Senior Technician, Quality Assurance

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.

Our Quality Assurance team works closely with Manufacturing Operations to ensure our products are made safely and to the highest quality standards. Working directly within our manufacturing plants, we embrace a "Safety First, Quality Always" mindset and are committed to continuous improvement. Through collaboration at the local plant level and across our global manufacturing network, we help ensure the highest quality standards for raw materials, intermediates, and finished products.

The Senior Technician, Quality Documentation position is available at our Animal Health facility in Worthington, Minnesota. This site manufactures vaccines for large and companion animals and operates within a collaborative, innovative, and highly regulated environment. Key technologies at the facility include biologics production through fermentation and cell culture platforms, along with filling and freeze-drying operations. As part of the Quality team, you will help ensure the integrity of documentation systems that support the production of safe, effective, and high-quality animal health products.

• Under general supervision, this position assists in maintaining quality expectations and regulations for a biological vaccine manufacturing site in accordance with GMP guidelines and site procedures.
• Use of electronic programs such as Word, Excel, and SAP pertaining to Quality functions
• Administer document control processes, including creation, review, approval, issuance, revision, and archival of controlled documents.
• Maintain quality systems documentation such as Standard Operating Procedures (SOPs), work instructions, forms, and batch records.
• Ensure documentation activities comply with GMP, regulatory requirements, and company quality standards.
• Work with cross-functional teams, including Manufacturing, Quality Assurance, Quality Control, and Technical Operations, for document revisions.
• Support document change control activities and ensure revisions are implemented accurately and on schedule.
• Monitor documentation metrics and identify opportunities for process improvements.
• Assist with internal and external audits, inspections, and regulatory requests by providing documentation and records as needed.
• Maintain electronic document management systems (MEDS) and ensure document records are complete, accurate, and readily retrievable.
• updates Organization, housekeeping and filing of site documents in QA areas, assist in maintenance and delivery of seed stocks.
• Will perform other duties as assigned.

Aseptic Manufacturing, Aseptic Manufacturing, Cell Cultures, Consulting, Corrective Action Management, Electronic Document Management System (EDMS), FDA Compliance, Global Manufacturing, GMP Compliance, Mammalian Cell Culture, Manufacturing, Manufacturing Audits, Manufacturing Environments, Materials Inspection, Operational Quality, Pilot Plant Operations, Process Improvements, Quality Improvement Programs, Quality Management Systems (QMS), Quality Process Development, Quality Standards, Quality Systems Documentation, Raw Materials, Standard Operating Procedure (SOP) Development, Standard Operating Procedure (SOP) Writing {+ 2 more}

• Ability to successfully assume/complete additional responsibilities with little supervision.
• Experience in document control, quality systems, or regulated manufacturing environments preferred.
• Quality, Biology or Microbiology experience or knowledge preferred.

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Employee Status:

Regular

Relocation:

No relocation