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Entry Level Fda Compliance Jobs (NOW HIRING)

Stark Pharma Solutions Inc

Manufacturing Engineer

Orlando, FL · On-site

$68K - $87K/yr

Ensure compliance with GMP, cGMP, FDA regulations, ISO standards, and company quality procedures ... entry-level roles in pharmaceutical, biotechnology, medical device, or regulated manufacturing ...

Neurology Rare Disease Center

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Clinical Research Coordinator (CRC)

Flower Mound, TX · On-site

$50K - $70K/yr

This is not an entry-level role and requires a high level of accountability, ownership, and the ... Ensure strict adherence to GCP, FDA regulations, and protocol requirements * Maintain high-quality ...

Tjoapack

Validation Writer

Clinton, TN · On-site

... FDA- and GMP-compliant documentation supporting primary and secondary pharmaceutical packaging operations as an entry level technical writer. Your primary responsibility is entry level Technical ...

Tjoapack

Validation Writer

Clinton, TN · On-site

... FDA- and GMP-compliant documentation supporting primary and secondary pharmaceutical packaging operations as an entry level technical writer. Your primary responsibility is entry level Technical ...

Todd's BBI

SANITATION

Madison, NE · On-site

$17.25 - $17.50/hr

None (entry-level candidates considered with proper training) Preferred: * 6 months experience in ... Compliance with GMP, FDA food-safety rules, and personal hygiene standards is mandatory REPORTING ...

mybakemark

04103A - Technician, QA

Spartanburg, SC

Participate in audits and compliance activities; prepare evidence and follow audit findings to ... Familiarity with relevant standards (ISO, GMP, FDA) depending on industry. (Qualifications ...

mybakemark

02203A - Technician, QA

Fresno, CA · On-site

Participate in audits and compliance activities; prepare evidence and follow audit findings to ... Familiarity with relevant standards (ISO, GMP, FDA) depending on industry. (Qualifications ...

mybakemark

04103A - Technician, QA

Spartanburg, SC

Participate in audits and compliance activities; prepare evidence and follow audit findings to ... Familiarity with relevant standards (ISO, GMP, FDA) depending on industry. (Qualifications ...

mybakemark

04103A - Technician, QA

Spartanburg, SC

Participate in audits and compliance activities; prepare evidence and follow audit findings to ... Familiarity with relevant standards (ISO, GMP, FDA) depending on industry. (Qualifications ...

mybakemark

02203A - Technician, QA

Fresno, CA

Participate in audits and compliance activities; prepare evidence and follow audit findings to ... Familiarity with relevant standards (ISO, GMP, FDA) depending on industry. (Qualifications ...

mybakemark

02203A - Technician, QA

Fresno, CA · On-site

Participate in audits and compliance activities; prepare evidence and follow audit findings to ... Familiarity with relevant standards (ISO, GMP, FDA) depending on industry. (Qualifications ...

mybakemark

02203A - Technician, QA

Fresno, CA

Participate in audits and compliance activities; prepare evidence and follow audit findings to ... Familiarity with relevant standards (ISO, GMP, FDA) depending on industry. (Qualifications ...

mybakemark

04103A - Technician, QA

Spartanburg, SC · On-site

Participate in audits and compliance activities; prepare evidence and follow audit findings to ... Familiarity with relevant standards (ISO, GMP, FDA) depending on industry. (Qualifications ...

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All JobsFda Compliance JobsEntry Level Fda Compliance Jobs

Entry Level Fda Compliance information

See salary details

$27K

$49.5K

$84K

How much do entry level fda compliance jobs pay per year?

As of Aug 12, 2026, the average yearly pay for entry level fda compliance in the United States is $49,486.00, according to ZipRecruiter salary data. Most workers in this role earn between $36,000.00 and $57,000.00 per year, depending on experience, location, and employer.

What is the difference between Entry Level Fda Compliance vs Entry Level Quality Assurance Specialist?

