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Fda Entry Level Jobs in Baltimore, MD (NOW HIRING)

Whole Foods Market

Flex Shopper - Part Time

Annapolis, MD · On-site

$17 - $25.40/hr

Exposure to FDA approved cleaning chemicals * May require use of ladders and other E-Commerce ... New entry level Team Members who successfully complete their first 90-days of employment and who ...

All JobsFda JobsFda Entry Level JobsFda Entry Level Jobs in Baltimore, MD

Fda Entry Level information

See Baltimore, MD salary details

$20.6K

$48.1K

$98K

How much do fda entry level jobs pay per year?

As of Aug 30, 2026, the average yearly pay for fda entry level in Baltimore, MD is $48,108.00, according to ZipRecruiter salary data. Most workers in this role earn between $35,183.00 and $51,770.00 per year, depending on experience, location, and employer.

What is an FDA entry level?

An FDA entry-level job is a starting position within the U.S. Food and Drug Administration, typically suited for recent graduates or individuals with minimal experience in regulatory affairs, public health, or scientific research. These roles can include positions in drug evaluation, food safety, compliance, and laboratory research. Responsibilities often involve data analysis, regulatory review, inspections, and assisting senior staff with policy implementation. Entry-level professionals gain valuable experience in federal regulations, public health policies, and scientific evaluations, which can lead to career advancement within the agency.

What are the typical responsibilities of an FDA entry level?

In an FDA Entry Level role, you may be tasked with supporting regulatory submissions, compiling and reviewing documentation, and ensuring compliance with FDA guidelines. Your responsibilities might also include data entry, assisting with laboratory tests or inspections, and helping prepare reports for internal and external stakeholders. You could work closely with scientists, regulatory affairs specialists, and quality assurance teams, which provides valuable exposure to the regulatory process and industry best practices. This hands-on experience helps you build foundational knowledge and opens the door to advancement to more specialized or senior roles over time.

What are the key skills and qualifications needed for an FDA entry level?

To thrive in an FDA Entry Level position, candidates typically need a bachelor’s degree in life sciences, pharmacy, or a related field, along with basic knowledge of regulatory processes. Familiarity with regulatory documentation, data entry systems, and software like Microsoft Office is important and some roles may require training in Good Laboratory Practice (GLP) or similar certifications. Detail orientation, analytical thinking, and strong written and verbal communication skills help candidates excel and collaborate effectively. These competencies ensure accuracy, compliance, and smooth communication in highly regulated environments.

What qualifications do I need for FDA entry level jobs?

FDA entry-level jobs typically require a bachelor's degree in a relevant field such as biology, chemistry, or health sciences. Strong attention to detail, good communication skills, and familiarity with regulatory guidelines and documentation are also important qualifications.

What are the most commonly searched types of Fda jobs in Baltimore, MD?

The most popular types of Fda jobs in Baltimore, MD are:

What are popular job titles related to Fda Entry Level jobs in Baltimore, MD?

For Fda Entry Level jobs in Baltimore, MD, the most frequently searched job titles are:

What job categories do people searching Fda Entry Level jobs in Baltimore, MD look for?

The top searched job categories for Fda Entry Level jobs in Baltimore, MD are:

What cities near Baltimore, MD are hiring for Fda Entry Level jobs?

Cities near Baltimore, MD with the most Fda Entry Level job openings:

Fda Entry Level jobs near you
Infographic showing various Fda Entry Level job openings in Baltimore, MD as of August 2026, with employment types broken down into 100% Temporary. Highlights an 100% In-person job distribution, with an average salary of $48,108 per year, or $23.1 per hour.

