S/he will report to the VP of Finance at HQ and dotted line into the Regional President of California, where they will serve on the state Leadership Team. This role will be responsible for the region’s three local facilities, the related distribution operation, and a wholesale network of 400+ dispensaries within California.

S/he will be responsible for overseeing quality-related activities at the facility associated with incoming inspection, sampling and inspection of finished products, customer complaint investigations, product investigations, and Corrective and Preventive Action (CAPA) plans.

S/he will develop sourcing roadmaps and comprehensive sourcing strategies for indirect spend categories while also implementing new and/or transforming existing internal processes and policies central to Cresco’s supply chain and sourcing / procurement capabilities.

S/he is responsible for developing the short-term and long-term production targets and production plans to satisfy customer demand within cost and capacity parameters, for all facilities, categories, segments, products and brands for California.

Cresco Labs is seeking a Senior Director of Distribution Operations to oversee distribution efforts across our California region, including the transportation, warehousing, inventory, and overall logistics for the multi-site operations and a network of 400+ retailers throughout the state.

Reporting to the Regional President of California, the VP of Operations will be based out of Los Angeles with travel and oversight of the California region. S/he is responsible for directing the day-to-day business activities across the region, including the management, development, and improvement of effective business strategies, programs, and procedures.

The Director of Pharmacovigilance will lead US-based pharmacovigilance, and global PV activities specifically in the analyzation of safety data, identifying, detecting and investigating safety signals, evaluating and proactively managing risk, and providing medical safety review for Greenwich Biosciences’ investigational compounds and market products.

The Associate Director, R&D Program Management Office (R&D PMO) will provide tactical and operational leadership to the R&D PMO staff who support individual project development teams.

Reporting directly to the Senior Director, Marketing, the Director, Product Marketing (MS) will play a key role within the Brand Team preparing to launch an exciting product candidate with an expected first indication in multiple sclerosis spasticity.

The Associate Director role leads and supports the business of the company specifically in respect to US regulatory policy and more generally in respect to global regulatory policy and intelligence. S/he represents the company externally in respect to advancing the policy objectives of Greenwich Biosciences.

Reporting to the VP of Clinical Research & Scientific Affairs, s/he will be a key member of Juul Labs Regulatory Science organization overseeing design and execution of clinical studies working with a talented team of clinical trial specialists, statisticians and data management scientists as well as external CRO’s and academic partners as needed.

S/he will build, develop, and lead the team of Supplier Quality engineers/technicians to support Manufacturing, Supplier Development, New Product Development, and Quality Systems at JUUL Contract Manufacturer (CM) sites.

Reporting to the Lab Manager and CSO, the Lab Technician will be responsible for testing ingredients and finished products to ensure correct composition and to identify any health or quality control issues that need to be corrected. S/he will participate in the R&D aspects of the job, including sample preparation, product testing, and new process trials.