CRISPR Therapeutics

Site Supply Chain Planning Specialist

Supply Chain - Framingham, MA - Full Time

Company Overview

Since its inception over a decade ago, CRISPR Therapeutics has transformed from a research-stage company advancing programs in the field of gene editing, to a company with a diverse portfolio of product candidates across a broad range of disease areas including hemoglobinopathies, oncology, regenerative medicine, cardiovascular and rare diseases. The Nobel Prize-winning CRISPR science has revolutionized biomedical research and represents a powerful, clinically validated approach with the potential to create a new class of potentially transformative medicines. To accelerate and expand its efforts, CRISPR Therapeutics has established strategic partnerships with leading companies including Bayer and Vertex Pharmaceuticals. CRISPR Therapeutics AG is headquartered in Zug, Switzerland, with its wholly-owned U.S. subsidiary, CRISPR Therapeutics, Inc., and R&D operations based in Boston, Massachusetts and San Francisco, California, and business offices in London, United Kingdom.

Position Summary

The Site Supply Chain Planning Specialist is responsible for establishing and maintaining material replenishment strategies to support the Internal Manufacturing schedule.  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 Site Supply Chain Planning Specialist 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 mange 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.
  • 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.
  • Minimum of 1 year experience working within a cGMP environment.
  • Minimum of 3 years’ experience in a related supply chain discipline; inventory management, planning, procurement, or warehouse operations.
  • 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.

Due to the nature of their work, our manufacturing and lab-based positions are located fully on-site.

CRISPR Therapeutics, Inc. is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law.

To view our Privacy Statement, please click the following link: http://www.crisprtx.com/about-us/privacy-policy

Apply: Site Supply Chain Planning Specialist
* Required fields
First name*
Last name*
Email address*
Location
Phone number*
Resume*

Attach resume as .pdf, .doc, .docx, .odt, .txt, or .rtf (limit 5MB) or paste resume

Paste your resume here or attach resume file

Will you, now or in the future, require immigration support from CRISPR Therapeutics to be able to work in the country this job is located? CRISPR Therapeutics will consider qualified applicants who require immigration support.*
If you currently reside outside of a commutable distance where the job is located, are you willing to relocate if offered a position with CRISPR Therapeutics?*
What salary are you looking for in your next position?
Are you willing to work onsite at our Framingham manufacturing facility?
Do you have previous cGMP Experience?
Have you previously worked with creating raw material forecasts to support manufacturing operations?
The following questions are entirely optional.
To comply with government Equal Employment Opportunity and/or Affirmative Action reporting regulations, we are requesting (but NOT requiring) that you enter this personal data. This information will not be used in connection with any employment decisions, and will be used solely as permitted by state and federal law. Your voluntary cooperation would be appreciated. Learn more.
Gender
Race/Ethnicity

Invitation for Job Applicants to Self-Identify as a U.S. Veteran
  • A “disabled veteran” is one of the following:
    • a veteran of the U.S. military, ground, naval or air service who is entitled to compensation (or who but for the receipt of military retired pay would be entitled to compensation) under laws administered by the Secretary of Veterans Affairs; or
    • a person who was discharged or released from active duty because of a service-connected disability.
  • A “recently separated veteran” means any veteran during the three-year period beginning on the date of such veteran's discharge or release from active duty in the U.S. military, ground, naval, or air service.
  • An “active duty wartime or campaign badge veteran” means a veteran who served on active duty in the U.S. military, ground, naval or air service during a war, or in a campaign or expedition for which a campaign badge has been authorized under the laws administered by the Department of Defense.
  • An “Armed forces service medal veteran” means a veteran who, while serving on active duty in the U.S. military, ground, naval or air service, participated in a United States military operation for which an Armed Forces service medal was awarded pursuant to Executive Order 12985.
Veteran status
I IDENTIFY AS ONE OR MORE OF THE CLASSIFICATIONS OF PROTECTED VETERAN LISTED ABOVE
I AM NOT A PROTECTED VETERAN
I DON’T WISH TO ANSWER

Voluntary Self-Identification of Disability
Voluntary Self-Identification of Disability Form CC-305
OMB Control Number 1250-0005
Expires 04/30/2026
Why are you being asked to complete this form?

We are a federal contractor or subcontractor. The law requires us to provide equal employment opportunity to qualified people with disabilities. We have a goal of having at least 7% of our workers as people with disabilities. The law says we must measure our progress towards this goal. To do this, we must ask applicants and employees if they have a disability or have ever had one. People can become disabled, so we need to ask this question at least every five years.

Completing this form is voluntary, and we hope that you will choose to do so. Your answer is confidential. No one who makes hiring decisions will see it. Your decision to complete the form and your answer will not harm you in any way. If you want to learn more about the law or this form, visit the U.S. Department of Labor’s Office of Federal Contract Compliance Programs (OFCCP) website at www.dol.gov/ofccp.

How do you know if you have a disability?

A disability is a condition that substantially limits one or more of your “major life activities.” If you have or have ever had such a condition, you are a person with a disability. Disabilities include, but are not limited to:

  • Alcohol or other substance use disorder (not currently using drugs illegally)
  • Autoimmune disorder, for example, lupus, fibromyalgia, rheumatoid arthritis, HIV/AIDS
  • Blind or low vision
  • Cancer (past or present)
  • Cardiovascular or heart disease
  • Celiac disease
  • Cerebral palsy
  • Deaf or serious difficulty hearing
  • Diabetes
  • Disfigurement, for example, disfigurement caused by burns, wounds, accidents, or congenital disorders
  • Epilepsy or other seizure disorder
  • Gastrointestinal disorders, for example, Crohn's Disease, irritable bowel syndrome
  • Intellectual or developmental disability
  • Mental health conditions, for example, depression, bipolar disorder, anxiety disorder, schizophrenia, PTSD
  • Missing limbs or partially missing limbs
  • Mobility impairment, benefiting from the use of a wheelchair, scooter, walker, leg brace(s) and/or other supports
  • Nervous system condition, for example, migraine headaches, Parkinson’s disease, multiple sclerosis (MS)
  • Neurodivergence, for example, attention-deficit/hyperactivity disorder (ADHD), autism spectrum disorder, dyslexia, dyspraxia, other learning disabilities
  • Partial or complete paralysis (any cause)
  • Pulmonary or respiratory conditions, for example, tuberculosis, asthma, emphysema
  • Short stature (dwarfism)
  • Traumatic brain injury
Please check one of the boxes below:
YES, I HAVE A DISABILITY, OR HAVE HAD ONE IN THE PAST
NO, I DO NOT HAVE A DISABILITY AND HAVE NOT HAD ONE IN THE PAST
I DO NOT WANT TO ANSWER

PUBLIC BURDEN STATEMENT: According to the Paperwork Reduction Act of 1995 no persons are required to respond to a collection of information unless such collection displays a valid OMB control number. This survey should take about 5 minutes to complete.

Name Date
Human Check*