Pharmacy Technician - Quality Assurnce Department (QA)
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.
Job role:
To provide effective administrative and documentation support for the Quality Assurance (QA) system, ensuring compliance with GxP requirements and facilitating ongoing coordination between the QA department and other departments in the company.
Job responsibilities:
1. Documentation Management
- Receiving, reviewing, and archiving production and control documentation (Batch Records, protocols, logs, checklists, etc.)
- Issuing production protocols upon approval by the QA Manager
- Verifying completeness and compliance of completed documentation prior to final QA review
- Archiving originals and scanning documents for entry into the electronic database
2. Labeling and Tagging Support
- Preparing and reviewing labels for semi-finished and finished products, raw materials, samples, and materials
- Issuing and recording labels in accordance with GMP procedures and with QA approval
- Maintaining a registry of used, returned, and damaged labels
3. Cross-Department Communication
- Coordinating with Production, Cultivation, and Logistics departments regarding documentation and forms
- Receiving and reviewing daily and weekly records from clean areas (logs, checklists, cleaning records, etc.)
- Supporting sample submission to the QC laboratory with accompanying documentation
4. QA Process Support
- Assisting in the preparation of documentation for inspections, audits, and internal reviews
- Keeping records of open/closed batches and the status of labels and documentation
- Checking for valid signatures and dates in documentation
- Supporting the review of Release Packages for batch release
5. Training and Compliance
- Adhering to GMP rules, wearing appropriate attire, and following cleanroom entry procedures
- Actively participating in internal training sessions on documentation and QA procedures
- Preparing and monitoring SOPs related to assigned tasks, and initiating updates when necessary
Qualifications:
- Minimum secondary education in pharmacy or a related field.
- Minimum 1 year of work experience in a production or pharmaceutical environment
- Good computer literacy (MS Office – Word, Excel, Outlook)
- English proficiency (at least intermediate level – reading and understanding documentation)
- Precision, organization, and attention to detail
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 at
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