Procurement Specialist II
Lexington, United States · Full-time
- Posted 3w ago
- From Genezen’s careers page
- Location
- Lexington, United States
- Type
- Full-time
- Experience
- 2+ years
- Department
- Supply Chain / Logistics / Procurement
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About the role
Job Summary
The Procurement Specialist II role is integral to the on-time delivery of compliant materials for Operations. This role supports the day-to-day purchasing of materials and management of vendors by working with internal stakeholders and managing external relationships. These activities are performed in accordance with cGMP guidelines and departmental and inter-departmental policies and standard operating procedures.
Job Responsibilities
- Assist in the procurement of GMP materials in compliance with company policies and procedures.
- Monitor inventory levels and support analysis of historical trends to help prevent stockouts.
- Support the tracking and reporting of supplier freight and expedite costs.
- Coordinate with vendors to gather quotes, confirm lead times, and process purchase orders.
- Assist in managing supplier documentation, including Vendor Change Notifications and Corrective Action Requests, under the guidance of senior staff.
- Maintain and update item master data in the ERP system as directed.
- Support internal teams by gathering information and helping assess material needs.
- Learn and apply GMP and procurement best practices through daily activities and team training.
- Meet with internal customers to assess needs and create forecasts.
- Work effectively with cross-functional teams including but not limited to Finance, Manufacturing, Quality Assurance, Quality Control, Planning/Scheduling and Warehouse.
Special Job Requirements
- Adaptability required as work schedule may change based on business needs.
- Criminal background check required.
- Other duties as assigned.
Education / Certifications / Licenses
- BS/MS degree in business or related field (e.g., Business Management, Supply Chain, or Finance)
- APICS Certification
On-the-Job Experience
- 2-4 years of relevant GMP experience in pharma/biotech company, working within a quality system and regulated GMP environment
- 1-2 years experience working with ERP systems
- Well versed in cGMP/ICH/FDA/EU regulations and guidelines
Physical Demands
Work Environment
- Regularly sit for long periods of time.
Movement
- Frequently required to stand; sit; walk; balance; stoop; kneel; crouch; use hands to finger, handle, or feel; reach with hands and arms
- Occasionally required to walk; climb or balance; and stoop, kneel, crouch, or crawl
Lifting
- Frequently lift and/or move up to 10 pounds.
- Frequently lift and/or move up to 25 pounds
Vision
- Frequently utilize close vision and the ability to adjust focus
Communication
- Frequently required to communicate by talking, hearing, using telephone and e-mail
Skills they ask for
Pick one to see other roles that ask for it.
- Supplier and vendor management
- Inventory management
- Excellent written and communication skills
- Ability to work independently with minimal supervision as well as working effectively as part of a team
- Ability to adapt quickly to change such as but not limited to ideas responsibilities and strategies
- Analytical problem solving
About Genezen
Viral vector and cell therapy manufacturingGenezen is a contract development and manufacturing organization providing viral vector and cell therapy services to advance gene and cell therapies.
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