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 Supervisor-2nd shift

Department: Operations

Purpose of Position:

Responsible for the implementation of production procedures and processes relating to DNA Synthesis and purification with the goal of optimizing the manufacturing process while meeting regulatory requirements. Provides line supervisory oversight of all unit operation activity on second shift for both synthesis and purification. Ensures compliance to internal and external regulatory policies and procedures.

Key Responsibilities:

  • Supervisors any critical unit operations occurring in production on the second shift.
  • Provides training and development of production personnel including, but not limited to, conducting midyear and annual job performance reviews for staff. Ensures that staff receives the training necessary to effectively perform their assigned tasks.
  • Assures batch records are appropriately followed and that all work performed is properly documented in batch records, equipment logbooks, etc.
  • Completes required deviations, change requests, or investigations for incidents that occur in the production area.
  • Assist with the development, execution, and communication of production schedule.
  • Communicates effectively and in a collaborative manner with staff, supervisor, and colleagues.
  • Ensures compliance to all GMP processes and procedures.
  • Ensures a safe work environment for all employees. This will be done by promoting a culture of safety awareness, implementing and supporting the site safety plan, addressing any safety audit findings, etc.
  • Performs other duties as required.

Job Knowledge Required:

  • This is specialist position requiring a comprehensive knowledge of the cGMP requirements for API manufacturing.
  • Minimum education requirements include a Bachelor’s degree, science or engineering preferred or equivalent work experience.
  • Must have a minimum of 2 years experience
  • Must be technically proficient on all unit operations associated with oligo manufacturing.
  • Experience managing and mentoring people.

Equal Opportunity Employer

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