Our client is the largest innovative pharmaceutical company in the Netherlands whose mission is to focus on being a global leader in generics and medicines which may help millions of people around the world. Based in Boxmeer, their mission is that everyone should have access to quality medicines.
You are going to be responsible for conducting routine audits, including data, information, procedures, equipment, systems, and facilities. These audits are conducted to ensure compliance with SOPs, Good GMPs, and global regulations. The role involves reviewing and approving production and analytical documentation related to the release of API, Safety Assessment, or clinical supply lots, both in bulk and packaged form, to ensure they adhere to relevant regulatory requirements.
-Assist various departments in Quality Improvement projects.
-Ensure compliance with regulatory standards and promote continuous improvement in quality processes.
-Review and authorize change documentation within the specified scope.
-Review and approve all qualification and validation documentation for processes and equipment
-Determine and establish quality and GMP requirements for new products and product introductions.
-Bachelor’s or Master’s degree or equivalent in a related field
-Minimum of 2 years of experience in a GMP/Quality-related role
-Results-driven and a collaborative team player
-Demonstrated commitment to continuous improvement and adaptability
-Key competencies include effective communication, problem-solving, people skills, task management, self-reflection, learning agility, flexibility, and leading by example.
We are currently seeking highly motivated talents to join our clients on an exciting journey. Our client is looking for people to fill various positions within their organization. If you are interested in this opportunity, or if you know of someone who may be, please do not hesitate to contact me through the apply button. I would be more than happy to discuss the details of this opportunity with you and explore the potential for your professional growth with our client
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Since 2012, SIRE Life Sciences is the most innovative and engaged consultancy company for the life sciences industries.
SIRE Life Sciences is proud of its ability to adapt to changing trends while always maintaining the highest level of quality for both our clients and our candidates.
Our team of knowledgeable professionals provides customized staffing services to clients and candidates, including secondment, direct hire, temporary-to-hire, temporary staffing, brokering, Statement of Work and we approach each type with the same degree of professional assessment. Our refined and collaborative style is unmatched in the staffing industry. We’re able to see beyond the surface to create matches that result in successful careers for our candidates and valuable talent for our clients.
Effective employment solutions need to put the right person in the relevant place every time, using advanced systems to streamline costs and time-frames for clients.