Quality Manager - PHIBRO ANIMAL HEALTH : Job Details

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About Phibro Animal Health Corporation

About Phibro Animal Health CorporationPhibro 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 to, Phibro's revenues are in excess of $1 billion and are supported by over 2,300 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.If you are interested in working for Phibro and feel that you do not meet all qualifications, we encourage you to apply as you might be the right candidate for this role or other positions.Phibro's Phibro-Tech (PTI) business unit recycles and manufacturers copper and iron-based products and recycles permitted waste primarily from the electronics industry.The Quality Manager is an integral part of our Manufacturing team based out of our US - Santa Fe Springs, CA site.Position OverviewWe are seeking a highly detail-oriented and organized Quality Engineer to join our team and specialize in technical documentation. This individual will be responsible for creating, maintaining, and ensuring the accuracy and integrity of documentation within the Rollup Regen (RUR) Business sector of the company. The ideal candidate will have a strong understanding of quality systems, regulatory requirements, and a passion for ensuring that documentation processes comply with internal standards and industry regulations.Key Responsibilities

• Write technical documents related to RUR business, including risk assessments, method statements, standard procedures, specifications, reports, and work instructions.
• Oversee the review and approval process for quality documentation to ensure compliance with company policies, industry standards, and regulatory requirements.
• Interact with external partners, customers, and authorities in a professional and effective manner to drive the business forward.
• Ensure proper version control for all documentation, tracking changes, approvals, and revisions in line with organizational and regulatory guidelines.
• Assist in internal and external audits by ensuring that all documentation is up-to-date, complete, and easily accessible for review.
• Provide guidance and training to team members on document control practices, procedures, and systems to ensure consistency and accuracy across departments.
• Continuously evaluate and improve the documentation control processes to enhance efficiency, accuracy, and compliance.
• Support change control activities by ensuring that any modifications to documentation are thoroughly documented and communicated to all relevant stakeholders.
• Become Grade II Drinking Water certified to assist process related tasks.
• Understand SBA resin pilot testing and regeneration equipment operation.
• Develop expertise in Ion Exchange Treatment and learn lab testing equipment (pH, conductivity, concentration) & procedures.

Qualifications

• Education: Bachelor's degree in Engineering, Quality Management, or a related field (or equivalent experience).
• Experience: Minimum of 3 years of experience in quality control or document management within a manufacturing, water treatment, pharmaceutical, or engineering environment.
• Knowledge: Understanding of quality management systems (ISO 9001, ANSI) and regulatory requirements (DDW, NSF, AWWA).

• Skills:
• Excellent organizational and time-management skills.
• Attention to detail with a focus on accuracy.
• Strong written and verbal communication skills.
• Proficiency in document control software and Microsoft Office Suite.
• Ability to manage multiple projects and priorities in a fast-paced environment.

Physical Demands

• Ability to work in an office environment for extended periods of time.
• Ability to occasionally lift objects weighing up to 50lbs.
• Occasional same day travel to other company locations or external facilities for audits or meetings. Must be able to drive up to 3 hours.

Key CompetenciesCommunicating EffectivelyPrioritizing and Organizing WorkDrivenAccountableCollaborativeDelivering High Quality WorkManaging TimeSupporting Organizational GoalsThinking GloballyUsing Computers and TechnologyEducation & Experience

• Bachelor's Degree in a relevant field
• Experience in pharmaceutical environments highly preferred

To learn more about Phibro Animal Health's competitive benefits package, please click here: Phibro Benefits .Phibro is an Equal Opportunity EmployerAll 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.Business Unit: Performance ProductsDivision: PhibroTechDepartment: ManufacturingLocation: US - Santa Fe Springs, CAWork Schedule: Monday - Friday (Standard Work hours)

Seniority level

• Seniority levelMid-Senior level

Employment type

• Employment typeFull-time

Job function

• Job functionQuality Assurance
• IndustriesPharmaceutical Manufacturing

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