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Nikky Vlemmix

Plv. Hoofd Geneeskundige Eenheid

Pharmaceutical Process Architect at Tebodin

Eindhoven Area, Netherlands

Section title

Nikky Vlemmix's Email Addresses & Phone Numbers

Nikky Vlemmix's Work Experience

Het Nederlandse Rode Kruis

Plv. Hoofd Geneeskundige Eenheid

March 2015 to Present

Tebodin

Pharmaceutical Process Architect

May 2013 to Present

Het Nederlandse Rode Kruis

SIGMA teamlid

July 2010 to Present

Nikky Vlemmix's Education

NODE / Het Oranje Kruis

Instructeur Eerste Hulp

2015 to 2016

BAs Biotechnology

1999 to 2003

Nikky Vlemmix's Professional Skills Radar Chart

Based on our findings, Nikky Vlemmix is ...

Troubleshooter
Maverick
Conceptual

What's on Nikky Vlemmix's mind?

Based on our findings, Nikky Vlemmix is ...

52% Left Brained
48% Right Brained

Nikky Vlemmix's Estimated Salary Range

About Nikky Vlemmix's Current Company

Het Nederlandse Rode Kruis

Frequently Asked Questions about Nikky Vlemmix

What company does Nikky Vlemmix work for?

Nikky Vlemmix works for Het Nederlandse Rode Kruis


What is Nikky Vlemmix's role at Het Nederlandse Rode Kruis?

Nikky Vlemmix is Plv. Hoofd Geneeskundige Eenheid


What is Nikky Vlemmix's personal email address?

Nikky Vlemmix's personal email address is n****[email protected]


What is Nikky Vlemmix's business email address?

Nikky Vlemmix's business email addresses are not available


What is Nikky Vlemmix's Phone Number?

Nikky Vlemmix's phone +44 ** **** *413


What industry does Nikky Vlemmix work in?

Nikky Vlemmix works in the Pharmaceuticals industry.


About Nikky Vlemmix

📖 Summary

Just take a step in the right direction, even a little step will eventually gets us there! - Started up a new Biotechnical USP facility for manufacturing pharmaceutical ingredients including process qualification and validation of equipment. - Led a team of about 10 (Sr.) Operators in a pharmaceutical USP facility. - Paricipant in improvement projects using Lean/Six-Sigma. - Quality Assurance in pharmaceutical biotechnology. - Assisted in introduction of new biotechnological products in USP and DSP facilies. - Continious Improvement using Lean Six Sigma and MPS - Medical assistant in Fire Safety and Emergency Management team at Organon (discontiniued 31-12-2010) - Medical assistant in SIGMA team Brabant Noord.Plv. Hoofd Geneeskundige Eenheid @ From March 2015 to Present (10 months) Pharmaceutical Process Architect @ As a Pharmaceutical Process Architect I'm responsible for the translation of the requirements of our (bio)pharmaceutical customers into workable processes and facilities which are in compliance with the cGMP regulations. From May 2013 to Present (2 years 8 months) SIGMA teamlid @ The Snel Inzetbare Groep ter Medische Assistentie (Rapid Deployable Group for Medical Assistance - SIGMA) is a group of volunteer helpers who can be deployed when the daily medical care is no longer sufficient due to a disaster or major accident. A SIGMA team is part of the Geneeskundige Combinatie (Medical Combination - GnK) and operates under the responsibility of the Geneeskundige Hulpverlening bij Ongevallen en Rampen (Medical Assistance in Accidents and Disasters - GHOR). SIGMA members operate as a volunteer of the Netherlands Red Cross. From July 2010 to Present (5 years 6 months) Process Engineer @ As a Process Engineer for MSD Animal Health I work together with our internal customers spread over our sites across Europe into expanding, upgrading, renewing and trouble shooting their facilities and equipment. I focus on clean utilities and biotechnological equipment, both Upstream as Downstream. From May 2012 to May 2013 (1 year 1 month) Sr. Investigator Quality Assurance Biologics @ As a Sr. Investigator QA-B I am the Quality Unit representative in our Operational Teams for all Q-related issues such as monitoring and safeguarding cGMP compliance. My goal is to involve everyone in the day to day quest for a higher level of compliance and make it a team effort. To achieve this besides being on the shop floor on a daily basis I write, assess and approve various sorts of documentation ranging from executed Batch Production Records and Master Production Instructions to Qualification and Validation reports and from assessing and approving the yearly reports from production to writing a Product Quality Report of the production process. Doing this my past positions as operator and technician in production give me the insight I need to have to fully understand the issue and support production when and where needed. Risk Analysis and Quality Approval of all events occured during the production processes and Impact Analysis of all Change Control documentation is also a key element in my job. Furthermore the preperation of the release of (Final) Intermediates is one of my most important tasks, because in the end that's where it's all about! From September 2009 to April 2012 (2 years 8 months) Proces technoloog USP @ From 2005 to 2009 (4 years) 1st Operator @ From 2004 to 2005 (1 year) Sr Operator @ From 2003 to 2004 (1 year) Instructeur Eerste Hulp @ NODE / Het Oranje Kruis From 2015 to 2016 BAs, Biotechnology @ From 1999 to 2003 Nikky Vlemmix is skilled in: Root Cause Analysis, Troubleshooting, Continuous Improvement, GMP, First Aid, Lean Manufacturing, Change Control, Six Sigma, Validation, Quality Assurance, Quality System, Manufacturing, Biotechnology, CAPA, Pharmaceutical Industry


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In a nutshell

Nikky Vlemmix's Personality Type

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

Average Tenure

2 year(s), 4 month(s)

Nikky Vlemmix's Willingness to Change Jobs

Unlikely

Likely

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