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MR Medical Recruiters:

Praca w różnych miejscach w Niemczech (Thüringen), w pełnym wymiarze godzin.

 

Państwa zadania:

  • Opieka medyczna różnych specjalności
  • Wywiad, rozpoznanie i leczenie
  • Wykonywanie procedur diagnostycznych i terapeutycznych

 

Państwa profil:

  • Tytuł lekarza
  • Zaangażowanie i umiejętność pracy w zespole
  • Kompetencje społeczne, profesjonalne, zaangażowanie i poczucie odpowiedzialności
  • Empatia i elastyczność
  • Znajomość języka niemieckiego w stopniu B2/C1

 

Oferujemy:

  • Stałe zatrudnienie, umowę o pracę na czas nieokreślony podpisaną bezpośrednio z niemieckim pracodawcą
  • Atrakcyjne wynagrodzenie od 6000-8000 €, atrakcyjne wynagrodzenie na zasadach umów taryfikacyjnych
  • emerytury pracownicze - dodatkowy fundusz emerytalny
  • Elastyczne modele pracy
  • Przyjazna atmosfera pracy
  • Praca z wykorzystaniem nowoczesnych urządzeń (high-tech)
  • Profesjonalne wdrożenie w proces pracy
  • Możliwości rozwoju zawodowego
  • Świadczenia pracownicze i inne socjalne
  • kursy języka niemieckiego dofinansowane przez niemiecki rząd
  • stopniowe wprowadzenie do obowiązków na stanowisku pracy oraz wsparcie osoby asystującej na miejscu
  • pomoc w znalezieniu pierwszego mieszkania / umeblowanego studia

 

Czy ta oferta pracy wzbudziła Państwa zainteresowanie? Jeśli tak, prosimy o wysłanie dokumentów.

Czekamy na Państwa zgłoszenie!

Prosimy o dopisanie następującej klauzuli: „Wyrażam zgodę na wykorzystanie i przetwarzanie danych osobowych do celów związanych z procesem rekrutacji oraz udostępnianie danych potencjalnym pracodawcom w ramach prowadzonych procesów rekrutacji zgodnie z Ustawą z dnia 29.08.1997 r. (Dz. U. z 2002 r. Nr 101, poz. 926 ze zm.) o Ochronie Danych Osobowych. Przysługuje mi prawo dostępu do moich danych, ich poprawiania oraz usunięcia."

SIRE Life Sciences®:

SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!

THE COMPANY

Our client is a professional Pharmaceutical organization, based in Limburg Belgium.

This company is an independent pharmaceutical contract-manufacturer and packer supplying a one-stop service for production and logistic for packaging their products.

ROLE DESCRIPTION

Are you ready for your first experience in a QP role for pharmaceutical manufacturing? Do you want a very important role in the quality? Then this is the job for you!

RESPONSIBILITIES

Ensure that each batch has been manufactured and checked in compliance with the laws in and in accordance with the requirements of the marketing authorization. Ensure timely and adequate batch disposition decisions. Next to that you will responsible for the following:
- Perform and/or assist with parts of various problem-solving duties which occur, including studying the situation, evaluation of possible solutions and options, deciding on most appropriate plan for solution, and approving plan of action
- Provide training to other employees by demonstration, repetition, modelling, large group training, etc.
- Coach staff in working with individuals on a regular basis to access, instruct and model
- Assist in controlling the correct working of the quality management system
- Batch documentation integrity, by means of batch record review, review of analytical records and other relevant batch information
- You will need to oversee the quality system, evaluation and approval of Change requests, CAPA plans and outcome of quality reviews.
- You will advice and approval of internal deviation handling and CAPAs

REQUIREMENTS

- Master degree, industrial pharmacist
- Completed with relevant training and courses
- Active in depth knowledge on international cGMP guidelines and pharmaceutical regulations
- Knowledge on HACCP and food regulations, Healthcare regulations, Medical Device regulations and Filling Weight regulations

- The following competences need to be included:
- Ownership
- Team player, able to work with all levels in the organization
- High level of integrity
- Think in processes
- Positive mind set / Think in solutions
- Decision maker
- Accurate
- Organized work processes / set priorities

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Valentijn de Krom.

SIRE Life Sciences®:

SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!

THE COMPANY

Our client is a professional Pharmaceutical organization, based in Noord-Brabant Netherlands.

The company produce products which are used both diagnostically and therapeutically in hospitals. These products are exported every week all over the world and has in recent years a significant growth. Candidates with the right background, but who don't have a QP certification yet, are also welcome to apply!

ROLE DESCRIPTION

In this job you will be responsible for the supervision, without any interference of third persons, of the business processes of pharmacy, related to the drug manufacturing license. With respect to the quality of the medicinal products, assurance of compliance to the Dutch Medicines Law and other applicable regulations. Together with the Head of Production maintaining an effective implementation, monitoring and maintenance of a GMP-compliant quality system.

RESPONSIBILITIES

- Design and implementation of a GMP - compliant quality system
- Auditing of contract manufacturers
- Assessment and release of manufactured medicinal products
- Release of incoming goods
- Assessment and processing of deviations and CAPA"s
- Training of employees with respect to GMP
- Provide support to QA on an "ad hoc" basis to assist in carrying out key QA responsibilities- including the provision of QA support to manage and escalate critical compliance issues through site QMS processes

REQUIREMENTS

- Experience with sterile product will be a plus
- Strong affinity with, and awareness of, quality issues
- QP Qualified (conform EU Directive 2001/83/EC) OR Candidates with the right background.
- Fluently in Dutch; good understanding of English
- Being flexible, assertive, can work with strict deadlines

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Valentijn de Krom.