Senior Project Engineering Manager

☞ Ferring Pharmaceuticals, Inc.

View: 142

Update day: 26-03-2024

Location: Saint-Prex Vaud VD

Category: Pharmaceutical / Chemical / Biotech

Industry:

Job type: Temps plein, Temps de travail : 90-100%

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Job content

Job Description:
Your Mission
The Senior Project Engineering Manager will be responsible for planning, leading and managing the engineering, EHS, construction, commissioning and qualification of the different projects within Ferring’s Global Engineering Department in close collaboration with other involved departments and stake holders (Country General Manager, Site Head, Production, QA, Finance, legal, procurement, CIS …) in a matrix organization. He will be the representative of Ferring Global Engineering for the day to day management of the projects, coordination with local Engineering Contractors, Control of the Budget & Schedule, Reporting of the project health, Monitor the Engineering, Construction, Commissioning and Qualification Activities. The Senior Project Engineering Manager will report to Ferring Global Engineering for the Technical and financial parts of the Project.
Your Responsibilities:
  • Plan and lead projects through the Engineering, Design, Construction, Commissioning and Qualification phases with the help of Local & Global Engineering, Contractors and Ferring involved departments
  • When relevant, build up the local Engineering and Maintenance Organisation for the new facility by hiring engineers / technicians for the various disciplines: Mechanical, HVAC, Electrical, Control Systems etc.
  • Provide Engineering Expertise and be the interface between Ferring Global Engineering and local Engineering / Maintenance, Contractors, other Ferring departments according to the project organisation set-up
  • EHS responsible for the duration of the project, provide technical support for the installation checks during the construction of the facility, provide support for the commissioning and star-up of the facility, provide qualification support for the new facility
  • Manage all contacts with local authorities for permitting, environmental, waste disposal, construction zone and facility cleaning etc.
  • Coordinate activities with the Engineering & Maintenance Department of the existing sites or neighbouring Production site
  • When needed (i.e. green field), provide support for all future maintenance activities and prepare maintenance schedule; Spare parts: support for the purchase and management
  • Prepare for the Maintenance Management System implementation in line with Ferring standards
  • Schedule and plan all future calibration activities – calibration schedule
  • Organise preparation of Maintenance and Calibration SOP’s for the new Facility
  • Coordinate the training of Engineering & Maintenance Personnel for the new Facility
  • Ensure good coordination between all Ferring’s involved departments (R&D, LQA & GQA, Legal, procurement, Production, LSC & GSC, organisation where required)
  • Apply LEAN methodology and tools
  • Facilitate LEAN activities and workshops including Visual management, Obeya, Gemba, Pull planning
  • Facilitate or support continuous improvement activities (A3, PDCA) and actively participate in the realization of solutions utilizing the appropriate Lean approach
Required Experience & Competences
  • Degree in Engineering, Pharmacy, Chemistry or Chemistry Engineering
  • 7-10 years’ experience in engineering related roles in the pharmaceutical industry
  • At least 5 years’ experience in manufacturing industry (preferably in API manufacturing) with demonstrated project execution experience
  • Broad technical knowledge of the Various Engineering Disciplines in the Pharmaceutical environment, both on clean and black utilities, process and packaging equipment, automation, Instrumentation and Civil Engineering
  • Using software such as MS-Word, Excel, Autocad, Product Design Specification (PDS) and should have extensively used Project IT Tools like MS- Projects, etc.
  • Deep knowledge of quality assurance and cGMP and good working knowledge of DS and DP manufacturing, GMPs, and FDA
  • Task orientated, analytical person who is very comfortable working towards set objectives and has a track record of achieving results in this regard
  • Team player happy to be in an international and multicultural environment
  • Excellent communication and presentation skills and able to communicate with stakeholders at all levels
  • Good knowledge of various types of pharmaceutical dosage form, in particular sterile products
  • Good command of English, French and any other language (verbal & written)
  • Good influencing and negotiation skills
  • Strong ability to plan, organize and set priorities
Location:
Switzerland HQ - St-Prex
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Deadline: 10-05-2024

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