Laboratory Technician

With sales of €700m and 3,300 employees worldwide, Nemera is one of the leading global manufacturers of complex drug delivery systems for the pharmaceutical industry, offering to patients a broad product portfolio which includes inhalation devices, injection devices, nasal and dermal pumps and ophthalmic delivery devices. Nemera has built very long lasting, strong relationships with the leading global pharmaceutical companies globally by providing high quality development, industrialization and manufacturing services. Nemera develops and manufactures its own IP product platforms but also offers also fully custom developments and contract manufacturing.

Nemera’s manufacturing sites are located in the US, France, Germany, Brazil and Poland. The headquarters and Innovation Center for early device design and development are located in France (Lyon).

We have big ambitions at Nemera! We are growing our franchises and strengthening our capabilities.

Responsibilities

Perform various testing on medical devices utilizing analytical equipment.; Analyse and interpret test results, ensuring data is within specification limits.; Document and report test findings and observations, maintaining accurate records according to documentation requirements.; Participate in the implementation of new testing methods and protocols.; Contribute to maintaining the cleanliness and orderliness of the laboratory.; Manage the stock of laboratory consumables.; Report any deviations, errors, failures, or OOS results and participate in the follow-up actions.; Comply with the Good Practices applicable to the laboratory.

Requirements

Bachelor’s degree in a scientific field.; Experience in a laboratory environment.; Self-motivated with good communication skills.; Excellent organization skills.; Strong attention to detail.; Ability to work independently and as part of a team.; Proficient with the MS Suite.

Nice to have

Ability to troubleshoot and maintain various laboratory equipment.; Experience in the pharmaceutical or medical device industry.; Familiarity with ISO standards and FDA regulations.