Flex Manager

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Project Manager

Project Manager

Work Experience

First 10 years project related experience in the chemical and petrochemical industries: project management, process engineering, commissioning and start-up management
Clients include: 3M, Borealis, Tecnimont, Broomchemie, BASF, Bayer, Kvaerner John Brown

Last 8 years: project related experience in the pharmaceutical industry: project management, conceptual studies, technical consulting and validation:
- manufacturing plants for sterile and non-sterile dosage forms
- infrastructure: clean rooms, HVAC, utilities,...

Clients include: Pharmacia/Pfizer, Janssen, GSK, Boehringer Ingelheim, Globopharm

DETAILS OF EXPERIENCE:
I. 3/2004 – now : Globopharm, A-VIENNA, Consultant for Basic Engineering
- Project : Major upgrade of the solids dosage facility of a third-party manufacturer
Reporting to : Project Manager of Pharmaplan Austria
- Responsibilities :
1. Conceptual study of the new plant
2. Specification of main equipment (Scope of Supply)

II. 5/2004 – 9/2004 : Glaxo-Smith-Kline, B-WAVRE, Consultant for Detailed Engineering
- Project : Thermal waste water decontamination system of a vaccine plant
Reporting to : Project Manager of Installation Subcontractor Fabricom GTI
- Responsibilities :
1. Review of data sheets and check consistency of all design information
2. Update of data sheets with vendor information
3. Calculation of heat exchangers / piping circuits / pumps

III. 2/2004 : GEA-Courtoy, B-Halle, Consultant for R&D of Tablet Press Manufacturer
- Project : Development of a new WIP tablet press
Reporting to : R&D Manager
- Responsibilities : Provide process knowledge for development of the new WIP press

IV. 10/2003 – 12/2003 : Pfizer, B-PUURS, Consultant for Specification of Equipment
- Project : Purchase of formulation vessels for sterile drugs
Reporting to : Pfizer Lead engineer
- Responsibilities : Inquiry documents (URS / Technical Spec / Scope book) and bid evaluation

V. 7/2003 – 9/2003 : Boehringer-Ingelheim, A-Vienna, Consultant for Quality Management
- Project: Writing of Quality Management Handbook for Project Execution
Reporting to: Boehringer-Ingelheim Project Manager


VI. 2/2003 – 6/2003 : Pfizer, B-PUURS, Consultant for Standardisation of Equipment
- Project : Standardisation of formulation vessel design specifications
Standardisation of sterile isolator specifications
Reporting to : Pfizer “Pharmaceutical Technical Support” Manager
- Responsibilities :
1. Collection of information on existing specifications in the plant
2. Bench marking on general industry practices
3. Production of the following standard documents for each of the 2 types of equipment
- User Requirements Specifications
- Technical specifications & Scope book
- Generic Project Validation Plan

VII. 1/2002 – 1/2003 : Pfizer, B-PUURS, Consultant for Equipment Design & Validation
- Project : Sterile suspension system: consisting of a sterile isolator to weigh and dispense highly toxic sterile powders that are brought into suspension in a connected high shear mixer system. Dedicated CIP and SIP facilities.
Reporting to : Pfizer Project Management
- Responsibilities :
1. Definition of operating principles of process and equipment and consultation with the various Pfizer departments involved
2. User Requirements Specifications and technical specifications of equipment
3. CGMP risk analysis of the process
4. Follow-up of detailed engineering of equipment
5. Project Validation Master Plan and validation strategy
6. Requirements for batch related tools, accessories and consumables
7. Preparation of budget

VIII. 9/2001 – 12/2001 : Pfizer, B-PUURS, Consultant for Equipment Design & Validation
- Project : Pre-engineering for upgrade of formulation department of sterile manufacturing facility with high containment design.
Reporting to : Pfizer Project Management
- Responsibilities :
1. Classification of products into groups according to quantity, toxicity, components, operations, …
2. Definition of operating principles of process and equipment for each group of products and consultation with the various Pharmacia departments involved
3. Requirements for batch related tools, accessories and consumables


