Senior Quality Manager

il y a 2 semaines


Bruxelles, Région de Bruxelles, Belgique SciNova Temps plein

Direct message the job poster from SciNova

Director @ SciNova - Science knows no boundaries, and neither do we

SciNova have exclusively partnered with one of Belgium's most Biopharmaceutical organisations specialising in clinical stage vaccine development and rare diseases. My client is searching for a Senior Quality Manager to manage and oversee all contract manufacturing activities, take ownership of all MBR matters and operate as the most senior POC in Quality for the entire European organisation. They will also be fully responsible for overseeing all QM related activities and direct team leadership - This includes internal and external audits, GMP compliance, QMS upgrades, validation/verification, deviation inspections and so on.

If you are passionate about working with ground-breaking, life-saving drugs and possess a wealth of experience working with Biologics, Vaccines and/or ATMP's, please apply ASAP.

Role responsibilities:

  • Develop and implement quality management systems and processes to ensure compliance with cGMP and other regulatory requirements.
  • Establish and maintain quality metrics and key performance indicators to monitor and improve quality performance.
  • Oversee all external manufacturing activities at key European CDMO hubs.
  • Conduct internal and external audits to assess compliance with regulatory requirements and company standards.
  • Investigate and resolve quality issues and non-conformances, implementing corrective and preventive actions as necessary.
  • Collaborate with cross-functional teams to support product development, manufacturing, and commercialisation activities.

Role requirements:

  • Bachelor's Degree in a Scientific discipline (minimum).
  • 8+ years' experience (minimum) working in QM within the Biotech/Biopharmaceutical industry - Experience working with complex biological products is essential.
  • Strong knowledge of cGMP and GMP regulations is mandatory.
  • Experience managing CDMO/CMO's, alternatively, working directly for one.
  • Excellent communication, interpersonal, and problem-solving skills.
  • Experience conducting audits and interacting with regulatory agencies.
  • Ability to work effectively in a fast-paced, dynamic environment and manage multiple priorities simultaneously.
  • Fluency in English is essential.

What my client offers:

  • Competitive salary and performance-based bonuses.
  • Opportunities for professional growth and career advancement.
  • A supportive and collaborative work environment.
  • Autonomy and independence.

How to apply:

  • Send your CV to lauren.howes@scinovasearch.com or instantly apply via LinkedIn.
Seniority level
  • Mid-Senior level
Employment type
  • Full-time
Job function
  • Quality Assurance
Industries
  • Biotechnology Research and Pharmaceutical Manufacturing
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