Quality Investigator
Job
Actalent
Wilson, NC (In Person)
$145,600 Salary, Full-Time
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Job Description
Job Title:
Quality Investigator Job Description As a Quality Investigator, you will be responsible for authoring and managing Quality Assurance Reports (QARs) and conducting deviation investigations related to manufacturing operations and process execution. You will play a pivotal role in supporting investigations for batch record discrepancies, process deviations, and manufacturing execution issues, while ensuring equipment or material impacts on operations are thoroughly examined. Responsibilities Lead root cause analysis using site-approved methodologies and ensure conclusions are accurate and defendable. Partner directly with Manufacturing, MSAT, Engineering, QA, and Operations leadership to gather accurate investigation details. Review and interpret batch records, manufacturing documentation, production logs, alarms, process data, SOPs, work instructions, and training records. Develop impact assessments and CAPAs aligned with operational risk and regulatory expectations. Ensure investigations are completed on time, accurate, and compliant with site procedures and GMP standards. Support regulatory inspections, internal audits, and quality metric reviews related to operations deviations. Essential Skills Bachelor's degree in Science, Engineering, or a related discipline, or equivalent GMP manufacturing experience. 2+ years of experience supporting operations-based deviations and quality investigations in a GMP manufacturing environment. Proven ability to independently write and close investigations tied to manufacturing processes. Strong understanding of batch record review, manufacturing workflows, and GMP documentation practices. Experience working in electronic quality systems (eQMS). Excellent technical writing, critical thinking, and stakeholder communication skills. Additional Skills & Qualifications Direct experience supporting aseptic or sterile manufacturing operations. Prior experience at a high-volume pharmaceutical manufacturing site. Experience supporting regulatory inspections or inspection readiness activities. Background in Manufacturing, MSAT, or Operations Quality. Work Environment This role is situated in a pharmaceutical manufacturing environment with an office area. You will be supporting critical backlog work to aid in getting products to patients on time, which are mission-critical to our healthcare system. Job Type & Location This is a Contract position based out of Wilson, NC. Pay and Benefits The pay range for this position is $60.00 - $80.00/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 Wilson,NC.
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