FDA Technical Consultant
Washington, DC · On-site +1
Prepare clients for inspections, provide inspection support (remote and on-site) * Provide technical support for remediation efforts in response to Form FDA 483s, Warning Letters, and other ...
Washington, DC · On-site +1
Prepare clients for inspections, provide inspection support (remote and on-site) * Provide technical support for remediation efforts in response to Form FDA 483s, Warning Letters, and other ...
Washington, DC · On-site +1
Prepare clients for inspections, provide inspection support (remote and on-site) * Provide technical support for remediation efforts in response to Form FDA 483s, Warning Letters, and other ...
Washington, DC · On-site
Prepare clients for inspections, provide inspection support (remote and on-site) * Provide technical support for remediation efforts in response to Form FDA 483s, Warning Letters, and other ...
Washington, DC · On-site
Prepare clients for inspections, provide inspection support (remote and on-site) * Provide technical support for remediation efforts in response to Form FDA 483s, Warning Letters, and other ...
... the Inspector General, Office for Civil Rights, the US Drug Enforcement Agency, and the US ... C. office seeks an experienced FDA regulatory associate to join our established Healthcare & Life ...
... the Inspector General, Office for Civil Rights, the US Drug Enforcement Agency, and the US ... C. office seeks an experienced FDA regulatory associate to join our established Healthcare & Life ...
Extensive experience interacting directly with FDA and supporting regulatory meetings and inspections. * Strong knowledge of: * FDA drug approval pathways * Generic drug regulations * CDER review ...
Extensive experience interacting directly with FDA and supporting regulatory meetings and inspections. * Strong knowledge of: * FDA drug approval pathways * Generic drug regulations * CDER review ...
Extensive experience interacting directly with FDA and supporting regulatory meetings and inspections. * Strong knowledge of: * FDA drug approval pathways * Generic drug regulations * CDER review ...
Extensive experience interacting directly with FDA and supporting regulatory meetings and inspections. * Strong knowledge of: * FDA drug approval pathways * Generic drug regulations * CDER review ...
Extensive experience interacting directly with FDA and supporting regulatory meetings and inspections. * Strong knowledge of: * FDA drug approval pathways * Generic drug regulations * CDER review ...
Quick apply
Extensive experience interacting directly with FDA and supporting regulatory meetings and inspections. * Strong knowledge of: * FDA drug approval pathways * Generic drug regulations * CDER review ...
Maintains all QA documents necessary to exceed Annual FDA Inspection requirements. * Is responsible for obtaining and maintaining ACR accreditation. Exceptional compensation for the right candidate!
Maintains all QA documents necessary to exceed Annual FDA Inspection requirements. * Is responsible for obtaining and maintaining ACR accreditation. Exceptional compensation for the right candidate!
Maintains all QA documents necessary to exceed Annual FDA Inspection requirements. * Is responsible for obtaining and maintaining ACR accreditation. Exceptional compensation for the right candidate!
Quick apply
Maintains all QA documents necessary to exceed Annual FDA Inspection requirements. * Is responsible for obtaining and maintaining ACR accreditation. Exceptional compensation for the right candidate!
Maintains all QA documents necessary to exceed Annual FDA Inspection requirements. * Is responsible for obtaining and maintaining ACR accreditation. Exceptional compensation for the right candidate!
New
Maintains all QA documents necessary to exceed Annual FDA Inspection requirements. * Is responsible for obtaining and maintaining ACR accreditation. Exceptional compensation for the right candidate!
New
Manassas, VA · On-site
The person will be responsible for managing and ensuring that facility meets all GMP, FDA and SOP requirements. * Managing all quality operations to include inspection of components, bulk, and final ...
Manassas, VA · On-site
The person will be responsible for managing and ensuring that facility meets all GMP, FDA and SOP requirements. * Managing all quality operations to include inspection of components, bulk, and final ...
Manassas, VA · On-site
The person will be responsible for managing and ensuring that facility meets all GMP, FDA and SOP requirements. * Managing all quality operations to include inspection of components, bulk, and final ...
Quick apply
Manassas, VA · On-site
The person will be responsible for managing and ensuring that facility meets all GMP, FDA and SOP requirements. * Managing all quality operations to include inspection of components, bulk, and final ...
The person will be responsible for managing and ensuring that facility meets all GMP, FDA and SOP requirements. * Managing all quality operations to include inspection of components, bulk, and final ...
The person will be responsible for managing and ensuring that facility meets all GMP, FDA and SOP requirements. * Managing all quality operations to include inspection of components, bulk, and final ...
Chantilly, VA · On-site
$115K/yr
The person will be responsible for managing and ensuring that facility meets all GMP, FDA and SOP requirements. * Managing all quality operations to include inspection of components, bulk, and final ...
