Process Engineer

Zoetis Spain SL; Union City (CA); On-site; USD 77,000 - 118,000; Full time

Benefits offered by this job

Healthcare benefits from day one

401K with match

Profit-sharing

4 weeks vacation

Job summary

Zoetis is seeking a qualified Process Engineer to measure and specify requirements for best-in-class quality products and manufacturing design. The role requires cross-functional collaboration to execute validation plans and material qualifications as needed.

The candidate will lead CAPA investigations, support manufacturing troubleshooting, and drive optimization of consumables for Zoetis diagnostic products, with emphasis on risk-based validation and change control.

Qualifications

• BS in Science or Engineering or equivalent years of experience in Process Engineering.
• Advanced degree or training / certification in Process Engineering preferred.
• 5+ years' experience in GMP manufacturing, preferably in diagnostics or biodevice industries.

Responsibilities

• Lead nonconformance investigations and drive CAPA using structured RCA (e.g., 5-Why, fishbone, fault tree) and Lean Six Sigma tools.
• Support manufacturing and troubleshoot process related issues.
• Lead projects relating to the development and optimization of consumables used in Zoetis' diagnostic products, ensuring deliverables and project timelines are met (30%).
• Implement changes including initiating change control, performing impact assessment and evaluating risk for non-conformances or process improvements.
• Assist vendor in completing deviations, CAPAs to meet delivery timelines.
• Develop and execute protocols and reports to quality equipment and processes.
• Use risk-based approaches for validation strategies, including acceptance criteria and sample sizes.
• Collaborate with site operations on projects to increase production capacity or deliver productivity savings of consumable components.
• Support continuous improvement projects.
• Collaborate with procurement to identify and qualify new vendors.

Skills

GMP manufacturing

Lean Six Sigma

cGMP knowledge

Project management

Data-driven decisions

Communication skills

English proficiency

DOE

Education

BS in Science or Engineering

Advanced degree or training in Process Engineering

Tools

Microsoft Office

DOE

Job description

Position Summary

The ideal candidate will use industry best practices and their expertise in regulatory requirements to measure, analyze and specify requirements that lead to best-in-class quality products and design for manufacturing. We are looking for a highly motivated candidate, who can work cross-functionally to execute to the validation plan as well as material qualifications that come up as required.

Position Responsibilities

• Lead nonconformance investigations and drive CAPA using structured RCA (e.g., 5-Why, fishbone, fault tree) and Lean Six Sigma tools.


• Support manufacturing and troubleshoot process related issues.


• Lead projects relating to the development and optimization of consumables used in Zoetis' diagnostic products, ensuring deliverables and project timelines are met (30%).


• Implement changes including initiating change control, performing impact assessment and evaluating risk for non-conformances or process improvements.


• Assist vendor in completing deviations, CAPAs to meet delivery timelines.


• Develop and execute protocols and reports to quality equipment and processes.


• Use risk-based approaches for validation strategies, including acceptance criteria and sample sizes.


• Collaborate with site operations on projects to increase production capacity or deliver productivity savings of consumable components.


• Support continuous improvement projects.


• Collaborate with procurement to identify and qualify new vendors.

Education and Experience

• BS in a field of Science or Engineering (Mechanical and Chemical preferred) or equivalent years of experience in Process Engineering.


• Relevant advanced degree or training / certification in Process Engineering preferred.


• 5+ years' experience in GMP manufacturing, preferably in diagnostics or biodevice industries.

Technical Skills Requirements

• Understanding of cGMP.


• Application of Lean/Six Sigma Manufacturing tools (Greenbelt is a plus).


• Project management experience.


• Able to work in a team and independently.


• Statistical analysis, including DOE, is a plus.


• Able to influence others with data-driven decisions.


• Good written and oral communication skills.


• Proficient in English.


• Proficient with Microsoft programs, Word, Excel, PowerPoint, etc.

Work Environment

This position requires on site presence in a manufacturing environment. Physical requirements include the ability to lift up to 50 pounds, stand or walk for extended periods, and work in areas with moving mechanical parts and varying noise levels. Personal protective equipment (PPE) is required in accordance with facility safety protocols, which may include safety glasses, hearing protection, steel-toed footwear, and other equipment as designated by area-specific requirements.

Salary and Benefits

The U.S. base salary range for this full-time position is $77,000 to $118,000. Our salary ranges are determined by role, level, and location. The range displayed on each job posting reflects the base pay target range for new hire salaries for the position. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. This position is also eligible for short-term incentive compensation.

In addition to compensation, Zoetis offers a comprehensive benefits package that supports the physical, emotional and financial wellbeing of our colleagues and their families including healthcare and insurance benefits beginning on day one, a 401K plan with a match and profit-sharing contribution from Zoetis, and 4 weeks of vacation. Visit zoetisbenefits.com to learn more.

Employment Type: Full time, Regular Colleague.

Equal Opportunity & Inclusion

Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability.

Company Culture

Join Zoetis – and build your career with a global animal health company dedicated to supporting its customers and their businesses.

Why Zoetis: Zoetis has more than 60 years of experience in delivering innovative, high-quality products and services that benefit our customers.

Zoetis work environment: At Zoetis, we take pride in a collaborative spirit and high-performing environment where every colleague is given room to learn and grow.

Your opportunities at Zoetis: We invest in our people and offer diverse and exciting opportunities to make a difference in a growing global industry while shaping the future of animal health.

Results that matter: Our colleagues make an impact by working hand-in-hand with those who raise and care for animals to better understand and address the unique real-world challenges they face.