R&D Associate - Condoms ( 1 year Contract)
ประกาศจากแหล่งภายนอกคุณสมัครได้โดยตรง — เราจะพาคุณไปยังหน้าสมัครงานของบริษัท ไม่ต้องสมัครสมาชิก ไม่มีคนกลาง ไม่ต้องล็อกอิน ThaiJobz
เกี่ยวกับตำแหน่ง
As an R&D Associate, you'll lead product development projects for Durex, from concept to launch, ensuring innovative and high-quality products. This role requires strong project management, technical expertise in healthcare/FMCG, and regulatory compliance knowledge.
รายละเอียดงาน
About the role
As an R&D Associate, you will play a key role in delivering product development projects across the Durex R&D portfolio. You will lead end-to-end (E2E) projects from concept through to market launch, or take ownership of a specific workstream within larger, more complex technical projects, depending on business needs. Your work will contribute directly to the development of innovative, consumer-preferred products and support their successful transition into full-scale production and commercial launch.
This role requires the ability to work independently while collaborating effectively within a multidisciplinary project team. You will be responsible for balancing project opportunities, costs, timelines, and technical constraints to deliver high-quality outcomes. Strong organizational, technical, and problem-solving skills are essential, along with the ability to take ownership of key project deliverables and drive progress in a dynamic environment.
The role may also involve coaching or line management responsibilities for R&D Assistants or junior R&D Associates. Success in this position requires both theoretical and practical expertise in relevant Durex technologies, such as formulation and process development, as well as a solid understanding of applicable regulatory and legislative requirements.
This is an exciting opportunity for someone who is passionate about innovation, enjoys solving technical challenges, and wants to make a meaningful impact through the development of products trusted by consumers around the world.
Your responsibilities
- Lead and execute product development activities in line with agreed project timelines, proactively identifying and escalating risks or issues to ensure successful delivery.
- Collaborate with cross-functional teams, both internal and external, to achieve technical milestones and project objectives.
- Plan, coordinate, and support factory trials, product qualification testing, and validation activities prior to commercialization.
- Ensure product specifications, technical documentation, and development records are accurate, complete, and approved before full-scale production.
- Provide guidance and support to R&D Assistants and junior Associates, including coaching and development opportunities where applicable.
- Apply consumer insights and market understanding to support the design and development of consumer-preferred products.
- Balance product performance, technical robustness, quality requirements, and cost targets throughout the development process.
- Develop and implement effective evaluation methodologies to support sustainable, consumer-relevant product claims.
- Contribute to idea generation, concept development, and continuous improvement initiatives.
- Ensure intellectual property (IP) considerations are appropriately assessed and addressed during product development.
- Prepare, review, and communicate technical reports and project updates throughout the product development lifecycle.
- Ensure all development activities comply with applicable regulatory, quality, safety, health, and environmental requirements.
The experience we're looking for
- Minimum of an undergraduate degree in a scientific field relevant to the product technologies within the portfolio.
- Minimum of 3 years’ experience in either healthcare/FMCG product development or in the medicaldevice industry, with focus on design control, risk management, or quality management.
- Experience in line management is preferred but not essential.
Knowledge or experience in the following areas is preferred:
- ISO 13485 – Quality management systems for medical devices, especially product realisation.
- ISO 14971 – Risk management for medical devices, or other riskmanagement methodologies (e.g., FMEA).
- BS EN 62366 – Usability engineering for medical devices.
- Design controls.
The skills for success
- Results-oriented with strong planning, time management, and organizational skills, along with the ability to work independently and take initiative.
- Experience working within large multinational organizations and complex cross-functional environments.
- Adaptable and open to change, with the ability to challenge conventional thinking and generate innovative solutions.
- Strong communication and stakeholder management skills, with the ability to perform effectively under pressure and manage competing priorities.
- A proactive and entrepreneurial mindset, coupled with a passion for innovation and continuous improvement.
- Strong analytical and problem-solving capabilities, with a structured approach to decision-making.
สวัสดิการที่ได้รับ
คุณสมบัติผู้สมัคร
- ประสบการณ์
- 3-5 ปี
- การศึกษา
- ปริญญาตรี
