INTERNSHIP DETAILS

MSAT Co-Op

CompanyBoehringerPRD
LocationGainesville
Work ModeOn Site
PostedJune 17, 2026
Internship Information
Core Responsibilities
Assist in the identification, development, and execution of pilot scale studies for production and analytical innovation. Responsibilities include writing experimental protocols, conducting bench studies, and analyzing data to facilitate change control execution.
Internship Type
full time
Company Size
46998
Visa Sponsorship
No
Language
English
Working Hours
40 hours
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About The Company
Our people are our strength. And together with over 54,000 colleagues, we're creating the next breakthrough in the world of healthcare and innovation for both humans and animals. Are you ready to join us? #LifeForward Privacy Notice: https://www.boehringer-ingelheim.com/privacy-notice Imprint: https://www.boehringer-ingelheim.com/imprint
About the Role

Description

Boehringer Ingelheim is currently seeking a talented and innovative Intern to join our Manufacturing Science and Technology (MSAT) department located at our Gainesville facility. As an Intern, you will assist in the identification, development, and execution of pilot scale studies related to production and analytical innovation and process development.

 

As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees

Duties & Responsibilities

  • Work alongside members of the MSAT team to facilitate collaboration and learning
  • Spend time on the production and quality control shopfloor to learn/observe the process for the purposes of identifying potential improvement initiatives
  • Write experimental protocols
  • Carryout bench/pilot scale studies
  • Analyze and review study and production/quality control data
  • Write technical reports to summarize study findings and facilitate change control execution

Requirements

    • Must be a current undergraduate, graduate or advanced degree student in good academic standing
    • Student must be enrolled at an accredited college or university for the duration of the Co-Op
    • Overall cumulative minimum GPA from last completed quarter/semester 3.0 GPA (on a 4.0 scale) preferred
    • Major or minor in related field of Co-Op
    • Undergraduate students must have completed at least 12 credit hours at current college or university
    • Graduate and advanced degree students must have completed at least 9 credit hours at current college or university


Eligibility Requirements:

  • Must be legally authorized to work in the United States without restriction.
  • Must be willing to take a drug test and post-offer physical (if required).
  • Must be 18 years of age or older.

Desired Skills, Experience and Abilities

  • Background in cell biology, microbiology, and/or virology
  • Understanding of aseptic principals as well as GLP and GMP standards
  • Laboratory experience with a background in execution of TCID50/EID50 titrations, PCR, ELISA, etc.
  • Proficient in the use of Microsoft Office applications
  • Desired experience with ViCell Cell Counter, Agilent, Cytation 5, and rapid sterility tools.
Key Skills
Cell BiologyMicrobiologyVirologyAseptic PrinciplesGLPGMPTCID50/EID50 TitrationsPCRELISAMicrosoft OfficeViCell Cell CounterAgilentCytation 5Rapid Sterility ToolsTechnical WritingData Analysis
Categories
Science & ResearchManufacturingEngineeringHealthcare
Benefits
Competitive CompensationBenefit Programs
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