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Olivier Trouillard

Qa Specialist @ GSK

QA Specialist

Rixensart, Wallonie, Belgium

Ranked #973 out of 19,460 for Qa Specialist in United States

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Olivier Trouillard's Email Addresses & Phone Numbers

Olivier Trouillard's Work Experience


Qa Specialist

July 2014 to Present


GSK Vaccines

QA Supervisor for aseptic operations

January 2013 to July 2014

GlaxoSmithKline Biologicals

QA Bulk Coordinator

December 2011 to December 2012


Olivier Trouillard's Education


Biotech Engineer - MS degree Biotechnology

2004 to 2007


Ingénieur biotechnologie Biotechnologie

2004 to 2007

Le Chesnoy


2001 to 2004

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About Olivier Trouillard's Current Company


Operational QA for whole process of production of Bordetela Pertussis antigens (from fermentation to antigens adsorption in aseptic environment). Week end shift.

Frequently Asked Questions about Olivier Trouillard

What company does Olivier Trouillard work for?

Olivier Trouillard works for GSK

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Olivier Trouillard is Qa Specialist

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What industry does Olivier Trouillard work in?

Olivier Trouillard works in the Pharmaceuticals industry.

About Olivier Trouillard

đź“– Summary

Qa Specialist @ Operational QA for whole process of production of Bordetela Pertussis antigens (from fermentation to antigens adsorption in aseptic environment). Week end shift. From July 2014 to Present (1 year 5 months) BelgiumQA Supervisor for aseptic operations @ QA for aseptic operations (production of biological substance) - Main Quality systems (review/approbal of deviations, CAPA, change controls, SOPs, batch records) - Validation activities (approval of validation plans, summary reports) - Maintenance and Calibration activities (evaluation and approval of technical modifications, Calibration deviations,...) - Shopfloor (implementation of the planning, follow up of the QA oversights on documentation and operations) QA change agent for the transformation program initiative started in july13 to increase the aseptic delivery capacity Training management (follow up of the training status of the QA team, SOP trainer) From January 2013 to July 2014 (1 year 7 months) QA Bulk Coordinator @ Operational QA activities for fermentation and purification process of Bordetella pertussis production including main quality systems (deviation, CAPA, documentation,...) and team management. From December 2011 to December 2012 (1 year 1 month) BelgiumQA/QP Associate @ Deviation, Change Control & Training management From May 2011 to December 2011 (8 months) Charleroi Area, BelgiumProject Associate Director @ Biotech project management including follow up of process, QC testing & release. Participation in production of retrovirus & lentivirus-based gene therapy vectors for preclinical & clinical use. From January 2011 to September 2011 (9 months) Charleroi Area, BelgiumProcess Engineer @ Participation in Factory Acceptance Tests of an oxidation skid unit using supercritical carbon dioxide to produce haemostatic tissue for compresses. 3 month contract From October 2010 to December 2010 (3 months) Nancy Area, FranceProduction Engineer @ As part of my duties, I had the opportunity to interact with all departments of the company and I worked on various topics including: Operational management of production project • Management of production projects under supervision of the Head of Production and in compliance with quality standards, procedures, specifications, timelines and costs • Implementation of action plans and production planning Process Engineering • Development and optimization of production processes in collaboration with R&D teams for a transfer to production plaform • Implementation of technology / process transfer and process validation • Manufacture of production batches (cell bank, virus seed and drug substance, proteins) for reproducibility studies, analytical methods development and preclinical studies Installation / Qualification / Validation • Specification drafting for conception of biotech equipments and systems • Installation and qualifications (DQ/IQ/OQ/PQ) of systems (HVAC, utilities) and equipments (autoclave, incubators and other lab equipments) • Implementation and validation of SIP and CIP processes of stainless steel equipments (bioreactors, tangential flow filtration skid, cell breakage skid) Quality • Implementation and continuous improvement of the production quality system in compliance with cGMP and French regulation (BPF – Afssaps) • Drafting, review and / or approval of SOPs and other quality documentation From July 2007 to August 2010 (3 years 2 months) Production Engineer (Internship) @ During this 7-months internship, I worked within the Production team in the pilot plant based on the site of Siena in Italy on: • the production and purification of group B Streptococcus polysaccharides at pilot scale (300L) in a cGMP environment in collaboration with the development department • the cleaning of the equipments and the validation of the cleaning-in-place of the fermentor in collaboration with the QC department From July 2006 to February 2007 (8 months) Biotech Engineer - MS degree, Biotechnology @ ENSTBB From 2004 to 2007 Ingénieur biotechnologie, Biotechnologie @ ENSTBB Bordeaux INP From 2004 to 2007 BS, BCPST @ Le Chesnoy From 2001 to 2004 Olivier Trouillard is skilled in: Biotechnology, CAPA, GMP, SOP, Validation, Change Control, Pharmaceutical Industry, Quality Assurance, Quality System

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In a nutshell

Olivier Trouillard's Personality Type

Introversion (I), Sensing (S), Thinking (T), Perceiving (P)

Average Tenure

1 year(s), 2 month(s)

Olivier Trouillard's Willingness to Change Jobs



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