VP, Quality Control & Analytical Development

Loyal

3d • $250,000 - $300,000

About The Position

The VP of QC & AD is responsible for the strategic leadership and execution of all analytical development and commercial quality control activities across Loyal’s pipeline and marketed products. This role owns the analytical and QC lifecycle from early development through commercialization, ensuring robust control strategies, regulatory compliance, and operational excellence for drug substance and drug product.
The VP of QC & AD will build and lead a scalable QC and analytical organization, establish fit-for-purpose operating models leveraging internal capabilities and external partners, and serve as a senior CMC thought partner to executive leadership. The role requires deep expertise in oral solid dosage (OSD) analytics, strong animal health regulatory acumen, and demonstrated success across early-stage, clinical, and commercial environments.
You will be reporting to our Chief Technical Operations Officer.

Requirements

• Ph.D., M.S., or B.S. in Analytical Chemistry, Chemistry, or a related scientific discipline.
• 18+ years of progressive experience in analytical development and quality control for pharmaceutical products, with deep expertise in small-molecule oral solid dosage forms.
• Demonstrated experience spanning early development, clinical programs, commercial launch, and post-approval lifecycle management.
• Proven success building and leading analytical and/or QC organizations, including hiring, mentoring, and developing senior technical leaders.
• Extensive experience with analytical method development, phase-appropriate validation, method transfer, and GMP QC operations.
• Strong knowledge of animal health regulatory requirements, including FDA CVM and relevant global guidelines (e.g., VICH; ICH as applicable), with direct experience supporting regulatory submissions and inspections.
• Track record of effective oversight of external GMP testing laboratories and analytical service providers, including governance, performance management, and quality issue resolution.
• Strategic mindset with the ability to translate scientific and regulatory complexity into clear, actionable business recommendations.
• Comfortable operating in a fast-paced, growth-stage environment, balancing hands-on technical leadership with executive-level decision-making.
• Excellent communication and influencing skills, with the ability to engage credibly with executive leadership, regulators, and external partners.

Nice To Haves

• Prior VP- or executive-level leadership experience in CMC, Analytical Development, or Quality Control.
• Experience supporting first-time commercial launches.
• Strong judgment in risk assessment, prioritization, and lifecycle decision-making.

Responsibilities

• Set and execute the global analytical development and quality control strategy aligned with Loyal’s corporate and CMC objectives.
• Own the end-to-end analytical and QC lifecycle from early development through commercialization, including commercial QC readiness, product release, stability programs, and post-approval lifecycle management.
• Serve as the accountable executive for GMP analytical and QC operations, ensuring inspection-ready systems and sustained regulatory compliance.
• Act as a senior CMC leader on cross-functional program teams, influencing development strategy, timelines, and investment decisions.
• Lead the development, validation, transfer, and lifecycle management of analytical methods and control strategies, with immediate focus on small-molecule oral solid dosage products, while supporting additional modalities as the pipeline evolves.
• Lead cross-functional identification and lifecycle management of CQAs, specifications, and control strategies.
• Establish and oversee commercial QC operations, including governance of external GMP testing laboratories and service providers.
• Provide executive oversight of deviations, investigations, OOS/OOT events, and CAPAs related to analytical and QC activities.
• Serve as a senior analytical subject-matter expert in interactions with FDA Center for Veterinary Medicine (CVM) and other global animal health regulatory agencies, including regulatory submissions, responses, and inspections.
• Select, manage, and govern external analytical laboratories, CDMOs (as applicable), and other partners to ensure technical performance, compliance, and cost effectiveness.
• Build, scale, and lead a high-performing QC and analytical development organization, including hiring, mentoring, and developing senior technical leaders.
• Establish operating models that balance internal capabilities with strategic outsourcing to support a growing and commercial portfolio.
• Manage resource planning, aligning analytical and QC investments with pipeline priorities and long-term business objectives.

Benefits

• Full-coverage health insurance — medical, dental and vision — for you and your dependents
• $1,000 home office equipment stipend
• $1,200/year learning budget for books, courses, etc.
• $250/month wellness budget for gym, cleaners, spa, food, etc.
• All 3-day weekends are turned into 4-day weekends 🎉
• Unlimited vacation and paid holidays
• Paw-ternity leave — adopt a dog and get a day off with your new family member 🐶
• Competitive salary
• Company equity options grant for new hires

What This Job Offers

• Job Type: Full-time
• Career Level: Executive
• Education Level: Ph.D. or professional degree
• Number of Employees: 101-250 employees