Compliance Director
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.
Make independent decisions on the implementation of the quality management system (QMS) at the site.
Managing the quality function including interacting/developing relationships with regulatory agencies in the Netherlands as well as EMA and the FDA.
A minimum of 8 eight years' experience in the FDA and/or EU regulated pharmaceutical environment, preferably in a manufacturing site in quality and/or manufacturing roles.
Demonstrated in-depth knowledge of global health authority regulations and quality and compliance requirements with the ability to effectively communicate these requirement
Demonstrated leadership and change management skills with focus on continuous improvement
Registration as Qualified Person is preferred
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
.Role Description
You will need to interface with all site functions and the global Quality organization and you will be responsible for oversight and activities related to the management of regulatory inspections, the site auditing program, significant investigations and recall execution, CAPA management, regulatory compliance, complaints management, site quality agreements and data integrity compliance.Responsibilities
Lead the site wide Permanent Inspection Readiness (PIR) program, influencing all IPT's (Integrated Process Team) and CoE's (Centre of Excellence) at the site. Report to Site Leadership Team on necessary GMP improvement programs for the site to remain permanent inspection ready.Make independent decisions on the implementation of the quality management system (QMS) at the site.
Managing the quality function including interacting/developing relationships with regulatory agencies in the Netherlands as well as EMA and the FDA.
Requirements
Master's Degree in Pharmacy, Life Sciences, EngineeringA minimum of 8 eight years' experience in the FDA and/or EU regulated pharmaceutical environment, preferably in a manufacturing site in quality and/or manufacturing roles.
Demonstrated in-depth knowledge of global health authority regulations and quality and compliance requirements with the ability to effectively communicate these requirement
Demonstrated leadership and change management skills with focus on continuous improvement
Registration as Qualified Person is preferred
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.
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