Quality Control Senior Analyst

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.

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.

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.

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.

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 prepare quality validation reports.

• To perform analytical validations and lab transfer analysis.

• 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 adhered to at all times.

• To ensure full traceability and reconciliation of samples.

• To monitor the analytical technique of other QC Analysts and guide them.

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 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.

• Good experience in the use of chromatographic equipment (HPLC, GC)

• Experience in analytical method validation is considered an asset.

• 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.

Offered: Minimum salary: €30,000 per year, depending on qualifications and experience.