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 teams—so we can solve problems in new ways.

Make it RIGHT – We hold ourselves to a high standard of excellence, fulfilling 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:

The Quality Engineer is responsible for equipment and system validation, qualification and change control by partnering with cross-functional teams (Engineering, Technical Services, Manufacturing, etc.) to ensure timely execution and approval.

The responsibilities:

Provides guidance and technical expertise in interpreting regulatory and Simtra requirements in validation strategy and processes.
Quality signatory responsible for providing leadership, guidance, quality oversight and approval of commissioning, qualifications, and validations related to equipment utilized in the manufacturing of pharmaceutical drug products.
Interfaces with Engineering, Technical Services, Manufacturing and Regulatory personnel as well as other technical disciplines to determine change control requirements. Assist and support the equipment and system validation activities.
Conducts assessments of quality systems, identifies and closes gaps related to validation and corporate procedures.
Guides peers, validation and engineering in the use of sound, statistically based quality engineering approaches in project and test planning and in the analysis and interpretation of test results. Studies and recommends improvements to existing products/processes.

The requirements:

Bachelor’s degree in engineering required
Experience working in a cGMP environment preferred.
American Society of Quality (e.g., CQE, CMQ/OE, etc.) and/or Six Sigma certification preferred.
Computer proficiency in Microsoft Word, Excel, and Outlook and the ability to use enterprise software (examples include: JDE, BPLM, 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 or standing for long hours.

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
- Employee Ownership Plan
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.

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Simtra BioPharma Solutions

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Quality Engineer