Fill/Finish Operations Supervisor - Night Shift The Fill/Finish Operations Supervisor is responsible for leading personnel, tasks, and activities associated with aseptic filling, finishing, and ...
Fill/Finish Operations Supervisor - Night Shift The Fill/Finish Operations Supervisor is responsible for leading personnel, tasks, and activities associated with aseptic filling, finishing, and ...
Biopharmaceutical Fill/Finish Operator - Night Shift As the Biopharmaceutical Fill/Finish Operator, you will be part of the Fill/Finish Operations team specializing in vial fill primary packaging and ...
Biopharmaceutical Fill/Finish Operator - Night Shift As the Biopharmaceutical Fill/Finish Operator, you will be part of the Fill/Finish Operations team specializing in vial fill primary packaging and ...
Fill-Finish Support * Serve as a technical lead for Aseptic Process Simulations (Media Fills). This includes designing "worst-case" simulation protocols, managing the incubation and inspection of ...
Fill-Finish Support * Serve as a technical lead for Aseptic Process Simulations (Media Fills). This includes designing "worst-case" simulation protocols, managing the incubation and inspection of ...
Manager, QC Microbiology (Sterile Drug Manufacturing & Fill Finish)
Danbury, CT · On-site
$116K - $174K/yr
Aseptic & Fill-Finish Support * Serve as a technical lead for Aseptic Process Simulations (Media Fills). This includes designing "worst-case" simulation protocols, managing the incubation and ...
Manager, QC Microbiology (Sterile Drug Manufacturing & Fill Finish)
Danbury, CT · On-site
$116K - $174K/yr
Aseptic & Fill-Finish Support * Serve as a technical lead for Aseptic Process Simulations (Media Fills). This includes designing "worst-case" simulation protocols, managing the incubation and ...
Sr. Fill Finish Process Engineer (Future Opportunities)
San Diego, CA · On-site
$110K - $142K/yr
We are seeking a Sr. Fill-Finish Process Engineer with strong experience in aseptic pharmaceutical or biologics manufacturing to support the capital project buildout of a new fill-finish suite within ...
Quick apply
Sr. Fill Finish Process Engineer (Future Opportunities)
San Diego, CA · On-site
$110K - $142K/yr
We are seeking a Sr. Fill-Finish Process Engineer with strong experience in aseptic pharmaceutical or biologics manufacturing to support the capital project buildout of a new fill-finish suite within ...
Sr. Fill Finish Process Engineer (Future Opportunities)
San Diego, CA · On-site
$110K - $142K/yr
We are seeking a Sr. Fill-Finish Process Engineer with strong experience in aseptic pharmaceutical or biologics manufacturing to support the capital project buildout of a new fill-finish suite within ...
Sr. Fill Finish Process Engineer (Future Opportunities)
San Diego, CA · On-site
$110K - $142K/yr
We are seeking a Sr. Fill-Finish Process Engineer with strong experience in aseptic pharmaceutical or biologics manufacturing to support the capital project buildout of a new fill-finish suite within ...
We are seeking a Sr. Fill-Finish Process Engineer with strong experience in aseptic pharmaceutical or biologics manufacturing to support the capital project buildout of a new fill-finish suite within ...
Quick apply
We are seeking a Sr. Fill-Finish Process Engineer with strong experience in aseptic pharmaceutical or biologics manufacturing to support the capital project buildout of a new fill-finish suite within ...
Sr. Fill Finish Process Engineer (Future Opportunities)
Boston, MA · On-site
$113K - $146K/yr
We are seeking a Sr. Fill-Finish Process Engineer with strong experience in aseptic pharmaceutical or biologics manufacturing to support the capital project buildout of a new fill-finish suite within ...
Sr. Fill Finish Process Engineer (Future Opportunities)
Boston, MA · On-site
$113K - $146K/yr
We are seeking a Sr. Fill-Finish Process Engineer with strong experience in aseptic pharmaceutical or biologics manufacturing to support the capital project buildout of a new fill-finish suite within ...
NY · On-site
The ideal candidate has over 8 years of experience, preferably in fill/finish manufacturing, and is skilled in leading teams through dynamic environments. A competitive salary and comprehensive ...
NY · On-site
Candidates should have at least 8 years in a relevant field, preferably in fill/finish manufacturing, with strong leadership skills in cGMP environments. A comprehensive benefits package, including ...
Fill Finish Cleanroom Technician (Biopharmaceutical) Job Summary Cleanroom technicians maintain critical areas of manufacturing/research facilities using specialized equipment and systematic cleaning ...
