IT Quality Assurance Manager
Warszawa, Warsaw
Boost your career with us
Polpharma Biologics is a state-of-the-art biological R&D and manufacturing facility, one of the most modern in Europe. We have a fantastic, international team of experienced experts and dynamic young scientists with common goals and values. Biotechnology is our passion.
Together we develop medicines, offering a new hope to patients suffering from serious diseases. We create a passionate and friendly workplace environment. Join us!
Together we develop medicines, offering a new hope to patients suffering from serious diseases. We create a passionate and friendly workplace environment. Join us!
We are currently seeking a skilled and experienced IT Quality Assurance Manager to join our dynamic team. As an IT Quality Assurance Manager, you will be responsible for ensuring the quality of our software and technology systems. Your attention to detail, analytical mindset, and strong leadership skills will be essential in driving our quality assurance efforts and ensuring the delivery of high-quality services and products to our stakeholders. In addition to the previously mentioned responsibilities, the following topics will also be covered:
Your responsibilities
- Develop and implement a comprehensive quality assurance strategy for our IT department, including managing deviations, investigations, and CAPAs
- Establish and maintain quality standards and procedures for the development and operation of computerized systems
- Providing guidance and support in testing methodologies, tools, and best practices for computerized systems
- Collaborate with software development, project management, and business teams to improve and implement quality standards and procedures for computerized systems
- Conduct risk assessments and establish mitigation strategies to address potential quality issues and project risks related to computerized systems
- Monitor and track deviations, investigations, and CAPAs, ensuring timely resolution and providing accurate reporting to stakeholders
- Review and support project phase activities as defined in computerized system validation plans
- Support life cycle processes such as change control and document management for computerized systems
- Provide training to team members and stakeholders related to computerized systems quality, compliance, and data integrity
- Support audits and inspections in IT related topics
If you have
- 5 years of IT related experience in pharmaceutical industry in IT Quality Assurance or Computerized System Validation roles
- Experience in stakeholder management
- Experience in managing quality activities, including deviations, investigations, and CAPAs in the pharmaceutical industry
- Experience in implementing quality standards and procedures for the development and operation of computerized systems
- Familiarity with reviewing risk assessment in relation to computerized systems
- Knowledge of project phase activities and computerized system validation plans
- Understanding of life cycle processes such as change control and document management for computerized systems
We offer
- Private healthcare
- Life insurance
- Pension plan above national standards
- Relocation package
- Additional free day
- and more…
