QC Analyst (Lates)

at  Dechra Pharmaceuticals PLC

Job Introduction
Thanks for checking out our vacancy, we’re delighted you want to learn more about Dechra.
Dechra are a growing, global specialist within the world of veterinary pharmaceuticals. Our expertise is in the development, manufacture, marketing and sales of high quality products exclusively for veterinarians worldwide.
Here at Dechra, our values are embedded within our culture and thrive within our family of almost 2000 colleagues globally. From manufacturing to marketing, (D)edication, (E)njoyment, (C)ourage, (H)onesty, (R)elationships and (A)mbition are at the heart of our everyday operations and the way we do business.

• Performing analytical and physical tests and evaluating the results obtained in order to guarantee the quality of packaging materials, semi-finished products, raw materials and end products, ie all Good Manufacturing Practice (GMP) requirements are met and all results are met.
• Meet established specifications and customer requirements.
• Collection, receipt and archiving of samples of raw materials, packaging, wage products, labels, semi-finished products, end products and water samples.
• Taking swab samples for monitoring and cleaning validations.
• Ensure an efficient division of the work, taking into account the production planning and agreed lead times.
• Performing regular maintenance and minor repairs, keeping clean and calibrating equipment, materials and spaces.
• Perform tests on raw materials, semi-finished products and packaging materials before use in production, using a wide range of analysis equipment.
• The release of raw materials, semi-finished products and packaging materials for use in production.
• Performing tests on end products for the release of products for the market, using a wide range of analysis equipment.
• Perform analysis for process, product, cleaning and equipment validation studies
• Conducting analysis for stability studies.
• Carry out analysis for method transfers to or from other laboratories.
• Checking and checking analysis data, documents, methods and procedures.
• Correct interpretation, processing and reporting of analysis data in electronic data systems and validation protocols.
• Preparing analysis certificates for customers.
• Conducting examinations as a result of Out-of-Specification results, deviations and other quality-related investigations.
• Keeping in touch with relevant departments to ensure that analytical tests are performed on time.
• Ensure the cleanliness in the laboratory rooms and the individual workplace.
• Keeping inventory and orders of chemicals, consumer goods and parts of equipment.
• Providing training / training to new employees or colleagues.
• Arranging the execution of external research, sending samples, processing reports and checking the progress of the work to be carried out.
• Drafting of specifications incl. Analytical regulations for raw materials, wage products, semi-finished products, packaging, labels and end products.
• Drafting of procedures relating to the departmental work and handling it according to the regulations.
• All other tasks that can reasonably be requested and approved by the management.
• Collaborate with team colleagues to ensure that the workplace environment remains at a high level regarding quality and cleanliness and complies with company and legislative standards at all times;
• Ensure both your own health and safety and that of others, ensure that all company safety and quality systems and relevant legislation are complied with, ask questions and report any incidents or suggestions to the manager;
• Ensure that all waste is safely removed and is in line with business processes.
• Stay abreast of developments in the field through training, reading of literature, documentation and the like