Intern, Manufacturing Specialist

BiogenResearch Triangle Park, NC
Onsite

About The Position

This application is for a 12-week internship role from June - August 2026. Resume review begins in January 2026. The Manufacturing Technical Operations (MTO) Team supports the Parenteral Facility Manufacturing Department. The group consists of specialists who serve the PF as process experts by managing various documentation and compliance needs of the Manufacturing team. Additionally, this team introduces new products to the facility and serve as project managers for continuous improvement projects. As an intern in this department, you will gain hands-on exposure to biotech manufacturing processes and learn how they are designed, documented, and implemented. You’ll work alongside experienced professionals to understand the fundamentals of process instructions, compliance documentation, training programs, and tech transfer activities.

Requirements

  • Knowledge of Biotech GMP manufacturing
  • Ability to absorb and communicate technical information
  • Ability to work independently once direction is given
  • Excellent written and verbal communication skills
  • Proficiency with Microsoft Word
  • Ability to assess workload and generate a plan to tackle work assigned
  • Legal authorization to work in the U.S.
  • At least 18 years of age prior to the scheduled start date.
  • Currently enrolled in an accredited community college, college, university or skills program/apprenticeship.
  • Minimum Sophomore year of their four-year degree or higher

Nice To Haves

  • technical writing skills preferred
  • Prior experience leafing projects is a plus
  • Science or Engineering major preferred

Responsibilities

  • Assist with documentation and compliance activities for manufacturing processes.
  • Support technology transfer initiatives for new product introductions.
  • Participate in continuous improvement projects to enhance operational efficiency.
  • Collaborate with cross-functional teams to maintain accurate records and workflows.
  • Learn and apply industry standards for biotech manufacturing operations.
  • Participate in Tech Transfer Meetings: Attend regular NPI Tech Transfer meetings to stay informed on project timelines, deliverables, and cross-functional needs.
  • Documentation Support: Assist Senior Specialists with the creation, review, and editing of technical documents related to the transfer process, ensuring accuracy and alignment with regulatory and operational standards.
  • Manufacturing Collaboration: Partner with Manufacturing teams to identify and implement continuous improvement opportunities, including updates to procedures and training materials that support efficient production of new products.

Benefits

  • Company paid holidays
  • Commuter benefits
  • Employee Resource Groups participation
  • 80 hours of sick time per calendar year

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What This Job Offers

Job Type

Full-time

Career Level

Intern

Education Level

Associate degree

Number of Employees

1,001-5,000 employees

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