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Fill Finish Cleanroom Technician (Biopharmaceutical) Job Summary Cleanroom technicians maintain critical areas of manufacturing/research facilities using specialized equipment and systematic cleaning ...
Sterling Fill Finish Manufacturing Rensselaer, NY 4 Months Contract Important Note Profiles focused mainly on CQV, utilities, validation, auditing or compliance without direct manufacturing ...
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Sterling Fill Finish Manufacturing Rensselaer, NY 4 Months Contract Important Note Profiles focused mainly on CQV, utilities, validation, auditing or compliance without direct manufacturing ...
The Sr. Manager, Fill & Finish, Pckg. & Inspection Production Engineering provides strategic leadership and governance for production engineering activities within pharmaceutical manufacturing ...
The Sr. Manager, Fill & Finish, Pckg. & Inspection Production Engineering provides strategic leadership and governance for production engineering activities within pharmaceutical manufacturing ...
Manufacturing Specialist - Aseptic - Fill Finish (Isolator Ops) GOFP
Charlottesville, VA · On-site
$30 - $34/hr
We are currently seeking a Manufacturing Specialist - Aseptic - Fill Finish (Isolator Ops) to support our growing biopharmaceutical operations at our on-site facility in Charlottesville, Virginia ...
Manufacturing Specialist - Aseptic - Fill Finish (Isolator Ops) GOFP
Charlottesville, VA · On-site
$30 - $34/hr
We are currently seeking a Manufacturing Specialist - Aseptic - Fill Finish (Isolator Ops) to support our growing biopharmaceutical operations at our on-site facility in Charlottesville, Virginia ...
The Sr. Manager, Fill & Finish, Pckg. & Inspection Production Engineering provides strategic leadership and governance for production engineering activities within pharmaceutical manufacturing ...
The Sr. Manager, Fill & Finish, Pckg. & Inspection Production Engineering provides strategic leadership and governance for production engineering activities within pharmaceutical manufacturing ...
Overview The Sr. Manager, Fill & Finish, Pckg. & Inspection Production Engineering provides strategic leadership and governance for production engineering activities within pharmaceutical ...
Overview The Sr. Manager, Fill & Finish, Pckg. & Inspection Production Engineering provides strategic leadership and governance for production engineering activities within pharmaceutical ...
Shape long-term DP/fill-finish strategic planning by translating program and pipeline demand into capacity scenarios, resource models, platform evolution needs, and operational roadmaps aligned with ...
Shape long-term DP/fill-finish strategic planning by translating program and pipeline demand into capacity scenarios, resource models, platform evolution needs, and operational roadmaps aligned with ...
This position will be responsible for facility start-up and execution of cGMP Drug Product Fill/Finish operations. The Drug Product Supervisor will be responsible for actively directing and engaging ...
This position will be responsible for facility start-up and execution of cGMP Drug Product Fill/Finish operations. The Drug Product Supervisor will be responsible for actively directing and engaging ...
Shape long-term DP/fill-finish strategic planning by translating program and pipeline demand into capacity scenarios, resource models, platform evolution needs, and operational roadmaps aligned with ...
Shape long-term DP/fill-finish strategic planning by translating program and pipeline demand into capacity scenarios, resource models, platform evolution needs, and operational roadmaps aligned with ...
This position will be responsible for facility start-up and execution of cGMP Drug Product Fill/Finish operations. The Drug Product Supervisor will be responsible for actively directing and engaging ...
This position will be responsible for facility start-up and execution of cGMP Drug Product Fill/Finish operations. The Drug Product Supervisor will be responsible for actively directing and engaging ...
Fill Finish information
What does a typical day look like for someone working in Fill Finish operations?
A typical day in Fill Finish involves preparing and operating specialized filling and packaging equipment in a cleanroom setting, following strict aseptic and safety protocols to handle pharmaceutical or biotech products. You may participate in setup, calibration, and troubleshooting of machinery, as well as perform quality checks and detailed documentation to comply with regulatory standards. Team members often work closely with quality assurance, maintenance, and production planning staff to ensure seamless workflow. This collaborative environment offers valuable experience in regulated manufacturing and can open doors to supervisory or technical specialist positions with continued training and experience.
What is a Fill Finish job?
A Fill Finish job involves the final stages of pharmaceutical manufacturing, where drug products are aseptically filled into vials, syringes, or other containers and then sealed for distribution. This process requires precision, sterile conditions, and adherence to strict regulatory guidelines to ensure product safety and efficacy. Fill Finish roles often include equipment operation, quality control, and compliance with Good Manufacturing Practices (GMP).
What are the key skills and qualifications needed to thrive in the Fill Finish position, and why are they important?
