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Manufacturing Supervisor – Downstream Bioprocessing (Night Shift
Job in
Overland Park, Johnson County, Kansas, 66213, USA
Listed on 2026-08-03
Listing for:
Elanco Tiergesundheit AG
Full Time
position Listed on 2026-08-03
Job specializations:
-
Manufacturing / Production
Production Manager, Manufacturing & Industrial Operations, Pharmaceutical Manufacturing, Production QC/QA
Job Description & How to Apply Below
## Manufacturing Supervisor – Downstream Bioprocessing (Night Shift)
Apply locations:
Elwood, KStime type:
Full time posted on:
Posted Yesterday job requisition :
R0026592
** At Elanco (NYSE: ELAN) – it all starts with animals!
**** As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.*
* ** At Elanco, we are driven by our vision of Food and Companionship Enriching Life and our purpose – all to Go Beyond for Animals, Customers, Society and Our People.
**** At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you’ll be part of a company that values and champions new ways of thinking, work with dynamic individuals, and acquire new skills and experiences that will propel your career to new heights.
**** Making animals’ lives better makes life better – join our team today!
**** Your Role:
Manufacturing Supervisor Night Shift – Downstream Bioprocessing
** The
** Manufacturing Supervisor – Downstream Bioprocessing
** is responsible for leading manufacturing personnel and daily operations supporting the bulk production of monoclonal antibody (mAb) products at Elanco's Elwood, Kansas manufacturing site. This role oversees production activities across downstream bioprocessing operations, ensuring production targets are achieved while maintaining the highest standards of safety, quality, regulatory compliance, and Good Manufacturing Practices (cGMP). The supervisor also plays a key role in developing team members, driving operational excellence, and fostering a culture of accountability and continuous improvement.
** Your Responsibilities:
*** Lead and oversee daily manufacturing operations supporting downstream bioprocessing activities, including buffer formulation, cell clarification, protein A chromatography, and Tangential Flow Filtration, while partnering with upstream and fill/finish and ensuring adherence to production schedules.
* Supervise, coach, and develop manufacturing personnel through performance management, training, and regular feedback to build a high-performing, engaged team.
* Ensure manufacturing activities are performed in compliance with USDA, EMA, and cGMP requirements, approved procedures, and batch production records.
* Maintain a strong presence on the production floor to promote safe work practices, operational excellence, and a culture of quality and accountability.
* Coordinate with Quality, Engineering, Maintenance, Validation, Supply Chain, and other cross-functional teams to support compliant and efficient manufacturing operations.
* Monitor production performance, equipment readiness, and schedule adherence while ensuring timely completion of batch records, SAP transactions, and manufacturing documentation.
* Lead or support investigations, root cause analyses, and corrective and preventive actions (CAPA) for operational events, deviations, and equipment or process issues.
* Drive continuous improvement initiatives that enhance manufacturing efficiency, strengthen compliance, and improve overall operational performance.
** What You Need to Succeed (minimum qualifications):**
* ** Education**:
High school diploma or equivalent
* ** Experience**: 3+ years experience in a regulated, commercial manufacturing environment.
* Must be able to wear appropriate gowning and personal protective equipment in manufacturing and support areas.
** What will give you a competitive edge (preferred qualifications):
*** Bachelor’s degree in biomanufacturing related field
* Biomanufacturing experience
* Monoclonal antibody manufacturing
* Understanding of USDA, FDA, EU GMP, cGMP regulatory standards
* Operational excellence, lean manufacturing, six sigma, TPS experience
* Demonstrated success in leadership
* Experience with SAP, OSI PI, VEEVA
** Additional Information:
*** Travel: minimal 0-5%
* Location:
Elwood, KS
* This role is a night shift 5p-5a 12 hour, 2 week rotation. (M,T,F,Sa,Su,W,R)
* Shift structure is subject to change with notice according to business demands
* Premiums…
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