documented and implemented in line with quality standards.
Collaborate with cross-functional teams (Engineering, Manufacturing, Supply Chain, Quality) to implement quality improvements, in line with the BioPure / WMFTS Quality Strategy.
Support validation activities by ensuring the development and maintenance of validation protocols, procedures, and documentation in line with global policy and process.
Be part of the internal audit team, conducting and generating audit reports to drive process improvements.
Provide training, coaching and guidance on quality tools, systems, and best practices to colleagues and stakeholders.
Promote a culture of quality, continuous improvement, and risk-based thinking throughout the product lifecycle and across all functions.
Skills/Experience:
Minimum of 3 years’ experience in Quality Assurance within a regulated industry.
Proven working knowledge of ISO 13485 and ISO 9001 standards.
Strong ability to engage and communicate effectively with cross-functional stakeholders.
Demonstrated expertise in product and process validation methodologies.
In-depth understanding of the design and development lifecycle.
Proficient in conducting internal audits; lead auditor certification is highly desirable.
Established track record in driving continuous improvement initiatives and applying lean methodologies.
Advanced problem-solving capabilities, including root cause analysis and effective CAPA (Corrective and Preventive Action) management.
Excellent communication, planning, and organisational skills
Resilient and delivery-focused, with a strong ability to manage change in dynamic environments
At Watson-Marlow, we believe in taking care of our colleagues. We offer a generous benefits package, including:
