extraordinary minds has a unique story to tell. Join us and contribute to our singular missionenabling our customers to make the world healthier cleaner and safer.
Apply today!
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
Employment Type
Full-Time
