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From Home Fda Consulting Jobs (NOW HIRING)

Alston

FDA Technical Consultant

Washington, DC · On-site +1

Alston & Bird is seeking an experienced FDA consultant to work with the Health Care team's FDA ... Interpersonal skills necessary in order to communicate and follow instructions effectively from a ...

AO Globe Life

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This entry-level role is ideal for individuals looking to start a career in sales while working from home. Training and ongoing support are provided to help you succeed. Key Responsibilities

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Fair Consultant - Work from Home

Westbury, NY · On-site

$26/hr

The Fair Consultant is responsible for owning a defined territory and portfolio of accounts, with ... This is a remote/home-based role that collaborates closely with cross-functional teams. These ...

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How much do from home fda consulting jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for from home fda consulting in the United States is $53.84, according to ZipRecruiter salary data. Most workers in this role earn between $53.61 and $58.89 per hour, depending on experience, location, and employer.

What are some common challenges faced by remote FDA consultants, and how can they be addressed?

Remote FDA consultants often face challenges such as staying updated on evolving regulations, managing client communications across time zones, and maintaining access to confidential documents securely. To address these, it's essential to establish clear communication protocols, utilize secure cloud-based document management systems, and participate in ongoing regulatory training. Building strong relationships with clients and leveraging digital collaboration tools can help ensure projects remain on schedule and compliant with FDA standards.

What are the key skills and qualifications needed to thrive as a from home FDA consultant?

To thrive as a From Home FDA Consultant, you need a solid background in regulatory affairs, scientific or medical expertise, and a thorough understanding of FDA guidelines and compliance, typically supported by relevant degrees and certifications such as RAC (Regulatory Affairs Certification). Familiarity with electronic submission systems like the FDA's Electronic Submissions Gateway (ESG), regulatory databases, and document management software is essential. Strong analytical thinking, attention to detail, and clear written and verbal communication help you effectively interpret regulations and interact with clients or regulatory agencies. These skills ensure accurate compliance guidance, successful submissions, and client satisfaction in a remote consulting environment.

How to become a from home FDA consulting?

To become a home-based FDA consultant, professionals typically need a background in life sciences, healthcare, or regulatory affairs, along with relevant experience in FDA regulations and compliance. Obtaining certifications such as RAC (Regulatory Affairs Certification) can enhance credibility, and strong knowledge of FDA guidelines, good communication skills, and familiarity with remote work tools are essential for success in this role.

What is a from home FDA consultant?

A 'From Home FDA Consultant' is a professional who provides expert advice and guidance on U.S. Food and Drug Administration (FDA) regulations and compliance requirements while working remotely. These consultants often help companies in the pharmaceutical, medical device, biotechnology, food, and cosmetic industries navigate the complex FDA approval and submission processes. Their responsibilities can include regulatory strategy, document preparation, product labeling reviews, and ensuring that products meet all necessary FDA standards. Working from home allows these consultants to offer their services flexibly to clients nationwide or internationally. This role requires strong regulatory knowledge, attention to detail, and effective communication skills.

What is the difference between From Home Fda Consulting vs From Home Fda Reviewer?

AspectFrom Home Fda ConsultingFrom Home Fda Reviewer
Required CredentialsTypically requires a background in life sciences, regulatory affairs, or related fields; certifications like RAC or CCRA are commonRequires a degree in life sciences or related fields; certifications like RAC or CCRA are often preferred
Work EnvironmentRemote consulting for clients, providing regulatory strategy and compliance adviceRemote review of regulatory submissions, ensuring compliance with FDA regulations
Employer & Industry UsageConsulting firms, pharmaceutical, biotech, and medical device companiesPharmaceutical and biotech companies, regulatory agencies, contract research organizations

From Home Fda Consulting involves advising clients on regulatory strategies and compliance, often on a freelance or consulting basis. In contrast, From Home Fda Reviewer focuses on evaluating regulatory submissions to ensure FDA compliance, typically within a company's regulatory team. Both roles require similar credentials but differ in daily tasks and work focus.

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From Home Fda Consulting jobs near you
Infographic showing various From Home Fda Consulting job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 73% Full Time, 22% Part Time, and 4% Contract. Highlights an 79% Physical, 1% Hybrid, and 20% Remote job distribution, with an average salary of $111,985 per year, or $53.8 per hour.

FDA Technical Consultant

Alston

Washington, DC • On-site, Remote

Full-time

Re-posted 11 days ago

Job description

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.

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