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Fda Consultant Jobs (NOW HIRING)

Spruce Infotech

SAP EWM Consultant

Dallas, TX · On-site

As Consulting Lead to partner with client leads for process and solution template governance on a ... Tailor EWM solutions to comply with Life Sciences GxP / validated environments including FDA / EMA ...

Resource Logistics Inc.

SAS Consultant

Rahway, NJ · On-site

... FDA/ICH guidelines Qualifications : Required : • Must have 6-8 yrs of exp in clinical domain • Strong knowledge of SDTM • Create advanced SAS macros, templates, and utilities for efficient data ...

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Fda Consultant information

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How much do fda consultant jobs pay per hour?

As of Jul 27, 2026, the average hourly pay for fda consultant in the United States is $41.55, according to ZipRecruiter salary data. Most workers in this role earn between $29.33 and $49.52 per hour, depending on experience, location, and employer.

What are the typical daily responsibilities of an FDA Consultant?

As an FDA Consultant, your days often involve preparing and reviewing regulatory submissions, advising clients on compliance strategies, and staying up-to-date with evolving FDA requirements. You'll work closely with clients in pharmaceutical, medical device, or biotech companies to interpret regulations, conduct gap analyses, and support product development from early stages through post-market compliance. Collaboration with cross-functional teams, such as research, quality assurance, and legal, is common to ensure all processes and documentation meet FDA standards. The work environment is typically a mix of independent analysis and interactive client meetings, offering a balance between technical expertise and strategic consulting.

What are the key skills and qualifications needed to thrive in the Fda Consultant position, and why are they important?

To thrive as an FDA Consultant, you need in-depth knowledge of FDA regulations and guidelines, regulatory submission processes, and a relevant science or healthcare background. Familiarity with regulatory databases, document management systems, and certifications like RAC (Regulatory Affairs Certification) are highly valued in this field. Strong analytical skills, attention to detail, and effective communication are key soft skills for advising clients and coordinating with multidisciplinary teams. These skills are essential for ensuring clients achieve compliance, avoid costly delays, and succeed in the highly regulated life sciences industry.

What is an FDA Consultant job?

An FDA Consultant helps businesses navigate FDA regulations to ensure compliance with federal laws related to drugs, medical devices, food, and other regulated products. They provide expert guidance on submissions, approvals, inspections, and regulatory strategies. Their role is crucial for companies seeking to bring products to market while meeting all legal requirements.

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Fda Consultant jobs near you
Infographic showing various Fda Consultant job openings in the United States as of July 2026, with employment types broken down into 1% Locum Tenens, 1% As Needed, 87% Full Time, 7% Part Time, and 4% Contract. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution, with an average salary of $86,430 per year, or $41.6 per hour.
Life Sciences Technical Consultant - Los Angeles

Life Sciences Technical Consultant - Los Angeles

Critical Mass Consulting

Los Angeles, CA

Full-time

Posted 2 days ago

Job description

Job Description: Life Sciences Technical Consultant – Los Angeles

Critical Mass Consulting, LLC is seeking individuals who want to learn and develop within a dynamic, start-up environment. We believe in our purpose: To develop a company which thrives on connectivity and engagement; to build a premier consulting organization, which rewards creativity, contribution, and growth.

Critical Mass Consulting, LLC is supporting Life Sciences clients in the areas of:

  • Project Management

  • Process Engineering

  • Quality Management Systems Development

  • Validation Program Development

  • GMP System Commissioning and Qualification

  • Cleaning and Process Validation

  • Computerized System Validation (CSV)

Our company places an emphasis on continuous personal development. This includes support/financing of technical training, mentorship, and development of high performance teams.

Job Description:

Critical Mass Consulting, LLC is recruiting Consultants to join its Los Angeles, CA field area. If you have a passion for Life Sciences and helping others, we are interested in discussing our company, our process and what it means to join our team-focused organization.

Expected Activities

Develop and execute commissioning/validation protocols, such as factory and site acceptance test (FAT, SAT), installation, operational and performance qualifications (IQ/OQ/PQ) on various critical systems, process equipment and supporting processes.

  • Develop and perform Risk Analyses

  • Support multiple client sites on validation projects throughout the Los Angeles area

  • Work on developing internal processes to increase quality of delivery, and increase team engagement

  • Consult clients on latest industry approaches to commissioning, qualification and validation

  • Develop standards and best practices for development and validation activities

  • Manage medium-small teams and/or projects

Additional Responsibilities

Participate in team-based projects, supporting life sciences clients in the areas of Quality Systems and Validation

  • Establish or maintain quality systems, including Change Control, Deviations, and CAPAs programs

  • Consult clients on latest industry approaches to commissioning, qualification and validation

Required Qualifications:

  • Belief in our Core Values. These 4 values provide the foundation for how we operate as a company. With these common shared values, we can effectively accomplish our mission of organizational excellence.

    • People Come First

    • We Build Together

    • Empowering Growth and Leading People to Make a Difference

    • Joy and Discipline, Life in Balance

  • Strong interest in Life Sciences and a passion for helping others

  • Excellent written and verbal communication skills, emphasizing strong technical writing skills

  • Minimum 2 years of experience working in the pharmaceutical, medical device or biotech industry

  • Strong understanding of Good Documentation Practices (GDP), and experience working in FDA regulated industries

  • Proficiency in no-code business intelligence tools is a nice to have (Power BI, Tableau, Looker, etc.)