At Bayer we’re visionaries, driven to solve the world’s toughest challenges and striving for a world where ,Health for all, Hunger for none’ is no longer a dream, but a real possibility. We’re doing it with energy, curiosity and sheer dedication, always learning from unique perspectives of those around us, expanding our thinking, growing our capabilities and redefining ‘impossible’. There are so many reasons to join us. If you’re hungry to build a varied and meaningful career in a community of brilliant and diverse minds to make a real difference, there’s only one choice.
Senior Principal Device Design Engineer (m/f/d)
Your tasks and responsibilities
You will plan, coordinate and execute Design Development and Life Cycle Engineering activities to successfully bring new Medical Device & Drug-Device Combination Products to the market and continuously improve the marketed Bayer Product Supply Product PortfolioYou will evaluate new and breakthrough technologies by applying theoretical engineering knowledge, to establish robust technical product requirements, and develop engineering design solutions to assure products maintain the required level of performance throughout the life of the productYou will provide author technical documentation (e.g. Design Development Plans, User Requirements Specifications, Design Inputs, Design Outputs, and DHF creation/ maintenance of DHF documentation), conformity assessments and risk management documentationYou will represent the design engineering team within global project teams and execute projects independently within the agreed time, quality, and cost constraints, resulting in state-of-the-art drug delivery systemsYou will actively offer technical consulting and manage the technical interfaces towards our internal and external development partnersYou will apply knowledge of the drug and medical devices regulatory landscape to ensure standard-compliant designs according to pharmacopeias (MDR, ISO 13485, 21CFR820, ISO14971, 21CFR820.30, ISO60601, ISO11608, ISO11040)You will ensure continuous improvement of our development and life cycle engineering processesYou will act as a recognized as global Subject Matter Expert to drive independent multiple technical activities like design transfers, root cause analysis and technical registration documentsYou will mentor/support less experienced design team members in complex projects and general skill development
Who you are
Bachelor’s degree in engineering or other science disciplines like pharmaceutical technology, mechanical engineering, pharmacy or equivalent required whereas Master’s degree in an engineering or scientific discipline is preferredMany years of work experience in the Medical Device & Drug-Device Combination Product industry (multiple Medical Device & Drug-Device Combination Product functions preferred, product development, new product introduction/ industrialization, design verification, design transfer)A few years of experience leading product development activities and projectsBroad and deep understanding of a variety of applicable standards and regulations (e.g., 21CFR820, ISO-13485, ISO-11607, ISO-14971, ISO-10993, ISO-11137, ASTM 4169, etc.) is requiredDemonstrated experience at utilizing Design Control processes to develop, launch and sustain medical devices and combination productsExperience with managing/coordinating the work of other internal and external design team members.Knowledge of multiple technologies, such as injection molding, tool design assembly (manual & automated), sterilization, labeling & packagingFamiliarity with equipment, test methods and best practices applicable to the verification of product designsStrong quantitative and qualitative analytical background and skills to understand and interpret analytical results (e.g. dissolution testing, functional and physical testing)Good statistical background and very good IT skills (e.g., Excel, Minitab)Experience leading small teams, demonstrating a collaborative leadership styleAbility to initiate and execute complex projects by leveraging cross-functional relationshipsFluency in English and German
What we offer
Our benefits package is flexible, appreciative, and tailored to your lifestyle, because: What matters to you, matters to us!
We ensure your financial stability through a competitive compensation package, consisting of an attractive base pay and our annual bonus. In addition, managers can recognize special contributions by granting an individual performance award.Whether it’s hybrid work models or part-time arrangements: Whenever it is possible, you will have the flexibility to work how, when and where it is best for you.Your family is a top priority. We offer loving company daycare centers at multiple locations, support in finding childcare, time off for the care of elderly or dependent family members, summer camps for children, and much more.We support your professional growth by providing access to learning and development opportunities, training programs through the Bayer Learning Academy, development dialogues, as well as coaching and mentoring programs.We embrace diversity by providing an inclusive work environment in which you are welcomed, supported, and encouraged to bring your whole self to work.
Be You. Be Bayer.
YOUR APPLICATION
This is your opportunity to tackle the world’s biggest challenges with us: Maintaining our health, feeding growing populations and slowing the rate of climate change. You have a voice, ideas and perspectives and we want to hear them. Because our success begins with you. Be part of something big. Be Bayer.
Bayer welcomes applications from all individuals, regardless of race, national origin, gender, age, physical characteristics, social origin, disability, union membership, religion, family status, pregnancy, sexual orientation, gender identity, gender expression or any unlawful criterion under applicable law. We are committed to treating all applicants fairly and avoiding discrimination.
Location: Germany : Berlin : Berlin
Division: Pharmaceuticals
Reference Code: 849997