Quick apply
Chantilly, VA · On-site
$115K/yr
The person will be responsible for managing and ensuring that facility meets all GMP, FDA and SOP requirements. * Managing all quality operations to include inspection of components, bulk, and final ...
Chantilly, VA · On-site
$115K/yr
The person will be responsible for managing and ensuring that facility meets all GMP, FDA and SOP requirements. * Managing all quality operations to include inspection of components, bulk, and final ...
Chantilly, VA · On-site
$115K/yr
The person will be responsible for managing and ensuring that facility meets all GMP, FDA and SOP requirements. * Managing all quality operations to include inspection of components, bulk, and final ...
The person will be responsible for managing and ensuring that facility meets all GMP, FDA and SOP requirements. * Managing all quality operations to include inspection of components, bulk, and final ...
The person will be responsible for managing and ensuring that facility meets all GMP, FDA and SOP requirements. * Managing all quality operations to include inspection of components, bulk, and final ...
FDA CDRH - Medical Officer (Gastroenterologist) SME Position Description The mission of the FDA ... recalls, allegations, Establishment Inspection Reports). Provides expert opinions and ...
FDA CDRH - Medical Officer (Gastroenterologist) SME Position Description The mission of the FDA ... recalls, allegations, Establishment Inspection Reports). Provides expert opinions and ...
FDA CDRH - Medical Officer (Gastroenterologist) SME Position Description The mission of the FDA ... recalls, allegations, Establishment Inspection Reports). Provides expert opinions and ...
Quick apply
FDA CDRH - Medical Officer (Gastroenterologist) SME Position Description The mission of the FDA ... recalls, allegations, Establishment Inspection Reports). Provides expert opinions and ...
FDA CDRH - Medical Officer (Gastroenterologist) SME Position Description The mission of the FDA ... recalls, allegations, Establishment Inspection Reports). Provides expert opinions and ...
FDA CDRH - Medical Officer (Gastroenterologist) SME Position Description The mission of the FDA ... recalls, allegations, Establishment Inspection Reports). Provides expert opinions and ...
... CBP officers, FDA district staff, CPSC analysts, EPA inspectors, and other PGA personnel • Coordinate logistics for cargo returns, CES pickup, drayage, and destruction with carriers, exam ...
... CBP officers, FDA district staff, CPSC analysts, EPA inspectors, and other PGA personnel • Coordinate logistics for cargo returns, CES pickup, drayage, and destruction with carriers, exam ...
... FDA district staff, CPSC analysts, EPA inspectors, and other PGA personnel Coordinate logistics for cargo returns, CES pickup, drayage, and destruction with carriers, exam facilities, and Amazon ...
... FDA district staff, CPSC analysts, EPA inspectors, and other PGA personnel Coordinate logistics for cargo returns, CES pickup, drayage, and destruction with carriers, exam facilities, and Amazon ...
$24.2K - $30.9K
3% of jobs
$30.9K - $37.6K
16% of jobs
$39.3K is the 25th percentile. Wages below this are outliers.
$37.6K - $44.3K
23% of jobs
The median wage is $46.3K / yr.
$44.3K - $51K
27% of jobs
$55.3K is the 75th percentile. Wages above this are outliers.
$51K - $57.7K
10% of jobs
$57.7K - $64.4K
4% of jobs
$64.4K - $71.1K
5% of jobs
$71.1K - $77.8K
2% of jobs
$77.8K - $84.5K
2% of jobs
$84.5K - $91.2K
2% of jobs
$91.2K - $97.9K
5% of jobs
$24.2K
$54.3K
$97.9K
FDA Inspectors routinely examine a variety of facilities, such as food processing plants, pharmaceutical manufacturers, medical device companies, and cosmetic production sites, to ensure compliance with federal safety and quality regulations. A typical inspection involves reviewing operational procedures, examining production environments, sampling products, and interviewing staff to identify potential violations or risks. Inspectors often work onsite, sometimes with travel required to cover multiple locations within their region, and collaborate closely with facility management to explain findings and recommend corrective actions. This role offers the opportunity to make a significant impact on public health and provides clear advancement pathways into specialized inspection or supervisory roles within regulatory agencies.
To thrive as an FDA Inspector, you need a solid background in science or public health, attention to detail, and thorough knowledge of regulatory standards, often supported by a relevant degree. Familiarity with inspection protocols, laboratory testing equipment, and digital reporting systems is commonly required, along with potential USDA or FDA certifications. Strong analytical thinking, effective communication, and integrity are important soft skills for this role. These competencies ensure accurate inspections, compliance with safety regulations, and clear reporting essential to public health and organizational accountability.
