Специалист по контролю качества лекарственных средств — работа в Финляндии
Pharmaceutical quality specialists perform inspections and precision measurements in order to test and ensure the quality of pharmaceutical products. They are involved in the whole development phase of a pharmaceutical product until it is ready for the market. This includes the process of acquiring clinical trial licences, advising the pharmaceutical development staff on regulatory requirements and evaluating the content of the package leaflet and other documentation on the product. Moreover, pharmaceutical quality specialists collect and evaluate information on side effects of the product and communicate this knowledge both internally and to the relevant authorities.
Специалист по контролю качества лекарственных средств - Какие навыки обязательны?
European and national legal framework for the development, distribution, and use of medicinal products for humans.
The offered pharmaceutical products, their functionalities, properties and legal and regulatory requirements.
Instruments and methods used to separate, identify and quanitfy matter - the chemical components of natural and artificial materials and solutions.
Test processed workpieces or products for basic faults.
Monitor quality standards in manufacturing and finishing process.
Analyse information flows to reconstruct messages quickly and precisely. Navigate a language to explain the same sense or feeling in situations where there is no definite word or literal translation.
The legal requirements and licenses required when handling controlled substances.
The technology that uses, modifies or harnesses biological systems, organisms and cellular components to develop new technologies and products for specific uses.
Pharmaceutical technology is the branch of pharmaceutics which deals with the technological design, development, manufacture, and evaluation of drugs and medicinal products.
Techniques applied in the different fields of natural science in order to obtain experimental data such as gravimetric analysis, gas chromatography, electronic or thermic methods.
Take the necessary precautions for storing, using and disposing chemical products.
The main stakeholders, companies and procedures in the pharmaceutical industry and the laws and regulations that govern the patenting, testing, safety and marketing of drugs.
The chemical aspects of identification and synthetic alteration of chemical entities as they relate to therapeutic use. The way various chemicals affect biological systems and how they can be integrated in drug development.
Специалист по контролю качества лекарственных средств - Какие навыки полезны, но не обязательны?
The offered chemical products, their functionalities, properties and legal and regulatory requirements.
Record data which has been identified specifically during preceding tests in order to verify that outputs of the test produce specific results or to review the reaction of the subject under exceptional or unusual input.
Transfer the chemical mixture from the mixing tank to the storage tank by turning on the valves.
Perform chemical experiments with the aim of testing various products and substances in order to draw conclusions in terms of product viability and replicability.
Pharmacology is a medical specialty mentioned in the EU Directive 2005/36/EC.
The relevant chemical processes used in manufacture, such as purification, seperation, emulgation and dispergation processing.
Use information technology to accurately record and analyse data from biomedical tests, writing reports on the data and sharing results with the appropriate persons.
The production and characteristisc of organic basic chemicals such as ethanol, methanol, benzene and inorganic basic chemicals such as oxygen, nitrogen, hydrogen.