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Job Description
Key responsibilities:
Serve as the primary QA contact for local R&D functions and IT regarding the implementation and validation of digital solutions and computerised systems.
Support digitalization by reviewing qualification and validation documents.
Provide expert guidance on policies and regulatory requirements in project teams.
Collaborate and communicate with stakeholders and global team members.
Conduct and manage audits for compliance with GLP and GCP regulations, specifically for clinical and preclinical studies.
Support during regulatory inspections and conduct supplier audits as required.
Develop and conduct training on compliance-related topics.
Qualifications & competences:
Bachelor’s or Master’s degree in Life Sciences, Information Technology, or a related field.
Minimum 3 years of experience in regulated GxP environment and QA auditing.
High affinity for digital solutions and technical knowledge of industry IT topics. Understanding of computerized systems validation and SDLC is a pro.
Mindset that demonstrates the confidence, resourcefulness and proactive acting.
Demonstrated ability to work as both a team player and independently.
Innovative problem-solving, critical thinking, compliance knowledge and high affinity for documentation requirements in regulated industry.
Benefits:
Flexible working hours (37.5 hours/week) and an attractive company pension scheme
Competitive salary package: 13 monthly salaries + holiday pay + target bonus
30 days holiday entitlement
Hybrid working model (up to 50 % remote)
Internal training and promotion opportunities
International co-operations
Training on the job
Contributing your own ideas to the process design
Insights into the development of veterinary medicinal products
Corporate benefits and free (electric) car parking
Good company canteen and a company health management program
Current Contingent Workers apply
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