An FDA Inspector is responsible for ensuring that companies comply with federal regulations related to food, drugs, medical devices, and other products overseen by the U.S. Food and Drug Administration. They conduct inspections, review records, collect samples, and assess manufacturing practices to ensure public health and safety. Inspectors may also investigate complaints, issue compliance notices, and recommend enforcement actions if violations are found.
The top searched job categories for Fda Inspector jobs in Woodbridge, VA are:
Cities near Woodbridge, VA with the most Fda Inspector job openings:

THE FIRM
As a leading international law firm, we are dedicated to excellence through impactful communication, collaboration, and community involvement. Our company culture has earned us one of the "100 Best Companies to Work For" for 27 consecutive years. This honor, along with many others, highlights our commitment to innovation and professional development. At Alston & Bird LLP, our foundation is made of trust, reliability, and compassion.
JOB DESCRIPTION
Alston & Bird is seeking an experienced FDA consultant to work with the Health Care team's FDA practice out of the Washington, D.C. Office. Qualified candidates will have at least 5 years' experience as an FDA investigator or a senior role in global quality, to assist our FDA team in responding to FDA inspections at pharmaceutical and medical device manufacturing sites. This role offers flexibility to work hybrid or a fully remote arrangement. Candidates should be self-starters, highly organized, and team players. Extended hours and regular domestic and international travel are often needed to meet client deadlines.
Key Responsibilities
Assist attorneys in supporting manufacturing clients on issues related to Current Good Manufacturing Processes (CGMP) compliance
Prepare clients for inspections, provide inspection support (remote and on-site)
Provide technical support for remediation efforts in response to Form FDA 483s, Warning Letters, and other enforcement actions
Extensive knowledge and experience related to quality systems, investigations, Corrective & Preventative Actions (CAPAs), contamination control, cleaning validation, and data integrity are essential for this role
Collaborate with cross-functional teams at the Firm and at the client including legal, regulatory, quality, manufacturing, and executive leadership teams
Draft memos regarding the status of projects
Maintain current and accurate daily time record
Perform special projects as assigned
SKILLS NEEDED TO BE SUCCESSFUL
Regular travel within the United States and Internationally. Regular travel 1-2 weeks a month with flexibility for more.
Ability to organize and prioritize numerous tasks and complete them under time constraints.
Interpersonal skills necessary in order to communicate and follow instructions effectively from a diverse group of clients, attorneys and staff and provide information with ordinary courtesy and tact.
Work typically requires more than 40 hours per week to perform the essential duties of the position; may require irregular hours.
Ability to travel to private and public buildings, domestically and internationally, via private or public conveyance to assist attorney in attending to client needs on legal matters.
EDUCATION & EXPERIENCE
Bachelor's degree in chemistry, biology, pharmacy, engineering, or a related field.
FDA experience required.
Minimum of 5 years as an FDA investigator or compliance officer, or industry senior position in global quality assurance.
In-depth knowledge of quality systems, regulatory requirements (21 CFR Parts 210, 211 and related guidance), quality management systems (QMS), and ISO standards.
Strong analytical skills with a focus on root cause analysis and problem-solving.
Excellent written and verbal communication skills, enabling effective interaction with various stakeholders.
Proficient in using quality management systems and documentation tools.
Ability to provide exceptional client service and manage multiple engagements in a fast-paced environment.
Willingness to frequently travel to international and domestic client sites to support inspections, audit, and remediation activities.
The salary range for this position in Washington D.C. is $200,000-$250,000 and represents the firm's good faith minimum and maximum range for this role at the time of posting. The actual salary offered will be dependent on various factors, including but not limited to, the candidate's experience, education, relevant certifications, geographic location, market demands, and specific business needs. Generally, candidates are considered for the higher end of the salary range when they bring the requisite level of experience and expertise to the role.
EQUAL OPPORTUNITY EMPLOYER
Alston & Bird LLP is an Equal Opportunity Employer does not discriminate on the bases of any status protected under federal, state, or local law. Applicants will be considered regardless of their sex, race, age, religion, color, national origin, ancestry, physical disability, mental disability, medical condition (associated with cancer, a history of cancer, or genetic characteristics), HIV/AIDS status, genetic information, marital status, sexual orientation, gender, gender identity, gender expression, military and veteran status, or other protected category under the law on the basis of race, color, religion, sex, age, sexual orientation, gender identity and/or expression, national origin, veteran status or disability in relation to our recruiting, hiring, and promoting practices.
The statements contained in this position description are not necessarily all-inclusive, additional duties and responsibilities may be assigned, and requirements may vary from time to time.
Professional business references and a background screening will be required for all final applicants selected for a position.
If you need assistance or an accommodation due to a disability you may contactdonavan.mclean@alston.com.
Alston & Bird is not currently accepting resumes from agencies for this position. If you are a recruiter, search firm, or employment agency, you will not be compensated in any way for your referral of a candidate even if Alston & Bird hires the candidate.