QA Remediation Specialist
Job
Actalent
Lake Villa, IL (In Person)
$119,600 Salary, Full-Time
Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
55
out of 100
Average of individual scores
Skill Insights
Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.
Job Description
Job Title:
QA Remediation Specialist Job Description We are seeking a dedicated QA Remediation Specialist to review and analyze FDA 483 observations and associated documentation. The role involves collaborating with cross-functional teams to develop and implement corrective and preventive actions (CAPAs), assisting in root cause investigations, and ensuring documentation meets regulatory expectations. Responsibilities Collaborate with cross-functional teams to develop and implement CAPAs. Assist in root cause investigations and ensure documentation meets regulatory expectations. Draft, revise, and manage SOPs, work instructions, and quality records to align with compliance requirements. Support training efforts related to new or revised procedures. Monitor progress of remediation activities and track CAPA effectiveness. Prepare and present status updates and reports to management and stakeholders. Ensure all remediation activities are completed within the defined timeline and meet FDA expectations. Essential Skills Quality assurance and FDA compliance expertise. Experience communicating with FDA inspectors to respond to regulatory inquiries. Proven experience with FDA 483 remediation and GMP regulations. Strong understanding of CAPA systems, deviation management, and documentation practices. Excellent communication, organizational, and analytical skills. Ability to work independently and in a fast-paced, deadline-driven environment. Additional Skills & Qualifications Bachelor's degree in Life Sciences, Engineering, or related field. Minimum 3-5 years of experience in pharmaceutical quality assurance or compliance. Experience with FDA audits and inspection readiness. Familiarity with electronic quality management systems (eQMS). Work Environment This is a full-time onsite position. The role requires comfort in working with a remote manager, providing weekly updates, and independently organizing your schedule. The work environment is fast-paced and deadline-driven, offering potential for extension based on the progress of work or projects. Job Type & Location This is a Contract position based out of Lake Villa, IL. Pay and Benefits The pay range for this position is $55.00 - $60.00/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
- Health Spending Account (HSA)
- Transportation benefits
- Employee Assistance Program
- Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Lake Villa,IL.
Similar jobs in Lake Villa, IL
Galati's Italian Restaurant & Pizzeria
Lake Villa, IL
Posted3 days ago
Updated14 hours ago
Similar jobs in Illinois
Plainfield Community Consolidated School District 202
Plainfield, IL
Posted2 days ago
Updated14 hours ago
Packaging Corp of America
Lake Forest, IL
Posted2 days ago
Updated14 hours ago