Process Engineer – Biological Manufacturing Upstream & Downstream at Zoetis

Lincoln, Nebraska, United States

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Not SpecifiedCompensation

Mid-level (3 to 4 years), Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Animal Pharmaceuticals, Biotechnology, ManufacturingIndustries

Requirements

Degree in Biological Sciences, Chemical Engineering, Biochemistry, or relevant disciplines
Experience: Bachelor + 6-8 years, Master + 3-5 years, or PhD + 1-2 years in relevant field
Experience working in a GMP environment (preferred)
Experience with mAb or biological production (upstream) and purification (downstream) at large or small scale
Knowledge of quality systems such as TrackWise (plus)
Ability to engage, collaborate, and lead projects
Analytical skills with understanding of data trending and statistics
Strong understanding of aseptic technique, cell culture, centrifugation, depth filtration, chromatography, tangential flow filtration, and nanofiltration
Knowledge of chromatography software such as AKTA Unicorn and automation (e.g., Delta V) (plus)
Demonstrated understanding of Lean Manufacturing concepts (preferred)
Excellent communication skills (written and oral) with attention to detail
Self-starter able to prioritize multiple concurrent projects with minimal guidance
Strong computer, scientific, and organizational skills
Demonstrated record of working in a team environment
Ability to wear appropriate gowning and PPE; tolerance for exposure to chemicals, fumes, odors, noise, live steam, temperature fluctuations, and biohazards

Responsibilities

Monitor monoclonal antibody (mAb) batch performance and investigate outliers
Assist with deviation resolution and effective CAPA implementation
Lead and drive technical improvements in mAb manufacturing processing area and troubleshoot complex technical challenges
Lead technical discussions between area team leaders, small scale process experts, and quality assurance delegates to assist with deviation closing
Participate in CAPA implementation and manage effectiveness checks
Monitor and report key process indicators (KPI)
Investigate outliers and implement lasting changes to drive process efficiency and robustness
Participate in introduction of new production processes and site-to-site transfers in collaboration with Global Manufacturing Technology
Maintain state-of-the-art competence on technological developments and recommend equipment/process enhancements for improved efficiencies, safety, and competitive advantage
Draft and manage SOPs, batch records, and risk assessments
Work cross-functionally with multiple teams to ensure highest quality products and provide tools, resources, and technical support
Assist with technical projects within the mAb area
Review automation recipes
May supervise up to 4 colleagues

Skills

Key technologies and capabilities for this role

monoclonal antibody manufacturingupstream processingdownstream processingbiologic manufacturingCAPA implementationdeviation resolutionprocess troubleshootingKPI monitoringtechnical leadershipprocess improvementprocess transferoutlier investigation

Questions & Answers

Common questions about this position

What benefits are offered for this position?

Benefits include 4 weeks accrued paid vacation and 13 paid holidays, 401(k) match with company profit sharing, tuition reimbursement and student loan repayment program, and great health, personal, and family benefits starting day 1.

Is this a remote position or does it require on-site work?

This is an on-site position at the Zoetis plant in Lincoln, NE, with 1st shift hours, on-call rotation, and possible weekends and holidays as needed.

What technical skills and experience are required for this role?

Required skills include experience with monoclonal antibody (mAb) production upstream and purification downstream at large or small scale, working in a GMP environment (preferred), and knowledge of quality systems like TrackWise (a plus). A degree in Biological Sciences, Chemical Engineering, Biochemistry, or relevant discipline is required, with experience varying by level: Bachelor + 6-8 years, Master + 3-5 years, PhD + 1-2 years.

What is the work environment like at Zoetis in Lincoln, NE?

The plant is a clean, modern site recognized as one of Nebraska’s Safest Companies, with a long-standing presence in the Lincoln community, focused on innovation, growth, and manufacturing high-quality animal medicines.

What makes a strong candidate for this Process Engineer role?

A strong candidate is a technical leader with experience in mAb manufacturing (upstream and downstream), GMP environments, and skills in deviation resolution, CAPA implementation, process improvements, and cross-functional collaboration; relevant degree with specified years of experience is required.