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Fda Entry Level Jobs in Georgia (NOW HIRING)

Manus Bio

Mechanical Designer

Augusta, GA

Ensure all mechanical designs adhere to FDA 21 CFR Part 210/211, ASME BPE, and other relevant ... design experience; entry-level candidates with strong internship or co-op experience will be ...

Momar Inc

Product Compliance Coordinator

Atlanta, GA · On-site

$24 - $26/hr

This is an excellent entry-level opportunity for someone who wants to build a career in chemical ... Familiarity with regulatory frameworks such as DOT, IMDG, IATA, GHS, FDA, CLP, TSCA, FIFRA, EPA ...

Cardinal Health

Chemist

Atlanta, GA · On-site

$27.30/hr

FDA, NRC, DOT) to support patient treatment through disease diagnosis, staging, and monitoring. Schedule * Full-time 40 hours per week. * The typical schedule is Monday through Friday with a start ...

Cardinal Health

Chemist

Chamblee, GA · On-site

$21.50 - $29/hr

FDA, NRC, DOT) to support patient treatment through disease diagnosis, staging, and monitoring. Schedule Full-time 40 hours per week The typical schedule is Monday through Friday with a start time ...

Cardinal Health, Inc.

Chemist

Atlanta, GA · On-site

$21.25 - $28.25/hr

FDA, NRC, DOT) to support patient treatment through disease diagnosis, staging, and monitoring. Schedule * Full-time 40 hours per week. * The typical schedule is Monday through Friday with a start ...

Cardinal Health

Chemist

Chamblee, GA · On-site

$21.50 - $29/hr

FDA, NRC, DOT) to support patient treatment through disease diagnosis, staging, and monitoring. Schedule * Full-time 40 hours per week. * The typical schedule is Monday through Friday with a start ...

Whole Foods Market

Flex Shopper - Part Time

Alpharetta, GA · On-site

$15 - $24.40/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 ...

Whole Foods Market

Flex Shopper - Part Time

Alpharetta, GA · On-site

$15 - $24.40/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 Georgia

Fda Entry Level information

See Georgia salary details

$15.9K

$37.2K

$75.9K

How much do fda entry level jobs pay per year?

As of Sep 2, 2026, the average yearly pay for fda entry level in Georgia is $37,235.00, according to ZipRecruiter salary data. Most workers in this role earn between $27,232.00 and $40,070.00 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 Georgia?

The most popular types of Fda jobs in Georgia are:

What are popular job titles related to Fda Entry Level jobs in Georgia?

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

What job categories do people searching Fda Entry Level jobs in Georgia look for?

The top searched job categories for Fda Entry Level jobs in Georgia are:

What cities in Georgia are hiring for Fda Entry Level jobs?

Cities in Georgia with the most Fda Entry Level job openings:

Fda Entry Level jobs near you
Infographic showing various Fda Entry Level job openings in Georgia as of August 2026, with employment types broken down into 100% Temporary. Highlights an 100% In-person job distribution, with an average salary of $37,235 per year, or $17.9 per hour.

Mechanical Designer

Manus Bio

Augusta, GA

Full-time

Re-posted 18 days ago

Job description

Position Summary

Manus works across industries and value chains to accelerate the transition to BioAlternatives better performing and more sustainable versions of complex molecules traditionally sourced from plants, animals, or fossil fuels. Our platform is proven to work across scales, bridging the Valley of Death between lab and manufacturing more efficiently and more reliably to deliver the benefits of synthetic biology today.

The Mechanical Designer supports the design, development, and documentation of mechanical systems, equipment, and facilities used in biotech and pharmaceutical manufacturing environments. Working under the direction of senior engineers and project leads, this role contributes to projects from concept through installation, ensuring designs comply with GMP regulations, FDA guidelines, and applicable industry standards. The ideal candidate brings solid AutoCAD and AutoCAD 3D proficiency, a foundational mechanical background, and an eagerness to grow within a regulated manufacturing setting.

Why work at Manus:
  • Opportunity For motivated, results-oriented team members, our growth creates opportunities for personal and professional advancement.
  • Accountability You are given the resources you need to succeed and the freedom to make it happen; in return, we hold each other accountable for our high expectations.
  • Passion We love what we do and enjoy working with others who feel the same way. We embrace the challenge and hard work that comes with working on the cutting edge.
Key Responsibilities

Design & Engineering

  • Develop 2D and 3D mechanical drawings, models, and assemblies using AutoCAD and AutoCAD 3D in compliance with GMP and cGMP standards.
  • Assist in the design of process equipment, piping systems, utility systems, and facility modifications for biotech/pharma manufacturing areas.
  • Produce and maintain engineering documentation including P&IDs, equipment layouts, installation drawings, BOMs, and design specifications.
  • Support design calculations, tolerance analyses, and material selections appropriate for cleanroom and regulated environments.
  • Review vendor drawings under guidance from senior staff; help verify equipment meets functional and regulatory requirements.

Project Execution

  • Support mechanical design workstreams on capital projects from initiation through commissioning and qualification (IQ/OQ).
  • Collaborate with process engineers, automation engineers, quality, and facilities to ensure mechanical designs align with operational requirements.
  • Assist with equipment procurement activities including RFQ preparation and participation in FATs/SATs.
  • Coordinate with contractors and construction teams during installation; provide field support as directed.
  • Track design deliverables, manage drawing revisions, and maintain controlled document packages in accordance with change control procedures.

Compliance & Quality

  • Ensure all mechanical designs adhere to FDA 21 CFR Part 210/211, ASME BPE, and other relevant standards under guidance from senior staff.
  • Participate in design reviews and risk assessments; document findings and follow up on assigned action items.
  • Support change control and deviation management processes from an engineering design perspective.
  • Maintain drawing and document archives in the company engineering document management system (EDMS).

Collaboration

  • Work closely with senior designers and engineers to develop technical skills and understanding of GMP design principles.
  • Follow established CAD standards, drawing templates, and best-practice documentation for the engineering team.
  • Participate actively in cross-functional project teams and communicate design status to team members and stakeholders.
Qualifications

Required

  • Associates or Bachelors degree in Mechanical Engineering Technology, Mechanical Design, or related field
  • 25 years of mechanical design experience; entry-level candidates with strong internship or co-op experience will be considered
  • Proficiency in AutoCAD 2D and AutoCAD 3D; ability to produce accurate, complete design packages independently
  • Basic understanding of GMP requirements and design documentation practices in a regulated environment
  • Working knowledge of GD&T, engineering calculations, and material selection
  • Strong attention to detail and ability to manage multiple drawing deliverables concurrently

Preferred

  • Experience in a GMP-regulated biotech or pharmaceutical manufacturing environment
  • Familiarity with ASME BPE piping standards and hygienic design principles
  • Exposure to cleanroom classifications (ISO 58) and HVAC/environmental control concepts
  • Experience with SOLIDWORKS or Inventor as a supplemental tool
  • Familiarity with engineering document management systems (EDMS)
  • Lean / continuous improvement mindset or coursework
Work Environment & Physical Requirements
  • Work is performed in a combination of office/CAD environment and active manufacturing/lab areas including cleanrooms.
  • Occasional gowning required when entering classified manufacturing spaces; adherence to site EHS and GMP protocols is mandatory.
  • May require occasional travel to vendor sites for FATs or to other company facilities.
  • Ability to lift up to 25 lbs and stand/walk on the production floor for extended periods during project support activities.

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