Quality Control Analyst
ZenPharm
Basis: Full-Time
Closing Date: 05-Dec-2024
Job Ref: KMP-95569
Job Description
BasisFull-Time |
Apply by05-Dec-2024 |
LocationUndefined |
SalaryUndefined |
ZenPharm is an established medicinal cannabis manufacturing company, regulated by the laws of Malta and of the European Union. The company has the facilities to manufacture Medicinal Cannabis products and has seen tremendous operational growth in the past months. ZenPharm Ltd is a sister operation to Natrix Sciences Ltd. which is an EU GMP-licensed CDMO which develops and manufactures oral solid dosage forms for the medicinal market.
We are looking for individuals who are ready to jumpstart their careers by immersing themselves in the traditional pharma and medicinal cannabis industries. Being a relatively small facility, we are ideally placed to provide new candidates expansive exposure to a wide field of skills, techniques and experiences. We are looking for a team player in a small team of chemistry analysts with a ‘can do’ attitude and a commitment to learn and develop within the company.
Specific Duties and Responsibilities
Reporting to the QC Manager, the successful candidate will be responsible for:
Requirements:
We are looking for individuals who are ready to jumpstart their careers by immersing themselves in the traditional pharma and medicinal cannabis industries. Being a relatively small facility, we are ideally placed to provide new candidates expansive exposure to a wide field of skills, techniques and experiences. We are looking for a team player in a small team of chemistry analysts with a ‘can do’ attitude and a commitment to learn and develop within the company.
Specific Duties and Responsibilities
Reporting to the QC Manager, the successful candidate will be responsible for:
- Sampling and analysis of raw materials, packaging, works in progress, finished goods and stability.
- To ensure that the company’s laboratory complies fully with good laboratory practice, including laboratory upkeep and cleanliness.
- To participate in the development of analytical methods.
- To perform analytical validation and lab transfer analysis.
- To participate in the procurement of laboratory reagents and consumables.
- To perform any necessary analytical documentation review in accordance with cGLP in a timely manner.
- To monitor environmental conditions in the laboratory.
- To ensure GMP compliance as per local procedures and Eudralex Volume 4 GMP guidelines.
- In case of handling of controlled drugs;
- To ensure that all safety and security regulations are abided to at all times.
- To ensure full traceability and reconciliation of samples.
Requirements:
- In possession of a degree in Chemistry, Biology, Medical Lab Science, or a related science subject. Candidates having a BTEC National Diploma in Applied Science will also be considered.
- At least 1 year of work experience in a QC chemistry laboratory with good understanding of analytical testing and equipment operation / troubleshooting; or an adequate combination of education and experience. However, fresh graduates are encouraged to apply as full training will be provided.
- Good time management skills.
- Good IT skills e.g. Microsoft Office (Word, Excel and Outlook).
- Ability to work in a team.
- Ability to communicate clearly and concisely in English, both orally and in writing.
- In possession of an EU working VISA.