More jobs:
Qa Associate
Job in
Centerbrook, Connecticut, 06409, USA
Listed on 2026-06-08
Listing for:
Actalent
Full Time
position Listed on 2026-06-08
Job specializations:
-
Quality Assurance - QA/QC
QA Specialist / Manager, Data Analyst, Quality Technician/ Inspector, Quality Control / Manager
Job Description & How to Apply Below
Quality Assurance Associate (Entry-Level / Early Career)
Launch your career in quality and compliance with hands-on experience in a regulated environment
About the Role
We're looking for a detail-oriented Quality Assurance Associate to help support our Quality Management System and ensure our products meet regulatory and internal standards. This is a great opportunity for recent graduates or early-career professionals to gain experience in cGMP, FDA regulations, and quality systems in the pharmaceutical/medical device space.
You'll work cross-functionally with teams in both office and lab environments, building valuable skills in compliance, documentation, and quality operations.
What You'll Do
In this role, you'll gain exposure to a wide range of quality functions while building a strong foundation in regulated environments:
* Support day-to-day activities of the Quality Management System (QMS) to maintain compliance with cGMP and FDA regulations
* Assist with document control, including organizing, reviewing, and updating SOPs, batch records, and quality documents
* Track and maintain documentation to ensure accuracy, consistency, and compliance
* Help prepare for and participate in internal audits, customer audits, and FDA inspections
* Assist in investigating customer complaints, deviations, and nonconformances with guidance from team members
* Support CAPA (Corrective and Preventive Action) processes, including documentation and tracking action items
* Maintain and update training records and help coordinate training programs
* Assist with regulatory documentation and customer requests
* Help collect and organize data for quality reports and compliance activities
* Collaborate with cross-functional teams to support quality initiatives and continuous improvement
* Stay informed on basic regulatory requirements and industry standards
What We're Looking For
Education & Experience
* Bachelor's degree (or pursuing) in a science, engineering, or related field
* Open to recent graduates or candidates with 0-2 years of experience
* Internship or academic experience in QA, lab environments, or regulated industries is a plus
Skills & Knowledge
* Basic understanding of quality systems, cGMP, or regulated environments (we'll help you learn!)
* Strong attention to detail and organizational skills
* Ability to manage multiple tasks and meet deadlines
* Comfortable using Microsoft Office (Excel, Word, etc.)
* Strong written and verbal communication skills
Nice-to-Have (Not Required!)
* Exposure to FDA regulations (21 CFR Part 111, 211, or 820)
* Familiarity with QA processes like document control, CAPA, or audits
* Experience in pharmaceutical, biotech, or medical device environments
Why Join Us?
Start Your Career Strong
Gain hands-on experience in quality assurance and regulatory compliance
Supportive & Collaborative Team
Work with experienced professionals who will mentor and guide you
Build In-Demand Skills
Develop expertise in cGMP, FDA regulations, and quality systems
Growth Opportunities
Clear path to expand your responsibilities and advance your career
Structured Work Environment
Exposure to both office and lab settings in a professional, team-focused culture
Work Environment
This role is based in a combined office and laboratory setting, where you'll work closely with quality, operations, and technical teams. You'll gain hands-on experience with quality documentation systems and processes while contributing to products that meet high regulatory standards.
Job Type & Location
This is a Contract position based out of Centerbrook, CT.
Pay and Benefits
The pay range for this position is $31.00 - $36.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
* Medical, dental & vision
* Critical Illness, Accident, and Hospital
* 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available
* Life Insurance (Voluntary Life & AD&D for the employee and dependents)
* Short and long-term disability
*…
Position Requirements
10+ Years
work experience
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