ZenPharm Ltd is a fully licensed vertically integrated seed to sale.  EU-cGMP pharmaceutical company specializing in the delivery of cannabis-based treatments that are routed in the fundamental medicinal standards of safety, quality and efficacy.

ZenPharm Ltd

Health insurance

Flexible working hours

&lt;p&gt;Natrix Sciences Limited is an EU cGMP-licensed pharmaceutical facility specializing in the development and manufacturing of generic medicines. Operating as a Contract Development and Manufacturing Organization (CDMO), Natrix focuses on Modified Release Solid Oral Dosage Forms - including powders, granules, and pellets - intended for filling into hard gelatin capsules and tablets.&lt;/p&gt;
&lt;p&gt;With a growing reputation for excellence, Natrix has also positioned itself as a strategic partner in innovative research and development projects, particularly from emerging and dynamic industries.&lt;/p&gt;
&lt;p&gt;In addition to its core pharmaceutical operations, Natrix Sciences provides specialized services as ZenPharm Limited, a licensed producer of medicinal cannabis. ZenPharm is well-placed to become a local industry leader, and this collaboration offers unique cross-sector experience.&lt;/p&gt;
&lt;p&gt;Our Quality Control department presents an excellent opportunity for professional development within a regulated, fast-paced environment. Laboratory analysts work within a single shift structure and benefit from flexible working hours. This role also includes the opportunity to gain hands-on experience in the medicinal cannabis industry, a rapidly growing and evolving sector. If you are a motivated QC professional with a strong GMP mindset and a can-do attitude, we would be pleased to hear from you.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Specific Duties and Responsibilities:&lt;/strong&gt;&lt;/p&gt;
&lt;p&gt;Reporting to the QC Manager, the successful candidate will be responsible for:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Sampling and analysis of raw materials, packaging, works in progress, finished goods, and stability.&lt;/li&gt;
&lt;li&gt;To ensure that the company’s laboratory complies fully with good laboratory practice, including laboratory upkeep and cleanliness.&lt;/li&gt;
&lt;li&gt;To participate in the development of analytical methods.&lt;/li&gt;
&lt;li&gt;To prepare quality validation reports.&lt;/li&gt;
&lt;li&gt;To perform analytical validations and lab transfer analysis.&lt;/li&gt;
&lt;li&gt;To perform any necessary analytical documentation review in accordance with cGLP in a timely manner.&lt;/li&gt;
&lt;li&gt;To monitor environmental conditions in the laboratory.&lt;/li&gt;
&lt;li&gt;To ensure GMP compliance as per local procedures and Eudralex Volume 4 GMP guidelines.&lt;/li&gt;
&lt;li&gt;In case of handling of Controlled Drugs.&lt;/li&gt;
&lt;li&gt;To ensure that all safety and security regulations are adhered to at all times.&lt;/li&gt;
&lt;li&gt;To ensure full traceability and reconciliation of samples.&lt;/li&gt;
&lt;li&gt;To monitor the analytical technique of other QC Analysts and guide them.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;Requirements:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;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.&lt;/li&gt;
&lt;li&gt;At least 2-year work experience in a QC Chemistry Laboratory with a good understanding of analytical testing and equipment operation/troubleshooting; or an adequate combination of education and experience.&lt;/li&gt;
&lt;li&gt;Good experience in the use of chromatographic equipment (HPLC, GC)&lt;/li&gt;
&lt;li&gt;Experience in analytical method validation is considered an asset.&lt;/li&gt;
&lt;li&gt;Good time management skills.&lt;/li&gt;
&lt;li&gt;Good IT skills, e.g., Microsoft Office (Word, Excel and Outlook).&lt;/li&gt;
&lt;li&gt;Ability to work in a team.&lt;/li&gt;
&lt;li&gt;Ability to communicate clearly and concisely in English, both orally and in writing.&lt;/li&gt;
&lt;li&gt;In possession of an EU working VISA.&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Offered: Minimum salary: €30,000 per year, depending on qualifications and experience.&lt;/p&gt;

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