Provide cross‑training, mentorship, and support to team members.
Actively contribute to continuous improvement in manufacturing, quality, and safety systems.
Requirements:
Degree in an engineering or scientific discipline.
3+ years' experience in validation/quality within medical device plastics processing, molding, or assembly operations.
Strong knowledge of c GMP and medical device regulatory requirements.
Excellent communication, organizational, and troubleshooting skills.
Ability to work independently and collaboratively, with strong prioritization and multitasking skills.
For a confidential conversation about the role please apply for the role or contact Owen Clancy at oclancy@sterlingengineeringeu.com By applying to this job post you agree that Sterling Engineering may process your personal data for recruitment.
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