CRISPR Therapeutics AG

Senior Specialist, Site Supply Chain Planning

CRISPR Therapeutics AG$110K — $120K *
Manufacturing & Automotive
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • 5-7 years of experience in supply chain, inventory management, planning, or procurement; 8-10+ years with lower educational qualifications
  • 3 years of experience in a cGMP environment
  • Advanced knowledge of ERP and WMS systems, particularly Oracle
  • Proficient in Microsoft Office Suite
  • Strong organizational and communication skills with a results-driven attitude

Responsibilities

  • Establish and manage material replenishment programs
  • Maintain vendor data and monitor replenishment parameters in Oracle SCM
  • Collaborate with vendors to maintain lead times and optimize stock levels
  • Create and manage purchase orders
  • Develop production supply forecasts and align site priorities with network planning
  • Drive procurement for raw materials and production supplies
  • Manage procurement of Leukopak materials

Benefits

  • Opportunity for career growth in a rapidly evolving biotech sector
  • Access to a collaborative and supportive work environment
  • Exposure to cutting-edge supply chain management practices
  • Comprehensive benefits package, including equity options
  • Participation in impactful projects that drive operational efficiency
Full Job Description
Job Description:

Position Summary

The Senior Specialist, Site Supply Chain Planning is responsible for establishing and maintaining material replenishment strategies to support the Internal Manufacturing and Quality Control schedules. This role collaborates with site and network stakeholders to ensure the uninterrupted supply of direct and indirect production materials. The incumbent will support operational readiness through the development of material forecasts, risk mitigation plans, and quality inspection queue oversight.

In support of site procurement activities, the Senior Specialist, Site Supply Chain Planning creates and manages vendor purchase orders. This role will maintain purchasing data in the Oracle Supply Chain Management module and drive projects to advance the supply chain systems roadmap.

As a member of Site Supply Chain, you will directly support materials management, site planning, procurement, supply chain systems, and compliance.

Responsibilities
  • Establish and manage material replenishment programs at the site.
  • Maintains vendor and procurement data within the Oracle SCM module. Monitors and adjusts replenishment parameters.
  • Proactively works with vendors to maintain lead times, pricing files, identify risks, and optimize stocking levels.
  • Create, track, and manage purchase orders.
  • Develops raw material, consumable, and production supply forecasts. Collaborates with network planning to connect site and network priorities.
  • Drives planning and procurement for raw materials, consumables, process aids, and production supplies.
  • Management of Leukopak procurement.
  • Monitor the quality inspection queue and manage priorities with cross-functional stakeholders (Manufacturing, Quality Control, and Quality Assurance).
  • Collaborate with the warehouse to resolve documentation or vendor related issues related to receipt, release, or material supply.
  • Support the department and site QMS through effective management of deviations, CAPA's, and change controls.
  • Maintain, update, and improve applicable Site Supply Chain procedures and documentation.
  • Participate in the development of scenario planning and production scheduling activities to drive operational readiness.
  • Manage transfers, chain of custody, and replenishment planning between Framingham warehouse and third-party storage partners.
  • Provides subject matter expert reviews of Supplier Change Notifications and assists with the development of impact assessments.
  • Supports the raw material program from material onboarding through lot release.
  • Assist stakeholders through the material onboarding process and provide review and subject matter approval for material specifications and onboarding documents.
  • Drives the supply chain systems roadmap through the completion of projects related to inventory control, master data, BOM lifecycle management, workflow planning, WMS, and material replenishment.


Minimum Qualifications
  • College degree or equivalent professional experience and Minimum of 5-7 years' experience in a related supply chain discipline; inventory management, planning, procurement, or warehouse operations.
  • Or high school / associate degree or higher and minimum of 8-10+ years' experience in a related supply chain discipline.
  • Minimum of 3 years' experience working within a cGMP environment.
  • Advanced knowledge of ERP and WMS systems (Oracle preferred).
  • Solid computer skills (Microsoft Office Suite) required.
  • Well organized, strong communication skills, and drives for results.


Preferred Qualifications
  • Bachelor's degree in business, supply chain, operations management, or related field.
  • APICS CPIM or CSCP preferred.
  • In-depth knowledge of GMP operations.
  • Demonstrates growing knowledge of regulatory compliance (FDA, GMP, etc.) in a biotech setting.
  • Previous experience procuring raw materials and consumables in a cGMP environment.
  • Comprehensive understanding of Inventory Management concepts.
  • Works independently, exercises sound judgment when troubleshooting.


Competencies
  • Collaborative - Openness, One Team
  • Undaunted - Fearless, Can-do attitude
  • Results Orientation - Delivering progress toward our mission. Sense of urgency in solving problems.
  • Entrepreneurial Spirit - Proactive. Ownership mindset.


Our manufacturing positions are located fully on-site at our Framingham manufacturing facility.

Senior Specialist: Base pay range of $110,000 to $120,000+ bonus, equity and benefits

The range provided is CRISPR Therapeutics' reasonable estimate of the base compensation for this role. The actual amount will be based on job-related and non-discriminatory factors such as experience, training, skills, and abilities.

About CRISPR Therapeutics AG

CRISPR Therapeutics AG, a gene editing company, focuses on developing transformative gene-based medicines for serious diseases using its proprietary CRISPR/Cas9 gene-editing platform. The company develops its products through in-house research programs and partnerships with biopharmaceutical companies and academic researchers. Its lead product candidate is CTX001, an ex vivo CRISPR gene-edited therapy for treating patients suffering from transfusion-dependent beta thalassemia or severe sickle cell disease in which a patient's hematopoietic stem cells are engineered to produce high levels of fetal hemoglobin in red blood cells. The company was formerly known as Inception Genomics AG and changed its name to CRISPR Therapeutics AG in April 2014. CRISPR Therapeutics AG was founded in 2013 and is headquartered in Zug, Switzerland.
Learn more about CRISPR Therapeutics AG
Size
473 employees
Market Cap
$3.3 billion
Industry
Net Income
-$348.8 million
Founded
2013
5 Year Trend
+181.6%
Revenue
$720,000
NASDAQ

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