Sr. QA Inspector - Label Control (2nd Shift)
Simtra US LLC | |
life insurance, parental leave, paid time off, paid holidays, 401(k)
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United States, Indiana, Bloomington | |
927 South Curry Pike (Show on map) | |
Aug 19, 2026 | |
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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: The Sr. Quality Inspector (Label Control) is a member of the Finishing Quality Assurance Team reporting directly to the Quality Finishing Line Operations Supervisor. They are responsible for printing, counting, inspecting, and issuing all client specific printed materials for pharmaceutical products. They are expected to meet client demand with first pass quality using controlled documentation (batch records, Finishing Specification Sheets, Master labels, standard operating procedures) and current Good Manufacturing Practices (cGMP) guidelines. In addition, they will ensure the accuracy of inventory counts and provide training for new Label Control employees. They are expected to contribute to an environment where teamwork, productivity, safety, identity, strength, purity and quality (SISPQ) are reflected in the finished product. The working hours for this role are Monday-Friday 2:45p-11:15p The responsibilities:
Required qualifications:
Physical / Safety Requirements
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/ | |
life insurance, parental leave, paid time off, paid holidays, 401(k)
Aug 19, 2026