Provide quality assurance and compliance expertise for Veterinary Medicine Research & Development (VMRD), including the design, execution, and transfer of new biological/biopharmaceutical products to ensure department and site objectives are achieved.
Responsibilities
Ensure VMRD production facilities and the transfer of newly developed and/or improved biological/biopharmaceutical products and processes comply with applicable USDA, EU, FDA, and Zoetis quality standards, as well as the regulatory requirements of destination countries.
Work in conjunction with VMRD Development Science & Technology (DST) colleagues on scale-up, technical transfers and coordination of regulatory issues.
Serve as QA consultant for development, clinical, and VICH batches/serials.
Support VMRD colleagues and initiatives by providing regulatory documents and manufacturing quality/compliance resources.
Review new product master batch records, manufacturing documents, and analytical documents for accuracy, completeness, and compliance with Outlines of Production/submissions, and provide QA approval.
Requirements
Bachelor's degree with 15 years' experience, or equivalent, in biological or pharmaceutical sciences, engineering, or related discipline.
Master's or PhD degree in a biological science or chemical/bioprocess engineering
The Microbiology Analyst I is responsible for performing routine microbiological testing and laboratory activities in support of quality control, manufacturing, and compliance requirements.
Responsibilities
Perform routine microbiological testing, including Bioburden, Endotoxin (LAL), Sterility Testing, and Growth Promotion Testing.
Conduct Environmental Monitoring activities in controlled manufacturing and laboratory areas.
Prepare culture media, reagents, and laboratory solutions according to approved procedures.
Operate laboratory equipment and maintain accurate test records and documentation.
Record and review laboratory data in compliance with Good Documentation Practices (GDP).
Provide quality assurance and compliance expertise for Veterinary Medicine Research & Development (VMRD), including the design, execution, and transfer of new biological/biopharmaceutical products to ensure department and site objectives are achieved.
Responsibilities
Ensure VMRD production facilities and the transfer of newly developed and/or improved biological/biopharmaceutical products and processes comply with applicable USDA, EU, FDA, and Zoetis quality standards, as well as the regulatory requirements of destination countries.
Work in conjunction with VMRD Development Science & Technology (DST) colleagues on scale-up, technical transfers and coordination of regulatory issues.
Serve as QA consultant for development, clinical, and VICH batches/serials.
Support VMRD colleagues and initiatives by providing regulatory documents and manufacturing quality/compliance resources.
Review new product master batch records, manufacturing documents, and analytical documents for accuracy, completeness, and compliance with Outlines of Production/submissions, and provide QA approval.
Requirements
Bachelor's degree with a minimum of 5 years of relevant experience
Master's degree with a minimum of 3 years of relevant experience
Equivalent combination of education and experience in biological or pharmaceutical sciences, engineering, or a related discipline
Nice to have: Master's degree in a biological science or chemical/bioprocess engineering
Dedicated Operating Room Assistant who supports surgical teams by preparing patients and procedure rooms, maintaining sterile technique, managing supplies and equipment, and ensuring efficient operating room workflow.
Compensation
$16.89 - $24.49
Responsibilities
Supports surgical teams by preparing patients and procedure rooms
Maintaining sterile technique
Managing supplies and equipment
Assists with patient transport, surgical skin preparation, and room turnover
Performs skills classified under sterile technique such as retractor, limb, and camera holding
The Certified Surgical Tech (CST) functions as a member of the Surgical Services Perioperative Team, performing duties as a Scrub Technologist or Second Assisting Technologist while maintaining a safe and sterile environment.
Compensation
Pay Range: $42.87 - $63.89. Shift differentials under the OFNHP: Evening: $2.50/hr. Weekend: $4/hr. Night: Starts at $10/hr.
Responsibilities
Functions duties to ensure patient care is accomplished in a safe, efficient, and cost-effective manner.
Ensures the perioperative regime for each patient is implemented as prescribed by the physician.
Prepares the operating room and obtains necessary equipment.
Drapes and covers operating and instrument tables; lays out supplies and equipment.
Assists and procures appropriate equipment that will be used during surgery, checks for any malfunctions.
Requirements
Graduate of a CAAHEP (Commission on Accreditation of Allied Health Education Programs) accredited program
ABHES (Accrediting Bureau of Health Education Schools) accredited program
Senior Technician responsible for executing downstream purification processes, ensuring GMP compliance, and supporting colleague development in a night‑shift manufacturing environment.
Responsibilities
Execute downstream purification processes including chromatography, filtration, and UF/DF
Operate chromatography systems and apply technical understanding
Ensure accurate GMP documentation and compliance with approved procedures and aseptic practices
Support troubleshooting, deviation investigations, and continuous improvement activities
Take ownership of training, technical qualifications, and development
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Certified Surgical Technologist in Operating RoomSt. Charles Health System · Bend, US
Quality Control Technician IITeva Pharmaceuticals
Senior Technician – Mammalian Downstream Manufacturing (Night Shift)AGC Biologics · Copenhagen, Denmark