Project Coordinator FDA
Wroclaw Project Coordinator FDA
Wroclaw
NR REF.: 1020702
For our client, an international well-known medical company, we are currentlylooking forProject Coordinator Quality Management with experience in FDA (food and drug administration).
The successful candidate will be responsible for project coordinator for implementation of FDA. Responsibilities will also include the following: research and development of new and actual medical products, review all components and tests, review all technology of production, create or review documentation of products according to relevant norms, introduce a new products or modificated products to the market, cooperate with another department: quality, regulatory, packaging, engineering, clinical, marketing.
Applications are invited from candidates with the following background/experience:study with scientific orientation or similar education (biomedical engineering), work experience in the field of Quality Management, experiences in medical industry are desirable, thorough knowledge of English, high potential of analytic approach to think and good problem-solving competence, pronounced communication and organisation skills.
For more details please contact: kowalczuk@hays.pl
Wroclaw
NR REF.: 1020702
For our client, an international well-known medical company, we are currentlylooking forProject Coordinator Quality Management with experience in FDA (food and drug administration).
The successful candidate will be responsible for project coordinator for implementation of FDA. Responsibilities will also include the following: research and development of new and actual medical products, review all components and tests, review all technology of production, create or review documentation of products according to relevant norms, introduce a new products or modificated products to the market, cooperate with another department: quality, regulatory, packaging, engineering, clinical, marketing.
Applications are invited from candidates with the following background/experience:study with scientific orientation or similar education (biomedical engineering), work experience in the field of Quality Management, experiences in medical industry are desirable, thorough knowledge of English, high potential of analytic approach to think and good problem-solving competence, pronounced communication and organisation skills.
For more details please contact: kowalczuk@hays.pl
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Opis stanowiska
Project Coordinator FDA
Wroclaw
NR REF.: 1020702
For our client, an international well-known medical company, we are currentlylooking forProject Coordinator Quality Management with experience in FDA (food and drug administration).
The successful candidate will be responsible for project coordinator for implementation of FDA. Responsibilities will also include the following: research and development of new and actual medical products, review all components and tests, review all technology of production, create or review documentation of products according to relevant norms, introduce a new products or modificated products to the market, cooperate with another department: quality, regulatory, packaging, engineering, clinical, marketing.
Applications are invited from candidates with the following background/experience:study with scientific orientation or similar education (biomedical engineering), work experience in the field of Quality Management, experiences in medical industry are desirable, thorough knowledge of English, high potential of analytic approach to think and good problem-solving competence, pronounced communication and organisation skills.
For more details please contact: kowalczuk@hays.pl
Wroclaw
NR REF.: 1020702
For our client, an international well-known medical company, we are currentlylooking forProject Coordinator Quality Management with experience in FDA (food and drug administration).
The successful candidate will be responsible for project coordinator for implementation of FDA. Responsibilities will also include the following: research and development of new and actual medical products, review all components and tests, review all technology of production, create or review documentation of products according to relevant norms, introduce a new products or modificated products to the market, cooperate with another department: quality, regulatory, packaging, engineering, clinical, marketing.
Applications are invited from candidates with the following background/experience:study with scientific orientation or similar education (biomedical engineering), work experience in the field of Quality Management, experiences in medical industry are desirable, thorough knowledge of English, high potential of analytic approach to think and good problem-solving competence, pronounced communication and organisation skills.
For more details please contact: kowalczuk@hays.pl
Dodatkowe informacje
- Ostatnia aktualizacja
- Wymiar etatu
- Pełny etat
- Rodzaj umowy
- Na czas nieokreślony
- Liczba wakatów
- 1
- Min. doświadczenie
- 1 rok
- Min. wykształcenie
- Policealne
- Branża / kategoria
- Praca Praca na produkcji
