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

Purpose of Position:

The QC Analyst (level TBD) is responsible for conducting routing analysis of raw materials, in-process samples and finished products in a strict GMP setting. The position involves working in the QC laboratory and in the manufacturing space on assigned tasks following written procedures and verbal instructions.

Key Responsibilities:

  •  Test and analyze samples
  •  Conduct environmental monitoring in the clean space
  •  Review data for compliance with specifications and GMP regulations
  •  Plan and schedule work assigned to them
  •  Writes/revises QC documents within their scope of expertise
  •  Performs experiments with guidance

Job Knowledge Required:

  •  BS in chemistry, biology or related discipline or equivalent combination of education and experience 
  •  0-5 years of experience in a laboratory environment 
  •  Familiarity with analytical testing equipment and methodology

Equal Opportunity Employer

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