Analytical Chemist / Chemist / Quality Control Chemist
Hunter International, Inc. (Akron, Ohio)

Salary:
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Salary Details:
NET, GROSS, EXCELLENT BENEFITS, FLEXIBLE WORK SCHEDULE
Position Type:
Fulltime
Ref Code:
71048691
Minimum Education Level:
Bachelors Degree
Minimum Career Level:
Experienced (Non-Manager)

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ANALYTICAL CHEMIST / PRODUCT DEVELOPMENT /

QUALITY CONTROL CHEMIST

 

Akron, Ohio

Cleveland, Ohio

 

Full-time Chemist

OR

Temporary Chemist

 

Analytical / QC Chemist Job Description:

The Product Development Chemist/ Quality Control Chemist may work within the Product and Process Development Department. Responsible for analytical test methods development, qualification and validation. Formulation and lyophilization cycle development and scale-up to production size. Evaluation of proposed formulation, processing procedure and selected container/closure system through pilot batch testing and development stability studies. Development batch, In-process testing, Final Product, Raw Material and various Stability tests, trouble shooting in HPLC and/ or GC.

 

 

Analytical / Quality Control Chemist Qualifications/Experience:

● Requires a (4) year degree in chemistry or closely related science.

● Requires a minimum of (2) years analytical chemistry experience in a pharmaceutical laboratory environment.

● Chemist must have demonstrated proficiency and trouble-shooting skills in HPLC & GC.

● Proven experience and trouble-shooting skills in IR, UV, KF and TLC.

● Chemist must have experience using electrochemical instrumentation.

● Chemist must have experience working with low molecular weight heprins and analytical techniques.

● Demonstrated proficiency with coagulation analysis and light scattering detection.

● Chemist must have demonstrated knowledge of formulation concepts, analytical method development, research, problem-solving skills and experimental design are required.

● Chemist must have experience in parenteral product development including lyophilization is desired.

● Computer literacy, documentation/report writing and cGMP experience is required.


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