Regulatory Affairs Manager Equipment
pbFrom Strategy to international Approval. /b You develop regulatory strategies for our electrical devices, coordinate international product registrations, and manage them throughout the entire product lifecycle. /p h3Your role /h3 ul liYou will support the implementation of regulatory requirements for our electrical equipment (ovens, milling machines, etc.) and share responsibility for creating and maintaining national and international technical documentation. /li liTogether with Product Development, Sales, and Marketing, you will develop the regulatory approval strategy, successfully implement it, and reliably manage deadlines and timelines. /li liYou will coordinate international product registrations—from new registrations and amendments to deregistration—in collaboration with subsidiaries, local partners, and regulatory authorities. /li liYou will use your expertise to support other departments with complaints, Non-Conformities (NCs), and Corrective and Preventive Actions (CAPA). /li liYou will monitor regulatory developments and assess the impact of changes on registrations. /li liYou will work as part of project teams. /li /ul h3Your profile /h3 ul liBachelor’s degree in medical technology, electrical engineering, electronics, mechanical engineering,
or a comparable qualification /li liSeveral years of experience in regulatory affairs for electrical devices and medical devices is a plus /li liIn-depth knowledge of regulatory requirements for electrical devices, machinery, and medical devices, as well as international approval requirements, is desired /li liA structured, independent work style and a passion for cross-functional collaboration /li liA pragmatic approach and a strong focus on finding solutions /li liExcellent German and English language skills, additional languages are a plus /li /ul h3What
We Offer
/h3 ul liA global, purpose-driven company with 3,700 employees. /li liA culture of innovation and collaboration. /li liLearning and development tailored to your growth. /li liAttractive benefits. /li /ul pFor this full-time position (40 hours per week), the gross annual salary starts at 44,000 EUR and a variable premio based on the company's earnings. Actual compensation will be determined based on professional qualifications, relevant work experience, and the skills required for the position. Salary classification is in accordance with the applicable working agreement for the rubber and plastics processing industry. /p #J-18808-Ljbffr
or a comparable qualification /li liSeveral years of experience in regulatory affairs for electrical devices and medical devices is a plus /li liIn-depth knowledge of regulatory requirements for electrical devices, machinery, and medical devices, as well as international approval requirements, is desired /li liA structured, independent work style and a passion for cross-functional collaboration /li liA pragmatic approach and a strong focus on finding solutions /li liExcellent German and English language skills, additional languages are a plus /li /ul h3What
We Offer
/h3 ul liA global, purpose-driven company with 3,700 employees. /li liA culture of innovation and collaboration. /li liLearning and development tailored to your growth. /li liAttractive benefits. /li /ul pFor this full-time position (40 hours per week), the gross annual salary starts at 44,000 EUR and a variable premio based on the company's earnings. Actual compensation will be determined based on professional qualifications, relevant work experience, and the skills required for the position. Salary classification is in accordance with the applicable working agreement for the rubber and plastics processing industry. /p #J-18808-Ljbffr