Operations Intern
Asahi Kasei

Cary, North Carolina

Posted in Manufacturing and Production


This job has expired.

Job Info


The Asahi Kasei Group operates with a commitment of creating for tomorrow. Our business sectors, Material, Homes, and Health Care, contribute to the development of society by anticipating the changing needs of those around the world. We look for candidates that offer a fresh perspective and a variety of skills to help us achieve our commitment.

Veloxis Pharmaceuticals is an Asahi-Kasei Group Company based in Cary, NC. Our purpose is to transform transplant medicine as the primary partner to the community of transplant healthcare providers and their patients; our focus is in developing new therapies and programs to help transplant healthcare providers and the patients they treat. Veloxis provides a dynamic and innovative place to work that encourages professional development and embraces diversity. We seek creative, intelligent, action-oriented, and passionate individuals who thrive in a collaborative team environment. If you are interested in being part of a patient-centric company, then we invite you to learn more about the employment opportunities available at Veloxis. Our success is tied to the contribution of every team member, which is why we provide a valuable and competitive compensation package that includes health and insurance benefits, training, and development opportunities, as well as performance-based bonus eligibility.

Company:
Veloxis Pharmaceuticals, Inc.

Job Description:

Summary of Key Responsibilities

  • Assist in setting up continuous process validation (CPV) for an existing commercial product. This involves reviewing all batch records and pulling out the critical process data.
  • Work with Subject Matter Experts (SMEs) to perform data trending and analytics to document the process performance has remained within critical process parameters.
  • Work with SMEs to set up a system to have all new batch values feed into these analytics and connect these analytics with our existing technical and management review cycle.
  • Assist in setting up key supplier data trending and analytics. This involves working with SMEs to identify the key parameters from each of the Company's high priority suppliers and where to obtain these inputs. Once identified, the intern will work with SMEs to set up automatic trending and monitoring similar to CPV project.
  • Work directly with the Company's Quality Assurance team to set up regulatory inspection dossiers and prepare PowerPoint documents that contextualize the layers of control. This involves organizing all technical reports and documents into an electronic folder and adding flow charts and support documentation to help regulatory inspectors understand the Company's controls systems.
  • Assist in setting up project management and metrics in the Company's continuous improvement plan.
  • Other duties, as assigned.

Required Qualifications and Skills

  • Major in Chemical Engineering, Biomolecular Engineering, Pharmaceutical Sciences, or related field at an accredited university.
  • Demonstrated attention to detail.
  • Excellent interpersonal (both written and oral) skills, with the ability to successfully interact with scientific and non-scientific personnel.
  • Ability to work in a dynamic, fast-paced environment with shirting priorities. Flexibility to adapt to changing priorities and manage activities to meet the needs of the business in a compliant manner.
  • Willingness to "roll up his/her sleeves" to get the job done.
  • Proficiency in MS Office Suite (Word, Excel, PowerPoint, Outlook), Adobe Pro.

As an equal opportunity employer, Asahi Kasei believes a diverse workforce will provide us with the ability to continuously support the changes in the economy, society, and environment.


This job has expired.

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