2026 Summer Internship CAPEX Expansion (ProjectProcess Engineering)

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profile Job Location:

Bloomington, IN - USA

profile Monthly Salary: Not Disclosed
Posted on: 06-11-2025
Vacancies: 1 Vacancy

Job Summary

Simtra BioPharma Solutions (Simtra) is a world-class Contract Development Manufacturing Organization partnering with pharmaceutical and biotech companies to bring their sterile injectable products to market. With facilities in Bloomington Indiana US and Halle/Westfalen Germany we offer a wide range of delivery systems including pre-filled syringes liquid/lyophilized vials diluents for reconstitution powder-filled vials and sterile crystallization.

Our product types include biologics and small molecules cytotoxics highly potent compounds diluents for reconstitution and vaccines which are all directly injected into patients worldwide. As such there is a strong emphasis on quality and continuous improvement at Simtra. We hold ourselves to the highest quality and regulatory standards.

While our primary focus is cGMP manufacturing we offer many support services including formulation and development lyophilization optimization global regulatory support and secondary packaging. Our teams are driven to help clients scale innovate and bring life-changing medicines to patients worldwide.

Why join Team Simtra Because we:

Make it HAPPEN We bring a growth mindset to every opportunity developing new skillsets and exceeding our expectations and those of our customers.

Make it TOGETHER We work as one respecting each voice and tapping into our unique strengths across teamsso we can solve problems in new ways.

Make it RIGHT We hold ourselves to a high standard of excellencefulfilling our commitments to the customer their patients and our team members.

Make it COUNT We take pride in our day-to-day work knowing the impact we make taking on challenges big and small to improve patient health.

The Role:
Simtra is seeking highly motivated undergraduate and students for our Summer Internship Program. We look for diverse students with inquisitive minds and the desire to challenge themselves. Our interns work closely with industry professionals and learn quickly how to problem solve on real-world projects that contribute to clinical research and manufacturing addition to on-the-job experience we offer learning sessions with top leadership site visits to local projects and social events

The Opportunity:
The CAPEX (Capital Expenditures)/Expansion Project Engineering Team develops and maintains the long-term CAPEX roadmap including but not limited to - identifying major facility expansions managing major equipment upgrades and supporting process improvement investments. They perform feasibility studies and business case development for capital projects while prioritizing projects using multi-criteria analysis. Other responsibilities include creating and implementing engineering and design specifications and manage project execution and oversight.

Responsibilities/Projects:
The intern will assist in leading and managing facility expansion projects - including developing and maintaining project tracker develop SOP changes support construction quality activities support turn-over package requirements and support all validation activities (writing protocols). They will coordinate internal stakeholders and external contractors. The intern will also troubleshoot and resolve technical challenges related to project implementation. Responsibilities include:

  • Develop upcoming years Engineering Capital Plan and ensure submitted projects contain a defined scope budget and schedule to sustain and support Site growth
  • Interacts with all functions and levels of management ensuring effective ongoing communications across teams and stakeholders
  • Assists Project Managers/Engineers on project deliverables
  • Participates in all collaborations with external engineering firms in feasibility assessments concept design basic design and detail design
  • Participates in technical review of all external engineering design reviews
  • Assist with work orders preventative maintenance plans P&ID redlines spare parts management among other activities related to project documentation.
  • Assists with project CQV (commissioning qualification and validation) activities


Required Qualifications:

  • Pursuing a BS or MS degree in Engineering Chemical Mechanical Electrical Packaging Pharmaceutical Biomedical) or a related technical field
  • Strong oral and written communication skills
  • Must be able to read mechanical electrical and P&ID drawings
  • Advanced proficiency in Microsoft Office Suite (Word Excel and Outlook)
  • Proficient in project management tools (MS Project Primavera JIRA etc.)
  • Experience and the ability to use enterprise software (examples include: JDE Microsoft Dynamics BPLM Veeva Trackwise etc.)


Onsite Campus Amenities:

  • Workout Facility
  • Cafeteria
  • Credit Union

Disclaimer

This job description is intended to provide the minimum knowledge skills and abilities necessary to perform the job. It may not be inclusive of all the duties and responsibilities of the job. Simtra reserves the right to make modifications based on business requirements.

Equal Employment Opportunity

Simtra is proud to be an equal opportunity employer. Simtra evaluates qualified applicants without regard to race color religion gender national origin age sexual orientation gender identity or expression protected veteran status disability/handicap status or any other legally protected characteristic.

Data Privacy

To learn more about Simtras approach to data privacy please review the Simtra Recruitment Platform Global Privacy Policy: Experience:

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Simtra BioPharma Solutions (Simtra) is a world-class Contract Development Manufacturing Organization partnering with pharmaceutical and biotech companies to bring their sterile injectable products to market. With facilities in Bloomington Indiana US and Halle/Westfalen Germany we offer a wide range ...
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