Base Career helps you apply smarter for this job.
Key skills for this role
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.
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 Bloomington facility is a full-service contract manufacturing plant providing formulation, aseptic filling and finishing services.
The Technical Services Director is a member of the plant senior leadership team and is responsible for the development, coordination and execution of clinical and commercial technical transfer and validation operations for syringe and vial filling/packaging activities.
Skip the repetitive application forms
Install the Base Career Chrome Extension and autofill job applications across major job boards with your profile.
Trusted by over 500,000 job seekers on Base Career
More from this employer
Bloomington, USA
Bloomington, USA
Bloomington, USA
Bloomington, USA
Bloomington, USA
Bloomington, USA
Bloomington, USA
Bloomington, USA
This includes providing guidance and technical expertise to multiple disciplines and serving as the technical liaison between the customer and manufacturing.
The Director is also responsible for the strategic planning of the department.
This position reports to the Site Director.
The responsibilities:
In return, you’ll be eligible for [1]:
[1] Current benefit offerings are in effect through 12/31/26
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.
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.
To learn more about Simtra's approach to data privacy, please review the Simtra Recruitment Platform Global Privacy Policy: https://simtra.com/privacy-policy/
Contract development and manufacturing organization (CDMO) specializing in sterile injectable drug products, serving pharmaceutical and biotech companies worldwide.
Visit company websiteJobs and hiring trendsDirector · 10+ years experience
Apply faster on company sites with our extension.