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.