Specialist, Bioprocess Engineer
EyeBio
Job Description
For over 130 years, we have pioneered groundbreaking science. Today, we are driven by continuous innovation to develop breakthrough medicines, vaccines and technology. Rooted in direct experience on the farm and in the clinic, we work hand in hand with our customers every step of the way.
Our singular focus is to empower those who care for animals, helping them manage their vital responsibility with confidence. Because when it comes to animal health, no one sees it like we do.
Specialist, Bioprocess Engineer - Vaccine Formulation, Fill-Finish, and Lyophilization
Join Us in Shaping the Future of Animal Health
Our Animal Health Division is investing $895 million through expansion of the manufacturing and research & development facilities in De Soto, Kansas — the state’s largest economic development project to date.
As a BioTechnology Solutions (BTS) Specialist and manufacturing process engineer, you will be part of a world-class team at our Center of Excellence in the Animal Health Corridor, contributing directly to the production of veterinary products that improve animal health and welfare globally.
The Specialist in the BTS Americas Strategic Projects team supports regional vaccine manufacturing technology assessments, transfers and associated technical activities. This individual contributor partners with Manufacturing, Quality, Process Development, Regulatory Affairs, Production Planning, Global Engineering Solutions and other stakeholders to help ensure compliant, efficient transfer execution and stable process performance at receiving sites. The role contributes to knowledge management implementation in the region, supports technical risk assessments and mitigation actions, and assists with post-transfer monitoring and continuous improvement. The Specialist may support onboarding/training activities and will escalate complex issues to senior team members as appropriate.
Key Responsibilities:
Support vaccine technology transfers by preparing technical inputs and documentation, coordinating readiness activities, and assisting during execution and start-up at receiving sites.
Contribute to technical risk assessments and mitigation by gathering data, supporting fit-gap evaluations, and helping implement agreed action plans prior to transfer runs.
Support cross-functional technical workstreams/projects that enable transfer success and improve process performance, escalating risks/issues when needed.
Support regional knowledge management implementation for assigned processes by maintaining transfer packages, playbooks, lessons learned, and best practices; coordinate updates and promote consistent adoption across sites.
Assist with post-transfer process robustness through monitoring/trending, troubleshooting support, and participation in investigations and continuous improvement in partnership with sites and Quality.
Contribute to training and onboarding by maintaining training materials and delivering selected training modules, as assigned.
Deliver compliant technical documentation and communication by drafting/reviewing protocols, reports, summaries, and trackers aligned with quality, regulatory, and internal governance expectations.
Job Requirements:
Education (Minimum)
Bachelor’s degree in Biotechnology, Biochemical Engineering, Chemical Engineering, Pharmacy, or related life science/engineering field.
A Master’s degree is preferred.
Required Experience and Skills
Minimum of 2 years experience in biopharmaceutical, antigen, or vaccine manufacturing, bioprocess engineering, process development, or technology transfer.
Working knowledge of upstream, downstream, fill-finish and lyophilization bioprocessing operations and fundamentals of process parameters definition and control strategies.
Experience working in a regulated (GxP) environment with strong attention to documentation and data integrity.
Demonstrated ability to support technical problem solving, investigations, and basic risk management tools (e.g., FMEA or similar).
Strong collaboration skills in cross-functional teams; ability to communicate clearly and escalate effectively.
Continuous improvement mindset with good organizational skills and ability to manage multiple priorities.
Preferred Experience and Skills
Exposure to process characterization, scale-up/scale-down concepts, and process robustness monitoring.
Familiarity with USDA regulatory expectations, related to technology transfers of antigens and vaccines.
Strong technical writing skills and comfort presenting technical content to diverse stakeholders.
Experience supporting project teams and delivering to timeline milestones and critical goals in a matrixed environment.
Ability to prioritize, focus on and obtain business results.
Schedule Requirements
Able to work first shift, Monday through Friday as base schedule.
Off-shift coverage may be required based on manufacturing/transfer activities.
What We’re Looking For
We seek individuals who:
Demonstrate execution excellence through effective problem-solving and critical thinking.
Embrace an entrepreneurial mindset, taking initiative and ownership of their work.
Adapt with agility and resilience in a dynamic, fast-paced environment.
Uphold a safety-first mindset, ensuring the well-being of themselves and their colleagues.
Why Join Us?
Be part of a transformative investment that will shape the future of animal health.
Work in a region renowned for its skilled workforce, strategic location, and robust infrastructure.
Contribute to cutting-edge research and manufacturing of large-molecule vaccines and biologic products.
Help us meet a growing global demand for our portfolio of animal health solutions
Required Skills:
Accountability, Adaptability, Applied Mathematics, Biomedical Engineering, Cell Culture Process Development, Construction Cost Estimating, Data Analysis, Documentations, Engineering Standards, Estimation and Planning, Information Systems Management, Maintenance Supervision, Manufacturing Processes, Manufacturing Quality Control, Process Improvements, Product Development, Product Formulation, Technical Problem-SolvingPreferred Skills:
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U.S. Hybrid Work Model
Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”.
The salary range for this role is
$87,300.00 - $137,400.00This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.
The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.
We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.
You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.
San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance
Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance
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Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
RegularRelocation:
No relocationVISA Sponsorship:
NoTravel Requirements:
10%Flexible Work Arrangements:
HybridShift:
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n/aJob Posting End Date:
04/9/2026*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.