Manager, Materials Management

Scorpion Therapeutics; Waltham (MA); Presencial; USD 110 000 - 150 000; Tempo integral

Resumo da oferta

Scorpion Therapeutics in Massachusetts seeks a Manager, Materials Management to oversee end-to-end materials operations at a biopharma manufacturing facility. The role includes receipt, storage, issuance, inventory control, GMP pack-out, shipping, and coordination with third-party logistics.

The candidate will interface with manufacturing, quality, validation, and facilities teams to drive operational excellence, maintain GMP standards, and optimize cross-functional processes on-site.

Qualificações

• Bachelor's degree with 6+ years of experience in materials or related operations.
• Advanced degree with proportional experience considered.
• Proven leadership and cross-functional collaboration skills, with strong GMP knowledge.

Responsabilidades

• Oversee receipt, storage, issuance, and inventory control of materials.
• Manage GMP pack-out, shipping, and coordination with 3PL providers.
• Ensure materials handling complies with GMP, chain of custody, and documentation standards.

Conhecimentos

Leadership

GMP knowledge

Formação académica

Bachelor's degree

Advanced degree

Ferramentas

SAP

Veeva

Kneat

Descrição da oferta de emprego

Role

Manager, Materials Management overseeing end-to-end materials operations at a biopharma manufacturing facility.

Primary responsibilities

Primary responsibilities include managing receipt, storage, issuance, inventory control, GMP pack-out, shipping, and coordination with third-party logistics.

Operations

Acts as a key interface for operational excellence, compliance, and continuous improvement across manufacturing, quality, validation, and facilities teams.

Materials handling

Ensures materials handling adheres to GMP regulations, chain of custody, and documentation standards, supporting both clinical and commercial manufacturing.

Validation

Manages validation activities, SOP documentation, and cross-functional investigations, driving process optimization.

Requirements

Bachelor's degree with 6+ years (or advanced degree with proportional experience), leadership skills, proficiency in SAP or similar ERP systems, experience with quality and validation tools like Veeva and Kneat, and strong GMP knowledge.

Preferred skills

Experience managing high-value materials, working with 3PL providers, and leading continuous improvement initiatives.

HighValue

Biopharma manufacturing (clinical and commercial), GMP compliance, inventory management, validation systems, cross-functional collaboration.

WorkSetup

On-site with physical requirements including standing, lifting, and PPE use.