Material Developer at Mölnlycke in Gothenburg

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Job Description

<h3>If you’re ready to have an impact in a career that makes a difference, Mölnlycke could be your next step. You’ll be helping to equip medical professionals around the world with solutions to improve outcomes for patients. And you’ll be developing yourself in a global environment with an inspirational culture, with lots of opportunities. All the while building a successful career, with real purpose.</h3><p>Mölnlycke is now looking for a <strong>Material Developer</strong> to join our R&D Wound Care team out of our headquarters in Gothenburg.</p><h3>About the job</h3><p>We are looking for a Material Developer to support the development and implementation of new and improved materials for Mölnlycke products in order to meet customer needs and improve product sustainability, as well as rationalizing and reducing the cost of products in order to improve profitability and to secure supply. You’ll be working in a fast-changing and exciting environment where, you will be both driving change projects and manning development projects with need for material expertise.</p><h3>These are the main accountabilities for this position</h3><ul><li>In this position you will be accountable to deliver in assigned design control roles and within the assigned material area to; plan, develop, deliver and document material solutions in assigned role in design control projects. You’ll have focus on material solutions in development and change projects.</li><li>You will ensure that material documentation for assigned materials is up to date and compliant and for maintaining and developing knowledge of materials within the assigned area. You’ll secure supply of existing materials by working with internal partners and material suppliers within the assigned material area and propose new product ideas leveraging on new material opportunities.</li><li>You will develop and improve existing material solutions and identify new potential suppliers within assigned area and continuously monitor and suggest new materials and/or alternative suppliers within the assigned area.</li></ul><h3>What you’ll need</h3><ul><li>Master's degree or Bachelor's degree in engineering, chemistry, life science or equivalent</li><li>Technical Knowledge in materials and related medical device</li><li>Understanding of Customer and end user needs including competitor knowledge</li><li>Knowledge of Global Regulatory Requirements and standards related to the material areas and related medical device.</li><li>Deep knowledge in QMS and Design control</li><li>Communication skills</li><li>Fluent English written and spoken</li><li>General business acumen</li></ul><h3>What you’ll get…</h3><ul><li>Wellness benefits</li><li>Flexible working hours</li><li>Great colleagues in a global company</li><li>An open, friendly and fair working atmosphere</li><li>Competitive compensation package including company pension plan, bonus, company health care</li></ul><h3>Our approach to diversity and inclusion</h3><p>At Molnlycke diversity is not just a vision, but our strength. We are dedicated to fostering an inclusive workplace that values and celebrates the power of diversity. At the heart of our commitment is the belief that diversity fuels innovation, creativity and problem-solving. We invite you to be a part of a team where authenticity is embraced, and every employee, regardless of background or any other traits, experiences a true sense of belonging. Your attitude, drive, enthusiasm, and eagerness to learn are just as important to us as the requirements for the role.</p><h3>About Mölnlycke</h3><p>Mölnlycke is a world-leading medical products and solutions company that equips healthcare professionals to achieve the best patient, clinical and economic outcomes. Our business is organized in the four business areas Wound Care, Operating Room Solutions, Gloves and Antiseptics, where customer centricity, sustainability and digitalisation are at the heart of everything we do.</p><p>Mölnlycke employs around 8,700 people. The company headquarters are in Gothenburg, Sweden and we operate in more than 100 countries worldwide. Mölnlycke is a founding partner of GoCo Health Innovation City, a world-class innovation cluster for health, and in early 2025 our headquarters will move there. Since 2007, the company has been part of Investor AB, an engaged owner of high-quality, global companies which was founded by the Wallenberg family in 1916. For more information, please visit <a href="http://www.molnlycke.com">www.molnlycke.com</a> and <a href="http://www.molnlycke.com/careers">www.molnlycke.com/careers</a></p><p>If this sounds like you and you feel you have what it takes to succeed in this role, we want to hear from you as soon as possible.</p>#LI-Hybrid

AI Powered Job Insights

Mölnlycke is seeking a Material Developer to join their R&D Wound Care team at their Gothenburg headquarters. This position offers an exciting opportunity to contribute to the development and implementation of innovative material solutions that enhance patient care and product sustainability.

📍 Location: Gothenburg  
💼 Position: Material Developer  
📅 Date Posted: 2024-07-03  

Role Summary:  
- Take technical ownership and build expertise within material technologies.  
- Collaborate within cross-functional teams and engage with various stakeholders and external suppliers.  
- Drive change projects and lead development initiatives focused on material expertise.

What You'll Do:  
- Develop and document material solutions within assigned design control projects.  
- Maintain and update material documentation to ensure compliance.  
- Collaborate with internal partners and suppliers to secure the supply of existing materials and propose new product ideas.  
- Identify and monitor new materials and potential suppliers.

What's Needed:  
- Master’s or Bachelor’s degree in engineering, chemistry, life science, or equivalent.  
- Technical knowledge in materials related to medical devices.  
- Understanding of customer needs and competitor insights.  
- Familiarity with global regulatory requirements and QMS.  
- Excellent communication skills and fluency in English.  
- General business acumen.

Top Interview Questions

  • Q: Can you describe your experience with materials development in a medical device context and how it relates to understanding customer needs?

    A: In my previous role, I was directly involved in developing biodegradable materials for wound care products. I conducted user interviews with healthcare professionals to understand their requirements, which allowed me to align our material selection with their needs for ease of use and patient safety. Additionally, I monitored competitive products to ensure our offerings were superior, demonstrating a balance between innovation and market demands.

  • Q: How do you ensure compliance with global regulatory requirements and standards for materials used in medical devices?

    A: To guarantee compliance, I stay updated on relevant regulations from agencies such as the FDA and ISO standards by attending workshops and engaging with professional organizations. In my past projects, I developed a comprehensive checklist aligned with these regulations and worked closely with the quality assurance team to review and update documentation. This proactive approach helped us achieve timely approvals for our products.

  • Q: Describe a time when you had to collaborate with cross-functional teams to drive a material development project. How did you ensure effective communication?

    A: In a recent project aimed at enhancing wound dressing materials, I collaborated with R&D, quality assurance, and marketing teams. I initiated weekly meetings to track progress and shared updates via a project management tool. To ensure everyone was aligned, I created visual materials summarizing key points and decisions, which helped maintain clarity and fostered a collaborative environment. This facilitated timely feedback and allowed us to meet our launch deadlines.

  • Q: What methods do you use to evaluate new material opportunities or potential suppliers in the medical device industry?

    A: When evaluating new materials, I conduct a thorough analysis that includes literature reviews, supplier assessments, and benchmarking against existing materials. I prioritize suppliers with a solid track record in the medical device realm. For instance, in a previous role, I developed a scoring system based on criteria such as cost, compliance, and performance to guide our supplier selection process, ensuring we chose the best partners for our material needs.

  • Q: How do you approach the challenge of improving product sustainability in material development while maintaining product performance?

    A: I believe that sustainability can be achieved without sacrificing performance by using innovative materials and technologies. In my last project, I explored alternative sources of biopolymers that not only met performance criteria like tensile strength and moisture control but also reduced our carbon footprint. We conducted extensive testing to ensure these materials performed as well as, or better than, traditional options, ultimately leading to a successful launch that resonated well with environmentally-conscious customers.

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