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.

Mfg. Purification Supervisor-2nd shift

Department: Manufacturing
Location: Milford, MA

2nd shift Supervisor-M-F 3:00-11:30pm, 10% shift differential


How can you make a difference in this role?

Responsible for the implementation of production procedures and processes relating to Purification with the goal of optimizing the manufacturing process while meeting regulatory requirements. Assists development personnel in developing new, scalable processes and procedures which improve product yield and reduce manufacturing costs. Assists in the maintenance of equipment used.

What are the key responsibilities of this role?

Maintain a safe working environment and follow all site safety procedures.

·         Assist in the development of new processes and procedures.

·         Operate and perform routine maintenance on equipment used.

·         Responsible for performing all work within Company and cGMP regulatory guidelines.

·         Develop production procedures and processes to improve the product yield and reduce manufacturing costs of current processes.

·         Evaluate data collected during process operations to verify validity and repeatability and find opportunities for improvement.

·         Performs all levels of work required in the Department.

·         Develop, Supervise and Train Staff assigned


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

BS Degree in Chemistry or related

Knowledge of chemical handling and basic lab safety required and experience in cGMP development setting preferred.

What other skills and competencies are required for you to succeed in this role?

Problem Solving: 

Must understand the properties of all chemicals being used, their interactions with other chemicals, and the impact of all processes on the each individual chemical and compound. Must be able to accurately collect and evaluate data to make judgments on the validity of the results achieved. Required to evaluate whether cGMP requirements are being met at all times and if not, to take appropriate action. Must be able to direct work of others.


Equal Opportunity Employer


Equal Opportunity Employer

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