engineering processes
The systematic approach to the development and maintenance of engineering systems.
Chemical engineers design and develop large-scale chemical and physical production processes and are involved in the entire industrial process required for transforming raw materials into products.
No competences in this bucket.
The systematic approach to the development and maintenance of engineering systems.
The process of creating chemical products that diminish or cancel the negative impact on the environment caused by the use of hazardous substances. It follows all the phases of chemical product generation from the design to the manufacturing and its disposal.
Oxidation and reduction are chemical processes characterised in terms of oxygen, hydrogen or electrons transfer that occurs during a reaction between a molecule, atom or ion.
The scientific field that focuses on investigating and measuring spectra that are produced through electromagnetic radiation either in the form of materials interaction with radiations or their emission.
Instruments and methods used to separate, identify and quantify matter-the chemical components of natural and artificial materials and solutions.
The composition, structure, and properties of substances and the processes and transformations that they undergo; the uses of different chemicals and their interactions, production techniques, risk factors, and disposal methods.
The engineering elements like functionality, replicability, and costs in relation to the design and how they are applied in the completion of engineering projects.
The study of existing materials and substances properties to produce new materials or enhance several existing properties such as chemical or physical ones. It involves knowledge on the structure, on the performance of diverse materials and on the transferability of the new or improved materials to different industries.
No competences in this bucket.
Develop new processes using controlled chemical processes in order to perform liquid or gases components separation or to generate electrical currents.
Adjust designs of products or parts of products so that they meet requirements.
Adhere to standards of hygiene and safety established by respective authorities.
Give consent to the finished engineering design to go over to the actual manufacturing and assembly of the product.
Monitor environmental impacts and carry out assessments in order to identify and to reduce the organisation's environmental risks while taking costs into account.
Analyse the operations and actions of a company in order to assess their repercussions, possible risks for the company, and to develop suitable strategies to address these.
Perform chemical experiments with the aim of testing various products and substances in order to draw conclusions in terms of product viability and replicability.
Gain, correct or improve knowledge about phenomena by using scientific methods and techniques, based on empirical or measurable observations.
Perform the testing procedures on the already prepared chemical samples, by using the necessary equipment and materials. Chemical sample testing involves operations such as pipetting or diluting schemes.
Handle chemicals and select specific ones for certain processes. Be aware of the reactions which arise from combining them.
No competences in this bucket.
Biological chemistry is a medical specialty mentioned in the EU Directive 2005/36/EC.
The rules and regulations of the European legislations and of the Food and Drugs Administration regarding clinical trials and drug development.
The way in which electrical and instrumentation engineering (E and I engineering) modernises the production infrastructure from design to preparation of execution phase and the execution phase itself followed by the after-sales services, improvements obtain by using the electrical and instrumentation engineering.
Regulatory requirements and Good Manufacturing Practices (GMP) applied in the relevant manufacturing sector.
Discipline that applies principles of physics, engineering and materials science to design, analyse, manufacture and maintain mechanical systems.
Microbiology-Bacteriology is a medical specialty mentioned in the EU Directive 2005/36/EC.
Be familiar with European and National legislation regarding the risk of pollution.
The characteristics and properties of different textile and fabric materials. These include strength, flexibility, elasticity, softness, durability, heat insulation, low weight, water absorbency/repellence, dyeability and resistance to chemicals. Moreover, the influence of chemical composition and molecular arrangement of yarn and fibre properties and fabric structure on the physical properties of textile fabrics; the different fibre types; the materials used in different processes and the effect on materials as they are processed.
The set of structures and models needed to understand or describe the software system, including the software elements, the relations between them and the properties of both elements and relations.
Types of plastic materials and their chemical composition, physical properties, possible issues and usage cases.
The production and characteristisc of organic basic chemicals such as ethanol, methanol, benzene and inorganic basic chemicals such as oxygen, nitrogen, hydrogen.
Tissues, cells, and functions of plant and animal organisms and their interdependencies and interactions with each other and the environment.
Process of adding chemical compounds to a product, such as food or pharmaceutical products, to prevent decay caused by chemical changes or microbial activity.
The properties of different materials developped in a laboratory, their usage per type of products, and how to create them.
