Philippe Granvillain

R&D and Site Manager, GREENSEA S.A.S.

34140MèzeLanguedoc-Roussillon - France

I used to be a Chemist in Research and Development, and I worked both in biotech and pharmaceutical sectors for 12 years in 3 start-up and restructuring companies (located in France and Canada). I now want to further my career by performing business development, or project management at a corporate level.

I am always reachable on philippe_granvillain@hotmail.com

(Please have a look on my extended network on LinkedIn)

Philippe Granvillain
51 contacts
Professional experience
2010 - 2011

As the general manager of Greensea site, I have been:

- Managing the overall operations on the Greensea site, at Mèze, France (F-34140): Personnel recruiting, raw material supplying, small and large scale microalgae cultivation, biomass extraction using tangential flow filtration (TFF)

- Setting the Quality Assurance system on site, and especially: employee security and hygiene, change control, raw material management, client claims, quality document system (protocols, manufacturing report)

- Developing/optimizing cultivation systems and strategies under controlled conditions: running tubular photobioreactors (200L, 2400L), applying physiological stress on microalgae cultures (oxidative stress, nitrogen limited, and high/low temperature modes), using LED

- Developing innovative ingredients and biological compounds from microalgaes and seaweeds for human food, nutraceuticals, feed, pet food, and aquaculture industries

- Developing business and international trade

www.greentech.fr

Biotech
2008 - 2010

Full time studying for 2 graduate diplomas (Master level):

- Graduate Diploma in Management - Treasury/Finance concentration (400h) - Granted on August 2010
- Graduate Diploma in Accounting (400h) - Granted on May 2010

www.mcgill.ca

Teaching - Research
2006 - 2008

I coordinated the handling of thousand of generic drug samples among the R&D Center, the manufacturing plant, and the technology transfer office for the 24-month regulatory Stability study purposes. I developed and managed the business process of those samples from manufacturing, through stability studies (under temperature and humidity stress), up to their ultimate destruction. Those drugs (in suspension, injection, and ophtalmological products) were involved in 80 commercial projects.

www.sandoz.ca/site/en/index.shtml

Pharmaceutical
2002 - 2005

I developed and managed the business process related to our internal bio-banking, from primary plant cells extraction, to high throughput LC separation (on Sepbox and Waters workstations), to ultimate isolation of natural active compounds to be tested on bio-assays. I developed LC-MS analytical runs to track natural compounds of interest. I daily organized the tasks to be performed and managed the Purification lab team.

http://bio-quan.com/technology.php

Biotech
1996 - 2002

I developped the production platform (2500L, 55m3) and managed the scaleup of marine microalgae industrial controlled cultures. I developped and produced an innovative portfolio of biomarine ingredients for the cosmetic sector. I was directly responsible of all chemistry issues (nutritive media, ingredient quality control, culture monitoring, algae extraction). I managed a 2-technician team, proactively did business intelligence, and built up our internal business network.

www.soliance.com/page.php?id=1

www.lvmh.fr/groupe/pg_societe.asp?int_id=27&rub...

Biotech
Education

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