Job Opportunities with Nitto Denko Avecia in the USA
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Why work at Avecia?

As a leading drug development services company for oligonucleotide therapeutics, the first step in our DNA/RNA sequence is to work with a great team of people.

At Avecia, our team approach allows you to excel in your individual area of expertise as well as to be part of a group of professionals that has the support of management and peers from various backgrounds. And while we’re focused on results, we still maintain our flexibility and enjoy camaraderie and the benefits of work/life balance. Make the next move in your progression of success and join Avecia.

At Avecia, we encourage and value people from diverse ethnic and cultural backgrounds to contribute to our collective success. It is Avecia’s policy to conduct business without regard to an individual’s disability or any other protected status. We are fully committed to the concept and practice of equal opportunity and affirmative action in all aspects of employment and encourage all to apply.

Quality Control Analyst

Department: QC
Location: Cincinnati, OH

Summary

  • This posting is for an Analyst position in a GMP pharmaceutical Quality Control Laboratory. The focus of this position would be support of microbiological testing but the responsibilities could include analytical chemistry testing based on the background and experience level of the candidate.

Key Responsibilities:

  • Performs microbiological testing on water and environmental samples following written procedures.
  • Performs sampling and chemical testing for raw materials following written procedures.
  • Provides analytical support to oligonucleotide manufacturing using various analytical instrumentation techniques including HPLC, UPLC, LCMS and NMR instrumentation.
  • Records and reports results in accordance with prescribed lab procedures and SOPs.
  • Maintains accurate and complete lab notebooks.
  • Reviews laboratory documentation for calculation, entry and cGMP compliance.
  • Participates in cGMP training and implements cGMP operating procedures.
  • Participates in and contributes to safety programs and maintains an orderly and safe laboratory environment.

Job Knowledge Required:

  • BS degree in Biology or Chemistry with at 0-5 years of experience or Master’s degree in Biology or Chemistry with 0 to 3 years of experience.
  • Excellent Communication Skills
  • Experience in a GMP/GLP environment following SOPs and/or compendial methods
  • Experience maintaining a laboratory notebook
  • Ability to work in a team oriented environment.

Equal Opportunity Employer

 

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