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.

Manufacturing Chemist-Purification

Department: Manufacturing
Location: Milford, MA

How can you make a difference in this role?

This role is responsible for the implementation of assigned production procedures working within defined production schedules. Responsible for performing all work within company and cGMP regulatory compliance. Operate and perform routine maintenance on equipment being used. Maintaining a safe work environment and following all site safety procedure. Performs routine, generally highly structure work. Responsible for staying current with the prescribed training curriculum specified for the job title.

What are the key responsibilities of this role?

  • Execute defined lab start up and shutdown procedures.
  • • Maintaining a clean and organized work environment in accordance with defined procedures.
  • • Assuring basic lab supply needs are met. • Qualify and maintain Qualification on all assigned manufacturing processes which may include: purification equipment cleaning and setup.
  • General solution preparation o Lab cleaning and changeover
  • Routine equipment monitoring or maintenance.
  • Monitor automated systems and record operational data.

  • Perform general routine or non technical operations including: pH measurements, UV determinations, Fraction collection


What experience and job knowledge do you need to excel in this role?

  • Must have Purification experience in a GMP manufacturing setting
  • Minimum education requirements high school diploma or equivalent, with college level chemistry or equivalent work experience.
  • A biotechnology certificate or college degree is preferred.

Equal Opportunity Employer

 

 

 

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