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Develop Quality Compliance Specialist
2 weeks ago
This placement offers the chance to apply knowledge of quality, regulatory, and legal frameworks in a medical device industry setting.
Key Responsibilities- Work with your team leader and supervisor to identify a Quality/Regulatory Affairs improvement project, including objectives, scope, milestones, and evaluation.
- Communicate project updates and present at review forums.
- Assist in developing regulatory procedures and best practices.
- Help prepare technical documentation and submission packages for regulatory agencies.
- Ensure compliance with quality and safety systems.
- Be adaptable and dependable, with initiative.
- Currently pursuing a degree in Engineering, Science, or related fields.
- Honesty and integrity; compliance with quality systems, regulations, and policies.
- Self-motivated, flexible, and hardworking; enjoy working in a dynamic environment.
- Reliable, dependable, and punctual.
- Organized, focused, and capable of multi-tasking.
- Good analytical and problem-solving skills.
- Good communication skills and basic computer skills.
- Team player capable of working in a multi-disciplinary team.
- Available for 6, 9, or 12 months, with duration and start date to be discussed.
