Senior Manager, Verification Programs

BioSpace; Rockville (MD); Remote; USD 131,000 - 171,000; Full time

Job summary

A leading organization in public health is seeking a Senior Manager for Verification Programs. This supervisory role involves managing verification programs, overseeing audits, and collaborating with stakeholders to ensure compliance. The ideal candidate will have a strong scientific background and extensive experience in cGMP environments. This position is primarily remote with occasional visits to the headquarters in Rockville, MD.

Benefits

Healthcare

Retirement Plans

Paid Time Off

Qualifications

• Extensive experience in cGMP environments.
• Knowledge of FDA regulations and GMP audits.

Responsibilities

• Lead the verification operational team, providing technical guidance.
• Ensure program integrity and develop staff.
• Engage with manufacturers for compliance.

Skills

Communication

Organizational Skills

Education

Bachelor’s Degree

Master’s Degree

Ph.D.

Job description

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About USP

The U.S. Pharmacopeial Convention (USP) is an independent scientific organization that collaborates with the world's leading health and science experts to develop rigorous quality standards for medicines, dietary supplements, and food ingredients. We are committed to scientific excellence, fairness, integrity, and global collaboration, with over 1,300 professionals across twenty global locations working to ensure the supply of safe, high-quality medicines worldwide.

USP values inclusive scientific collaboration and promotes diversity to strengthen public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. USP is an equal employment opportunity employer dedicated to fair, merit-based hiring processes and providing accommodations for individuals with disabilities.

Job Overview

This supervisory role in USP's Global Laboratory and Technical Operations division involves managing verification programs, including overseeing cGMP site audits, product documentation reviews, and test design. The role includes developing new tools and procedures to support team growth. This is primarily remote, with mandatory visits to the Rockville, MD headquarters once or twice a month. Applicants must reside in MD, DC, VA, WV, PA, IL, MI, MN, KS, FL, NC, or OR.

Impact and Responsibilities

You will play a vital role in advancing scientific rigor and public health standards, increasing access to high-quality medicines, and supporting USP’s mission through leadership, collaboration, and continuous improvement initiatives.

Key Responsibilities

• Lead the verification operational team, providing technical guidance and mentorship.
• Ensure program integrity, develop staff, and collaborate with other departments.
• Engage with manufacturers and industry stakeholders to ensure compliance and continuous improvement.
• Represent USP through outreach, presentations, and publications.
• Monitor industry trends and implement operational enhancements.

Candidate Profile

Ideal candidates will have a scientific degree (Bachelor’s, Master’s, or Ph.D.) with extensive experience in cGMP environments, knowledge of FDA regulations, and experience with GMP audits. Additional preferences include management experience, familiarity with ISO standards, and relevant certifications. Strong communication, organizational skills, and ability to handle multiple priorities are essential.

Supervisory Role

Yes, with at least five direct reports including scientists and GMP auditors.

Benefits and Compensation

USP offers comprehensive benefits, including healthcare, retirement plans, and paid time off. The salary range is USD $131,500 - $170,500 annually, with bonuses based on role and performance.

Additional Information

USP does not accept unsolicited resumes from third-party agencies. We are an equal opportunity employer committed to diversity and inclusion.