Technical Services Associate I (Risk Management)

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profile Job Location:

Bloomington, IN - USA

profile Monthly Salary: Not Disclosed
Posted on: 25-10-2025
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.

This role:

The Technical Services Associate I (Risk Management) is responsible for risk management activities associated with non-conformances complaints equipment validation qualification and change control activities at the BPS site. This position interacts with clients regulatory agencies and cross-functional teams (Engineering Technical Services Manufacturing etc.) to ensure timely approval of all associated documents. This position reports to the Technical Services Validation Sr. Manager.

The responsibilities:

  • Provide guidance and technical expertise of regulatory and Baxter requirements in Risk Management strategies and processes.
  • Assess risk associated with non-conformances complaints audits change control etc. and update the site process FMEA with new risks as needed.
  • Approve risk forms submitted with newly identified risk submitted via non-conformance investigations complaints audits change control etc.
  • Author and/or approve applicable risk assessment documents for equipment and manufacturing process related changes.
  • Author and/or approve applicable deviation reports for product and process related deviations.
  • Help lead Risk Management activities for sustaining Engineering/Manufacturing projects
  • Provide SME input to risk remediation activities.
  • Support risk assessment of new processes to be validated.
  • Uses statistical tools to analyze data.
  • Performs annual reviews of all process FMEAs.
  • Participates in regulatory inspections.

Desirable qualifications:

  • Bachelors degree required preferably in a science or engineering related field
  • Pharmaceutical industry experience in parenteral manufacturing a plus
  • American Society of Quality (e.g. CQE CMQ/OE etc.) and/or Six Sigma certification a plus.
  • Computer proficiency in Microsoft Word Excel and Outlook and the ability to use enterprise software (examples include: JDE Pilgrim Trackwise etc.)

Physical / Safety Requirements:

  • Must be able to wear appropriate personal protective equipment.
  • 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.
  • Must be able to gown for Grade C area

In return youll 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
    • Short and Long-Term Disability 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
    • 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 12/31/25

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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THIS IS WHERE IT ALL BEGAN Did you know that Baxter is the first commercial manufacturer of prepared IV solutions? It all started in 1931 in Iowa when Dr. Ralph Falk and Dr. Donald Baxter launched the Don Baxter Intravenous Products Company. Hillrom’s roots go back to when Bill Hille ... View more

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