Quality Manager
- Denmark
- Contract
- Compliance / Quality Assurance
Our client, a global CDMO in pharmaceutical manufacturing, is recruiting for a Quality Manager to join their new and exciting large-scale CAPEX investment programme. With a mission to provide process development and cGMP production in cell culture, microbial fermentation, and gene therapies, this is an outstanding opportunity make a genuine contribution to the biopharmaceutical industry.
Main Responsibilities
- Develop project and ensure resolution of all quality related issues on Sample Booth project
- Develop Validations plans together with QA and RA
- Alignment with both and external stakeholders to ensure all process requirements are met.
- Assist Sample Booth Project manager.
- Contribute to time schedule for project both design and execution.
- Highlight as early as possible any challenges in achieving the goals.
- Coordinate all process related issues with the whole team.
- Follow up on actions.
- Review for potential problems in risk areas
Personal skills:
- Experienced Quality and/or Process Manager with a background from pharmaceutical industry
- +10 years of experience on complex industry project
- Knowledge of cleanroom design
Requirements:
- Bachelor or master in contract law or similar degree
- Fluent Danish/English.
If this role is of interest to you, please apply now!
#LI-AS1
We have worked together with QCS Staffing for seven years now and have always received a professional service. QCS Staffing's speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of QCS Staffing's people and their ability to deliver.
Global Pharmaceutical firm
I have always received a highly professional & personable service from the team at QCS Staffing. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
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Abigail
I manage this role.