QC Data Reviewer I

Pharmaceutics International Inc

Hunt Valley, MD • On-site

Other

Re-posted 18 days ago

Job description

Job Summary:
The Quality Control Data Reviewer I is responsible for the accurate and timely review of analytical data generated in the QC laboratory. This entry-level role ensures all documentation meets regulatory, internal, and client requirements in support of pharmaceutical product development and manufacturing. The Data Reviewer I will verify compliance with Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP), and related company standard operating procedures (SOPs), state, FDA, local laws and international (e.g., EU, Chinese, Japanese) as applicable to maintain data integrity across analytical activities.
Duties/Responsibilities:
  • Perform thorough review of analytical chemistry testing data for completeness, accuracy, and compliance with SOPs, test methods, and applicable regulatory standards.
    1. High-performance Liquid Chromatography (HPLC)
    2. Gas chromatography (GC)
    3. Dissolution
    4. Integrated Software Empower 3.
    5. UV-Vis Spectrophotometer
    6. Mastersizer 3000 for Particle Size Distribution (PSD)
    7. Karl Fischer (KF)
    8. pH
  • Data Review of Analytical Chemistry Testing:
    1. Raw Material (RM) including API (active pharmaceutical ingredients) and excipients
    2. In Process (IP) Testing
    3. Clinical Verification
    4. Packaging Material
    5. Components
  • Review the data to Comply with GLPs, cGMPs, and GDP (Good Documentation Practice).
  • Confirm that calculations, units, and transcriptions are correct and traceable.
  • Ensure chromatographic integrations and results are scientifically sound and compliant with established protocols.
  • Verify that all test methods and procedures are properly followed and documented.
  • Identify, document, and escalate any data discrepancies or deviations for investigation.
  • Maintain a thorough understanding of current USP, EP, and ICH guidelines related to QC testing.
  • Support audit readiness and participate in internal/external audits as needed.
  • Collaborate closely with analysts, supervisors, and QA to resolve issues and ensure timely batch release.
  • Maintain good documentation practices (GDP) and support data archival processes.
  • Continuously improve and educate analytical chemists to improve analytical data reporting, adhering to GDP and cGMP to increase efficiency, compliance, and Quality.
  • Review analytical data to ensure ALCOA+.
  • Ensure compliance of testing with laboratory procedures, test methods, and protocols. Work with laboratory personnel to correct any errors and omissions in GMP documentation and promote a cGMP culture. Ability to pay attention to detail, focus, and multitask on review of analytical laboratory data.
  • Adhere to the Safety and Health Program and associated plans.
  • Review time of use logs on cGMP instrumentation and other analytical equipment.
  • Completion of work within the assigned time frame, to perform or assist in general organizational tasks including open tasks and timelines and tracking of tasks.
  • Knowledge of QA events/deviations/Investigations.
  • Any other responsibilities are assigned by the manager or department head.
Required Skills/Abilities:
  • Demonstrates excellent personal organizational skills
  • Knowledgeable in Pharmaceutical industry regulations
  • Health and Safety Awareness
  • Must work as a team member in the QC Lab environment
Education and Experience:
  • Bachelor's degree or higher, in Chemistry, Pharmacy, Sciences, or Quality (QA/QC), or equivalent work experience
  • 0-3 years of relevant work experience in Quality Assurance/Data review of Chemistry QC in the pharmaceutical industry.
  • Experience in all areas of Pharmaceutical, e.g., CMO, CDMO, Clinical and commercial products is preferred.
  • Experience with MS Programs such as Word, Excel, PowerPoint, Access, Project, Proofreading skills, etc.
  • Knowledge of Quality Management Systems such as Master Control.
  • Knowledge of current federal, local, and international regulations regarding the Testing, production, and release of drug substances and products.
  • Basic understanding of analytical techniques (e.g., HPLC, GC) and laboratory data documentation requirements.
  • Familiarity with cGMP, GLP, and regulatory compliance standards (FDA, EMA, ICH).
  • Proficient in Microsoft Office (Word, Excel, Outlook); experience with electronic laboratory systems (e.g., Empower, LIMS, LabWare) is an advantage.
  • Strong communication, organizational, and time management skills.
  • Ability to manage multiple priorities and re-prioritize tasks as required.
  • Strong attention to detail and ability to detect data inconsistencies.
  • Excellent problem-solving skills.

Physical Requirements:
• Fluent in English
• Ability to travel between and within facilities to visit staff, operations, projects, etc.
• Ability to sit, stand, climb stairs, and climb ladders to mezzanines (when necessary).
• Ability to lift up to 40 pounds on occasion.
• Ability to use PPE (safety shoes, goggles, respirators, gloves, etc. when necessary).
All job requirements in the job description provided indicate the level of knowledge, skills, and/or abilities deemed necessary to perform the job competently. Job descriptions are an overview of the duties, responsibilities, and requirements of the position. Employees may be required to perform other job-related assignments as requested.

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