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.

PD Process Validation Technical Writer

Department: Process Development
Location:

Process Validation Technical Writer

Reporting to the Technical Manager, Process Validation, this role will provide support of Process Validation activities for Avecia’s manufacturing processes.

Key job responsibilities:

  • Preparation of process validation documentation in accordance with SOPs in support of Process Development deliverables across multiple projects. Documentation includes, but is not limited to, process development/validation risk assessments, protocols and reports.

  • Contribute to the standardization of approaches to process validation across projects.

  • Contribute to activities executed to support process design/characterization, process risk assessments and process monitoring.

  • Coordinate documentation review with the Quality Unit to ensure documents meet established procedures.

Qualifications/skills/experience required:

BSc in Chemistry or related field and 2 years relevant experience
Knowledge of cGMP
Proficiency in MS Word and MS Excel and in the preparation of technical reports in the English language
Excellent communication skills and ability to interact with technical laboratory staff at all levels to discuss the content of technical documentation
Ability to work under minimal supervision with excellent judgement in problem solving and elevating issues when necessary.
Experience with Statistical Analysis software is not required but is beneficial

 

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