Engineering discipline that combines computer science with electrical engineering to develop computer hardware and software. Computer engineering occupies itself with electronics, software design, and the integration of hardware and software.
The elements used in design such as unity, scale, proportion, balance, symmetry, space, form, texture, colour, light, shade and congruence and their application into practice.
The field of engineering that deals with the study and application of electricity, electronics, and electromagnetism.
The principles of electricity and electrical power circuits, as well as the associated risks.
The science that studies the human organs and its interactions and mechanisms.
The selection of software that aids in estimating, managing and scheduling industrial processes such as design, work flow and production improvement.
The regulations that govern the set of rights protecting products of the intellect from unlawful infringement.
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.
The steps required through which a material is transformed into a product, its development and full-scale manufacturing.
The behaviour of solid objects when subjected to stresses and strains, and the methods to calculate these stresses and strains.
Theoretical and practical applications of the science studying the action of displacements and forces on physical bodies to the development of machinery and mechanical devices.
Technologies, science, and engineering activities conducted on a nanoscale, where material or extremely small components are manipulated on an atomic, molecular, or supramolecular scale.
Subdiscipline of engineering that deals with the development of optical instruments and applications, such as telescopes, microscopes, lenses, lasers, fibre optic communication, and imaging systems.
The processes of packaging or protecting products for distribution, storage and sale.
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.
Drug manufacturing phases: pre-clinical phase (research and tests on animals), clinical phase (clinical trials on humans) and the sub-phases required to obtain as an end product a pharmaceutical drug.
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.
European and national legal framework for the development, distribution, and use of medicinal products for humans.
The quality systems model that apply in pharmaceutical manufacturies. The most common system ensures quality in facilities and equipment system, laboratory controls system, materials system, production system and packaging and labelling system.
Pharmaceutical technology is the branch of pharmaceutics which deals with the technological design, development, manufacture, and evaluation of drugs and medicinal products.
Pharmacology is a medical specialty mentioned in the EU Directive 2005/36/EC.
Regulations used to control and monitor adverse drug reactions at EU level.
The natural science involving the study of matter, motion, energy, force and related notions.
Quality assurance principles, standard requirements, and the set of processes and activities used for measuring, controlling and ensuring the quality of products and processes.
The national and international requirements, specifications and guidelines to ensure that products, services and processes are of good quality and fit for purpose.
The study of the risks associated with engineered designs and systems, accident prevention as well as the safety benefits of reducing deaths and injuries. The discipline focuses on analysing and mitigating potential hazards in engineering processes.
Semiconductors are essential components of electronic circuits and contain properties of both insulators, such as glass, and conductors, such as copper. Most semiconductors are crystals made of silicon or germanium. By introducing other elements in the crystal through doping, the crystals turn into semiconductors. Depending on the amount of electrons created by the doping process, the crystals turn into N-type semiconductors, or P-type semiconductors.
The flow of goods in the supply chain, movement and storage of raw materials, work-in-process inventory, and finished goods from point of origin to point of consumption.
Types of materials of which the physical state changes when exposed to heat, as well as the specific manner in which the materials react to heat exposure.
The negative effects of chemicals on living organisms, their dose and exposure.
Qualities, specifications, applications and reactions to different fabricating processes of various types of metal, such as steel, aluminium, brass, copper and others.
Properties of materials that make them suitable for packaging. Conversion of raw materials into packaging materials. Different types of labels and materials used which comply with the correct storage criteria depending on the goods.
No competences in this bucket.
Compare technological and economic characteristics of different options to produce hydrogen. This includes comparing sources (natural gas, water and electricity, biomass, coal) and related technologies.
Evaluate the ongoing pharmaceutical production process against the latest developments on the market regarding the mixing, compounding and packaging, ensuring the necessary updates are implemented.
Prepare tissue, blood or skin samples for examination procedures and analyse them by running chemical and biological tests.
Perform the evaluation and assessment of the use of hydrogen as an alternative fuel. Compare costs, technologies and available sources to produce, transport and store hydrogen. Take into account the environmental impact to support the process of decision making.
Explain to patients the basis of their disease from the molecular and metabolic points of view and how therapies can affect their lifestyles.
Manage the design and construction of pharmaceutical production facilities making sure the facilities and process validation are according to the planning and conform to FDA and GMP.
