Jobs · Manufacturing · Massachusetts

Raw Material Manager

Actalent · Norwood, MA · 1 mo ago
On-siteManufacturing$35–$40/hrFull-time

Responsibilities

  • Assist the material supplier management process for all raw material and consumable suppliers including onboarding and qualification activities.
  • Support the supplier change notification process and ensure notifications are assessed for impact based on risk.
  • Support Supplier Corrective Action Request (SCAR) process by issuing supplier complaints and drive for resolution and corrective actions.
  • Support quality agreement execution including coordination of negotiations with suppliers, customers and or partners, documentation of those quality agreements, and tracking adherence to quality agreement requirements.
  • Support raw material qualification program and management of raw materials used in clinical and commercial programs.
  • Support the material onboarding process ensuring all relevant GxP regulations, guidelines, and company policies are followed and in compliance.
  • Support change controls, deviations, corrective and preventative actions (CAPAs), and quality investigations involving raw materials by completing assigned actions.
  • Review quality plans.
  • Support investigations to provide root cause analysis and ensure effective corrective actions are taken.
  • Ensure compliance and drive improvement plans where needed.
  • Follow all relevant GxP regulations, guidelines, and company policies to ensure compliance with regulatory and internal requirements.
  • Execute tasks precisely as defined in internal guiding documents including but not limited to standard operating procedures (SOPs) and work instructions.
  • Follow Good Documentation Practices and Data Integrity requirements to ensure data, documentation, and records are completed and maintained for use by the business and available to support audits or inspections.
  • Complete training in assigned required learning plan according to the defined timing and the prescribed requalification cadence.

Requirements

BA/BS in a scientific or engineering discipline. 1-3 years of experience in pharmaceutical / biotech industry with Quality Assurance exposure preferred. Demonstrated aptitude or ability to learn in order to gain a strong understanding of GxP regulations. Entry level position.

Skills

  • raw material
  • CAPA
  • Deviation
  • change control
  • SCAR (Supplier Corrective Action Request)
  • material supplier management
  • GDP (Good Documentation Practices)
  • GXP

Benefits

  • 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)

Pay

The pay range for this position is $35.00 - $40.00/hr.

Workplace

This is a fully onsite position in Norwood, MA.

Application Deadline: Sep 29, 2026.

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