To thrive in a Fill Finish role, you should have a background in life sciences or manufacturing, strong attention to detail, and experience working in Good Manufacturing Practice (GMP) environments. Familiarity with automated filling equipment, aseptic techniques, and relevant quality control systems or certifications (such as GMP or ISO) is often required. Strong teamwork, communication skills, and the ability to follow strict protocols set outstanding candidates apart. These skills ensure that pharmaceutical or biotechnology products are safely and efficiently filled, sealed, and packaged with the highest standards of quality and safety.
Fill/Finish Operations Supervisor - Night Shift
Elwood, KS • On-site
Full-time
Retirement
Posted 2 days ago
Elanco rating
7.8
Based on 25 frontline employees who took The Breakroom Quiz
44th of 74 rated pharmaceutical
Job description
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: Fill/Finish Operations Supervisor - Night Shift
The Fill/Finish Operations Supervisor is responsible for leading personnel, tasks, and activities associated with aseptic filling, finishing, and secondary packaging operations at the Elwood, Kansas monoclonal antibody (mAb) manufacturing facility. This role provides day-to-day leadership for shop floor manufacturing operations, ensuring safe, compliant, and efficient production of sterile injectable products while driving team performance, operational excellence, and continuous improvement.
Your Responsibilities:
- Lead daily fill / finish manufacturing operations, ensuring production activities are executed safely, efficiently, and in alignment with cGMP, USDA, EMA, and company standards.
- Oversee aseptic filling, finishing, and secondary packaging activities to meet production schedules, quality expectations, and operational targets.
- Maintain strong shop floor presence to monitor operations, reinforce safety and quality culture, troubleshoot issues, and support manufacturing teams in real time.
- Ensure accurate execution and review of batch records, manufacturing documentation, SOPs, and SAP production transactions.
- Partner cross-functionally with Quality, Engineering, Maintenance, Supply Chain, and Technical Services teams to resolve manufacturing challenges and implement process improvements.
- Support equipment troubleshooting, maintenance coordination, deviation investigations, and root cause analysis activities to minimize downtime and manufacturing variability.
- Lead, coach, and develop manufacturing personnel through training, performance management, and talent development initiatives while fostering a collaborative, high-performing team environment.
- Act as a change agent by driving operational excellence initiatives, continuous improvement efforts, and adherence to safety and compliance standards.
What You Need to Succeed (minimum qualifications):
- Education: High School Diploma or equivalent.
- Experience: 3+ years of experience in a regulated commercial GMP biomanufacturing environment, including aseptic processing, fill / finish, formulation, or secondary packaging operations.
- Strong technical knowledge of manufacturing equipment, troubleshooting, and shop floor operations in a sterile manufacturing environment.
- Ability to interpret and follow SOPs, batch records, and manufacturing documentation with a high level of accuracy and compliance.
- Demonstrated ability to work effectively in a fast-paced team environment while maintaining strong safety and quality standards.
What Will Give You a Competitive Edge (preferred qualifications):
- Education: Associate's or Bachelor's degree in biology, chemistry, engineering, biomanufacturing, or a related scientific discipline.
- Demonstrated success leading operational or manufacturing teams within a GMP-regulated environment.
- Understanding of USDA, FDA, and EU GMP regulatory requirements for veterinary biologics manufacturing.
- Experience performing or supporting investigations, root cause analysis, and continuous improvement initiatives.
- Familiarity with manufacturing systems and tools such as SAP, OSI PI, Veeva, CMMS, and Microsoft Office applications.
- Strong communication, problem-solving, and organizational skills with the ability to lead through influence and collaboration.
Additional Information:
- Location: Elwood, Kansas (on-site position)
- Shift: Day Shift (1st Shift); occasional overtime may be required to support production operations
- Travel: 0-5%
Don't meet every single requirement? Studies have shown underrecognized groups are less likely to apply to jobs unless they meet every single qualification. At Elanco we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles!
Elanco Benefits and Perks:
We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights include:
- Multiple relocation packages
- 8-week parental leave
- 9 Employee Resource Groups
- Annual bonus offering
- Flexible work arrangements
- Up to 6% 401K matching
Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status
Elanco may use automated tools, including AI, to support parts of our recruitment process, such as reviewing applications against job-related criteria and/or transferrable skills. These tools help ensure a consistent, structured evaluation, but they do not make hiring decisions. All decisions involve a human reviewer. For more information on how we handle personal data, please see our Elanco Workforce Privacy Notice.
About Elanco
Sourced by ZipRecruiter
Industry
Pharmaceutical and medicine manufacturing
Company size
5,001 - 10,000 Employees
Headquarters location
Greenfield, IN, US
Year founded
1954