Francesc Pont

Francesc Pont Email and Phone Number

QA oversight for Engineering and CAPEX projects @
Francesc Pont's Location
Marburg an der Lahn, Hesse, Germany, Germany
Francesc Pont's Contact Details

Francesc Pont personal email

n/a
About Francesc Pont

A hands on and highly committed manager (director level) and experienced leader of production and quality management units in the GMP field of the pharmaceutical industry with increasing responsibilities in the manufacturing of plasma-derived and recombinant therapeutic products including but not limited to: chromatographic purification, formulation, aseptic filling, lyophilization, visual inspection and labeling & packaging. I am a diplomatic and supportive leader with excellent communication skills and a proven record of building, inspiring and motivating teams to innovate and achieve the highest standards through effective line management.

Francesc Pont's Current Company Details
CSL Behring

Csl Behring

QA oversight for Engineering and CAPEX projects
Francesc Pont Work Experience Details
  • Csl Behring
    Global Quality Engineering Lead
    Csl Behring Sep 2021 - Present
    Providing Quality Assurance Oversight for Engineering and capital investment projects.
  • Csl Plasma
    Global Lead Quality Csl Plasma
    Csl Plasma Feb 2018 - Sep 2021
    Quality Assurance and Quality Control for collection centers, plasma logistics and release, supplier quality management, and lab QA, ensuring all plasma for further manufacture supplied meets the requirements of licensed CSL Behring product dossiers and all processes are in compliance with relevant quality standards, regulations, legal and company-specific requirements.
  • Csl Behring
    Head Of Quality Final Product
    Csl Behring Nov 2015 - Jan 2018
    Melbourne, Victoria, Au
    Leadership, management and development of the Quality Assurance department for final product (Quality Final Product) at the CSL Behring GmbH site in Marburg in line with company strategies to ensure compliance with current regulatory / GMP requirements. Accountable for batch- and validation-related QA support, deviation management, operational Quality support to projects in R&D and Production, stability studies, Quality-related crisis management for all final products manufactured and /or released or distributed in the responsibility of CSL Behring GmbH, including products for clinical trials.
  • Csl Behring
    Head Of Quality Management Production
    Csl Behring Apr 2010 - Oct 2015
    Melbourne, Victoria, Au
    Leader of the Quality Management Delegates in Marburg supporting the Marburg manufacturing departments. Responsible for developing and driving continuous improvement initiatives in collaboration with other departments to ensure drug safety, Legality, and Quality through effective Quality Systems and coordinate respective actions for the site products in compliance with relevant quality, regulatory, and company-specific requirements and guidelines.
  • Csl Behring
    Head Of The Filling Department
    Csl Behring Aug 2007 - Apr 2010
    Melbourne, Victoria, Au
    Leader of the of the Filling areas in building H69 (Marburg site). Responsible for business results of Infusion Bottle, Vial, and Syringe Filling operations including safety, quality, compliance, supply, and financial results. Accountable for the processes to ensure operations of the manufacturing facilities and equipment of filling areas in H69 within proper control and in a continued validated state. Planning of investment requirements in cooperation with the engineering, QA, and controlling departments.
  • Csl Behring
    Head Of Production Refludan & Streptase
    Csl Behring Nov 2005 - Jul 2007
    Melbourne, Victoria, Au
    Leader of the Refludan manufacturing plant (recombinant Hirundin purification from intermediate to Bulk Drug Substance) and Streptase manufacturing plant (fermentation and purification of streptokinase to Bulk Drug Substance). Responsible for business operations of both areas including safety, quality, supply and financial results. Responsible for interrelation and coordination with subcontractor for manufacturing of the Refludan intermediate (Aventis Pharma site at Romanville) and the product MAH (Bayer Schering) as Alliance Manager.
  • Csl Behring
    Mgr. Quality Management Delegate Production
    Csl Behring Aug 2004 - Oct 2005
    Melbourne, Victoria, Au
    Start up and implementation of the Quality management Delegates concept at the Marburg site. Responsible for the operational quality management of the manufacturing plants of plasmatic FVIII and FIX drug products in Marburg including deviation investigations and change controls. Developing and driving continuous improvement initiatives. Providing input into development protocols for new and improved processes in manufacturing. Participate in innovation projects, including provide assistance and recommendations regarding GMP.
  • Aventis Behring
    Laboratory Head General Pharmacology
    Aventis Behring Jan 2004 - Aug 2004
    Us
    Leader of the group General Pharmacology with responsibilities for the research in the area of wound healing and protease inhibitors. Responsible for the pharmacological and toxicological development of new surgical sealants (e.g. liquid fibrin sealant) including the contracting out of GLP compliant, toxicological studies and pharmacological research to contract research organizations. Responsible for planning, conduct and reporting pharmacological investigations in animals as study director for in-house studies and writing regulatory documents for submissions of development products to regulatory agencies.
  • Aventis Behring
    Assistant Plant Manager Haemaccel
    Aventis Behring Nov 1999 - Dec 2003
    Us
    Ensure the Haemaccel manufacturing (Active ingredient, drug substance, filling, visual inspection and packaging) according to planned production schedule. Responsible for ensuring Product Safety, Legality and Quality through effective Quality Systems in compliance with relevant quality, regulatory and company specific requirements and guidelines. Managing the discontinuation of the manufacturing activities for the transition of the plant following the divestiture of Haemaccel to TheraSelect.

Francesc Pont Skills

Gmp Pharmaceutical Industry Deviation Management Capa Internal Audit Aseptic Processing Sop Biotechnologie Pharmaindustrie Validation Quality Assurance Biotechnology

Francesc Pont Education Details

  • University Of Bremen
    University Of Bremen
    Organic Chemistry
  • Universitat De Barcelona
    Universitat De Barcelona
    Organic Chemistry
  • Queen Mary University Of London
    Queen Mary University Of London
    Organic Chemistry
  • Universitat De Barcelona
    Universitat De Barcelona
    Organic Chemistry
  • Escola Jungfrau
    Escola Jungfrau

Frequently Asked Questions about Francesc Pont

What company does Francesc Pont work for?

Francesc Pont works for Csl Behring

What is Francesc Pont's role at the current company?

Francesc Pont's current role is QA oversight for Engineering and CAPEX projects.

What is Francesc Pont's email address?

Francesc Pont's email address is fr****@****ing.com

What schools did Francesc Pont attend?

Francesc Pont attended University Of Bremen, Universitat De Barcelona, Queen Mary University Of London, Universitat De Barcelona, Escola Jungfrau.

What skills is Francesc Pont known for?

Francesc Pont has skills like Gmp, Pharmaceutical Industry, Deviation Management, Capa, Internal Audit, Aseptic Processing, Sop, Biotechnologie, Pharmaindustrie, Validation, Quality Assurance, Biotechnology.

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