Investigation & Deviation Specialist

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About Phibro Animal Health Corporation:
Phibro Animal Health Corporation is a publicly traded, global organization with a rich history in animal health and nutrition as a manufacturer and marketer of medicated feed additives, vaccines, nutritional specialty products, and mineral nutrition. We strive to be a trusted partner with livestock producers, farmers, veterinarians, and consumers who raise or care for farm and companion animals by providing solutions to help them maintain and enhance the health of their animals.

Phibro is a diversified company in manufacturing and marketing products for ethanol performance, microbials for plants, home and industrial applications, and specialty chemicals for various industrial markets. In addition, Phibro’s revenues are in excess of $1 billion and are supported by over 2,400 employees worldwide. At Phibro, people are our greatest asset. We strive to develop a diverse workforce that fosters an environment where people feel supported in openly sharing their creativity and skills that allows them to be the most successful that they can be.

Position Details:

• Location:
  
  US – Chicago Heights, IL
• Compensation range: $74,000 – $90,000
• Work schedule:
  
  Monday – Friday (Standard Work hours)
• Business Unit:
  Animal Health & Mineral Nutrition
• Division:
  Animal Health & Nutrition
• Department:
  Manufacturing

Key Responsibilities:

• Lead, author, and manage manufacturing deviations and investigations, ensuring compliance with cGMP, site procedures, and corporate standards.
• Conduct structured root cause analyses (5‑Why, Fishbone, Fault Tree, Human Error Analysis) to identify true root causes and define effective CAPAs.
• Write clear, concise, and scientifically sound investigation reports that withstand regulatory review.
• Collaborate cross‑functionally with Quality, Process Technical/CI, Engineering, and Operations to ensure timely and thorough closure of all investigations.
• Track, trend, and communicate investigation metrics to site leadership and support reduction of repeat deviations. Work cross‑functionally with Engineering and Production teams to help steer process improvements.
• Participate in internal audits and external inspections as a subject matter expert for the investigation process.

Secondary Responsibilities (as workload permits):

• Provide technical writing support for protocols, risk assessments, change controls, and manufacturing documentation.
• Assist in deviation reduction initiatives, human error analyses, and procedure optimizations.
• Partner with manufacturing to improve data integrity, record‑keeping, and alignment of shop‑floor practices with cGMP expectations.
• Contribute to training initiatives aimed at strengthening root cause and investigation competencies across departments.
• Participate in special projects such as technology transfers, new equipment qualification, or process robustness studies.

Education & Experience:

• Bachelor’s degree in Engineering, Microbiology, Biotechnology, or a related technical/scientific discipline. Relevant experience in lieu of a Bachelor’s degree will be considered.
• Minimum 2‑5 years of experience in a cGMP pharmaceutical or biotechnology manufacturing environment.
• Demonstrated experience in authoring and leading investigations and CAPAs.
• Exceptional technical writing and documentation skills.
• Strong analytical and problem‑solving ability with a holistic understanding of manufacturing systems.
• Knowledge of fermentation or biologics processes preferred.
• Familiarity with electronic Quality Management Systems (Track Wise, Veeva, etc.) and data analysis tools.
• Ability to work independently, manage multiple priorities, and collaborate cross‑functionally.

Competencies:

• Technical acumen and data‑driven mindset
• Strong technical writing and verbal communication skills
• Cross‑functional collaboration and influencing ability
  
  Quality and compliance focus
• Adaptability and initiative to add value beyond primary scope

To learn more about Phibro Animal Health's competitive benefits package, please visit our benefits page.

Phibro is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, national origin, gender, age, religion, disability, sexual orientation, gender identity, veteran status, marital status or any other characteristics protected by law.

• Mid‑Senior level

• Full‑time

• Legal
• Industries:
  Pharmaceutical Manufacturing