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Director, Operational Excellence

Simtra BioPharma Solutions

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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 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.

 


 

This role:

Simtra Biopharma Solutions is seeking a dynamic and experienced Director of Operational Excellence (OpEx) to lead performance improvement initiatives across the Bloomington site partnering with manufacturing, quality, and supporting departments. This role is pivotal in driving operational discipline, lean execution, and data-informed performance management to ensure consistent, high-quality production and timely delivery of life-saving pharmaceutical products. The Director, OpEx is a member of the site senior leadership team, and reports to the Site Head.

The responsibilities:

Leadership and Strategy:

 

Process Improvement and Lean Execution:

 

Performance Management and Reporting & Analytics

Required qualifications:

• Bachelor’s degree in Engineering, Life Sciences, Operations management or related field
• 10+ years of experience in pharmaceutical or similarly regulated manufacturing operations with 5+ years of experience in a people leadership role, with a strong track record in operational excellence and performance improvement
• Proven experience in leading cross-functional teams and driving change in high-complexity environments
• Excellent communication and stakeholder engagement skills
• Proficiency in Microsoft 365 (Word, Excel, Powerpoint, Outlook) and the ability to use enterprise and AI software (e.g., D365, SAP, TrackWise, ServiceNow, Veeva, Claude, ChatGPT)

 

Preferred Qualifications:

• Master’s Degree equivalent or higher
• Strong knowledge of sterile manufacturing processes and regulatory requirements (FDA, cGMP, etc.)
• Experience with software such as Quality Management Systems, ERPs, OT
• Lean Six Sigma Green Belt or Black Belt
• Strong analytical skills with proficiency in data visualization and performance reporting tools (e.g., Power BI, Tableau, Excel)
• Project Management Professional (PMP)

 

 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 or standing for long hours

 

In return, you’ll be eligible for[1]:

[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/

 

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Listed on greenhouse · posted 2026-09-23. ApplySarthi collects openings and links to application pages; the role is advertised by Simtra BioPharma Solutions, not by us.