QAV Specialist - Buffer
- Denmark
- Contract
- Compliance / Quality Assurance
This vacancy has now expired
Our client, a global CDMO in pharmaceutical manufacturing, is recruiting for a QAV Specialist to join them on their new expansion project. Based in a charming Nordic location, this on a contractual basis, and will involve significantly growing the sites capacity for the manufacture of Biologics.
The successful QAV Specialist will be responsible for:
- Provide quality and cGMP input and oversight for all start-up project activities.
- Provide QA support for risk-based verification activities in the capacity of Quality Assurance Subject Matter Expert. Review and approval clean utility documentation from design to post execution.
- Participate in verification quality risk assessments and provide quality oversight to ensure verification quality risk assessments are effectively maintained/controlled.
- Review and approval of engineering functional area documentation (SOP, Work Instructions, Criticality Assessments, technical report and protocols).
- Complete on behalf of Quality Engineering Vendor assessments.
- Authoring, review and approval of QA-related procedures.
- Oversee the effective documentation and tracking of quality management system activities including deviations and change controls and CAPA.
- Review and approve Validation protocols as required.
- Support the vendor quality management programme.
- Participate in regulatory inspections as required.
- Develop and report quality metrics.
- Represents Quality Assurance to guide various projects and technical meetings, as needed.
- Responsible for documenting and reporting compliance issues to management.
The ideal candidate will possess:
- Extensive QAV experience in a pharmaceutical manufacture/biopharmaceutical environment. (BDS experience is essential).
- Must have strong process knowledge to include buffer prep/ buffer hold.
- An ability to work independently, as well as a member of a team in a dynamic, fast-paced environment.
- Excellent communication & presentation skills are essential.
- Excellent time management organisational skills along with a proven ability to multi-task.
- Must have experience of working from initial project phases through to final hand over, engaging with Stakeholders/ User Groups/ Procurement/Suppliers.
- This individual must have had experience of a similar project with a multi-million capital spend.
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
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
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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