QC Inspector
Job
Actalent
Bedford, MA (In Person)
$61,360 Salary, Full-Time
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Job Description
Quality Control Incoming Inspector Second Shift | Monday-Friday, 1:00 PM-9:30 PM Position Summary The Quality Control Incoming Inspector is responsible for completing all activities required to approve incoming raw materials for use in manufacturing. This role also supports quality inspection activities during in‑process manufacturing to ensure products meet established specifications, procedures, and quality standards. This position is second shift, Monday through Friday from 1:00 PM to 9:30 PM . Key Responsibilities Perform quality line clearances and in‑process inspections during inspection and packing operations in accordance with approved SOPs Issue lot numbers and control labels for incoming raw materials and perform inspections per internal procedures and specifications Release approved raw materials for manufacturing use, including completion of required documentation, bin cards, and inventory relabeling Review Manufacturing Process Sheets (MPS) prepared by other incoming inspectors for approval and release Monitor and perform annual retain sample inspections; coordinate required retesting with Quality Control and complete associated documentation Perform Out‑of‑Specification (OOS) investigations and participate in Material Review Board (MRB) activities for rejected materials, as required Act as a Subject Matter Expert (SME) for incoming inspection activities and provide training to new employees, contractors, and QA personnel Conduct biennial reviews of assigned procedures and MPS documents as needed Author and complete Document Change Requests (DCRs) in alignment with document control processes Accurately document all work activities in compliance with Good Documentation Practices (GDP) Maintain current training on all assigned procedures, including read‑and‑understood reviews, skills development, and classroom training Participate in additional projects and support activities as assigned Job Complexity This position performs work that is routine in nature and receives detailed instructions for tasks and responsibilities. Supervisory Responsibilities None Required Qualifications Associate's degree in life sciences or a related field, or equivalent relevant work experience 0-1 year of experience in a cGMP environment or prior QA/QC experience within a regulated industry (internship experience considered) Proficiency with Microsoft Office applications and/or ERP systems Preferred Qualifications Bachelor's degree in a scientific discipline Experience working in a cleanroom or controlled manufacturing environment Strong written and verbal communication skills with attention to detail and documentation accuracy Job Type & Location This is a Contract position based out of Bedford, MA. Pay and Benefits The pay range for this position is $27.00 - $32.00/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 Bedford,MA.
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