Associate Director Quality Assurance (hybrid in Europe- onsite when needed for audits and inspections)
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Job Location:
Monthly Salary:
Posted on:
5 hours ago
Vacancies:
1 Vacancy
Job Summary
The Associate Director of Quality Assurance ensures continuous quality improvement through effective management and oversight of audits and inspections. Identifies and implements IT solutions and process efficiencies. Facilitates ongoing quality improvement measures through communication of audit & Inspection intelligence analytics reports and compliance guidance/training.
The Associate Director of Quality Assurance drives ongoing quality improvement initiatives by disseminating audit and inspection intelligence delivering comprehensive analytics reports and providing expert compliance guidance and training.
The Associate Director of Quality Assurance leads the audit and inspection hosting team.
As a leader the Associate Director of Quality Assurance cultivates a high-performing team fostering their development into subject matter experts through education mentorship and empowerment.
Role and Responsibilities
- Works with the Director of Quality Assurance to drive excellence and optimize audit and Inspection hosting.
- Participate in audits and inspections including document request provision front and back-room activities and follow-up of audit and inspection findings and completion of client questionnaires and RFP/RFI when needed.
- Drives ongoing quality improvement measures through communication of audit results and compliance guidance/training.
- Identifies and implements process improvements and efficiencies via IT solutions.
- Works with the Quality Assurance Manager to develop and train the hosting team in all activities associated with hosting.
- Works with the Quality Assurance Manager to continually develop and maintain training material for audit & Inspection attendees.
- Monitors and communicates trends seen in audits and Inspections to the Director of Quality Assurance.
- Works with the hosting team to develop and maintains an Inspection knowledge library.
- Proactively prepares the company and clients for regulatory inspections and audits
- Collaborates and guides operational personnel to ensure effective audit and Inspection attendance.
- Generates metrics on audits and Inspections for Global Quality Council Quality Leadership Senior Leadership and Management review purposes.
- Manages the electronic quality management system (EG-QMS) Audits module. Identifying process improvements and initiating these changes with the relevant IT SME to EG-QMS
- Fosters a culture of quality within the organisation as led by members of the Quality Leadership Team.
- Acts as a Subject Matter Expert and client point-of-contact for Quality including attendance at operational and quality governance meetings.
- Assists in the development maintenance and management of mechanisms that assure ongoing monitoring and compliance with all applicable laws and regulations including but not limited to EU GVP US FDA CFRs JMPA and ICH-E6.
- Manages the audit and inspection hosting team
- Conducts other ad hoc activities as requested by Director of Quality Assurance and/or VP of Quality.
Qualifications :
- A university degree in a healthcare discipline or equivalent scientific area
- Substantial experience in pharmaceutical/biotechnology pharmacovigilance with an in depth understanding of GVP/GCP-related Quality Management and Assurance
- Sound knowledge of international regulations related to Pharmacovigilance and Medical Information
- Significant experience of participating in audits and inspections
- Excellent communication and facilitation skills within a global organization
- Proactive and self-motivated
SPECIAL SKILLS
- Strong organizational and planning abilities
- Excellent problem-solving and decision-making skills
- Ability to lead mentor and develop teams
- Strong communication and interpersonal skills
- Attention to detail and commitment to high standards
- Ability to analyze data and prepare detailed reports
- Knowledge of quality management principles and practices
Additional Information :
We prioritize diversity equity and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds genders and ages can contribute and grow.
To succeed we must work together with a human first approach. Why because our people are our greatest strength leading to our continued success on improving the lives of those around us.
We offer:
Training and career development opportunities internally
Strong emphasis on personal and professional growth
Friendly supportive working environment
Opportunity to work with colleagues based all over the world with English as the company language
Our core values are key to how we operate and if you feel they resonate with you then PrimeVigilance could be a great company to join!
Quality
Integrity & Trust
Drive & Passion
Agility & Responsiveness
Belonging
Collaborative Partnerships
We look forward to welcoming your application.
Remote Work :
No
Employment Type :
Full-time
Key Skills
- Quality Assurance
- FDA Regulations
- ISO 9001
- Root cause Analysis
- Biotechnology
- Clinical Trials
- Quality Systems
- Food Processing
- Quality Control
- Quality Management
- cGMP
- HACCP
About Company
Ergomeds fast-growing services business includes an industry-leading suite of specialist pharmacovigilance solutions, integrated under the PrimeVigilance brand and a full range of high-quality clinical research and trial management services under the Ergomed Clinical Research brand. ... View more