Provide organisations and individuals searching for alternative energy fuels information on costs, benefits, and negative aspects of the use of hydrogen. Inform about what one must take into account when considering the implementation of hydrogen solutions.
Test the systems used to manufacture pharmaceuticals measuring and analysing the processes to ensure that the products are produced according to specifications.
Test the supplied materials prior to their release into processing, ensuring the results are complying with GMP (Good Manufacturing Practices) and to the suppliers` COA (Certificate of Analysis).
Advise individuals and organisations on the development and implementation of actions which aid in the prevention of pollution and its related risks.
Advise organisations on the implementation of waste regulations and on improvement strategies for waste management and waste minimisation, to increase environmentally sustainable practices and environmental awareness.
Analyse production processes leading toward improvement. Analyse in order to reduce production losses and overall manufacturing costs.
Interpret and analyse data collected during testing in order to formulate conclusions, new insights or solutions.
Study developments and innovation proposals in order to determine their applicability in the business and their feasibility of implementation from various fronts such as economic impact, business image, and consumer response.
Speak in public and interact with those present. Prepare notices, plans, charts, and other information to support the presentation.
Participate in the registration process that allows the sale and distribution of substances that treat or prevent human and animal diseases or enable medical diagnosis.
Solve problems which arise in planning, prioritising, organising, directing/facilitating action and evaluating performance. Use systematic processes of collecting, analysing, and synthesising information to evaluate current practice and generate new understandings about practice.
Define, in collaboration with managers and quality experts, a set of quality standards to ensure compliance with regulations and help achieve customers' requirements.
Design and develop optical and imaging systems, products, and components, such as lasers, microscopes, optical fibre, cameras, and magnetic resonance imaging (MRI) machines.
Design production control systems which involve all processes from pharmaceutical production process to pharmaceutical stocks with the purpose of providing the correct input for the development of pharmaceutica manufacturing plant software packages.
Design prototypes of products or components of products by applying design and engineering principles.
Research and create new chemicals and plastics used in the production of a variety of goods such as pharmaceuticals, textile, building materials and household products.
Develop testing protocols in collaboration with engineers and scientists to enable a variety of analyses such as environmental, chemical, physical, thermal, structural, resistance or surface analyses on a wide range of materials such as metals, ceramics or plastics.
Develop new therapeutic products according to the potential formulas, studies and indications recorded during the research process which involved also collaboration with physicians, biochemists and pharmacologists.
List the design specifications such as materials and parts to be used and a cost estimate.
Monitor activities and perform tasks ensuring compliance with standards involving environmental protection and sustainability, and amend activities in the case of changes in environmental legislation. Ensure that the processes are compliant with environment regulations and best practices.
Implement safety programmes to comply with national laws and legislation. Ensure that equipment and processes are compliant with safety regulations.
Establish a connection between organisations or individuals which may benefit from communicating with one another in order to facilitate an enduring positive collaborative relationship between both parties.
Analyse the principles that need to be considered for engineering designs and projects such as functionality, replicability, costs and other principles.
Collect data required to make improvements or modifications to chemical processes. Develop new industrial processes, design new process plants/equipment or modify existing ones.
Assist with the integration of new systems, products, methods, and components in the production line. Ensure that production workers are properly trained and follow the new requirements.
Manage the procedures to be used in chemical testing by designing them and conducting tests accordingly.
Monitor plant processes and efficiency set-up to ensure the maximum output of production levels.
Carry out tests in a laboratory to produce reliable and precise data to support scientific research and product testing.
Provide expert knowledge in a particular field, especially concerning mechanical or scientific subjects, to decision makers, engineers, technical staff or journalists.
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.
Test the composition, characteristics, and use of materials in order to create new products and applications. Test them under normal and extraordinary conditions.
Use computer-aided design (CAD) systems to assist in the creation, modification, analysis, or optimisation of a design.
Use the laboratory equipment such as Atomic Absorption equimpent, PH and conductivity meters or salt spray chambre.
Create technical designs and technical drawings using specialised software.
Write reports on the manufactured batches history taking into account the raw data, tests performed and compliance to Good Manufacturing Practices (GMP) of each batch of product.
Compose technical customer reports understandable for people without technical background.