A pioneering med-tech company developing innovative inhalation technologies for precise drug delivery. Our mission is to enhance patient care by leveraging breakthrough technology to improve treatment outcomes.
We are looking for a cQP (Cannabis Qualified Person) & cRP (Cannabis Responsible Person) to join our Tiberias site. As cQP (Cannabis Qualified Person) youll ensures that each batch of product released for marketing is produced and tested in accordance with the quality and regulatory requirements.
As cRP (Cannabis Responsible Person) youll be responsible for drugs inventory movements in the facility and for fulfilling regulatory requirements. Moreover, ensures that each batch of product released for marketing is produced and tested in accordance with the quality and regulatory requirements.
Key Responsibilities
Responsibilities as cQP
Releasing cartridge production batches to the market after approval of quality assurance, ensuring compliance with regulatory and quality requirements, adhering to Eudralex volume 4, annex 16, guidelines.
Batch release approval documents will be personally kept by the CQP, available for authorities review, for a period of no less than 5 years.
Supervision of the production of cannabis products.
Change controls regarding manufacturing process review and, when applicable, plan approval.
Participation in solving quality issues and deviations in production.
Responsibilities as cRP
Contact with the relevant district pharmacist on issues related to the production or release of products.
Dangerous Drugs inventory log management.
Dangerous Drugs annual report to the IMCU: Preparation of annual reports for submission to the district pharmacist.
Control over the receipt of cannabis into the warehouse.
Supervising the preparation of shipments of finished products.
Preparation of rejected cannabis for destruction including full documentation.
Carrying out a monthly and annual cannabis inventory count.
Change controls regarding inventory management and procedural cannabis movements review and, when applicable, plan approval.
Control of procedures as needed.
Requirements: Bachelor's degree in a relevant scientific discipline (e.g., Chemistry, Pharmacy, Biology), and has a pharmacist's certificate.
Proven experience of at least two years in a manufacturing facility for the production of preparations or in a facility for the production of cannabis products.
Experience in the activity of quality tests of raw materials and preparations, in quantitative tests of raw materials and finished products, and in the tests required to ensure the quality of the preparation;
Thorough understanding of Good Manufacturing Practices (GMP).
Preferred Qualifications:
Advanced degree (e.g., Master's or PhD) in a relevant scientific discipline.
Experience in the pharmaceutical cannabis industry.
This position is open to all candidates.