Resolian
Senior QA Advisor
Fordham
$80k – $108k/yr
Posted 2 days ago
How your CV stacks up
1Upload CV
2Analyse CV
3Improve CV
Upload your CV to see how well it fits this job role
?%
Responsibilities
- Conduct study, process, and facility audits according to the audit programme and study timelines in accordance with GLP and GCP requirements.
- Collaborate with QA and Operational teams across Resolian to enhance quality standards, streamline processes, and drive operational efficiencies.
- Maintain strong and up-to-date knowledge of applicable regulations, standards, and industry guidance.
- Provide expert advice and interpretation of regulatory requirements.
- Support the maintenance and continual improvement of Quality Management Systems (QMS).
- Support external inspections, customer audits, and customer enquiries.
- Contribute to the delivery and improvement of training modules.
- Identify, propose, and drive continuous improvement initiatives.
- Support the internal self-inspection programme by performing process and facility audits.
- Assist with deviation and Quality Incident investigations.
- Participate in external sponsor audits, ensuring feedback is captured and fed into process improvements.
- Build and maintain effective working relationships with suppliers, acting as a key point of contact for external communications.
Reasons to use Rodeo
Start with a chat, not a search bar
Grad scheme, placement, apprenticeship? Not sure what you want yet — that's fine. Your agent talks it through with you and turns "I have no idea" into a shortlist.
It searches the market for you
Every day your agent scans the market matching roles against what actually matters to you, not just keywords on a CV.
Only hits
No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.
Skills, Education & Qualifications
- Strong knowledge and understanding of working within a GCP/GLP regulated environment.
- Demonstrable audit skills that can be practically applied to auditing activities as a sole auditor or as part of a team.
- Experience of establishing audit scope and developing relevant audit schedules and checklists.
- An understanding of the function of the QMS and actively supporting QMS systems such as Deviations, Change Control and CAPA.
- Able to demonstrate strong customer (internal and external) and regulator interaction skills.
- Experience working within the pharmaceutical industry is preferable.
- Previous experience working in a bioanalytical laboratory is preferable but not essential.
Get help with your application
Your very own career expert that helps elevate your application to the next level.
Qualifications
- Minimum level of BSc in scientific field, recognised auditor certification, or equivalent industry experience.
Trusted by 25,000+ job seekers
“It took my CV and asked me questions relevant to understanding what kind of jobs to suggest for me. Suggestions were almost perfect. Jobs were exactly what I’ve been looking for.”
Jessica, London
Skills
GCP
GLP
Audit Skills
Quality Management Systems
Customer Interaction
Pharmaceutical Industry
Bioanalytical Laboratory
Regulatory Requirements
Continuous Improvement
Training Modules
Deviation Investigations
Process Audits
Facility Audits
Operational Efficiencies
Quality Standards
Location