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Internship R&D Software Engineer Jobs in Bloomington, IN

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D., or equivalent studies/experience. Graduate of Construction Management or Construction ... Proficiency with Engineering & Virtual Design Software platforms, Autodesk Construction Cloud ...

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Python Tutor

Bloomington, IN ยท Remote

$40/hr

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Internship R D Software Engineer information

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How much do internship r&d software engineer jobs pay per hour?

As of May 28, 2026, the average hourly pay for internship r&d software engineer in Bloomington, IN is $23.51, according to ZipRecruiter salary data. Most workers in this role earn between $19.13 and $26.68 per hour, depending on experience, location, and employer.

What is the difference between Internship R&D Software Engineer vs Software Developer Intern?

AspectInternship R&D Software EngineerSoftware Developer Intern
FocusResearch and development, innovation, prototypingApplication development, coding, feature implementation
Work EnvironmentLabs, R&D departments, experimental projectsDevelopment teams, product teams, software projects
Required SkillsProgramming, research methods, problem-solvingProgramming, debugging, software design
Industry UsageTech companies, research institutionsTech companies, startups, software firms

Internship R&D Software Engineers focus on innovative research and prototyping, often working in labs or research settings. In contrast, Software Developer Interns primarily work on developing and coding software applications. Both roles require programming skills, but the R&D role emphasizes research and experimentation, while the Developer role emphasizes application development.

What cities near Bloomington, IN are hiring for Internship R&D Software Engineer jobs? Cities near Bloomington, IN with the most Internship R&D Software Engineer job openings:

Computer Systems Validation Associate II

Simtra BioPharma Solutions

Bloomington, IN โ€ข On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post hasย expired today.ย Applications are no longer accepted.


Job description

For over 65 years, pharmaceutical and biotech companies have partnered with Simtra BioPharma Solutions (Simtra) to bring their sterile injectable products to market.
Simtra is a world-class Contract Development Manufacturing Organization with facilities in Indiana, US and Halle/Westfalen, Germany. We offer a wide-range of delivery systems including prefilled-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, at Simtra, there is a strong emphasis on quality and continuous improvement. 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.
In addition to unmatched expertise and experience, we offer a uniquely collaborative approach. Clients look to Simtra as an extension of their own companies.
It is very rewarding industry to work in. Our teams are driven to help clients scale, innovate, and bring-life changing medicines to patients worldwide.
The Validation Associate II is a key member of the Computer Systems Validation team within the Technical Services organization. The Validation Associate II must have a working knowledge of the overall requirements dictated by worldwide regulatory agencies with respect to computer systems validation. This position works directly with the Information Technology department and other functional areas and is considered the lead validation resource. The Validation Associate II understands industry best practices and maintains a state of audit readiness always. This position reports to the Manager, Computer Systems Validation.
What you'll be doing:
  • Validation document author/reviewer - VP, URS, FS/DS, TM, IQ, OQ, PQ using established templates
  • Technical writing proficiency - VP, URS, FS/DS, TM, IQ, OQ, PQ using established templates.
  • Entitlement Reviews - Coordinates user access reviews for recertification and authorization
  • Local Change Control owner
  • CSV periodic reviews - to maintain the validated state, the Associate will perform periodic reviews of validation packages per established procedures
  • Validation lead GAMP Category 1 - 4
  • Client audits - The Associate will participate in client audits, responding verbally to auditor's questions.
  • Global Change Control task owner
  • System assessments - Quality, Regulatory, Risk, Gap CAPA owner
  • NCR/SNCR investigator
  • Validation Lead for implementation of major and minor software applications or modules for Good Manufacturing Practices (GMP) use
  • Completes detailed risk assessment and 21 CFR part 11 Gap analysis
  • Maintains departmental compliance with regulations and corporate procedures
  • Coordinates computer systems implementation activities with Vendors and other non-BPS resources
  • Creates/Reviews validation documentation, templates, procedures, and all documentation generated during a computer systems validation project
  • Participates in Internal/Client/Corporate Audits
  • Represents validation department as validation expert in cross-functional work teams
  • Advocates and understands best practices for system validations and processes
  • Articulates complex systems and communicates to technical and nontechnical management

What you'll bring:
  • BS in Electronic or Software Engineering, Information Systems, or a related field, preferred
  • 3+ years experience of working within a regulated environment (worldwide regulatory agencies), particularly in computer systems validation or other validation discipline
  • Ability to use enterprise software (i.e., ERP, EDMS, QMS, JDE, Trackwise, etc.)
  • Experience with Microsoft Project
  • Technical writing skills

Physical / Safety Requirements
  • Duties may require overtime work, including nights and weekends
  • Use of hands and fingers to manipulate office equipment is required
  • Position requires sitting for long hours, but may involve walking or standing for periods of time

In return, you'll be eligible for[1]:
  • Day One Benefits
    • Medical & Dental Coverage
    • Flexible Spending Accounts
    • Life and AD&D Insurance
    • Supplemental Life Insurance
      • Spouse Life Insurance
      • Child Life Insurance
    • 401(k) Retirement Savings Plan with Company Match
    • Time Off Program
      • Paid Holidays
      • Paid Time Off
      • Paid Parental Leave and more
    • Adoption Reimbursement Program
    • Education Assistance Program
    • Employee Assistance Program
    • Community and Volunteer Service Program
  • Additional Benefits
    • Short and Long-Term Disability Insurance
    • Voluntary Insurance Benefits
      • Vision Coverage
      • Accident
      • Critical Illness
      • Hospital Indemnity Insurance
      • Identity Theft Protection
      • Legal and more
    • Onsite Campus Amenities
      • Workout Facility
      • Cafeteria
      • Credit Union

[1] Current benefit offerings are in effect through 12/31/26
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 Simtra's approach to data privacy, please review the Simtra Recruitment Platform Global Privacy Policy: https://simtra.com/privacy-policy/