Skill Set Overview:
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1. Demonstrate a strong understanding of cGMP and regulatory requirements.
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2. Show evidence of excellent analytical and problem-solving skills.
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3. Possess strong communication and interpersonal skills.
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4. Demonstrate ability to work effectively in a team environment.
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5. Hold a qualification and/or degree in engineering or a scientific discipline.
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6. Have 3+ years of validation/Quality experience in medical device plastics processing, moulding, or assembly operations.
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About This Opportunity:
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This QAV Engineer role offers a unique opportunity to apply your technical expertise and problem-solving skills to drive process improvements and ensure compliance with industry regulations. As a key member of our team, you will have the chance to work on challenging projects, develop your skills, and contribute to the success of our organization.