AspectEntry Level Fda ComplianceEntry Level Quality Assurance Specialist
Required CertificationsFDA compliance training, sometimes GMP or HACCP certificationsGMP, HACCP, or ISO certifications often preferred
Work EnvironmentRegulatory departments, manufacturing facilities, laboratoriesManufacturing plants, laboratories, quality departments
Employer & Industry UsagePharmaceutical, biotech, food, and beverage industriesFood, pharmaceutical, and manufacturing sectors

Entry Level Fda Compliance roles focus on ensuring products meet FDA regulations, often involving documentation and regulatory submissions. Entry Level Quality Assurance Specialists concentrate on product quality, testing, and process improvements. While both roles require knowledge of GMP and FDA regulations, compliance roles are more regulatory-focused, whereas QA roles emphasize product quality assurance.

More about Entry Level Fda Compliance jobs
What are the most commonly searched types of Fda Compliance jobs? The most popular types of Fda Compliance jobs are:
What job categories do people searching Entry Level Fda Compliance jobs look for? The top searched job categories for Entry Level Fda Compliance jobs are:
Entry Level Fda Compliance jobs near you
Infographic showing various Entry Level Fda Compliance job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 11% Part Time, and 4% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $49,486 per year, or $23.8 per hour.

Manufacturing Engineer

Stark Pharma Solutions Inc

Springfield, MA • On-site

$72K - $93K/yr

Contractor

Re-posted 6 days ago

Job description

Hi,

My name is Sravani Dasari from Stark Pharma Solutions Inc. We are hiring talent for our client and are currently working on a Manufacturing Engineer position. Please send me your updated resume if you have relevant experience and are interested in this opportunity. The detailed job description is as follows.

Job Title: Manufacturing Engineer
Location: USA
Duration: Long Term

Position Overview

We are seeking a motivated Manufacturing Engineer with 0–1 year of experience to support manufacturing operations within the pharmaceutical, biotechnology, or medical device industry. This entry-level role is ideal for recent graduates or candidates with internship or co-op experience who are eager to build a career in regulated manufacturing. The selected candidate will assist with process improvements, manufacturing support, equipment qualification, documentation, and quality compliance while working closely with cross-functional teams.

Key Responsibilities

  • Support daily manufacturing operations to ensure safe, efficient, and compliant production.
  • Assist in monitoring and improving manufacturing processes to enhance productivity and product quality.
  • Support equipment installation, qualification, troubleshooting, and maintenance activities.
  • Assist with process validation, equipment qualification (IQ/OQ/PQ), and manufacturing documentation.
  • Prepare and maintain SOPs, work instructions, batch records, and engineering documentation.
  • Collaborate with Manufacturing, Production, Quality Assurance, Validation, Engineering, and Regulatory teams.
  • Collect and analyze manufacturing data to identify process improvement opportunities.
  • Assist with deviation investigations, CAPA activities, and change control documentation.
  • Ensure compliance with GMP, cGMP, FDA regulations, ISO standards, and company quality procedures.
  • Participate in Lean Manufacturing and continuous improvement initiatives.

Required Qualifications

  • Bachelor's degree in Mechanical Engineering, Manufacturing Engineering, Industrial Engineering, Chemical Engineering, Biomedical Engineering, Biotechnology, or a related engineering discipline.
  • 0–1 year of experience through internships, co-op programs, academic projects, or entry-level roles in pharmaceutical, biotechnology, medical device, or regulated manufacturing environments.
  • Basic understanding of manufacturing processes and engineering principles.
  • Familiarity with GMP/cGMP, FDA regulations, ISO 13485, or regulated manufacturing practices is preferred.
  • Basic knowledge of process validation, equipment qualification, and quality systems is a plus.
  • Strong analytical, troubleshooting, and problem-solving skills.
  • Excellent written and verbal communication skills.
  • Ability to work effectively in a cross-functional team environment.
  • Proficiency in Microsoft Office applications.
  • Eagerness to learn and grow in a regulated manufacturing environment.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/