Opis stanowiska pracy
SIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences 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!Our client is a professional Pharmaceutical organisation, based in Netherlands.
The CompanyThis company has a particular focus in commercial manufacturing within an cGMP environment. There are facilities available such as inhouse QA and QC
Role DescriptionYou will be responsible for making sure that every operation of and every decision made regarding the QA department is in line with all regulations within the Netherlands, the relevant authorities and EMA. Furthermore it it your responsibility to maintain the the good image of the company towards our customers and authorities, thereby maintaining the companies cGMP compliance.
ResponsibilitiesMaintain and manage the resources within the QA group.
Responsible for hiring within your particular departments
Arrange that objectives related tot site manages are in line with the objectives of your team
Discuss and initiates career development and training of QA staff.
Responsible for setting up structures in terms of roles, responsibilities and competency profiles for QA staff
Setting up projects together with the project manager, thereby making full use of attributes and resources available.
Setting KPI's and follow up every three months with the QA Team
Reports regularly to Site Manager on all relevant matters.
RequirementsMinimum 15 years’ experience working in biological or pharmaceutical industry
Minimum 10 years’ experience managing/leading a Quality/Manufacturing team/unit
Preferable certification as “qualified person”.
Thorough understanding of pharmaceutical industry
Knowledgeable in the manufacturing science and monoclonal antibodies
Knowledgeable in Lean
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Greg Silberstein.
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. Rozwiń
- Ostatnia aktualizacja:
- Wymiar etatu:
- Pełny etat
- Rodzaj umowy:
- Własna działalność gospodarcza
- Liczba wakatów:
- Min. doświadczenie:
- 2 lata
- Min. wykształcenie:
- Wyższe licencjackie
- Branża / kategoria:
Praca Kontrola jakości