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.

Sr. Quality Control Manager

Department: QC

Purpose of Position:

The Quality Control Manager position manages all of the QC activities for the Milford site. The position assists and supports the development, implementation, and maintenance of Quality Control systems and activities for the site.

Key Job Responsibilities:

  • Ensure timely analysis of samples and release of products while adhering to procedures and regulations.

  • Develop and / or review departmental documentation including SOPís, test methods, protocols, and material specifications.

  • Responsible for leading QC efforts versus QA and customer audits.

  • Direct and develop Quality Control Department personnel and ensure department consistency across multiple shifts

  • Coordinate with associated departments: manufacturing, QA, process development, facilities, etc. in order to ensure QC provides data in a timely and consistent manner.

  • Oversee testing of release samples, stability, and environmental samples to determine suitability versus pre-established written specifications.

  • Oversee the maintenance of laboratory systems including but not limited to: reference standards, reagent log-in, column tracking, retain storage, stability storage.

  • Assist the Director / Associate Director of Quality Control in the management of the physical analytical laboratory.

  • Manage day to day lab operations to ensure efficient use of resources across the different QC subgroups.

Job Knowledge Required:

  • BS in chemistry, biology or related discipline

  • 5+ years of experience in a laboratory environment

  • Working knowledge of cGMP.

  • Strong leadership skills

  • 7+ years Quality Systems experience in an FDA regulated industry.

  • Experience and familiarity with analytical testing equipment and methodology

Problem Solving:

  • This position involves problems of diverse scope. The position exercises judgment within broad technical and practical parameters to determine the appropriate policy,

Equal Opportunity Employer

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