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
In this position, you will be responsible for the daily receiving, inspection, storage, and distribution activities for a cGMP warehouse. The position will be required to perform and document daily warehouse operations in a cGMP environment, while maintaining high level of attention to detail, good documentation practices, and ability to follow procedures as written. This position requires daily interactions with manufacturing staff, Quality Control, Quality Assurance, and other Materials Management staff to ensure material needs are met.
Responsibilities
Receiving, inspection, labeling, and storage of incoming materials per cGMP guidance and applicable procedures.
Execute cold chain pack-out and shipment of drug product and samples.
Execute material picking, verification, and delivery to Internal Manufacturing
Perform cycle counts and physical inventory maintenance activities.
Transact material requests and transfers between warehouse and third-party storage.
Support PCMS alarm management.
Manage the Returned Goods process according to the Returned Goods SOP.
Assists in record storage and retrieval process as needed.
Ensures accurate inventory is maintained and inventory discrepancies are communicated/investigated
Ensures materials are shipped in correct temperature conditions and are handled appropriately.
Demonstrate proficiency in the use of the ERP system (Oracle) and execute real time transactions.
Safely operate all motorized equipment including forklift trucks, electric pallet jacks, lifts, and company vehicles.
Use PPE, where required, ensures proper safety practices, and identifies safety/hazard risks.
Maintain a state of compliance in the warehouse.
Minimum Qualifications
High School Degree
Minimum of 3-5 years' experience working within a cGMP supply chain environment and/or with GCP regulations.
Strong understanding of storage and shipping of cold chain products in the Biotech/Lifesciences industry and the associated documentation requirements.
Knowledge of warehouse and distribution business processes.
Knowledge of common ERP systems.
Ability to perform the physical demands of the role, including lifting moderately heavy boxes.
Well organized, strong communication skills, and drives for results
Valid and active Driver's License.
Preferred Qualifications
College Degree (Bachelor's degree in Business, Supply Chain, Operations Management, or related field) or relevant experience
Exhibits a "can-do" attitude.
Demonstrates growing knowledge of applicable regulations.
Works independently, exercises sound judgment when troubleshooting.
Previous experience in Logistics, Distribution, Warehousing, and Supply Chain preferred.
In-depth knowledge of warehouse operations in a GMP as well as a non-GMP setting.
Strong knowledge of good documentation practices.
DOT, IATA, OSHA certification a plus.
Experience in gene therapy highly preferred.
Competencies
Collaborative - Openness, One Team
Undaunted - Fearless, Can-do attitude
Results Orientation - Delivering progress toward our mission. Sense of urgency in solving problems.
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
