Requirements: English
Company: Hays
Region: Lombardy
La tua nuova aziendaOur Client, is a leading pharmaceutical company, organization located in the Mediterranean. It focuses on the development and production of high-quality pharmaceutical products, utilizing advanced technologies and modern facilities. Committed to innovation and regulatory compliance, it collaborates with global partners and continuously invests in infrastructure and sustainability.Il tuo nuovo ruoloIn view of expanding our workforce, we are seeking a QC Supervisor. For this role, the following responsibilities are expected:Quantitative and qualitative analysis of Active Pharmaceutical Ingredients (APIs).Analysis of raw materials and starting materials received by the warehouse; analysis of intermediates and finished products (APIs) from internal production; emission of approved and rejected labels for these materials.Management of chemical-physical standards.Management of department documentation.Management of stability data.Study and execution of analytical methods.Carrying out analysis for cleaning validation.Update list of qualified suppliers and suppliers in phase of qualification by the quality control laboratory.Preparation and analysis of various reagents.Management of retention samples.Carrying out the re-controlling (or retesting) of warehouse materials.Management of non-conforming analytical results. Carrying out the resulting investigation.Execution of internal periodic calibration of the instruments according to procedures currently in force.Preparation of samples for consignment.Activation & Deactivation of laboratory utilities.Management of solid/liquid laboratory waste.Management of laboratory supplies.Contacts with external laboratories for product analysis and release.Validation of analytical methods.Relationships with analytical equipment suppliers in order to solve any emerging issues.Sampling operations for intermediates, finished goods, raw materials and packaging materials.Execution of analytical method transfer.Emission of approved and rejected labels.Assignment and management of codes for analytical methods, impurities, reagents, reference standards and finished micronized products.Analyst status in relation to the software for the management of chromatographic data.Recording of analytical results.Cleaning the working environment.Control and substitution of silica gel used for the purpose of storing reference standard, retention samples and products under stability study.Compilation of the certificate of analysisVerification of the compiled in process control data sheetDi cosa hai bisogno per aver successoFor this role, the following qualifications are required:A Scientific Degree (e.g., Pharmaceutical Chemistry and Technology, Pharmacy, Biology, etc.);At least 2 years of solid experience in a pharmaceutical production environment (preferably APIs);Fluent knowledge of the English language is mandatory.Cosa devi fare oraIf you are interested in this opportunity, click on "Apply Now" to submit an updated copy of your CV. If this opportunity does not align with your expectations, but you are looking for a new job, visit our website to discover new opportunities. Candidates of both sexes, after viewing the mandatory privacy notice on the website www.hays.it, are requested to send their CV in Word format, indicating the reference (Ref. 948042) and their consent to the processing of personal data pursuant to D.LGS. 196/03. Min. Auth. No. 13/I/0007145/03.04 of April 1, 2008.#LI-DNI#948042 - Martina D''andrea#J-18808-Ljbffr