Lead Quality Training - Gent, België - MindCapture
Beschrijving
LEAD QUALITY TRAINING
- Biotech
- GhentWHAT IS OFFERED
We reward you with competitive wages and offer a strong package with additional legal benefits such as meal vouchers, eco vouchers, high health insurance (DKV) and group insurance.
We provide personalised training to let you grow in the area of
- What you like to do
- What you are good at
- Where and how you want to have an impact
ABOUT THE COMPANY
MindCapture collabs with a global immunology company committed to improving the lives of people suffering from severe autoimmune diseases and cancer.
Together, we are looking to strengthen their internal quality management with a motivated and experienced Lead Quality Training.
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QMS Training Strategy: Develop and execute a global QMS training strategy for quality assurance and compliance, aligning with business goals and regulatory requirements.
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Program Development: Design and deliver engaging and effective training materials, courses, and workshops that cover GMP, quality systems, SOPs, and relevant regulations.
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Internal Staff Training: Train and educate internal staff members on GMP principles, QMS procedures, and quality compliance standards.
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Cross-functional Collaboration: Partner with various departments to understand their training needs and tailor programs that address specific quality-related challenges.
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Compliance Oversight: Monitor and stay up-to-date with evolving regulations and industry trends to ensure training materials and programs remain compliant and reflect best practices.
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Performance Evaluation: Implement mechanisms to assess the effectiveness of training initiatives, collecting feedback and metrics to continuously improve training outcomes.
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Team Leadership: Lead a team of training specialists, providing mentorship, guidance, and fostering a culture of continuous learning and development.
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Documentation: Maintain thorough and accurate records of training activities, ensuring documentation for compliance purposes.
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Stakeholder Communication: Regularly communicate training updates, achievements, and challenges to senior management and relevant stakeholders.
REQUIRED COMPETENCES & SKILLS
- Bachelor's or Master's degree in a relevant scientific field or equivalent experience.
- Minimum of 5 years of progressive experience in quality, SOP design and review and training staff.
- Deep understanding of GMP, quality systems, and regulatory guidelines within the context of drug development and manufacturing.
- Strong leadership skills with the ability to inspire and guide a team of training specialists.
- Excellent communication and interpersonal skills, capable of collaborating effectively with diverse crossfunctional teams.
- Proficiency in learning management systems and training development tools.
- Detailoriented mindset with exceptional organizational and problemsolving abilities.
- Adaptability to changing priorities and the capacity to thrive in a fastpaced, dynamic environment.
- Relevant certifications in quality assurance, training, or regulatory affairs are a plus.
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