Quality Supply Chain Manager
Location: NetherlandsSIRE® 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.
- Quality Systems implementation, maintenance and introduction of improvements
- Responsible for all QA associated activities: documentation, complaints, internal/ external audits, deviations, recalls, CAPA management...)
- Perform risk assessments
- Provide Regulatory compliance
- Management of regional and cross-functional projects
- Background in a relevant scientific field
- Previous experience in Quality within the pharmaceutical industry
- Experience in a GDP distribution environment
- Solid problem solving, negotiation skills and ability to perform under tight deadlines
- Proficient English (Dutch is NOT a requirement)
- Type of contract: temp-to-perm (after 4-6 months depending on performance)
- Location: Amsterdam
- Full-time: 40 hours/ week, flexible working arrangements possible
Please contact Iselde van Beurden via +31 (0)20 658 9800 for more information, or apply via the link below.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Seppe Verhoeven.
The Company
Internationally operating pharmaceutical manufacturer.Role Description
Management of all GMP/GDP related activities and ensure compliance with local and global regulations. You will working closely together with Supply Chain in order to maintain quality oversight.Responsibilities
Responsibilities- Quality Systems implementation, maintenance and introduction of improvements
- Responsible for all QA associated activities: documentation, complaints, internal/ external audits, deviations, recalls, CAPA management...)
- Perform risk assessments
- Provide Regulatory compliance
- Management of regional and cross-functional projects
Requirements
Requirements- Background in a relevant scientific field
- Previous experience in Quality within the pharmaceutical industry
- Experience in a GDP distribution environment
- Solid problem solving, negotiation skills and ability to perform under tight deadlines
- Proficient English (Dutch is NOT a requirement)
Other information
Additional information- Type of contract: temp-to-perm (after 4-6 months depending on performance)
- Location: Amsterdam
- Full-time: 40 hours/ week, flexible working arrangements possible
Please contact Iselde van Beurden via +31 (0)20 658 9800 for more information, or apply via the link below.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Seppe Verhoeven.
Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.
Job Description
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.
- Quality Systems implementation, maintenance and introduction of improvements
- Responsible for all QA associated activities: documentation, complaints, internal/ external audits, deviations, recalls, CAPA management...)
- Perform risk assessments
- Provide Regulatory compliance
- Management of regional and cross-functional projects
- Background in a relevant scientific field
- Previous experience in Quality within the pharmaceutical industry
- Experience in a GDP distribution environment
- Solid problem solving, negotiation skills and ability to perform under tight deadlines
- Proficient English (Dutch is NOT a requirement)
- Type of contract: temp-to-perm (after 4-6 months depending on performance)
- Location: Amsterdam
- Full-time: 40 hours/ week, flexible working arrangements possible
Please contact Iselde van Beurden via +31 (0)20 658 9800 for more information, or apply via the link below.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Seppe Verhoeven.
The Company
Internationally operating pharmaceutical manufacturer.Role Description
Management of all GMP/GDP related activities and ensure compliance with local and global regulations. You will working closely together with Supply Chain in order to maintain quality oversight.Responsibilities
Responsibilities- Quality Systems implementation, maintenance and introduction of improvements
- Responsible for all QA associated activities: documentation, complaints, internal/ external audits, deviations, recalls, CAPA management...)
- Perform risk assessments
- Provide Regulatory compliance
- Management of regional and cross-functional projects
Requirements
Requirements- Background in a relevant scientific field
- Previous experience in Quality within the pharmaceutical industry
- Experience in a GDP distribution environment
- Solid problem solving, negotiation skills and ability to perform under tight deadlines
- Proficient English (Dutch is NOT a requirement)
Other information
Additional information- Type of contract: temp-to-perm (after 4-6 months depending on performance)
- Location: Amsterdam
- Full-time: 40 hours/ week, flexible working arrangements possible
Please contact Iselde van Beurden via +31 (0)20 658 9800 for more information, or apply via the link below.
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Seppe Verhoeven.
Additional Information
- Last updated
- Employment type
- Full time
- Contract type
- Self employed
- Number of vacancies
- 1
- Min. experience
- Two years
- Min. education
- Bachelor
- Industry / category
- Jobs in Quality Control
