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Director, Manufacturing


Biogen is looking for a Director Manufacturing for the Large Scale Manufacturing plant in Hillerød.

Job Category


Requisition Number


Job Description

The Director Manufacturing is responsible for leading the manufacturing operations in the Large Scale Manufacturing plant. Manufacturing operations include personnel and activities related to the areas Cell Culture, Purification, Dispensary and Compliance. The Director is responsible for directing all strategic, tactical and operational aspects of the group. 

You manage the department budget, which includes developing, implementation, and tracking of department expenditures. You collaborate closely with our Corporate Headquarters and other sites to develop and implement systematic approach to continuous improvement. 
As a Director Manufacturing you insure the harmonization of practices across manufacturing groups/functions and across other Biogen manufacturing organizations. 
Additionally you provide global guidance in standards and practices.

The Director will provide overall directing for an organization encompassing up to 175 FTEs:
1. Develops and executes performance and organizational management for a staff composed of Manufacturing Associates, Supervisors and Managers. Directs tactical and operational activities for the manufacturing staff. Ensures personnel are adequately trained on processing activities and safety requirement to execute their roles per established procedures
2. Develops and maintains budget (expense and capital) for Bulk DS manufacturing. Performs budgetary tracking and decision making for department expenses, and capital expenditures for the site. Ensures review of batch records and resolution of manufacturing related issues for release of batches. Responsible for overall compliance with personnel and work place safety standards 
3. Develops capacity and resource assessments, which includes equipment capacities and human resource allocation and planning to ensure adequate staffing to meet production schedules. Provides leadership in the area of environmental and safety compliance, and ensures implementation of safety programs in manufacturing. Supports regulatory submissions and inspections.
4. Establishes metrics for the manufacturing group, and tracks progress against the target. Interfaces with cross functional department heads to oversees activities for manufacturing areas such as validation,maintenance, calibrations,up-grades,sampling and others. Participates on CMC core teams and lead team as required. 



You are able to influence without authority, facilitate groups with diverse perspectives and bring teams to consensus.
• Able to lead change and manage resistance to change.
• Ability to communicate effectively at all levels and present complex and/or new ideas with darity and simplicity.
• Excellent planning and organizational skills.
• Have a strong understanding of the finance/budgeting processes.
• Must be customer focused and able to deal with ambiguity.
• Able to develop a culture of continuous improvement across the site.

Fluency in written and spoken English is essential.


The ideal candidate has a Master's degree in a related Science /Engineering field with at least 12 years of strong leadership skills from a global pharmaceutical or biotech company.

Employment Category

Full-Time Regular

Experience Level


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