Business Planning

1 week ago


Paisley, Renfrewshire, United Kingdom MM Search Full time
MM Search are delighted to be working with Turemo Aortic on their new Director of Manufacturing Operations role

The director of manufacturing will provide leadership to the manufacturing team while managing personnel and processes involved in their assigned area of responsibility.

The director is responsible for creating a culture of continuous improvement by developing people who are capable of problem solving to achieve strategic and business objectives.

The position is based in the Glasgow facility.

Develop and execute a manufacturing strategy to achieve key long-term growth, profitability, and capability goals.

  • Collaborate with cross-functional teams to integrate manufacturing processes with other departments such as HR, R&D, Quality, Regulatory, and Supply chain.
  • Ensure that manufacturing capability best supports internal and external customer requirements for safety, quality, speed, and cost.
Provide leadership to the Manufacturing departments to ensure consistent behaviours and progress to department strategic goals.

  • Management of manufacturing costs ensuring that they track in line with Manufacturing P&L requirements
  • Reporting and tracking of all KPI's for Manufacturing Departments in line with business goals
  • Supporting the transfer of projects/devices into full manufacturing
  • Lead the team to meet Safety, Quality, Delivery, Inventory, and Productivity goals (SQDIP).
  • Ensure an effective site daily management system is in place.
  • Oversee the day-to-day operations of the manufacturing team.
Champion lean manufacturing principles throughout the organization, creating a continuous improvement culture.

  • Seek new methods of manufacture to improve quality, reduce cost, improve efficiency or shorten cycle time in close collaboration with engineering and quality.
Talent Development

  • Lead the teams ensuring goals and objectives are in place to support the business goals and progress both team and individual development delivering high performance Lead, develop, and mentor managers, engineers, supervisors, and other professional staff.
  • Regulatory and Quality System compliance
  • Maintain a robust quality management system to support and improve product quality while ensuring regulatory compliance.

QUALITY REQUIREMENTS:
Ensure compliance with all quality systems regulatory requirements such as, but not limited to, ISO 13485, 21 CFR Part 820, MDSAP, MDD (93/42/EEC) and MDR (EU 2017/745)
Ensure compliance with all Environmental Health and Safety regulatory requirements.
Ensure related Risk Assessments are completed, accidents raised and action hazards.

Applies business understanding.

o High level of financial acumen including understanding of operations impacts to the income statement, statement of cash flow, and the balance sheet.

o Completes individual and leads large project teamwork activities as assigned demonstrating ability to effectively manage overall productivity and deliver strong results.

Bachelor's degree or appropriately equivalent experience in the industry,

  • Experience in leading a structured strategy deployment process.
  • Ability to organize and manage projects and work independently.
  • Excellent oral and written communication skills (English)
  • Working knowledge of an ERP software such as SAP, Oracle, or JD Edwards, etc
  • At least 7 years in a biotechnology/medical device industry
  • At least 5 years' experience in manufacturing management
  • Deep understanding of quality system regulations (ISO13485, 21CFR820)


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