Top 26 Laboratory director Jobs in Gaithersburg Md

Senior Director, Global Programs (Regulatory and Laboratory)
The U.S. Pharmacopeia (USP) —Rockville, MD
- $208,060 - $262,150 a year
- Full-time
- 5 years
- Bachelor's degree
- Travel
- Paid time off
12d
Sr. Director, Biotherapeutic Sciences
BASI GAITHERSBURG LLC —Rockville, MD
- $167,000 - $227,000 a year
- Full-time
- 3 years
- Bachelor's degree
- Doctor of Philosophy
- Paid parental leave
- Disability insurance
Quick Apply
Manufacturing QMS Consultant_Pharma/Life Sciences & Med Device_Director
PRICE WATERHOUSE COOPERS —Washington, DC
- $155,000 - $410,000 a year
- Master's degree
- Analysis skills
- Bachelor's degree
- Paid holidays
- Health insurance
Director of Lab Services, Capital Choice Pathology Lab
Adventist HealthCare —Silver Spring, MD
- $105,664.42 - $158,496.00 a year
- Full-time
- 5 years
- Pass drug screening
- Master's degree
- Free parking
- AD&D insurance
Associate Director, AS&T Lifecycle Management (Biological Method Expert)
BioNTech AG —Gaithersburg, MD
- $146,300 - $234,100 a year
- Full-time
- Senior level
- Commercial
Associate Director, Clinical Outcomes Assessment - Quantitative Research - Digital Health R&D Oncology – Evinova
AstraZeneca —Gaithersburg, MD
- $151,227.20 - $226,840.80 a year
- Hybrid work
- Office
- Master's degree
- Bachelor's degree
- Health insurance
- Dental insurance
Director of Quality Assurance – Clinical Diagnostic Laboratories
nuCare Medical Solutions —Frederick, MD
- $150,000 - $185,000 a year
- Full-time
- Hybrid work
- Master's degree
- Bachelor's degree
- Team management
- Health insurance
- Dental insurance
Quick Apply
9d
Director Planetary Science Division
US Headquarters, NASA —Washington, DC
- $210,812 - $217,332 a year
- Online Application
- Background check
- Computer Science
- Pass drug screening
Clinical Assistant Director
GeneDx, Inc —Gaithersburg, MD
- Full-time
- Mid-level
- 2 years
- Communication skills
Quick Apply
Senior Director, Companion Diagnostics
Precision Medicine Group —Frederick, MD
- $203,200 - $304,800 a year
- Online Application
- Microsoft Word
- Microsoft Excel
- 11+ years
Executive Director/Site Head
Precision Medicine Group —Frederick, MD
- $203,200 - $304,800 a year
- Online Application
- Microsoft Word
- Microsoft Excel
- 11+ years
Senior Director, Companion Diagnostics
Precision for Medicine —Frederick, MD
- $203,200 - $304,800 a year
- Online Application
- Microsoft Word
- Microsoft Excel
- 11+ years
Quick Apply
Associate Director, AS&T Lifecycle Management (Chemical Method Expert)
BioNTech AG —Gaithersburg, MD
- $146,300 - $234,100 a year
- Full-time
- Senior level
- Commercial
Head of Global Quality Systems
Merck KGaA —Rockville, MD
- $154,700 - $290,300 a year
- English
- 8 years
- Bachelor's degree
- Health insurance
- Paid time off
DIRECTOR OF RESEARCH
Whitman-Walker Health —Washington, DC
- $108,000 - $133,000 a year
- Weekends as needed
- 5 years
- Word processing
- Writing skills
Quick Apply
Director, Quality Assurance (Bioservices)
Precision for Medicine —Frederick, MD
- $162,000 - $243,000 a year
- Online Application
- 5 years
- English
- Driver's License
Quick Apply
Executive Director/Site Head
Precision for Medicine —Frederick, MD
- $203,200 - $304,800 a year
- Online Application
- Microsoft Word
- Microsoft Excel
- 11+ years
Quick Apply
Director, Quality Assurance (Bioservices)
Precision Medicine Group —Frederick, MD
- $162,000 - $243,000 a year
- Online Application
- 5 years
- English
- Driver's License
Director, Product (Labs)
Bully Pulpit International —Washington, DC
- $160,000 - $185,000 a year
- Full-time
- Hybrid work
- Office
- 8 years
- Product management
- Paid parental leave
- Health insurance
Quick Apply
Director, FCC Evaluations Research and Services
W. R. Grace & Co. —Columbia, MD
- Management
- 11+ years
- Doctor of Philosophy
- Wellness program
- Paid holidays

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Senior Director, Global Programs (Regulatory and Laboratory)

The U.S. Pharmacopeia (USP) -
Rockville, MD

Apply Now

Job Details

Full-time
$208,060 - $262,150 a year
12 days ago

Benefits

Paid time off

Qualifications

Staff supervision
Scientific publications
GxP
Pharmaceutical regulatory compliance
Scientific and medical presentations experience
Global team management
Content creation for professionals
Leading team collaboration initiatives
Senior leadership

Full Job Description

Description

Who is 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. At USP, we believe that scientific excellence is driven by a commitment to fairness, integrity, and global collaboration. This belief is embedded in our core value of Passion for Quality and is demonstrated through the contributions of more than 1,300 professionals across twenty global locations, working to strengthen the supply of safe, high-quality medicines worldwide.

At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health.

USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific minds—regardless of background—to contribute to advancing public health solutions worldwide. We provide reasonable accommodations to individuals with disabilities and uphold policies that create an inclusive and collaborative work environment.

Brief Job Overview

This role, a critical member of the Global Health and Manufacturing Services (GHMS) leadership team, is responsible for developing and implementing a global growth strategy for USP’s externally funded regulatory and laboratory programs. The incumbent will be primarily responsible for developing long-term strategic relationships with potential funders and partners which drive towards shaping and ultimate realization of new opportunities for programming in the United States and internationally. Additionally, she/he, will represent USP externally as a thought leader in a variety of forums and will supervise a global team across Africa and Asia.

How will YOU create impact here at USP?

As part of our mission to advance scientific rigor and public health standards, you will play a vital role in increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards.

Additionally, USP’s People and Culture division, in partnership with the Equity Office, invests in leadership and workforce development to equip all employees with the skills to create high-performing, inclusive teams. This includes training in equitable management practices and tools to promote engaged, collaborative, and results-driven work environments.

The Senior Director, Global Programs (Regulatory and Laboratory) has the following responsibilities:

Develop and continuously adjust USP’s growth strategy for regulatory and laboratory programming.
Interface and partner with external and internal stakeholders, including potential funders, to understand evolving regulatory and laboratory technology landscape and customer needs.
Align existing USP offerings and solutions to meet customer needs and develop new offerings in the regulatory and laboratory space to address gaps.
Represent USP externally as a thought leader in technical discussions and in external forums to advance programming growth.
Provide technical support and input to relevant funding proposals; and lead the develop of proposals with a primary focus on growing the regulatory and laboratory program.
Manage and deploy global team to support growth strategy and implementation of secured programming.
Support and / or oversee implementation of funded programming including providing strategic and technical oversight for specialized health systems programming, with a strong focus on regulatory strategies, strengthening National Regulatory Authorities (NRAs), pharmacovigilance (PV), post-market surveillance systems, and clinical study capacity for Bioequivalence/Bioavailability (BE/BA) trials.
Be a thought partner to other leaders within the GHMS team as we collectively advance USP’s mission and broader strategic goals.
Other duties as assigned.

Who is USP Looking For?

The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience:

Bachelor's or advanced degree in scientific, regulatory or related field.
Minimum of five (5) years’ experience in regulatory role within or interfacing with stringent regulatory authority/authorities.
Minimum of ten (10) years’ experience in Good Practice guidelines and regulations in pharmaceuticals and/or biologics (GxPs).
Experience with/ understanding of WHO regulatory processes.
Minimum of five (5) years in roles with international scope.
Minimum of seven (7) to nine (9) years of people management experience.
Proven track record of thought leadership as evidenced by speaking engagements/ panel roles and/ or publications/ other content generation.
Willingness/ ability to travel at least 25% domestically and internationally.

Additional Desired Preferences

Demonstrated ability to design, manage, and implement complex projects.
Active network with potential funding sources / entities, including global (such as Gates, Global Fund) and domestic funders (such as Department of War, Health and Human Services, etc.).
Experience and/or exposure with the changing landscape of regulatory and laboratory science as applied to new manufacturing and quality modalities (e.g., advanced manufacturing, AI-enabled processes, non-destructive testing).
Relevant work experience in a lower middle income country (LMIC).
Experience working in program / project management or other relevant technical area in DARPA, BARDA, JPEO-CBRAND or similar.

Supervisory Responsibilities

Yes, the following direct reports:

Director / Sr Manager, International regulatory and laboratory programs
Senior Pharmacovigilance Manager
Senior Technical Advisor

Benefits

USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected.

Compensation

Base Salary Range: USD $208,060.00 – $262,150.00 annually.

Target Annual Bonus: % Varies based on level of role.

Individual compensation packages are based on various factors unique to each candidate’s skill set, experience, qualifications, equity, and other job-related reasons.

Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP.

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities

This employer is required to notify all applicants of their rights pursuant to federal employment laws.

For further information, please review the Know Your Rights (https://www.eeoc.gov/poster) notice from the Department of Labor.

Job Category Ext. Affairs, Regulatory, & Communications

Job Type Full-Time

Apply Now

Refine Your Search

laboratory director jobs in gaithersburg md

Senior Director, Global Programs (Regulatory and Laboratory)

Sr. Director, Biotherapeutic Sciences

Manufacturing QMS Consultant_Pharma/Life Sciences & Med Device_Director

Director of Lab Services, Capital Choice Pathology Lab

Associate Director, AS&T Lifecycle Management (Biological Method Expert)

Associate Director, Clinical Outcomes Assessment - Quantitative Research - Digital Health R&D Oncology – Evinova

Director of Quality Assurance – Clinical Diagnostic Laboratories

Director Planetary Science Division

Clinical Assistant Director

Senior Director, Companion Diagnostics

Executive Director/Site Head

Senior Director, Companion Diagnostics

Associate Director, AS&T Lifecycle Management (Chemical Method Expert)

Head of Global Quality Systems

DIRECTOR OF RESEARCH

Director, Quality Assurance (Bioservices)

Executive Director/Site Head

Director, Quality Assurance (Bioservices)

Director, Product (Labs)

Director, FCC Evaluations Research and Services

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