(Temp) Quality Manager Supply Chain - 3 Months
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 Noord-Holland Netherlands.
A worldwide sustainable partner in healthcare.
May be asked to act as a Responsible Person (RP)
- Coordinating and supporting the GMP/GDP Quality Systems related to distribution and manufacturing
- Analyzing GDP/GMP compliance processes (Change requests and Deviations)
- Legal and Regulatory compliance and Risk Management
- Managing complex cross functional/regional projects
- leading a multi-functional team
- Strong planning en people management abilities
- 5 years of Pharmaceutical experience in a similar position
- Proven experience in process improvement, compliance and auditing activities
- Experience with GMP or GDP and Quality Management Systems is a must
The Company
The company is a leading global pharmaceutical company with offices in over 100 countries. The company does research, development, production and marketing for medicines.A worldwide sustainable partner in healthcare.
Role Description
You will be responsible for all GMP/GDP related activities. Overseeing the legal and regulatory compliance regarding Global Supply Chain Quality is part of the job.May be asked to act as a Responsible Person (RP)
Responsibilities
- Implement and maintaining the Quality Systems (QMS)- Coordinating and supporting the GMP/GDP Quality Systems related to distribution and manufacturing
- Analyzing GDP/GMP compliance processes (Change requests and Deviations)
- Legal and Regulatory compliance and Risk Management
- Managing complex cross functional/regional projects
- leading a multi-functional team
Requirements
- Analytical and problem solving mindset- Strong planning en people management abilities
- 5 years of Pharmaceutical experience in a similar position
- Proven experience in process improvement, compliance and auditing activities
- Experience with GMP or GDP and Quality Management Systems is a must
Prosimy o aplikowanie poprzez przycisk znajdujący się po prawej stronie ogłoszenia.
Opis stanowiska
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 Noord-Holland Netherlands.
A worldwide sustainable partner in healthcare.
May be asked to act as a Responsible Person (RP)
- Coordinating and supporting the GMP/GDP Quality Systems related to distribution and manufacturing
- Analyzing GDP/GMP compliance processes (Change requests and Deviations)
- Legal and Regulatory compliance and Risk Management
- Managing complex cross functional/regional projects
- leading a multi-functional team
- Strong planning en people management abilities
- 5 years of Pharmaceutical experience in a similar position
- Proven experience in process improvement, compliance and auditing activities
- Experience with GMP or GDP and Quality Management Systems is a must
The Company
The company is a leading global pharmaceutical company with offices in over 100 countries. The company does research, development, production and marketing for medicines.A worldwide sustainable partner in healthcare.
Role Description
You will be responsible for all GMP/GDP related activities. Overseeing the legal and regulatory compliance regarding Global Supply Chain Quality is part of the job.May be asked to act as a Responsible Person (RP)
Responsibilities
- Implement and maintaining the Quality Systems (QMS)- Coordinating and supporting the GMP/GDP Quality Systems related to distribution and manufacturing
- Analyzing GDP/GMP compliance processes (Change requests and Deviations)
- Legal and Regulatory compliance and Risk Management
- Managing complex cross functional/regional projects
- leading a multi-functional team
Requirements
- Analytical and problem solving mindset- Strong planning en people management abilities
- 5 years of Pharmaceutical experience in a similar position
- Proven experience in process improvement, compliance and auditing activities
- Experience with GMP or GDP and Quality Management Systems is a must
Dodatkowe informacje
- Ostatnia aktualizacja
- Wymiar etatu
- Pełny etat
- Rodzaj umowy
- Własna działalność
- Liczba wakatów
- 1
- Min. doświadczenie
- 2 lata
- Min. wykształcenie
- Wyższe licencjackie
- Branża / kategoria
- Praca Kontrola jakości
