Senior Manager of Quality Management

Posted 8 Days Ago
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Hiring Remotely in Kraków, Małopolskie
Remote
Senior level
Biotech • Pharmaceutical
The Role
The Senior Manager of Quality Management leads Quality Management teams, ensuring compliance with regulatory standards in Pharmacovigilance and Medical Information activities. Responsibilities include managing quality system activities, addressing non-conformities, maintaining oversight of controlled procedures, and ensuring training compliance effectively.
Summary Generated by Built In

Company Description

We are PrimeVigilance (part of Ergomed Group), a specialised mid-size pharmacovigilance service provider initially established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance. 

PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and becoming one of the global leaders in its fields. We cover all therapy areas including medical devices. 

We love investing in our staff by providing an excellent training and development platform. We value employee experience, well-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high-quality client service can be achieved. 

Come and join us in this exciting journey to make a positive impact in patient’s lives.

Job Description

The Senior Manager of Quality Management is responsible for leading one or more teams within Quality Management in line with global strategic objectives. The Senior Manager of Quality Management collaborates with global operational functions to ensure Pharmacovigilance and Medical Information activities are conducted in compliance with GVP regulations, the International Conference on Harmonization (ICH) and PrimeVigilance requirements. The Senior Manager of Quality Management leads, educates, mentors and develops the Quality Management function to ensure their competence and confidence in developing skills to become subject matter experts.

Role and Responsibilities

  • The Senior Manager of Quality Management has a managerial position responsible to ensure that assigned Quality Management System activities are managed in compliance with regulations and company policies and in accordance with any agreements.
  • The Senior Manager of Quality Management maintains oversight of one or more departments within the Quality Management function to ensure that the quality of PrimeVigilance’s Pharmacovigilance and Medical Information activities are in compliance with applicable regulatory requirements, and that its clients’ Sponsor and Marketing Authorisation Holder Obligations are fulfilled. This may include but is not limited to the following:
  • Deviations, non-conformities and issue management
    • Supporting PrimeVigilance operational departments in assessing, reporting and addressing deviations, non-conformities and issues within timelines mandated by PrimeVigilance procedures
    • Elevating serious and/or systemic issues with appropriate recommendations to Senior Leadership for immediate and long-term resolution
    • Trending deviation, issue and compliance assessment data for discussion and agreement of recommendations for risk mitigation
  • Controlled Procedures
    • Maintaining oversight of the status and quality of applicable PrimeVigilance controlled procedures
  • Training
    • Maintaining oversight of training compliance
    • Managing training relating to Quality Management responsibilities
  • Electronic Quality Management System
    • Oversight of assigned areas of the system and assisting in maintaining the system
    • Providing user administration and support
    • Managing and testing the Business Continuity Plan for the system
  • Change management of controlled systems
    • As required reviewing and assessing changes and upgrades to the system
  • Audits and Inspections

Supporting audits and inspections of PrimeVigilance as a Subject Matter Expert for the PrimeVigilance Quality Management department.

Qualifications

  • Life science graduate, pharmacy, nursing or other healthcare related qualification
  • Demonstrated line management experience
  • Extensive applicable pharmaceutical and/or biotech pharmacovigilance experience with a solid understanding of GVP-related Quality Management and Assurance
  • GxP Knowledge: In-depth knowledge of the applicable GxP regulations and ICH Guidelines.
  • Auditing Knowledge: Demonstrates advanced knowledge in the conduct and reporting of audits and the translation of findings into corrective actions plans that mitigate risks to the company, to safety and data integrity.
  • ASQ Certified Quality Auditor (CQA), ASQ Certified Manager of Quality/Organizational Excellence, SQA Registered Quality Assurance Professional or similar recognised professional status, Quality Management Systems Auditor/Lead Auditor (ISO 9001)
  • Negotiation Skills: Demonstrates proficiency in negotiation and conflict resolution.
  • Pharmacovigilance Development: Understands the phases, processes and techniques used to execute a Pharmacovigilance development program.
  • Product Knowledge: Understands the medical/therapeutic impact of products.
  • Scientific Knowledge: Possesses the necessary science education and knowledge to manage quality management and assurance oversight
  • Communication skills: Must communicate professionally, clearly, concisely and consistently to external and internal customers, both verbally and in writing. Must demonstrate professional presentation skills and deliver informative and balanced presentations and, when applicable, facilitate resolution of differing opinions.
  • Project Management: Must demonstrate proficiency in managing complex projects, delivering all expected deliverables in a timely manner, and proactively communicating changes in pre-established goals and deadlines.
  • Organizational skills: Must be able to prioritize work effectively to meet timelines.
  • Must be able to manage all tasks assigned and effectively deliver all expected deliverables in an organized and a timely manner and proactively communicate changes in pre-established goals and deadlines.

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. 

The Company
HQ: Raleigh, NC
535 Employees
On-site Workplace
Year Founded: 1997

What We Do

Founded in 1997, Ergomed is a global provider of high-quality services to the biopharmaceutical industry, spanning all phases of clinical trials, post-approval pharmacovigilance, and medical information. Ergomed’s fast-growing services business includes an industry-leading suite of specialist pharmacovigilance (PV) solutions, integrated under the PrimeVigilance brand, and Ergomed Clinical Research, a complete, global Phase I-IV clinical development and trial management services with a strong heritage in the development of drugs in rare diseases and oncology.

• 1,400+ highly qualified professionals
• Global full-service CRO
• 25+ years of experience
• Therapeutic specialization in oncology
• Strong expertise in rare disease trials
• Robust clinical safety system
• Choice of leading drug safety databases

Our key services include:
• Clinical Research Services
• Pharmacovigilance
• Medical Information
• Regulatory
• Medical Writing
• Site Management
• Study Physician Support
• Biostatistics
• Patient Study Support

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