Quality Management System Specialist
Location: GermanySIRE 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. 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!
THE COMPANY
Our client is a professional Pharmaceutical organization, based in Hessen Germany.
Within a competitive industry, this pharmaceutical company has been able to ensure a solid market share. The organization empowers the employees to work independently and invest in good leader who can help team members to grow into the next step.
ROLE DESCRIPTION
The Quality Management System Specialist will be responsible for maintaining and reinforcing the current QMS system. THE QMS Specialist has a solid knowledge of all Quality subsystems (CAPA, deviation, change control, documentation...).
As part of your responsibilities, you will join the Quality Compliance and ensure that the local and global guidelines are met.
Together with the rest of the team, the QMS Specialist will develop a training program. The training program needs to be consistent, complete, unambiguous, effective and clear for employees within different levels in the organization.
RESPONSIBILITIES
- Challenge the current QMS and introduce improvements to make it more effective
- Ensure that the regulations at a local and global level are compliant
- Develop a training program clear for employees within different organizational scales
- Create and review Quality agreements with external partners
REQUIREMENTS
- Bachelor or Master within a relevant scientific degree
- +4 years of relevant experience within the pharmaceutical industry (drug products)
- Ability to work within a team
- Native German and proficient English
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Patricia Oses Equiza.
