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GROSSE-SCHUETTE-CONSULTING.COM

GROSSE-SCHUETTE-CONSULTING

My added value for your company. We support or take over your. Objectives to achieve or adhere to EN ISO 9001, EN ISO 13485 and CFR 21 Part 820 QSR. Planning, organisation, implementation, documentation, review and release activities for equipment and facility qualifications together with process validations (DQ, IQ, OQ, PQ). CAPA management activities, document control activities, process management activities, audit management activities. For my personal references, please contact me or click in "xing"...

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Grosse-Schuette Consulting

Grosse-Schuette Rico

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Obe●●●den , 8942

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Zu●●ch , 8001

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GROSSE-SCHUETTE-CONSULTING | grosse-schuette-consulting.com Reviews
<META>
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My added value for your company. We support or take over your. Objectives to achieve or adhere to EN ISO 9001, EN ISO 13485 and CFR 21 Part 820 QSR. Planning, organisation, implementation, documentation, review and release activities for equipment and facility qualifications together with process validations (DQ, IQ, OQ, PQ). CAPA management activities, document control activities, process management activities, audit management activities. For my personal references, please contact me or click in xing...
<META>
KEYWORDS
1 Singapore
2 Singapur
3 Consulting
4 Medizinprodukte
5 medical device
6 Grosse-Schuette
7 Validation
8 CAPA
9 Quality Management
10
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GROSSE-SCHUETTE-CONSULTING | grosse-schuette-consulting.com Reviews

https://grosse-schuette-consulting.com

My added value for your company. We support or take over your. Objectives to achieve or adhere to EN ISO 9001, EN ISO 13485 and CFR 21 Part 820 QSR. Planning, organisation, implementation, documentation, review and release activities for equipment and facility qualifications together with process validations (DQ, IQ, OQ, PQ). CAPA management activities, document control activities, process management activities, audit management activities. For my personal references, please contact me or click in "xing"...

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GROSSE-SCHUETTE-CONSULTING GmbH

http://www.grosse-schuette-consulting.com/profile.php

Experienced project leader in the development, qualification and validation, optimization of tools (mould injection), machine-tool, equipments and facilities as well as manufacturing procedures. Highly qualified in quality management and manufacturing of medical devices. Responsible, trustful leader. Manager with a creative and sustainable approach in solving problems. Good knowledge in English and German. Knowledge in Russian, Spanish and Chinese(Mandarin). Die casting of disposables and medical devices.

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My added value for your company. We support or take over your. Objectives to achieve or adhere to EN ISO 9001, EN ISO 13485 and CFR 21 Part 820 QSR. Planning, organisation, implementation, documentation, review and release activities for equipment and facility qualifications together with process validations (DQ, IQ, OQ, PQ). CAPA management activities, document control activities, process management activities, audit management activities. For my personal references, please contact me or click in "xing"...

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