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:

Key Responsibilities:

  • Provides analytical support to small molecule and oligonucleotide manufacturing groups utilizing various analytical instrumentation techniques including HPLC, UPLC, LCMS and NMR instrumentation.
  • Records and reports results of analyses in accordance with prescribed lab procedures and SOPs.
  • Maintains accurate and complete lab notebooks.
  • Reviews laboratory documentation for calculation, entry and cGMP compliance.
  • Develops and/or modifies test methods.
  • Documents and reports results of development and experimentation in technical reports if needed.
  • Participates in cGMP training and implements cGMP operating procedures.
  • Participates in and contributes to safety programs and maintains an orderly and safe laboratory environment.
  • Performs qualification testing of laboratory instruments.

Job Knowledge Required:

  • BS degree with concentration in Analytical Chemistry including HPLC and GC skills and 2+ years of experience or Masterís degree with concentration in Analytical Chemistry including HPLC and GC analysis.
  • Excellent Communication Skills.
  • Experience in a GMP/GLP environment following SOPs and/or compendial methods.
  • Experience with HPLC and/or UPLC.
  • Experience maintaining a laboratory notebook.
  • Experience with the analysis of oligonucleotides is a plus.
  • Ability to work in a team oriented environment.

Equal Opportunity Employer

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