The company
Nedcann is a company dedicated to human health.
Our goal is to provide premium and sustainably grown products that will help people who suffer from diseases and make their conditions easier.At Nedcann we prioritize safety, transparency, and community, ensuring every experience is as exceptional as the plants we cultivate.
Join us on a journey to wellness and explore the natural benefits of cannabis with Nedcann
We make no concessions in our endeavor to be the best supplier in the medical cannabis market worldwide. Our production facility is located in Ohrid and we are currently seeking for new team members who will help us build our organization.
QC Specialist
Job role
As a member of the Nedcann team, the QC Specialist would take active role in the process of controlling and maintaining the quality of medicinal cannabis growth and processed on-site. The position is accountable for development, implementation and ongoing participation of the quality control program and control systems in compliance with the Nedcann polices and procedures.
Job Responsibilities
- Develop and follow SOP and standard analytical procedures to meet Good Laboratory Practices and Good Manufacturing Practices Compliance
- Performing Quality control of the resulting final product.
- Preparing certificate of analysis (CoAs) for all conducted analyses and keep records for all activities and processes according to established Standard Operating Procedures (SOPs).
- preparing specifications for all raw materials, packing materials, finished products, intermediates and solvents, and reagents used in analyses according to established Standard Operating Procedures (SOPs).
- Preparing analysis reports for the tested samples, and recording and investigating any results that are Out Of Specifications (OOS).
- Inspecting, sampling, and testing of all starting materials including packaging materials, intermediate and finished products as per procedures defined in the Standard Operating Procedures (SOPs).
- Monitoring environmental conditions are met as per current Good Manufacturing Practices (cGMP) requirements.
- Responsible for ensuring compliance with internal Standard Operating Procedures (SOP’s)
- Ensures that the final product is safe to release for sale or distribution
- Monitoring of storage conditions for materials and products
- Monitoring of contract manufacturers and providers of other GMP related outsourced activities
- Work with HPLC, GC and MC methods/techniques
- Responsible for hygiene, organization, and overall appearance of laboratory.
- Responsible for product development procedures to ensure that products meet quality and efficiency standards.
- Preparation of daily work reports
Requirements
- Degree in Pharmacy or Chemistry;
- Relevant experience in quality control in the GMP area;
- Knowledge of various analytical methods (HPLC, GC, LC-MS, etc.);
- Knowledge of method transfer, validation, qualification, calibration as well as the applicable GMP guideline;
- Experience in development and updating of specifications, analytical methods and procedures relating to laboratory activities;
- Specialization in pharmaceutical technology/Drug testing and control (preferred but not required).
- In-depth knowledge of pharmaceutical regulations;
- Attention to Detail- Strong attention to detail and commitment to maintaining high standards.
- Communication Skills- Effective communication and collaboration with cross-functional teams.
- Experience in development of sampling methods;
- Experience in validation of analytical methods according to ICH guidelines;
- Fluent knowledge of the English language, both written and spoken.
Our Offer:
In return for your expertise and commitment, we will provide a stimulating international environment, which will stretch your abilities and channel your talents. We also offer competitive salary and benefits combined with outstanding career development opportunities.
Interested? Then make sure to send us your CV and cover letter in English today via Fast Apply.
Contact phone: +389 76 777 223
