Responsibilities:
Drive validation activities across the product lifecycle, including IQ/OQ/PQ protocol development and execution.
Apply APQP methodologies to support new product introductions.
Perform statistical analysis on product and process data to ensure compliance with internal and external standards.
Collaborate with cross-functional teams to optimize manufacturing processes and support quality assurance deliverables.
Contribute to continuous improvement and quality strategy initiatives. Requirements:
3+ years of experience in a quality engineering role, ideally within medical or pharmaceutical manufacturing.
Strong understanding of validation processes and advanced proficiency in Minitab (not just basic knowledge).
Familiarity with plastic injection moulding and GD&T is a plus.
Excellent communication skills, including a clear and confident speaking voice for customer interactions.
Bachelor's degree in engineering or a related technical discipline.