Natrix Sciences Limited is an EU cGMP-licensed pharmaceutical facility specialising in the development and manufacturing of generic medicines. Operating as a Contract Development and Manufacturing Organisation (CDMO), Natrix focuses on Modified Release Solid Oral Dosage Forms - including powders, granules, and pellets -intended for filling into hard gelatine 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 specialised 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.
Ensuring 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 abided by 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 years of 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.

Senior Quality Control Analyst

Job Description