Altasciences

Veterinarian

• Serve as a Clinical Pathologist on nonclinical safety studies
• Evaluate clinical pathology data and prepare GLP and nonGLP reports
• Collaborate with Study Directors, Anatomic Pathologists, and other relevant personnel
• Support Study Directors in addressing clinical pathology-related data and issues with sponsors
• Support client development through discussions with sponsors about study goals and designs
• Implement or support company-wide scientific initiatives involving the Clinical Pathology department
• Support continuing development of Study Directors and other Safety Assessment personnel
• Perform other duties as assigned

Veterinary Clinical Pathologist

Marketing

• Develop B2B and internal marketing campaigns showcasing Altasciences’ brand, people, expertise, and services
• Create content including email marketing, blog articles, social media posts, ads, and infographics
• Produce videos and podcasts, including concepts, scripts, interviews, filming, editing, captioning, and promotional content
• Coordinate and produce the Off-Label With Altasciences podcast
• Support social media optimization strategies and content planning
• Write and edit blogs, articles, and press releases
• Manage project timelines, schedules, deliverables, and review cycles
• Collaborate with subject matter experts to translate scientific information into engaging content
• Apply SEO and AIO best practices
• Identify and engage vendors for advertising and article publication
• Ensure brand unity across Altasciences’ sites and locations
• Keep marketing literature up to date
• Contribute to monthly and quarterly marketing reports
• Format presentations, brand documentation, update or build templates, and proofread/copyedit as needed

Marketing Specialist

QA Engineer

• Carry out systematic and independent audits of study-related activities and documents
• Determine compliance with protocols, SOPs, GLP (21 CFR Part 58 and Part 11), and applicable regulatory requirements
• Report findings to Study Directors, Responsible Persons, and Testing Facility Management
• Audit nonclinical and laboratory study phases, reports, disciplines, facilities, vendors, equipment, and software validations
• Perform in-life audits, process audits, vendor qualifications, facility audits, and validation audits
• Act as lead auditor on studies and projects
• Maintain computerized audit files, QA records, and study documentation
• Support project planning and implementation
• Provide risk-based compliance opinions and guidance
• Write and issue inspection reports and evaluate responses to findings
• Review SOPs and ensure they are current and practiced
• Identify and communicate process improvement opportunities
• Notify management of quality and compliance trends
• Perform SOP QA reviews, client hosting, regulatory agency hosting, and external site qualifications
• Interpret FDA regulations and regulatory guidance under supervision
• Perform project management, quality issue investigations, and QA data collection, trending, and analysis under supervision
• Recommend procedure modifications and support process improvement and resolution
• Interpret and train staff on GLP and associated regulatory documents
• Complete self-development efforts and assist with regulatory training

Veterinary Clinical Pathologist

Marketing Specialist

Senior QA Auditor