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Director Manufacturing Engineering

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1 Vacancy
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Job Location drjobs

Cincinnati, OH - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Work Schedule

Standard (MonFri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards Fluctuating Temps hot/cold Loud Noises (Equipment/Machinery) Office

Job Description

Thermo Fisher Scientific Inc. is the world leader in serving science with annual revenue exceeding $40 billion. Our Mission is to enable our customers to make the world healthier cleaner and safer. Whether our customers are accelerating life sciences research solving complex analytical challenges improving patient diagnostics and therapies or increasing efficiency in their laboratories we are here to support them.

Group/division summary

The Pharma Services Group (PSG) is redefining the way pharmaceuticals are made with a simplified endtoend supply chain for pharmaceutical and biopharmaceutical companies of all sizes.

Position summary

The Director Engineering will operate within the organizational structure to provide direction and management guidance to Capital Engineering Validation Utilities Automation and Maintenance activities. In addition to leading the development and implementation of technical support strategies this role sits on the sites leadership team and interacts with the other directors and site General Manager to realize complimentary overall site strategies that meet the shortterm and longerterm goals and objectives. Extensive customer interaction is required related to business development proposals opportunities audits and regulatory authorities.

Key Responsibilities:

  • Provides leadership to their team specifically: leading organizational change; developing and empowering staff; cultivating relationships; putting staff in a position to succeed by facilitating their personal career goals while also achieving organizational goals; building effective teams that apply their diverse skills and perspectives to achieve common goals; driving engagement and creating a climate where employees are motivated to do their best.
  • Set tactical and strategic policy leadership and direction in engineering validation utilities and systems in compliance with SOPs GAPs cGMPs and other site procedures.
  • Lead the Site Master Planning to assure site can achieve STRAP this includes utility/facility/equipment planning.
  • Responsible for site CAPEX planning in a 5year view and . CAPEX in excess of $25M per year investment in the site.
  • Build socialize and deliver on cases for growth sustainment compliance and efficiency projects.
  • Ensures that all parties interacting with technical support are aligned in shared tactical & strategic approaches.
  • Develops capital and expense budgets.
  • Ownership of the site coop program.
  • Directs and leads the technical aspects (process equipment automation cleaning validation programs process maintenance and process and project engineering functions) supporting the business strategy.

Qualifications:

BS in Engineering

8 years of shown experience in a relevant field that includes at least 8years of management experience

Pharmaceutical manufacturing experience in OSD preferred

Effective written interpersonal and presentation skills

Ability to work on multiple projects simultaneously

Equivalent combinations of education training and meaningful work experience may be considered

Ability to drive functional technical and operational excellence.

Ability to inspire and champion innovation teamwork clarity and team effectiveness.

Analytical mentality

Ability to handle ambiguity.

Experience with influencing within cross function teams


Required Experience:

Director

Employment Type

Full-Time

Company Industry

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