Clinical Veterinarian. Location. Illinois. Weekly Hours. ~10 (Fluctuations based on animal health cases and training). Emergency Calls. Occasional phone consultations (~3x per week), in-person visits (~1-2x per month). Main Purpose of Role. The Clinical Veterinarian provides clinical veterinary support to Abbott’s animal care and use program, ensuring the humane treatment of animals and compliance with regulatory requirements. This role involves ...
We are seeking a highly skilled. Sr. Global Market Access Manager. to join our team at Viltis. We are dedicated to developing innovative technologies that improve patient outcomes and transform lives. Job Responsibilities. The. Sr. Global Market Access Manager. will be responsible for. Developing Global Market Access strategies and deliverables for priority pipeline and on-market products within the Infectious Disease portfolio. Leading cross-fun...
Viltis is a global leader in healthcare, and we are seeking an experienced. Sr. Global Market Access Manager. to join our team. We are committed to improving patient outcomes and transforming lives through innovative technologies. Job Description. The. Sr. Global Market Access Manager. will be responsible for developing Global Market Access strategies and deliverables for priority pipeline and on-market products within the Infectious Disease port...
We are looking for a skilled. Sr. Global Market Access Manager. to join our team at Viltis. Viltis develops innovative technologies that improve patient outcomes and transform lives. Job Responsibilities. The. Sr. Global Market Access Manager. will be responsible for. Developing Global Market Access strategies and deliverables for priority pipeline and on-market products within the Infectious Disease portfolio. Leading cross-functional teams to e...
Viltis is seeking a. Regulatory Consultant for GLP. to support our clients' facilities in Hopewell, NJ. As a Regulatory Consultant, you will be responsible for ensuring compliance with. 21 CFR Part 58. regulations and Good Laboratory Practice (GLP) standards. The ideal candidate will have extensive experience in GLP QA auditing, with a strong understanding of. 21 CFR Part 58. Hands-on experience with phase audits, data audits, and facility audits...
We are looking for a. Quality Assurance Auditor. to support our clients' facilities in Hopewell, NJ. As a Quality Assurance Auditor, you will be responsible for conducting phase audits, data audits, and facility audits to ensure compliance with. 21 CFR Part 58. regulations and Good Laboratory Practice (GLP) standards. The ideal candidate will have hands-on experience with phase audits, data audits, and facility audits in a GLP environment. Additi...
At Viltis, we are seeking a. GLP Compliance Specialist. to join our team. In this role, you will be responsible for ensuring compliance with. 21 CFR Part 58. regulations and Good Laboratory Practice (GLP) standards. You will conduct phase audits, data audits, and facility audits to assess compliance and identify areas for improvement. The ideal candidate will have extensive experience in GLP QA auditing, with a strong understanding of. 21 CFR Par...
As a. Good Laboratory Practice Expert. you will be responsible for ensuring compliance with. 21 CFR Part 58. regulations and Good Laboratory Practice (GLP) standards. You will conduct phase audits, data audits, and facility audits to assess compliance and identify areas for improvement. The ideal candidate will have extensive experience in GLP QA auditing, with a strong understanding of. 21 CFR Part 58. Hands-on experience with phase audits, data...
Job Title. Quality Assurance GLP Consultant. Job Type. Contract (40 hours/week, hybrid onsite with a minimum of 3 days onsite per week). Location. Hopewell, NJ. Job Overview. We are seeking a. QA GLP Consultant. to support. Good Laboratory Practice (GLP) compliance. activities at our clients facility in Hopewell, NJ. This contract position requires non-clinical (GLP) experience. Candidates must have a strong understanding of. 21 CFR Part 58. regu...
Job Title: Clinical Data Systems Analyst II. Location. Sylmar, CA. Hours. Business Hours. Onsite/Remote. Initially onsite. potential for hybrid after performance evaluation. Duration. 12-month contract with potential for extension. Interview Process. Two managers will conduct interviews, either together or separately. Job Summary. Working under general supervision, the Clinical Data Systems Analyst II will be responsible for special projects rela...
Job Title: Clinical Data Systems Analyst II. Location. Sylmar, CA. Hours. Business Hours. Onsite/Remote. Initially onsite. potential for hybrid after performance evaluation. Duration. 12-month contract with potential for extension. Interview Process. Two managers will conduct interviews, either together or separately. Job Summary. Working under general supervision, the Clinical Data Systems Analyst II will be responsible for special projects rela...
