Quality Assurance Engineer

Stark Pharma Solutions Inc

  • Indianapolis, IN
  • 5 days ago

    Highlights

    We provide specialized consulting and staffing solutions across Quality & Validation, Regulatory Affairs, R&D, Manufacturing, Supply Chain, Project Management, and IT, with a focus on delivering tailored solutions that drive growth, operational excellence, and long-term client success. We are seeking a Quality Assurance Engineer with strong experience in regulated manufacturing environments to support quality systems, compliance, documentation, and quality improvement activities.

    Numbers & Facts

    LocationIndianapolis, IN

    Description

    About the Company

    Stark Pharma Solutions Inc. is a global consulting and staffing partner established in 2014, serving the Pharmaceutical, Medical Device, Biotech, and IT industries across the USA, Canada, and India. We provide specialized consulting and staffing solutions across Quality & Validation, Regulatory Affairs, R&D, Manufacturing, Supply Chain, Project Management, and IT, with a focus on delivering tailored solutions that drive growth, operational excellence, and long-term client success.

    Position: Quality Assurance Engineer

    Location: Indiana

    Duration: Long Term

    Job Overview

    We are seeking a Quality Assurance Engineer with strong experience in regulated manufacturing environments to support quality systems, compliance, documentation, and quality improvement activities.

    Key Responsibilities

    Support quality assurance activities and maintain quality system documentation.
    Review and maintain quality records, procedures, and manufacturing documentation.
    Support deviations, CAPA, change controls, and root-cause investigations.
    Assist with internal and external quality audits.
    Work with Manufacturing, Engineering, Quality Control, and Regulatory teams to resolve quality issues.
    Ensure processes and documentation comply with GMP, FDA, and ISO requirements.
    Support continuous improvement and quality compliance activities.
    Prepare and maintain quality reports and records.

    Required Qualifications

    Bachelor's degree in Engineering, Life Sciences, or a related technical field.
    3+ years of experience in Quality Assurance within a pharmaceutical, medical device, biotech, or regulated manufacturing environment.
    Experience with GMP and quality systems.
    Knowledge of deviations, CAPA, change controls, and root-cause analysis.
    Experience with quality documentation and compliance requirements.
    Strong analytical, documentation, communication, and problem-solving skills.
    Ability to work effectively with cross-functional teams.

    How to Apply

    Apply Now: Submit your updated resume to Stark Pharma Solutions Inc. for consideration.

    Stark Pharma is an Equal Opportunity Employer and welcomes qualified candidates from diverse backgrounds.

    Similar Jobs

    See more jobs