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Technical transfer technician (pharma manufacturing)

Barberà del Vallès
Siegfried
Publicada el 24 octubre
Descripción

PAt its locations around the world, Siegfried offers employees exciting career opportunities in international settings. We cultivate multidisciplinary cooperation and encourage our staff to actively shape and influence their careers. This approach, coupled with our dynamic working environment, make Siegfried an attractive employer. /ppbr/ppstrongYour role: /strong /ppbr/pulliComprehensive Product Management: Oversee the entire commercial lifecycle of the product, from its transfer by development to the present date, acting as the Single Point of Contact (SPOC). /liliRisk Analysis and Quality Control: Create, update, and monitor the product-specific Quality Risk Analysis (QRA) and ensure compliance with quality standards. /liliData Monitoring and Analysis: Evaluate critical and key variables through statistical analysis, track data trends, and review the Annual Product Quality Review (APQR) to make informed decisions regarding control status. /liliInspection Readiness: Ensure all aspects related to the product process are prepared for audits and regulatory inspections. /liliPerformance Monitoring and Improvement: Identify trends, detect issues, and lead the implementation of corrective and preventive actions (CAPAs) to enhance products. /liliDeviation Management and Improvement Projects: Investigate process deviations, lead optimization projects, and engage cross-functional teams in improvement initiatives. /liliIn-Process Controls (IPC) Monitoring: Ensure the tracking of critical parameters in laboratories and guarantee that data is visible and communicated at the plant level. /liliTechnical Change Assessment: Analyze the impact of process modifications, determine their feasibility, and manage the quotations associated with these changes. /liliProcess and Product Validation: Ensure continuous validation status, alignment with the APQR, and implementation of control strategies based on Critical Quality Attributes (CQA), Critical Process Parameters (CPP), and Critical Material Attributes (CMA). /liliProduct Launch and Transfer: Facilitate product transfers by ensuring technical documentation and providing necessary support to the receiving plant. /liliManufacturing Optimization and Excellence: Lead improvement projects to enhance the robustness and sustainability of pharmaceutical processes in collaboration with Operational Excellence (OPEX). /li /ulpbr/ppstrongYour profile: /strong /ppbr/pulliUniversity degree in a scientific field or related, or a higher vocational training degree in a scientific field with previous experience in a similar position. /liliHigh level of English. /liliExperience in a similar technical position and in the pharmaceutical sector. /liliKnowledge of data management and application of statistical techniques. /li /ulpbr/ppbr/ppstrongWorking at Siegfried /strong /ppbr/ppstrongBenefits: /strong /ppbr/pulliAnnual Bonus: 7.5% /liliTwo days of home office per week /liliFree parking /liliGood public transport available to reach the site /liliSubsidized canteen on-site or restaurant ticket: to use when eating out or working from home /liliMedical, life, and accident insurance /liliAccess to "Club Siegfried": an exclusive platform with discounts and offers on over 400 services /li /ulpbr/ppSiegfried's work environment is dynamic and international. With a highly professional and motivated team, the company operates in a future-oriented business field. Siegfried possesses a unique culture that leverages cultural differences to create a competitive advantage. Siegfried places highest priority on providing a flexible, diverse and discrimination-free working environment in which employees can develop personally and professionally, advance innovation and deliver superior performance. We strive to provide a work environment where employees can take on challenging jobs and associated responsibilities that best serve their personal and technical development and can benefit from the success of our company. The company regulations in respect of compensation and career development opportunities apply to all Siegfried sites. Additional conditions of employment are governed by location-specific circumstances, legislation and customs. /ppbr/ppbr/ppIn the Midst of People’s Lives – Across the Globe /ppThe Siegfried Group is one of the world’s leading Custom Development and Manufacturing Organizations (CDMOs) developing and producing active pharmaceutical ingredients (API), intermediates and finished dosage forms. As our core competence, we successfully integrate chemical and pharmaceutical capabilities into a single business model. /ppThe Siegfried name stands for highest quality, efficiency, flexibility and safety. Present in Europe, Asia and North America, we serve a broad global customer base from major international pharmaceutical companies down to small biologic-pharmaceutical organizations. For them we develop and produce product innovations on a large scale to finished products. We integrate our offer seamlessly into the customers’ value chain. Our comprehensive services range from early-stage Research Development services such as synthesis, scale-up, formulation development, stability studies and method development all the way through to manufacturing services, ranging from preclinical RD material for clinical trial purposes to commercial production. /ppWe are able to produce about 200 of the approximately 1500 registered drug substances used in medicine. Moreover, we produce 20 percent of global demand for caffeine. Consequently, nearly 1 billion individuals come into contact with Siegfried products. /p

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