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Fda Entry Level Jobs in Massachusetts (NOW HIRING)

Assembler

Mansfield, MA · On-site

$17 - $21/hr

We are searching for entry level Assemblers to work 1st shift (7:00 am - 3:30 pm) Monday through ... Requires adherence to Good Manufacturing Practices (GMP) and FDA, ISO, and environmental ...

Assembler

Mansfield, MA

$17 - $21/hr

We are searching for entry level Assemblers to work 1st shift (7:00 am - 3:30 pm) Monday through ... Requires adherence to Good Manufacturing Practices (GMP) and FDA, ISO, and environmental ...

Ensure materials and services comply with all applicable regulatory and quality standards (e.g., FDA, ISO 13485). * Develop and maintain strong supplier relationships; conduct performance reviews ...

Material Handler

Chelsea, MA · On-site

$18.25 - $22/hr

This entry-level role focuses on accurate material handling, inventory support, and maintaining a ... Experience in GMP/FDA-regulated or biotechnology environments (preferred) * Forklift experience ...

This entry-level Production Worker role offers hands-on training and the opportunity to build ... FDA Regulated Facility, Production/Manufacturing environment, Manufacturing equipment operation ...

New

FDA. * Successful candidate will be: * Skilled with Fidessa's Expression valuator configuration language * familiar with Fidessa internal Real-time Database (RTD) * Fidessa constructs such as ...

Material Handler

Chelsea, MA · On-site

$18.25 - $22/hr

This entry-level role focuses on accurate material handling, basic inventory tasks, and maintaining ... GMP, FDA-regulated, biotechnology environment is preferred. • Fork lift experience required ...

Assembler

Mansfield, MA · On-site

$17 - $21/hr

We are searching for entry level Assemblers to work 1st shift (7:00 am - 3:30 pm) Monday through ... Requires adherence to Good Manufacturing Practices (GMP) and FDA, ISO, and environmental ...

Assembler

Mansfield, MA · On-site

$17 - $21/hr

We are searching for entry level Assemblers to work 1st shift (7:00 am - 3:30 pm) Monday through ... Requires adherence to Good Manufacturing Practices (GMP) and FDA, ISO, and environmental ...

An entry level role that applies broad theoretical job knowledge typically obtained through ... to FDA Good Clinical Practice (GCP) guidelines. Physical Requirements: 1. This is largely a ...

Flex Shopper - Part Time

Sudbury, MA · 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 ...

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Fda Entry Level information

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 Massachusetts?

The most popular types of Fda jobs in Massachusetts are:

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

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

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

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

Infographic showing various Fda Entry Level job openings in Massachusetts as of August 2026, with employment types broken down into 100% Temporary. Highlights an 100% In-person job distribution.

Manufacturing Engineer

Springfield, MA • On-site

$72K - $93K/yr

Contractor

Re-posted 24 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/