IX. 12/98 – 8/2001 : Janssen Pharmaceutica, B-BEERSE, Project & Technical Manager, Solids Pilot Plant
- Project : Grass Roots Pilot Plant for Pharmaceutical Product Development
Oral solids dosage facility with high containment design (OEL3 compounds)
Equipment: isolators, DFB’s, powder handling, IBC’s, blender, granulation, tabletting, coating, capsule filling, spray liquid prep., solvent recovery, …
Reporting to : Janssen Pharmaceutica Project Director
- Responsibilities :
1. Supervision of 5 project & validation engineers
2. Design and layout of production areas
3. Specification and procurement of equipment (contained design)
4. Installation and commissioning of equipment
5. Validation & CGMP Risk Analysis of process equipment
6. Project organisation, planning, cost control and Progress reporting

X. 5/97 – 12/98 : Pfizer, B-PUURS, Project Manager
- Project : Modification and upgrading of sterile manufacturing facility: clean room remodelling, HVAC and utilities upgrade, relocation of existing equipment and installation of new equipment:
(1) Washing, sterilising and filling line for vials
(2) Capping and AOV lines
- Reporting to : Pfizer Engineering Management
- Responsibilities :
1. Co-ordination of the different project disciplines
2. Project organisation, planning, cost control & Progress reporting
3. Construction co-ordination and supervision
4. Validation of infrastructure and clean utilities

XI. 5/96 – 5/97 : KVAERNER JOHN BROWN / B-ANTWERP, Project Manager
- Project : Revamp acetylene converters / Fina Naphta Cracker 2
- Reporting to : John Brown Antwerp Office General Manager
- Responsibilities :
1. Co-ordination of the different project disciplines
2. Client contacts
3. Project organisation and planning / Monthly progress reporting
4. Process work during basic and detailed engineering and safety studies




XII. 12/95 - 4/96 : BAYER / B-ANTWERPEN, Project Engineer
- Project : DM 70 MM expansion project of the polycarbonate plant
- Reporting to : Project Manager
- Responsibilities :
1. Co-ordination with the engineering office and review of P&I D’s, equipment drawings,...
2. Project organisation and planning, monthly progress reporting
4. Assistance for processing of P&I D’s

XIII. 11/94 - 11/95 : BASF / B-ANTWERPEN, Assistant Project Manager
- Project : DM 75 MM debottlenecking of Caprolactam / Hydroxylamine /
Anon plants
- Reporting to : Project Manager
- Responsibilities :
1. Perform process study work / Calculations on selected items
2. Check data sheets and ordering of equipment
3. Follow-up of detailed engineering
4. Replace the project manager during his absence

XIV. 5/94 - 9/94 : BROOMCHEMIE / HOLLAND, Commissioning & Start-up Supervisor
- Process : Bromium Compounds : Slurry Batch Process
- Reporting to : Technical Manager
- Responsibility : Supervision of the start-up of a major extension of the plant

XV. 11/93 - 3/94 : TECNIMONT / IRAN, Start-up Supervisor
- Process : Polypropylene : Sferipol (Himont license)
- Reporting to : Commissioning Manager
- Responsibility : Supervision of acceptance testing for the new plant

XVI. 5/91 - 10/93 : BOREALIS Chemicals, B-BERINGEN, Process Design Engineer
- Processes : High Density Polyethylene : slurry loop reactor
Polypropylene : Sferipol (Himont)
- Reporting to : Engineering Manager
- Responsibilities :
1. Process studies and design
2. Trouble shooting

XVII. 11/89 - 4/91 : BOREALIS, B-BERINGEN, Commissioning & Start-up supervision
- Process : High Density Polyethylene : low pressure slurry loop reactor
- Reporting to : Start-up Manager
- Responsibilities : Catalyst Preparation Section
1. Supervision and training
2. Pre-commissioning
3. Commissioning
4. Supervision of the start-up

XVIII. 12/87 ? 10/89: 3M Belgium, B-ANTWERPEN, Project and Construction Management
- Process : Chemical plant / Low pressure batch reactors
- Reporting to : Engineering Manager
- Responsibilities : Overall project responsibility for concept/execution/budget
1. Process design and cost estimate
2. Follow-up of detailed design
3. Equipment specification and vendor contacts
4. Safety
5. Procurement and construction
6. Planning and cost control


Education

MSc Chemical Engineering
MBA

Skills

Design of plants for processing of potent (both sterile and non-sterile)compounds in the pharmaceutical industry

Languages

Working languages: German, English, French, Dutch
Basic skills: Italian, Arabic, Persian

Other

GMP training
CIP training
Computer literacy

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