02.05.24 | Vollzeit, Praktikum | Main-Kinzig-Kreis | Procter & GambleIn P&G Health. In a dedicated team of scientists (pharmacists, nutritionist and other life sciences), you will work on diverse tasks concerning medicinal products and food supplements or cosmetics. You will work in an international environment in Regulatory Affairs on product life cycle management
Später ansehen28.04.24 | Vollzeit | Wertheim | www.gerresheimer.com1. Job details Head Regulatory Affairs (m/f/d) Solothurnerstrasse 235, Switzerland Olten Full-time Job Description As Head of Regulatory Affairs you will manage a team of currently 4 internal employees. The group is responsible for global submissions and requirements related to Class I, II and III
Später ansehen21.04.24 | Vollzeit | Wertheim | www.gerresheimer.comHead Regulatory Affairs (m/f/d) Solothurnerstrasse 235, Switzerland Olten Full-time Job Description As Head of Regulatory Affairs you will manage a team of currently 4 internal employees. The group is responsible for global submissions and requirements related to Class I, II and III medical devices
Später ansehen02.05.24 | Vollzeit, Praktikum | Main-Taunus-Kreis | Procter & GambleConcerning Rx and Over-the-counter medicinal products and food supplements. You will work in an international environment together with other departments like Regulatory Affairs, Marketing, Legal, Quality etc. on product ideas, product offers, evaluation of marketing concept and new product developments
Später ansehen28.04.24 | Vollzeit | Wertheim | www.gerresheimer.comLaw and regulatory compliance - May evaluate, select, and oversee vendors that provide supplemental HR processes and services - Coordinates with HR support staff to process and maintain employment, attendance, and other records - Review timesheets, code in HRIS, and submit to payroll for processing
Später ansehen28.04.24 | Vollzeit | Wertheim | www.gerresheimer.comFocus - Experienced in the FMEA method for medical devices - Practical experience in the application of quality and problem-solving techniques - Knowledge of the interpretation and implementation of regulatory requirements for medical devices (MDR, EN ISO 14971, 21 CFR 820, EN 13485) - Experience
Später ansehen28.04.24 | Vollzeit | Wertheim | www.gerresheimer.comFocus - Experienced in the FMEA method for medical devices - Practical experience in the application of quality and problem-solving techniques - Knowledge of the interpretation and implementation of regulatory requirements for medical devices (MDR, EN ISO 14971, 21 CFR 820, EN 13485) - Experience
Später ansehen28.04.24 | Vollzeit | Wertheim | www.gerresheimer.comTests Perform a variety of laboratory tests and analyses to assess the quality and performance of raw materials, intermediate products, and finished goods. - Quality Assurance Procedures Execute and maintain quality assurance procedures and protocols to ensure compliance with regulatory standards
Später ansehen28.04.24 | Vollzeit | Wertheim | www.gerresheimer.comDisciplines. - Lead and coordinate cross-functional project teams consisting of engineers, designers, regulatory experts, quality assurance specialists, and manufacturing personnel. - Develop project plans, timelines, and budgets, and ensure adherence to project milestones and deadlines. - Collaborate
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